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Meta_analysis

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Meta_analysis Powered By Docstoc
					Reg. HighReg. LowReg. Avg.gene
  -1000             -1000
    -500             -500
    -350             -350 IL-10
    -200             -200 beta-glucuronidase
    -200             -200 beta-glucuronidase
    -150             -150
    -100             -100 apo[a]
    -100             -100 cholesterol 7-alpha hydroxylase
    -100             -100 Ty2-917
    -100             -100
    -100             -100
     -70              -70 RALDH2
    -100      -20     -60 c-myc
     -60              -60 epididymal proenkephalin
     -50              -50
     -50              -50
     -74       -7     -41
     -40              -40 CPT-I
     -40              -40 Wnt5a
     -35              -35 BCL-6
     -35              -35 histone
     -30              -30 2Apro
     -30              -30 IL-1alpha
     -30              -30 L-14
     -50      -10     -30 phytochrome
     -43      -16     -30
     -25              -25
     -25              -25
     -30      -15     -23 H1
     -22              -22
     -30      -10     -20 FXIII
     -20              -20 OP-1
     -20              -20 Se-GPx1
     -20              -20
     -20              -20
     -20              -20
     -20              -20
     -20              -20
     -20              -20
     -30      -10     -20
     -19              -19 bcl-2
     -17      -15     -16 albumin
     -17      -15     -16 albumin
     -16              -16 SSG1
     -16              -16
     -15              -15 alphaMyHC
     -15              -15 alpha-subunit
     -15              -15 biglycan
     -15              -15 DHFR
     -20      -10     -15 estrogen-dependent
     -20      -10     -15 MK
  -15         -15   PBP
  -20   -10   -15   virus L
  -15         -15
  -15         -15
-12.5         -13   OPN
   -4   -22   -13   VDR
  -12         -12   beta-galactosidase
  -12         -12
  -11         -11
  -10         -10   ALPL steady-state
  -10         -10   CHK2
  -10         -10   Drosophila hsp70
  -10         -10   EGF receptor
  -10         -10   Fgf10
  -10         -10   fos
  -10         -10   FPPS
  -10         -10   GPD1
  -10         -10   hla
  -10         -10   hycA
  -10         -10   iNOS
  -10         -10   IRF-1
  -10         -10   mdr1
  -10         -10   NA-specific
  -10         -10   p53
  -10         -10   PDGF
  -10         -10   phy
  -12    -7   -10   RHAMM
  -10         -10   SWI4
  -10         -10   TGF-beta type II
  -10         -10   TIMP
  -10         -10   TNF
  -10         -10   toxin
  -10         -10   Type II procollagen
  -10         -10   UCP1
  -10         -10
  -10         -10
  -10         -10
  -10         -10
  -10         -10
  -10         -10
  -10         -10
  -10         -10
  -15    -3    -9   bcr/abl
  -10    -8    -9   EGF-R
   -9          -9   Fas ligand
  -10    -7    -9
  -10    -5    -8   ADA-specific
   -8          -8   BRCA1
  -10    -5    -8   fiber
   -8          -8   GLUT1
   -8          -8   IFN-gamma induced IAb
   -8          -8   involucrin
 -10    -5    -8   Mac-2
  -8          -8   macrophage I-A alpha
  -8          -8
  -8          -8
  -8          -8
 -10    -5    -8
  -7          -7   c-myc
 -10    -3    -7   c-myc
  -7          -7   inhibitor-1
  -7          -7   rac2
 -11    -3    -7   TFF
-6.5          -7   TPA
 -10    -3    -7   VEGF
  -7          -7
  -7          -7
  -6          -6   albumin
  -6          -6   c-fos
  -6          -6   estrogen receptor
  -6          -6   galanin
  -6          -6   IGF-I
  -6          -6   mdr-1
-7.7   -2.8   -6   ODC
  -6          -6   P450R
-5.8          -6   trk C
  -6          -6
  -6          -6
  -6          -6
  -6          -6
  -6          -6
-5.5          -6
  -7    -5    -6
  -8    -4    -6
-4.2          -5   24-hydroxylase
  -5          -5   24-OHase
  -5    -4    -5   adipsin
  -5          -5   albumin
  -5    -4    -5   alpha 1I3
  -5          -5   AR
  -5          -5   BBEC PAI-1
  -5          -5   c-myc
  -5          -5   collagen alpha 1(III)
  -5          -5   CSP
  -5          -5   EF-1
  -5          -5   fliC
  -5          -5   HS-P LRP
  -5          -5   I-24-OHase
  -5          -5   IGF-binding protein-5 (IGFBP-5)
  -5          -5   IGFBP-2
-4.4          -5   IGFBP-5
  -5          -5   IGF-I
  -5          -5   IGFII
  -5          -5   metallothionein
  -5          -5   mP2
  -5          -5   NHE-1
-4.5          -5   PAM
  -5          -5   PEPCK
  -5          -5   PSA
  -5          -5   S5
  -5          -5   synthase
  -5          -5   TGF-beta 1
  -5          -5   topoisomerase II
  -5          -5   type II collagen
  -5          -5   VEGF
  -6    -4    -5   ZnT1
  -5          -5
  -5          -5
  -5          -5
  -5          -5
  -5          -5
  -5          -5
-4.6          -5
  -5    -4    -5
  -5    -4    -5
  -4          -4   aggrecan
  -4          -4   alpha 1I3
  -4          -4   alpha 2(V)
  -6    -2    -4   alpha actin
  -4          -4   Apo B
-3.6          -4   ApoA1
  -4          -4   apoA-IV
  -4          -4   AR
  -4          -4   AT(1)R
  -4          -4   bcl-X(L)
-3.4          -4   BDNF
-3.6          -4   calcitonin
  -4    -3    -4   ERG3
  -4          -4   ET(B) receptor
  -4          -4   hAR
  -4          -4   IRF-1
  -4          -4   M-CSF
  -4          -4   mdr1
  -4          -4   Mramp/y39
  -4          -4   myostatin
-3.8   -3.4   -4   NT-3
  -4          -4   P-450c11AS
-3.3          -4   PMCA1b
  -4          -4   POMC
  -4          -4   pp63
  -4          -4   reg
  -5    -3    -4   Star
  -4          -4
  -4          -4
  -4          -4
  -4          -4
  -5     -3   -4
  -5   -1.5   -4
  -3          -3   5alphaR1
-2.5          -3   alk4-1
  -3          -3   amastin
  -3          -3   antithrombin
  -3          -3   antral somatostatin
-2.3          -3   apoA-I
  -3          -3   AT2
  -3          -3   AVP
  -3          -3   beta-globin
  -3    -2    -3   CD13/APN
  -3          -3   Col1A1
  -3          -3   collagen I
-2.9          -3   cortical COX-2
-2.7          -3   cortical NaSi-1
-2.2          -3   cortical NaSi-1
-2.7          -3   COX-2
  -3          -3   DSC1
  -3          -3   EGF receptor
  -3          -3   FBP
  -3          -3   fibronectin
  -3          -3   Fibronectin
  -3          -3   fixBCX
  -3    -2    -3   gamma-zein
  -3          -3   GAP43
  -3          -3   GAP-43
  -3          -3   glomerular iNOS
-2.5          -3   GnT-I
  -3          -3   HSC70
  -3          -3   Insl3
  -3          -3   LNGFR
-2.5          -3   MMP-9
  -3          -3   mP2
  -4    -2    -3   P-450 2c
-2.4          -3   P-450f
  -3    -2    -3   PATR
  -3          -3   PGHS-2
  -3          -3   PKAc
  -3          -3   POMC
  -3          -3   PRL
  -3          -3   procollagen
  -3          -3   ribosomal S2
-2.5          -3   topoisomerase II alpha
-2.5          -3   topoisomerase IIalpha
  -3          -3   TPA
  -3          -3   t-PA
  -3   -1.5   -3   uidA
  -3          -3   VLDLR
  -3          -3   XD
  -3          -3
-2.6          -3
  -3          -3
  -3          -3
  -3          -3
  -3          -3
  -3          -3
  -3          -3
  -3          -3
  -3          -3
  -3          -3
  -3          -3
  -3          -3
  -3          -3
  -3          -3
  -3    -2    -3
-2.5          -3
-2.5          -3
-3.6   -1.2   -3
  -2          -2   Ad2+ND5-specific
  -2          -2   adipsin
  -2          -2   apoA-I
  -2          -2   apoAIV
  -2          -2   ASF/SF2
  -2          -2   beta 3-AR
  -2          -2   beta-CGRP
  -2          -2   beta-globin
-1.8          -2   BNP
-1.9          -2   cardiac alpha-actin
  -2          -2   c-myc
  -2          -2   COL1A1
  -2          -2   CPA1
  -2          -2   DHFR
  -2          -2   E1A
  -2          -2   ecNOS
  -2          -2   GHR
  -2          -2   glucoamylase specific
  -2          -2   glucokinase
  -2          -2   HCR
  -2          -2   hsp90
  -2          -2   IGFBP-6
-1.7          -2   IGF-I
-1.5          -2   IL-1 beta
  -2          -2   insulin
  -2          -2   insulin receptor
  -2          -2   insulin receptor substrate-1
  -2          -2   kallikrein
  -2          -2   Kv4 subfamily
  -2          -2   lacZ
  -2          -2   leukotoxin
  -2          -2   L-PGDS
  -2          -2   MMP-9
  -2          -2   PGDH/GAPDH
  -2          -2   RBP
   -2          -2   renin
   -2          -2   rPLII
   -2          -2   SPO13
   -2          -2   SRB1/PSA1
   -2          -2   talin
   -2          -2   TGF-beta 1
 -1.7          -2   topoisomerase II
   -2          -2   topoisomerase II alpha
   -2   -1.5   -2   TPA
   -2          -2   UCP2
   -2          -2
   -2          -2
   -2          -2
   -2          -2
   -2          -2
   -2          -2
   -2          -2
   -2          -2
   -2          -2
   -2          -2
   -2          -2
   -2          -2
   -2          -2
   -2          -2
 -0.1          -1   D2
-0.41          -1   thrombospondin-1
  0.4           0   GFAP
  0.5           0   GFAP
  0.5           0
  1.9           1   4.8-kb TGF-alpha
  1.8           1   ABCA1
  1.5           1   alpha
  1.7           1   alpha subunit
  1.6           1   alpha1a-AR
  1.7           1   alpha2,8-sialyltransferase III
  1.8           1   angiotensinogen
  1.8           1   angiotensinogen
  1.6           1   angiotensinogen
  1.8           1   ApoB-100
  1.5   1.4     1   apoC-III
  1.6   1.6     1   APP
    1           1   AR
  1.3           1   AR
    2   1.7     1   Bcl-2
  1.5           1   beta-globin
  2.6   1.1     1   beta-PPT
  1.5           1   bFGF
  1.8           1   BMP-2
  1.5           1   C/EBP beta-mediated
  1.6           1   Ca(2+)-ATPase
  1.9           1   cACT
  1.8           1   CD40L
 1.8         1   c-fos
 1.2         1   citrate synthase
 1.8         1   c-jun
 1.6         1   CK-M
 1.8         1   c-myc
 1.8         1   cortical EP3 receptor
 1.6         1   CYP2B1/2
 1.7   1.4   1   CYP4A8
 1.5         1   DBH
 1.2         1   DHPR
1.24         1   enoyl-CoA hydratase (ECH)
 1.4         1   ER
 1.5         1   ER
 1.7         1   ERalpha
 1.5         1   fatty acid binding protein
 1.3         1   fibronectin
 1.5         1   FMRFamide
 1.4         1   FN
 1.5         1   FSH beta
 1.5         1   GALP
 1.6   1.3   1   gamma-GCS
 1.4         1   GFAP
 1.8         1   GHR
 1.9         1   ghrelin
 1.6         1   glomerular TGF-beta
 1.5         1   GLUT4
 1.5         1   GRalpha
 1.5         1   H4
 1.3         1   H4 histone
 1.8         1   HCN4
 1.8         1   HDAC1
 2.5   1.4   1   HL
 1.6         1   HO-1
 1.9         1   IAPP
 1.8         1   ICAM-1
 1.8         1   ICAM-1
 1.6         1   IGFBP-2
 2.2   1.7   1   IGF-I receptor
 1.4         1   IL-1alpha
 1.9         1   IL-1Ra
 1.9         1   IL-6
 1.5         1   ileum apo A-IV
 1.7         1   laminin
 1.3         1   LCAT
 1.5         1   LCAT
 1.5         1   LDL-receptor
 1.6         1   lipase
 1.2   2.6   1   MCP-1
 1.8         1   MCP-1
 1.2         1   m-CSF
 1.4         1   MDR1
 1.7         1   MMP2
 1.3         1   MMP-9
 1.8         1   MRP1
 1.5         1   MRP3
 1.5         1   Na-K-ATPase beta1-subunit
 1.3         1   NaPi-2
 1.9         1   NE
 1.7         1   NGF
 1.5         1   NHE-1
 1.5         1   NHE2 and NHE3
 1.8         1   NPT2
 1.5         1   NPY
 1.9         1   O6-AGT
1.75   1.2   1   ob
 1.8         1   ODC
 1.9         1   osteocalcin
 1.5         1   OT
 1.5         1   p21WAF1/CIP1
1.75         1   P450C21
 1.4         1   P450scc
   1         1   PAI-1
 1.9         1   PCNA
 1.6         1   PGHS-1
 1.4         1   PGHS-2
 1.7         1   PGIS
 1.8         1   PPE
   2   1.5   1   PPE
 1.5         1   preproET-1
   1         1   proenkephalin
 1.9         1   PSA
 1.5         1   rabCyP18
 1.9         1   rap1a
 1.5         1   ras
 1.9         1   RB
 1.4         1   renin
 1.5         1   renin
 1.8         1   rGSTA1/A2
 1.9         1   RhoA
 1.9         1   RhoA
   2   1.5   1   rpoB
 1.8         1   sgk1
 1.5         1   SP-A SP-B
 1.5         1   TGF-alpha
1.66         1   TGF-beta 1
 1.7         1   TIMP-3
 1.5         1   transferrin receptor
 1.9         1   transforming growth factor-beta1
 1.8         1   transin
 1.4         1   type I procollagen
 1.8         1   tyrosinase
 1.5         1   UVA-induced HO-1
 1.5         1   uvi15(+)
 1.8         1   uvi15(+)
1.85         1   vasopressin
 1.8         1   VEGF
 1.2         1   VP
 1.6         1   VP
1.85         1   VP
 1.8         1   VPF
1.25         1
 1.2         1
   2   1.5   1
 1.5         1
 1.7         1
 1.5         1
 1.5         1
 1.6         1
 1.6         1
 1.6         1
 1.6         1
 1.7         1
 1.7         1
 1.7         1
 1.8         1
 1.9         1
   2   1.5   1
   2         2   3 beta HSD
 2.5         2   5-LO
   2         2   92-kDa
 2.7         2   A3AR
   2         2   ABP
 2.8         2   ACE
   3    2    2   ACLP
   2         2   ACP-22
 2.3         2   ACS
   2         2   ACTH-R
   2         2   actin
   2         2   ADH
   2         2   ADH5
 2.2         2   ADM
   2         2   ADM
   2         2   adrenalectomized rat lung GS
 2.1         2   Adx
   2         2   Agrp
   2         2   ALAS
   2         2   alpha
   2         2   Alpha
 2.5         2   alpha
 2.3         2   alpha 1
   2         2   alpha 1(II)
   2         2   alpha 1PI
   2         2   alpha-casein
   2         2   alpha-subunit
   2         2   alpha-subunit
 2.5         2   androgen receptor
  2         2   Angiotensin type 1
2.4         2   angiotensinogen
  2         2   angiotensinogen
2.7         2   angiotensinogen
  2         2   ANP
2.7         2   ANP
  3    2    2   APLP2
  2         2   apo A-I
  3    2    2   apo A-I
2.3         2   apo A-I
2.5         2   ApoA1
  2         2   apoA-IV
  2         2   apoB
  2         2   apoC-III
  2         2   apoE
  2         2   apoE
  2         2   apolipoprotein A-I (apoA-I)
2.3   2.3   2   APP
  2         2   APP-751 mRNA/APP-695
1.8   2.2   2   AQP2
  2         2   AR
  2         2   argininosuccinate synthetase
2.4         2   aromatase
2.5         2   AT(1)
  2         2   AT(1A)
  2         2   AT1
2.3         2   AT1
  2         2   AT2 receptor
  2         2   A-utrophin
2.2         2   AVP
2.6         2   BACE-2
2.1         2   Bcl-2
  2         2   Bcl-XL
  2         2   BDNF
  3    2    2   beta
  2         2   beta 1
  2         2   beta 1
  2         2   beta 2AR
2.3         2   beta 3-AR
  2         2   beta 3-AR
  2         2   beta 3-AR
  2         2   beta actin
  2         2   beta APP
2.5         2   beta G-GA
  2         2   beta glycan
  2         2   beta1-AR
  2         2   betaA
2.3         2   beta-actin
2.3         2   beta-actin
2.5         2   beta-actin
  2         2   beta-myosin heavy chain
  2         2   beta-pol
  2       2   bFGF
  2       2   bFGF
2.5       2   bFGF
  3   2   2   bFGF and NGF
  3   2   2   bFGF and NGF
  2       2   bGH
  2       2   BGP
  3   2   2   BMP-2
2.2       2   BNP
  2       2   BSP
  2       2   C/EBP alpha
  2       2   C/EBP alpha
2.7       2   C4BP
  2       2   CaBP
2.5       2   calbindin protein and
2.6       2   calcitonin
  2       2   calmodulin-specific
  2       2   CASR
2.4       2   catalase
  2       2   cathepsin L
2.6       2   cAT-III
  2       2   CCTalpha
  2       2   CEH/HSL
  2       2   ceruloplasmin
  2       2   c-fos
  2       2   c-fos
2.5       2   C-fos
  2       2   CGRP
  2       2   cholesterol esterase
  2       2   c-jun
2.4       2   c-jun
  2       2   c-jun
2.5       2   c-jun
2.2       2   CK-B
  2       2   c-met
  2       2   c-myc
2.1       2   c-myc
  2       2   c-myc
  2       2   CNTF
  3   2   2   collagen
  2       2   collagen
  2       2   collagen IV
2.3       2   collagen IV
2.1       2   Connexin43
2.6       2   cortex CRH
  2       2   cortical IGFBP-1
  2       2   COT1
  2       2   Cox-2
  2       2   COX-2
  2       2   Cox-2
  2       2   COX-2
  2       2   CPT
2.3         2   CPT I
  2         2   CPT I
  2         2   CRABP-II
2.3         2   CRBP
2.5         2   CRBP-I
2.1         2   CRF
2.5         2   CRF
  2         2   CRH
  2         2   CRP reporter
  2         2   c-ski
  2         2   c-src
  2         2   CT
  2         2   CT
  2         2   CTGF
2.8         2   Cyclin D1
2.7         2   cyclin E
2.5         2   CYP2J4
  2         2   CYP3A7
2.7         2   Cyp4a14
  2         2   CYP7A1
  2         2   D2
2.6         2   D2
  2         2   decorin
2.2         2   decorin
2.7         2   desaturase
2.2         2   DHP receptor
  2         2   DMP1
2.5         2   DNase I
  2         2   dopamine D2-receptor (D2-R)
2.4         2   duodenal CCK
  2         2   dynorphin
  2         2   dynorphin
2.7         2   EC PAI-1
  2         2   E-Cad
2.2         2   ecNOS
  2         2   ecNOS
  2         2   EGF
  2         2   EGF
  2         2   EGFR
  3     2   2   EGF-R
  2   3.5   2   elastin
  2         2   endoglin
2.5         2   endothelin B
  3    2    2   ENK
  3    2    2   eNOS
  2         2   eNOS
2.8         2   eNOS
2.8         2   eNOS
  2         2   EPCR
2.2         2   epicardial ANP
2.1         2   Epiregulin
  2         2   ER
2.5       2   ER
2.7       2   ET(A)-receptor
  2       2   ET(B) receptor
  2       2   ET-1
  2       2   ET-1
2.3       2   ET-1
  2       2   ET-1
2.5       2   ET-1
  2       2   ETA receptor
  2       2   ETB receptor
  2       2   F1/GAP-43
2.5       2   FAS
2.5       2   Fc gamma RII
  2       2   Fd-dependent glutamate synthase
2.5       2   ferritin heavy chain
  2       2   FGF-2
  2       2   Fibronectin
  2       2   fibronectin
2.6       2   fibronectin
  2       2   follistatin
2.7       2   follistatin
  2       2   FSH beta
2.7       2   FSH beta
2.8       2   FSH beta
  2       2   FSH-beta
2.3       2   G gamma
  2       2   G6Pase
  2       2   GAD67
  2       2   galanin
  2       2   galanin
  2       2   gamma
  2       2   gamma/gamma + beta
2.5       2   gamma-actin
  2       2   gamma-globin
  2       2   gamma-globin
  2       2   GAP-43
  2       2   GAPDH
2.5       2   GAPDH
2.1       2   GCR
2.7       2   GCS
  2       2   gec1
2.1       2   GH
2.3       2   GH
2.5   2   2   GH
2.5       2   GH
2.5       2   GH receptor
2.5       2   GHF-1
  2       2   GH-rec
2.3       2   Gi alpha(2)
2.9       2   Gi2 alpha
  2       2   GIP
  2       2   GLCLC
   2         2   globin
   2         2   Glu-6-Pase
 2.5   2.7   2   glucagon
   2         2   glucagon receptor
   2         2   glucocorticoid receptor
   2         2   glucokinase
 2.5         2   glucose-6-phosphatase
   2         2   GLUT1
 2.1         2   GLUT1
 2.2         2   GLUT1
   2         2   GLUT1
 2.4         2   GLUT1/actin
 2.3   1.7   2   GLUT2
   3     2   2   GLUT2
   2         2   GLUT2
 2.5         2   GLUT2
   2         2   GLUT4
   2         2   GLUT4
   2         2   GLUT4
   2         2   GLUT4
   2         2   GLUT4
 2.1         2   GLUT4
 3.5    2    2   GLUT5
   2         2   glutaminase
   2         2   glutaminase
   3    2    2   GLVR-2
   2         2   GnRH receptor
   2         2   GnRH receptor
   2         2   GnRH receptor
 2.7         2   GnRH receptor
   2         2   gp130
   2         2   GRbeta
   2         2   GS
 2.3         2   GS
 2.7         2   Gs alpha
   2         2   GST
 2.5         2   GT
   2         2   H
   3    2    2   Has2
   2         2   HAS3
   2         2   HBV
   3    2    2   hCG
   2         2   hCRH
   2         2   HHC289
 2.1         2   HIF-1alpha
   2         2   histone
   2         2   HKII
2.26         2   HKII
 2.7         2   HKII
 2.7         2   HO isozyme
 2.6         2   HO-1
 2.7         2   HO-2
2.5         2   HOXA5
2.3         2   hREN
  2         2   HSL
2.7         2   hsp10
  2         2   Hsp23
  2         2   HSP27
2.5         2   HSP27
  2         2   hsp60
2.3         2   HSP70
  3    2    2   hsp70
  2         2   HSP70
  2         2   hsp70c
  2         2   hTERT
2.3         2   IAPP
2.7   2.4   2   IAPP
  2         2   iBAT
2.5         2   ICE
  2         2   ICER
2.8         2   IGF I
  2         2   IGF-binding protein-2 (IGFBP-2)
  3    2    2   IGFBP-1
  2         2   IGFBP-1
2.5         2   IGFBP-1
2.7         2   IGFBP-1
2.8         2   IGFBP-1
  2         2   IGFBP-3
  3    2    2   IGFBP-3
  2         2   IGFBP-5
  2         2   IGFBP-5
  2         2   IGF-I
  2         2   IGF-I
  2         2   IGF-I
  2         2   IGF-I
2.4         2   IGF-I
  2         2   IGF-I
  2         2   IGF-I receptor (IGF-IR)
2.1         2   IGF-I receptor (IGF-IR)
  2         2   IGF-IR
  2         2   IGFR-I
  2         2   IL-1 beta
  2         2   IL-15
  2         2   IL-18
2.5         2   IL-1ra
  2         2   IL-6
  2         2   IL-6
2.1         2   IL-6R
2.5         2   IL-8
2.8         2   IL-8
  2         2   ileum mucosal IGF-I
  2         2   inhibin alpha-subunit
2.5         2   inhibin-alpha
  2         2   insulin
  2         2   insulin
2.5         2   junD
  2         2   Kv1.5
  2         2   L
  2         2   lactate dehydrogenase
  2         2   lactate dehydrogenase
  2         2   LAMP-1
  2         2   larger VEGF
3.3   1.8   2   LCB2
  2         2   LDL-receptor
2.5         2   LDL-receptor
  2         2   L-FABPc
  2         2   lipoprotein lipase
  2         2   LNGFR
  3    2    2   LO
  3    2    2   LPL
  2         2   LPL
2.3         2   L-PRLR
2.2         2   LT-beta
  2         2   MAT2A
2.5    2    2   MCAD and mMDH
  2         2   m-calpain
  2   2.9   2   MCAM
  2         2   MCP-1-to-glyceraldehyde-3-phosphate dehydrogenase
2.5         2   M-CPT-I (muscle-type CPT-I)
  2         2   mdr1
  2         2   metallothionein
2.5         2   metallothionein
  2         2   mHS
  2         2   MIF
  2         2   MME
  2         2   MnSOD
  2         2   mPPAR gamma
2.5         2   MT
2.5   1.8   2   MTase
  2         2   MUC2
  2         2   mucin
2.5         2   murine C4BP
  2         2   Mx
  2         2   Na(+)-Ca2+ exchanger
  3    2    2   Na-channel
2.4         2   NAIP
2.2         2   NaPi-2
  3    1    2   natriuretic peptide (ANP)
  2         2   NCX
  3   1.5   2   NF-H
  2         2   NFIL-6
  2         2   NGF
  2         2   NGF
  3    2    2   NGF
2.7         2   NGFI-B
  2         2   NHE3
  2       2   NHE3
  2       2   NHE3
  2       2   NK2-receptor
2.5   2   2   Nm23-R1
  2       2   NPFF
  2       2   NPY
  2       2   NPY
  3   2   2   NPY
  2       2   NPY
2.7       2   NPY
  2       2   Nramp1
  2       2   Ntcp
2.5       2   ob
  2       2   OB NPY
  2       2   occludin
  2       2   OPM-2 GR
2.4       2   OPN
  2       2   OPN
2.2       2   osteocalcin
2.6       2   Osteocalcin
  2       2   OT
  2   3   2   OT
  2       2   OT
  2       2   OTR
2.5       2   OTR
2.5       2   oxide synthase
  2       2   p100
  2       2   p100
  2       2   p21(WAF1/CIP1)
  2       2   p21WAF1/CIP1
2.8       2   P2Y(2)
2.7       2   P2Y2-receptor
2.7       2   p36
  2       2   P450 3A
  2       2   P450IA1
  2       2   P-450sc
  2       2   P450scc
2.9       2   P-450scc
  2       2   p46
  2       2   p53
  2       2   p53
  2       2   p85alphaPI 3-K
  2       2   PAF receptor
2.5       2   PAH
  2       2   PAI-1
  2       2   PAI-1
  2       2   PAI-1
  2       2   PAI-1
  2       2   PAI-1
  2       2   PAI-1 antigen and
  2       2   pancreatic GLUT-2
  2       2   Pancreatic PC1 and PC2
  2         2   PAR-1
  2         2   PAR-1
2.5         2   PCK
2.2         2   PDGF
  2         2   PDGF
  3    2    2   PDGF B
2.5         2   PDGF-B
2.6         2   PDGF-B steady state
2.5         2   PDGF-specific
2.5         2   PDI
  2         2   PE
  2         2   PEPCK
  3    2    2   PEPCK
  2         2   PEPCK
  2         2   perlecan
2.5         2   pGFAP-MT-I
2.5         2   phospholamban
2.7         2   pIgR
  2         2   Pit2 receptor
  2         2   PKC-delta
  3    2    2   pmAAT
  2         2   PNMT
2.3         2   PNMT
  3    2    2   polyUb
  3    2    2   polyUb
  2         2   POMC
  2         2   POMC
  3    2    2   POMC
2.5         2   POMC
3.3   1.6   2   PPE
2.4         2   PPT
  2         2   preapo-C-III
  2         2   preapolipoprotein AiV
  2         2   Pref-1
  2         2   preproET-1
  2         2   PreproET-1
2.3         2   preproinsulin
  2         2   preprolactin
  2         2   preproNPY
  3    2    2   preproNPY
  2         2   preprotachykinin A
  2         2   PRL
  2         2   PRL
2.6         2   PRL
  2         2   PRLR
  2         2   PRLR
2.3         2   PRLR
2.5         2   PRL-R(L)
2.5         2   pro alpha1(I) collagen
  2         2   pro-alpha 1(I) collagen
  2         2   procollagen production and
  2         2   ProEnk A
  2         2   ProEnk A
2.4         2   proinsulin
  2         2   proTRH
  2         2   proTRH
2.5   1.5   2   PrP
2.4         2   pS2
  3    2    2   psbA2
2.3         2   PSP1
  2         2   PTG
  2         2   PTH/PTHrp receptor
  2         2   PTH/PTHrp receptor
  2         2   PTH/PTHrP receptor
  2         2   PTHrP
  2         2   PTHrP
  2         2   PTP1
  2         2   RAR alpha
  2         2   RARbeta
  2         2   RAR-gamma
2.5         2   rbcL
  2         2   RC3
  2         2   Renal renin
  2         2   renin
2.3         2   renin
  2         2   renin
  2         2   RERG
2.4         2   resistin
2.6         2   Resistin
  2         2   RFC
  3    2    2   RGS2
  3    2    2   RGS4
  2         2   ribosomal protein
  2         2   RNA
  2         2   rPLI
  2         2   SCD1
2.9         2   SGP-2
  3   1.8   2   SNAP-25
  2         2   somatostatin
3.5    2    2   SP-22
2.7         2   SP-A
2.4         2   SPARC
2.7         2   SPARC
  2         2   SP-B
  2         2   SP-C
  3    2    2   SP-C
  2         2   SP-encoding PPT
2.5         2   SPR
  3    2    2   SR-BI
  3    2    2   ST6Gal I
  2         2   StAR
  2         2   stored beta-F1-ATPase
  2         2   syndecan-4
  2         2   synthesis and its
  2         2   TAFI
  2         2   TbetaRII
  2         2   TF
  2         2   TfR
  3    2    2   TfR
  2         2   TGF-alpha
  2         2   TGF-alpha
  2         2   TGF-alpha
  2         2   TGF-alpha
  3    2    2   TGF-alpha
  2         2   TGFB1
2.5         2   TGF-beta
  2         2   TGF-beta 1
  2         2   TGF-beta 1
  2         2   TGF-beta 1
  2         2   TGF-beta 1
  2         2   TGF-beta 1
  2         2   TGF-beta 1
  2         2   TGF-beta 1
  2         2   TGF-beta 1
  2         2   TGF-beta 1
2.5         2   TGF-beta 1
  2         2   TGF-beta 2
  2         2   TH
  2         2   TH
  2         2   TH
  3    2    2   TH
2.5         2   thrombin receptor
  2         2   Thyroglobulin
  2         2   thyroglobulin
  2         2   thyroparathyroid PTH
  3    2    2   tigA
  2         2   Tim23
2.7         2   Tim23
2.9         2   TIMP
  2         2   TIMP-1
  2         2   TNF-alpha
2.2         2   TNF-alpha
2.2         2   topoIIalpha
  3   1.5   2   topoIIalpha
  2         2   tPA
  2         2   tPA
  2         2   tPA
2.5         2   TPA
  2         2   TR beta-2
  2         2   transferrin
  3    2    2   transferrin receptor
2.7         2   TrkA
  3    2    2   trkB
  2         2   TSH receptor
2.2         2   tubulin
2.9         2   type IIx MyoHC
  2         2   ubiquitin
  3    2    2   UCP
  2         2   UCP2
  2         2   UCP2
2.5    2    2   UCP2
2.5    2    2   UCP3
  3    2    2   UCP3
  2         2   UCP3
  3    2    2   UOxase
  2         2   uterine IGF-I
2.5         2   utrophin
  2         2   VDR
2.7   1.8   2   VDR
2.5         2   VDR
  2         2   VEGF
  2         2   VEGF
  2         2   VEGF
  2         2   VEGF
  2         2   VEGF
2.4         2   VEGF
2.5         2   VEGF
2.2         2   VEGF-C
  2         2   VIM
2.6         2   VLDLR
  2         2   VP
2.3         2   XVI collagen
2.6         2   Y1R
  2         2   zif-268
3.5   0.5   2
  2         2
  3    2    2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  3    2    2
  2         2
  2         2
2.4         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  3    2    2
  3    2    2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
2.2         2
2.9   1.5   2
  3     2   2
  3     2   2
  3     2   2
  3     2   2
  3     2   2
  3     2   2
   3     2   2
   3     2   2
 3.4   1.8   2
2.75         2
 2.7         2
 2.5         2
 2.5         2
 2.5         2
 2.5         2
 2.5         2
 2.5         2
 2.5         2
 2.5         2
2.51         2
 2.6   3.1   2
 2.6         2
 2.6         2
 2.8         2
 2.8         2
   3   2.5   2
   5     2   3   (prepro)insulin
   3         3   12-LO
   3         3   24-hydroxylase
   3         3   24-hydroxylase
   3         3   3 beta-HSD
   3         3   52-kDa SS-A/Ro
   3         3   ABP
   4    2    3   ACTH-R
   4    3    3   adhesion molecule-1
   3         3   ADNP
   3         3   adrenalectomized rat lung GS
   4    3    3   ahp
   3         3   ALAS2
   3         3   alkaline phosphatase
   4    2    3   alpha
   3         3   alpha 1
   3         3   alpha 1(I) procollagen
   3         3   alpha 2
   3         3   Alpha 5
   3         3   alpha rENaC
   3         3   alpha-1
   3         3   alpha1a-AR
 5.5   1.3   3   alpha2-Laminin
   4     3   3   alpha-MHC
   3         3   alpha-subunit
   4    3    3   ANF
 3.5         3   angiotensinogen
   3         3   ApoA-I
   3         3   apoE
   3         3   APP
   3         3   Aquaporin-1
 3.5         3   arginase
  3         3   ATB(0)
  3         3   atrial natriuretic factor
  3         3   AVP
  4    3    3   Bag-1
  3         3   bax
  3         3   B-CK
  4    2    3   BDNF
  3         3   BDNF
3.7         3   BDNF
  3         3   beta 2AR
  4    3    3   beta 2AR
  3         3   beta-actin
3.5         3   beta-APP
  3         3   beta-globin
  3         3   beta-tubulin
  3         3   bFGF
  3         3   bFGF
  3         3   bFGF
3.5         3   bFGF
3.6         3   BNP
  3         3   C/EBP alpha
3.5         3   calbindin-D28k
  3         3   calcitonin-related peptide
  4    3    3   Carbonyl reductase
  3         3   cardiac ACE
  3         3   cardiac ANP
  3         3   cardiac AT1
  3         3   caspase-1
  3         3   catalase
3.7         3   cathepsin B
  4    3    3   CCTalpha
  4    3    3   CCTbeta
  3         3   CD23
  3         3   CEA
  4    3    3   CETP
  4    3    3   CFI
  3         3   c-fos
  3         3   c-fos
  3         3   c-jun
  3         3   c-jun
  3         3   c-jun
3.5         3   c-Jun
3.2         3   CK 20
3.5   2.5   3   CKB
  3         3   CK-B
  3         3   clusterin
3.6         3   cMoat
  4    3    3   c-myb
  5    2    3   c-myc
  3         3   c-myc
  3         3   c-myc
  3         3   c-myc
3.2         3   c-myc
  3         3   cNOS
3.5    3    3   COL1A2
  3         3   collagen I
  3         3   collagen type II
  3         3   COX-2
  4    2    3   Cp
  3         3   CPS
  3         3   CPT
3.5         3   CRF
  3         3   CRH
  3         3   CSF-1 receptor (CSF-1r)
  4    3    3   CT
  3         3   CTH2
  3         3   Cx43
  3         3   cyclin D1
  3         3   cydAB
3.3         3   CYO-II
  3    4    3   CYP2A1
3.3         3   CYP2E1
  3         3   CYP3A4
  3         3   cytidyltransferase
  4   3.5   3   delta protein
3.8         3   depolarization-activated NF-kappaB-dependent
  3         3   DHCR
  3         3   DHFR
  3         3   DOR
  3         3   DPPIV
  3         3   EC
  3         3   E-Cad
  3         3   ECE-1 beta
  3         3   ecNOS
  3         3   EDG4 receptor
  5    2    3   efp
  3         3   efp
3.9         3   EGF-R
  3         3   eNOS
  3         3   epoxide hydrolase
  3         3   ERK1/2
6.3   1.4   3   ET-1
  3         3   ET-1
  3         3   ETBR
  3         3   F3
  4    2    3   Fas
  3         3   FAS
  3         3   FAS
  4    3    3   FAS
  3         3   Fas and MnSOD
  3         3   Fas/CD95
  3         3   Fas/CD95
  3         3   fibrinogen Bbeta
4.9   1.5   3   fibronectin
  3       3   fibronectin and alpha5
  3       3   FKBP51
  3       3   flt-1
  5   2   3   FMR1
  3       3   FN
  3       3   FOS
  3       3   G alpha i2
  3       3   G alpha i-2
  3       3   G3PDH
  3       3   GABAB receptor
  3       3   GAL
  3       3   galanin
  4   3   3   galanin
3.8       3   galectin-3
  3       3   gamma-zein
  3       3   Gap43
  3       3   gastrin
  3       3   G-CSF
  3       3   GDNF
  3       3   GFAP
  3       3   GH
  3       3   GH
  3       3   GH
3.5       3   GH-R
  3       3   Gi alpha
  3       3   Gi-2 alpha
  3       3   Glc-6-Pase
3.5       3   glomerular TGF-beta1/beta-actin
3.9       3   GLT-1
  3       3   glucagon receptor
  3       3   GLUT1
3.4       3   GLUT1
3.5       3   GLUT1
  3       3   GLUT2
3.2       3   GLUT2
  4   3   3   GLUT2
  3       3   Glut4
  3       3   GLUT4
  3       3   Glutamine synthetase
  3       3   glutamine transporter ATB(0)
3.2       3   glutathione S-transferase
  3       3   GnRH receptor
  3       3   GnRH receptor
3.5       3   GnRH receptor
3.8       3   groESL
  3       3   H+/K(+)-ATPase
3.2       3   hAGT
  3       3   hBD2
  3       3   heat shock protein
  3       3   hemopexin
3.9       3   hGSTA1 steady-state
  4   3   3   HIF-1alpha
  3         3   HK II
  3         3   HKcbeta
  3         3   HMG-CoA reductase
  5    2    3   hMTII
  3         3   hMT-IIa
  3         3   HO-1
3.9         3   HO-1
  3         3   HSL
  3         3   HSP70
  3         3   HSP70
  3         3   HSP70
  4   2.7   3   HSS
  3         3   ICL2
  4    2    3   IFN-beta promoter
  3         3   IFN-gamma
3.6    3    3   IFN-gamma
  3         3   IGF-1
  3         3   IGFBP-1
  3         3   IGFBP-1
  3         3   IGFBP-2
  3         3   IGFBP-3
  3         3   IGFBP-3
3.9         3   IGFBP-3
3.3         3   IGFBP-4
3.8   2.7   3   IGFBP-4
  3         3   IGFBP-4
  3         3   IGFBP-5
  3         3   IGF-I
  4   2.5   3   IGF-I
  3         3   IGF-I
3.7         3   IGF-I
  3         3   IGF-I receptor
  3         3   IGF-I receptor
  3         3   IGF-Ib
  3         3   IkappaBalpha
  3         3   IL 1
  3         3   IL-1 beta
3.6    3    3   IL-10
3.6    3    3   IL-12p35
  3         3   IL-15
  3         3   IL-6
  3         3   IL-6
3.9         3   IL-6
  3         3   IL-8
  4    3    3   IL-8
3.8         3   inducible NOS
3.8         3   inhibin alpha
3.8         3   inhibin beta
  4    3    3   insulin
  4    3    3   insulin receptor
  3         3   interleukin-6
  3         3   IR
  3         3   kallikrein
  3         3   KDR
  3         3   laminin A chain
  3         3   LDL-receptor
  3         3   LDL-receptor
3.6         3   LFABP
  3         3   L-ferritin
  3         3   LPL
  3         3   L-pyruvate kinase
  3         3   M1
  3         3   MCAF
  3         3   MCP-1
  3         3   MCP-1
  3         3   MCP-1
3.4         3   MCP-1
3.6         3   MCP-1
  3         3   MDR1
  3         3   mdr2
  3         3   mEH
3.6         3   METHODS AND RESULTS: MCP-1
  3         3   MHA2
  3         3   MHC-A
  3         3   mitosis and DOR
3.8         3   MMP-3
  3         3   MnSOD
  3         3   MnSOD
3.4         3   MnSOD
  3         3   MRP
  4   3.8   3   myocilin/TIGR
  3         3   Na/H antiporter
  3         3   Na+/H+ antiport (NHE-1)
  3         3   NaPi-4
  3         3   natriuretic factor (ANF)
  3         3   NCAM protein and
  3         3   NEP
  3         3   nerve growth factor
3.4         3   NFkappaB-dependent
  4    3    3   NFM
  3         3   NGF
  3         3   NGF
  3         3   NHE-1
  3         3   NHE-1
  3         3   NHE3
  3         3   NHE3
  3         3   nNOS
  3         3   NOS
  3         3   NPY
  3         3   NPY
  3         3   NT
  3         3   OPN
3.5         3   OPN
  3         3   oxidase (ACO)
 3.5         3   OXPHOS
   3         3   P120
   3         3   P450(17alpha)
   3         3   P450(SSC)
   3         3   P4502C7
 3.5         3   P450arom
   3         3   P450c17
   3         3   P450IIE1
3.48         3   P450scc
3.31         3   P450SCC
   2    5    3   p53
   3         3   p53
   3         3   p75LNGFR
   3         3   PAI-1
 3.1         3   PAI-1
   4     3   3   PAI-1
   4     3   3   PAI-1
 3.7   3.7   3   PAI-1
   3         3   PCPE
   3         3   PDGF alpha-receptor
   3         3   PDGF-A
   3         3   PDGF-A
   3         3   PDGF-A
   3         3   PDGF-BB
   4    3    3   pdiA
   3         3   PEPCK
 3.1         3   PEPCK
   3         3   PGF(2alpha)-R
 3.4         3   PGHS-1
   3         3   PHGPX
   3         3   PhLP
 3.5         3   pim-1
   3         3   PKCbetaII
   4    3    3   PLP
 3.7         3   PNMT
   3         3   POMC
   3         3   POMC
   3         3   POMC
 3.3         3   PR
   3         3   predominant 4.5-kb PDG
   4    3    3   prepro-NPY
   3         3   PRL-R
 3.1         3   proANH
   3         3   proenkephalin A
   3         3   pS2
 3.1         3   PSA
   3         3   PSA
   3         3   PTHrP
   3         3   PTHrP
   3         3   pyruvate kinase L
 3.4         3   Relaxin
   3         3   renal kallikrein
   3       3   renin
   3       3   renin
   3       3   renin
   3       3   renin
   3       3   renin
   3       3   renin
 3.5       3   resistin
   3       3   retinal VEGF/VPF
 3.5       3   S100P
   3       3   silique ACC oxidase
   3       3   SNAP-25
   3       3   SP-A
 3.9       3   SPARC
 3.2       3   SP-B
   3       3   SPT
 3.5       3   SRA
   4   3   3   SR-BI
   3       3   SRE-dependent
   4   2   3   SSAT
3.25       3   sst2
   3       3   StAR
   3       3   STC2
 3.5       3   striatal proenkephalin
   3       3   subunit
   3       3   SULT60
   3       3   TERP-1
   3       3   tet(L)
   3       3   TFPI
   3       3   TfR
   3       3   TfR
 3.6       3   TGF
   3       3   TGF-alpha
   4   2   3   TGF-beta 1
   3       3   TGF-beta 1
   3       3   TGF-beta 1
   3       3   TGF-beta 1
   3       3   TGF-beta 1
   3       3   TGF-beta 1
   3       3   TGF-beta 1
   3       3   TGF-beta 1
   4   3   3   TGF-beta 1
   3       3   TGF-beta 2
   3       3   TH
 3.5       3   TH
   3       3   thioredoxin
 3.4       3   Tie2
   3       3   TIMP
   3       3   TIMP-1
 3.4       3   TIMP-3
   3       3   TK
 3.5       3   T-KG
   3       3   TM
  3         3   TNF-alpha
  3         3   TNF-alpha
  3         3   TNF-alpha
  3         3   TNF-alpha
  3         3   topoisomerase I
3.5         3   tPA
  3         3   t-PA synthesis and
  3         3   TPH
  3         3   transferrin
3.5         3   transferrin
  4    3    3   transferrin receptor
  3         3   tropoelastin
  3         3   tropoelastin
  3         3   type X collagen
  4   2.5   3   ubiquitin
  4     3   3   UCP
  3         3   UCP1
  3         3   UCP2
  3         3   UCP2
  3         3   UCP3
  3         3   UCP3
  3         3   UCP3
3.4         3   UCP3
  3         3   UCP3L
  3         3   UCP3S
3.4         3   UGT1*1
  3         3   UGT1A1
  3         3   UGT1A1
  3         3   UGT2B15
  3         3   uterine ER
3.7         3   VCAM-1 (P<0.01)
3.8         3   VDR
  3         3   VEGF
  3         3   VEGF
  3         3   VEGF
  3         3   VEGF
  3         3   VEGF
  3         3   VEGF
  3         3   VEGF
3.7         3   VEGF
3.7         3   VEGF
3.5         3   VEGF
  5     1   3
  4     2   3
  4     2   3
  5     2   3
  2     5   3
  4     2   3
  4     2   3
  4     2   3
4.8   1.8   3
  5     2   3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  4   3   3
  3       3
  4   3   3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
3.2       3
3.2       3
 3.4         3
 3.8   2.6   3
   4     3   3
   4     3   3
   4     3   3
   4     3   3
   4     3   3
   4     3   3
 3.9         3
 3.5         3
 3.6         3
 3.6         3
 3.8         3
 3.9         3
 3.9         3
   4         4   3alpha-HSD/DD
   4         4   3B
   4         4   5S
 4.1         4   ABC1
   4         4   actin
   4         4   ada
   4         4   adipocyte leptin
   4         4   Adipose tissue GLUT4
   4         4   adipose tissue LPL
   4         4   aggrecan
   4         4   AhR
   4         4   AlaAT-2
   4         4   alcohol dehydrogenase
   4         4   alpha 1B-receptor
   4         4   alpha 1III procollagen
   4         4   alpha 2M
   4         4   amylase
   4         4   androgen receptor (AR)
 4.5         4   angiotensinogen
   4         4   Ank
 4.7         4   apelin
   4         4   APN
   4         4   apo A-I
   4         4   apoE
   4         4   AQP5
   4         4   AR
 4.5         4   AR
   4         4   Bag-1
   4         4   bcl-x
   4         4   BDNF
 4.7         4   beta 1
   4         4   beta(1)AR
   4         4   bFGF
   4         4   BHMT
4.72         4   C3
   4         4   C4BP
   4         4   CaBP
  5    3    4   cad
4.6         4   cardiac IGF-I
4.5         4   CART
  4         4   cat
  5    4    4   CAT
  4         4   cFABP
  4         4   c-fos
  5    4    4   c-fos
  4         4   c-fos
  4         4   c-fos
  4         4   c-fos
  5    4    4   c-fos
4.6         4   CINC
  6   3.9   4   CKII alpha
  6     2   4   c-myc
  4         4   c-myc
  4         4   c-myc
  6    2    4   Col I
  5    3    4   COL3A1
  4         4   colonic H+-K+-ATPase
  5    3    4   COX-2
  4         4   CPT
  4         4   CRF
  4         4   CRF
  4         4   CT
  5    3    4   Cx43
  4         4   Cx43
  4         4   CXCR4
  4         4   cyclin D1
  4         4   CYP3A1
  4         4   decorin
  4         4   delta subunit
  8   0.6   4   delta-subunit
  6     3   4   EGF
  4         4   EGFR
4.2         4   EGFR
  4         4   Egr-1
  5    3    4   enzyme level and
  4         4   ET-1
  4         4   ET-1
  4         4   ETA
  4         4   EXCH
4.7         4   FasL
6.5   2.2   4   fatty acid translocase
  4         4   ferritin H
4.8         4   fibrinogen
  6    3    4   fibronectin
  4         4   Fralpha
  7    2    4   FSH beta
  4         4   G6PDH
  4         4   galanin
  4         4   galanin
4.5         4   galectin-1
  4         4   GAP-43
4.5         4   GAPDH
4.4         4   GCS
7.1   1.9   4   G-CSF
  5     4   4   GCS-LS
  4         4   GFAP
  4         4   GH
  4         4   GH
  4         4   Gi alpha 1
  4         4   glpD
  4         4   Glu-6-Pase
  4         4   glucocorticoid receptor
  4         4   glucokinase
  4         4   glucokinase
  4         4   glucokinase
  4         4   GLUT1/actin
  4         4   GLUT3
  5    4    4   GLUT3
  5    4    4   GLUT4
4.5         4   glutamate dehydrogenase
4.5         4   GRO-alpha
  6    3    4   GRP78
  4         4   H chain
  4         4   hBD-2
4.7         4   HB-EGF
4.9         4   HB-EGF
4.7         4   HCN2
  4         4   HDC
  4         4   H-FABP
  4         4   ICE
  4         4   IFN-gamma
4.3         4   IGF1
  4         4   IGFBP-3
  4         4   IGFBP-4
  4         4   IGFBP-5
  4         4   IGF-I
  4         4   IGF-I class 1
4.4         4   IGF-IR
  4         4   IL-1
4.5         4   IL-1 beta
  5   3.4   4   IL-10
  4         4   IL-11
  5   3.4   4   IL-12p35
  4         4   IL-17R
  4         4   IL-18
  5   3.4   4   IL-6
  4         4   IL-6
4.5         4   IL-6
4.7         4   IL-6
4.2         4   IL6-R
  4         4   IL-8
   4          4   IL-8
   4          4   IL-8
 4.1          4   iNOS
   4          4   insulin
   4          4   insulin receptor
   4          4   kinase 1
   4          4   K-ras
   4          4   lactase
   4          4   lactase-phlorizin hydrolase
   5     4    4   LH receptor
   4          4   liver phosphofructokinase
   4          4   L-kininogen
   4          4   LPL
 4.4          4   LT-beta
   4          4   MCAD
   4          4   mCG alpha
   4          4   MCM
   4          4   MCP-1
 4.5          4   M-CPT-I
   4          4   Mdr1
   4          4   MEK1,2-dependent PAI-1/luciferase
   4          4   mHS
   4          4   MMP-9/GAPDH
   4          4   MnSOD
 4.5          4   MRP
5.88   2.36   4   MT
   4          4   Mx
   4          4   Myf5
   4          4   Na,K-ATPase
   5     4    4   NF-kappa B1
   4          4   NGF
   4          4   NK2-receptor
 4.8          4   norA
   4          4   NQO1
   4          4   OAT
   4          4   ob
   5     3    4   ODC
   4          4   ODC
   4          4   ODC
   4          4   ODC
   4          4   OLE1
   5     4    4   osteocalcin
 4.4          4   oxytocin receptor
   4          4   p48
   4          4   p85alpha
   4          4   PAF receptor
   4          4   PAI-1
   4          4   PAI-1
   4          4   PCK
   4          4   PDGF
 4.3          4   PDGF-C
 4.4          4   PGC-1
  4       4   PGHS-1 mRNA; PGHS-1
  4       4   POA ERbeta
  5   3   4   POMC
  6   3   4   PPARgamma2
4.2       4   preproendothelin-1
  4       4   PRL
  4       4   pro-alpha 2 (I)
  4       4   proenkephalin
  4       4   proenkephalin
  4       4   proenkephalin
  4       4   proinsulin
  4       4   PrP
  4       4   PSA
  4       4   PTH
  4       4   PTH
  4       4   PTHrP
  4       4   PTP-PEST
  4       4   RA binding protein (CRABP)
  5   4   4   RAR gamma
  6   3   4   REN
  4       4   renal CaBP
  4       4   renin
  4       4   RIP140
  4       4   rNLRR-3
  4       4   ROMK2
  4       4   rpsL-bmpD
4.5       4   RWB
  4       4   SAA
4.5       4   SCP-x
  4       4   serotonin transporter
4.1       4   SHP
  4       4   skeletal alpha-actin (SK)
  4       4   SLF
  4       4   somatostatin
  4       4   SOX4
  4       4   SP-A
  4       4   SP-A
  4       4   SP-B
  4       4   SP-D
  4       4   ST6Gal I
  4       4   sTnC
  4       4   SULT-20/21
  4       4   T alpha 1
  4       4   TAXREB107
  4       4   TfR
  6   3   4   TGF-alpha
  4       4   TGF-beta
  4       4   TGF-beta 1
4.1       4   TGF-beta 1
  4       4   TGF-beta1 and CTGF
  4       4   TH
  4       4   TH
  4         4   TH
4.5   4.2   4   TH
  4         4   thioredoxin reductase
  5    3    4   Thy-1
  4         4   TIMP
  4         4   TIMP-1
  5    3    4   tissue growth factor
  4         4   TM
  4         4   TNF
  4         4   TNF
  4         4   TNF-alpha
  4         4   TNF-alpha
  4         4   TNF-R1
4.4         4   todC1
  4         4   t-PA
  4         4   transferrin
4.8         4   TRH
  4         4   TSC-22
  4         4   TSG6
  4         4   TSH beta
  4         4   TSH-R
  4         4   type 2 17beta-HSD
  4         4   type X collagen
  4         4   ubiquitin
  4         4   UCP1
  5    4    4   UCP1
  4         4   UGT1A7
  4         4   UGT1A8
4.9         4   u-PA
  4         4   uPA and uPAR
  4         4   uPAR
  4         4   u-PAR
  4         4   VCAM-1
  5    4    4   VDR
  5    3    4   VEGF
4.2         4   VEGF
  4         4   VEGF
  4         4   VEGF
  4         4   VEGF
4.6         4   VEGF
  4         4   Vn
  4         4   WAF1
  4         4   zif/268
  7     2   4
  6     3   4
  5     3   4
  5     3   4
  5     3   4
  6     3   4
  6   2.5   4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
4.2         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
  4         4
4.4         4
4.4         4
  5     4   4
5.1   3.5   4
4.5         4
4.5         4
4.5         4
4.6         4
4.6         4
  5         5   (HN) Epo
  5         5   5 alpha-reductase
  5         5   5-HT1c
  3    7    5   7alpha-hydroxylase
  5         5   Acyl-CoA oxidase
  5         5   adhesion molecule (VCAM)-1
5.4         5   ADRP
  5         5   AFP
7.4   3.2   5   A-IV
  5         5   alpha
  5         5   alpha
  6    5    5   alpha 1(I)
5.3         5   alpha 2A receptor
  5         5   alpha-actin
  5         5   alphaENaC
  5         5   alpha-ENaC
  5         5   androgen receptor
  6    5    5   Ann-II
  5         5   ANP
  5         5   ANP
  6    5    5   Apaf1
  5         5   apo E
  5         5   apoD
  5         5   APP
  5         5   AT1
  5         5   AT1R
  5         5   betaA
  5         5   C3
  5         5   CA12
  5         5   calreticulin
  5         5   Cap G
  5         5   CCR1
  5         5   CD95L
  5         5   Cdk4
  5         5   cervical IGF-I
  5         5   CETP transgene
  5         5   c-fos
  5         5   c-fos
  5         5   c-fos
  5         5   c-fos
  5         5   c-fos
  5         5   c-fos
  5         5   c-fos
  5         5   c-fos
  5         5   c-jun
  5         5   c-jun
  5         5   c-jun
5.4         5   c-jun
5.2         5   c-jun
  6   4   5   c-myc
  5       5   c-myc
  5       5   c-myc
  5       5   c-myc
  5       5   collicular KCC2
  8   3   5   cotransporter
  5       5   COX-2
  5       5   COX-2
  5       5   COX-2
5.5       5   CRBP
  5       5   CRBP1
  5       5   CT
  5       5   Cx26
5.3       5   cytochrome P450c
  5       5   cytokeratin 14
  5       5   DNA polymerase beta
5.8       5   DT-diaphorase
  5       5   E1A
5.7       5   EGF receptor
  5       5   elastin
  5       5   EP(2)
  5       5   epididymal Epo
  5       5   ER
  5       5   ERbeta
  5       5   erythropoietin
  5       5   erythropoietin
  5       5   erythropoietin
  5       5   ET-1
  5       5   Ets-1
  5       5   FAS
  5       5   FAS
  6   4   5   ferritin H
  5       5   FGF receptor
  5       5   fibronectin
  5       5   fibronectin-specific
  6   5   5   GAD67
  5       5   galanin
  5       5   galanin
  5       5   gamma-Actin
  5       5   GAP-43
  5       5   GCS
  5       5   GFR alpha-2
5.9       5   GHR
  5       5   GH-R
  5       5   GHRH
  6   4   5   glucose transporter
  3   8   5   GLUT1
  5       5   glutamine synthetase
  5       5   GM-CSF
  5       5   GPI-PLD
5.8       5   growth factor receptor
  5       5   GT
5.4       5   HB-EGF
  5       5   hemopexin
  5       5   histone
  5       5   hMT-le
  5       5   HO-1
  5       5   hPRL
  5       5   hsp-70
  5       5   hsp-70-like
  5       5   human growth hormone
  5       5   IGFBP-5
  5       5   IGFBP-5
  5       5   IGF-I
  5       5   IGF-I
5.6       5   IGF-IIR
  5       5   IL-1ra
  5       5   inhibin alpha-subunit
  5       5   inhibin-alpha
  5       5   iNOS
  5       5   IR
  5       5   kallikrein
  5       5   leptin
  5       5   Lerk-5
  5       5   lipo I
  5       5   LPL
  6   5   5   L-type enzyme
  5       5   LV
  5       5   MCP-1
  5       5   MCP-1
  5       5   MCP-1
  5       5   MHC class I
  5       5   MMP-9
  5       5   MnSOD
5.6       5   MT
  5       5   mucin
  5       5   neurons expressing trkA
  5       5   NGF
5.1       5   Nkx2-5
  7   4   5   NNT-1/BSF-3
  5       5   nrdDG
  5       5   nrdIEF
  5       5   ob
  5       5   ODC
  5       5   OTR
  5       5   PAGE-1
  5       5   PAI-1
  5       5   PAI-1
  5       5   PAI-1
  5       5   PAI-1
  5       5   PAI-1
  5       5   PAI-1
  5       5   PAO
  5       5   PAR-1
   8    2    5   PDGF-B
   5         5   PDGF-B
   5         5   PDGF-R alpha
   5         5   PEPCK
   5         5   phosphorylase
   5         5   PI-6
   6    4    5   PPARalpha
   5         5   PR
   6    5    5   predominant PR
 5.6         5   prodynorphin
   5         5   proenkephalin (Penk)
   5         5   progelatinase
   5         5   PTH
   5         5   PTN
   6    4    5   pup MT-3
   5         5   PYC1
   5         5   R2
   5         5   RAD23
   5         5   RANK
   5         5   RANTES
   5         5   RANTES
   5         5   renin
   5         5   renin
   5         5   Resistin
   8    3    5   rGH
   5         5   rpoB
   5         5   RV irANP
   5         5   SAA
   5         5   SCD4
   5         5   SKM UCP3
   5         5   SOCS3
   5         5   somatostatin
   5         5   SP(NK(1)) receptor
   5         5   SPARC
 5.2         5   SP-B
   5         5   Spec3
   5         5   SR Ca(2+)-ATPase
 5.5         5   SSAT
  10   1.5   5   Stat5
   5         5   TGF-alpha
   5         5   TGF-beta
5.01         5   TGF-beta 1
   5         5   thioredoxin
 5.1         5   THRP
   5         5   TKT
   5         5   TNF
   6    5    5   TNF-alpha
   5         5   to resection; IGF-I
   5         5   TPH
   5         5   tryptophan oxygenase
   5         5   TyrATase
   5         5   UCP2
  5         5   UCP2
  5         5   uncoupling protein
5.9         5   u-PA activity
  5         5   VEGF
5.2         5   VEGF
7.5    3    5   VP
  5         5   Yc2
  8     3   5
  4   6.3   5
  6     4   5
  6     4   5
  7     4   5
  7     4   5
  5         5
  5         5
  5         5
  5         5
  6    5    5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
  5         5
   5         5
   5         5
5.13         5
   6     5   5
   6     5   5
   6     5   5
   6   4.8   5
   6   4.5   5
 5.5         5
 5.5         5
   6         6   1.8-kb HO-1
   8    4    6   5-HT1A-R
   6         6   5-lipoxygenase
   6         6   ACC-alpha
   6         6   AhR steady state
  10    2    6   alb
 6.6         6   ANG II receptor
   8    4    6   apo A-I
   6         6   apoB-100
   6         6   atrial natriuretic factor
   6         6   BDNF
   6         6   beta 2AR
   6         6   beta-fibrinogen
 6.9         6   BMP-3b
   6         6   BNP
   6         6   bone morphogenetic protein-7
   6         6   Ca(2+)-Mg(2+)-ecto-adenosinetriphosphatase
   6         6   CaBP9K
   6         6   ceruloplasmin
   4    8    6   c-fos
   6         6   c-fos
   6         6   ChAT
   6         6   c-myc
   6         6   COX-2
 6.7         6   cph
   6         6   cTnI
  10    2    6   cyclin B2
 6.2         6   Cyclin E
   6         6   CYP1A1
   6         6   D3
   6         6   eotaxin
   6         6   ER beta
   7    6    6   factor H
   6         6   Fas
   6         6   fibronectin
   6         6   FN
   7    5    6   G6PD
   6         6   G-CSF
  11     2   6   GdA
 7.2   5.5   6   GFAP
   6         6   GH receptor-encoding
   6         6   GLUT1
  6         6   GnRH receptor
  8    4    6   growth hormone
6.8         6   HB-EGF
  6         6   hepcidin
  6         6   HGF
  6         6   HL
  6         6   HSP70
6.5         6   Hsp72
  7    5    6   IEX-1L
  6         6   IGFBP-1
  6         6   IGFBP-1
  8    4    6   IGFBP-2
  7    5    6   IGFBP-5
  6         6   IGF-II
  6         6   IL-4
  6         6   iNOS
  6         6   iNOS
  6         6   iNOS
  6         6   mannose receptor
  6         6   MCP-1
  6         6   MCP-3
  6         6   M-CSF
  6         6   metallothionein
  6         6   mGPDH
  6         6   MT-MMP-1
  6         6   Nox4
  6         6   NRF-1
  8    5    6   OST-PTP
6.5         6   OTR
  6         6   p21WAF1/CIP1
  6         6   p21WAF1/CIP1
  6         6   PAI-1-tPA
  6         6   PC1
  6         6   PC2
  7    5    6   PFK-A
  6         6   preproenkephalin
6.4         6   preproET-1
  6         6   preproIGF-I
  6         6   procollagen I
  6         6   proenkephalin
  6         6   PTH-related protein
 10    2    6   PTP alpha
  6         6   RAG-1
6.8         6   renin
  6         6   rGSTA2
  6         6   RII51
  7   5.8   6   synapsin I
  6         6   TF
  8    4    6   TGF-alpha
  6         6   TGF-alpha
  6         6   TGF-beta 1
  6         6   TKT
  6         6   trehalase
  6         6   UCP3
  6         6   VIP
 11   2.5   6   VWF
  6         6   Y2 receptor
  6         6   ZO-1
  8    4    6
  7    5    6
  7    5    6
  7    5    6
  7    6    6
  6         6
  7    6    6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  6         6
  7    6    6
  7    6    6
6.5         6
 10    5    7   11beta-HSD2
7.6         7   3 beta HSD
 10    5    7   A1
  7         7   adipocyte PAI-1
  7         7   adrenal 5 alpha-reductase
  7         7   ALAD
  7         7   albumin
  7         7   ANP
  7         7   ASBT steady-state
  7         7   AT1
  7         7   AVP
  7         7   beta-actin
   7        7   calbindin-D 9k
 7.6        7   calbindin-D 9k
  13   2    7   calcitonin
   8   6    7   CAT
  10   5    7   c-fos
   7        7   class mu GST
  10   5    7   c-myc
 7.4        7   c-myc
 7.5        7   c-myc
   7        7   collagen
   7        7   collagenase (MMP-1)
7.09        7   COX-2
 7.4        7   COX-2
 7.7        7   COX-2
  10    4   7   CRH
   4   11   7   cripto
   7        7   cyclase
   8   6    7   E-FABP
  13   2    7   FAS
   8   6    7   fibromodulin
  10   4    7   FPGS
  11   3    7   gastrin
   7        7   GFR alpha-1
   8   7    7   GnRH receptor
   7        7   gp91(phox)
   7        7   GS
  10   5    7   HBsAg
   7        7   HNF-3g
 7.5        7   I-BABP
   7        7   IGFBP-3
  10   4    7   IL-8
   7        7   insulin receptor
   7        7   LDL-receptor
   7        7   LDL-receptor
  10   5    7   LIF
   8   7    7   long-chain acyl-CoA synthetase
   8   7    7   MDR1
   7        7   mdr1
 7.2        7   monocyte chemotactic protein 1
   7        7   MT
   7        7   MT
   7        7   NSP-A
   8   6    7   P450R
   7        7   PAI-1
 7.8        7   PAI-1
   7        7   PAI-2
 7.8        7   PAI-I
   7        7   PGHS-2
   7        7   pIgR
   7        7   PKC-eta
   7        7   PRA
   8   6    7   RARalpha
  7         7   RAR-beta
  7         7   renin
  7         7   SCD1
  7         7   SMG NGF
  7         7   SP-A
 10    5    7   T alpha 1
  7         7   TGF-alpha
  7         7   TNF-alpha
  7         7   TS
  7         7   UCP3
 13   1.6   7
  8     6   7
  8     6   7
  8     6   7
  7         7
  7         7
  7         7
  7         7
  7         7
  7         7
  7         7
7.3         7
7.5         7
  8         8   4.4-kb
  8         8   ABCA1
  8         8   ACE
  8         8   adrenal PNMT
  8         8   alpha 1IV collagen
  8         8   alpha 2
  8         8   ANP
  9    7    8   ANT2
  8         8   APP
  8         8   BDNF
8.5         8   cat-specific
  8         8   CGRP
 10    7    8   c-myb
  8         8   colonic H+-K+-ATPase
  8         8   Cox
  8         8   COX-2
  8         8   cPLA(2)
  8         8   Delta6 desaturase
  8         8   deltaEF1
  8         8   DNA ligase
  8         8   DT-diaphorase
  8         8   EGF-R
  9    8    8   FS
  8         8   Gadd45
8.3         8   GH
  8         8   glucokinase
  8         8   glyceraldehyde-3-phosphate dehydrogenase (GAPDH)
 10    7    8   GTP cyclohydrolase I
  8         8   htrA
  8.5          8   IGFBP-1
    8          8   IGF-I
    8          8   IGF-I
    8          8   IL-6
   10     7    8   IP-10
    8          8   junD
    8          8   LRP16
    8          8   MCT2
    8          8   mEH
    8          8   mgrA
15.26   1.71   8   MT
    8          8   neutrophil IL-8
    4    12    8   NGFI-B
    8          8   NGF-R
    8          8   OCN
    8          8   p16(INK4a)
    8          8   PAI-1
    8          8   PAI-1
    8          8   PBP-C1
    8          8   PEPCK
    8          8   PlGF
    8          8   preproenkephalin
    8          8   RAR-alpha
  8.6          8   renin
    8          8   Retinal ceruloplasmin
    8          8   RII beta
    8          8   SCF
    8          8   Tac
    8          8   TBM
    8          8   TGF-beta 1
    8          8   TGF-beta 3
    8          8   TM
    8          8   TNF-alpha
   12     4    8   TSH beta
  8.1          8   UCP3
    8          8   UCP3
   10     7    8
    8          8
    8          8
    8          8
    8          8
    8          8
    8          8
    8          8
    8          8
    8          8
    8          8
    8          8
    8          8
    8          8
  8.1          8
    9          9   AP-1
   9        9   calcyclin
   9        9   CAT
   9        9   ceruloplasmin
   9        9   c-jun
   9        9   csp
   9        9   CT
   9        9   cyclin E
   9        9   epidermal TNF
   9        9   ET-1
   9        9   ET-1
   9        9   gamma RII beta
  10   8    9   GH
  10   8    9   GluR1 FLOP
  11   7    9   HB-EGF
   9        9   hMT-IIa
   9        9   HSP27
 9.5        9   IGFBP-1
   9        9   IL-12 p40
   9        9   LOX-1
   9        9   mdr1
   9        9   mEH
 9.5        9   MMP-1
   9        9   MnSOD
   9        9   MT-III
  15   3    9   OGG1
   9        9   Ornithine decarboxylase (ODC)
   9        9   p21(WAF1)
   9        9   P-450f
   9        9   PAI-1
   9        9   PLA2
 9.8        9   preproET-1
12.7   7    9   renin
  10   8    9   somatostatin
  10   8    9   SP-B
  10   8    9   TAT
 9.3        9   TNF-alpha
   9        9   TPH
   9        9   TSH beta
   9        9   VEGF
  16   2    9
  12   6    9
  10   8    9
   9        9
   9        9
   9        9
   9        9
   9        9
   9        9
   9        9
   9        9
  10       10   1.9-kb
  13   7   10   AHRR
  10         10   albumin
  10         10   alkaline phosphatase
  10         10   alpha 1
  10         10   alpha 1I3
  10         10   alpha-subunit
  10         10   AM
  10         10   ANF reporter
  10         10   barnase
  10         10   bcl-2 p2 site 1
  12    9    10   c49a
  10         10   calcyclin
  10         10   CAT
  18   3.8   10   cat-1
  10         10   CBG hepatic
  10         10   CD40
  10         10   c-fos
  10         10   c-fos
  10         10   c-fos
  10         10   c-Fos
  10         10   cIGFBP-5
  10         10   c-met
  10         10   c-myc
  10         10   collagen alpha1(I)
  10         10   cotransporter
  10         10   COX-2
  10         10   cyclooxygenase (COX)-2 steady-state
  10         10   DHFR
  10         10   E3
  10         10   EGF
  10         10   EGF-R
10.9         10   Egr-1
  10         10   emc
  12    8    10   ENC-1
  10         10   Epo
  11    9    10   fatty acid-binding protein
  10         10   fibronectin
  10         10   FN
  10         10   Fructose-1,6-bisphosphatase
  16    5    10   galanin
  10         10   galanin
  10         10   gelsolin
  10         10   GFAP
  10         10   GFAP
  10         10   GLUT4
  10         10   GM-CSF
  10         10   GnT-I
  10         10   growth factor
  10         10   hippocampal AChE
  10         10   HMG-CoA reductase
  10         10   hPKC alpha
  10         10   HSP70
  10         10   hsp70
  17   3   10   IFI27
  10       10   IFN-gamma
  10       10   IFN-gamma
  10       10   IGF-I
  10       10   IGF-I
  10       10   IGF-I receptor
  10       10   IL-1ra
  10       10   IL-6-specific
  10       10   iNOS
10.5       10   IPF-1
  10       10   IR
  10       10   ISG
  10       10   keratinocytes hINV
  10       10   KGF
  10       10   Ltype calcium channel
  10       10   MHC-A
  10       10   MMP-3
  10       10   MT-1 and -2
  10       10   Mx
  10       10   MxA
  10       10   NaS(i)-1 and sat-1
  10       10   nascent IGF-II
  10       10   NCX
  10       10   NF-M
  10       10   NOS
  10       10   NPR-A
  10       10   NPY
  10       10   Ntcp
  10       10   ob
  10       10   ODC
  10       10   ODC
  10       10   p21
  10       10   p21WAF1/CIP1
  10       10   P-450 1A1
  15   6   10   p52(PAI-1)
  10       10   PB2
  10       10   PEPCK
  10       10   PGHS
  10       10   P-glycoprotein
  10       10   PKA-stimulated PEPCK-C
  10       10   PPT-A
  10       10   preproNPY
  10       10   PTHrP
  10       10   PVY CP
  15   6   10   pyruvate kinase
  10       10   RBP
  10       10   renin
  10       10   S100 beta
  10       10   SAA
  10       10   SCD1
  10       10   SN1
  10       10   sodCp
  10       10   TGF-beta
  10       10   TGF-beta 1
  10       10   TGF-beta igh3
  12   8   10   TNF-alpha
  10       10   TNF-alpha
  10       10   TNF-alpha
  10       10   TPH
  10       10   transferrin
  10       10   tTG
  10       10   type II
  10       10   UCP3
  10       10   UCP3
  10       10   u-PA
  10       10   uPAR
  10       10   VDR
  10       10   vitellogenin
  10       10   YMR26
10.8       10   ZAKI-4
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
  10       10
11.5       11   10-fold and
  11       11   alpha 1B receptor
  11       11   Cat3
  11       11   CR1
  11       11   CYP4A
11.3       11   Egr-1
  11        11   FATP
  11        11   hsp-72
  11        11   ICAM-1
  11        11   IGF-I
  11        11   IL-12Rbeta2
  11        11   IL-1alpha
  11        11   IL-6
11.5        11   KLK8
  11        11   LPL
  11        11   MT-2
  15   7    11   P450IA
  11        11   PAI-1
  11        11   pnp
  11        11   todC1
  11        11   uPAR
  20    3   11
  15   10   12   4-nitrophenol GT
  12        12   ADM
  22   2    12   alpha-ENaC
  12        12   CYP3A
  12        12   dpsA
  12        12   Egr-1
  15   10   12   ermC
  12        12   ET(B)-R
  12        12   Fibronectin
  15   10   12   FOSP-1
  12        12   G6PD synthesis and
  12        12   GLUT5
  12        12   GRP mRNA:GAPDH
  12        12   GS
  12        12   HPTP beta
  15   10   12   hsp70
  12        12   hsp70
  12        12   IGF-I
  12        12   IGF-I
  12        12   IL-8
12.8        12   IL-8
  12        12   KGF
  23    2   12   laminin-receptor-precursor
  15   10   12   mGPDH
12.5        12   NGF
  12        12   ODC
  15   10   12   ornithine decarboxylase (ODC)
  12        12   OX(1) receptor
  15   10   12   PAI-2
12.4        12   PAI-2
  12        12   PKCtheta
  17   8    12   ras
12.5        12   VPF
  10   15   12
  15   10   12
  15   10   12
  12         12
  12         12
  12         12
  12         12
  12         12
  12         12
  12         12
  14   12    13   1.9-kb ADH
  13         13   C3
  18    9    13   CFTR
  13         13   hexokinase II
  13         13   IGF-II/CIMPR
  13         13   IL-6
  16   10    13   mEH
  13         13   multidrug resistance-associated protein
  13         13   PLA2
  13         13   urokinase
  16   10    13
  13         13
  13         13
  14         14   aFGF
  14         14   apoD
  14         14   BMP-2
14.9         14   Egr-1
  14         14   Epoxide hydrolase
  24    5    14   GH
14.9         14   glomerular Egr-1
14.6         14   hSK4
  14         14   IL-2R beta
14.5         14   metallothionein
  14         14   ompT
  14         14   PEPCK
  14         14   thioredoxin
  14         14   TIMP-1
  28   1.9   14
  16    12   14
  14         14
  15         15   19S
  15         15   3.2-kilobase
  15         15   4.7-kb
  15         15   5.5-kilobase poly(A)+
  15         15   Actin
  15         15   Agrp
  15         15   al-3
  15         15   ANPR-C
  15         15   bFGF
  15         15   CD59
  15         15   chloramphenicol acetyl transferase
  28    3    15   class II
  15         15   COX-1
  15         15   cprBA
  20   10    15   cryIA(c)
  20    10    15   desmin
  15          15   Fas
  15          15   GADD45
  15          15   gelatinase B
  15          15   gene 33
  15          15   Grp78
  20    10    15   HB-EGF
  15          15   HB-EGF
  15          15   Hsp70
  15          15   HSP82
  20    10    15   ICAM-1
  15          15   IGFBP-1
  20    10    15   IL-8
  20    10    15   iNOS
  15          15   LmGT2
15.8          15   MBP
  15          15   murinoglobulin
15.3          15   OP
  20    10    15   OrnDCase
  15          15   P450
  25     5    15   PDGF A chain
  15          15   SHR
  15          15   TNF-alpha
  20    10    15   tPA
  20    10    15   UCP3
  15          15   UDPGT
  20    10    15
  20    10    15
  20    10    15
  20    10    15
  20    10    15
  15          15
  15          15
  16          16   islet amyloid polypeptide
  16          16   LH beta
  16          16   MCAF/MCP-1
  16          16   metallothionein
  16          16   MnSOD
  16          16   PEPCK
  16          16   prodynorphin
  16          16   TPH
  16          16   UMP synthase
  16          16   UMP synthase
  16          16
  16          16
  22    12    17   amphoR
  17          17   beta-actin
  17          17   bolA1p
17.3   17.6   17   c-jun
  25     10   17   GLUT1
  20     14   17   LBP
  17          17   mEH
  20   15    17   PA
  17         17   UMP
  33    2    17
  30    5    17
  20   15    17
  17         17
  17         17
  18         18   beta TSH
   4   33    18   gene 33
  18         18   HSP70
  18         18   procollagen-alpha1(I)
  18         18   TRAIL-R1/DR4 and TRAIL-R2/DR5
  18         18   UCP3
  30    7    18
  18         18
  18         18
  18         18
19.7         19   alpha 2M
  19         19   calculated
  19         19   Fas antigen
19.6         19   glucokinase
30.2   7.9   19   hpa
  19         19   PAPP-A
  19         19   TGF-beta 1
  19         19   TGF-beta 1
  19         19
  20         20   2700-base
  20         20   4F2HC
  20         20   alpha 1-acid glycoprotein
  20         20   alpha 1-acid glycoprotein-1
  20         20   alpha 2
  20         20   ANF
  20         20   apoB
  20         20   arylsulfatase A
  20         20   beta-casein
  20         20   calbindin
  20         20   Calmodulin
  20         20   c-fos
  20         20   c-fos
  30   10    20   CMP-NeuAc synthetase
  20         20   c-myb
  20         20   c-myc
  20         20   collagenase
  20         20   cyclin D1
  20         20   EPO
  20         20   FasL
  20         20   flagellar
  20         20   Galanin
  20         20   GFAP
  20         20   GGT
  20         20   HO-1 1.8-kb
  20         20   HPRT
  20        20   IL-6
  20        20   kin1
  20        20   LDL-receptor
  20        20   legumin
  20        20   malic enzyme
  20        20   malic enzyme
  20        20   mdr
  20        20   mesangial MCP-1
  20        20   MMP-1
  20        20   MnSOD
  20        20   MRP
  20        20   NPY
  20        20   PAF-acetylhydrolase
  20        20   PAI-1
  20        20   PB P-450
  20        20   PLRP-2
  20        20   psaB
  20        20   renin
  20        20   serum amyloid A3
  20        20   u-PAR
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  21        21   bGT 2.9 Kb
  21        21   Cyp2a-4/5
  21        21   erp72 and HO-1
21.6        21   IL-1Ra
  23   20   21   ilv
21.4        21   ob
  21        21   tPA
  21        21
  21        21
  22        22   CYP2B1/2
  22        22   mEH
  23        23   c-fos
  23        23   CYP2B1/2
  23        23   cytochrome P-450b
  23        23   ER
  23        23   pyruvate carboxylase
  24        24   AT(2) receptor
  24        24   AT2 receptor
24.4        24   Ckidelta
  24        24   CT
  24        24   ENA-78
  24        24   GRP
  24        24   HO-1
  25        25   ATP-citrate lyase
  30   20   25   calbindin-D28K
  25        25   eotaxin
  30   20   25   FAS
  30   20   25   fatty-acid synthase
  25        25   FSH beta
  25        25   hTERT
  25        25   IkappaBalpha
  25        25   IL-6
  25        25   LDH-H
  40   10   25   PBE
  25        25   RFP
  25        25
  26        26   P450cc24
  26        26   TF
  26        26
  30   25   27   c-myc
  27        27   IL-12 p40
  27        27
  28        28   apo A-IV
  28        28   MCP-1
  28        28
  38   20   29   COL1A1 and COL6A3
  29        29   CYP1A1
29.3        29   ETA receptor
  29        29   Krox-20
  48   10   29   PAI-1
  30        30   24-hydroxylase
  30        30   AT
  50   10   30   beta-myosin heavy chain
  30        30   CaT1
  30        30   CNTF
  30        30   collagenase
  30        30   COX-2
  30        30   globin
  30        30   glutamine synthetase
  30        30   GMP-r
  30        30   N/OFQ
  30        30   OPN
  30        30   procollagen-alpha1(I)
  50   10   30   RAR beta
  30        30   TK
  40   20   30   TNF-alpha
  30        30   type I collagen
  30        30   Ucp
  40   20   30   urokinase
  45   15   30
  40   20   30
  30        30
  30        30
  30        30
  30        30
  30        30
  30        30
  31        31
  40   25   32   beta-casein
32.4        32   betaig-h3
  32        32   collagenase-3
  33        33   HO-1
  33        33   P450scc
  33        33
  34        34   betaFSH
  34        34   TF
34.9        34   u-PA receptor
  34        34
  34        34
  40   30   35   CYP1A5
  50   20   35   hsp 108
  35        35   HSP70
  35        35   IL-1 beta
  35        35   Na+/K+ ATPase alpha-subunit
  35        35   Pem
  50   20   35   TK
  40   30   35
  40   30   35
  40   30   35
  35        35
  35        35
  36        36   EGF-R
  36        36   mdm-2
36.7        36   NK-1R
  37        37   1.8-kb HO-1
  37        37   beta-casein
  50   25   37   P450IIE1
  38        38   PGHS-2
  50   30   40   4.5 kb
  40        40   adrenomedullary ppEnk
  40        40   CD11a
  40        40   CD-RAP
  40        40   COX-2
  40        40   CPT-Ialpha
  40        40   IGF-I
  40        40   MRP
40        40   netrin-1
40        40   NGF
40        40   p75NTR
40        40   PAI-1
40        40   PAI-1
40        40   POMC
40        40   relaxin
40        40   rGAL-encoding
40        40   SOCS-3
40        40   ST6Gal I
40        40   TGF-beta 1
40        40
40        40
40        40
40        40
40        40
60   23   41   immunoglobulin (Ig) mu
42        42   CYP3A1
43        43   IL-10
45        45   ATPase alpha-subunit
45        45   Cox-2
45        45   CYP3A1
50   40   45   DipEAAT1
45        45   GHBP-encoding
50   40   45   HSP-70A
45        45   SCD1
50   40   45
45        45
46        46   IGF-II
47        47   c-fos
48        48   PDGF-B
49        49
49        49
50        50   5'DI
50        50   cathepsin L
50        50   c-fgr
50        50   COX-2
50        50   gp30
50        50   IL--6
50        50   inducible NO synthase
50        50   LCB2
50        50   PTHrP
50        50   rGH
50        50   smc01944
50        50   TYRP2
50        50
50        50
50        50
50        50
50        50
50        50
50        50
 50         50
 50         50
100   5     52   IL-2
 52         52   PDGF-B
 54         54   intramonocyte 85B
 71   37    54   PGHS-1
 60   50    55   4F2HC
 55         55   osteocalcin
100   10    55
 59         59   GLUT1
 59         59
 60         60   4F2HC
 60         60   alpha 1-acid glycoprotein
 60         60   Epo
 60         60   epsilon-globin
100   20    60   histone
 60         60   IGF-I
 60         60   metallothionein and its
 60         60   MIP-2
 60         60   PRL-R
 60         60   reelin
 60         60   VEGFR-1
 62         62   leptin
 75   50    62   TRAP
100   30    65   metallothionein
 66         66   alpha 2-macroglobulin
 66         66   P450 2B1/2
 75   60    67   IGFBP-3
 69         69   POMC
 70         70   beta-MHC
100   40    70   IGF-II
 70         70   PGHS-2
 70         70   TP
 73         73
 75         75   CyP40
 80   70    75   elastin
100   50    75   Epo
 77         77   MGF
 79         79   Gs alpha
 80         80   CYP1A1 and CYP1A2
 80         80   GRP78
 80         80   IL-6
 80         80   knox-24
 80         80   mdr
100   70    85   CYP1A2
 85         85   CYP1A2
100   75    87
 90         90
 90         90
110   73    91   matrix metalloproteinase-9
100        100   AS alpha 1
100        100   AVP
100        100   c-fos
100        100   COX-2
100        100   CYP1A1
100        100   HIOMT
100        100   hREN
100        100   IL-13
100        100   IL-6
100        100   PGHS-2
100        100   PNMTase
100        100   PRL
100        100   TF
100        100   TS
100        100
100        100
100        100
100        100
100        100
100        100
100        100
100        100
100        100
100        100
100        100
210   3    106   afp
120        120   AdoMetDC
120        120   IL-2R alpha
120        120   IL-6
120        120
121        121   Membrane type-1-MMP (MT1-MMP)
121        121   POMC
125        125   IFN-gamma
125        125   TF
130        130   glutamine synthetase
135        135   calbindin9K-to-beta-actin
140        140   PDGF-A
144        144   PRC
144        144   renin
230   60   145   FIT3
150        150   beta-tropomyosin
150        150   IL-6
150        150
210   95   152   CYP2C45
160        160   KGF
170        170   AdoMetDC
188        188   c-fos
200        200   AT2
200        200   c-sis
200        200   c-sis
200        200   cytochrome P-450d
200        200   Epo
200        200   MTase
200        200   osteocalcin
      200             200
      200             200
      214             214   alpha 2-macroglobulin
      218             218
      280             280   MCP-1
      288             288   cyclin D1 specific
      300             300   glucoamylase
      300             300   IE94-IFN-specific
      300             300
      350             350   lux
      430   270       350   tetA
      400             400   proU
      419             419   CXCR1
    1,000   100       550
     1200    10       605
      612             612   CCR5
     1000            1000
     1393            1393   IFN-gamma
     1500            1500
     3400    23      1711   alphafp
    2,000            2000   SAA
     5000   200      2600
    3,000            3000   galanin
     7600     5      3802   afp
     4500            4500   hepcidin
  20,000    2000    11000   ER
   50000       5    25002   iNOS
 400,000           400000   I-TAC
1000000      10    500005   alb
sentence                                                                     PMID                      validation?
                                                                                           Year Microarray?
least a 1000-fold decrease in viral transcription after 8-MOP Using             7975222 1994         0      1
in the medium and reduced its gene expression 500-fold (P =.04),              11231848 2001          0      0
by exogenous (>350-fold reduction of IL-10 mRNA level), as well as              9425923 1998         0      0
a > 200-fold decrease in beta-glucuronidase mRNA levels and virtually no 8101990 1993                0      0
                                                                                2495302 1989
greater than 200-fold reduction in the beta-glucuronidase mRNA concentration in mutant               0      0
on MUP mRNA levels. MUP mRNA was reduced 150-fold                               6656765 1983         0      0
a approximately 100-fold fall in hepatic apo[a] mRNA levels and >60-fold 10357831 1999               0      0
                                                                              12492453 2003
caused a 100-fold reduction of cholesterol 7-alpha hydroxylase mRNA levels in mice                   0      0
                                                                                9271107 1997
causes a 100-fold decrease in transcription of Ty2-917. Activation by the isolated                   0      0
about a 100-fold decrease in gene expression in the lung as                     9349425 1997         0      0
Furthermore, a 100-fold reduction in the transcription efficiency of the Cdc612006585 2002           0      1
and a 70-fold decrease in RALDH2 mRNA in testis. In each                      11169459 2001          0      0
                                                                                7564322 1995
20- to 100-fold decrease in c-myc mRNA transcripts, respectively. This inhibition                    0      1
                                                                                2325661 1990
to a 60-fold decrease in epididymal proenkephalin mRNA levels. Testosterone replacement              0      0
in a 50-fold decrease in accumulated mRNA level. We show that                   1398070 1992         0      0
                                                                                8289800 1994
an average 50-fold reduction of the basal transcription level, while the dexamethasone-stimulated 0         0
in a 7-74-fold decrease in reporter gene expression depending on the cell 11318112 2001              0      0
In hypothyroid rats, the CPT-I mRNA levels decreased 40-fold                    8003033 1994         0      1
The level of Wnt5a mRNA expression was decreased 40-fold                        9367869 1997         0      0
                                                                                8652841
five-fold to 35-fold decrease in BCL-6 mRNA levels. Similar downregulation of BCL-6 1996             0      0
a rapid 35-fold decrease in the histone mRNA concentration which our            2017161 1991         0      0
was cleaved and the 2Apro mRNA was reduced 30-fold                              1713590 1991         0      0
KO mice, whereas expression of IL-1alpha mRNA decreased >30-fold                9565638 1998         0      0
by a 30-fold decrease of L-14 mRNA levels. Removal of retinoic                  8135794 1994         0      0
10- to 50-fold decrease in mature phytochrome mRNA levels, suggesting that      2879299 1986         0      0
16- to 43-fold reduction of gene expression in infected cells transduced      12908971 2003          0      0
Expression of this mRNA was also reduced 25-fold                                1713590 1991         0      0
an approximately 25-fold decrease in the rate of transcription was observed, 2436040 1987            0      0
15- to 30-fold decrease in steady-state H1 mRNA levels in randomly              2896124 1988         0      0
replication and 22-fold reduction in transcription by RNA polymerase II from 1713590 1991            0      0
10- to 30-fold reduction in FXIII mRNA levels. This is also                     8025280 1994         0      0
the ischemic medulla, OP-1 mRNA was strikingly downregulated 20-fold            9697668 1998         0      1
                                                                                transcription-PCR
an approximately 20-fold reduction in Se-GPx1 mRNA abundance. Reverse 9566912 1998 analyses          0      1
an approximately 20-fold reduction in the specific transcription of the tk      2842233 1988         0      0
                                                                                8393767 1993
elicited a 20-fold decrease in mRNA S14 concentrations. An elevated intracellular                    0      0
                                                                                7499353 1995
for the 20-fold decrease in transcription. Accordingly, transcription in the mutant                  0      0
in a 20-fold reduction in reporter gene expression in HepG2                     9716591 1998         0      0
induced a 20-fold decrease in the mRNA level of both calpain                  11350751 2001          0      1
showed a 20-fold decrease in transcription when its kappaB sites were           9188623 1997         0      0
10- to 30-fold reduction in alpha1AT gene expression in cell                    9927755 1999         0      0
to a 19-fold reduction of bcl-2 mRNA levels and only barely                   15000830 2003          0      0
                                                                                3179336 1988
approximately a 15-17-fold decrease in albumin mRNA relative to total cytoplasmic                    0      0
for the 15-17-fold decrease in albumin mRNA abundancy caused by tryptophan      3179336 1988         0      0
with SSG1 mRNA expression, SSG1 protein was decreased 16-fold                 11357054 2001          0      1
to a 16-fold reduction in initiation of transcription of this                   2916325 1989         0      0
myocardium and that alphaMyHC mRNA expression is decreased 15-fold 10700442 2000                     0      0
                                                                                 JEG-3
mutation of this element decreases alpha-subunit gene expression 15-fold in7518566 1994              0      0
                                                                                9536978 1998
statistically significant 15-fold decrease in biglycan mRNA expression was observed in AAA           0      1
RNase protection assays showed DHFR mRNA levels decreased 15-fold 2592372 1989                       0      1
                                                                                2335521 1990
to the NF1 transcription activator reduced estrogen-dependent transcription 10-20-fold in both       0      0
10- to 20-fold reduction in MK mRNA levels was observed in mammary              8944070 1996         0      0
found a 15-fold down-regulation of PBP mRNA by differential Regulation 14673015            2004   0   0
showed a 10-20-fold reduction of hybridizable virus L mRNA in infected          9010295    1997   0   0
greater than 15-fold decrease in mRNA encoding the catalytic unit of the 11516168          2001   0   0
of a 15-fold decrease in the rate of transcription of the maltase               6352680    1983   0   0
same rachitic bones, while OPN mRNA was reduced 12.5-fold                       9933476    1999   0   0
22), a 4-fold decrease in VDR mRNA was observed, accompanied by                 1647304    1991   0   1
                                                                              11696239
derepression with galactose, beta-galactosidase gene expression is reduced 12-fold         2001   0   0
in the unfertilized eggs. This mRNA pool decreased 12-fold                      3972162    1985   0   0
specific suppression of collagen expression. mRNA levels dropped 11-fold 12559975          2003   0   0
demonstrated a 10-fold reduction of ALPL steady-state mRNA and enzyme activity, 8682172    1996   0   0
gives a >10-fold reduction in CHK2 mRNA and protein. This level               14514889     2003   1   0
heat-shock conditions, Drosophila hsp70 mRNA translation is reduced 10-fold     6821336    1982   0   0
least a 10-fold reduction of EGF receptor mRNA levels in tumor                  9935207    1999   0   1
as a 10-fold decrease in mRNA expression level of Fgf10 but                   11404268     2001   0   1
by a tenfold reduction of the fos mRNA level and a twofold                      3904752    1985   0   0
induced a 10-fold down-regulation of FPPS mRNA within 24 h in the             11566436     2001   0   1
a transient 10-fold drop of the GPD1 mRNA level. Neither the HOG              10217506     1999   0   0
the cellular concentration of hla mRNA was reduced 10-fold                      7556100    1995   0   0
hypophosphite-dependent activation of hycA gene expression was reduced 10-fold  8022272    1994   0   0
revealed about 10-fold inhibition of iNOS gene expression by As               10574472     1999   0   1
RESULTS: A 10-fold reduction in full length IRF-1 mRNA was detected           15082491     2004   0   0
cause a 10-fold decrease in mdr1 mRNA level. However, this specific             9627221    1998   0   0
an approximate 10-fold reduction of NA-specific mRNA and protein levels (Fodor10675411     2000   0   0
                                                                                9445014
greater than 10-fold reduction in p53 transcription activity. Using Ga14-p53 fusion        1998   0   0
A 10-fold reduction in the amount of mRNA for the PDGF                          7718626    1995   0   0
more than tenfold reduction in maize phy mRNA abundance occurs in seedlings     2628175    1989   0   1
levels were analysed. Transcription of RHAMM was decreased 7-12-fold 10607311              1999   0   0
SWI4 UAS decreases the level of SWI4 mRNA 10-fold in asynchronous               8497280    1993   0   0
to a 10-fold decrease in mRNA levels of TGF-beta type II                        8020609    1994   0   1
Concomitantly, a 10-fold reduction in TIMP protein and mRNA levels by           2174435    1990   0   1
a specific, 10-fold decrease in TNF mRNA half-life. Here we show                1310308    1992   0   0
A 10-fold reduction in toxin mRNA production and a 25-fold                    15033232     2004   0   0
Type II procollagen mRNA levels decreased 10-fold                               4033659    1985   0   0
In AKR/J mice, UCP1 mRNA was decreased 10-fold                                12421846     2002   0   0
mature male rats reduces the 1.5 kb mRNA 10-fold in the seminal                 3758473    1986   0   0
                                                                              10811657
a central subdomain of intron 1 inhibited transcription >/=10-fold in transiently          2000   0   0
region in 10-bp steps. Two mutations reduced transcription 10-fold or more, 1406648        1992   0   0
had the dual effect of reducing gene expression 10-fold and of producing 10391325          1999   0   0
in a 10-fold decrease in reporter mRNA accumulation. The removal of the 8394439            1993   0   0
and a 10-fold reduction in translatable mRNA for two collagen                     198783   1977   0   0
a relative 10-fold decrease in mRNA levels after 6 days of treatment.         10618640     1999   0   1
least a 10-fold reduction in transcription rate. The half-life of stb           1706707    1991   0   1
IL-2, a 3-15-fold reduction of bcr/abl mRNA accumulation was demonstrated7885040 by        1995   0   0
8- to 10-fold reduction in EGF-R mRNA copies per cell in dormant                7678348    1993   0   1
was a ninefold decrease in Fas ligand mRNA expression between GD                9558079    1998   0   0
causes a 7-10-fold decrease of both the mRNA that codes for                     6323236    1984   0   0
a 5-10 fold reduction in ADA-specific mRNA which is also more                   3306603    1987   0   0
with an eightfold decrease in BRCA1 mRNA compared to normal breast              9778046    1998   0   0
                                                                                2
5- to 10-fold reduction in fiber mRNA levels. Previously Anderson and Klessig 778880       1989   0   0
An eight-fold decrease in Glut1 mRNA was observed when glucose                  8208668    1994   0   0
six- to eightfold reduction in IFN-gamma induced IAb mRNA levels, and comparable9529320    1998   0   0
Both involucrin mRNA and protein levels were decreased 8-fold                   1657375    1991   0   0
5- to 10-fold decrease in Mac-2 mRNA levels in cancer compared                    7682704 1993  0   0
Peritoneal macrophage I-A alpha mRNA levels decreased 8-fold                      8361168 1993  0   1
An 8-fold decrease in the rate of transcription of this                           1382604 1992  0   0
                                                                                   and prtM
an approximately eightfold decrease in mRNA production. Furthermore, prtP8626277 1996           0   0
seven- to eightfold reduction in transcription as well as a significant           9367984 1997  0   0
5- to 10-fold reduction in the transcription of the gC and U(L)47               11336552 2001   0   1
five- to sevenfold reduction in c-myc mRNA through a decreased rate               3881681 1985  0   0
                                                                                  9624173 1998  0
multinucleated myotubes decrease their levels of c-myc mRNA 3-10-fold through posttranscriptional   0
                                                                                10675497 2000
beta1 (TGF-beta1) and plasminogen activator inhibitor-1 gene expression sevenfold at two        0   0
RT-PCR demonstrated that rac2 mRNA expression was reduced 7-fold                12471136 2002   1   1
3- to 11-fold reduction in TFF mRNA expression, displayed in real-time          12297725 2002   0   0
protein and 6.5-fold decrease in TPA mRNA were found in brain                     8614937 1996  0   0
3- to 10-fold down-regulation of VEGF mRNA expression in endostatin-treated     12354694 2002   0   0
>2 to 7-fold reduction in cytokine mRNA half-lives. In contrast, SB202190 10563470 1999         0   0
Alpha transcription in isolated nuclei is decreased sevenfold                     3023910 1986  0   0
of human albumin mRNA sequence, editing is reduced 6-fold                         8286418 1994  0   0
caused a 6-fold decrease in c-fos mRNA levels. In addition, nuclear               1568207 1992  0   1
in a six-fold decrease in estrogen receptor mRNA half-life from 4                 9719445 1998  0   0
Steady-state anterior pituitary galanin mRNA levels decreased 6-fold              9427502 1997  0   0
approximately a 6-fold decrease in IGF-I mRNA and IGF-I nuclear                   9048599 1997  0   1
A sixfold reduction of mdr-1 mRNA expression by 8-Cl-cAMP began                   7543490 1995  0   0
decarboxylase (ODC) mRNA level and activity are decreased 2.8-7.7-fold 11139396 2001            0   0
                                                                                11961126
the T3-dependent 6-fold decrease in cytoplasmic P450R mRNA half-life, from a basal 2002         0   1
was a 5.8-fold reduction of trk C mRNA levels, which reached                      9865928 1998  0   1
                                                                                11058715
a approximately six-fold decrease of mRNA expression and a approximately two-fold 2000          0   0
A six-fold decrease in transcription of 4.5S RNA was observed                     2450810 1987  0   0
extracts and 6-fold drop in liver. Transcription in both extracts was             9332728 1997  0   0
japonicum; a sixfold reduction in transcription from the highest (250 microM) 8380149 1993      0   0
                                                                                10203333 1999
reflecting a 6-fold decrease in mRNA expression. Interestingly, TIMP-4 also differed            0   0
Mutation of this site decreases reporter gene expression 5.5-fold in the Burkitt  8197157 1994  0   0
5 to 7-fold reduction in steady-state transcription from cycA::lacZYA operon 1320126 1992       0   0
                                                                                  7047528 1982
4- to 8-fold decrease in relative read-through transcription was observed in response           0   0
The half-life of 24-hydroxylase mRNA is reduced 4.2-fold                        12520520 2003   0   0
showed a fivefold decrease in renal 24-OHase mRNA compared with rats 8760262 1996               0   0
was a 4-5-fold decrease of adipsin mRNA level. In contrast, actin,                1985940 1991  0   1
proteins, a 5-fold reduction in albumin mRNA relative to total RNA,               6822503 1983  0   0
the relative abundance of alpha 1I3 mRNA decreased 4-5-fold                       2450089 1988  0   1
and a 5-fold reduction in AR mRNA expression was detected in TNF-alpha-treated    8646686 1996  0   1
observed that BBEC PAI-1 mRNA levels were decreased fivefold                      7519664 1994  0   0
Five-fold reduction of c-myc mRNA and a marked decrease                           8393433 1993  0   0
Wistar hearts, collagen alpha 1(III) mRNA levels decreased fivefold               1423932 1992  0   0
                                                                                   2
to a fivefold reduction in translatable mRNA for CSP. Reconstitution of isolated 91364 1978     0   0
three to five-fold decrease in the steady-state mRNA level of EF-1                9568107 1998  0   0
                                                                                fljBA(ON)
operon demonstrated that while FljA inhibits fliC transcription fivefold in the 12775694 2003   0   0
with a fivefold decrease in HS-P LRP mRNA expression as measured                10531236 1999   0   1
< 0.001) 5-fold reduction in I-24-OHase mRNA expression. These data suggest       7956916 1994  0   0
and a fivefold decrease in IGF-binding protein-5 (IGFBP-5) mRNA levels in primary 9491783 1998  0   0
demonstrated a 5-fold decrease in IGFBP-2 mRNA (P < 0.001) and a                  7525636 1994  0   1
in a 4.4-fold decrease in IGFBP-5 mRNA levels. When added together                9642243 1998  0   0
in a fivefold reduction in hepatic IGF-I mRNA levels (optical density             1476613 1992  0   1
and a 5-fold reduction of IGFII mRNA derived from the P4                          9502429 1998  0   0
above adult levels. Maternal liver metallothionein mRNA decreased fivefold 6840062 1983         0   0
assays, a 5-fold decrease in mP2 transcription is seen when both                     9341127 1997       0   0
                                                                                     9040047
a progressive five-fold reduction in NHE-1 mRNA expression in ventricular myocardium 1997               0   0
4.5 +/- 0.5-fold decrease in total PAM mRNA and a 2-fold                             9389509 1997       0   0
                                                                                     1719385 1991
produced a 5-fold decrease in phosphoenolpyruvate carboxykinase (PEPCK) mRNA levels, which              0   0
A fivefold decrease in PSA mRNA was also detected in IL-2-treated                    8646686 1996       0   1
analysis showed that S5 mRNA expression is reduced 5-fold                            9202169 1997       0   1
was a 5-fold decrease of synthase mRNA within 3 These                                2877984 1986       0   0
showed a fivefold reduction in TGF-beta 1 mRNA and 15-fold reduction                 1730743 1992       0   0
demonstrates a 5-fold reduction in topoisomerase II mRNA isolated from log1660341 1991                  0   1
with a fivefold reduction in type II collagen mRNA and a cessation                   4033660 1985       0   0
regimen, a fivefold decrease in VEGF mRNA expression was observed from              11413193 2001       0   0
to a 4-6-fold reduction in ZnT1 mRNA levels and a loss                              10952993 2000       0   0
an approximately fivefold decrease in the cellular transcription carried out by 1385385 1992            0   0
in a 5-fold decrease in reporter gene mRNA accumulation, but did                     7641691 1995       0   0
shows a 5-fold reduction in the translatable mRNA for cell surface                    198783 1977       0   0
in a 5-fold inhibition of transcription in a transient transfection assay           11684679 2002       0   0
in a fivefold decrease in transcription from the major initiation site               2247077 1990       0   0
to a five-fold reduction in transcription rate of both the IL-3                      8641331 1996       0   0
than a 4.6-fold decrease in expression of mRNA (size, approximately 5.1 12134233 2002                   0   1
4- to 5-fold decrease in the transcription rate. Further deletion of -99             8819312 1996       0   0
Steady-state Hmga2 mRNA levels in NIH3T3 cells decreased 4-5-fold                   12799440 2003       0   0
a nearly four-fold decrease in aggrecan mRNA levels compared to control 14624453 2003                   0   1
The fourfold reduction of alpha 1I3 mRNA concentrations in FAO1                      1699110 1990       0   0
and a fourfold decrease in alpha 2(V) mRNA observed after treatment                  9443080 1998       0   0
a 2-6 fold decrease in alpha actin mRNA levels and an                                1875785 1991       0   0
Apo B mRNA abundance was decreased fourfold                                          1591230 1992       0   0
with a 3.6-fold reduction in ApoA1 mRNA in young rats, but                           8997358 1996       0   0
In hypothyroid rats, apoA-IV gene expression was decreased fourfold                  8429259 1993       0   0
h after castration reduced ventral prostate AR mRNA 4-fold within 8                  2325667 1990       0   1
detectable in the adrenal medulla. AT(1)R mRNA decreased 4-fold                     10684814 2000       0   0
in a fourfold downregulation of bcl-X(L) mRNA and protein levels followed 9141616 1997                  0   0
                                                                                    10762711
demonstrate a 3.4-fold decrease in brain-derived neurotrophic factor mRNA levels in the2000             0   0
adrenalectomy, a 3.6-fold decrease in the calcitonin mRNA level was observed         2599094 1989       0   1
UAS1 which when deleted reduces ERG3 gene expression 3-4-fold but maintains          8772195 1996       0   0
isolated cells, mRNA for the ET(B) receptor decreased 4-fold                         9409812 1997       0   1
revealed a 4-fold reduction of hAR gene transcription 96 h after                     8413317 1993       0   1
                                                                                    12358902
Surprisingly, fourfold reduction of full-length IRF-1 mRNA expression was established 2002              0   0
showed a fourfold decrease in M-CSF mRNA expression in both unstimulated             7994042 1994       0   1
A 4-fold decrease in the mdr1 gene transcription rate was                            7838133 1995       0   0
demonstrate a fourfold decrease in Mramp/y39 mRNA ratios from organisms grown       10477555 1999       0   1
A fourfold decrease in myostatin mRNA in the mdx muscle                             12133862 2002       0   0
induced, a 3.4-3.8-fold decrease in NT-3 mRNA was observed by Northern 9221916 1997                     0   1
three- to fourfold decrease in P-450c11AS mRNA without a change in the 8872624 1996                     0   1
namely, a 3.3-fold decrease in PMCA1b mRNA and a 3.7-fold increase                  10642281 2000       0   1
Glucocorticoids rapidly inhibited POMC gene transcription fourfold in the anterior   3500023 1987       0   0
a approximately 4-fold decrease in pp63 mRNA level was detected at                   1659407 1991       0   0
to a fourfold decrease in reg mRNA levels (23 +/- 12%                                8070617 1994       0   0
produced a 3-5-fold decrease in Star mRNA along with a loss                          9516465 1998       0   0
an approximately fourfold reduction in transcription from the major surface antigen  1651407 1991       0   0
and a fourfold reduction in transcription in vitro. Another mutation in the         11238896 2001       0   0
in a fourfold decrease in the mRNA half-life, demonstrating the importance 12949089 2003                0   0
                                                                                     7964636
three- to fourfold inhibition of transcription in transfected cells. Inhibition of transcription 1994   0   0
caused a 3-5-fold reduction in mRNA levels for the other extracellular      2914960 1989   0   0
                                                                           12393792 2002
1.5- to 5-fold reduction in mRNA abundance. All truncating mutations located               0   0
five- and three-fold reduction in the mRNA expression of 5alphaR1 after 15004407 2004      0   0
a significant 2.5-fold decrease of mRNA for alk4-1 type I activin          11069203 2000   0   1
caused a 3-fold decrease in amastin mRNA and a 7-fold increase              7673251 1995   0   0
                                                                            7495074 1995
cause a 3-fold decrease in antithrombin mRNA levels, suggesting that the hormone           0   1
by a threefold decrease in antral somatostatin mRNA levels that began       2901431 1988   0   0
with a 2.3-fold decrease in hepatic apoA-I mRNA abundance. Our findings 12364558 2002      0   0
an approximate threefold reduction of AT2 mRNA levels, and also increased7580938 1995      0   0
in CRH peptide levels. AVP mRNA levels fell three-fold                      2576125 1989   0   0
beta-globin marker gene from this mRNA was reduced 3-fold                   1713590 1991   0   0
in a 2-3-fold decrease in CD13/APN mRNA expression and near ablation 7658720 1995          0   0
two- to threefold decrease in Col1A1 mRNA in lungs of homozygous            9584177 1998   0   1
An average 3-fold reduction in collagen I mRNA expression was seen         11371952 2001   0   0
In contrast, cortical COX-2 mRNA levels decreased 2.9-fold                  9530264 1998   0   0
and a 2.7-fold decrease in cortical NaSi-1 mRNA abundance, as determined9727363 1998       0   1
and a 2.2-fold decrease in cortical NaSi-1 mRNA abundance. The inhibitory  10362603 1999   0   0
                                                                            8958057 1996
hr incubation (2.7-fold decrease of mRNA COX-2 transcripts); and about a threefold         0   1
that a threefold decrease in DSC1 mRNA is accompanied by a threefold 12196396 2002         0   0
                                                                           10837364 2000
a significant 3-fold decrease in EGF receptor mRNA levels in the antisense-treated         0   0
an approximately 3-fold decrease in FBP mRNA levels per KB1BT               1299378 1992   0   1
and about 3-fold decrease of fibronectin mRNA level in diabetic ulcers     12906161 2002   0   0
                                                                            1423932 1992
spontaneously hypertensive rat (SHR). Fibronectin mRNA expression decreased threefold      0   0
in a three-fold reduction of the fixBCX mRNA level, which in turn           2503674 1989   0   0
2- to 3-fold reduction in gamma-zein mRNA and protein synthesis and reduces 7892202 1995   0   0
that the rate of GAP43 transcription was reduced threefold                  9143270 1997   0   0
observations, a three-fold decrease in GAP-43 mRNA in the adrenal gland 7842514 1994       0   0
two- to threefold reduction in glomerular iNOS mRNA levels. iNOS activity 10589693 1999    0   1
subclass of GnT-I mRNA in rat liver decreased 2.5-fold                      9781684 1998   0   0
two- to threefold decrease in HSC70 mRNA levels in the human               10967038 2000   0   1
in a three-fold decrease in Insl3 mRNA expression level (P<0.005), at      10650968 2000   0   0
displayed a 3-fold decrease in LNGFR mRNA expression compared to untreated  1473271 1992   0   0
revealed a 2.5-fold decrease of MMP-9 mRNA and a 4.5 fold                  11471571 2001   0   1
about a 3-fold reduction of mP2 transcription in vitro. Although the PAF-1  9341127 1997   0   0
2- to 4-fold decrease in P-450 2c mRNA levels after castration              1691818 1990   0   0
caused a 2.4-fold reduction in P-450f mRNA which was partially reversed 2303159 1990       0   1
2- to 3-fold decrease in PATR mRNA in a time- and dose-dependent            8600159 1996   0   1
we found that PGHS-2 mRNA levels were reduced threefold                     8892355 1996   0   1
that, following partial hepatectomy, PKAc mRNA is decreased 3-fold          2306720 1990   0   1
was a 3-fold decrease in POMC mRNA in the IL in ADX                         3374760 1988   0   0
in a 3-fold reduction in PRL mRNA and CgB mRNA, whereas                     7912292 1994   0   0
Greater than threefold downregulation of procollagen mRNA levels was seen 247814454 1995   0   0
to the internal control ribosomal S2 mRNA decreased threefold              11792652 2002   0   0
                                                                            8267650 1993
indicated a 2.5-fold reduction in topoisomerase II alpha mRNA in etoposide-resistant       0   1
                                                                            A comparison
and approximately 2.5-fold decrease in topoisomerase IIalpha mRNA level.11901227 2002      0   0
twofold to threefold decrease of TPA mRNA levels with increasing in vitro 9108786 1997     0   0
to a 3-fold decrease of t-PA mRNA stability. The insertion of this          8554675 1995   0   0
1.5- to 3-fold decrease in uidA mRNA levels and a 1.5-                     12690442 2003   0   0
The VLDLR mRNA expression was down-regulated 3-fold                        10488949 1999   0   0
controls (20% oxygen). Conversely, XD mRNA was decreased threefold          8914935 1996   0   1
to a threefold reduction in target mRNA accumulation in the tissues        12753592 2003   0   1
of translational efficiency of capped mRNA was reduced 2.6-fold             8125928 1994   0   0
and a 3-fold reduction in its cognate mRNA level. However, apo                   1329783 1992       0   0
in a 3-fold decrease in total transcription activity. Surprisingly, the decrease 3755688 1986       0   0
and a threefold decrease in mRNA encoding MHC-B. Using SDS polyacrylamide        1999462 1991       0   0
in a 3-fold decrease in transcription in a nuclear extract and a                 1990266 1991       0   0
in a threefold reduction in the mRNA level of interleukin-1 beta-induced         8630528 1996       0   0
in a three-fold reduction of the transcription of the It                         8980537 1996       0   0
of GGT mRNA in mutant kidney is reduced 3-fold                                  10474818 1999       0   1
promoter determinants, because when mutated, transcription is reduced 3-fold     6552939 1983       0   0
showed a threefold decrease in mRNA level in the (Hyp) mice                      8070635 1994       0   1
to a 3-fold reduction in gene expression as well as a significant                2041767 1991       0   0
to a threefold reduction of mRNA and protein levels of acyl                     10751229 2000       0   0
two- to threefold decrease of transcription from most yeast promoters and a     10581267 1999       0   0
                                                                                 1413541 1992
two- to three-fold reduction in transcription. Transcription decreased to an almost                 0   0
in a 2-3-fold reduction in gene expression in wild type                          9565583 1998       0   0
in a 2.5-fold decrease in the mRNA half-life. These results underscore          12949089 2003       0   0
produced a 2.5-fold decrease in mRNA translation rate in both rabbit             7979405 1994       0   0
tumors, a 1.2-3.6-fold reduction of mRNA signals of the 5 genes                 12385006 2002       0   0
However, the level of Ad2+ND5-specific mRNA was depressed twofold                2999436 1985       0   0
observed a 2-fold decrease in adipsin mRNA in the obese rats                     2930496 1989       0   0
in a 2-fold decrease in apoA-I mRNA with no significant change                   9169468 1997       0   0
in total intestine. Rat hepatic apoAIV mRNA decreased twofold                    8020488 1994       0   0
                                                                                10590230
to 12-O-tetradecanoylphorbol-13-acetate (TPA). ASF/SF2 mRNA levels were decreased1999      2-fold   0   1
a 2 fold decrease in beta3-adrenoceptor (beta3-AR) mRNA levels and a 2 10217540 1999                0   0
2 groups; however, beta-CGRP mRNA levels were reduced 2-fold                    10642343 2000       0   1
caused a twofold inhibition of beta-globin mRNA levels, and 5-azacytidine had   10648397 2000       0   1
hours (5.2-fold, P<0.001). Thereafter, BNP mRNA levels decreased (1.8-fold      11897768 2002       0   0
and a 1.9-fold decrease of cardiac alpha-actin mRNA (p < 0.001),                 7680287 1993       0   0
a nearly twofold decrease of basal c-myc mRNA (P< .05) and a                     8614006 1996       0   1
to 1.7-fold above control values. COL1A1 mRNA decreased 2-fold                  10430646 1999       0   0
Moreover, the half-life of CPA1 mRNA is reduced twofold                          2406564 1990       0   1
However, steady-state levels of total DHFR mRNA decreased 2.0-fold               2592384 1989       0   0
(a transient twofold decrease in E1A mRNA accumulation was observed in CREF      2972843 1988       0   0
whereas levels of ecNOS mRNA transcripts were reduced twofold                    8594908 1995       0   1
noted a twofold reduction of hepatic GHR mRNA in the transgenic                 12423624 2002       0   0
due to twofold reduction in the glucoamylase specific mRNA This                  2848632 1988       0   0
about a 2-fold decrease in insulin and glucokinase mRNA levels compared 8070343 1994                0   0
A 2-fold downregulation of HCR mRNA expression was observed on                  14675183 2003       0   1
2-fold decrease in hsp90 mRNA levels is observed after                           1525042 1992       0   0
and a twofold reduction in IGFBP-6 mRNA in the lungs, but                       12775111 2002       0   0
hormone receptor and IGF-I mRNA levels were reduced 1.7-fold                     9398004 1997       0   1
expression of IL-1beta mRNA in the diencephalon decreased 1.5-fold               9565638 1998       0   0
about a 2-fold decrease in insulin and glucokinase mRNA levels compared 8070343 1994                0   0
the suckling-weaning transition, insulin receptor mRNA level decreased 2-fold    7750897 1995       0   1
                                                                                10096790 1999
produced a twofold reduction in insulin receptor substrate-1 mRNA expression in the                 0   0
in a twofold decrease in kallikrein mRNA levels. These findings suggest          8738807 1996       0   0
                                                                                 in atrial
an approximately twofold decrease in total Kv4 subfamily mRNA expression 8033339 1994               0   0
only a 2-fold drop in lacZ mRNA or galactoside transacetylase                    6319355 1984       0   0
                                                                                 8179822
caused a two-fold reduction of leukotoxin transcription in Escherichia coli, suggesting 1994        0   0
Surprisingly, L-PGDS gene expression is reduced 2-fold                          12518068 2003       1   0
Constitutive mRNA expression of MMP-9 was reduced twofold                        9210959 1997       0   0
found a 2-fold reduction in placental PGDH/GAPDH mRNA concentrations (0.28 +/-  11238526 2001       0   1
In cyclic animals, RBP mRNA expression decreased two-fold                        8049061 1994       0   0
only a twofold decrease in kidney renin mRNA content, as compared              3049341 1988   0   0
a two fold decrease in rPLII mRNA levels. Using DNA transfection               9790263 1998   0   0
in a 2-fold reduction in SPO13 mRNA levels during meiosis, indicating          9303311 1997   0   0
and a twofold reduction of the steady-state SRB1/PSA1 mRNA In                 10075413 1999   0   0
an approximate 2-fold reduction in talin mRNA levels compared with stromal 9738453 1998       0   1
TGF-beta1 was downregulated and the TGF-beta1 mRNA decreased twofold          10637094 2000   0   0
to a 1.7-fold decrease in topoisomerase II mRNA stability with no              8267650 1993   0   1
gene and two-fold reduction of topoisomerase II alpha mRNA content were 10496023 1999         0   0
1.5- to 2-fold decrease of TPA mRNA levels in passage 1,                       9108786 1997   0   0
provoked a 2-fold decrease in UCP2 mRNA levels. Human recombinant leptin      10066437 1999   0   0
7 bases of the AP-1 site reduced transcription two-fold and ablated            8756333 1996   0   0
A 2-fold decrease in mRNA abundance was observed after irradiation,           10517849 1999   0   1
                                                                               7979405 1994
A corresponding 2-fold reduction in mRNA binding affinity for reticulocyte eucaryotic         0   0
A further 2-fold drop in transcription activity was attributed to the region   7803234 1994   0   0
A twofold decrease in mRNA expression of an isoform of alternative            10022522 1999   0   0
an estimated two-fold decrease in mRNA level and a 65-fold decrease            2174744 1990   0   0
by the 2-fold decrease in mRNA stability observed. This is consistent          2444925 1987   0   0
II alpha mRNA were noted to be reduced 2-fold                                  7712479 1995   0   1
is a 2-fold decrease in the mRNA for the glycolytic enzyme,                    3078566 1988   0   1
                                                                               9223489 1997
of transcription efficiency. However, transcription efficiency was reduced twofold            0   0
                                                                               8819312 1996
resulted in 2-fold decrease in the transcription rate. The core light-responsive              0   0
to a two-fold decrease in mRNA levels for all genes studied,                   3047675 1988   0   0
to a twofold reduction in transcription and a preferential use of upstream     8076817 1994   0   0
was a twofold decrease in transcription (AC 63.1 +/- 9.3) accompanied          9879497 1998   0   0
excess of D3 mRNA and reduced D2 mRNA (0.1-fold of normal pituitaries).12072042 2002          0   0
VEGF decreased thrombospondin-1 mRNA 0.41-fold after 4                        10027393 1999   0   0
fibrillary acidic protein (GFAP) mRNA were significantly increased 0.4-fold 9219877 1997      0   0
The level of GFAP mRNA was significantly increased 0.5-fold                    9219877 1997   0   0
less than 0.5-fold increase in transcription rates of these genes under        9345268 1997   0   0
in a 1.9-fold increase in the 4.8-kb TGF-alpha mRNA transcript, and TGF-alpha  8368318 1993   0   0
HF diet increased the hepatic ABCA1 mRNA 1.8-fold in WT,                      12487373 2002   0   0
and Go alpha mRNA levels were transiently increased 1.5-fold                   7873600 1995   0   0
only a 1.7-fold increase in alpha subunit mRNA levels. Down regulation         2516449 1989   0   0
a 1.6 fold upregulation of the alpha1a-AR mRNA without significant effects 11693201 2001      0   1
                                                                              12235144 2002
also demonstrated that alpha2,8-sialyltransferase III mRNA expression increased 1.7-fold      0   0
                                                                                 effect
caused a 1.8-fold increase in angiotensinogen mRNA accumulation, and this2839039 1988         0   0
for a 1.8-fold increase of angiotensinogen mRNA at week The                   11401419 2001   0   0
groups, but kidney angiotensinogen mRNA level was increased 1.6-fold           9176018 1997   0   1
We found that indeed ApoB-100 mRNA increased 1.8-fold                          1417837 1992   0   0
1.4- to 1.5-fold increase in hepatic apoC-III mRNA levels, by Northern         7868970 1994   0   1
                                                                              11101207
showed a 1.6-+/-0.1-fold increase in APP mRNA compared to untreated nonimpacted 2000          0   1
induced a 1-fold increase of AR mRNA compared with unexposed cells,            8804569 1996   0   0
produced a 1.3-fold increase in AR mRNA and a 2.2-fold increase               12692781 2003   0   0
1.7- to 2-fold increase in caspase-1 mRNA. Bcl-2 mRNA decreased 2.4- 14691177 2004            0   1
and a 1.5-fold elevation of beta-globin mRNA when assayed by RNA              11074543 2000   0   1
1.1- to 2.6-fold increase in steady-state lung beta-PPT mRNA and a 50          9252538 1997   0   0
and transient 1.5-fold increase in bFGF mRNA while shear of 36                 8408655 1993   0   0
produced a 1.8-fold increase in BMP-2 mRNA expression by the                   9587316 1997   0   1
in a 1.5-fold increase of C/EBP beta-mediated transcription in insulin-treated1372389 1992    0   1
probes revealed that the Ca(2+)-ATPase mRNA levels increased 1.6-fold 8287415 1993            0   1
Atrial levels of cACT mRNA were increased 1.9-fold                             9539873 1998   0   0
                                                                              10415005 1999
an approximately 1.8-fold increase in CD40L mRNA abundance. In response to trinitrophenol     0   0
 When preload was increased, c-fos mRNA rose 1.8-fold                      8287409    1993   0   1
and a 1.2-fold increase in citrate synthase mRNA from late foetal          8158120    1994   0   1
hour after E2 injection, c-jun mRNA levels increased 1.8-fold             11193187    2001   0   1
a significant 1.6-fold increase in CK-M mRNA and a 2.2-fold increase       1887884    1991   0   1
The mRNA of c-myc was increased 1.8-fold                                   8287409    1993   0   1
showed an 1.8-fold increase of cortical EP3 receptor mRNA expression as 14636300      2003   0   0
a small 1.6-fold increase in CYP2B1/2 mRNA levels. 6. Precision-cut lung 12893519     2003   0   0
A similar 1.4-1.7-fold increase in CYP4A8 mRNA was also found in 3-        9281597    1997   0   0
of reserpine (10 mg/kg i.p.) elevates DBH mRNA 1.5-fold by 6               7984052    1994   0   0
Relative mRNA levels for DHPR were increased 1.2-fold                     10423342    1999   0   1
and a 1.24-fold increase in enoyl-CoA hydratase (ECH) mRNA in rats,       14669153    2003   0   0
a limited 1.4-fold increase in ER mRNA at 10(-7) In                        9328213    1997   0   1
in 3 days. The ER mRNA level increased 1.5-fold                            7974526    1994   0   0
reveal a 1.7-fold increase in ERalpha mRNA that was not significant,      14654987    2004   0   1
adipocyte fatty acid binding protein mRNA levels increased (1.5-fold      11473052    2001   0   0
diabetes, the levels of fibronectin mRNA were increased 1.3-fold           8603829    1996   0   0
0.8 kb for ELH. FMRFamide mRNA level increased 1.5-fold                    1912481    1991   0   1
P<0.05), and 1.4+/-0.09-fold increase in FN mRNA compared with 5 mmol/l11522874       2001   0   1
culture for 72 h increased FSH beta mRNA 1.5-fold (P less                  1370794    1992   0   0
in a 1.5-fold increase in hypothalamic GALP mRNA levels. Next, GALP       12746327    2003   0   1
                                                                          11972604
(12.8 +/- 1.0). Similarly, gamma-GCS mRNA expression increased 1.3-1.6-fold           2002   0   1
with 6-hydroxydopamine (6-OHDA), GFAP mRNA level is increased 1.4-fold 2496892        1989   0   1
the LLC of cattle. Furthermore, GHR mRNA increased 1.8-fold                8886596    1996   0   0
in a 1.9-fold increase in ghrelin mRNA levels relative to control         11517195    2001   0   0
and a 1.6-fold increase in glomerular TGF-beta mRNA expression (4          7731171    1995   0   0
caused a 1.5-fold increase in expression of GLUT4 mRNA and protein         7846068    1995   0   0
to a 1.5-fold increase in GRalpha mRNA and a 2.0-fold increase            11381138    2001   0   0
and a 1.5-fold increase of H4 mRNA in the cytoplasm after                  3038171    1987   0   1
in a 1.3-fold increase in nuclear H4 histone mRNA levels and a             3038171    1987   0   1
demonstrated a 1.8-fold elevation of HCN4 mRNA and no significant change  11534852    2001   0   1
of HDAC1 mRNA in GC tissue was increased 1.8-fold                         11749695    2001   0   1
found 1.4-2.5 fold elevation of HL mRNA with concomitant lowering of HDL11451387      2001   0   0
In addition, HO-1 mRNA transiently increased 1.6-fold                     12392996    2002   0   1
At low glucose, IAPP mRNA levels were increased 1.9-fold                   9142872    1997   0   0
demonstrated a 1.8-fold increase in ICAM-1 mRNA when compared with control14507893    2003   0   0
                                                                           8794821
sustained, approximately 1.8-fold increase in ICAM-1 mRNA levels in 11% strained      1996   0   1
levels and mRNA expression of IGFBP-2 were increased 1.6-fold              9398004    1997   0   1
1.7 to 2.2-fold increase in IGF-I receptor mRNA levels in kidney,          8695914    1996   0   1
IFN-alpha mRNA at both concentrations. IL-1alpha mRNA increased 1.4-fold   8836922    1996   0   0
                                                                          whereas
h almost completely blocked induction of IL-1Ra mRNA (1.9-fold induction) 14598021    2004   0   0
renal TNF-alpha or IL-6 mRNA level significantly increased 1.9-fold       11928713    2002   0   0
and a 1.5-fold increase in ileum apo A-IV mRNA levels, although            8412754    1993   0   0
only a 1.7-fold increase in laminin mRNA between the two cell              2885332    1987   0   0
increased 1.4-fold and LCAT mRNA levels were increased 1.3-fold            8808761    1996   0   0
                                                                           9687543
in a 1.5-fold increase in hepatocyte LCAT mRNA accumulation, whereas butyrate         1998   0   0
In mouse liver, too, LDL-receptor mRNA levels increased 1.5-fold           8375391    1993   0   0
Diabetes, independent of diet, also increased lipase mRNA 1.6-fold (P <    7524347    1994   0   0
2.6-fold and 1.2-fold induction of MCP-1 mRNA expression in HUVECs,       11866893    2000   0   0
                                                                           strained
mainly serum-independent 1.8-fold induction of MCP-1 mRNA levels in ECs 8967390       1996   0   1
tissue, a 1.2-fold increase in the expression of mRNA for m-CSF           12202518    2002   0   1
normal pancreas, MDR1 mRNA levels were only increased 1.4-fold            11039467    2000   0   1
as upregulation of pro-MMP2. MMP2 mRNA was upregulated 1.7-fold           12844104    2003   0   1
+ V stimulation, and MMP-9 mRNA was elevated 1.3-fold                       12485640 2003    0   0
and a 1.8-fold induction of MRP1 mRNA levels were seen in the               11697747 2001    0   1
a corresponding 1.5-fold induction of MRP3 mRNA levels (p <                 11697747 2001    0   1
                                                                            11404249 2001
showed a 1.5-fold increase in the Na-K-ATPase beta1-subunit mRNA levels and up               0   0
mice) and a modest increase in NaPi-2 mRNA (1.3-fold in both                  8927512 1996   0   0
sulfoxide, the rate of NE gene transcription increased 1.9-fold               1586720 1992   0   0
achieve a 1.7-fold increase in NGF mRNA compared to control in the            9120757 1997   0   0
NHE-1 mRNA in human lymphocytes increased 1.5-fold                            7511337 1994   0   0
states, both NHE2 and NHE3 mRNA levels increased 1.5-fold                     8779923 1996   0   0
4 days, the NPT2 mRNA level was increased 1.8-fold                          10497181 1999    0   0
measured by ribonuclease protection assay, NPY mRNA increased 1.5-fold12008019 2002          0   0
A 1.9-fold increase in O6-AGT mRNA was observed after partial               11599795 2001    0   0
1.2-, and 1.75-fold increase in ob mRNA expression and a 3.8-,              10098489 1999    0   0
a further 1.8-fold increase in ODC mRNA was observed at 8                     2082182 1990   0   0
and a 1.9-fold increase in osteocalcin mRNA above untreated controls at 12923462 2003        0   0
with a 1.5-fold increase in OT mRNA after 7 days of osmotic                   3780571 1987   0   1
                                                                              9
only a 1.5-fold increase in p21WAF1/CIP1 transcription but a three- to six-fold513045 1998   0   0
to a 1.75-fold increase of P450C21 mRNA and a 3.31-fold increase              9888542 1998   0   0
                                                                            11226075 24
toxin-stimulated cAMP synthesis. Cholera toxin increased P450scc mRNA 1.4-fold after 2001    0   0
1-fold increase in PAI-1 mRNA expression, its effect underwent              10432384 1999    0   1
The PCNA mRNA level was also increased 1.9-fold                             14614307 2000    0   0
within 180 min. PGHS-1 mRNA level was increased 1.6-fold                    10367586 1999    0   0
combined IL-1 and TGF-alpha. PGHS-2 mRNA was increased 1.4-fold               8079657 1994   0   1
determination of luciferase activity. PGIS gene expression increased 1.7-fold9202659 1997    0   1
found a 1.8-fold increase in PPE mRNA levels in the VMH                       8717366 1996   0   0
A 1.5-2-fold increase in PPE mRNA levels was observed in estradiol-treated 9449413 1997      0   0
1.5 +/- 0.1-fold upregulation of preproET-1 mRNA (p = The                     9861306 1998   0   0
approximately 1 fold increase in proenkephalin gene expression in the NTS, 7898313 1994      0   0
compared to 1.9-fold increase in IAS-treated mice. PSA mRNA expression levels 8809195 1996   0   0
in a 1.5-fold increase in rabCyP18 transcription and an increased PPIase 10611060 2000       0   0
1.9 +/- 0.5-fold increase in rap1a mRNA was observed at 14                    8832211 1996   0   1
induction of ras mRNA. ras mRNA level increased 1.5-fold                      1551479 1992   0   0
                                                                              8242609 1993
demonstrated a 1.9-fold increase in RB mRNA following castration that parallels              0   0
to a 1.4-fold increase of renin mRNA in the kidneys of sham-treated           8203557 1994   0   0
caused a 1.5-fold increase in the kidney renin mRNA content, as               3049341 1988   0   0
showed a 1.8-fold increase in rGSTA1/A2 transcription rates in ischaemic lobes9461493 1998   0   0
older rats (19 months ole), RhoA mRNA increased 1.9-fold                    11557278 2001    0   0
RT PCR revealed that RhoA mRNA concentration increased 1.9-fold             14556075 2003    0   1
1.5- to 2-fold increase in the transcription of the rpoB and C                 368011 1979   0   0
(1) a 1.8-fold increase of sgk1 mRNA at 3 h (150                            11961006 2002    0   0
to 10(-7) M increased SP-A and SP-B mRNA 1.5-fold and SP-C                  12538780 2003    0   0
in a 1.5-fold increase in TGF-alpha mRNA levels within 4 h                    8398905 1993   0   0
                                                                              9356238
showed a 1.66-fold increase in TGF-beta1 mRNA levels when compared to ischemic 1997          0   0
stimulated a 1.7-fold increase in mRNA encoding TIMP-3 compared with          8699421 1996   0   1
displayed a 1.5-fold increase in transferrin receptor mRNA and protein and a7671248 1995     0   0
                                                                            10633010 1999
in a 1.9-fold increase in transforming growth factor-beta1 mRNA level compared               0   0
promoter activity, and transin mRNA levels were increased 1.8-fold            9357821 1997   0   0
The type I procollagen mRNA was elevated 1.4-fold                             2383596 1990   0   0
caused a 1.8-fold increase in tyrosinase mRNA levels. A tumor promoter, 1823929 1991         0   1
a further 1.5-fold rise in the UVA-induced HO-1 mRNA In                     12057767 2002    0   0
The half-life of uvi15(+) mRNA was also increased 1.5-fold                  10954610 2000    0   0
that the rate of uvi15(+) transcription was increased 1.8-fold              10954610 2000    0   0
                                                                                 7683841 1993
by hypothalamic vasopressin mRNA concentrations was significantly increased 1.85-fold           0   0
After hypoxia, VEGF mRNA levels increased 1.8-fold                              10634417 2000   0   1
1.2 +/- 0.03-fold increase in rat VP mRNA seen in normal                         8100353 1993   0   1
and a 1.6-fold increase in VP mRNA levels of the                                 3772378 1986   0   0
in a 1.85-fold increase in VP mRNA levels of the SON                             3772378 1986   0   0
caused a 1.8-fold increase in VPF mRNA levels after 4 hours,                     1719968 1991   0   0
was a 1.25-fold increase in both transcription and steady-state mRNA             3122771 1987   0   0
                                                                                12906923 2003
on transcription (1.2-fold increase in transcription vs. 5.5-fold increase in ppET-1            0   0
1.5- to 2-fold increase in extractable mRNA was observed. These data              903378 1977   0   0
(-453 to -184) show modest increases in transcription (1.5-fold or less)         2016766 1991   0   0
a significant 1.7-fold increase in renal cortical mRNA expression of alpha(v)12629275 2003      0   0
and renin mRNA level in the kidney increased 1.5-fold                            2405694 1990   0   1
Ca2+ produced 1.5-fold increase in mRNA levels for the DHP                       9236134 1997   0   1
activity and 1.6-fold increase in mRNA in response to 10 ng/ml                   7814638 1995   0   0
and a 1.6-fold increase in mRNA levels. No change in biosynthesis               11668031 2001   0   0
induce a 1.6-fold increase in transcription activity, whereas a large family     8631965 1996   0   0
to a 1.6-fold increase in mRNA encoding for type IV                              2383596 1990   0   0
a 1.7 fold increase in the rate of transcription for the pro-alpha               8835848 1996   0   0
A 1.7-fold induction of mRNA expression and a 3.5-fold induction                10814841 2000   0   0
caused a 1.7-fold increase in the mRNA level. This procedure was                 8228572 1993   0   1
produced a 1.8-fold increase in the amount of mRNA for the normal                2496935 1989   0   0
in a 1.9-fold increase in mRNA expression of the nucleotide excision            12359362 2002   0   0
1.5- to 2-fold increase in transcription of this gene in virulent                9724875 1998   0   1
Insulin increased 3 beta HSD mRNA twofold over basal                             9420856 1995   0   0
about a 2.5-fold increase in 5-LO mRNA and triggered a redistribution           12671301 1998   0   0
demonstrated a twofold increase in the 92-kDa mRNA level in response             9357863 1997   0   1
2.7 +/- 0.3-fold increase in A3AR mRNA in RBL-2H3 cells treated                  7730645 1995   0   1
in a 2-fold increase of ABP mRNA as revealed by Northern                         1511092 1992   0   1
found a 2.8-fold increase of ACE mRNA (n = 3; P                                  7485557 1995   0   0
muscle cells, ACLP mRNA and protein were up-regulated 2-3-fold                   9624159 1998   0   0
a rapid 2-fold increase in ACP-22 mRNA and is not able                           9087546 1993   0   0
2.3 +/- 0.1-fold increase in ACS mRNA levels and induced ACS                     8967477 1996   0   0
only a 2-fold increase in ACTH-R mRNA and a small decrease                       7588377 1995   0   0
with a 2-fold increase in actin gene transcription and a 10-                     8021252 1994   0   0
indicated a 2-fold increase in ADH mRNA in the treated animals                   1626640 1992   0   1
codons in the ADH5 mRNA increased gene expression twofold in CV-1, 11368338 2001                0   0
12 h increased expression levels of ADM mRNA 2.2-fold and fivefold              10477134 1999   0   0
showed a 2-fold increase in ADM gene transcription which was suppressed10980200 2000            0   0
short-term endotoxemia, adrenalectomized rat lung GS mRNA increased twofold      9435573 1997   0   0
and a 2.1-fold increase in Adx mRNA levels, and in the Z-F-R                     2626031 1989   0   1
of hypothalamic Pomc to Agrp mRNA was elevated two-fold                         14636173 2003   0   0
blood cells, 2-fold increase in the ALAS mRNA and increase from                 10215191 1999   0   0
A two-fold increase in alpha mRNA occurred between 0800-2000 h                   2428604 1986   0   0
Alpha and FSH-beta mRNA concentrations increased 2-fold                          7545437 1995   0   0
2- to 2.5-fold, while alpha mRNA levels increased 2.5-fold                       2751830 1989   0   0
caused a 2.3-fold increase in the alpha 1 mRNA and a 4.7-fold                    8238401 1993   0   0
greater than 2-fold increase in alpha 1(II) mRNA at Day 7                        7944410 1994   0   1
acute-phase response alpha 1PI mRNA levels were increased twofold                2473162 1989   0   0
                                                                                 1572409
approximately a twofold increase in the alpha-casein mRNA transcription rate in cells 1992      0   0
a selective twofold increase in alpha-subunit mRNA (from 266 +/- 18              3337227 1988   0   0
pulsatile GnRH, while alpha-subunit gene transcription was elevated 2-fold 2126596 1990         0   0
104-R cells, the androgen receptor mRNA level increased 2.5-fold                 7511045 1994   0   0
RESULTS: Angiotensin type 1 mRNA was maximally upregulated 2-fold 11986592 2002          0   0
caused a 2.4-fold increase in angiotensinogen mRNA level. We conclude from8142296 1994   0   0
A twofold induction of hepatic angiotensinogen mRNA levels in E2-OVX      1316402 1992   0   1
adrenal glands, the hepatic angiotensinogen mRNA levels increased 2.7-fold2192214 1990   0   0
age, whereas levels of ANP mRNA were elevated twofold                     7573495 1995   0   1
After 3 weeks hypoxia ANP mRNA had increased 2.7-fold                     9094257 1997   0   0
2- to 3-fold increase in the gene expression of both APLP2                9121703 1997   0   1
in a 2-fold induction of apo AI mRNA and, a one-third                     1811554 1991   0   0
the half-life of apo AI mRNA was increased 2-3-fold                       7628462 1995   0   0
The apo A-I mRNA level was increased 2.3-fold                             1654887 1991   0   0
with a 2.5-fold increase in ApoA1 mRNA in young rats and a                8997358 1996   0   0
The sucrose-rich diet increased apoA-IV gene expression twofold in both   8408629 1993   0   0
and editing of the endogenous apoB mRNA increased 2-fold                  8051066 1994   0   0
reduced to half and apoC-III mRNA was increased two-fold                 10805503 2000   0   0
for a 2-fold increase of the apoE mRNA level. The increase                8297388 1994   0   0
The 2-fold increase in translatable apoE mRNA correlates with a similar   2722811 1989   0   0
drug, a 2-fold induction in apolipoprotein A-I (apoA-I) mRNA levels       8900208 1996   0   0
was a 2.3-+/-0.2-fold increase in APP mRNA in the thalamus of treated    11101207 2000   0   1
If this twofold increase in the APP-751 mRNA/APP-695 mRNA ratio results 2460367 1988     0   0
                                                                         Sham-operated
2.2- and 1.8-fold increase in AQP2 mRNA expression when compared with15010283 2004       0   0
2.0 +/- 0.5-fold increase in AR mRNA level was observed, without          1315310 1992   0   0
In contrast, argininosuccinate synthetase mRNA was induced 2-fold         2547341 1989   0   0
                                                                         14654987 2004
demonstrate a 2.4-fold increase in aromatase mRNA level which is confirmed               0   1
                                                                         12433659 2003
an approximately 2.5-fold increase in AT(1) mRNA levels, which was markedly              0   0
whereas a twofold increase in AT(1A) mRNA level but not in AT(1B)         8698443 1996   0   0
caused about 2-fold increase in AT1 mRNA levels, and this increase       11108153 2000   0   1
and a 2.3-fold increase in AT1 mRNA (P<.05). Tumor necrosis factor-alpha 9231818 1997    0   0
AT2 receptor mRNA was then increased 2-fold                              10190134 1998   0   0
vitro, a 2-fold increase in A-utrophin mRNA level was Expression         11726694 2001   0   0
basal and stimulated conditions. Brain AVP mRNA increased 2.2-fold        8203636 1994   0   1
revealed a 2.6-fold increase in BACE-2 mRNA levels in the DS             12895444 2003   0   0
observed a 2.1-fold increase in Bcl-2 mRNA levels in the Akt             10753867 2000   0   0
an approximately twofold increase in mRNA level of Bcl-XL by 6            9393984 1997   0   0
level of brain-derived neurotrophic factor (BDNF) mRNA increased two-fold 8510496 1993   0   1
The beta mRNA abundance also increased 2-3-fold                           2846580 1988   0   0
an approximate two-fold increase in beta 1 mRNA accumulation. A maximum   8408640 1993   0   0
overall approximately 2-fold increase in mRNA beta 1 content with no     10091577 1999   0   1
and a twofold increase in beta 2AR mRNA levels. Exposure of cells         1320040 1992   0   0
caused a 2.3-fold increase in beta 3-adrenoceptor mRNA levels, which was 8706762 1996    0   0
in a twofold increase in beta 3-AR mRNA and a fivefold                    7733267 1995   0   0
produced a two-fold increase in beta 3-AR mRNA in ob/ob mice              9347404 1997   0   0
found a twofold increase in beta actin mRNA and a four-                   1730382 1992   0   0
a significant two-fold increase in total beta APP mRNA in nucleus         2513588 1989   0   0
However, only the beta G-GA mRNA is increased 2.5-fold                    8760253 1996   0   0
at lower levels. beta glycan mRNA levels increased 2-fold                11897700 2002   0   0
a 2 fold increase in beta1-AR mRNA levels. 3. Binding studies            10217540 1999   0   0
demonstrated by RT-PCR. Expression of betaA mRNA increased 2-fold 14738881 2004          0   0
only a 2.3-fold increase in the beta-actin mRNA level. Although the rat  10488052 1999   0   1
showed a 2.3-fold increase in beta-actin mRNA and a 2.5-fold increase     8951105 1996   0   1
Both beta- and gamma-actin mRNA are elevated 2.5-fold                     6548547 1984   0   0
greater than twofold increase in beta-myosin heavy chain mRNA and an      8508529 1993   0   0
An almost 2-fold increase in beta-pol mRNA was observed 18-24 h           2736248 1989   0   0
a modest twofold increase in bFGF mRNA (P < Rats                            11509513 2001   0   0
elicited a 2-fold increase in bFGF mRNA in the cortex and hippocampus.        8381505 1993  0   0
caused a 2.5-fold increase in bFGF mRNA and considerable bFGF protein 8545077 1995          0   1
elicited a 2-3-fold increase in bFGF and NGF mRNA content in rat              8381505 1993  0   0
elicited a 2-3-fold increase in bFGF and NGF mRNA in the cerebral             8381505 1993  0   0
made chronically acidotic, the bGH mRNA was increased twofold                 8770165 1996  0   0
showed a 2-fold increase in mRNA level for BGP, and a greater                 8453631 1993  0   1
2-fold to 3-fold up-regulation of BMP-2 mRNA expression in bovine capillary 12045566 2002   0   0
The left ventricular BNP mRNA levels increased 2.2-fold                     11897768 2002   0   0
a approximately 2-fold increase in the transcription of the BSP gene,         9178100 1997  0   0
h a twofold increase in C/EBP alpha mRNA was Treatment                        9349591 1997  0   0
produced a twofold induction of C/EBP alpha mRNA after 8                      9349591 1997  0   0
produced a 2.7-fold induction of C4BP mRNA levels. In the absence             1339286 1992  0   0
less than 2-fold increase in CaBP mRNA levels. Previous studies have          3691957 1987  0   0
D-replete rats, renal calbindin protein and mRNA increased 2.5-fold           2460748 1988  0   1
wt), a 2.6-fold rise in calcitonin mRNA occurred in adrenalectomized rats     2599094 1989  0   1
                                                                               muscle
an approximate two-fold increase in calmodulin-specific mRNA in dystrophic 2965585as 1988   0   0
parathyroid, thyroid, and kidney CASR mRNA levels increased 2-fold          12036954 2002   0   0
treatment, a 2.4-fold increase in catalase mRNA was observed, which was 10802226 2000       0   0
to a twofold increase in cathepsin L mRNA expression, whereas TGF-beta 10849756 2000        0   0
                                                                              8424948 1993
2.6 +/- 0.5-fold increase in steady-state cAT-III mRNA levels. Assay of functional          0   1
increased PtdCho synthesis (2-fold). CCTalpha mRNA was increased 2-fold     12659631 2003   0   0
protein and mRNA levels. CEH/HSL mRNA levels increased twofold                8527515 1995  0   0
by 18 h. Hepatic ceruloplasmin mRNA content increased 2-fold                  3360784 1988  0   0
although a twofold increase of the c-fos mRNA level immediately after         9655520 1998  0   0
and a 2-fold increase in c-fos mRNA levels. In comparison, stimulation        8752305 1996  0   0
                                                                            12632510 2003
control-animals (0.74+/-0.22, P<0.01). C-fos mRNA levels were increased 2.5-fold            0   1
elicited a 2-fold increase in CGRP mRNA and a 9-fold increase                 8061571 1994  0   1
of a 2-fold increase in cholesterol esterase mRNA was observed after          8138719 1994  0   0
only a 2-fold increase in c-jun mRNA levels. In transient transfection        8838143 1996  0   0
A 2.4 fold increase in c-jun mRNA was apparent after 4                        9258340 1997  0   0
Also, BN transiently increased c-jun mRNA twofold and the increase            7784258 1995  0   0
                                                                            12324757 2002
RESULTS: A 2.5-fold increase in c-jun mRNA expression was detected in Ad5aTGF-beta1-infected0   1
and a 2.2-fold increase of CK-B mRNA 5 h after insulin                        1887884 1991  0   1
The c-met mRNA expression was increased twofold                             11669338 2001   0   1
A small, twofold increase in c-myc mRNA levels and transcription levels       8149351 1994  0   0
6. The c-myc mRNA level increased 2.1-fold                                    8187933 1994  0   0
In contrast, ventricular c-myc mRNA content increased twofold                 8313569 1994  0   0
and a two-fold up-regulation of CNTF mRNA levels, trophic factors that      12076088 2002   0   1
2- to 3-fold increase in collagen mRNA levels upon acetaldehyde               8048746 1994  0   0
was essentially unchanged, whereas collagen mRNA content increased 2-fold     8587226 1995  0   0
the levels of collagen IV mRNA were increased twofold                         8282817 1994  0   1
alpha 1 collagen IV mRNA levels were increased 2.3-fold                       8973474 1996  0   0
thyroid hormone-treated Wistar rats. Connexin43 mRNA was elevated 2.1-fold  11076030 2000   0   0
In ischemic cortex CRH mRNA levels were elevated 2.6-fold                     8541482 1995  0   0
greater than 2-fold increase in cortical IGFBP-1 mRNA and a 75%               7536658 1995  0   0
in a twofold increase in COT1 mRNA abundance. The gene encodes                1508175 1992  0   0
a transient 2-fold increase in Cox-2 mRNA was noticed bilaterally in the      9561138 1997  0   0
and PAF increased the transcription of COX-2 mRNA two-fold after 8          10338371 1999   0   0
caused a two-fold increase in Cox-2 mRNA in both normal and transformed 9111217 1997        0   0
revealed a twofold increase in COX-2 mRNA that reached baseline again 9892042 1998          0   1
exhibited a 2-fold increase in hepatic CPT transcription rate and CPT         2543360 1989  0   0
and a 2.3-fold elevation of muscle CPT I mRNA levels, as                    11158930     2001   0   0
a 2 fold increase in mRNA and activity of CPT I                               9546617    1998   0   0
an approximate two-fold increase of CRABP-II mRNA levels was seen in cells    8179592    1994   0   1
The level of lung CRBP mRNA increased 2.3-fold                                3190677    1988   0   0
CRABP-II mRNA and CRBP-I mRNA were modestly elevated (2.5-fold                1332208    1992   0   0
in a 2.1-fold increase in CRF mRNA levels in the parvocellular                8401558    1993   0   0
was a 2.5-fold increase in CRF mRNA derived from polyadenylation at           7877440    1994   0   0
in a twofold rise in CRH mRNA content (P less than                            2333962    1990   0   0
Levels of CRP reporter gene expression were increased 2-fold                  9395482    1997   0   0
                                                                              skeletal
revealed a two-fold increase in c-ski mRNA during terminal differentiation of 8573720    1995   0   1
The two-fold increase in mRNA synthesis of c-src oncogene after               8054999    1993   0   0
A 2-fold increase in CT mRNA level measured by dot-blot                       3838942    1985   0   0
We found that CT mRNA increased 2-fold                                        8615772    1996   0   0
greater than 2-fold increase in CTGF mRNA levels, which was attenuated 14592956          2004   0   1
Cyclin D1 mRNA levels were increased 2.8-fold                                 8761413    1996   0   1
The cyclin E mRNA level was increased 2.7-fold                              14614307     2000   0   0
polyclonal anti-CYP2J4 antibody. CYP2J4 mRNA levels were increased 2.5-fold 10497137     1999   0   0
                                                                            12673034
approximately a 2-fold induction of the CYP3A7 mRNA level. Treatment with rifampicin     2003   0   0
In wt mice, dietary feeding up-regulated Cyp4a14 mRNA 2.7-fold and increased12829994     2003   0   0
LXR-alpha, reflected activation. CYP7A1 mRNA and activity increased twofold 14684380     2004   0   0
a nearly two-fold increase in gene expression of the D2 dopamine            10320779     1999   0   0
with normal pituitaries. D2 mRNA was also increased 2.6-fold                12072042     2002   0   0
than a twofold increase in decorin mRNA after 1, 2, 3,                        9815141    1998   0   0
Approximately a 2.2-fold increase in decorin mRNA levels, was found by        7625849    1995   0   1
Stearoyl-CoA desaturase mRNA levels were transiently increased (2.7-fold 11172741        2001   0   0
produced a 2.2-fold increase in DHP receptor mRNA levels at 2                 8609220    1996   0   1
Expression of DMP1 mRNA in osteocytes increased 2-fold                      12733719     2003   0   0
caused a 2.5-fold increase in DNase I mRNA within 30 min                    12514269     2003   0   0
a concomitant 2-fold increase in dopamine D2-receptor (D2-R) mRNA Despite     9147288    1997   0   0
and a 2.4-fold increase in duodenal CCK mRNA levels. Simultaneous intravenous 1969232    1990   0   0
A 2-fold induction of dynorphin mRNA by 24 hours, followed                    9587487    1997   0   1
A two-fold induction of dynorphin mRNA by 24 h, followed                      9243520    1997   0   0
as a 2.7-fold increase in specific EC PAI-1 mRNA expression after             8172858    1994   0   1
was a 2-fold increase in E-Cad mRNA concentrations between postnatal ages     7679970    1993   0   1
a 2.2 fold increase in ecNOS mRNA levels. These findings suggest              9449657    1998   0   1
iNOS were found. mRNA levels for ecNOS increased 2-fold                       9735341    1998   0   1
and a twofold increase in liver EGF mRNA between 3 and 10                     3260454    1988   0   0
An approximately twofold increase in intestinal EGF mRNA and protein was    10484377     1999   0   0
greater than 2-fold increase in EGFR mRNA and 50% more EGFR                   7606741    1995   0   0
TGF alpha also increased transcription of EGF-R mRNA 2-3-fold in KB           9839451    1998   0   0
                                                                              7626022
3.5- and 2-fold increase in elastin synthesis, elastin mRNA level and transcriptional    1995   0   0
induced a 2-fold increase in endoglin mRNA levels in both Eng(+/+)          12411467     2002   0   1
was a 2.5-fold increase in endothelin B mRNA expression after MI            11113050     2000   0   0
about a 2-3-fold increase in mRNA ENK which was abolished by                  2435729    1987   0   0
produced a 2-3-fold increase in eNOS mRNA and protein levels as             10690351     1999   0   1
protein and mRNA expression levels. eNOS mRNA increased two-fold            10235453     1999   0   0
and a 2.8-fold increase in eNOS mRNA half-life. Induction of eNOS           10679488     2000   0   0
was a 2.8-fold rise in eNOS mRNA abundance. Thus eNOS gene                    8928825    1996   0   0
an approximately 2-fold increase in EPCR mRNA and soluble Incubation 10688825            2000   0   1
caused a 2.2-fold increase in epicardial ANP mRNA levels (P <                 8005862    1994   0   0
recombinant human epiregulin. Epiregulin mRNA levels were increased 2.1-fold10891365     2000   0   0
in combination increased ER 5-fold and ER mRNA 2-fold compared with control   7931002    1994   0   0
caused a 2.5-fold increase in ER mRNA (6.6 kilobases) levels after          2785242   1989   0   1
The amount of ET(A)-receptor mRNA increased 2.7-fold                       11078385   2000   0   0
altered whereas ET(B) receptor mRNA levels were up-regulated twofold 11827687         2002   0   0
and a 2.0-fold increase in ET-1 mRNA content in the hippocampus            12401340   2002   0   0
revealed a twofold increase in ET-1 mRNA in the ischemic myocardium         7728993   1995   0   1
By contrast, ET-1 mRNA was induced 2.3-fold                                10625580   2000   0   1
than a twofold increase in mRNA expression of ET-1 as well                 12710522   2003   0   0
a > 2.5-fold induction of ET-1 mRNA in that kidney, which                   7485537   1995   0   0
Whereas ETA receptor mRNA expression increased 2-fold                      14605251   2004   0   0
and a 2-fold increase in ETB receptor mRNA expression at 48                14605251   2004   0   0
F1/GAP-43 mRNA expression was also increased 2-fold                         8510501   1993   0   0
and a 2.5-fold increase in FAS gene transcription (P <                      9227460   1997   0   0
showed a 2.5-fold increase in Fc gamma RII mRNA levels that                 2531041   1989   0   1
leaves, the Fd-dependent glutamate synthase mRNA is induced twofold         9057836   1997   0   0
with a 2.5-fold induction of ferritin heavy chain mRNA and ferritin         9441903   1997   0   0
an approximately 2-fold increase in FGF-2 mRNA level in the hypothalamus 7590624      1995   0   0
for TGF-beta 3 message. Fibronectin mRNA levels increased twofold           1535758   1992   0   0
                                                                           12906161
showed about 2-fold increase of fibronectin mRNA level in hypertrophic scars          2002   0   0
in a 2.6-fold increase in fibronectin mRNA expression within 15 minutes;    7636394   1995   0   0
elicited a 2-fold elevation in follistatin mRNA levels between 1600-2000 h  8612495   1996   0   0
showed a 2.7-fold increase in follistatin mRNA accumulation within 6        7789314   1995   0   0
In contrast, FSH beta mRNA increased 2-fold                                 2502379   1989   0   0
only a 2.7-fold increase in FSH beta mRNA was observed when                 1505470   1992   0   0
h for 10 h increased FSH beta mRNA 2.8-fold (P less                         1370794   1992   0   0
Alpha and FSH-beta mRNA concentrations increased 2-fold                     7545437   1995   0   0
The G gamma mRNA level increased 2.3-fold                                   9502623   1998   0   0
The G6Pase mRNA level was increased twofold                                10459573   1999   0   0
A maximum two-fold increase of GAD67 mRNA was found on the day              9777631   1998   0   1
showed a two-fold increase in galanin mRNA 7 days, but not                  7518895   1994   0   0
of galanin mRNA in GnRH neurons first increased twofold                     9425013   1998   0   0
a near twofold increase in gamma mRNA during a 10-day infusion              7524768   1994   0   0
the ratio of gamma/gamma + beta mRNA increased twofold                      7524768   1994   0   0
Both beta- and gamma-actin mRNA are elevated 2.5-fold                       6548547   1984   0   0
                                                                            9763579
interactions were examined. Expression of gamma-globin mRNA increased twofold         1998   0   0
twofold, and the level of gamma-globin mRNA increased twofold               7677966   1993   0   0
in a twofold increase in GAP-43 mRNA levels. Given this evidence,          12957493   2003   0   0
Glut 4 and GAPDH mRNA were increased 2-fold                                 1301380   1992   0   0
levels were measured. GAPDH mRNA levels were increased 2.5-fold             7931002   1994   0   0
caused a 2.1-fold increase in lung GCR mRNA expression, but GCR            12948937   2004   0   0
Concomitantly, whole brain GCS mRNA levels were increased 2.7-fold          8806884   1996   0   1
A 2-fold increase in the gec1 mRNA level was achieved                       8495796   1993   0   1
to a 2.1-fold increase in the GH mRNA level. Altogether, the present        1955080   1991   0   0
induced a 2.3-fold increase in GH mRNA expression, which could result 14755131        2004   0   1
2- to 2.5-fold increase in GH mRNA levels, and the maximal                  6424119   1984   0   0
only a 2.5-fold increase in GH mRNA. GH mRNA levels were                   12706289   2003   0   0
induced a 2.5-fold increase in GH receptor mRNA levels, and a weak          8365359   1993   0   0
and dose-dependent fashion. GHF-1 mRNA levels were increased 2.5-fold 7649093         1995   0   0
The levels of GH-rec mRNA increased two-fold                               10990448   1998   0   0
A corresponding 2.3-fold increase in Gi alpha(2) mRNA was observed as 1689305         1990   0   0
had a 2.9-fold increase in Gi2 alpha mRNA (p < 0.001)                       8488974   1993   0   0
of GIP mRNA in the duodenum were increased twofold                          1476614   1992   0   0
was a 2-fold induction in GLCLC: mRNA and protein in the gd                10966520   2000   0   1
a further 2-fold increase in globin mRNA content. During the 44               1150671 1975      0    0
blot analysis indicated that Glu-6-Pase mRNA abundance increased 2-fold 11092693 2000           0    1
2.7- and 2.5-fold increase in steady-state glucagon mRNA levels at 24         2879843 1987      0    0
A 2-fold induction in glucagon receptor mRNA levels was obtained              7541048 1995      0    0
                                                                              3274898 1987
an approximately 2-fold increase in glucocorticoid receptor mRNA concentrations. This effect    0    1
rise in the glucokinase mRNA content was increased twofold                  11149749 2000       0    0
                                                                              7980534 1994      0
a concomitant 2.5-fold increase in glucose-6-phosphatase mRNA abundance. In addition, protein-free   0
2-fold increase in GLUT1 mRNA half-life. GLUT1 protein, detected              2025645 1991      0    1
to a 2.1-fold increase in GLUT1 mRNA but did not alter                        1372573 1992      0    0
although the steady-state levels of GLUT-1 mRNA increased 2.2-fold            8226960 1993      0    0
denervation, by which time GLUT-1 mRNA was increased 2-fold                   1396328 1992      0    0
2.4 +/- 0.2-fold increase in the GLUT1/actin mRNA ratio versus control        8098356 1993      0    1
by a 1.7-2.3-fold increase in cytoplasmic GLUT2 mRNA levels. To determine7929431 1994           0    0
and a 2-3-fold increase in glut-2 mRNA (p<0.01). Induction of glut-2        10625094 2000       0    0
GLUT-2 and PEPCK mRNA concentrations increased 2-fold                         1463468 1992      0    0
showed a 2.5-fold induction of GLUT2 mRNA apparent after only 8               8349038 1993      0    0
a approximately 2-fold increase in GLUT4 mRNA and a 50% increase              8182045 1994      0    0
caused a 2-fold increase in GLUT4 mRNA at 1 day, and a                        1381614 1992      0    0
Furthermore, GLUT4 mRNA and protein increased twofold                       12827286 2003       0    0
in a twofold increase in GLUT4 protein and mRNA and a sixfold                 7869920 1995      0    0
with a twofold increase in GLUT-4 protein and mRNA in mixed                   1767839 1991      0    0
Thus the GLUT-4 protein-to-GLUT-4 mRNA ratio was increased 2.1-fold           8447397 1993      0    0
fructose exposure, GLUT5 mRNA and protein levels increased 2-3.5-fold 9606981 1998              0    0
in Km (enzyme affinity). Endotoxin increased glutaminase mRNA twofold at 2    8343065 1993      0    1
                                                                              1641766 1992
were also determined. RESULTS. Dexamethasone increased glutaminase mRNA (twofold at 4           0    1
a 2-3 fold increase in GLVR-2 mRNA levels in CD34+ cells                    10440910 1999       0    0
A two-fold increase in GnRH receptor mRNA expression was also                 8404635 1993      0    0
Concentrations of GnRH receptor mRNA increased 2-fold                         7925096 1994      0    1
steady-state amounts of GnRH receptor mRNA were increased twofold             9861165 1998      0    0
2.7 +/- 0.29-fold increase in GnRH receptor mRNA levels in the pituitary      9397947 1994      0    1
                                                                            10080949
induced a twofold increase in gp130 mRNA levels; however, alpha-thrombin inhibited 1999         0    0
and a 2.0-fold increase in GRbeta mRNA in HeLaS3 cells, which               11381138 2001       0    0
an approximately twofold increase in GS mRNA half-life caused by              8772537 1996      0    0
RESULTS: GS mRNA levels were increased 2.3-fold                               9095109 1997      0    1
and a 2.7-fold increase in Gs alpha mRNA (p < 0.03)                           8488974 1993      0    0
an approximately 2-fold increase in the rate of transcription of GST          7488239 1995      0    0
2.8 kb species of GT mRNA that increased 2.5-fold                             2556143 1989      0    1
duodenum, a twofold increase in both H and mRNA and subunit                   8638717 1996      0    0
3 (Has1 and Has3), whereas Has2 mRNA increased 2-3-fold                     11262389 2001       0    1
a delayed, 2-fold up-regulation of HAS3 mRNA was observed. The HAS1 12620932 2003               0    0
                                                                            10559356 1999
less than twofold increase in HBV transcription rates and steady-state levels                   0    0
to a 2-3-fold increase in hCG mRNA levels, whereas treatment with both        2844818 1988      0    0
in a twofold increase in hCRH mRNA levels, while infection with an          12062896 2002       0    0
revealed a 2-fold increase in transcription of the HHC289 gene during         1993178 1991      0    1
showed that the levels of HIF-1alpha mRNA increased 2.1-fold                12780343 2003       0    1
with a twofold increase in both histone gene transcription and cellular       1429875 1992      0    0
velocity were also determined. HKII mRNA was increased 2-fold               10877213 2000       0    0
2.26 +/- 0.36-fold increase in HKII mRNA previously reported for healthy 11319725 2001          0    0
even though the endogenous HKII mRNA was induced 2.7-fold                   14746909 2004       0    0
                                                                            14654370 2003
controls), in association with increased HO isozyme mRNA (2.7-fold increase as                  0    1
point, a 2.6-fold increase in HO-1 mRNA in the descending aorta               8667253 1996      0    0
observed a 2.7-fold increase in HO-2 mRNA in homogenized spinal cord 10686338 2000              0    1
A 2.5-fold increase in HOXA5 mRNA expression was demonstrated by             11238043   2001   1   0
A 2.3-fold increase in hREN mRNA half-life was also observed                 10082506   1999   0   0
HSL immunoreactive protein and HSL mRNA levels increased twofold              8141275   1994   0   0
blot analysis revealed that hsp10 mRNA was increased 2.7-fold                10925156   2000   0   1
in a twofold increase in Hsp23 mRNA in polysomes. Hsp23 mRNA                  2388629   1990   0   1
in hypertonic medium. HSP27 mRNA abundance was increased twofold              9736278   1998   0   0
(HSP) 27 mRNA level was increased 2.5-fold                                   10686387   2000   0   0
                                                                              8576930
transient, approximately two-fold elevation in hsp60 mRNA occurred following 5 min      1995   0   1
normal groups (P<0.05). HSP70 mRNA induction was increased 2.3-fold 11431153            2001   0   0
to a 2-3-fold increase in the relative hsp70 mRNA level in bloodstream        8919995   1996   0   0
The HSP70 mRNA level was increased two-fold                                   8614568   1995   0   1
showed a two-fold increase in hsp70c mRNA and protein These                   9515035   1998   0   1
provoked a 2-fold increase in hTERT mRNA and protein expression (P           12843187   2003   0   1
caused a 2.3-fold increase in IAPP mRNA levels; this effect was               9110380   1997   0   0
2.4- and 2.7-fold increase in IAPP mRNA levels in the low                     9110380   1997   0   0
Steady-state iBAT mRNA levels were increased twofold                          9252527   1997   0   1
< 0.01) 2.5-fold increase in ovarian ICE gene expression as compared         10660263   1999   0   0
                                                                             12641739
immunoreactivity of the inhibitory transcription factor ICER increased twofold          2003   0   0
IGF I mRNA in collecting ducts were increased 2.8-fold                        1985106   1991   0   0
Mammary IGF-binding protein-2 (IGFBP-2) mRNA levels increased twofold 7690391           1993   0   0
2- to 3-fold elevation of IGFBP-1 mRNA in liver and                          12933666   2003   0   0
less than 0.001), while IGFBP-1 mRNA was increased 2-fold                     1709855   1991   0   1
A 2.5-fold induction of IGFBP-1 mRNA occurred within 1 week                  11044255   2000   0   0
additive with octreotide. IGFBP-1 mRNA expression was induced 2.7-fold 1385103          1992   0   0
was a 2.8-fold increase in IGFBP-1 mRNA expression in the livers              9362393   1997   0   1
than a two-fold increase in both hepatic IGFBP-3 mRNA and serum               7694822   1993   0   0
2- to 3-fold increase in IGFBP-3 mRNA was observed when cells                 1714831   1991   0   0
induced a twofold increase in IGFBP-5 mRNA based on RNase protection 11011784           2000   0   0
in a 2-fold increase in mRNA levels of both IGFBP-5 and the                  12176674   2002   0   1
and have 2-fold elevation of both hepatic IGF-I mRNA levels and circulating 3383777     1988   0   0
an approximately twofold increase in abundance of IGF-I mRNA in the aorta.2140801       1990   0   0
in a twofold induction of IGF-I mRNA in both nodules and liver.               2372370   1990   0   1
In brain, IGF-I mRNA levels rose 2-fold                                       2721444   1989   0   0
d 28, local muscle IGF-I mRNA levels increased 2.4-fold                      14677858   2003   0   1
A significant 2-fold increase in myocardial IGF-I mRNA was found after       12550078   2003   0   1
caused a twofold induction of IGF-I receptor (IGF-IR) mRNA in the heart 12775111        2002   0   0
IGF-I receptor (IGF-IR) mRNA was induced 2.1-fold                            10567181   1999   0   0
DES treatment increased the level of IGF-IR mRNA 2-fold compared with that    7788852   1995   0   1
produced a twofold increase in IGFR-I mRNA levels compared with untreated     9010034   1997   0   1
and a twofold increase in interleukin-1 beta mRNA levels. During the course 8625556     1996   0   0
in a twofold increase of IL-15 mRNA transcripts as measured by               11134253   2001   0   1
induced a 2-fold increase in IL-18 mRNA and elevated the levels              10859481   2000   0   1
Finally, IL-1ra mRNA levels were elevated 2.5-fold                            7921651   1994   0   0
an approximately 2-fold increase in steady-state IL-6 mRNA levels that peaked 8703029   1996   0   0
                                                                             11102468
human IL-6 promoter. Membrane depolarization raised IL-6 transcription twofold to       2000   0   0
showed a 2.1-fold increase in IL-6R mRNA expression. This stimulation was 8580365       1995   0   0
1.4-fold at 10 micrograms/ml. IL-8 mRNA was upregulated 2.5-fold              8836922   1996   0   0
to a 2.8-fold increase in IL-8 gene transcription and a 3.6-fold             10655985   1999   0   0
mucosal glutaminase and ileum mucosal IGF-I mRNA increased twofold 12901621             1999   0   0
produced a two-fold increase in inhibin alpha-subunit mRNA levels, and small  8397120   1993   0   0
a significant 2.5-fold increase in inhibin-alpha mRNA levels 5 days after    10579342   1999   0   1
in a twofold increase in insulin mRNA levels and did not                      7685720   1993   0   0
Steady-state insulin mRNA levels were elevated twofold                      9703324 1998        0   1
and a 2.5-fold increase in Jun D mRNA in the right                          8951105 1996        0   1
                                                                          12668525 2003
transcripts: approximately 2-fold increase of Kv1.5 mRNA from trough at Zeitgeber               0   0
A two-fold increase in L mRNA level was found in both                       8439658 1993        0   0
                                                                            6271788 1981
indicated a 2-fold increase of lactate dehydrogenase mRNA molecules in stimulated               0   1
The 2-fold increase of lactate dehydrogenase mRNA was confirmed by          6271788 1981        0   1
was a twofold upregulation of LAMP-1 mRNA but no alteration in LAMP-2 9767233 1998              0   0
demonstrated a 2-fold increase in the larger VEGF mRNA isoform (189         8752153 1996        0   1
1.8 to 3.3-fold increase in LCB2 mRNA levels (P < 0.01)                     9788249 1998        0   1
hepatic LDLr mRNA; linoleic acid increased LDLr mRNA 2-fold (P <            8978483 1996        0   1
                                                                          11728391 3
Atorvastatin and lovastatin increased low-density lipoprotein receptor mRNA (2.5-fold at 2001   0   1
A two fold increase in I and L-FABPc mRNA occurs in starved                 1905184 1991        0   1
                                                                            2322580 1990
is a 2-fold increase in lipoprotein lipase mRNA abundance, whereas lipoprotein                  0   0
over a 2-fold increase in the LNGFR mRNA level was found                    1337936 1992        0   1
showed a 2-3-fold increase in LO mRNA in MPM, but not                       9261183 1997        0   0
2- to 3-fold increase in LPL mRNA level in brown adipose                    8864952 1996        0   0
and a twofold increase in LPL gene expression in both the innervated        9688627 1998        0   0
tissue, the level of L-PRLR mRNA expression increased 2.3-fold            11014209 2000         0   0
with portal fibrosis, LT-beta mRNA levels were elevated 2.2-fold          12912866 2003         0   0
in a 2-fold increase in MAT2A mRNA levels and a 2-fold                    11115410 2001         0   0
Both MCAD and mMDH mRNA levels increased 2-2.5-fold                         2808399 1989        0   0
                                                                            9695025 1998
regulatory subunit ATPases. m-calpain mRNA concentration also increased two-fold                0   0
2.9-fold and 2.0-fold increase in MCAM mRNA expression in COPD patients   14516134 2003         1   0
                                                                          10417339 1999
caused a 2-fold increase in the MCP-1-to-glyceraldehyde-3-phosphate dehydrogenase mRNA The      0   0
caused a 2.5-fold induction in M-CPT-I (muscle-type CPT-I) mRNA In        11470240 2001         0   0
proliferation, a 2-fold increase of mdr1 mRNA levels was observed in the    7838133 1995        0   0
in a 2-fold increase of metallothionein mRNA levels in the primary          2357467 1990        0   0
showed a 2.5-fold induction of metallothionein mRNA (P < 0.05), and a     10357793 1999         0   0
a significant 2-fold increase in liver mHS mRNA compared to NAL-fed       12049798 2002         0   0
caused a twofold increase in MIF mRNA expression in NRK52E and MCT 12631343 2003                0   0
DEM, the level of the MME mRNA increased 2-fold                           10216232 1999         0   1
Splenic MnSOD mRNA levels were increased twofold                            8179009 1994        0   0
proliferator, a 2-fold increase in mPPAR gamma mRNA was observed in the8262913 1993             0   1
                                                                            8722222
statistically significant 2.5-fold increase in MT mRNA in exposed compared to control 1996      0   1
1.8- to 2.5-fold increase in MTase mRNA levels in colon carcinoma           8816806 1996        0   1
induced about two-fold increase of MUC2 mRNA level in LS174T              12848848 2003         0   0
A 2-fold increase in mucin mRNA (rat Muc5ac) expression was               11588000 2001         0   0
hepatic levels of murine C4BP mRNA are elevated 2.5-fold                    1339286 1992        0   0
in a two-fold increase in Mx mRNA levels compared to bred,                11479146 2001         0   1
induced a twofold increase in Na(+)-Ca2+ exchanger mRNA accumulation in9007674 1997             0   1
2- to 3-fold increase in muscle Na-channel mRNA levels, suggesting that     2446331 1987        0   0
caused a 2.4-fold increase in NAIP gene expression in the                 10471469 1999         0   0
with a 2.2-fold increase in renal cortical NaPi-2 mRNA and a 4.9-fold       7977794 1994        0   0
Atrial natriuretic peptide (ANP) mRNA was increased 1-3-fold                9004160 1996        0   0
of a two-fold increase in NCX mRNA in these 4.                            10474782 1999         0   1
1.5- to 3-fold increase in NF-H mRNA within 2-4 h of hormone              10439464 1999         0   1
MC3T3-E1 cells, bFGF (10(-8) M) increased NFIL-6 mRNA 2-fold at 30          8725173 1996        0   0
in a two-fold increase in both NGF mRNA and NGF                             8137156 1994        0   0
an approximate twofold increase in NGF mRNA in both the hippocampus 8405292 1993                0   0
to a 2-3-fold increase in NGF mRNA content after an additional              1875907 1991        0   0
                                                                            9027329
effective concentrations, AII produced increases in NGFI-B mRNA 2.7-fold larger than 1996       0   0
cause a twofold increase in NHE3 mRNA abundance. In the absence             9927505 1999        0   0
in a twofold increase in NHE3 mRNA abundance and a threefold                7771509 1995     0   0
showed a twofold increase in NHE3 mRNA expression with MP                   9435499 1997     0   1
NK1- and NK2-receptor mRNA expression was increased twofold                 7573463 1995     0   0
2- and 2.5-fold upregulation of the Nm23-R1 mRNA and protein, respectively,11082283 2000     0   0
A twofold increase in NPFF mRNA was observed after 72                      12354280 2002     0   1
A smaller two-fold increase in NPY mRNA was observed in cells               3427446 1987     0   0
to the two-fold increase in NPY mRNA in the same                           10036310 1999     0   1
2- to 3-fold increase in NPY mRNA levels in the telencephalon/POA,          8119148 1994     0   1
After weaning NPY mRNA levels were increased 2-fold                         8401561 1993     0   0
that a 2.7-fold increase of NPY mRNA was induced by starvation             11438937 2001     0   1
                                                                            maximum
but reproducible twofold induction of Nramp1 mRNA expression. In addition, 9261342 1997      0   0
and a 2-fold increase in Ntcp protein. Ntcp mRNA remained significantly 11124830 2001        0   0
stimulated a 2.5-fold increase in ob mRNA within 1 h of treatment,         10909960 2000     0   0
in a two-fold increase in OB NPY mRNA over copper adequate                 10036310 1999     0   1
A similar two-fold increase in occludin mRNA was observed by real-time 11841574 2002         0   0
mRNA than OPM-1. OPM-2 GR mRNA was induced 2-fold                           2106390 1990     0   0
PDGF, a 2.4-fold increase in OPN mRNA expression was observed at            8911275 1996     0   1
rats, OPN mRNA in the kidney was increased 2-fold                          11431195 2001     0   1
                                                                            9578515
an approximately 2.2-fold increase in osteocalcin mRNA levels (determined by reverse 1998    0   0
proliferation by day 8. Osteocalcin mRNA was up-regulated 2.6-fold         12485640 2003     0   0
but not 0.1 microg/g genistein elevated OT mRNA (2-fold P<0.05), OTR 12504828 2003           0   0
3- and 2-fold increase of OT mRNA and VP mRNA, respectively,                3342761 1988     0   1
weeks, a 2-fold increase in the OT mRNA content was found                   3780571 1987     0   1
During the estrous cycle, OTR mRNA levels increased 2-fold                  7588281 1995     0   0
                                                                           11270639 2001
serine phosphorylation inhibitors), respectively. RESULTS: OTR mRNA increased 2.5-fold       0   0
endothelial nitric oxide synthase mRNA levels were increased 2.5-fold      11788426 2002     0   0
and a two-fold increase in p100 mRNA stability. Furthermore the p100        9529131 1998     0   0
by a two-fold increase in the p100 transcription rate and a two-fold        9529131 1998     0   0
                                                                            9637781 1998
arrest, a twofold increase in p21(WAF1/CIP1) transcription and expression, and a threefold   0   0
than a 2-fold increase in p21WAF1/CIP1 gene transcription was observed as   8895764 1996     0   0
showed a 2.8-fold increase in P2Y(2) mRNA levels from P9 to P24            11299315 2001     0   1
P2X1- and P2Y2-receptor mRNA levels which were increased 2.7-fold          10503935 1999     0   1
caused a 2.7-fold increase in p36 mRNA but barely increased p46            10872801 2000     0   0
although the 2-fold increase in P450 3A mRNA detected after repeated        8043019 1994     0   0
an approximately 2-fold increase in P450IA1 mRNA at 4 h and a               2387012 1990     0   0
in a 2-fold increase in mRNA encoding P-450scc, as revealed by              1660516 1991     0   1
with normal ovarian stroma, P450scc mRNA was increased twofold              9988407 1999     0   1
provoked a 2.9-fold increase in P-450scc mRNA level in the Z-G              2626031 1989     0   1
a approximately 2-fold increase in the mRNA abundance of p46 was           10567346 1999     0   0
induced a 2-fold increase in p53 mRNA levels and a 2-                      12145335 2002     0   0
                                                                           11697199 2001
Approximately a 2.0-fold increase in p53 gene expression was observed following              0   0
induced a 2-fold increase in p85alphaPI 3-K mRNA abundances (118 +/- 10567366 1999           0   0
was a 2.0-fold increase in PAF receptor mRNA at 60 minutes                  7957648 1994     0   1
and 2.5 fold rise of PAH mRNA concentrations in rats fed                    9028150 1996     0   0
a concomitant twofold increase of endothelial PAI-1 mRNA levels (P <        9108786 1997     0   0
fold to 2-fold increase of endothelial PAI-1 mRNA levels (P <               9108786 1997     0   0
Hepatocyte PAI-1 mRNA levels are increased 2-fold                           2536889 1989     0   0
an approximately twofold increase of PAI-1 mRNA levels, as well as          9108786 1997     0   0
Levels of PAI-1 mRNA were elevated 2-fold                                   1712775 1991     0   0
four- and twofold increase in PAI-1 antigen and mRNA levels, respectively, 10102708 1999     0   0
Total pancreatic GLUT-2 mRNA was increased twofold                          1644920 1992     0   0
Pancreatic PC1 and PC2 mRNA increased >2-fold                              10749575 2000     0   0
induced a 2-fold increase in both PAR-1 mRNA and protein                    11711494 2001       0   0
muscle cells in irradiated intestine. PAR-1 mRNA increased twofold          12057911 2002       0   0
exhibit a 2.5-fold increase in PCK mRNA when transferred to acidic           8770165 1996       0   0
II nuclear receptors. PDGF mRNA levels are elevated 2.2-fold                11739278 2001       0   0
and a twofold rise in mRNA levels for PDGF in                                7923630 1994       0   0
2- to 3-fold increase for PDGF B mRNA (P less than                           1996708 1991       0   0
levels of PDGF-B mRNA in lung were elevated 2.5-fold                         2696512 1989       0   1
in a 2.6-fold increase in PDGF-B steady state mRNA and immunoreactive 9514402 1998              0   0
                                                                             at
reflected a 2.5-fold increase in PDGF-specific mRNA synthesis, and peaked 3598461 1987          0   0
is a 2.5-fold increase in PDI mRNA that is maintained by                     2383249 1990       0   0
be relatively short: PE mRNA levels were increased 2-fold                    2927283 1989       0   0
GLUT-2 and PEPCK mRNA concentrations increased 2-fold                        1463468 1992       0   0
                                                                             Glycogenolysis
in a 2-3-fold increase in hepatic phosphoenolpyruvate carboxykinase mRNA 9813020 1998           0   0
and old CR mice. Phosphoenolpyruvate carboxykinase mRNA increased 2-fold    11795521 2001       0   0
A 2.0-fold induction of perlecan mRNA occurred by 24 hours                   8231112 1993       0   0
with the pGFAP-MT-I plasmid led to increased mRNA (2.5-fold in astrocytes   10668428 1999       0   1
The steady state level of phospholamban mRNA rose 2.5-fold                   8287415 1993       0   1
induced a 2.7-fold increase in the pIgR mRNA and a 2.2-fold                  9612336 1998       0   0
shows a two-fold increase in Pit2 receptor mRNA and causes some             10910141 2000       0   0
an additional two-fold increase in steady state PKC-delta mRNA (and protein) 8902852 1996       0   0
induced a 2-3-fold increase in pmAAT mRNA level in both rat                  2355732 1990       0   0
a 1.7-to 2.0-fold rise in PNMT mRNA at 8 In                                  8859016 1996       0   0
transcription: a 2.3-fold increase in PNMT transcription persists for 18 hr  1358447 1992       0   0
2- to 3-fold increase in polyUb mRNA also occurred within 1                  1724903 1991       0   0
a progressive 2-3-fold increase in polyUb mRNA for 1-3 days, whereas         7741690 1995       0   0
was a 2-fold increase in POMC mRNA in the arcuate nucleus                   11701716 2001       0   0
                                                                            10657504 1999
was a twofold increase in POMC mRNA levels and [(35)S]-methionine incorporation                 0   0
caused a 2-3-fold increase in the POMC mRNA level in rat                     3474031 1987       0   0
+/- 0.3 ng/mL, P <.05). POMC mRNA increased 2.5-fold                        10964021 2000       0   0
1.6- and 3.3-fold increase in PPE mRNA levels after 24 and 48                9001946 1996       0   0
mRNA analysis revealed that PPT mRNA levels increased 2.4-fold               1698245 1990       0   1
in a 2-fold increase in intestinal preapo-C-III mRNA accumulation but no     6698975 1984       0   0
in a 2-fold increase in preapolipoprotein AiV mRNA after 4                   6897360 1982       0   0
observed a 2-fold increase in Pref-1 mRNA on E17 and a 5-fold                9275085 1997       0   0
However, myocardial preproET-1 mRNA expression increased twofold            10749728 2000       0   0
growth in DOCA-salt rats. PreproET-1 mRNA was increased 2-fold               9774378 1998       0   1
                                                                             in the beta-cell
glucose concentration increased the content of preproinsulin mRNA 2.3-fold 1322137 1992         0   0
studies, a 2-fold increase in preprolactin mRNA activity was obtained in male 911801 1977       0   0
                                                                             2373052
an approximate 2-fold increase in preproNPY mRNA content, whereas obese animals 1990            0   0
2- to 3-fold increase in preproNPY mRNA levels in the hypothalamus           2373052 1990       0   0
caused a twofold increase in preprotachykinin A mRNA in the limbic           8281296 1993       0   0
of morning values, and PRL mRNA levels increased 2-fold                      2924734 1989       0   0
and a 2-fold increase in PRL mRNA in 4 h, while                              1446607 1992       0   0
in the same cytosols, E2 increased PRL mRNA 2.6-fold in the low              1874194 1991       0   0
an approximate two-fold increase in PRLR mRNA after 24 hr of treatment 1457040 1992             0   0
lactation, whereas PRLR mRNA within the epithelia increased twofold         11572793 2001       0   0
was a 2.3-fold increase in PRLR mRNA levels, and in cells                    8806706 1996       0   0
been weaned for 24 h, PRL-R(L) mRNA increased 2.5-fold                       9256361 1997       0   0
                                                                            12163502 2002
synthesis and 2.5-fold increase in pro alpha1(I) collagen mRNA expression, without              0   0
a two fold increase of pro-alpha 1(I) collagen mRNA in cells                 8227157 1993       0   0
2-fold increase in procollagen production and mRNA levels when               2364107 1990       0   0
more than 2-fold increase in cellular ProEnk A mRNA levels with a            2082202 1990       0   0
in a 2-fold increase in ProEnk A mRNA but had no                            1850066 1991   0   0
fatty acids (FFA) the proinsulin mRNA ratio rose 2.4-fold                   9325287 1997   0   0
and thyroid hormone levels. Hypothalamic proTRH mRNA increased twofold 8699147 1996        0   0
A nearly twofold increase in proTRH mRNA was observed in hypothyroid        3116669 1987   0   1
1.5- to 2.5-fold increase in PrP mRNA levels 1 and 3h                      10757517 2000   0   1
receptor concentration increased 2.6-fold and pS2 mRNA increased 2.4-fold  10967555 2000   0   0
UV-B irradiation increases the level of psbA2 mRNA 2-3-fold and, more       9651331 1998   0   0
concentration of PSP1 mRNA in rat liver increased 2.3-fold                 10101265 1999   0   0
deprivation, a two-fold increase in PTG mRNA and a decrease of mRNAs 12383246 2002         0   0
                                                                            7649081 1995
an approximately 2-fold increase in PTH/PTHrp receptor mRNA expression in the kidneys      0   0
                                                                            7649081 1995
an approximately 2-fold increase in PTH/PTHrp receptor mRNA was also observed              0   0
rate of PTH/PTHrP receptor gene transcription was increased twofold         9550631 1998   0   0
caused a twofold increase in PTHrP mRNA at six hours, without              11532093 2001   0   0
had a two-fold increase in PTHrP mRNA stability (from 45 to 90             11911944 2002   0   0
PTP1 expression at the mRNA level was elevated twofold                      1373143 1992   0   0
the 2.7 kb RAR alpha mRNA was increased two-fold                            8208594 1994   0   1
a rapid 2-fold increase in RARbeta mRNA levels in A2780 cells,             10328240 1999   0   0
Lung RAR-gamma mRNA levels were also induced 2-fold                         1719965 1991   0   0
The stability of rbcL mRNA increased 2.5-fold                               8329684 1993   0   0
in a 2-fold increase in RC3 mRNA in EDL with no                             9852215 1998   0   1
RESULTS: Renal renin gene expression increased twofold                     11919408 2002   0   0
by Northern blotting. 3. Renal renin mRNA increased 2-fold                  9176018 1997   0   1
induced a 2.3-fold increase in the renin mRNA in adult kidney,              8719773 1995   0   0
induced a twofold increase in steady-state renin mRNA levels above control 8023970 1994    0   0
a nearly twofold increase in RERG mRNA as cells differentiate from         10084682 1999   0   0
values, a 2.4-fold induction in resistin mRNA levels was observed in white 12647275 2003   0   0
the adipose tissue were investigated. Resistin mRNA increased 2.6-fold 11684088 2001       0   0
showed a twofold increase in RFC mRNA levels over Similarly,                9458739 1998   0   1
but RGS2 and -4 mRNA levels are increased 2-3-fold                         12653973 2003   0   0
LV myocardium RGS4 mRNA and protein was upregulated 2-3-fold               12176127 2002   0   0
show that ribosomal protein mRNA levels are increased twofold               8114723 1994   0   0
than a 2-fold increase in RNA transcription and had no effect               2498320 1989   0   0
a two fold increase in endogenous rPLI mRNA levels, and a two               9790263 1998   0   0
induced a 2-fold increase in SCD1 mRNA within 6 h and a                     7961698 1994   0   0
a significant, 2.9-fold increase in SGP-2 mRNA during the same              9408256 1997   0   1
1.8- to 3-fold increase in SNAP-25 mRNA and protein as determined          11277561 2001   0   1
                                                                            8099701 1993
a significant 2-fold increase in somatostatin mRNA accumulation, with a maximal            0   1
The expression of SP-22 mRNA increased 2.0-3.5-fold                         9890990 1999   0   0
was a 2.7-fold increase in fetal lung SP-A mRNA (P <                       10070110 1999   0   1
with a 2.4-fold increase in SPARC gene expression in STNx compared          9294828 1997   0   0
Relative levels of SPARC mRNA were increased 2.7-fold                      10484471 1999   0   0
was a twofold increase in SP-A mRNA. SP-B mRNA levels also                 10749753 2000   0   0
DEX increased fetal lung SP-C mRNA 2-fold over the level                    9475281 1998   0   0
2) a 2-3-fold increase in SP-C mRNA levels was observed in response         8618787 1995   0   1
                                                                            8301359 1994
approximately a twofold increase in SP-encoding PPT mRNA expression in the ipsilateral     0   0
to a 2.5-fold increase in SPR mRNA levels (4.7 kb band)                     9484906 1997   0   1
2- to 3-fold increase in SR-BI mRNA and protein levels, in association     10508199 1999   0   0
2- to 3-fold elevation of overall ST6Gal I mRNA abundance by               10570225 2000   0   0
by Northern blotting. Levels of StAR mRNA increased 2-fold                  9116155 1997   0   1
(ii) a 2-fold increase of the stored beta-F1-ATPase mRNA being rapidly      8420961 1993   0   0
                                                                           11598898 2001
induce a two-fold increase in syndecan-4 mRNA (P < 0.0001) and significantly               0   0
showed a 2-fold increase in synthesis and its mRNA levels during            2307121 1990   0   0
in a 2-fold increase of both TAFI mRNA levels and promoter                 12645517 2003      0     0
assessed a twofold increase in TbetaRII mRNA levels in treated cases        9759702 1998      0     0
most a 2-fold increase in transcription of the TF gene following            1693617 1990      0     1
induced a twofold increase in TfR mRNA levels in both the duodenum          8944690 1996      0     0
2- to 3-fold increase of TfR mRNA of NKM-1 cells cultured                   1701357 1990      0     1
exhibited a 2-fold increase in TGF alpha mRNA and a 3-fold                  1518840 1992      0     0
A 2-fold increase of TGFalpha mRNA and a 10-fold increase                  11989832 2002      0     1
                                                                           11692060 2001
a significant two-fold increase in TGF-alpha mRNA expression was obtained at                  0     0
was a twofold increase in TGF-alpha mRNA levels at 2 h                      1886882 1991      0     0
2- to 3-fold increase of TGF-alpha mRNA levels, in relation to incubation   7512173 1994      0     1
An approximately twofold increase in the TGFB1 mRNA in irradiated cells 10521925 1999         0     0
Ang II at 10(-6) M increased TGF-beta mRNA 2.5-fold compared to control 10426193 1999         0     0
in a 2-fold increase of TGF beta 1 mRNA and more                            9325190 1997      0     0
Steady-state TGF-beta 1 mRNA level increased 2-fold                         1732279 1992      0     0
and a twofold increase in TGF-beta 1 mRNA expression (p <                  11583905 2001      0     0
greater than 2-fold increase in TGF-beta 1 mRNA was quantitatively measured 7639112 1995      0     0
hybridization; here, expression of TGF-beta 1 mRNA increased 2-fold         9659584 1998      0     1
induced a two-fold increase in TGF-beta 1 mRNA levels within 4              8576949 1995      0     0
over a two-fold increase in TGF-beta 1 mRNA in the                          8292830 1993      0     1
transforming growth factor (TGF)-beta 1 mRNA were elevated twofold          7653628 1995      0     0
transforming growth factor beta1 (TGF-beta1) mRNA was increased twofold    10216135 1999      0     0
with a 2.5-fold increase in TGF-beta 1 gene expression during a 16-week 9150473 1997          0     0
was a 2-fold increase in mRNA for TGF beta 2, a 5-fold                      8765316 1996      0     0
(1 microM) induced c-fos and TH gene transcription fivefold and twofold,    7609611 1995      0     0
a significant 2-fold rise in TH mRNA levels (p <                            7898980 1994      0     0
with a twofold rise in TH mRNA level, indicating the absence               10386968 1999      0     0
2- to 3-fold increase in TH mRNA levels in LC and A1                        1350653 1992      0     0
caused a 2.5-fold increase of thrombin receptor mRNA within 24 h,           9415277 1997      0     1
effects were additive. Thyroglobulin mRNA content was increased twofold 8040191 1994          0     0
indicated a twofold increase in thyroglobulin mRNA content compared with 7937323 1994         0     1
to a twofold increase in thyroparathyroid PTH mRNA levels. This increase 8772488 1996         0     0
stress-inducible alfalfa, G1. Transcription of tigA is induced 2-3-fold     9256071 1997      0     0
                                                                           11165051
mice, the administration of cortisol increased Tim23 mRNA 2-fold but with progesterone,2001   0     0
On day 13 of pregnancy, Tim23 mRNA increased 2.7-fold                      11165051 2001      0     0
cells, in which TIMP mRNA levels were increased 2.9-fold                    2558843 1989      0     0
                                                                            9033278 1997
alpha plus tumor necrosis factor-alpha increased TIMP-1 mRNA twofold above constitutive       0     0
treatment with GdCl(3), TNFalpha mRNA transcripts were increased 2-fold 11141354 2001         0     0
found 2.2 fold increase in TNF-alpha mRNA at diestrous, in SP               9143232 1997      0     1
                                                                           10648639 2000      0
and approximately 2.2-fold increase in topoIIalpha mRNA levels. Furthermore, CEM/ICRF-8 expresses   0
The amount of topoIIalpha mRNA was increased 1.5-3-fold                     9553115 1998      0     0
a sustained 2-fold increase in tPA mRNA accumulation. Dexamethasone and cA  1738371 1992      0     0
A twofold increase in content of tPA mRNA was observed                      9798919 1998      0     0
only a 2-fold increase in tPA mRNA and a 5-fold increase                    2157975 1990      0     0
The levels of TPA mRNA increased 2.5-fold                                  10819311 2000      0     0
and a two-fold increase in TR beta-2 mRNA levels after incubation           8472843 1993      0     0
was a twofold increase in both transferrin mRNA and transcription of the    3785157 1986      0     0
2- to 3-fold increase in transferrin receptor mRNA expression. A motif     10446188 1999      0     0
that NGF and TrkA mRNA levels were increased 2.7-fold                      10561305 1999      0     1
2- to 3-fold increase in full-length trkB mRNA expression starting 2        8743749 1996      0     0
in a 2-fold increase in TSH receptor mRNA expression, which was             8408457 1993      0     0
with a 2.2-fold increase in tubulin transcription as well as suppressed     8694278 1996      0     1
                                                                           10747199 2000
and exercise training upregulated type IIx MyoHC mRNA 2.9-fold and 1.2-fold,                  0     0
revealed a twofold increase in the ubiquitin mRNA content of neurons           7898620 1994     0   0
the injection, whereas the UCP mRNA abundance increased 2-3-fold               3192531 1988     0   0
less consistent twofold increase in muscle UCP2 mRNA levels was observed       9519732 1998     0   0
UCP2 mRNA and protein were increased twofold                                  11289045 2001     0   0
a similar 2-2.5-fold increase in UCP2 and -3 mRNA levels in lean               9389729 1997     0   0
a similar 2-2.5-fold increase in UCP2 and -3 mRNA levels in lean               9389729 1997     0   0
despite a 2-3-fold increase in UCP3 mRNA and protein expression in skeletal   10995775 2000     0   0
and a 2-fold increase in UCP-3 mRNA levels in white adipose                   10403804 1999     0   0
2- to 3-fold increase in UOxase mRNA content, whereas the fatty                3194410 1988     0   0
The uterine IGF-I mRNA level increased two-fold                                7974526 1994     0   0
                                                                              10077665 1999
a approximately 2.5-fold increase in utrophin mRNA levels. Transient transfection experiments   0   0
blot analysis showed that intestinal VDR mRNA increased 2-fold                 7754807 1995     0   1
in normal mice, VDR mRNA levels were up-regulated 1.8-2.7-fold                 1335319 1992     0   0
with a 2.5-fold increase in intestinal VDR mRNA which was accompanied 2551904 1989              0   1
protein kinase C (PKC) activator, increased VEGF mRNA 2-fold and PKC 10882716 2000              1   0
189 was detectable. The mRNA for VEGF increased 2-fold                         9665344 1998     0   1
demonstrated a 2-fold increase in the VEGF transcription rate 2 h              9794479 1998     0   1
in a two-fold induction of VEGF mRNA and 1.3-2-fold increase in protein, 11518466 2001          0   0
increase in capillary length density, VEGF mRNA increased >2-fold             10417401 1999     0   0
in a 2.4-fold increase in VEGF mRNA expression after 3                        12087245 2002     0   1
The half-life of VEGF mRNA was increased 2.5-fold                             12147617 2002     0   1
an approximately 2.2-fold increase in VEGF-C mRNA transcript in the cancer    11291931 2001     0   1
hybridization, at 4 days post-ECL, VIM mRNA increased two-fold                 7822482 1995     0   0
revealed a 2.6-fold increase in VLDLR mRNA at term compared to that            7828550 1995     0   1
The VP mRNA levels of the SCN increased 2-fold                                 2716958 1989     0   1
Type XVI collagen mRNA level was elevated 2.3-fold                            10469311 1999     0   0
                                                                               8978705 1997
rapid, transient 2.6-fold increase in Y1R mRNA levels. However, all trans-retinoic              0   0
A 2-fold increase in zif-268 mRNA was seen, while increases                    1388031 1992     0   0
about 0.5-3.5 fold increase in the levels of mRNA for c-myc                   11111017 2001     0   0
showed a two-fold increase in the level on mRNA Also,                          8647234 1996     0   1
protein, mRNA levels and transcription rate were increased 2-3-fold            2775196 1989     0   0
at 48 h, while the 1.4-kb mRNA increased twofold                               8323294 1993     0   1
caused a twofold increase in the 2.5-kb mRNA in liver at                       8323294 1993     0   1
caused about 2-fold increase in the activity and mRNA Dibutyryl                2837211 1988     0   0
carboxykinase activity and mRNA abundance were concordantly elevated 2-fold    1733721 1992     0   0
with salt intake, and mRNA abundance was increased twofold                    10432392 1999     0   0
in lung, and its mRNA levels were induced 2-fold                               1654565 1991     0   1
greater than twofold increase in aortic mRNA encoding the myosin regulatory    7653526 1995     0   0
and a 2-3-fold increase in brain mRNA is observed in tubby                     8606774 1996     0   0
A twofold increase in gene transcription is detected within two                6319718 1984     0   0
The level of the gene expression increased 2-fold                              7548221 1995     0   0
                                                                               7678798 1993
accumulation was due in part to increased transcription (2.4-fold relative to that              0   1
the -686 to -553 region increased intestinal transcription 2-fold and decreased2161843 1990     0   0
by a 2-fold increase in its mRNA level. Hepatocytes prepared from             11559709 2001     0   0
the level of only one mRNA was increased two-fold                             12436262 2002     1   0
about a 2-fold increase in relative mRNA synthesis rates in primary            8502238 1993     0   0
Reporter gene expression was also increased 2-fold                             9395482 1997     0   0
observed a twofold increase in the steady-state mRNA levels of both            1848408 1991     0   0
cells, the level of this mRNA maximally increased 2-3-fold                     2420802 1986     0   0
that corresponds to a mRNA that is induced 2-3-fold                            2211664 1990     0   0
the respective transporter mRNA levels. Betaine uptake increased twofold 9862864 1999           0   0
a nearly twofold increase in abundance of the mRNA encoding the catalytic 7762619 1995          0   0
a significant 2-fold increase in CAT reporter gene expression and the antagonist1779976 1991     0   0
A two-fold increase in mRNA L-FABPc occurred in differentiated Caco-2           8232271 1993     0   1
A two-fold increase in the mRNA levels of the EGF                               7572213 1995     0   0
about a twofold increase in the mRNA expression levels compared with the 7579405 1995            0   1
                                                                                9767233 1998
an almost twofold increase in tyrosinase activity and gene expression with increased             0   0
                                                                                7699198 1994
an approximate 2-fold increase in transcription rate within two hours of stimulation             0   0
                                                                                7768793 1995
an approximate twofold increase in bacteriochlorophyll and carotenoid gene expression under      0   0
                                                                               12163594 2002
an approximately twofold increase in basal activity. Reporter gene expression was                0   0
an approximately twofold increase in the abundance of mRNA coding for           9530269 1998     0   0
and renin mRNA level in the kidney increased twofold                            2405694 1990     0   1
approximately 2 fold increase in the transcription rate of the full-length      9450651 1997     0   0
approximately a twofold increase in mRNA in resistant clone 7                   2897875 1988     0   1
but a 2-fold increase of mRNA stability under the influence of IL-10.          10820228 2000     0   0
by a 2-fold increase of the mRNA level of nucleotide excision                  14670002 2003     0   0
by a twofold increase in mRNA levels and an 83% increase                       14720206 2004     0   0
by a two-fold increase in mRNA of endothelial constitutive nitric oxide         7528018 1994     0   0
by a twofold increase in transcription per copy of X-linked genes               7926760 1994     0   0
cause a two-fold increase in target gene expression throughout the genome      12723697 2003     0   0
despite a twofold increase in gene expression of MMP-2. Concanavalin A 10855539 2000             0   0
displayed a 2-fold increase in mRNA transcripts; in contrast, despite failure 12619927 2003      0   0
greater than 2-fold increase in reporter gene expression in human corneal 10415459 1999          0   0
in a twofold increase in mRNA abundance. In contrast, the activation            3279055 1988     0   0
in a two-fold increase in mRNA and protein expression. High glypican-1         15016071 2004     0   0
In contrast, the mRNA of LH-beta was increased twofold                          2547009 1989     0   0
involves a 2-fold increase in transcription from the single male X             10882077 2000     0   0
mediate the 2-fold induction in gene expression seen with cAMP alone,           8070363 1994     0   0
mediating the 2-fold increase in transcription that is characteristic of dosage 7796814 1995     0   0
mRNA levels for cyclin E increased twofold                                      9071705 1997     0   1
mucosal glutaminase mRNA in the study group increased twofold                   8582226 1995     0   0
obtain a 2-fold increase in gene expression compared to delivery of the        12408981 2002     0   0
oleic acid medium, transcription of both genes increased 2-fold                12748191 2003     0   1
produced a 2-fold increase in the mRNA content of the high-mobility-group 12785009 2003          0   0
showed a >2-fold increase of gene expression compared with AD                  14657882 2003     1   1
showed a twofold increase in mRNA for both heat shock proteins                  9881488 1998     0   1
showed a twofold upregulation in the mRNA levels of biglycan and collagen10607916 1999           0   1
                                                                               12634920 2003
statistically significant two-fold increase in gene expression of the pGL3-insertion construct   0   0
statistically significant, >2-fold increase of gene expression compared with In14657882 2003     1   1
than a 2-fold increase in transcription from the cloned tk gene                 3244356 1988     0   0
the proper two-fold increase in gene expression needed for X chromosomal       12723697 2003     0   0
up to twofold increase in transcription corresponding to the increase in mRNA   7601099 1995     0   1
which a 2-fold rise in transcription was accompanied by a 12-fold               3785172 1986     0   0
with a 2-fold increase in the mRNA level, completely account for                6133859 1983     0   0
with a 2-fold increase in transcription rate and the formation of a             8294491 1994     0   0
with a 2-fold increase of the mRNA levels of both cytochrome                    8631925 1996     0   0
(i) The half-life of the mRNA pool increased 2.2-fold                           8181721 1994     0   0
1.5- to 2.9-fold increase in the mRNA and protein levels of alpha3,            11742036 2001     0   1
2- to 3-fold increase in mRNA levels at 20 degrees                             12754279 2003     0   0
2- to 3-fold increase in mRNA levels of osteocalcin compared with controls 8352780 1993          0   1
2- to 3-fold increase in the level of mRNA encoded by                           7685914 1993     0   0
and that the rate of transcription remains elevated 2-3-fold                    1359399 1992     0   0
conditions, with 2-3-fold increase in mRNA expression by TGF-beta These 11310348 2001            0   0
exhibit a 2-3-fold increase in transcription during S phase. Northern blot      1993178 1991     0   1
induces a 2-3-fold increase in mRNA transcripts in both However,             12949077 2003       0   0
reveal a 2-3-fold increase in transcription in response to There              7947392 1994       0   0
1.8- to 3.4-fold increase in the levels of mRNA encoding the alpha-subunit 8225223 1993          0   1
to adrenalectomy, the level of hybridizable mRNA increased 2.75-fold          3262055 1988       0   1
                                                                              8720280 1996
expressed a 2.7-fold increase in steady state mRNA levels compared to unexposed                  0   0
showed a 2.5-fold increase in translatable mRNA for the receptor, whereas 2985960 1985           0   0
and 2.5 fold increase in mRNA for both TS and DNA                             8355415 1993       0   1
and a 2.5-fold rise in mRNA for transforming growth factor alpha              9426692 1998       0   0
Interestingly, the mRNA transcript levels increased 2.5-fold                  1586720 1992       0   0
                                                                             11591374 2001
measured a 2.5-fold increase in mRNA level for mitochondrial encoded cytochrome                  0   0
                                                                              2.5-fold
micrograms.kg-1.min-1), angiotensinogen mRNA level in the liver increased 2405694 1990           0   1
                                                                             11273776 2001
revealed a 2.5-fold increase in gene expression and increased therapeutic efficacy               0   0
revealed a 2.5-fold increase in mRNA alpha 1 and a 3.4-fold                   8201010 1994       0   1
2.51 +/- 0.21-fold increase in the mRNA level of alpha(1A)-AR was            12784082 2003       0   0
3.1- and 2.6-fold increase of mRNA alpha and mRNA beta content,               2460453 1988       0   0
in a 2.6-fold increase in mRNA levels at the middark phase                    8404679 1993       0   1
in a 2.6-fold increase in mRNA levels for IL-8. IL-8 levels                  10688536 2000       0   0
                                                                             10920222
a cell-specific 2.8-fold increase in collagen gene expression in mature, matrix-depositing2000   0   0
                                                                              9171421 1997
showed a 2.8-fold increase in transcription with alginate production under the same              0   0
2.5- to 3-fold increase in the mRNA in muscle and                             8695914 1996       0   1
2- to 5-fold elevation in (prepro)insulin mRNA levels within 60-90            9689076 1998       0   0
a approximately 3-fold increase in 12-LO mRNA levels. In conclusion, we 12806174 2003            0   0
> or =3-fold increase in 24-hydroxylase mRNA expression was observed for     12972708 2003       0   0
                                                                              8137741 1994
elicited a 3-fold increase in renal 24-hydroxylase mRNA abundance relative to that               0   0
P450scc and 3 beta-HSD mRNA levels were increased 3-fold                      8793056 1996       0   1
to a 3-fold increase in 52-kDa SS-A/Ro mRNA levels in human                   9833039 1998       0   0
showed a three-fold increase in the mRNA level for ABP (expressed             7540162 1995       0   0
of human ACTH-R mRNA in H295 cells increased 2-4-fold                         8187950 1994       0   0
vascular cell adhesion molecule-1 mRNA and protein increased 3-4-fold 10521464 1999              0   0
two- to threefold increase in ADNP mRNA in astrocytes, suggesting that 11193814 2000             0   0
long-term endotoxemia, adrenalectomized rat lung GS mRNA increased threefold  9435573 1997       0   0
3- to 4-fold induction of ahp mRNA after heat or salt                         8932314 1996       0   0
up to 3-fold up-regulation of ALAS2 mRNA levels and an increase              12393745 2003       0   0
                                                                              2165496 1990
that a 3-fold increase in alkaline phosphatase gene transcription was detectable                 0   0
2- to 4-fold rise in alpha mRNA was sustained for 18                          2538310 1989       0   0
in a threefold increase in alpha 1 mRNA accumulation. The increased           8408640 1993       0   0
                                                                              7593596 1995
more than threefold increase in alpha 1(I) procollagen mRNA levels and collagenous               0   0
two- and threefold increase in alpha 2 mRNA was evident when                  7804325 1994       0   1
Alpha 5 mRNA expression was also increased 3-fold                            10564567 1999       0   0
The alpha rENaC mRNA (3.7-kb transcript) increased 3-fold                     7667305 1995       0   0
and sustained 3-fold induction in alpha-1 mRNA accumulation within 6          1646819 1991       0   0
                                                                              9737938 1998
two to three-fold increase in alpha1A-adrenergic receptor mRNA with a concomitant                0   0
alpha2-Laminin mRNA expression and protein increased 1.3-5.5-fold            11038071 2000       0   0
The abundance of alpha-MHC mRNA was also increased 3-to-4-fold                1705119 1991       0   0
plating (about 3-fold increase of the alpha-subunit mRNA level). The effect 2586755 1989         0   0
in primary cultures, ANF mRNA levels are increased 3-4-fold                   1835978 1991       0   0
                                                                              3533999 1986
demonstrated that renal cortical angiotensinogen mRNA concentrations increased 3.5-fold          0   1
was lower (1.6-fold). ApoA-I mRNA abundance was increased threefold           8399088 1993       0   0
Dexamethasone (DEX) treatment selectively increased apoE mRNA 3-fold in outer 1373819 1992       0   0
                                                                             10582586 1999
an approximately threefold elevation of APP mRNA levels in differentiating rat                   0   0
to CPB/HCA and reperfusion. Aquaporin-1 mRNA levels increased 3-fold 9323711 1997                0   0
conjugating enzyme (E2). The up-regulation of arginase mRNA (3.5-fold after 2 9502196 1997       0   0
by a threefold increase of ATB(0) mRNA levels in PMA-treated                  12127819 2002     0   0
including a threefold increase in atrial natriuretic factor mRNA and a sixfold11299205 2001     0   0
in a 3-fold increase of AVP mRNA to 35 +/- 5                                   3759944 1986     0   0
                                                                              12180851 2002
revealed a three-four-fold up-regulation of Bag-1 mRNA expression in anti-CD4 mAb-treated       0   0
a nearly 3-fold increase in bax mRNA levels within the mouse                   7675327 1995     0   0
a roughly threefold increase in B-CK mRNA levels and a decrease               11068189 2000     0   0
2- to 4-fold increase in BDNF mRNA expression which had its                    8743749 1996     0   0
a nearly threefold increase in BDNF mRNA concentrations in the dentate         9514826 1998     0   0
                                                                              10837866
Brain-derived neurotrophic factor (BDNF) mRNA was transiently upregulated 3.7-fold 2000         0   1
beta 2-Adrenergic receptor mRNA levels increased 3-fold                        1690708 1990     0   0
3- to 4-fold increase in steady-state beta 2AR mRNA These                      2472635 1989     0   0
showed a three-fold increase in beta-actin mRNA after either DC shock          8745214 1996     0   1
we demonstrate that beta-APP mRNA content is increased 3.5-fold                7595528 1995     0   0
was a 3-fold elevation of beta-globin mRNA when assayed by RT-PCR             11074543 2000     0   1
in a threefold increase in two beta-tubulin mRNA species, suggesting that 3785170 1986          0   0
and a 3-fold increase in bFGF mRNA compared with cells grown                   1518840 1992     0   0
maintained for 21 days. bFGF mRNA levels increased threefold                   7637645 1995     0   0
and a 3-fold increase in steady state mRNA levels for bFGF,                    8463321 1993     0   0
Maximal bFGF mRNA levels were elevated 3.5-fold                               12133549 2002     0   1
a 3.6-fold increase in BNP mRNA levels in left atria                           8194476 1994     0   0
to a threefold increase in C/EBP alpha mRNA within 4                           9349591 1997     0   0
was followed by the induction of calbindin-D28k mRNA (3.5-fold 3 h             9221916 1997     0   1
                                                                              11459783
strikingly, a 3-fold induction in calcitonin gene-related peptide mRNA expression in the 2001   0   0
Carbonyl reductase mRNA could be induced 3-4-fold                              2182121 1990     0   0
two- to threefold increase of cardiac ACE mRNA and fourfold stimulation        7670928 1995     0   0
the water-replete controls. T4 increased cardiac ANP mRNA 3-fold in dehydrated 2969452 1987     0   0
in a three-fold increase in cardiac AT1 mRNA levels in both                    9040029 1997     0   1
twofold to threefold increase of caspase-1 mRNA mean level was found 10567499 1999              0   0
A 3-fold induction of catalase mRNA was seen at a nontoxic                     1761541 1991     0   0
an average 3.7-fold increase in cathepsin B mRNA levels in the cancerous 10374777 1999          0   0
3- to 4-fold increase in mRNA levels of CCTalpha and CCTbeta                  11892987 2002     0   1
3- to 4-fold increase in mRNA levels of CCTalpha and CCTbeta                  11892987 2002     0   1
analysis showed that CD23 mRNA levels were increased three-fold                8380367 1993     0   1
with the 3-fold increase in CEA mRNA seen in differentiated Caco-2             7876096 1995     0   0
and concentration-dependent 3-4-fold induction of CETP mRNA by sodium CETP     8281947 1993     0   0
a 3-4 fold increase in the transcription rate of CFI gene                     10630630 1999     0   0
induced a threefold increase of c-fos mRNA after 30 min and a                  8287409 1993     0   1
following: (1) Pituitary c-fos and c-jun mRNA increased 3-fold                 9655081 1998     0   0
In contrast, c-jun mRNA levels were increased >3-fold                         10799339 2000     0   0
induced about three-fold increase in c-jun mRNA levels. This increase was 10964049 2000         0   0
following: (1) Pituitary c-fos and c-jun mRNA increased 3-fold                 9655081 1998     0   0
repression by UV irradiation. c-Jun mRNA was induced 3.5-fold                  9439681 1997     0   1
exhibited a 3.2-fold increase in CK 20 mRNA by comparison with respective     10537351 1999     0   1
2.5- and 3.5-fold induction of CKB mRNA was observed 2 and 24                  8472861 1993     0   0
05). Steady state CK-B mRNA increased three-fold                               9344761 1997     0   0
while a three-fold induction of clusterin mRNA was observed in astrocytes 8963451 1996          0   1
A 3.6-fold increase in cMoat mRNA levels and a 2.5-fold                       10377250 1999     0   0
After serum stimulation, levels of c-myb mRNA increased 3-4-fold               1537845 1992     0   0
a 2-5 fold increase of the c-myc mRNA level. H2O2 also                         9278255 1997     0   0
and a threefold increase of c-myc mRNA after 90 When                           8287409 1993     0   1
concentration of c-myc mRNA in RA-treated cultures increased 3-fold            3078960 1988     0   0
control by 56 days. c-myc mRNA expression increased 3-fold                    10430646 1999     0   0
exposure with much larger increases in c-myc transcription (3.2-fold over   9848127 1998       0       0
produced a threefold increase in cNOS mRNA at all O2 concentrations,        8675632 1995       0       0
                                                                           10498651 1999
showed a 3-and-a-half-fold increase in COL1A2 transcription in the cells expressing            0       0
more than three-fold elevation of collagen I mRNA levels in SSc             1649227 1991       0       0
A three-fold increase in collagen type II mRNA expression is               14964721 2004       0       1
induced a 3-fold elevation of COX-2 transcription in Int 407 cells         12604350 2003       0       0
                                                                           12029093 2002
caused a 2-4-fold induction in Cp mRNA expression. The mechanism of induction                  0       0
diabetic animals (3-fold increase in CPS mRNA with no change in OCT         3754512 1986       0       0
was increased 4-fold and CPT mRNA was increased 3-fold                      2543360 1989       0       0
was a 3.5-fold increase in CRF mRNA levels in the medulla                   7494465 1995       0       0
in a threefold rise in the CRH mRNA content of anatomic                     2333962 1990       0       0
induced a threefold increase in CSF-1 receptor (CSF-1r) mRNA expression as  8781300 1996       0       1
A 3-4-fold rise in translatable CT mRNA activity was observed               3838942 1985       0       0
least a threefold increase in CTH2 mRNA accumulation. No change in phenotype8890739 1996       0       0
caused a 3-fold increase in Cx43 mRNA levels by 2                           9562438 1998       0       0
                                                                           11872077
a greater-than-or-equals 3-fold increase in cyclin D1 mRNA was observed compared 2001          0       1
two- to threefold increase in cydAB gene expression observed upon reduction11717265 2001       0       0
                                                                           11229430 2001
to a 3.3-fold increase in islet CYO-II mRNA expression compared with mother-fed                0       0
4-fold and 3-fold increase in CYP2A1 mRNA and CYP3A1 mRNA was               8347134 1993       0       1
showed a 3.3-fold increase in CYP2E1 mRNA level in the                     11181486 2001       0       1
resulted in >/=3-fold induction of CYP3A4 mRNA and protein as assessed 12470639 2002           0       1
                                                                            8048539
chain reaction (RT-PCR) analysis, cytidyltransferase mRNA content increased three-fold1994     0       0
Both PKC delta protein and mRNA expression increased 3.5-4-fold            10854711 2000       0       0
                                                                           12475794 2002       (3.8-fold at 45
experiments showed that KCl induced depolarization-activated NF-kappaB-dependent transcription 0       0
approximately a 3-fold induction of DHCR mRNA and a 5-fold increase        10329655 1999       0       1
that a threefold increase in DHFR mRNA levels following growth stimulation 6736126 1984        0       0
RA a 3-fold increase in DOR mRNA at 48 h, and later                         8866697 1996       0       1
Northern hybridization demonstrated that DPPIV mRNA was increased 3-fold   12239451 2002       0       1
2-fold increase in protein, while EC increased mRNA 3-fold and protein      1539169 1992       0       0
was a 3-fold increase in E-Cad mRNA concentrations between 7-14 days; 7679970 1993             0       1
greater than threefold increase in ECE-1 beta mRNA at 12-24 h               9595399 1998       0       0
two- to threefold increase of ecNOS mRNA content quantified by Northern 8572165 1995           0       1
EDG4 receptor mRNA expression was increased 3-fold                         11291053 2001       0       0
2- to 5-fold induction of efp mRNA levels whereas UDCA did                  9855000 1998       0       1
low stringency RT-PCR. efp mRNA levels were induced 3-fold                  9855000 1998       0       1
a concomitant 3.9-fold increase in EGF-R mRNA levels in these               8621250 1996       0       1
caused a 3.0-fold increase in eNOS gene transcription and a 2.8-fold       10679488 2000       0       0
level of translatable epoxide hydrolase mRNA is increased 3-fold            6785755 1981       0       0
                                                                           11741826 2002
regulating gene expression after TGF-beta1. ERK1/2 phosphorylation increased threefold         0       0
1.4-fold and 6.3-fold increase in ET-1 mRNA levels in endothelial cells,    8454558 1993       0       1
was a threefold increase in ET-1 mRNA and a simultaneous threefold          7485537 1995       0       0
diet exhibited 3-fold increase in ETBR mRNA levels with little change       8440682 1993       0       1
more than threefold increase in F3 mRNA levels in response to stimulation. 9651216 1998        0       0
Fas mRNA and protein levels are increased two-to-fourfold                  10208933 1999       0       0
by a threefold increase in FAS mRNA and a 2.5-fold increase                 9227460 1997       0       0
five- and three-fold increase in FAS mRNA content in adipocytes and hepatoma9644037 1998       0       0
                                                                            9067276 1997
causes a 3-4-fold increase in FAS mRNA levels. Concomitantly with the increase                 0       1
induced a >3-fold increase in Fas and MnSOD mRNA expression in wild-type   10909967 2000       0       1
                                                                           p53-bearing
an approximately 3-fold increase in Fas/CD95 mRNA expression in mutant 14719118 2004           0       0
to an ~3-fold increase in Fas/CD95 mRNA expression in mutant p53-bearing   14719118 2004       0       0
                                                                           mice
approximately a 3-fold increase in fibrinogen Bbeta mRNA in heterozygous 11434679 2001         0       1
In SSc fibroblasts, fibronectin mRNA levels were induced 1.5-4.9-fold       8615828 1996       0       0
two to three-fold increase in fibronectin and alpha5 mRNA abundance at         9529009 1998     0   0
FKBP51 mRNA and protein levels were increased 3-fold                          12746298 2003     0   0
The mRNA levels of flt-1 were up-regulated threefold                           9027720 1997     0   0
2- to 5-fold increase in FMR1 mRNA levels obtained with 5-azadC               10545613 1999     0   0
shown a 3-fold increase in FN mRNA in liver that is                            7862527 1995     0   1
Gy/h transiently increased the level of FOS mRNA 3-fold after 0.5             11025647 2000     0   1
relative content of G alpha i2 mRNA increased threefold                        7954628 1994     0   0
                                                                               8227026 1993
gene, forskolin treatment increased G alpha i-2 transcription 3-fold but inhibited              0   0
resulted in 3-fold increase in G3PDH gene transcription as measured by         1668204 1991     0   1
was a 3-fold increase in GABAB receptor mRNA levels in the caudal              9931160 1999     0   0
two- to threefold increase in GAL gene expression compared to wild-type        8088514 1994     0   1
observed a 3-fold induction of galanin mRNA in the GnRH neurons                8730652 1996     0   0
3- to 4-fold increase in galanin gene expression in these                     11016971 2000     0   0
and a 3.8-fold increase of galectin-3 mRNA (p < 0.01) in CP                   10950114 2000     0   1
twofold to threefold increase in gamma-zein gene expression in both opaque-2   1821766 1991     0   0
detected a three-fold increase in Gap43 mRNA levels in the brains              1838777 1991     0   1
                                                                               7
stimulates a three-fold increase in gastrin mRNA levels and that the response573458 1995        0   0
in a 3-fold increase in G-CSF mRNA levels. These data suggest                  9168062 1997     0   0
that GDNF mRNA and protein levels were elevated threefold                     11573987 2001     0   1
60% of AL levels. Hypothalamic GFAP mRNA increased 3-fold                      7723929 1995     0   0
an almost 3-fold increase in rat (r) GH mRNA levels; IGF-I                     3948790 1986     0   0
A nearly 3-fold increase in GH mRNA accumulation was observed in GX            8325953 1993     0   0
induced a 3-fold rise of GH mRNA concentration after 8 h                       3680275 1987     0   0
IGF-I and 3.5-fold increase in GH-R mRNA at day 4 versus                       9039091 1997     0   0
in a 3-fold increase in Gi alpha mRNA as well as                               3100330 1987     0   0
during 1,25-(OH)2D3 treatment, whereas Gi-2 alpha mRNA increased 3-fold8033808 1994             0   0
                                                                               9604863 1998
induced a threefold increase in Glc-6-Pase mRNA concentration. Both stimulation of Glc-6-Pase   0   0
                                                                               9375822 1997
microscopy, a 3.5-fold increase of glomerular TGF-beta1/beta-actin mRNA ratio in the moderate   0   0
a 3.9 fold increase in levels of GLT-1 mRNA was observed                      12533722 2003     0   0
an approximately 3-fold increase in glucagon receptor mRNA in islets cultured  7534705 1995     0   0
an approximately 3-fold increase in GLUT1 mRNA levels. (Bu)2cAMP (1 mM),       1319316 1992     0   0
and normal hearts. GLUT1 mRNA expression was increased 3.4-fold                9220353 1997     0   1
a marked 3.5-fold increase in GLUT-1 mRNA in red and 2.2-fold                  7762639 1995     0   0
GLUT2 mRNA levels were also increased threefold                               11804845 2002     0   1
induced a 3.2-fold increase in GLUT2 mRNA levels compared with hepatocytes     1727734 1992     0   0
we showed that glucose induced GLUT2 gene transcription 3-4-fold in INS-17929431 1994           0   0
a significant threefold increase in Glut 4 mRNA while leptin mRNA              8755631 1996     0   1
in 13-day-old hypothyroid rats, GLUT4 mRNA levels increased 3-fold             8119934 1994     0   0
Glutamine synthetase mRNA and enzyme activity were elevated threefold 1362040 1992              0   0
and a threefold increase in glutamine transporter ATB(0) mRNA IGF-2           14746834 2004     0   0
in a 3.2-fold increase in glutathione S-transferase mRNA over levels found 6273441 1982         0   0
of progesterone increased amounts of GnRH receptor mRNA threefold (P < 9861165 1998             0   0
was a three-fold increase in GnRH receptor mRNA levels on the afternoon 8404635 1993            0   0
observed a 3.5-fold increase in GnRH receptor mRNA levels after 48             8793112 1996     0   1
The amount of groESL mRNA was increased 3.8-fold                              12092841 2002     0   0
was a 3-fold increase in H+/K(+)-ATPase mRNA from the 140-day-old fetus 1347009 1992            0   0
produced a 3.2-fold increase in hAGT mRNA peaking at 96 h                     11222745 2001     0   0
An average 3-fold increase in hBD2 mRNA occurs 24 h after                     10882713 2000     0   0
min of reperfusion, heat shock protein mRNA rose threefold                     9881488 1998     0   1
                                                                                TRUNCATED AT
showed a 3-fold increase in hepatic hemopexin mRNA content.(ABSTRACT 1988069 1991               0   0
                                                                              11134551 2001
and a 3.9-fold increase in hGSTA1 steady-state mRNA expression. Exposure to 250                 0   0
The mRNA for HIF-1alpha subunit was increased 3-4-fold                        10926858 2000     0   1
an approximately threefold increase in HK II mRNA in the absence            10658036      2000   0   0
testis and lung. HKcbeta mRNA abundance is upregulated threefold             9950762      1999   0   1
and 65%, respectively. HMG-CoA reductase mRNA levels increased 3-fold 1431598             1992   0   0
2- to 5-fold increase in hMTII mRNA levels after 6-8 h                       2974926      1988   0   0
                                                                             7511778
revealed a 3-fold increase in hMT-IIa transcription rate. Basal hMT-IIa steady            1994   0   0
to control cells: HO-1 mRNA levels were increased 3-fold                     9852279      1998   0   0
At day 1, HO-1 mRNA was increased 3.9-fold                                  12392996      2002   0   1
more than threefold elevation of HSL mRNA levels. The induction was         11574402      2001   0   1
in a threefold increase in HSP 70 mRNA (P less than                          1985091      1991   0   1
isolated perfused heart, HSP 70 mRNA was increased threefold                 1752959      1991   0   1
over a threefold increase in HSP 70 mRNA after 2 h                           9887036      1999   0   0
2.7- and 4.0-fold increase of HSS mRNA was observed when HepG2               7685352      1993   0   1
threefold induction of ICL2 mRNA levels and of 2-methylisocitrate           11092862      2000   0   0
A 2-4-fold increase in IFN-beta promoter transcription was observed in Sendai1782151      1991   0   0
mRNA and 3-fold induction of IFN-gamma mRNA in the spinal cord              11120847      2000   0   0
3- to 3.6-fold increase in mRNA levels for IFN-gamma, IL-12p35, and IL-10. 8975902        1997   0   0
IGF-I mRNA in the bladder was elevated 3-fold                                7511339      1994   0   0
from furosemide-treated kidney cortices, IGFBP-1 mRNA was increased threefold7538611      1995   0   0
                                                                             7538611
glucocorticoids or arginine vasopressin. That IGFBP-1 mRNA increased threefold            1995   0   0
at 144 h IGFBP-2 mRNA level was increased three-fold                        12450627      2003   0   1
two- to threefold elevation of IGF BP-3 mRNA levels, obtained by             9655767      1998   0   0
a approximately 3-fold increase in expression of IGFBP-3 mRNA after         15020235      2004   1   1
3.9 +/- 1.1 (n = 3)fold increase in IGFBP-3 mRNA and protein. This effect 8913883         1996   0   1
h caused 3.3-fold increase in IGFBP-4 mRNA levels which was determined 9217275            1997   0   0
                                                                             9138096
2.7 +/- 0.3- and 3.8 +/- 0.5- (n = 3) fold increase in IGFBP-4 mRNA and protein, This     1997   0   1
caused a 3-fold increase in liver IGFBP-4 mRNA (P: < 0.001)                 11145587      2001   0   0
type IV collagen. IGF-I increased IGFBP-5 gene expression 3-fold in the cells9535886      1998   0   0
An approximately 3-fold increase in IGF-I mRNA abundance was seen 6          8625897      1996   0   1
2.5- to 4-fold increase in IGF-I mRNA levels after 8 h                      11787055      2002   0   0
15% and the mean IGF-I mRNA had increased 3-fold                             2127500      1990   0   0
beta mRNA expression. RESULTS: IGF-I mRNA was increased 3.7-fold             8335195      1993   0   0
(IGF-I) and IGF-I receptor mRNA levels were elevated 3-fold                  1315253      1992   0   0
caused a threefold increase in IGF-I receptor mRNA and protein in infarct, 12754294       2003   0   0
liver, the fold increase in IGF-Ib mRNA levels was approximately three       3419435      1988   0   0
only a 3-fold increase in IkappaBalpha mRNA at 24 h, indicating              9573251      1998   0   0
twofold to threefold increase in IL 1 mRNA compared with                     2883234      1987   0   1
release and hematopoiesis. IL-1beta mRNA levels were increased threefold    10029158      1999   0   0
3- to 3.6-fold increase in mRNA levels for IFN-gamma, IL-12p35, and IL-10. 8975902        1997   0   0
3- to 3.6-fold increase in mRNA levels for IFN-gamma, IL-12p35, and IL-10. 8975902        1997   0   0
demonstrated that the expression of IL-15 mRNA increased 3-fold              9482906      1998   0   0
with a threefold increase of IL-6 mRNA in the bone marrow                    1372159      1992   0   0
revealed a threefold increase in mRNA for IL-6 by AIgG in vitro.             8455353      1993   0   1
by a 3.9-fold increase in mRNA levels for IL-6, 3.7-fold for                11837796      2002   0   0
to 3 fold upregulation in IL-8 mRNA and protein. Tumor necrosis             10376933      1999   0   0
3- to 4-fold increase of IL-8 mRNA and an enzyme-linked immunosorbent 8621523             1996   0   1
However, a 3.8-fold increase in inducible NOS mRNA and a 61%                12770931      2003   0   0
ovarian inhibin alpha- and beta A-subunit mRNA increased 3.8-fold            2458912      1988   0   0
ovarian inhibin alpha- and beta A-subunit mRNA increased 3.8-fold            2458912      1988   0   0
3- to 4-fold increase in insulin mRNA and protein. These results             2226773      1990   0   0
that the 3-4-fold increase in insulin receptor mRNA could be attributed      3047118      1988   0   0
                                                                             8123203
demonstrated a threefold increase in interleukin-6 mRNA expression in contractile cells   1993   0   0
an approximately three-fold increase in IR mRNA in liver, but not            7704100      1994   0   1
two- to threefold increase in kallikrein and renin mRNA levels in 2        9392495     1997   0   0
demonstrated a 3-fold increase in KDR mRNA levels following VEGF           9792718     1998   0   0
about a three-fold increase of laminin A chain mRNA In                     9291467     1997   0   1
a further 3-fold increase in LDL receptor mRNA levels. The increase        2086705     1990   0   0
with a three-fold increase in LDLr mRNA in the Using                      11726974     2001   0   0
(100 ng/ml) for 3 days. LFABP mRNA increased 3.6-fold                     11551854     2001   0   0
3 +/- 0.14-fold increase for L-ferritin mRNA 24 h after the end           12468600     2002   0   0
was a 3-fold increase in LPL mRNA and a 4-fold rise                        1384715     1992   0   0
                                                                           1314202
insulin administration (60 h) raised L-pyruvate kinase mRNA three-fold above control   1992   0   1
have a 3-fold increase in M1 mRNA expression relative to parental          7882331     1995   0   0
                                                                           9620840
and a 3-fold increase in MCAF mRNA level. Immunohistochemical analysis of the          1998   0   0
smooth muscle cells (VSMC), PTHrP(1-36) increased MCP-1 mRNA (3-fold at 6 12805493     2003   0   0
induced a 3-fold increase in MCP-1 mRNA in rat vascular smooth            12377739     2002   0   0
induced a 3-fold increase of MCP-1 mRNA expression in HMC-1 cells         11378326     2001   0   1
and a 3.4-fold increase in MCP-1 mRNA expression in macrophages and a 9258404          1997   0   1
detected a 3.6-fold increase in MCP-1 mRNA in the aortas of hypertensive 9403559       1997   0   1
only a 3-fold increase in MDR1 mRNA level in HP-gp cells                   8562335     1996   0   0
                                                                           9514072
revealed a 3-fold increase in mdr2 mRNA levels after dexamethasone administration      1998   0   0
caused a 3-fold elevation in the hepatic mEH mRNA Furthermore,             9146707     1997   0   0
METHODS AND RESULTS: MCP-1 mRNA increased 3.6-fold                        14684425     2004   0   0
and root epidermal cells. MHA2 mRNA was induced threefold                  8837507     1996   0   0
in a threefold increase in the mRNA encoding MHC-A and a threefold         1999462     1991   0   0
0.009) during mitosis and DOR mRNA level increased threefold              10931523     2000   0   0
and a 3.8-fold increase in MMP-3 mRNA levels, while virtually no           9478985     1998   0   0
                                                                           8432858
despite a threefold increase of MnSOD mRNA concentration; addition of a reducing       1993   0   0
                                                                           1
The 3-fold induction of MnSOD mRNA was dose-dependent, reaching a peak 761541          1991   0   0
a similar trend. In contrast, Mn-SOD mRNA increased 3.4-fold               8940825     1996   0   0
resistant cell line 30.3M, MRP mRNA is elevated 3-fold                     7860142     1995   0   0
3.8- and 4-fold increase in myocilin/TIGR mRNA expression was Expression  10509652     1999   0   1
two- to threefold increase in Na/H antiporter mRNA (mRNANa/H) abundance 4  1310692     1992   0   0
induced a threefold increase in Na+/H+ antiport (NHE-1) mRNA at 24         8201001     1994   0   1
two- to threefold increase in NaPi-4 mRNA abundance. The increase in NaPi-49887079     1999   0   0
of atrial natriuretic factor (ANF) mRNA were elevated threefold            8013079     1994   0   1
two- to threefold increase in NCAM protein and mRNA abundance in both 2380247          1990   0   0
Left ventricular NEP mRNA content was increased 3-fold                    11804980     2002   0   1
elicited a 3-fold increase of nerve growth factor mRNA levels in both      1712487     1991   0   0
                                                                           <
binding and 3.4-fold increase in NFkappaB-dependent gene transcription (p10506215      1999   0   0
reveals a 3-4-fold increase of medium neurofilament (NFM) mRNA in wobbler  8793115     1996   0   0
caused a 3-fold increase of NGF mRNA levels at 24                          8177507     1994   0   0
elicited a threefold increase in NGF mRNA expression which was limited     7720824     1995   0   0
caused a threefold increase in NHE (NHE-1) mRNA levels. CONCLUSIONS: The  10504492     1999   0   0
with a threefold elevation in NHE1 mRNA expression in control animals      9950878     1999   0   0
                                                                           8648261
that in tunicamycin-treated cells, NHE-3 mRNA expression increased threefold           1996   0   1
two- to threefold increase in NHE-3 mRNA abundance. This increase was 8769835          1996   0   0
show a threefold increase in nNOS mRNA expression, more modest nNOS 9134969            1997   0   0
rats a 3-fold increase in NOS mRNA was observed in the PVN                 7688585     1993   0   0
and statistically not significant. NPY mRNA was increased threefold       11466452     2001   0   0
P < 0.02), while NPY mRNA was increased 3-fold                             7682936     1993   0   1
the steady-state levels of NT mRNA were increased threefold                8179005     1994   0   1
stimulated a 3-fold increase in OPN mRNA which was reflected in a          8841428     1996   0   0
observed in the ischemic cortex. OPN mRNA increased 3.5-fold               9482794     1998   0   0
Hepatic acyl-CoA oxidase (ACO) mRNA levels were increased 3-fold           9989264     1999   0   0
a compensatory 3.5-fold induction of nuclear OXPHOS gene mRNA and regions     1383759 1992   0   0
more than threefold increase in the P120 transcription rate and an            8707886 1996   0   0
was increased twofold and P450(17alpha) mRNA was increased threefold 9988407 1999            0   1
all postmenopausal ovaries studied. P450(SSC) mRNA was increased threefold   12517592 2003   0   1
solution hybridization assay, P4502C7 mRNA levels were induced 3-fold         8246923 1993   0   1
a transient 3.5-fold increase in P450arom mRNA and protein, most likely       2759040 1989   0   0
in a 3-fold increase in P450c17 mRNA within 12 h (10(-7)                      8381079 1993   0   0
caused a 3-fold increase in the liver P450IIE1 mRNA An                        2116767 1990   0   0
ng DDE ml(-1). Cholera toxin increased P450scc mRNA 3.48-fold after 48 11226075 2001         0   0
and a 3.31-fold increase of P450SCC mRNA compared to unstimulated             9888542 1998   0   0
A 2-fold increase in p53 mRNA and protein amounts was                         8895543 1996   0   1
Levels of p53 mRNA were also increased 3-fold                                10630619 1999   0   0
two- to threefold increase in level of p75LNGFR mRNA (the low-affinity        8522994 1996   0   0
Northern blots showed that PAI-1 mRNA increased threefold                     9665808 1998   0   1
in a 3.1+/-0.4-fold increase in PAI-1 mRNA levels (P < 0.01)                 10905498 2000   0   0
3- and 4-fold increase in PAI-1 mRNA and protein, respectively, in cocultured11157728 2001   0   0
approximately 3-4 fold increase in PAI-1 transcription rates. These in vitro 10595645 1999   0   0
3.7 (+/- 0.9)-fold increase in PAI-1 mRNA as measured by northern             8611700 1996   0   1
The expression of PCPE mRNA was increased threefold                           9303490 1997   0   1
                                                                              8530514
PDGF alpha-receptor expression. PDGF alpha-receptor mRNA levels increased 3-fold 1995        0   0
in a 3-fold increase in PDGF-A mRNA expression. Thrombin also regulates 7863965 1995         0   0
                                                                              1423927 1992
prevented the threefold increase in expression of PDGF-A mRNA characteristically exhibited   0   0
The mRNA for PDGF-A chain was increased threefold                            10362700 1999   0   0
platelet-derived growth factor-BB (PDGF-BB) mRNA was also induced 3-fold9468491 1998         0   0
the pdiA promoter. Transcription of pdiA is induced 3-4-fold                  9021130 1997   0   1
inducing a 3-fold increase in the rate of transcription of the PEPCK          1848696 1991   0   0
                                                                              9611146
content of phosphoenolpyruvate carboxykinase (PEPCK) mRNA was increased 3.1-fold 1998        0   0
                                                                             11058550 2000
with a threefold increase in PGF(2alpha)-R mRNA production, indicating that the regulation   0   0
increased 9-fold at 15 min, PGHS-1 mRNA increased 3.4-fold                   10691023 1999   0   0
hypophysectomized rats testicular PHGPX mRNA levels were increased 3-fold    12544360 2003   0   1
to a 3-fold increase in PhLP mRNA levels. Induction of PhLP                   8248177 1993   0   0
exhibited a 3.5-fold induction of pim-1 mRNA within 4 h of stimulation.       1940364 1991   0   0
Mature PKCbetaII mRNA and protein rapidly increased >3-fold                   9422749 1998   0   0
3- to 4-fold increase in PLP mRNA expression in Actin                         7509847 1994   0   0
by a 3.7-fold increase in PNMT mRNA at 8 In                                   8859016 1996   0   0
a 3 fold increase in anterior pituitary POMC mRNA To                          8246667 1993   0   0
A three-fold increase in POMC mRNA was observed in the pituitary             12520768 2002   0   0
those of controls. POMC mRNA levels were increased 3-fold                     2797383 1989   0   0
and a 3.3-fold increase in PR mRNA in the ventrolateral aspect                1876238 1991   0   0
cells, the predominant 4.5-kb PDG mRNA is increased threefold                10662727 2000   0   0
3- to 4-fold increase in prepro-NPY mRNA levels in the samples                2404748 1990   0   0
an unexpected threefold rise in PRL-R mRNA in the female kidney               1543535 1992   0   0
reaction revealed that proANH gene expression was increased 3.1-fold         14577601 2003   0   0
in a 3-fold increase in proenkephalin A mRNA levels in this                   3538020 1986   0   0
in a 3-fold increase in pS2 mRNA expression. 5 alpha-dihydrotestosterone (5   9164678 1997   0   1
RESULTS: A 3.1-fold increase in PSA mRNA was observed following T            12529988 2002   0   0
cell growth rates. PSA gene expression was increased threefold                9581866 1998   0   0
revealed a 3-fold increase in PTHrP gene transcription 1 h after              8420973 1993   0   0
revealed a 3-fold increase in PTHrP gene transcription 4 h after              8756533 1996   0   0
caused a 3-fold increase in transcription of the pyruvate kinase L            2414297 1985   0   0
RESULTS: Relaxin gene expression was up-regulated 3.4-fold                   12237664 2002   0   1
                                                                              8342612 1993
5-day-old newborn, steady-state renal kallikrein mRNA levels increased threefold             0   0
two- to threefold increase in kallikrein and renin mRNA levels in 2         9392495 1997     0   0
after clipping, intrarenal renin mRNA levels were elevated threefold        7506697 1994     0   0
In the kidney renin mRNA was increased 3.0-fold                             3893995 1985     0   0
2 days after clipping, renin mRNA levels increased 3-fold                   8039838 1994     0   0
caused a 3-fold increase in renin mRNA and protein over 36                 11116131 2000     0   0
                                                                            7690309
concentration-dependent maximal threefold increase in renin mRNA in the cultures after1993   0   0
The level of resistin mRNA increased 3.5-fold                              11684088 2001     0   0
analysis revealed that retinal VEGF/VPF mRNA expression increased 3-fold 7846076 1995        0   0
Levels of S100P mRNA were increased 3.5-fold                               12711858 2003     0   0
the same time, silique ACC oxidase mRNA increased three-fold               12092614 2002     0   0
The threefold increase of SNAP-25 mRNA shortly after birth compared        10842212 2000     0   0
and a threefold increase in fetal lung SP-A mRNA levels when                8291690 1993     0   0
a maximum 3.9-fold increase in SPARC mRNA being reached at 24               1709099 1991     0   1
and a 3.2-fold increase in SP-B mRNA (P < 0.01) in the                     10070110 1999     0   1
produced a 3-fold increase in SPT mRNA in HepG2 cells, and the              9714132 1998     0   0
                                                                           11435347
expression was analyzed. Mechanical strains induced SRA mRNA (3.5+/-0.6-fold at 3% 2001      0   0
in a 3-4-fold increase in both SR-BI mRNA and protein levels,              11707442 2002     0   0
                                                                           10490632 1999
to a threefold increase in SRE-dependent transcription over the level induced                0   0
indicated a 2-4-fold increase in the transcription rate of the SSAT         8360194 1993     0   1
Compared with 2-day-old pituitaries, sst2 mRNA abundance rose 3.25-fold 10499533 1999        0   0
3',5'-cyclic monophosphate for 24 hr increased StAR mRNA 3-fold or          7761400 1995     0   0
showed a 3-fold induction of STC2 mRNA expression in MCF-7 cells           11888893 2002     1   0
a 3.5 fold increase in striatal proenkephalin mRNA and a 30%                3434462 1987     0   1
an approximately 3-fold increase in subunit mRNA levels in intact but       2163314 1990     0   0
TX rat by 25%. SULT60 mRNA expression increased 3-fold                     10821164 2000     0   1
plus E also suppressed ERbeta. TERP-1 mRNA increased 3-fold                10830306 2000     0   0
two- to threefold increase in tet(L) mRNA stability. Using a plasmid-borne 11807047 2002     0   0
with a 3-fold increase in TFPI mRNA 24 hours after release                  9851943 1998     0   0
detected a 3-fold increase of TfR mRNA despite a decrease of iron          10446187 1999     0   0
revealed a 3-fold increase in TfR gene transcription and a 6-fold           8514748 1993     0   0
nearly a 3.6-fold increase in mRNA and a 2.5-fold increase in TGF           8179588 1994     0   0
The same treatment increased TGF alpha mRNA 3-fold above untreated          2524651 1989     0   0
2- to 4-fold increase in TGF-beta 1 mRNA levels due to both                 7570983 1995     0   0
by a 3-fold increase in TGF beta 1 mRNA expression in these                 8937504 1996     0   0
TGF beta 1 mRNA expression increased threefold                              7719414 1995     0   0
factor-beta 1 (TGF-beta 1) mRNA levels were increased threefold             8760166 1996     0   1
about a three-fold increase of TGF-beta 1 mRNA in the regenerating          7572285 1995     0   0
electrophoresis and Western blots. TGF-beta 1 mRNA increased threefold 7688761 1993          0   0
entorhinal cortex lesioning (ECL), TGF-beta 1 mRNA increased threefold 8491285 1993          0   0
renal hypertrophy, TGF-beta 1 mRNA levels were increased threefold          7810696 1994     0   0
provoked a 3-4-fold rise in TGF-beta1 mRNA levels within 30                 8772189 1996     0   0
                                                                           12369727 2001
with a 3-fold increase in protein. TGF-beta2 mRNA increased approximately 6%                 0   0
by a 3-fold increase in TH mRNA levels in the ipsilateral                   7696617 1994     0   0
In the arcuate nuclei, TH mRNA levels increased 3.5-fold                    1686424 1991     0   0
                                                                            9464857 1997
solution hybridization technique. The thioredoxin mRNA level increased 3-fold                0   0
h, in the jeopardized myocardium. Tie2 mRNA increased 3.4-fold             12737621 2003     0   1
of collagenase gene activity. TIMP mRNA level increased three-fold          2175694 1990     0   1
Time-course studies revealed that TIMP-1 mRNA was induced threefold         9472898 1998     0   0
The mRNA level of TIMP-3 increased 3.4-fold                                10765925 2000     0   1
showed a 3-fold increase in TK mRNA levels after growth induction           9776764 1998     0   0
Steady state T-KG mRNA levels increased 3.5-fold                            1287554 1992     0   1
in cultured BASMCs that TM mRNA is increased threefold                      9178727 1997     0   0
Moreover, the 3-fold increase in TNF alpha mRNA caused by WY-14,643 9348444                1997   0   0
In total PBL, TNF-alpha mRNA accumulation increased threefold                8727080       1996   0   0
in a 3-fold increase in TNF-alpha gene expression driven by the gadd        11593333       2001   0   0
                                                                             8615653
TPA stimulation, transcription of TNF-alpha (constitutively present) increased threefold   1996   0   0
24 h, and topoisomerase I mRNA levels increased 3-fold                       8938795       1996   0   0
inducing a 3.5-fold increase in steady state tPA mRNA levels and forskolin 2506174         1989   0   0
about a threefold increase in t-PA synthesis and mRNA expression in HMC 8945961            1996   0   0
elicited a threefold rise in TPH mRNA in median raphe nucleus               14744469       2004   0   0
responded by increasing the level of transferrin mRNA 3-fold as determined 2342475         1990   0   1
a specific 3.5-fold increase in the transferrin mRNA levels in the mammary 8297471         1993   0   0
to a 3-4-fold increase in transferrin receptor mRNA and a coordinate         2016326       1991   0   0
about a threefold increase in tropoelastin mRNA levels at 19 days            7900831       1995   0   0
in a threefold increase in tropoelastin mRNA levels in both the SHR          1943085       1991   0   0
the level of type X collagen mRNA increased threefold                        2124188       1990   0   0
2.5- to 4-fold increase in ubiquitin mRNA in muscle. There was               8182144       1994   0   0
3- to 4-fold increase in UCP mRNA levels in hypothyroid rats                 3211156       1988   0   1
produced a 3-fold increase in UCP1 mRNA in brown adipose tissue             10938091       2000   0   0
induced a 3-fold rise in UCP-2 mRNA levels possibly through transcriptional 11278377       2001   0   0
two- to threefold increase in UCP-2 and UCP-3 mRNA levels in nondiabetic10567009           1999   0   0
two- to threefold increase in UCP-2 and UCP-3 mRNA levels in nondiabetic10567009           1999   0   0
two- to threefold increase in both mRNA and protein levels of UCP3          12721157       2003   0   0
causes a threefold increase in UCP-3 mRNA and a 1.5-fold increase           10950831       2000   0   0
In contrast, UCP-3 mRNA levels were induced 3.4-fold                        11311126       2001   0   0
an approximately threefold increase of UCP3L and UCP3S mRNA The              9686925       1998   0   0
an approximately threefold increase of UCP3L and UCP3S mRNA The              9686925       1998   0   0
in a 3.4-fold induction of UGT1*1 mRNA levels (P<0.001) but only             9737578       1998   0   0
A 3-fold increase in UGT1A1 mRNA was produced by PCN                        11854140       2002   0   0
show a 3-fold increase in UGT1A1 transcription after T3 treatment and a      9202038       1997   0   0
and 3 fold increase of UGT2B15 mRNA expression following treatment with aFGF 9569009       1998   0   0
about a 3-fold increase in rat uterine ER mRNA levels, and these             8418920       1993   0   0
and a 3.7-fold increase in VCAM-1 (P<0.01) mRNA expression in cancer 11815996              2002   0   1
a significant 3.8-fold increase in intestinal VDR mRNA was observed in rats 1647304        1991   0   1
of the most sensitive. Lead induced VEGF mRNA 3-fold and VEGF               10882716       2000   1   0
culture, a threefold increase in VEGF mRNA (P < 0.001) was                   9836521       1998   0   1
Likewise, VEGF mRNA expression was induced 3-fold                           11059786       2000   0   0
maintained in room air, VEGF mRNA levels rose threefold                     11413193       2001   0   0
mRNA remained unchanged. VEGF mRNA and protein increased 3-fold 10468530                   1999   0   0
results showed that VEGF mRNA abundance was increased three-fold            11401064       2001   0   0
than a threefold increase in VEGF mRNA abundance (3.40 +/- 1.45;             9729593       1998   0   0
in a 3.7-fold increase in VEGF mRNA expression after 6 hours                12087245       2002   0   1
showed a 3.7-fold increase in VEGF mRNA when analyzed by Northern            9039936       1997   0   1
muscle VEGF mRNA (via Northern blot) was upregulated 3.5-fold               12086595       2002   0   1
day before birth. These mRNA then further increased 1-5-2-fold               7651752       1995   0   0
culture, SGP-2 protein and mRNA levels were increased 2-4-fold               7974249       1994   0   0
2- to 4-fold increase in expression from an mRNA containing an              10908358       2000   0   0
2- to 5-fold increase in receptor mRNA levels as assessed by                 8119774       1994   0   0
5- and 2-fold increase in mRNA levels in the supraoptic and paraventricular 6514139        1984   0   0
2- to 4-fold increase in mRNA is observed 1 h after                          1374011       1992   0   0
2- to 4-fold induction of transcription by agents that elevate cAMP          2472635       1989   0   0
only a 2-4-fold increase in the rate of transcription of the gene            3571271       1987   0   0
weight and 1.8-4.8-fold increase in the mRNA levels of UCP2 and UCP3 11307932              2001   0   0
a 2--5 fold increase in transcription at the nonpermissive Co-infection        215330      1978   0   0
the control level, while its mRNA expression increased threefold             11769734 2001        0       1
In contrast, exchanger mRNA levels were increased threefold                   8620603 1996        0       0
gene in TT cells. Basal transcription was elevated 3-fold                     8232320 1993        0       0
produced a 3-fold increase in basal transcription as compared to the 2.1 11311550 2001            0       0
measured by run-on transcription of isolated nuclei, increased 3-fold         3379039 1988        0       0
the amount of the 1.9 kb mRNA increased 3-fold                                3017758 1986        0       1
the control group, and its mRNA was induced threefold                         9531255 1998        0       0
in rich media, but its transcription is increased threefold                  11059492 2000        0       0
                                                                              9204001 1997
transcription, assessed by nuclear run-on transcription assay, increased 3-fold                   0       1
by a 3-fold increase in the corresponding mRNA in aldosterone-salt compared  10205234 1999        0       0
the level of the corresponding mRNA is increased 3-fold                       1830489 1991        0       0
3- to 4-fold increase in de novo mRNA synthesis. In contrast,                 2157495 1990        0       0
induced a 3-fold increase in exon II mRNA on postnatal day                   10465264 1999        0       0
of TTF-1 and PKA-cat increased fusion gene expression 3-4-fold as compared    9468516 1998        0       0
                                                                              8887271 1996
A significant threefold increase in renal cortical mRNA levels for transforming                   0       0
C/EBP alpha expression vector, reporter gene expression increased 3-fold 11024036 2001            0       0
two- to threefold increase in steady-state mRNA levels (whether or not        1996672 1991        0       1
express the enzyme. The transcription activity was increased 3-fold           8563137 1995        0       0
and a threefold increase in translatable mRNA for the 23,000 dalton           3141556 1988        0       0
1.8 kb) cDNA, whose corresponding mRNA is increased 3-fold                    2137012 1994        0       0
an approximately threefold increase of mRNA XRCC1/mRNA beta actin as early    9399634 1997        0       0
and a 3-fold increase of mRNA content, measured in the hepatopancreas 9166890 1997                0       1
by 48 hours. mRNA levels for c-jun increased threefold                        7752577 1995        0       1
by a 3-fold elevation in the mRNA levels in those fetuses                     8723735 1996        0       1
by a 3-fold increase in the mRNA expression of endogenous K-ras               9373177 1997        0       0
caused a 3-fold increase in mRNA abundance, primarily through transcriptional 9396552 1997        0       0
cells a 3-fold increase in the amount of mRNA was observed                    1397262 1992        0       0
developing rat lung, mRNA for fatty-acid synthase increased 3-fold            2574595 1989        0       0
                                                                              3422447 1988        0       0
exhibited a 3-fold increase in mRNA for both dihydrofolate reductase (5,6,7,8-tetrahydrofolate:NADP+-oxidoreductase,
experiments, the transcription rate and protein levels increased three-fold 11943172 2002         0       0
fnbB, but not fnbA, mRNA were co-coordinately increased >3-fold              14699158 2004        0       0
greater than threefold increase in the expression of mRNA for cell           12483023 2002        0       1
greater than threefold increase in the mRNA and protein levels of the         8971097 1997        0       0
in a threefold increase in gene expression in transient In                    8995616 1997        0       0
in a threefold increase in transcription of a galF::lacZ chromosomal         12581358 2003        0       0
induced a 3-fold increase in the transcription of both the endogenous         1710218 1991        0       0
induced a 3-fold increase of mRNA for PG-S1, collagen I and III               1870448 1991        0       0
induces a 3-fold increase in stability of mRNA for tyrosine hydroxylase       7908289 1994        0       0
Isk mRNA levels in the uterus increased threefold                             7943198 1994        0       0
only a 3-fold increase in the transcription of p33-mRNA. The insulin          2643510 1989        0       0
produced a 3-fold increase in the level of mRNA encoding sodium               1331749 1992        0       0
protein and mRNA increased significantly, and RV16 induced 3-fold            12751040 2003        0       0
reported a threefold increase of mRNA for the elastase specific alpha         2421641 1986        0       1
revealed a 3-fold increase of tyrosine hydroxylase gene expression after 5 9578138 1998           0       0
showing a 3-fold increase in transcription frequency of the SERCA1 gene 7980406 1994              0       0
the macrophage and renal enzymes. mRNA levels rose three-fold                10759775 2000        0       0
to a 3-fold increase in the mRNA levels of fatty acid                         7910458 1994        0       0
two- to three-fold increase in levels of mRNA and protein for                 1701330 1990        0       1
two- to threefold induction of transcription when stimulated with These       8867808 1996        0       0
with a 3-fold increase in mRNA and a 6-fold increase in MT                    1539169 1992        0       0
estrogen receptor mRNA (62%). Progesterone receptor levels increased 3.2-fold 8207012 1994        0       0
Levels of mRNA for CRF-R1 were increased 3.2-fold                            11043535 2000        0       0
and a 3.4-fold increase in mRNA beta 1 in diabetic rats                       8201010 1994       0    1
2.6- to 3.8-fold induction of mRNA levels in human adrenocortical H295R 8619637 1996             0    1
3- to 4-fold increase in mRNA levels for these enzymes compared               7479800 1995       0    0
average of 3-4-fold increase in gene expression compared with the normal 12067970 2002           0    0
causes a 3-4-fold increase in the rate of transcription of the malic          3192523 1988       0    0
exhibited a 3-4-fold increase in transcription 2 h after the injection,       3192531 1988       0    0
more persistent 3-4-fold increase in transcription rate than either treatment 2404015 1990       0    0
The 3-4-fold increase in the transcription rate occurred with a half-time     3192523 1988       0    0
up to 3.9-fold elevation of the steady state mRNA levels for                  8832987 1996       0    1
showed a 3.5-fold upregulation of insulin gene expression in response to the9005977 1997         0    0
from a 3.6-fold increase in mRNA for this enzyme. Glutathione peroxidase 3127038 1988            0    0
with a 3.6-fold increase in the mRNA at 24 h, whereas                        11295257 2001       0    0
cells, a 3.8-fold increase in mRNA level and a 2.4-fold increase             12376346 2002       0    0
of PCNA mRNA was found to be increased 3.9-fold                               7505276 1994       0    1
with a 3.9-fold rise in mRNA levels but cholesterol 7 alpha-hydroxylase       7814648 1995       0    0
steady state levels of 3alpha-HSD/DD mRNA were increased 4-fold               9495812 1998       0    0
to a 4-fold increase in H3. 3B mRNA levels within 2                           9445389 1998       0    0
                                                                              2686985
wild-type tRNA genes and increase 5S gene transcription 4-fold compared with extracts 1989       0    0
in a 4.1-fold increase in ABC1 mRNA level and also increased                 10896940 2000       0    0
twofold to fourfold increase in actin mRNA levels. In situ hybridizations     1867323 1991       0    1
caused a 4-fold increase in ada mRNA while total alkyltransferase activity 2185901 1990          0    0
in a fourfold increase in steady-state adipocyte leptin mRNA levels compared  9500564 1998       0    0
Adipose tissue GLUT4 mRNA was increased 4-fold                                8495814 1993       0    0
and a fourfold elevation in adipose tissue LPL mRNA steady-state levels,      1657130 1991       0    0
showed a 4-fold increase in levels of aggrecan mRNA (P <                     14558092 2003       0    0
greater than fourfold elevation of AhR mRNA and protein levels, whereas 9706865 1998             0    0
showed a 4-fold increase of a single AlaAT-2 mRNA band after                  8123785 1994       0    0
two- to fourfold increase in alcohol dehydrogenase mRNA levels as estimated   3369866 1988       0    1
more than 4-fold increase in mRNA for the alpha 1B-receptor in the            8307096 1993       0    0
BALB/c mice, whereas alpha 1III procollagen mRNA increased 4-fold             2457084 1988       0    0
AIR, the level of alpha 2M mRNA increased fourfold                            2473162 1989       0    0
with a fourfold increase in steady-state amylase mRNA levels in comparison 1696755 1990          0    0
4.0 +/- 0.3-fold up-regulation of androgen receptor (AR) mRNA was observed,   1315310 1992       0    0
was a 4.5-fold increase in angiotensinogen mRNA by 8 h which                  3793733 1987       0    0
                                                                             12056852 perichondrium
an approximately four-fold induction of Ank mRNA in prehypertrophic chondrocytes and 2002        0    1
analysis, left ventricular apelin mRNA levels were increased 4.7-fold        12914775 2003       0    1
more than 4-fold increase in their APN mRNA content. In the course            8920985 1996       0    1
explain the 4-fold induction in apo A-I mRNA levels caused by                 8003099 1994       0    0
showed a 4-fold increase in apoE mRNA and a 10 to 50-fold                     1932138 1991       0    0
causes a 4-fold increase in AQP5 mRNA and protein levels and induces 12783871 2003               0    0
more than 4-fold increase in mRNA for AR in IMCD cells                        9949255 1998       0    0
maximum of 4.5-fold induction of AR mRNA by MG was accompanied               11961137 2002       0    0
                                                                             11870624 2002
three- to fourfold up-regulation of Bag-1 mRNA expression in anti-CD4 mAb-treated                0    1
(P < 0.001), bcl-x mRNA half-life was elevated 4-fold                         8959331 1996       0    0
two- to four-fold elevation of BDNF mRNA and increased plasma levels         10686079 2000       0    0
and a 4.7-fold increase in the beta 1 mRNA accumulation with peak             8238401 1993       0    0
and a fourfold increase in beta(1)AR mRNA levels. Increased calcium channel  12624436 2002       0    0
found a four-fold increase in bFGF mRNA in tissue surrounding focal           8804711 1996       0    1
                                                                             10075673 1999
betaine-homocysteine methyltransferase (BHMT) mRNA content and activity increased 4-fold         0    0
had a 4.72-fold increase in C3 mRNA and a 19.5-fold increase                  9633921 1998       0    0
a synergistic 4-fold induction of C4BP mRNA levels was In                     1339286 1992       0    0
was a 4-fold increase in CaBP mRNA levels in the kidney                       2411531 1985       0    0
3- to 5-fold increase in cad mRNA levels in both cell                        12746293    2003   0   0
                                                                               1518079
in a 4.6-fold increase in cardiac IGF-I mRNA levels compared to hypophysectomized        1992   0   0
in a 4.5-fold increase in CART mRNA levels after 6 h                         11948252    2002   0   0
to the fourfold increase in stability of cat mRNA in the stationary-phase      9534243   1998   0   0
a 4-5 fold increase in CAT mRNA levels in Kst-6                                1356336   1992   0   1
three- to fourfold increase of total cFABP mRNA in two transgenic              7586757   1995   0   0
to a 4-fold induction of c-fos transcription stimulated by G17 and to          9950815   1999   0   0
                                                                               2535780
expression of c-fos mRNA by increasing c-fos transcription 4-5-fold and slightly         1989   0   0
cardiac pressure overload. The c-fos mRNA was increased fourfold               8620603   1996   0   0
in a four-fold increase in hepatic c-fos mRNA and c-fos                        1322568   1992   0   0
c-myc, and GAPDH. mRNA levels for c-fos increased fourfold                     7752577   1995   0   1
by a 4-5-fold rise in mRNA expressions of c-fos and c-jun,                     9722577   1998   0   0
the phenomenon of culture activation. CINC mRNA rose 4.6-fold                  9756517   1998   0   0
3.9- to 6.0-fold increase in CKII alpha mRNA in the infected                   8467809   1993   0   1
2- to 6-fold increase in c-myc mRNA at 2 weeks, and a                          3479800   1987   0   0
A 4-fold increase in c-myc mRNA expression at 30 min                           8187952   1994   0   0
                                                                             12742828
with a fourfold increase in c-myc transcription. Transcription rate assays performed     2003   0   0
2- to 6-fold increase of myocardial Col I mRNA abundance (P<0.01),           10351968    1999   0   0
induced a 3-5-fold increase in COL3A1 mRNA that was paralleled by            10831628    2000   0   0
by a fourfold increase in colonic H+-K+-ATPase mRNA in rats treated            9083276   1997   0   1
a significant 3-5-fold induction of COX-2 mRNA (p < COX-2                    12837757    2003   0   0
and a 4-fold increase in CPT mRNA by 90-120 The                                2543360   1989   0   0
precipitated a 4-fold increase in CRF mRNA expression relative to sham-operated2795152   1989   0   0
three- to four-fold increase in CRF mRNA                                       3265687   1988   0   1
The amount of CT mRNA increased 4-fold                                         1653227   1991   0   0
An approximately 3-5-fold increase in Cx43 mRNA levels was observed in cultured9788101   1998   0   1
by a fourfold increase in Cx43 mRNA of SMC but not                           11900482    2002   0   1
                                                                             10411001
three- to fourfold induction of CXCR4 mRNA occurred in macrophage-derived foam           1999   0   0
to four fold increase in cyclin D1 mRNA expression, but blocked                7589260   1995   0   0
3 consecutive days. CYP3A1 mRNA levels were increased 4-fold                 11714877    2001   0   0
and high glucose (450 mg/dl) increases decorin mRNA fourfold compared with 100 9815141   1998   0   0
level of the delta subunit mRNA is increased fourfold                          9572274   1998   0   0
                                                                               2155926
0.6-fold, despite 8-fold upregulation of delta-subunit mRNA and reciprocal effects on    1990   0   0
and 3-6 fold increase in renal EGF mRNA relative to controls                   9243098   1997   0   0
by a 4-fold increase in EGFR mRNA levels, maximal at 6-12                      9269899   1997   0   1
EGFR mRNA in DOCA-salt aorta was increased 4.2-fold                          11751714    2001   0   0
in a 4-fold increase in Egr-1 mRNA at 30 min, as                             10829028    2000   0   0
Thymidylate synthase enzyme level and mRNA content increased 3-5-fold 2826452            1988   0   0
revealed a fourfold rise in ET-1 mRNA transcripts, whereas levels of ecNOS8594908        1995   0   1
three- to fourfold increase in ET-1 mRNA in atria and a progressive            7656280   1995   0   0
two- to fourfold increase in ETA mRNA levels were observed in CDH              9473106   1998   0   1
from end-stage heart failure, EXCH transcription was increased fourfold 11013973         2000   0   1
but a 4.7-fold increase in FasL mRNA 3 h after serum                         11159354    2001   0   0
signaling capability; fatty acid translocase mRNA was increased 2.2-6.5-fold 10497230    1999   0   0
produced a 4-fold increase in brain ferritin H mRNA (p <                     12608735    2003   0   1
                                                                               6896326
a median 4.8-fold increase in fibrinogen mRNA species after defibrination compared       1982   0   0
A 3-6-fold increase in fibronectin mRNA was observed in aortic                 2254339   1990   0   0
showed a 4-fold increase in FRalpha gene expression level and 9-fold         11925593    2002   0   1
2- to 7-fold increase in FSH beta mRNA compared to control                     2118538   1990   0   0
caused a fourfold increase in G6PDH mRNA while insulin caused about            6386474   1984   0   0
different; 2) pituitary galanin mRNA concentrations are increased 4-fold       7512494   1994   0   0
observed a 4-fold increase in signal for galanin mRNA in the GnRH              7512492   1994   0   0
revealed a 4.5-fold increase of galectin-1 mRNA (p < 0.01) and a            10950114 2000    0   1
two- to four-fold increase in GAP-43 mRNA in ALS that localized              1387517 1992    0   1
with a 4.5-fold increase in GAPDH mRNA levels in UAEC, although              9408883 1997    0   1
Renal GCS mRNA is maximally elevated 4.4-fold                                1351382 1992    0   0
1.9- to 7.1-fold increase in G-CSF mRNA levels in the lung                   9374735 1997    0   0
4- to 5-fold increase in hepatic GCS-LS mRNA levels by 9                     7910420 1994    0   1
induced a 4-fold increase in GFAP mRNA levels in the hilus                   8062084 1994    0   0
three- to fourfold induction of cytoplasmic GH mRNA by hydrocortisone (1 3882504 1985        0   0
was a 4-fold induction of GH mRNA after incubation with 1                    1900776 1991    0   1
two- to fourfold increase in Gi alpha 1 mRNA Furthermore,                    1315851 1992    0   0
that repressor-mediated control of glpD transcription was increased fourfold 8955388 1996    0   0
causes a fourfold increase in Glu-6-Pase mRNA at 3 h in FAO                  8866562 1996    0   0
and a 4-fold increase in glucocorticoid receptor mRNA within 12              2001346 1991    0   0
caused a 4-fold increase of glucokinase mRNA in liver which was              7755556 1995    0   1
caused a 4-fold induction of glucokinase mRNA within 48 h, which             6323405 1984    0   0
                                                                            11389922
h following feeding. Feeding transiently induced glucokinase mRNA fourfold in control 2001   0   0
three- to fourfold increase in the GLUT1/actin mRNA ratio in ECL             8189217 1994    0   1
induced a fourfold increase in placental GLUT3 mRNA and protein with no 7615800 1995         0   0
placental GLUT3 mRNA and protein levels were increased four-to-fivefold 7615800 1995         0   0
                                                                             8407939 1993
displayed a 4-5-fold increase in GLUT4 mRNA compared with undifferentiated myoblasts         0   0
but the glutamate dehydrogenase mRNA level was elevated 4.5-fold            12164789 2002    0   0
revealed a 4.5-fold increase in GRO-alpha mRNA over basal levels (p          7551561 1995    0   1
elevation and phorbol ester. GRP78 mRNA was induced 3-6-fold                 1655795 1991    0   0
3% DMSO or IFN-gamma increased H chain transcription four-fold and sevenfold,1737936 1992    0   0
an average 4-fold increase in hBD-2 mRNA 18 h after challenge,              14703118 2003    0   1
was a 4.7-fold increase in HB-EGF mRNA levels in human gastric               8621250 1996    0   1
showed a 4.9-fold increase in HB-EGF gene transcription within 2 h           9468491 1998    0   0
caused a 4.7-fold increase in myocardial HCN2 mRNA expression level and only10488052 1999    0   1
had a 4-fold increase in HDC mRNA expression and histamine contents          8828505 1996    0   0
a nearly four-fold increase of the H-FABP mRNA level. Similarly, at          9250607 1997    0   0
We show that ICE mRNA expression is increased 4-fold                         8905663 1996    0   0
associated with fourfold increase in IFN-gamma mRNA in lymph node cells 2104918 1990         0   0
in viable myocytes biventricularly. Moreover, IGF1 mRNA increased 4.3-fold 7505276 1994      0   1
Time-course studies indicated that IGFBP-3 mRNA was increased fourfold 9659296 1998          0   0
concentrated around the injury. IGFBP-4 mRNA levels increased 4-fold         8793117 1996    0   0
and a 4-fold increase in IGFBP-5 mRNA (P < 0.01) in BPH                      7525636 1994    0   1
The level of IGF-I mRNA was maximally increased (4-fold                      1712481 1991    0   0
with a fourfold increase in IGF-I class 1 mRNA and an                       10343285 1999    0   0
exhibited a 4.4-fold increase in IGF-IR mRNA levels. These findings suggest7743492 1995      0   0
respectively; (2) pituitary IL-1 and IL-6 mRNA increased 4-fold              9655081 1998    0   0
IL-1 beta mRNA in BLM-treated mice was increased 4.5-fold                    8617091 1996    0   0
3.4- to 5-fold increase in mRNA levels for IL-10, IL-12p35, IL-6,            8975902 1997    0   0
A Northern analysis showed that IL-11 mRNA increased 4-fold                 10620068 1999    0   1
3.4- to 5-fold increase in mRNA levels for IL-10, IL-12p35, IL-6,            8975902 1997    0   0
                                                                            11966773 2002
induced a fourfold increase of IL-17R mRNA expression and augmented the IL-17-stimulated     0   1
induced a 4-fold increase in IL-18 mRNA levels and elevated the content 10859481 2000        0   1
3.4- to 5-fold increase in mRNA levels for IL-10, IL-12p35, IL-6,            8975902 1997    0   0
respectively; (2) pituitary IL-1 and IL-6 mRNA increased 4-fold              9655081 1998    0   0
RESULTS: Compared to shams, IL-6 mRNA levels increased 4.5-fold             12943813 2003    0   1
induced a 4.7-fold increase in IL-6 mRNA (P < 0.05) with a                  10362698 1999    0   0
that rat liver IL6-R mRNA concentrations were increased 4.2-fold             2174054 1990    0   0
10 micrograms/ml after 6 h. IL-8 mRNA increased 4-fold                       8061117 1994    0   0
of 4 h duration increased IL-8 gene transcription fourfold above            10409244 1999      0   0
mRNA, a fourfold increase in induced IL-8 mRNA and less than                  7751024 1995     0   0
A 4.1-fold increase in iNOS mRNA was observed in the old                    11207215 2001      0   1
only a four-fold increase in insulin mRNA levels. Pancreatic islet amyloid    2612759 1989     0   0
beta actin mRNA, insulin receptor mRNA levels increased 4-fold                7750897 1995     0   1
whereas thymidine kinase 1 mRNA levels were up-regulated 4-fold             11358795 2001      0   0
sevenfold by 8 h; K-ras mRNA was induced fourfold                             8436603 1993     0   0
                                                                            11825065 2002
identified a 4-fold induction of lactase mRNA abundance in intestinal epithelial               1   1
                                                                              7508390 1994
by a fourfold increase in lactase-phlorizin hydrolase mRNA levels, suggesting transcriptional  0   0
The LH receptor mRNA was increased 4-5-fold                                   2226328 1990     0   0
The liver phosphofructokinase mRNA level increased 4-fold                     2969893 1988     0   0
to cyclic gilts, endometrial L-kininogen gene expression increased fourfold 13679312 2004      0   0
causes a 4-fold increase in LPL mRNA accompanied by a 3-                    10067830 1999      0   0
subjects with bridging fibrosis, LT-beta mRNA levels increased 4.4-fold     12912866 2003      0   0
the cortex, the levels of MCAD mRNA rose 4-fold                               8615829 1996     0   0
an approximately 4-fold increase in mCG alpha mRNA levels within 6            1612035 1992     0   0
induced a fourfold increase in MCM mRNA on Northern blots from                8929440 1996     0   1
in a fourfold induction of MCP-1 mRNA expression. The time course             9409217 1997     0   1
In vivo, M-CPT-I mRNA levels increased (4.5-fold                            11473052 2001      0   0
observed a 4-fold increase in Mdr1 mRNA expression in the intestines          9097955 1997     0   0
                                                                            14656894 angiotensin
mediated a 4-fold increase of MEK1,2-dependent PAI-1/luciferase mRNA expression by2004         0   0
a selective fourfold increase in mHS mRNA abundances in both neonatal 9798904 1998             0   0
was a fourfold elevation in MMP-9/GAPDH mRNA transcript levels in 5.0- 9337194 1997            0   0
showed a 4-fold increase in islet MnSOD mRNA content after a 90-min           1533363 1992     0   1
the MRP mRNA and protein levels were increased 4.5-fold                     11206006 2000      0   1
In vivo TPA induced hepatic MT mRNA 2.36-5.88-fold (dot blot)                 1397494 1992     0   1
showed a four-fold increase in Mx mRNA levels in PBMC from                  11479146 2001      0   1
an approximately 4-fold increase in Myf5 mRNA levels, but similar effects 11148132 2001        0   0
induce a similarly rapid increases in Na,K-ATPase mRNA (4-fold within 6       7478810 1995     0   0
4- to 5-fold increase of NF-kappa B1 gene expression at both                  7905283 1993     0   1
level of NGF mRNA in total embryo increased four-fold                         3416767 1988     0   0
                                                                              7573463 1995
containing membranous airways, NK2-receptor mRNA expression was increased fourfold             0   0
but the half-life of norA mRNA was increased 4.8-fold                       11244079 2001      0   0
three- to fourfold increase in NQO1 mRNA expression. We found that          11275421 2001      0   0
H4 cells only. cAMP increased endogenous OAT mRNA 4-fold in HepG2             1845993 1991     0   0
two- to fourfold increase in ob mRNA and a twofold increase                 10334301 1999      0   0
3- to 5-fold increase in ODC mRNA occurred in kidney of rats                  8380973 1993     0   0
and a fourfold increase in ODC mRNA transcripts in the                        1564558 1992     0   0
synchronized MCF-7 cells. ODC mRNA and activity increased four-fold           8012036 1994     0   0
and a 4-fold increase in steady-state ODC mRNA levels. In contrast,           2055284 1991     0   0
an approximate 4-fold increase in OLE1 mRNA half-life in the absence          8824209 1996     0   0
PTH increased the levels of osteocalcin mRNA 4-5-fold in both               14634012 2004      0   0
observed a 4.4-fold increase in oxytocin receptor mRNA levels in the VMH 9032770 1997          0   0
fibroblasts, a 4-fold increase in p48 mRNA amount was observed 38           10777490 2000      0   0
with type 2 diabetes. p85alpha mRNA was elevated fourfold                   12397383 2002      0   0
caused a fourfold increase in PAF receptor mRNA expression that was           9725815 1998     0   0
and transient 4-fold increase in PAI-1 mRNA that was maximal at               8816919 1996     0   0
caused a four-fold increase in specific PAI-1 mRNA and a three-fold           8259551 1993     0   0
The PCK mRNA is initially increased 4-fold                                    1851745 1991     0   0
demonstrate a fourfold increase in cell PDGF mRNA immediately after exposure  1490932 1992     0   1
as a 4.3-fold increase in PDGF-C mRNA was detected in microdissected 12707385 2003             0   1
In isolated white adipocytes, PGC-1 mRNA increased 4.4-fold                 11108270 2000      0   0
three- to fourfold increase in PGHS-1 mRNA; PGHS-1 mRNA remained elevated   8215426 1993        0   0
whereas a 4-fold increase in POA ERbeta mRNA expression was observed12810577 2003               0   0
3- to 5-fold increase in POMC mRNA level in the                             6572972 1983        0   0
                                                                            9950217
h, a 3-6-fold increase of PPARgamma2 mRNA was observed, whereas PPARgamma1 1999                 0   0
                                                                           12409963 2002
synthase (2.1-fold increase, 0.05), or preproendothelin-1 gene expression (4.2-fold increase,   0   0
in a fourfold increase in PRL mRNA levels. No interactions were            12804517 2003        0   0
demonstrated a 4-fold increase in pro-alpha 2 (I) mRNA that was             8906362 1996        0   0
                                                                            24
an approximately fourfold increase in the proenkephalin mRNA levels within 7894225 1994         0   0
                                                                            KCl,
and a 4-fold increase in proenkephalin mRNA (mRNAenk). These effects of 2458344 1988            0   0
show a fourfold increase of proenkephalin mRNA content in striatum but      6190182 1983        0   0
three- to fourfold increase in proinsulin mRNA levels relative to total     6761201 1982        0   0
demonstrated a 4-fold increase of PrP mRNA in relation to cellular          7912403 1994        0   1
found a fourfold increase in the PSA mRNA level in prostatic               11791186 2002        1   0
calcium and phosphate. PTH mRNA levels were elevated 4-fold                 9165053 1997        0   1
to a fourfold increase in PTH mRNA and calcitonin mRNA                      1469095 1992        0   0
                                                                            8624779 1996
situ hybridization demonstrated that PTHrP mRNA expression increased fourfold                   0   0
an approximately 4-fold induction of PTP-PEST mRNA within 36                8454633 1993        0   0
Cellular RA binding protein (CRABP) mRNA rose fourfold                      7485518 1995        0   0
to a 4-5-fold increase in the RAR gamma mRNA level, but                     8394693 1993        0   1
3- to 6-fold upregulation of REN mRNA binding proteins. RNase degradation  12600897 2003        0   0
renal CaBP and renal CaBP mRNA levels increased 4-fold                      2411531 1985        0   0
to a fourfold increase in renin mRNA levels without changing AT1            7675636 1995        0   0
A rapid, fourfold induction of RIP140 mRNA was detected within 3           11467847 2001        1   0
two- to fourfold increase in rNLRR-3 mRNA in rat normal fibroblasts        11549284 2001        0   0
and downregulated thereafter, while Kir1.1b (ROMK2) mRNA increased fourfold12466933 2002        0   1
and a fourfold increase in rpsL-bmpD mRNA compared to growth of B.         12010998 2002        0   0
probasin and RWB mRNA levels. Probasin mRNA increased 4.5-fold              7628369 1995        0   1
an approximately fourfold increase in SAA mRNA levels in non-regenerating  12543124 2003        0   0
had a 4.5-fold increase in SCP-x mRNA transcript levels. Western blot      10191285 1999        0   0
                                                                            9154218
an approximately four-fold increase of serotonin transporter mRNA in Brodmann's area 1997       0   0
size increased nearly 2-fold. SHP mRNA levels increased 4.1-fold           12897188 2003        0   0
The abundance of skeletal alpha-actin (SK) mRNA increased fourfold          7653628 1995        0   0
While SLF mRNA expression was increased four-fold                           7507856 1994        0   0
caused a 4-fold increase in somatostatin mRNA levels within 4 hr            2875459 1986        0   0
in a 4-fold increase in SOX4 mRNA levels within 4 h                        10343288 1999        0   0
greater than 4-fold increase in the rate of transcription of SP-A           2848814 1988        0   0
the amount of mRNA for SP-A was increased 4-fold                            8408275 1993        0   0
saline-treated or uninjected animals. SP-B mRNA was increased fourfold 8291690 1993             0   0
induced at 2 days. SP-D mRNA was increased fourfold                        11159007 2001        0   0
greater than 4-fold elevation in liver ST6Gal I mRNA was                   10521536 1999        0   0
An approximately four-fold increase of sTnC mRNA level in the transfected 12062407 2002         0   0
in a 4-fold increase in SULT-20/21 mRNA in HX GH                            9566754 1998        0   0
increased seven-fold, and T alpha 1 mRNA increased four-fold                1348250 1992        0   0
showed a fourfold increase in TAXREB107 mRNA after 1 hr of erythropoietin  10082121 1999        0   1
a approximately 4-fold increase in TfR mRNA levels within 2-6 h,           11264285 2001        0   0
                                                                            2033054 1991
3- to 6-fold increase in TGF-alpha mRNA expression. Increased production of TGF-alpha           0   0
                                                                            2257881 1990
induced a four-fold increase in TGF-beta mRNA transcript levels. This increase                  0   0
two to fourfold increase in TGF-beta 1 mRNA in activated as                 1939646 1991        0   1
caused a 4.1-fold increase in TGF-beta 1 mRNA associated with an            7929822 1994        0   1
biliary fibrosis TGF-beta1 and CTGF mRNA levels increased fourfold         11290541 2001        0   0
(0.5-2.0 x 10(6) cells/cm2) TH mRNA levels increased 4-fold                 1685006 1991        0   0
Forskolin (10 microM) also increases TH transcription (fourfold in 15       1359019 1992        0   0
report a 4-fold increase in TH mRNA half-life in DMPP-treated cells           14741398    2004   0   0
4.2- and 4.5-fold increase of TH mRNA which was maximal 2                       2872048   1986   0   0
a transient 4-fold increase in thioredoxin reductase mRNA at 1 hour             9042207   1996   0   0
inducing a 3-5-fold increase in the steady-state Thy-1 mRNA level, concomitant  7649169   1995   0   0
whereas the amount of TIMP mRNA was increased fourfold                          8006459   1994   0   1
TIMP-1 mRNA levels also significantly increased 4-fold                          9127337   1997   0   0
demonstrated connective tissue growth factor mRNA was increased 3-5-fold      10845662    2000   0   1
in a 4-fold increase in TM mRNA at 4 and 8                                      9409303   1997   0   0
A 4-fold increase in TNF mRNA levels was demonstrated after                     1722107   1991   0   0
TNF mRNA in peritoneal macrophages rose fourfold                                8015310   1994   0   0
Tumour necrosis factor-alpha mRNA levels were increased fourfold                8384958   1993   0   0
Approximately a four-fold increase in TNF alpha mRNA levels was observed9106252           1997   0   1
vein endothelial cells (HUVEC), TNF-R1 mRNA is increased four-fold            10880244    2000   0   0
putida F1 cultures, todC1 mRNA levels increased 4.4-fold                        9835608   1998   0   0
with a 4-fold induction in t-PA gene transcription and a 3-fold               11279071    2001   0   0
to a fourfold increase in transferrin mRNA synthesis at As                      3785157   1986   0   0
A 4.8-fold increase in TRH mRNA and a 4-fold increase                           2471071   1989   0   0
primary Sertoli cell cultures. TSC-22 mRNA transiently increased 4-fold         8161377   1994   0   1
confirmed a 4.0-fold increase in steady state mRNA for TSG6 following         11278699    2001   1   1
a maximum 4-fold increase in TSH beta mRNA and a 2-fold                         1446607   1992   0   0
an average 4-fold increase of TSH-R mRNA levels in the thyroids                 8981006   1996   0   0
A four-fold increase in type 2 17beta-HSD mRNA levels was                     14672737    2003   0   0
three- to fourfold increase in type X collagen mRNA within 24                   9257195   1997   0   0
three- to fourfold increase in mRNA levels for ubiquitin and HC3                9005983   1997   0   1
produced a 4-fold increase in UCP1 mRNA levels in Dbh+/- mice                 10499537    1999   0   0
4- to 5-fold increase in UCP1 mRNA levels in both interscapular                 9886838   1999   0   0
3-MC and PCB each increased UGT1A7 mRNA 4-fold but did                        11854140    2002   0   0
showed a 4-fold increase in UGT1A8 transcription after treatment with         11992647    2002   0   1
urokinase-type PA (u-PA) activity and mRNA are increased 4.9-fold               1328201   1992   0   0
and a fourfold increase in uPA and uPAR mRNA levels in pancreatic               9020484   1997   0   1
showed a 4-fold increase in uPAR mRNA transcription and approximately 40%       9824646   1998   0   0
primary cell culture. RESULTS. Thrombin increased u-PAR mRNA 4-fold in RPE      7558719   1995   0   1
greater than 4-fold up-regulation of VCAM-1 mRNA was seen in rabbits          10552999    1999   0   0
a 4-5 fold increase in the VDR mRNA level. VDR mRNA                             7686756   1993   0   1
induced a 3-5-fold increase in VEGF mRNA expression in all cell                 8706019   1996   0   0
Submaximal exercise for 1 h increased VEGF mRNA 4.2-fold and TGF-beta(1)      10749807    2000   0   1
greater than fourfold increase of VEGF mRNA levels. ZR-75 breast cancer 14647449          2004   0   0
two to fourfold increase in retinal VEGF protein gene expression (p           11126403    2000   0   1
an approximately fourfold increase in VEGF protein and mRNA expression,10444484which      1999   0   1
a significant 4.6-fold increase in VEGF mRNA expression over time in culture    9039936   1997   0   1
the steady-state level of hepatic Vn mRNA increased 4-fold                      7519600   1994   0   0
which the WAF1 mRNA steady-state level is upregulated fourfold                10327058    1999   0   0
three- to fourfold induction of zif/268 mRNA levels was observed 45             8654528   1996   0   1
                                                                                9
stimulated a 2-7-fold increase in steady state mRNA levels for the parathyroid397968      1994   0   0
ODC activity and mRNA levels were elevated 3-6-fold                             8495425   1993   0   0
3- to 5-fold increase in mRNA expression during maturational growth of the10224672        1999   0   0
3 to 5-fold increase in mRNA levels for the M2 subunit,                       10076525    1998   0   0
3- to 5-fold increase in the transcription rate. In the fgdA                    9342838   1997   0   0
with a 3-6-fold increase in gene expression for oncogenes, DNA repair           2092869   1990   0   0
in a 2.5-6-fold increase in transcription over controls with hepatocyte nuclear 9931303   1999   0   0
                                                                              12736183
twofold and fourfold increase in enzyme mRNA levels. BAT hemidenervation resulted         2003   0   0
three- to fourfold increase in Purkinje cell mRNA for the 67                    8774452   1996   0   0
                                                                               10320799 1999
an almost fourfold increase of the corresponding mRNA levels compared to sham-operated          0     0
three- to fourfold induction of fusion gene mRNA and secreted human              2769161 1989   0     0
at 0.1 ppm as selenite increased muscle mRNA 4-fold relative to a                7568010 1995   0     1
to a 4-fold increase in its transcription rate. Levels of NF-H                   2928342 1989   0     0
an abrupt 4-fold increase in ovarian mRNA levels occurred between days 8462476 1993             0     0
by a 4.2-fold increase in steady state mRNA levels for the beta                  2298754 1990   0     0
a transient four-fold increase in the transcription level of both genes        10517332 1999    0     0
about a 4-fold increase of the reporter gene expression Primer                 11556716 2001    0     0
an approximately 4-fold induction of reporter gene expression due to             8972864 1996   0     0
an approximately fourfold increase in the abundance of mRNA coding for 9038833 1997             0     0
and a 4-fold increase in the mRNA levels for the                                 7674372 1995   0     0
                                                                                 8118044
approximately a four-fold rise in transcription from the endogenous or a heterologous 1994      0     0
contrast, a fourfold increase in the mRNA level of CL100 (3CH134),               7798338 1995   0     1
elicits a 4-fold increase in the rates of transcription of the two               1684180 1991   0     0
                                                                                 1782151 1991
extract, a 4-fold increase in transcription was observed. These experiments demonstrate         0     0
                                                                                 9065445 1997
greater than 4-fold increase in transcription from potentially functional L1 elements           0     0
in a 4-fold increase in the rate of transcription of the rat                     8174761 1994   0     0
                                                                               11985711 2002
in a fourfold increase in transcription of the sigma28-dependent major flagellin                1     0
in a fourfold induction of reporter gene expression during CONCLUSIONS: 12127821 2002           0     0
In proliferating cells, mRNA levels are increased 4-fold                       10506483 1999    0     0
mediate a 4-fold induction in reporter gene expression by retinoic               8832580 1996   0     0
point taken (15 min). Transcription rate was increased 4-fold                    2543360 1989   0     0
produced two-to fourfold elevation of the mRNA in both normal and mutant 2033473 1991           0     0
                                                                               10666313 2000
produces a fourfold increase in transcription of the fibronectin gene in cultured               0     0
response (> 4-fold increase in mRNA level) at 1 ng/ml                          12540490 2003    1     1
RESULTS: The mRNA abundance of hepatic Glu-6-Pase increased fourfold           10912855 2000    0     0
revealed a 4-fold increase in transcription observed as early as 1               2153135 1990   0     0
show a fourfold increase in the rate of transcription of the fliC              11790733 2002    0     0
showed a 4-fold increase in mRNA after 8 days Protein                            7612002 1995   0     1
showed a 4-fold increase in mRNA expression, peaking within 4 hr                 9568675 1998   0     1
                                                                                in AM
significant maximum 4.0-fold up-regulation of NF-kappa B gene expression10541885 1999           0     0
The copy number of the mRNA was increased 4-fold                               10715550 2000    0     0
The four-fold increase in mRNA correlates with and is sufficient                 7509203 1993   0     0
The R-2/3 mRNA content in the liver increased fourfold                           8476059 1993   0     1
                                                                               12606504 2003    0     0
three- to fourfold increase in mRNA expression of glutamine:fructose-6-phosphate aminotransferase (GFAT),
three- to fourfold increase in mRNA stability but not by changes                 1847169 1991   0     0
three- to fourfold increase in the mRNA encoding the catalytically active        8917676 1996   0     0
three- to fourfold increase in the rate of transcription of the endogenous       8392622 1993   0     0
threefold to fourfold increase in mRNA abundance for two transgenes and an     11752382 2001    1     0
                                                                               11551827 2001
to a four-fold increase in transcription of this S-adenosyl-L-methionine binding                0     0
treatment, Northern blot hybridization indicated that mRNA increased fourfold  10208301 1999    0     1
two- to fourfold increase in the level of mRNA for both                          8823493 1996   0     0
two- to fourfold increase in transcription in several cell types, including      8083955 1994   0     0
where a 4-fold increase in mRNA was paralleled by a 20-fold                      2208584 1990   0     0
with a 4-fold increase in abundance of the mRNA for the alpha                    2554299 1989   0     0
with a fourfold increase in transcription rates of the TNF-alpha gene,           8898955 1996   0     0
A 4.4 fold increase in the mRNA level was observed after                         2435283 1987   0     0
The relative content of the mRNA increased 4,4-fold                               407223 1977   0     0
4- to 5-fold increase in the expression of mRNA for the ATP                    12897186 2003    0     0
3.5- and 5.1-fold increase in mRNA alpha 1 and mRNA beta                         2156438 1990   0     1
by a 4.5-fold increase in the initial transcription rate and a 2.4-fold        12095688 2002    0     0
thaliana is light-regulated, with its mRNA level increased 4.5-fold              8401602 1993   0     0
a maximal 4.5-fold increase in mRNA after 8 h with AAT                        9256066 1997   0   0
highest activity in reporter assays. Transcription was induced 4.6-fold      10224410 1999   0   0
up to 4.6-fold increase in gene expression of the transcription factor        9737890 1998   0   0
5-7 days before hemorrhage (HN) Epo mRNA increased 5-fold                     8734478 1996   0   0
Thus, the 5-fold rise in 5 alpha-reductase mRNA concentrations that occurred  1505481 1992   0   1
2-fold between E17 and P27, 5-HT1c mRNA increased 5-fold                      2015654 1991   0   1
                                                                              9006961 1997
hepatoma cells increased the content of 7alpha-hydroxylase mRNA 3-fold above the levels      0   0
of these parameters. Acyl-CoA oxidase mRNA levels increased 5-fold           11162775 2001   0   0
vascular cell adhesion molecule (VCAM)-1 mRNA expression increased 5-fold    11950695 2002   0   0
adipophilin in humans). ADRP mRNA was specifically upregulated 5.4-fold 15075187 2004        1   0
At 10(-7) M, c-RA increased AFP mRNA 5-fold and chloramphenicol               7539613 1995   0   1
3.2 to 7.4-fold increase of A-IV mRNA in the To                              12924437 2003   0   1
of TNF alpha mRNA in corneal explants increased fivefold                      8641833 1996   0   0
and by day 20 alpha mRNA was increased 5-fold                                 2426086 1986   0   0
with a 5-6-fold increase in alpha 1(I) mRNA levels. PGE2 at                   2676997 1989   0   0
5.3 +/- 0.8-fold increase in alpha 2A receptor mRNA abundance as              1848558 1991   0   0
Skeletal/cardiac alpha-actin mRNA isoforms were already increased fivefold 7680287 1993      0   0
with a 5-fold increase in alphaENaC mRNA expression that could be            10212217 1999   0   0
three- to fivefold increase in alpha-ENaC mRNA (but not in those             10232677 1999   0   1
                                                                             12624436
produced a fivefold increase in androgen receptor mRNA levels. Testosterone treatment2002    0   0
5- to 6-fold increase in new 32P-labeled Ann-II mRNA levels, compared        10888061 2000   0   0
a selective 5-fold increase of ANP mRNA in Dox-treated dog hearts            11715857 2001   0   1
twofold and RV irANP and ANP mRNA increased fivefold                          9249516 1997   0   0
                                                                             11591730
apoptosis a 5-6-fold upregulation of Apaf1 mRNA was detected. Induction of neuronal 2001     1   0
four- to fivefold increase of apo E mRNA abundance. The addition              7635986 1995   0   0
10(-11) M of this retinoid induced apoD mRNA 5-fold over the control,         8943263 1996   0   1
to a fivefold increase of total APP mRNA without change in the                2205513 1990   0   1
In the liver, AT1 mRNA levels increased fivefold                              8432862 1993   0   1
in a fivefold increase in AT1R mRNA expression at 24 hours                   14675034 2004   0   0
Four- to fivefold induction of betaA mRNA was observed in postconfluent 10644566 2000        0   1
least a fivefold increase in C3 mRNA in LPS-treated monolayers, which         3900137 1985   0   1
showed a five-fold increase in the CA12 mRNA level with no                   12676895 2003   0   1
                                                                              9245785 1997
revealed a fivefold increase in calreticulin mRNA levels. Thapsigargin also induced          0   1
and a 5-fold increase of Cap G mRNA were observed in cells                   12754261 2003   0   0
we found that CCR1 mRNA expression was increased 5-fold                      11556842 2001   0   0
three- to five-fold increase in CD95L mRNA levels within 6 hours,             9425938 1998   0   0
and a 5-fold increase in Cdk4 mRNA abundance was observed within              7669723 1995   0   0
was a 5-fold increase in the cervical IGF-I mRNA level 12                    11377977 2001   0   0
by a fivefold increase in transcription rate of the CETP transgene,           1401066 1992   0   0
an approximate 5-fold increase in c-fos mRNA levels within 90 min             2496305 1989   0   0
two- to fivefold increase in c-fos mRNA levels was observed in plateau        9451418 1997   0   1
When noradrenaline was infused, c-fos mRNA was increased fivefold             8287409 1993   0   1
BN (10 nM) increased c-fos mRNA fivefold using NCI-H345                       7784258 1995   0   0
PACAP-27 (100 nM) increased c-fos mRNA 5-fold using NCI-N417                  8761002 1996   0   0
(1 microM) induced c-fos and TH gene transcription fivefold and twofold,      7609611 1995   0   0
and transient 5-fold increase in c-fos and c-jun mRNA levels, followed        1331650 1992   0   0
was a 5-fold increase of c-fos and c-myc mRNA within 30                       9426692 1998   0   0
and transient 5-fold increase in c-fos and c-jun mRNA levels, followed        1331650 1992   0   0
after K+/serum deprivation. Levels of c-jun mRNA increased fivefold           8922404 1996   0   0
an about 5-fold increase in c-jun mRNA level in response to cell              7619047 1995   0   0
Under these conditions, the c-jun mRNA was increased 5.4-fold                 1448115 1992   0   0
or a 5.2-fold increase of maximal c-jun mRNA expression respectively         11720885 2001   0   0
4- to 6-fold increase in c-myc mRNA levels. Additivity is also                2674692 1989      0       0
was a 5-fold increase of c-fos and c-myc mRNA within 30                       9426692 1998      0       0
The level of c-myc mRNA was increased five-fold                               2450880 1988      0       0
TAM treatment for 72 hours increased c-myc mRNA five-fold (from a relative8614006 1996          0       1
that a fivefold increase in collicular KCC2 mRNA levels was associated       11445278 2001      0       0
                                                                              7531177
induced a 3-8-fold increase in cotransporter mRNA levels suggesting that the increase 1994      0       0
an approximately 5-fold rise in expression of COX-2 mRNA detected by         11285187 2001      0       1
fetal lambs to NB2. COX-2 mRNA levels increased fivefold                      9458802 1998      0       0
three- to fivefold induction of COX-2 mRNA and protein expression but        14988266 2004      0       0
(0.1%) or all-trans retinol (1.6%) induced CRBP mRNA 5.5-fold (p <            7615982 1995      0       0
A fivefold increase in CRBP1 mRNA levels was observed 32-48                   8382159 1993      0       0
to a 5-fold increase in CT gene transcription after a lag                     3258183 1988      0       0
                                                                             11900482 2002
by a fivefold increase in Cx26 mRNA of urothelium. Scrape-loading of propidium                  0       1
                                                                              2916850 1989      0
assays, treatment with 1,2-benzanthracene induced cytochrome P450c transcription 5.3-fold over untreated1
                                                                             12517797 2003
identified a 5-fold up-regulation of cytokeratin 14 mRNA expression in ZD:p53-/-                0       0
A 5-fold increase in DNA polymerase beta mRNA was observed                    1397262 1992      0       0
in a 5.8-fold elevation of steady-state DT-diaphorase mRNA levels. Both enzyme9815750 1997      0       0
                                                                              2943984 1985
induced a fivefold increase in E1A transcription rate. Deletion analysis suggested              0       0
exhibited a 5.7-fold increase in EGF receptor mRNA concentrations, and 20 7959207 1994          0       1
the highest concentration used, elastin mRNA levels increased 5-fold          9426317 1998      0       1
expressed throughout the gut. Intestinal EP(2) mRNA increased fivefold 12431904 2003            0       0
induced a 5-fold increase in the epididymal Epo mRNA transiently, which 12147241 2002           0       0
that the 5-fold increase in ER mRNA levels in endometrium of ovariectomized  12554762 2003      0       0
variants were found. After denudation, ERbeta mRNA increased five-fold 11500242 2001            0       0
                                                                              9514014 1998
All these compounds induced erythropoietin gene expression 5-fold at concentration              0       0
                                                                              9644066 1998
These compounds induced erythropoietin gene expression 5-fold at a concentration                0       0
                                                                             10075801 1999
This compound induced erythropoietin gene expression fivefold at a concentration                0       0
two- to fivefold elevation in ET-1 mRNA levels in aorta, liver,              12490547 2003      0       0
least a fivefold increase in Ets-1 mRNA at 3 h of phorbol                     9595399 1998      0       0
despite a 5-fold increase in FAS mRNA. FAS mRNA stability as                  8463228 1993      0       1
Hepatic FAS mRNA levels were elevated five-fold                               1552231 1992      0       0
muscle cells increase expression of ferritin H mRNA 4-6-fold after 48         3410854 1988      0       0
in a 5-fold increase in FGF receptor mRNA levels at 6-8                       1846535 1991      0       1
showed that left ventricular fibronectin steady-state mRNA increased fivefold8137508 1994       0       1
                                                                             12507307 2003
could be shown that C5a upregulated fibronectin-specific mRNA five-fold whereas entactin,       0       1
A 5-6-fold increase in the expression GAD67 mRNA was found                   12367554 2002      0       0
and a 5-fold increase in the galanin mRNA signal content of GnRH              8730651 1996      0       0
showed a 5-fold induction of galanin mRNA in GnRH neurons (68                 8730652 1996      0       0
beta- and gamma-Actin gene expression was also induced 5-fold                 8482333 1993      0       0
About five fold increase in GAP-43 mRNA in the colchicine-treated hypothalamic7637588 1995      0       1
a rapid 5-fold increase in hepatic GCS mRNA levels reaching maximal           7910420 1994      0       1
contrast, the 5-fold increase in GFR alpha-2 mRNA after 24 hr                11319768 2001      0       0
revealed that synthesis of GHR mRNA was increased 5.9-fold                   11369615 2001      0       1
IGF-I and five-fold increase of GH-R mRNA expressions versus sham-operated    9039091 1997      0       0
showed a 5-fold elevation in GHRH mRNA expression in the ARC-VMH              8580424 1995      0       0
4-, and 6-fold increase in glucose transporter mRNA induced by glucose        2649505 1989      0       1
8- and 3-fold induction in GLUT1 mRNA and GLUT1 protein,                      8892317 1996      0       0
nearly a 5-fold increase in glutamine synthetase mRNA levels in lung          7630137 1995      0       1
by a 5-fold increase in cells expressing mRNA for GM-CSF (p                   9876226 1998      0       0
their lean littermates. Islet GPI-PLD mRNA was increased 5-fold              11735099 2001      0       0
beta-type platelet-derived growth factor receptor mRNA was increased 5.8-fold10212001 1999      0       0
about a 5-fold increase in GT mRNA in adipocytes, whereas insulin             2656715 1989      0       0
HB-EGF optimally increased the levels of HB-EGF mRNA 5.4-fold at 1             8051092 1994   0   1
in a 5-fold increase in hepatic hemopexin mRNA content within 48               1988069 1991   0   0
a specific fivefold increase in histone mRNA in 30 The                         6209555 1984   0   0
and a 5-fold increase in hMT-le mRNA levels in SCC25/CP cells,                 7511778 1994   0   0
at 5 hr. HO-1 mRNA was maximally induced fivefold                             11258550 2000   0   0
quantitative RT-PCR revealed that hPRL gene expression increased 5-fold 11701738 2001         0   1
                                                                               2193225 1990
The mean 5-fold increase in (-)-gossypol-induced hsp-70 mRNA appears coincident with a        0   1
5 +/- 2-fold increase in hepatic hsp-70-like mRNA was observed 9               3274897 1987   0   0
to five fold induction of human growth hormone mRNA and a similar              7116452 1982   0   0
and a fivefold increase of IGFBP-5 mRNA levels on day                         11739080 2002   0   0
that a 5-fold increase in IGFBP-5 mRNA levels observed in RRO-I                1280130 1992   0   0
muscle a fivefold increase in IGF-I mRNA levels associated with an            11739080 2002   0   0
and a 5-fold increase in liver IGF-I mRNA concentrations saline-treated        1375898 1992   0   1
exhibited a 5.6-fold increase in IGF-IIR mRNA levels, whereas in 3             9361090 1997   0   0
Furthermore, IL-1ra mRNA levels were elevated 5-fold                           7921651 1994   0   0
caused a 5-fold increase in relative inhibin alpha-subunit mRNA levels and a2744212 1989      0   0
model, a 5.0-fold increase in inhibin-alpha mRNA levels, similar to that      10579342 1999   0   1
four- to fivefold increase in iNOS mRNA was observed in wild                  10562585 1999   0   0
induce a 5-fold increase in IR mRNA levels. Studies of IR                      2407479 1990   0   1
dot blot analysis, kallikrein mRNA levels were increased 5-fold                3643103 1987   0   1
                                                                              11387233 2001
but transient fivefold increase in leptin mRNA levels. This transcriptional control           0   0
showed a 5-fold increase in Lerk-5 mRNA expression when it was                 9533549 1998   0   0
levels of lipo I mRNA and protein increased 5-fold                             1827255 1991   0   0
                                                                               9150252 1997
rapid, transient, 5-fold increase in LPL mRNA level. Norepinephrine (NE) injection            0   0
5- to 6-fold increase in the L-type enzyme mRNA level after                    6526814 1984   0   1
by a 5-fold upregulation of LV mRNA expression of atrial natriuretic          12403658 2002   0   0
of nephritic kidneys mRNA for MCP-1 was increased 5-fold                      10862646 2000   0   1
showed a 5-fold increase of MCP-1 mRNA when compared with cells                9861781 1998   0   0
However, mRNA levels for MCP-1 were increased fivefold                        14522423 2003   0   0
expressed a fivefold increase in MHC class I mRNA over vector-treated         10201945 1999   0   0
caused a fivefold increase in MMP-9 mRNA that was associated with increased   11839551 2002   0   0
in a 5-fold induction of specific MnSOD mRNA levels following the third        9886257 1999   0   0
and a 5.6-fold increase in MT mRNA levels (p<0.002) compared to control 9838151 1998          0   0
three to five-fold increase in mucin transcription as determined by nuclear 10738897 1999     0   0
caused a five-fold increase in neurons expressing trkA mRNA and a two-fold9283812 1997        0   0
caused a fivefold increase in NGF mRNA after 8 Stimulation                     1951711 1991   0   0
the NK family homeodomain. Nkx2-5 mRNA levels increased 5.1-fold               9612365 1998   0   0
4- to 7-fold induction in NNT-1/BSF-3 mRNA expression was observed between    14605001 2004   0   1
to a fivefold increase in nrdDG and nrdIEF transcription under anaerobic 11717286 2001        0   1
to a fivefold increase in nrdDG and nrdIEF transcription under anaerobic 11717286 2001        0   1
a mean 5-fold increase in ob mRNA within 3 h after                             8702391 1996   0   0
for growth factor supply. ODC mRNA was elevated 5-fold                         8519686 1995   0   0
OTR gene expression in chorio-decidual tissue increased fivefold               8200965 1994   0   1
cell sublines, while PAGE-1 mRNA levels were elevated 5-fold                   9651357 1998   0   1
an approximate 5-fold increase in PAI-1 mRNA levels at 4 h,                    1701436 1990   0   0
an approximately 5-fold increase in PAI-1 mRNA levels and in PAI-1             1701436 1990   0   0
fourfold to fivefold increase of PAI-1 mRNA levels, as well as                 9108786 1997   0   0
two- to five-fold induction of PAI-1 mRNA expression in HT-1080 and Hep 1652590 1991          0   0
induces a 5-fold increase in PAI-1 gene transcription and does not             1738371 1992   0   0
more than 5-fold increase in the PAI-1 gene transcription The                  3262618 1988   0   0
in approximately 5-fold induction of PAO mRNA and a >3-fold induction         11454677 2001   0   0
found a 5-fold increase in PAR-1 mRNA in cervical spinal cords                10952021 2000   0   0
2- to 8-fold increase in PDGF-B mRNA positive cells, significant in all      8463938 1993       0   1
and a 5-fold increase of PDGF-B mRNA (P < 0.05) as                           7702206 1995       0   0
PDGF-R alpha gene expression was increased 5-fold                            7546776 1995       0   0
caused a 5-fold induction of PEPCK mRNA within 6 h in these                  7945224 1994       0   0
By contrast, the phosphorylase mRNA level was increased 5-fold               8125170 1994       0   0
showed a 5-fold increase in PI-6 mRNA and a 7-fold increase                  9851866 1998       0   0
4- to 6-fold increase in PPARalpha mRNA and a 1.8-fold increase            11373342 2001        0   0
an approximately 5-fold increase of the PR mRNA levels occurred after        2915647 1989       0   0
5- to 6-fold increase in the predominant PR mRNA transcripts (5.1          10218985 1999        0   1
                                                                             2178216 1990
a transient 5.6-fold increase in steady state prodynorphin mRNA levels relative                 0   1
up to 5-fold increase in proenkephalin (Penk) mRNA levels. After an          2229066 1990       0   0
levels of the chicken progelatinase mRNA are increased 5-fold                8010954 1994       0   1
up to 5-fold increase in PTH mRNA at 1 h, thus                               2737148 1989       0   0
level by immunohistochemistry. Quantity of PTN mRNA increased 5-fold 11999218 2002              0   0
4- to 6-fold increase in pup MT-3 mRNA abundance on the day                10407136 1999        0   0
caused a fivefold increase in PYC1 mRNA in less than 30                    11082192 2000        0   0
or = 5-fold increase in R2 mRNA and an 18-fold increase                      9605773 1998       0   0
The RAD23 mRNA levels are elevated 5-fold                                    2204027 1990       0   0
gave a fivefold increase in RANK mRNA levels. In contrast to RANKL         14653607 2003        0   0
responsible for IL-1beta action. RANTES mRNA was induced 5-fold            11600537 2001        0   0
compared to controls. mRNA for RANTES was increased 5-fold                 10862646 2000        0   1
Moreover, a 5-fold increase of renin mRNA was observed in hearts           11300225 2001        0   0
to a 5-fold rise of renin mRNA levels in the ipsilateral                     8058474 1994       0   0
SD and F344 animals. Resistin gene expression increased fivefold           11832366 2002        0   0
enzymes MspI and HpaII. 5-Azacytidine increased rGH mRNA 3-8-fold in GH3D6   6206070 1984       0   0
a rapid fivefold increase in the transcription of the rpoB and C              368011 1979       0   0
twofold and RV irANP and ANP mRNA increased fivefold                         9249516 1997       0   0
We found that SAA mRNA could be increased fivefold                           2747640 1989       0   0
polyunsaturated fatty acids. SCD4 mRNA levels were elevated 5-fold         12815040 2003        0   0
skeletal muscle (SKM) expression. SKM UCP3 mRNA rose fivefold              10913045 2000        0   0
a large, 5-fold increase in SOCS3 mRNA in the liver, brain,                12550079 2003        0   0
                                                                             2879843 1987
inducing a 5-fold increase in somatostatin mRNA levels and 4.8-fold stimulation                 0   0
However, SP(NK(1)) receptor mRNA levels increased fivefold                 10516226 1999        0   0
                                                                             8644857
of experimental mesangioproliferative glomerulonephritis, SPARC mRNA was increased1996 5-fold   0   0
and SP-B cDNA probes. SP-B mRNA levels increased 5.2-fold                    1996658 1991       0   0
four- to fivefold increase in Spec3 mRNA levels, implying that the Spec3     2828169 1987       0   0
of total SR Ca(2+)-ATPase mRNA content and increased 5-fold                  1301393 1992       0   0
The natural polyamine, spermine, also increased SSAT mRNA (5.5-fold at 24    8360194 1993       0   1
1.5- to 10-fold increase in a Stat5 transcription complex, which binds       9602424 1998       0   0
Furthermore, TGF-alpha mRNA expression was also elevated fivefold            2064727 1991       0   0
                                                                             3133414
three- to fivefold up-regulation of intracellular TGF-beta mRNA and TGF-beta biologic 1988      0   1
TGF-beta1 mRNA levels in rhM-CSF-treated wounds increased 5.01-fold 9356238 1997                0   0
depot, the amount of thioredoxin mRNA was increased five-fold              10416835 1999        0   0
                                                                             9630690 1998
associated with 5.1-fold increase in THRP mRNA and 3.7-fold increase in protein                 0   0
In addition, TKT mRNA levels were elevated fivefold                        11095059 2000        0   1
of potentially toxic chemicals, TNF mRNA was elevated fivefold               1644919 1992       0   0
5- to 6-fold induction of TNF-alpha mRNA and 3-fold induction of IFN-gamma 11120847 2000        0   0
colon due to resection; IGF-I mRNA was increased 5-fold                    11668024 2001        0   0
supplemental P treatment, TPH mRNA signal was increased fivefold             8824338 1996       0   1
tyrosine aminotransferase and tryptophan oxygenase mRNA had increased five-fold 26567 1978      0   0
a rapid 5-fold increase in TyrATase mRNA concentration in rat                6149549 1984       0   0
despite a fivefold increase of UCP2 mRNA in BAT of UCP1-deficient          11001779 2000        0   0
than pair-fed controls. UCP2 mRNA levels were increased 5-fold                  11843026 2002       0   0
and a fivefold increase in uncoupling protein mRNA in brown adipose               7733267 1995      0   0
added rhHGF also increased u-PA activity and mRNA 5.9-fold in MDCK                1328201 1992      0   0
vivo about 10-fold. The VEGF mRNA was up-regulated fivefold                       9027720 1997      0   0
revealed a 5.2-fold increase in VEGF mRNA transcript in the cancer                9815813 1997      0   1
3- to 7.5-fold increase in VP mRNA levels. Long term treatment                    1717834 1991      0   0
The GST Yc2 steady-state mRNA level was induced 5-fold                            8625305 1996      0   0
3O-C(12)-HSL, an 8-fold induction in mRNA and a 35-fold increase in protein     12193735 2002       0   0
A fourfold induction in fusion gene mRNA in the liver                             2769161 1989      0   0
causes a 4-6-fold increase in the rate of transcription of pro-alpha              6333422 1984      0   1
causes a 4-6-fold increase in the synthesis of mRNA coding for                    2415156 1985      0   0
4- and 7-fold increase in transcription levels was observed after wounding 7916213 1994             0   0
4-fold to 7-fold increase in luciferase gene expression in tumor tissue         14961303 2001       0   0
The full-length (7.9 kb) mRNA increased 5-fold                                  10521420 1999       0   0
in a fivefold increase in the 2.4-kb mRNA as well as                              2175615 1990      0   1
                                                                                  7688356 1993
induced a fivefold increase in its transcription rate. Posttranscriptionally, IFN-beta and -gamma   0   1
disclosed a 5-fold increase in receptor mRNA activity over untreated control 2432610 1987           0   0
5- to 6-fold increase in the relative transcription rate of the beta               341156 1977      0   0
                                                                                  9699483
three- to fivefold increase in smooth muscle-specific transcription over that stimulated 1998       0   0
confirmed a fivefold induction of this mRNA transcript between fetal day 11741818 2002              0   1
a nearly 5-fold increase in proTRH gene expression in neurons of the              8874872 1996      0   0
and a 5-fold increase in the mRNA concentration of the                            2663078 1989      0   1
because the 5-fold increase in mRNA levels in response to TNF-alpha             10820282 2000       0   0
                                                                                10644908
causes a fivefold increase in mRNA expression of monocyte chemoattractant protein 2000              0   0
Cbeta subunit mRNA in these cells was increased fivefold                        10581157 1999       0   0
demonstrate a fivefold increase in the transcription rate of beta(1)AR          12742828 2003       0   0
                                                                                  7690720
demonstrate a five-fold increase in transcription by calcitonin. Similar increases were 1993        0   1
dexamethasone, as a positive control, increased the transcription fivefold to 8282344 1994          0   0
four- to fivefold increase in mRNA expression levels of both ATP-binding 14529830 2003              0   0
four- to fivefold increase in the mRNA levels coding for the proenkephalin 3681292 1987             0   0
in a 5-fold increase in the rate of transcription of the HMG-CoA                  3410847 1988      0   0
in a 5-fold increase in the transcription of the endogenous n-cam                 8071351 1994      0   0
In addition, mRNA corresponding to pUDPGTr-2 was elevated 5-fold                  6207173 1984      0   0
induced a 5-fold increase in mRNA and protein expression of                     10400916 1999       0   1
is a 5-fold increase in mRNA for TNF in adherent cells                            8476631 1993      0   0
is a five-fold upregulation of the mRNA for thymosin beta4 (Tbeta4)             14517430 1999       0   0
least a 5-fold increase in mRNA levels likely accounted for this                  9237866 1997      0   0
mRNA encoding EGRF 1 was increased fivefold                                     10432383 1999       0   0
produced a 5-fold increase in transcription (P < 0.05) from the thyroid           8346251 1993      0   0
showed a 5-fold increase in mRNA hybridizing to pGT16.4 72 h                      8489258 1993      0   1
showed a five-fold increase of the mRNA level between 11 dpc                      2178193 1990      0   1
steady-state amount of mRNA for gamma-GCS was increased 5-fold                    7568279 1995      0   0
The level of mRNA recovered and increased 5-fold                                  2241969 1990      0   1
The level of mRNA was induced fivefold                                            1980193 1990      0   1
three- to fivefold increase in the transcription of MT2 and HLA                   3990797 1985      0   0
three- to fivefold increase in transcription directed by wild-type P2 but         8887629 1996      0   0
to a 5-fold increase of transcription rate (run-on assay) without a change 10769164 2000            0   0
to a fivefold increase in transcription rate, without altering start site         8552077 1996      0   0
two- and fivefold increase in mRNA encoding collagenase 3 and TIMP-1, 11226050 2001                 0   1
two- to five-fold up-regulation of the mRNA expression of the alpha1,           11869073 2002       0   0
VEGF mRNA by increasing the rate of transcription (5-fold after 4                 8910616 1996      0   0
while a five-fold induction of transcription occurs in M. domesticus, none        1766361 1991      0   0
with a five-fold increase in mRNA coding for fibronectin. Elastin mRNA        2414324 1985    0       1
with approximately 5-fold increase in gene expression in ErbB2(+) cell as 11571533 2001       0       0
6.64-fold at 60 min. mRNA for c-myc increased 5.13-fold                       8897947 1996    0       0
caused a 5-6-fold increase in transcription initiated from both the P1        9685226 1998    0       1
to a 5-6-fold increase in mRNA level over a 15-fold range                     9139747 1997    0       0
                                                                              9852109 1998
with a 5-6-fold increase in mRNA level. Reverse transcriptase-polymerase chain reaction       0       0
4.8- and 6-fold increase in mRNA amounts encoding TGF-beta1 and TGF-beta3,    9139831 1997    0       1
                                                                              7848525
4.5- to 6-fold increase in the transcription with ERE-containing promoters in comparison 1994 0       0
                                                                             5.5-fold
RESULTS: Cathelicidin mRNA in cholesteatoma epithelium was increased 12616192 2003            0       0
to a 5.5-fold increase in transcription from the E3 In                       12502827 2003    0       0
average a sixfold increase in the 1.8-kb HO-1 mRNA level compared             8455037 1993    0       1
4 to 8-fold increase in 5-HT1A-R mRNA was observed both in hippocampus 7674372 1995           0       0
in a 6-fold increase in 5-lipoxygenase mRNA and a 1.3-fold increase           8380989 1993    0       0
The sixfold increase in total ACC-alpha mRNA expression in mammary           11719287 2001    0       0
produced a 6-fold increase in AhR steady state mRNA levels and a              9415701 1997    0       0
for 53 healthy/non-HCC controls, alb- mRNA levels increased 2-10-fold        11369140 2001    0       0
with a 6.6-fold increase in ANG II receptor mRNA in myocytes                  8456979 1993    0       0
4-fold and 8-fold increase in apo A-I mRNA and secreted protein               8003099 1994    0       0
and the concentration of apoB-100 mRNA was increased sixfold                  3782476 1986    0       0
an approximately sixfold increase in atrial natriuretic factor mRNA in left   8508529 1993    0       0
demonstrated a sixfold increase of BDNF mRNA in the immediate plaque 15014117 2004            0       1
                                                                              9305915 1997
treatment, while beta2-adrenoreceptor mRNA levels were potently induced (6-fold               0       0
of 10(-6) M dexamethasone beta-fibrinogen mRNA levels increased 6-fold 2454192 1988           0       0
to the primary osteoblast culture, BMP-3b mRNA increased 6.9-fold            10079200 1999    0       0
of ANF were minimally affected. BNP mRNA increased 6-fold                     8264660 1993    0       0
approximately a 6-fold increase in bone morphogenetic protein-7 mRNA In 9621899 1998          0       0
                                                                              9038875 1997    0       0
for 7 days) increased expression of Ca(2+)-Mg(2+)-ecto-adenosinetriphosphatase mRNA sixfold and increased
in a 6-fold increase in CaBP9K mRNA after 3 h and a                           1695565 1990    0       0
five- to sixfold induction of ceruloplasmin mRNA in lung tissue within        1996664 1991    0       0
8- and 4-fold increase in c-fos mRNA level after 30 min                       7903543 1993    0       0
five- to sixfold elevation of c-fos mRNA levels in rat frontal                7612155 1995    0       0
led to six-fold increase in ChAT mRNA without a concomitant increase          7914755 1994    0       0
Steady-state levels of c-myc mRNA increased 6-fold                            2721228 1989    0       0
as the induction medium. COX-2 mRNA was elevated 6-fold                       9242685 1997    0       0
Steady-state levels of cph mRNA increased 6.7-fold                            9989819 1999    0       0
showed a six-fold increase in cTnI mRNA from day 3 to day                     8072015 1994    0       1
(13%) a 2-10-fold increase of cyclin B2 mRNA which was not                   11960377 2002    0       0
Cyclin E mRNA levels were increased 6.2-fold                                  8761413 1996    0       1
produced a 6-fold induction of CYP1A1 mRNA in MCF-7 2-Nitrofluoranthene      12107646 2002    0       0
was not detected. In contrast, D3 mRNA increased sixfold                      8922433 1996    0       0
lungs from saline-challenged animals, eotaxin mRNA levels increased sixfold   7869037 1995    0       0
                                                                             11922631 2002
induce a 6-fold increase in ER beta mRNA transcription, indicating the coregulation           0       0
a 6-7 fold increase in both factor H mRNA species, and a                      2972796 1988    0       0
100% at 24 h. Fas mRNA levels increased 6-fold                               14625471 2003    0       0
found a 6-fold increase in fibronectin mRNA levels in fibroblasts cocultured 14978126 2004    0       0
with a sixfold increase in FN mRNA by Day Experiments                         1577188 1992    0       0
5- to 7-fold increase in G6PD mRNA in rat This                                9788241 1998    0       0
more than 6-fold increase in the G-CSF mRNA half-life (20 minutes             7684703 1993    0       0
production rate (2-6-fold). The GdA mRNA concentrations increased 2-11-fold  10321810 1999    0       0
5.5-fold and 7.2-fold increase in the GFAP mRNA in the ischemic              10707898 1999    0       1
The GH receptor-encoding mRNA (4.2 kb) increased sixfold                      7511151 1994    0       1
                                                                              8892317
a approximately 6-fold increase in GLUT1 mRNA content. Moreover, incubation of cells 1996     0       0
induced a 6-fold increase in GnRH receptor mRNA (0.4 +/- 0.1               8788193 1996    0   0
4- to 8-fold increase in growth hormone mRNA in GH1                        2424908 1986    0   0
hours after UVB treatment. HB-EGF mRNA was elevated 6.8-fold              12547714 2003    1   0
induced a sixfold increase in liver hepcidin mRNA levels and a twofold    12370282 2002    0   0
exclusively in endothelial cells. HGF mRNA levels rose sixfold             7683700 1993    0   0
threefold to sixfold elevation in liver HL mRNA and a fourfold             1657130 1991    0   0
                                                                           7721395 1995
fivefold to sixfold increase in aortic HSP70 mRNA expression. Chronic exposure             0   0
Skeletal muscle Hsp72 mRNA expression increased 6.5-fold                  11795476 2001    0   0
                                                                          10720500 2000
respiratory syncytial virus (RSV). IEX-1L mRNA expression increased 5-7-fold               0   0
the abundance of hepatic IGFBP-1 mRNA was increased 6-fold                 7694841 1993    0   1
was a 6-fold increase in IGFBP-1 mRNA abundance, a lower induction         7679969 1993    0   0
were unchanged, whereas IGFBP-2 mRNA levels were increased 4-8-fold 10985759 1998          0   0
5- to 7-fold increase in IGFBP-5 mRNA levels after 16-24                   7536661 1995    0   1
IGF-I mRNA had increased eightfold and IGF-II mRNA sixfold in skeletal     3177637 1988    0   0
IL-2 mRNA levels, IL-4 mRNA transcripts were increased six-fold            7535208 1995    0   0
a 6 fold increase in iNOS mRNA transcript (P<0.05), which returned         9257899 1997    0   1
A sixfold increase in the iNOS mRNA levels was observed                    9749707 1998    0   0
of 100 microM mevalonate. iNOS mRNA levels increased sixfold              14757118 2004    0   1
                                                                          10438721 1999
showed a 6-fold increase in mannose receptor mRNA expression in the nonparenchymal         0   1
induced a sixfold increase in MCP-1 mRNA levels. The amount of MCP-1 8622597 1996          0   0
Steady-state MCP-3 mRNA levels were elevated 6-fold                       12235260 2002    0   0
and a 6-fold increase in M-CSF mRNA and protein levels after               9278333 1997    0   0
with a 6-fold increase in metallothionein mRNA 5 h after injection,        4015627 1985    0   0
fast (4-6 h). Furthermore, mGPDH mRNA is induced 6-fold                    8760382 1996    0   0
METHODS AND RESULTS: MT-MMP-1 mRNA levels increased sixfold                9443435 1998    0   0
h), Nox1 and Nox4 mRNA levels were increased 6-fold                       11728818 2001    0   1
to a 6-fold increase of NRF-1 mRNA level. The upregulation of TFAM        11457459 2001    0   0
well as cyclic AMP analogues, increase OST-PTP mRNA 5-8-fold in UMR 7527035 1994           0   0
and a 6.5-fold increase in OTR mRNA levels, respectively. Progesterone was 9112379 1997    0   1
a five-to six-fold increase in p21WAF1/CIP1 mRNA levels and a three-       9513045 1998    0   0
                                                                            p21WAF1/CIP1
three- to six-fold increase in p21WAF1/CIP1 mRNA stability. The increase in9513045 1998    0   0
was a sixfold increase in PAI-1-tPA mRNA ratio in patients with MN        11920334 2002    0   0
We found that PC1 mRNA was increased 6.0+/-0.02-fold                      11730986 2001    0   0
                                                                          11730986 2001
increased 6.0+/-0.02-fold (P<0.05) and PC2 mRNA was increased 1.80+/-0.01-fold             0   0
                                                                           8110779 1994
myoblast differentiation to myotubes. PFK-A gene transcription increased 5-7-fold          0   0
in a 6-fold increase in preproenkephalin mRNA in hypox glands cultured     3412328 1988    0   0
                                                                           9861306 1998
6.4 +/- 0.8-fold upregulation of preproET-1 mRNA in the noninfarcted and the               0   0
that the level of preproIGF-I mRNA is increased 6-fold                     2628735 1989    0   1
procollagen I mRNA in papillary dermal fibroblasts increased sixfold       8085868 1994    0   0
                                                                           3368036
greater than six-fold increase in proenkephalin mRNA (mRNA(enk)) was observed by 1988      0   0
four- to sixfold increase in PTH-related protein mRNA levels in smooth     9814617 1998    0   1
level, a 2-10-fold increase in PTP alpha mRNA was detected in 10           7621435 1995    0   0
The amount of RAG-1 mRNA was increased sixfold                             8020549 1994    0   0
diet, whereas renal cortex renin mRNA levels increased 6.8-fold            3533999 1986    0   1
caused a 6-fold increase of rGSTA2 mRNA in the liver (100                  9920464 1998    0   0
demonstrated that the concentration of RII51 mRNA increased 6-fold         3032573 1987    0   0
5.8- and 7-fold increase of synapsin I mRNA levels in the locus            8750825 1995    0   0
induced a 6-fold increase of TF mRNA and reduced time until               10233435 1999    0   0
4- to 8-fold increase in TGF alpha mRNA levels and secrete                 1981145 1990    0   0
exhibited a sixfold increase in TGF alpha mRNA concentrations. In situ     7959207 1994    0   1
TGF-beta 1 mRNA was able to be induced six-fold                            1314170 1992    0   0
for the -510/+91 fragment. TKT mRNA levels increased sixfold               9521875 1998    0   0
about a 6-fold increase in trehalase mRNA content in ovaries 4                7519445   1994   0   1
However, UCP3 mRNA expression was upregulated 6-fold                        14970361    2004   0   0
HPRL, a 6-fold increase in VIP mRNA can be seen in E2-treated                 7606249   1995   0   1
2.5- to 11-fold increase in VWF mRNA in normal canine heart,                12649145    2003   0   0
A 6-fold increase in Y2 receptor mRNA was observed in the                   11287094    2001   0   0
Expression of ZO-1 mRNA was increased sixfold                               11590321    2001   0   1
4 to 8-fold increase in transcription of stably transfected c-myc fusion      2284094   1990   0   0
5- to 7-fold elevation of functional mRNA coding for tyrosine aminotransferase 24052    1978   0   0
                                                                              1547909
5- to 7-fold increase in transfected glucocorticoid receptor gene expression relative   1992   0   0
contrast, osteoprotegerin mRNA and protein levels were induced 5-7-fold 10811631        2000   0   1
rats, a 6-7-fold increase in both mRNA and the transcription rate             1536642   1992   0   1
less than sixfold increase in the corresponding gene transcription The        2470563   1989   0   0
a dose- and time-dependent increase in both mRNA (6-7-fold increase at 8662783          1996   0   0
was a 6-fold induction of the two mRNA species hybridizable to HLp            3460094   1986   0   0
A 6-fold increase in transcription activity of the reporter was             11750763    2001   0   0
A 6-fold increase in transcription of the adult alpha and beta                7794810   1995   0   0
A2 receptor mRNA was found to be upregulated sixfold                          9494030   1998   0   0
and a 6-fold increase in mRNA (P = 0.002). After birth,                       9609733   1998   0   1
and a sixfold increase in leptin promoter-reporter gene expression at 1     12169453    2002   0   0
                                                                            11310348
conditions; a 6-fold increase in mRNA expression was observed using serum-free          2001   0   0
gave a 6-fold increase in mRNA levels at 300 microM, followed                 8169528   1994   0   0
in a sixfold increase in luciferase gene expression in C6                     8592113   1996   0   0
in the crypts, and the mRNA abundance increased 6-fold                        1764071   1991   0   0
indicated a sixfold increase in steady-state levels of mRNA for collagen      2145089   1990   0   1
Levels of mRNA for alpha2(IV) procollagen increased sixfold                   9847287   1998   0   0
mediated a sixfold increase in transcription in response to forskolin, but    1349342   1992   0   0
revealed a sixfold increase in transcription by 30 min and a return           8175144   1994   0   1
showed a 6-fold increase in mRNA for specific chemokines in the brain       11138923    2000   0   1
than six fold increase in SV-40 late gene expression in cells               10071986    1999   0   0
The 6-fold increase in mRNA was paralleled by an equivalent                 11736658    2001   0   0
The level of mRNA for V(H)HAR+ IgG increased 6-fold                         10428261    1999   0   0
The mRNA level for transferrin was increased six-fold                         7540162   1995   0   0
The sixfold increase in mRNA did not translate into an                      10640418    2000   0   0
twofold to sixfold increase in mRNA was observed in the thymus              10194439    1999   0   0
vector, a sixfold increase in mRNA levels was seen. Actinomycin D             1717710   1991   0   0
with a 6-fold increase in the transcription rate of this                      2007095   1991   0   0
with a sixfold rise in mRNA levels for TGF-beta 1 and a                       7923630   1994   0   0
6- to 7-fold increase in the transcription of new t-PA and u-PA               9660311   1998   0   0
a 6-7 fold increase in PAI-1 gene expression in both lean                   11755928    2002   0   0
and a 6.5-fold increase in mRNA (30 nM dexamethasone for 72                   7814638   1995   0   0
a 5-10 fold increase in 11beta-HSD2 mRNA as determined by semiquantitative    9888553   1998   0   0
plus FSH, 3 beta HSD mRNA expression increased 7.6-fold                       9420856   1995   0   0
5- to 10-fold increase in A1 mRNA levels in peritoneal cells                10384143    1999   0   0
secretion and adipocyte PAI-1 mRNA levels were increased seven-fold           9498632   1998   0   0
in a sevenfold increase in adrenal 5 alpha-reductase mRNA content compared    2043243   1991   0   0
shows a 7-fold increase in ALAD mRNA at 2 h into                              7894023   1995   0   0
caused a sevenfold increase in translatable albumin mRNA and a threefold 3141556        1988   0   0
was a 7-fold increase of ANP mRNA in LV at day                              10525429    1999   0   0
was a sevenfold increase in ASBT steady-state mRNA levels in the kidney 8770054         1996   0   1
an almost sevenfold upregulation of AT1 mRNA levels in the clipped            7630117   1995   0   0
detected a sevenfold increase of AVP mRNA in the SON, a fivefold              3712004   1986   0   1
During this time, beta-actin mRNA levels increased 7-fold                     1761163   1991   0   0
                                                                             1988453 1991
greater than 7.0-fold increase in calbindin-D 9k mRNA without stimulating intestinal        0   0
                                                                             1988453 1991
caused a 7.6-fold increase in calbindin-D 9k mRNA without significantly increasing          0   0
caused a 2-13-fold increase in calcitonin mRNA and a 40-60% decrease         3491070 1986   0   1
CAT gene expression in lungs was increased 6-8-fold                          8913866 1996   0   0
                                                                             1677643 1991
was a 5-10-fold induction of c-fos mRNA and phosphatidylinositol 4-kinase activity          0   0
                                                                             1472074
an approximately 7-fold increase in class mu GST mRNA levels in ionophore-treated 1992      0   1
of 2.5 kb c-myc mRNA are transiently elevated 5-10-fold                      3817014 1987   0   0
In contrast, c-myc mRNA was elevated 7.4-fold                                2113532 1990   0   0
induced a 7.5-fold increase in c-myc mRNA accumulation as analyzed on 2439522 1987          0   1
caused a 7-fold induction of collagen mRNA levels and a greater              2188970 1990   0   0
                                                                             with primary
produce a 7-fold elevation in collagenase (MMP-1) mRNA levels, consistent 9407397 1997      0   0
with non-ALS spinal cord, COX-2 mRNA was upregulated 7.09-fold             11571316 2001    0   1
and a 7.4-fold increase in expression of COX-2 mRNA (P <                   11317684 2001    0   0
A low-salt diet increased COX-2 mRNA 7.7-fold in MD                          9530264 1998   0   0
4- to 10-fold increase in CRH mRNA levels, which was rapid                   2558296 1989   0   1
11- and 4-fold increase in cripto mRNA levels in pancreatic cancer           8314343 1994   0   1
I adenylyl cyclase mRNA in the hippocampus increased 7-fold                  7782295 1995   0   0
6- and 8-fold induction of E-FABP mRNA and protein, Up-regulation          10762707 2000    0   0
Insulin increased the abundance of FAS mRNA 2-13-fold and fatty              9560309 1998   0   0
revealed a 6-8-fold increase in the fibromodulin mRNA level from day         8760363 1996   0   1
was a 4-10-fold increase in FPGS mRNA and folypolyglutamate formation (Glu   8217815 1993   0   1
An 11-fold increase in gastrin mRNA expression was recorded in the           9051591 1997   0   0
induced a 7-fold increase in GFR alpha-1 mRNA levels. These changes 11319768 2001           0   0
7- to 8-fold increase in GnRH receptor mRNA activity. Treatment with both 1964491 1990      0   0
and a 7-fold increase in gp91(phox) mRNA in diabetic In                    11157681 2001    0   0
rapid, transient sevenfold increase in GS mRNA (P < or =                     9435573 1997   0   0
5- to 10-fold increase in HBsAg mRNA levels. In addition, adult              2760988 1989   0   0
7-fold increase in HNF-3g mRNA in the liver and did                        11018767 2000    0   0
a remarkable 7.5-fold increase in the I-BABP mRNA level over the control 9461519 1998       0   1
in a sevenfold increase in steady-state IGFBP-3 mRNA and a 1.8-fold        10199564 1999    0   0
4- to 10-fold increase in IL-8 mRNA expression but not in the                8417753 1993   0   1
six- to sevenfold increase in insulin-receptor mRNA due to the prolongation 1849849 1991    0   1
with a 7-fold increase in the LDL-R mRNA level in LDL-IC                     9034205 1997   0   1
and a sevenfold rise in liver LDL-receptor mRNA is attained with a           2401854 1990   0   0
to study this regulatory mechanism. LIF mRNA increased five-to-tenfold       8891691 1996   0   0
level of long-chain acyl-CoA synthetase mRNA is increased 7-8-fold           2341402 1990   0   0
7- to 8-fold increase in MDR1 mRNA levels. MDR1 RNA levels                   1967174 1990   0   0
The level of mdr1 gene expression was increased sevenfold                    2224796 1990   0   0
in a 7.2-fold induction of mRNA for monocyte chemotactic protein 1           1752961 1991   0   0
a nearly seven-fold elevation in MT mRNA                                     7881512 1994   0   0
had a 7-fold increase in MT mRNA and a 2-fold increase                       1539169 1992   0   0
and 95% (P<0.0001) respectively, while NSP-A mRNA increased 7-fold         12844347 2003    0   0
6- to 8-fold increase in P450R transcription rate within 12 h,             11306680 2001    0   1
a transient sevenfold increase in PAI-1 mRNA 6 h after injection             9227364 1997   0   0
7.8 +/- 3.3-fold increase in PAI-1 mRNA expression. The PAI-1 antigen      10432384 1999    0   1
7-fold increase in PAI-2 mRNA and protein levels in HT-1080                10075998 1999    0   0
PRL, a 7.8-fold increase in PAI-I mRNA levels is observed as               11324510 1998    0   0
produced a sevenfold increase in PGHS-2 mRNA by 1 h that                     8989914 1996   0   1
initial lag of 12 hr, pIgR mRNA increased seven-fold                         8455639 1993   0   0
exhibited a sevenfold increase in PKC-eta mRNA when cultured in medium 1379814 1992         0   1
to 7 fold elevation of PRA and renin mRNA Mibefradil                         9647484 1998   0   0
                                                                           10979975
6- to 8-fold increase in steady-state RARalpha mRNA compared with vector-transfected 2000   0   0
showed a 7-fold increase in liver RAR-beta mRNA levels as compared            1654565 1991   0      1
to 7 fold elevation of PRA and renin mRNA Mibefradil                          9647484 1998   0      0
and a 7-fold induction of SCD1 mRNA levels, respectively, as determined 9070250 1997         0      0
in a 7-fold increase in SMG NGF mRNA levels. A signal                         1547729 1992   0      0
increase in tissue SP-A. SP-A mRNA was increased 7-fold                       2619999 1989   0      0
5- to 10-fold increase in T alpha 1 mRNA levels in developing                 1975243 1990   0      1
by 0.5 h; TGF alpha mRNA was induced sevenfold                                8436603 1993   0      0
                                                                             12388149 2002
tibialis anterior muscle. Endotoxin rapidly increased TNF-alpha mRNA (7-fold at 1            0      0
cells, a 7-fold increase of TS mRNA in DLD-1/FdUrd cells, and a              10891536 2000   0      0
7-fold induction in UCP-3 mRNA levels in skeletal muscle                     10403804 1999   0      0
1.6- and 13-fold increase in mRNA levels were observed. Both of these         6185489 1983   0      0
that corresponds to an mRNA that is induced 6-8-fold                          1894636 1991   0      0
rapid 6-8 fold increase in transcription of the c-fos gene was                2114401 1990   0      0
The mature form of mRNA (1.3 kb) increased 6-8-fold                           9397163 1998   0      0
five- to sevenfold increase in mRNA occurring 9-12 h after temperature       11251819 2001   0      0
in a 7-fold increase in mRNA coding for the alpha-subunit, whereas            4032011 1985   0      0
levels were low. After axotomy, mRNA levels increased sevenfold              12898535 2003   0      0
                                                                              1448077
sequence mediate sevenfold induction of reporter gene expression when present in two 1992    0      0
                                                                             11027684 2001
stimulates a 7-fold increase in transcription of the acetyl-CoA carboxylase-alpha (ACCalpha) 0      0
Two- to sevenfold induction of the endogenous gene expression was observed   10559334 1999   0      0
with a 7-fold increase in gene expression using a NLS peptide/DNA            14733595 2004   0      0
by a 7.3-fold increase in mRNA alpha and no change in mRNA                    2460453 1988   0      0
causing a 7.5-fold rise in mRNA levels in primary adipocytes and a            7706939 1995   0      1
hybridizes to a 4.4-kb mRNA that is induced eightfold                        10710546 2000   0      1
4.1-fold while CYP8B declined 64%. ABCA1 mRNA rose 8-fold                    12897188 2003   0      0
in an 8-fold increase of ACE mRNA expression, whereas ACE mRNA               12504823 2003   0      0
show an 8-fold elevation in adrenal PNMT mRNA at 6 h                          8063705 1994   0      0
six- to eightfold increase in alpha 1IV collagen mRNA in the glomeruli        8468927 1993   0      1
and 8 fold elevation in alpha 2 mRNA levels compared with age-matched 1662123 1991           0      0
and an eightfold increase in left ventricular ANP mRNA levels in RHRs,        2136812 1990   0      0
whereas the amount of ANT2 mRNA is increased 7-9-fold                         8760382 1996   0      0
five- to eight-fold increase in APP mRNA levels which peaked at               8046777 1994   0      0
At this time, BDNF mRNA level was increased eight-fold                       11457573 2001   0      0
                                                                              3900035 1985
an about 8.5-fold increase in cat-specific mRNA in cells expressing the resistance           0      0
and an eightfold increase in CGRP mRNA occurred 3 days after                  1493379 1992   0      1
7- to 10-fold increase in c-myb mRNA was detected in late                     1730880 1992   0      0
an approximately 8-fold increase in colonic H+-K+-ATPase mRNA in the          9083276 1997   0      1
in an 8-fold induction of Cox mRNA within 1-2 h which                         1400321 1992   0      0
and an 8-fold increase in COX-2 transcription that was temporally preceded 9266823 1997      0      0
failed to alter [Ca(2+)](i). BK increased cPLA(2) mRNA eightfold by 15       10458930 1999   0      0
                                                                             11327701 2001
administration to diabetic rats induces Delta6 desaturase mRNA eightfold within 24           0      0
report demonstrates that transcription factor deltaEF1 is induced eightfold 10207083 1999    0      0
elicits an eightfold increase in DNA ligase mRNA                              3885010 1985   0      0
to an eight-fold elevation in functional DT-diaphorase mRNA at 8 h            6430240 1984   0      0
contrast, an 8-fold increase in EGF-R mRNA copies per cell was                7678348 1993   0      1
8- to 9-fold increase in the FS mRNA level after 4                            1375907 1992   0      0
five- to eightfold increase in Gadd45 mRNA levels and a two-                  9356304 1997   0      0
Pituitary growth hormone (GH) mRNA expression was increased 8.3-fold 12076076 2002           0      0
euthyroid rats the mass of glucokinase mRNA increased 8-fold                  2584235 1989   0      0
                                                                              8727080 1996   0      0
Interestingly, a eightfold increase in glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA accumulation was
Levels of GTP cyclohydrolase I mRNA were increased 7-10-fold                  7512954 1994   0      0
over an eightfold increase in the htrA transcription level, was found         9829922 1998   0      0
was an 8.5-fold increase in IGFBP-1 mRNA expression in the livers                1371449 1992   0   1
By day 80 IGF-I mRNA had increased eightfold                                     3177637 1988   0   0
4 days) to ovariectomized rats increased IGF-I mRNA 8-fold to levels             2718698 1989   0   0
                                                                                 8592115 1996
demonstrated an eightfold increase in IL-6 mRNA concentration and IL-6 immunoreactivity,        0   1
7- to 10-fold increase in the steady state mRNA expression of IP-10              9218606 1997   0   0
a nearly 8-fold increase in junD mRNA levels in the rat                          1489400 1992   0   0
five- to eightfold increase in LRP16 mRNA levels in MCF-7 cells;               12790785 2003    0   1
in an 8-fold increase in testicular MCT2 mRNA levels. Conversely, FSH          12773420 2003    0   1
an approximately 8-fold increase in hepatic mEH mRNA levels after three 8043012 1994            0   1
four- to eightfold increase in mgrA transcription in strain Thus,              12813062 2003    0   1
In vitro TPA induced MT mRNA 1.71-15.26-fold in EC3                              1397494 1992   0   1
the steady-state level of neutrophil IL-8 mRNA increased 8-fold                11509634 2001    0   0
12-fold and 4-fold increase of NGFI-B mRNA in the ischemic cortex                9037528 1996   0   1
in an 8-fold increase in NGF-R mRNA in adult rat spinal                          2560649 1989   0   0
PTH/PTHrP receptor and OCN mRNA expression increased 8-fold                      8585429 1995   0   1
                                                                               with control
exhibited an eightfold increase in p16(INK4a) mRNA level when compared 10942530 2000            0   0
Kidney PAI-1 mRNA expression was increased eightfold                           10972684 2000    0   0
on Matrigel: the PAI-1 mRNA level was increased eightfold                        7822431 1995   0   1
to an 8-fold increase in PBP-C1 mRNA levels. While the pure                      2138099 1990   0   0
                                                                                 1
caused an 8-fold induction of phosphoenolpyruvate carboxykinase mRNA in 6282847 1982            0   0
P < 0.05). In Calu-3, PlGF mRNA increased 8-fold                               11948135 2002    0   0
In the striatum, preproenkephalin mRNA abundance linearly increased 8-fold3219577 1988          0   0
PAD cells expressed RAR-alpha mRNA which was upregulated eightfold               8127013 1994   0   1
Renal renin gene expression was increased 8.6-fold                             10069682 1999    0   0
RESULTS: Retinal ceruloplasmin mRNA was upregulated eight-fold                 12724641 2003    1   1
An approximately 8-fold induction of RII beta mRNA and a 3-fold                  8793051 1996   0   0
was an eight-fold increase in the SCF mRNA level in the bone                   12662436 2003    0   0
with an eightfold increase in Tac mRNA production. Tac expression was            2789338 1989   0   1
induced an eight-fold increase in TBM transcription as determined by reporter    9161404 1997   0   0
BEA injection, the mRNA for TGF-beta1 was increased eightfold                  10411687 1999    0   0
cells into myotubes, TGF-beta 3 mRNA levels increased eightfold                  1710772 1991   0   0
with an eightfold increase in measured TM transcription at 90                    7665981 1995   0   1
was an eight-fold increase in TNF-alpha mRNA expression on postburn day        11571581 2001    0   0
these agents induced human TSH beta gene expression 4-12-fold in GH3 1310694 1992               0   0
UCP3 mRNA and protein levels increased 8.1-fold                                10823916 2000    0   0
in an 8-fold induction in UCP-3 mRNA levels in preadipocytes compared 10933891 2000             0   0
7- to 10-fold increase in transcription in response to increases in the          3141381 1988   0   0
poor and remained fairly constant, but transcription increased eightfold       12773103 2003    0   0
to an 8-fold increase in specific mRNA over a 48-h observation                   1572298 1992   0   0
                                                                                 2583674 1989
inhibit the eightfold increase in translatable mRNA elicited by calcium administration          0   0
despite an 8-fold increase in ventricular mRNA for atrial natriuretic            9261135 1997   0   0
about an eightfold increase in mRNA levels, and an increased enzyme              6152283 1984   0   0
an approximate 8-fold increase in mRNA was observed in tat-transformed Raji      2243081 1990   0   0
approximately an 8-fold increase in mRNA coding for IL-1 itself, we              7507497 1994   0   0
beta 2-adrenoceptor mRNA was found to have increased 8-fold                      9203993 1997   0   0
caused an 8-fold increase in transcription rate by 90 min and a                  2543360 1989   0   0
causes an eight-fold increase of transcription efficiency, although it has only 3359915 1988    0   0
epoxide hydrolase mRNA level in liver was increased eight-fold                   8750907 1995   0   0
three- to eightfold increase in transcription relative to the wild-type promoter 2325201 1990   0   0
which an 8-fold rise in transcription was associated with a 27-fold              3785172 1986   0   0
By comparison, mRNA for fibronectin increased 8.1-fold                           1550689 1992   0   1
more than ninefold induction of transcription factor AP-1 activity to be       12209633 2002    0   0
level and 9-fold increase in calcyclin mRNA level in BGC823 cells          11925593     2002   0   1
The 9-fold increase in CAT mRNA levels attained with the -533              11223948     2001   0   0
seven- to ninefold increase in ceruloplasmin mRNA content in each tissue 1996664        1991   0   0
an approximately ninefold induction of c-jun mRNA at 1 h, followed           9657066    1997   0   0
seven- to ninefold induction of csp mRNA after a temperature shift         10508072     1999   0   1
and a 9-fold increase in CT mRNA steady state levels after                   8061571    1994   0   1
to nine fold increase in cyclin E mRNA and about 50%                         9604788    1997   0   1
Furthermore, epidermal TNF mRNA was elevated ninefold                        1644919    1992   0   0
challenge, a ninefold increase in hepatic ET-1 mRNA occurred within 3        9124581    1997   0   1
rat, a ninefold increase in hepatic ET-1 mRNA occurs within 3                9696707    1998   0   0
of Fc gamma RII beta mRNA was increased 9-fold                               2550246    1989   0   1
8- to 10-fold induction of GH mRNA after 6 h.(ABSTRACT TRUNCATED             1779974    1991   0   0
8- to 10-fold increase in the GluR1 FLOP mRNA and a twofold                  9826784    1998   0   0
In addition, HB-EGF mRNA levels were increased 7-11-fold                     8349708    1993   0   0
found a 9-fold increase in basal hMT-IIa mRNA levels and a 5-fold            7511778    1994   0   0
in a ninefold upregulation of HSP27 mRNA and protein in axotomized           9671676    1998   0   0
9.5 +/- 2.0-fold increase in hepatic IGFBP-1 mRNA abundance (P less          1703482    1991   0   0
induced a 9-fold increase in IL-12 p40 mRNA levels. This was                 8606072    1996   0   0
analysis revealed that LOX-1 gene expression was up-regulated 9-fold         9837956    1998   0   1
possessed a 9-fold increase in mdr1 mRNA and increased P-glycoprotein without1717144    1991   0   0
in a 9-fold increase in the mEH mRNA level at 24                             9146707    1997   0   0
                                                                           10464329
up to 9.5-fold increase in matrix-degrading metalloprotease-1 (MMP-1) mRNA A            1999   0   0
                                                                             7967352
two- to ninefold increase in Mn-SOD mRNA expression associated with significantly       1994   0   0
in a 9-fold elevation of MT-III mRNA in cortex, a 3-5-fold                   7655346    1995   0   0
with a 3-15-fold increase in mRNA of OGG1 as compared to liver             12509275     2002   0   1
Ornithine decarboxylase (ODC) mRNA was elevated ninefold                     3691536    1987   0   0
to a 9-fold increase in p21(WAF1) mRNA and protein, which is,              10954755     2000   0   0
caused a 9-fold increase in P-450f mRNA in hypophysectomized male rats 2303159          1990   0   1
six- to ninefold increase in PAI-1 mRNA at 1 to 3                          11133880     2001   0   0
stimulation of thrombin, cytosolic PLA2 (cPLA2) mRNA increased 9-fold 10691023          1999   0   0
                                                                           14654371
9.8 +/- 2.3-fold upregulation of preproET-1 mRNA assessed by real-time quantitative     2003   0   0
7- and 12.7-fold increase in total renin mRNA in kidneys of ADX,             3032710    1987   0   1
                                                                             2885756
cells, and cAMP also induces somatostatin gene transcription 8-10-fold in transfected   1987   0   0
8- to 10-fold increase in SP-B mRNA after 3 days that                        1733279    1992   0   1
to a 8-10-fold increase in TAT mRNA level, cAMP to a 20-30-fold              2885194    1987   0   0
and a 9.3-fold increase in the TNF-alpha mRNA levels was observed            8569176    1996   0   1
revealed a ninefold increase in TPH mRNA in E-treated macaques compared      8824338    1996   0   1
and a 9-fold increase in TSH beta gene expression from TSS                   2210030    1990   0   1
and a ninefold elevation in skeletal muscle VEGF mRNA expression (P        12763746     2003   0   0
2- to 16-fold increase in the level of mRNA encoding the alpha               2831539    1988   0   0
a 6-12 fold increase in amount of mRNA for the mu                            6818319    1982   0   0
to an 8-10-fold increase of mRNA detected in dot-blots. In contrast,         8756755    1996   0   1
and a 9-fold increase in hybridizable mRNA levels. Within 2 h                2413017    1985   0   0
a 9 fold increase in the expression of mRNA sequences for                    6689125    1983   0   0
                                                                             8621726
causes a 9-fold increase in steady-state levels of mRNA for UDP-Gal:beta-D-Gal          1996   0   0
CdCl2, a ninefold increase in MT gene expression was observed in lymphocytes,1716322    1991   0   1
                                                                            epidermal
elicits a ninefold increase in expression of mRNA encoding heparin-binding11943653      2002   0   0
on a 9-fold increase in the level of mRNA transcribed from                   6693434    1984   0   0
The mRNA level of PC12-PTP1 is increased 9-fold                              7814416    1995   0   1
The transcription rate for arginase mRNA increased 9-fold                    8460937    1993   0   0
a time-dependent 10-fold increase in a 1.9-kb mRNA in response to a          8554317    1995   0   0
The AHR repressor (AHRR) mRNA level was induced 7-13-fold                  12520768     2002   0   0
than 10 fold induction of albumin mRNA in cultures maintained in steroid       3010979 1986   0   0
                                                                                24-h
demonstrate a 10-fold increase in alkaline phosphatase mRNA levels after a2165496 1990        0   0
caused a 10-fold increase in the alpha 1 mRNA expression, and the              8238401 1993   0   0
of age when alpha 1I3 mRNA levels increased 10-fold                            2450089 1988   0   1
of age, testis levels of alpha-subunit mRNA increased 10-fold                  9041125 1997   0   0
an approximately 10-fold increase in steady-state AM mRNA levels was observed, 9746563 1998   0   0
to Gq/PLC, carbachol increased ANF reporter gene expression 10-fold and also   7721739 1995   0   0
with a 10-fold induction of barnase mRNA expression. Directing tTA expression 11504884 2001   0   0
promoter, this bcl-2 p2 site 1 increased transcription 10-fold in the presence11704864 2001   0   0
9 to 12-fold elevation of rat c49a mRNA at 12 h                               10381256 1999   0   1
The level of calcyclin mRNA is increased 10-fold                               9321910 1997   0   0
an approximately 10-fold increase in CAT activity and mRNA in EL-4             1917935 1991   0   0
and NRK kidney cells, cat-1 mRNA levels increased 3.8-18-fold                 10521420 1999   0   0
greater than 10-fold increase in CBG hepatic mRNA in day-18.5 embryonic 10509797 1999         0   0
induced a 10-fold increase in CD40 mRNA and protein Furthermore,               7554483 1995   0   0
an approximately 10-fold increase in c-fos mRNA levels. Pretreatment of MCF-7  8125161 1994   0   0
contrast, a 10-fold increase in c-fos mRNA expression was evident in 20        8847708 1995   0   0
more than 10-fold increase of the c-fos mRNA level as well                     9655520 1998   0   0
than that observed initially. c-Fos mRNA was increased 10-fold                 9439681 1997   0   1
an approximately 10-fold increase in cIGFBP-5 mRNA relative to embryonic 9149401 1997         0   1
HGF, a 10-fold increase in c-met mRNA levels was observed 30                   7526865 1994   0   0
Steady-state c-myc mRNA levels were increased 10-fold                          7955204 1994   0   1
RESULTS: The collagen alpha1(I) mRNA was increased 10-fold                     9927153 1999   0   0
isotonic to hypertonic medium, cotransporter mRNA abundance rose 10-fold8430828 1993          0   0
produces a 10-fold induction of COX-2 mRNA and an 8-fold increase              9266823 1997   0   0
                                                                               8897833 1996
stimulated a 10-fold increase in cyclooxygenase (COX)-2 steady-state mRNA levels in 18Co      0   0
The rate of DHFR transcription increased 10-fold                               8765160 1996   0   0
induced a 10-fold increase in E3 mRNA levels. E3 transcripts are               8839844 1996   0   0
demonstrates a tenfold increase in EGF mRNA following retinoic acid treatment  1748717 1991   0   1
ER transcription rate. Levels of EGF-R mRNA increased 10-fold                  8836162 1996   0   0
diminished in PKC-depleted cells. AVP induced Egr-1 mRNA 10.9-fold in control  1415734 1992   0   0
revealed that the level of emc mRNA increased 10-fold                          9611245 1998   0   1
ENC-1 mRNA levels are transiently increased 8-12-fold                         10828068 2000   0   0
only a 10-fold increase in Epo gene transcription in response to these         1985693 1991   0   1
plasma membrane fatty acid-binding protein mRNA was increased 9-11-fold       10497230 1999   0   0
least a 10-fold increase in fibronectin mRNA and a 2-fold increase             2180962 1990   0   0
of lavaged cells expressing FN mRNA was increased 10-fold                      1419030 1992   0   0
                                                                               2847161 1988
not in nongluconeogenic tissues. Fructose-1,6-bisphosphatase mRNA was increased 10-fold       0   0
5- to 16-fold increase in galanin mRNA levels, measured by Northern            8751287 1995   0   1
                                                                               1
Furthermore, a 10-fold increase in galanin mRNA levels seen in the presence 385097 1992       0   0
carcinoma cell lines. Levels of gelsolin mRNA increased 10-fold                2546951 1989   0   0
in a 10-fold increase in GFAP mRNA by 1 day and a                              9668663 1998   0   1
was a 10-fold increase in GFAP mRNA levels in these same                       8062084 1994   0   0
least a 10-fold increase in GLUT 4 mRNA and protein detected                   1584210 1992   0   1
a concentration-dependent, >10-fold induction of GM-CSF mRNA after 4 A 11752025 2002          0   1
the minor subclasses of GnT-I mRNA was induced 10-fold                         9781684 1998   0   0
Hepatocyte growth factor mRNA levels were increased 10-fold                    7954397 1994   0   1
In contrast, hippocampal AChE mRNA increased 10-fold                           7834388 1994   0   1
greater than 10-fold increase in HMG-CoA reductase mRNA levels, LPS had7595071 1995           0   0
showed a 10-fold increase in the transcription of hPKC alpha mRNA              1616823 1992   0   0
an over 10-fold increase in HSP 70 mRNA was observed, which                    7810720 1994   0   0
in a 10-fold increase of hsp70 mRNA in the mucosal and in                     12403938 2002   0   0
A 3-17-fold upregulation of IFI27 mRNA expression was observed when 15086558 2004                0   1
demonstrated a 10-fold increase in IFN-gamma mRNA levels at 7 days            12757624 2003      0   1
express a 10-fold increase in mRNA and produce high titers of IFN-gamma. 8955202 1996            0   0
after GH administration, hepatic IGF-I mRNA had increased 10-fold              8840951 1996      0   0
injections, a 10-fold increase in IGF-I mRNA was seen 24 h                     7974526 1994      0   0
after day 10. IGF-I receptor mRNA levels increased 10-fold                     1324154 1992      0   0
of IL-1 beta mRNA. IL-1ra mRNA levels increased tenfold                        9106226 1997      0   0
by a tenfold increase of IL-6-specific mRNA following UVA Induction            7688402 1993      0   1
over a 10-fold increase in iNOS mRNA content in glomeruli and the              7516453 1994      0   1
confirmed a 10.5-fold increase in IPF-1 mRNA levels after 3 days              11016451 2000      0   0
reveal a 10-fold increase in IR mRNA after differentiation. These studies      2407479 1990      0   1
                                                                               2108862
an approximately 10-fold increase in ISG transcription. ISG transcription is dependent 1990      0   0
In cultured keratinocytes hINV mRNA levels are increased 10-fold              10970794 2000      0   0
is a 10-fold increase in KGF mRNA by 72 h of culture.                          9788959 1998      0   0
mRNA, a tenfold increase in Ltype calcium channel mRNA accumulation, and a    12624436 2002      0   0
In contrast, nonmuscle MHC-A mRNA increased 10-fold                            1550206 1992      0   0
injury in bovine cartilage, MMP-3 mRNA levels increased 10-fold               12746902 2003      0   1
PCR, a 10-fold increase in MT-1 and -2 mRNA levels was                        10884303 2000      0   0
pregnant cows, steady-state levels of Mx mRNA increased 10-fold               12817504 2003      0   1
concentrations, the amount of MxA mRNA was induced 10-fold                     7679692 1993      0   0
a maximal tenfold increase in NaS(i)-1 and sat-1 mRNA levels compared 10603126 1999              0   0
                                                                               8469241 1993
greater than 10-fold rise in nascent IGF-II mRNA during cellular differentiation,                0   0
Fetal bovine serum increased NCX mRNA 10-fold in 4                             7961668 1994      0   0
and a 10-fold increase in the NF-M mRNA levels after 24                        8381895 1993      0   0
was a 10-fold increase in NOS mRNA in granulation tissue of both              12384060 2002      0   0
by a 10-fold increase in NPR-A mRNA levels and ANP stimulation                 7911451 1994      0   0
elevated compared to controls. mRNA for NPY increased 10-fold                  1954911 1991      0   1
                                                                               7945260 1994      0
ovariectomized rats with ovine prolactin increased Ntcp mRNA 10-fold compared with solvent-treated   1
A ten-fold increase in ob mRNA was detected in white                           7488081 1995      0   1
that the ODC mRNA level, that was increased 10-fold                            9194572 1997      0   1
two- to 10-fold increase in ODC mRNA with a maximum after                      1745018 1991      0   0
Upon temperature shift, p21 mRNA was upregulated 10-fold                      10050041 1999      0   0
                                                                                less than
an approximately 10-fold increase in p21WAF1/CIP1 mRNA levels, whereas8895764 1996               0   0
BA treatment, tenfold induction of P-450 1A1 mRNA after BA treatment           9452186 1997      0   0
6- to 15-fold increase in lung p52(PAI-1) mRNA content was evident             8368324 1993      0   0
about a 10-fold increase in PB2 mRNA and protein The                           2989815 1985      0   0
                                                                               7587654 1995
Following hormonal stimulation, cAMP induces PEPCK gene expression 10-fold within 20-30          0   0
a > 10-fold increase in PGHS mRNA over the control (169                        8473524 1993      0   0
six- to ten-fold increase in mRNA for P-glycoprotein and expression of the 8098991 1993          0   0
                                                                              11443121
more than 10-fold induction of PKA-stimulated PEPCK-C gene transcription caused by 2001          0   0
a relative 10-fold increase in PPT-A mRNA in smokers with chronic             11555376 2001      0   0
an about ten-fold increase of preproNPY mRNA levels over the dentate           8090071 1994      0   0
of PTHrP mRNA and secreted PTHrP were increased 10-fold                        7717970 1995      0   1
in a 10-fold increase in the PVY CP mRNA steady-state levels,                  7990802 1994      0   1
L-type pyruvate kinase mRNA concentration was increased 6-15-fold              6546383 1984      0   0
to male X. laevis induces hepatic RBP mRNA 10-fold from its                    3558378 1987      0   0
In aorta-coarctated rats ischemic kidney renin mRNA increased 10-fold          3531004 1986      0   0
an approximately 10-fold increase in S100 beta mRNA and protein levels         8965656 1996      0   1
more than 10-fold increase in SAA mRNA expression, but it is                  10831790 2000      0   1
and a 10-fold increase in SCD1 transcription within 24 Additionally,           7961698 1994      0   0
caused a 10-fold increase in whole kidney SN1 mRNA level and a                12372777 2002      0   0
in a 10-fold increase of sodCp mRNA whereas the sodB transcript                9177032 1997      0   0
with a tenfold increase in TGF-beta mRNA (TGF-beta mRNA at 6                 11849412     2002   0   0
to the vessel's media. TGF-beta 1 mRNA increased 10-fold                      9409216     1997   0   0
in a 10-fold increase in TGF-beta igh3 mRNA levels. Zta was                   7769680     1995   0   1
8- to 12-fold increase in TNF-alpha mRNA compared to lymphocytes activated    1708843     1990   0   0
an approximately 10-fold increase in TNF-alpha mRNA and a 35-fold increase    9378369     1997   0   1
for a 10-fold increase in TNF-alpha mRNA stability by reducing poly(A)        8089495     1994   0   0
six- or ten-fold rise in TPH mRNA in median raphe nucleus                    10381000     1999   0   0
                                                                              a
synthesis, a 10-fold increase in the steady-state transferrin mRNA level, and 1315521     1992   0   0
by a 10-fold increase in tTG mRNA level, which is followed,                   1672508     1991   0   0
with a 10-fold increase in type II mRNA levels at 48                          7905505     1994   0   0
that a 10-fold increase in UCP3 mRNA levels occurs in rat                     9519732     1998   0   0
                                                                             had
produced a 10-fold increase in UCP-3 mRNA expression, but rosiglitazone 12630940          2003   0   0
of about tenfold increase in steady-state u-PA mRNA at 3 hr                   2500450     1989   0   0
(b) a 10-fold increase in steady state mRNA levels of uPAR                    8391387     1993   0   1
a synergistic 10-fold induction of VDR mRNA and the appearance of a           9397948     1994   0   0
to a 10-fold increase in vitellogenin mRNA                                      652525    1978   0   0
The amount of the YMR26 mRNA was increased 10-fold                            2017142     1991   0   1
rats, the fold increase in ZAKI-4 mRNA level from E18 to P17 was 10.8        11316738     2001   0   1
was a 10-fold increase in the 1.4-kb mRNA by 1 week                           8323294     1993   0   1
the cells with 30 microM forskolin increased transcription 10-fold within 30 2481819      1989   0   0
with ethacrynic acid or dimethyl maleate increased mRNA 10-fold and 5-fold,7515059        1994   0   0
embryo, and the level of its mRNA increased tenfold                           9778036     1998   0   1
the most sensitive and its transcription was increased 10-fold               14559238     2003   1   0
an approximate 10-fold increase in specific transcription using a 5 S         1939109     1991   0   0
up to 10-fold increase of specific mRNA was seen, as was                     12558136     2003   0   0
mass, a 10-fold increase in steady-state mRNA levels, and a 3.4-fold          1995604     1991   0   0
to a 10-fold increase in steady-state mRNA levels compared to the wild-type 9447962       1998   0   0
found a 10-fold increase in this mRNA following 60 min of insulin             2643510     1989   0   0
a > 10-fold increase in mRNA expression in response to LPS                    7790054     1995   0   0
a 10 fold increase of transcription is obtained at the higher                 6292834     1982   0   0
about a 10-fold increase in mRNA levels in both epidermis and gut,            8353525     1993   0   0
an approximately tenfold increase in reporter gene expression in Caco-2 11111045          2000   0   0
at the level of transcription and is induced 10-fold                         10564515     1999   0   1
by cell type, transcription from the locus increased 10-fold                  3313002     1987   0   0
                                                                             site
caused a 10-fold upregulation of luciferase reporter gene expression at the 10609662      1999   0   0
five- to 10-fold increase in transcription along the entire length of the     8649860     1996   0   0
induced a 10-fold increase in mRNA levels of the proto-oncogene,             10064622     1999   0   0
                                                                              7779861
induced a tenfold increase in the transcription of the pulmonary vasoconstrictor          1995   0   0
induction, a ten-fold increase in the mRNA for each gene was                  2454872     1988   0   0
                                                                              8655488
is a 10-fold increase in transcription from three different sigmaD-dependent promoters,   1996   0   0
pylori, the 10-fold induction in transcription of a second copy of HP1043    12169605     2002   0   0
The transcription efficiency of IVa2 is increased 10-fold                     6593702     1984   0   0
to a 10-fold increase in reporter gene expression levels when compared 14684287           2004   0   0
to the 1,25-dihydroxyvitamin D3 receptor. mRNA levels increased 10-fold 2481316           1989   0   1
with a 10-fold increase in the gene expression of Increased                  12032186     2002   0   0
with a 10-fold increase in transcription of the flgMN operon compared         9765570     1998   0   0
was increased 10-fold and mRNA levels were increased 11.5-fold               10837498     2000   0   0
induced an 11-fold increase in alpha 1B receptor mRNA The                     7989580     1994   0   0
mRNA increased 2-fold, whereas Cat3 mRNA levels increased 11-fold             9614060     1998   0   1
induces an 11-fold increase in CR1 mRNA expression in K-562 erythroleukaemia 10023854     1999   0   0
                                                                              8187072
analysis demonstrated that DHEA induces CYP4A gene expression 11-fold at the level        1994   0   1
An 11.3-fold increase in Egr-1 transcription rate was observed as             8214093     1993   0   0
in an 11-fold up-regulation of FATP mRNA expression in adipose                8843418 1996         0       0
Shock-induced transcription of hsp-72 was elevated elevenfold                 1379380 1992         0       0
Expression of ICAM-1 mRNA was increased 11-fold                               7507856 1994         0       0
was an 11-fold increase in liver IGF-I mRNA abundance in the GH               1315260 1992         0       0
had an 11-fold increase in IL-12Rbeta2 mRNA levels while porcine blasts 12383645 2002              0       1
induced an eleven-fold increase in IL-1alpha mRNA in the hypothalamus relative9622598 1998         0       1
caused an 11-fold increase in IL-6 mRNA in both cell                        12733076 2003          0       0
demonstrate an 11.5-fold increase in KLK8 mRNA levels in AD hippocampus     11522960 2001          0       1
in fetal and neonatal hearts. LPL mRNA increased 11-fold                      1550225 1992         0       0
metallothionein-2 (MT-2) genes. Levels of mRNA were increased 11-fold         2066364 1991         0       0
7- to 15-fold induction of P450IA mRNA expression. Northern blot analysis 1855491 1991             0       1
                                                                              mRNA content reflected a 15-fold
late-passage senescence-associated 11-fold elevation in steady-state PAI-1 9397159 1998            0       0
steady state level of the pnp mRNA increased 11-fold                          3308454 1987         0       0
to uninduced TVA8 cultures, todC1 mRNA levels increased 11-fold               9835608 1998         0       0
in higher-grade gliomas. uPAR mRNA level was increased 11-fold              11234878 2001          0       0
3-fold and 20-fold elevation of their respective mRNA levels. The major       7775439 1995         0       0
The level of 4-nitrophenol GT mRNA is elevated 10-15-fold                     2504523 1989         0       0
a time-dependent 12-fold upregulation of ADM mRNA in AVSMCs that was 11799096 2002                 0       0
                                                                            12948937 2004
2- and 22-fold increase in lung alpha-ENaC mRNA expression compared with saline-treated            0       0
A 12-fold increase in the CYP3A mRNA signal (approximately 2.4              10570035 1999          0       1
under metal-ion limitation, because dpsA mRNA levels increased 12-fold 10896214 2000               0       0
produces a 12-fold increase in Egr-1 mRNA within 30 Pretreatment              2005129 1991         0       0
in a 10-15-fold increase in ermC mRNA half-life in Bacillus                   7682278 1993         0       0
                                                                             control)
responded with an increase both in ET(B)-R mRNA (12-fold compared with11457849 2001                0       0
mice compared to BALB/c mice. Fibronectin mRNA increased 12-fold              2457084 1988         0       0
10 to 15-fold increase in FOSP-1 mRNA by 60 h, whereas                        2210028 1990         0       0
how a 12-fold increase in G6PD synthesis and mRNA (measured by                2039474 1991         0       0
A 12-fold increase in GLUT5 mRNA levels was detected at                       7619068 1995         0       0
with a 12-fold rise in GRP mRNA:GAPDH mRNA between days 17                    9614367 1998         0       1
induce a 12-fold increase in GS mRNA in murine skeletal muscle,               2904387 1988         0       0
A 12-fold increase in HPTP beta mRNA expression was detected                  7575486 1995         0       1
10- to 15-fold increase in the rate of transcription of the hsp70             3862119 1985         0       0
an almost 12-fold increase in hsp70 mRNA levels, but a significant          11259510 2001          0       0
to a 12-fold increase in IGF-I mRNA and enhanced IGF-I promoter             11390399 2001          0       0
was a 12-fold increase in IGF-I mRNA levels in the GH                         1315260 1992         0       0
to a 12-fold increase in interleukin 8 (IL-8) mRNA as compared              11591715 2001          0       1
(100 ng/mL) increased the expression of IL-8 mRNA 12.8-fold after 3         12594001 2003          0       1
Whole lung KGF mRNA expression was increased 12-fold                          9887062 1999         0       1
                                                                              1824600 1991
2- to 23-fold increase in levels of laminin-receptor-precursor mRNA in the cancer                  0       0
demonstrated the 10-15-fold induction of mGPDH mRNA in rat liver after        8760382 1996         0       0
and a 12.5-fold induction in NGF gene transcription was obtained after        1547729 1992         0       0
In contrast, ODC mRNA level increased 12-fold                                 8273569 1993         0       1
                                                                               in DF-40
induces a 10-15-fold increase in ornithine decarboxylase (ODC) mRNA level7954361 1994              0       0
rats, pituitary OX(1) receptor mRNA levels were increased 12-fold           12639903 2003          0       0
Peak expression of PAI-2 mRNA is increased 10-15-fold                         2498314 1989         0       1
12.4 +/- 3.2-fold increase in PAI-2 mRNA in RME cells and rat                 7883982 1995         0       0
into myotubes, PKCtheta mRNA and protein were increased 12-fold             10919262 2000          0       0
human genomic ras sequence. ras mRNA was increased 8-17-fold                  8626688 1996         0       0
caused a 12.5-fold increase in VPF mRNA levels at 24 hours,                   1719968 1991         0       0
15-, and 10-fold increase in the mRNA levels encoding the EGF                 1401070 1992         0       1
in a 10-15-fold increase in the level of transcription of a chimeric          1325459 1992         0       0
                                                                            11069927 2001
induce a 10-15-fold increase in the rate of transcription of the phosphoenolpyruvate               0       0
on chromosome V, and its transcription is increased 12-fold                   1377774 1992       0   0
the transient assay system. Reporter gene expression increased 12-fold        2011579 1991       0   0
and a 12-fold increase in the level of mRNA for the F                       11922631 2002        0   0
by a 12-fold increase in mRNA content. In the kidney and lung                 3785172 1986       0   0
                                                                            12011978 2002
to a 12-fold increase of reporter gene expression (luciferase) with progesterone                 0   0
Transcription of this gene is induced 12-fold                                 8670196 1996       0   0
with a 12-fold increase in the mRNA level. TGF-beta 1 also                    1655420 1991       0   0
The 1.9-kb ADH mRNA levels were increased 12-14-fold                          1370936 1992       0   0
an 11-to 13-fold increase in C3 synthesis. C3 mRNA levels were                8344703 1993       0   0
causes a 9-18-fold increase in CFTR mRNA abundance versus the mRNA 1705554 1991                  0   0
4 and hexokinase II mRNA levels were elevated 13-fold                       12766179 2003        0   0
to the 13-fold rise in IGF-II/CIMPR mRNA levels, transcript levels for        1722618 1991       0   0
showed a 13-fold increase in IL-6 mRNA on day IL-6                            1544451 1992       0   0
The levels of mEH mRNA were increased 10-16-fold                              8117322 1994       0   1
EHR2, the multidrug resistance-associated protein mRNA was increased 13-fold10856431 2000        0   0
caused a 13-fold increase in mRNA for this PLA2. Timecourse studies           2803314 1989       0   0
induced a 13-fold increase in urokinase mRNA synthesis in colon carcinoma2107972 1990            0   0
in a 10-16-fold increase in gene expression of the ubiquitin ligases        12672461 2003        0   0
a transient 13-fold increase in transcription by day 14 with return           2509021 1989       0   1
conferred a 13-fold increase in the reporter gene expression in vivo        11115610 2001        0   0
exhibited a 14-fold increase in aFGF mRNA levels, and 19 of 21                7507297 1994       0   1
course analysis demonstrated that apoD mRNA was induced 14-fold               8943263 1996       0   1
                                                                            12593849 2003
inhibitor lovastatin (34 microM) increased BMP-2 gene transcription >14-fold as measured         0   1
A 14.9-fold increase in Egr-1 mRNA was observed 6 days                        9139213 1997       0   0
chemical carcinogenesis procedure. Epoxide hydrolase mRNA is increased 14-fold2295064 1990       0   0
5- to 24-fold rise in total GH mRNA levels by 48-72                           2583364 1989       0   0
a maximal 14.9-fold increase in glomerular Egr-1 mRNA at day 6                9067901 1997       0   1
In activated lymphoblasts, hSK4 mRNA increased 14.6-fold                    10329683 1999        0   0
and a 14-fold increase in IL-2R beta mRNA levels. A large                     8056031 1994       0   0
In the liver metallothionein mRNA was increased 14.5-fold                     2980792 1988       0   1
expression and demonstrated that ompT transcription is upregulated 14-fold  11952906 2002        0   0
caused a 14-fold induction of PEPCK mRNA in 6 This                            7727519 1995       0   0
in a 14-fold increase in thioredoxin mRNA by 16 hours, and a                  9042207 1996       0   0
showed that lung steady-state TIMP-1 mRNA levels increased 14-fold          11350830 2001        0   1
1.9- to 28-fold increase of the mRNA and protein levels of the              12594236 2003        0   1
12- to 16-fold increase of the 2.7 kb mRNA in response                        3454871 1987       0   0
                                                                            10642578
indicated a 14-fold increase in ovarian mRNA for carbonyl reductase, with expression 2000        0   1
A 15-fold increase in rat 19S mRNA and only a 3-fold                          6547088 1984       0   1
hybridized to a 3.2-kilobase mRNA whose level increased 15-fold               3393528 1988       0   0
2.8-kb transcript, expression of the 4.7-kb mRNA increased 15-fold            8175144 1994       0   1
clone revealed a 5.5-kilobase poly(A)+ mRNA that increased 15-fold            3276692 1988       0   0
with a 15-fold increase in ODC activity. Actin mRNA levels were               8319826 1993       0   0
causes a 15-fold elevation of hypothalamic Agrp mRNA levels but has         10218993 1999        0   0
the al-3 mRNA was shown to be increased 15-fold                               2524647 1989       0   0
Steady-state ANPR-C mRNA level was increased 15-fold                          8349696 1993       0   1
exhibited a 15-fold increase in bFGF mRNA levels. In situ hybridization       7507297 1994       0   1
caused a 15-fold up-regulation of CD59 mRNA in these cells, implying          7543447 1995       0   0
                                                                            10998151     -308A
produced a 15-fold increase in chloramphenicol acetyl transferase transcription from the2000     0   0
3- to 28-fold increase in class II mRNA in SFC and an                         9436470 1997       0   0
a 15 fold increase in COX-1 mRNA including an alternatively spliced           9562240 1998       0   0
                                                                            11004165 2000
tetracistronic cprBACD transcript. Transcription of cprBA was induced 15-fold                    0   1
10-fold to 20-fold increase in cryIA(c) mRNA and protein levels compared 1515613 1992            0   0
10- to 20-fold increase in desmin mRNA is observed in myogenic              6594672 1984     0   0
insulin-producing RINm5F cells. Fas mRNA expression was increased 15-fold  11473033 2001     0   0
a subsequent 15-fold increase in GADD45 mRNA levels, neither the chromatin 10481028 1999     0   0
                                                                            9325284 1997     0
a approximately 15-fold increase in gelatinase B mRNA expression, dexamethasone down-regulated   0
demonstrated a 15-fold increase in gene 33 mRNA after 1 h                   8156927 1994     0   0
The level of Grp78 mRNA rose 15-fold                                        9310369 1997     0   0
                                                                            7629148 1995
in a 10-20-fold increase in endogenous HB-EGF mRNA levels; ii) co-transfection               0   0
HB-EGF mRNA abundance was also increased 15-fold                            7929446 1994     0   0
in a fifteen-fold increase in Hsp70 mRNA levels. The return of stressed    12212628 2002     0   0
with HSP82, and while HSP82 transcription is induced 15-fold                8675027 1996     0   0
In A549 cells, ICAM-1 mRNA is increased 10-20-fold                          7911467 1994     0   0
severe energy restriction: IGFBP-1 mRNA abundance was increased 15-fold7679969 1993          0   0
10- to 20-fold increase in IL-8 mRNA abundance when compared with the 10226079 1999          0   0
revealed a 10-20-fold increase in iNOS mRNA in spinal cords during          8982114 1996     0   1
                                                                            9786920 1998
the approximately 15-fold up-regulation of LmGT2 mRNA levels in promastigotes compared       0   1
showed a 15.8-fold increase in MBP mRNA between 12 and 18                   8951645 1996     0   1
                                                                            7544347 1995
The impressive 15-fold increase in maternal liver murinoglobulin mRNA at partum              0   0
AP mRNA decreased 48%, and OP mRNA increased 15.3-fold                      7573489 1995     0   1
10- to 20-fold increase in OrnDCase mRNA concentration in normal animals,   6366788 1984     0   0
in a 15-fold induction of P450 gene expression within 26                    1855491 1991     0   1
PDGF A chain mRNA levels were increased 5-25-fold                           3478335 1987     0   0
relative abundance of this mRNA in SHR increased 15-fold                   10342790 1999     0   1
post-TPA treatment TNFalpha mRNA levels were increased 15-fold             10953159 2000     0   1
10- to 20-fold increase in tPA mRNA and protein. Regulation of both         2157975 1990     0   0
10- to 20-fold increase of UCP3 gene expression is achievable through      14673524 2004     0   0
In normal rats, 3-MC-inducible UDPGT mRNA concentration increased 15-fold   2113060 1990     0   0
10- to 20-fold increase in kidney steady-state mRNA levels for genes        1281619 1992     0   0
with a 10-20-fold increase in both gene transcription and mRNA levels       1690720 1990     0   0
by a 10-20-fold increase in their stability. This mRNA stabilization is     2559736 1989     0   0
10- to 20-fold increase in mRNA produced by strain C600F(pKC30STb) over2318537 1990          0   1
10- to 20-fold increase in transcription of MGSA/GRO alpha, -beta and -gamma8264646 1994     0   1
caused a 15-fold increase in the transcription rate of the lysozyme         9590245 1998     0   1
Nuclear transcription rates for the transporter increased 15-fold           7860756 1995     0   1
analysed, a 16-fold elevation in islet amyloid polypeptide mRNA was observed2612759 1989     0   0
mRNA was increased 5-fold and LH beta mRNA 16-fold over values              2426086 1986     0   0
                                                                           10068207 1999
blotting analysis revealed that MCAF/MCP-1 mRNA expression increased 16-fold                 0   1
result: a 16-fold increase in hepatic metallothionein mRNA was observed 7h 4015627 1985      0   0
for a 16-fold increase in Mn SOD mRNA concentration. Mn SOD                10330025 1999     0   0
                                                                            7916534
After NH4Cl, phosphoenolpyruvate carboxykinase (PEPCK) mRNA increased 16-fold 1994           0   0
caused a 16-fold increase in prodynorphin mRNA levels which comprised all 7898656 1994       0   0
was a 16-fold increase in TPH mRNA in the pineal gland                      9332732 1997     0   1
have a 16-fold increase in UMP synthase mRNA but a 40-fold                  6546385 1984     0   0
indicates a 16-fold increase in UMP synthase mRNA in the resistant          6134725 1983     0   0
by a 16-fold increase in the transcription rate of mouse B2                 2470009 1989     0   0
with a 16-fold increase in mRNA expression in advanced stage carcinomas11063652 2000         0   1
12- to 22-fold increase in amphoR mRNA in HSCs from cryopreserved          10372116 1999     0   0
                                                                            2255185 1990
infiltration without crescent formation, beta-actin mRNA were increased 17-fold              0   0
in a 17-fold increase in mRNA levels derived from bolA1p 1                 10361282 1999     0   0
                                                                           11720885
17.6-fold and 17.3-fold increase of c-jun mRNA expression respectively (P<0.001) was 2001    0   0
10- to 25-fold increase in GLUT-1 mRNA levels in endothelial and Kupffer 8928796 1996        0   0
                                                                            8418776
14-, and 20-fold upregulation of hepatocyte LBP mRNA following treatment with LPS, 1993      0   1
The level of mEH mRNA increased 17-fold                                     7689039 1993     0   1
in a 15-20-fold increase in cellular PA mRNA content. The effect           3933492   1985   0   0
have a 17-fold increase in translatable mRNA activity coding for UMP       6134725   1983   0   0
A 2-33-fold increase in mRNA levels was found in colorectal                8275492   1994   0   1
5- to 30-fold increase in reporter gene expression in OMEC II             11318110   2001   0   0
in a 15-20-fold increase in transcription in NIH3T3 and Hep1-6 cells      10721719   2000   0   0
The level of specific mRNA for aromatase increased 17-fold                 1694074   1990   0   0
however, a 17-fold increase in the level of mRNA encoding the chemokine 10729341     2000   0   1
euthyroid rats (= 1.0). beta TSH mRNA increased 18-fold                    2294008   1990   0   0
Vanadate (10(-3) M) maximally increased gene 33 transcription 4-fold at 15 1472065   1992   0   0
and a 18-fold increase in HSP70 mRNA expression, whereas HSP40 levels11855822        2002   0   1
showed an 18-fold increase in procollagen-alpha1(I) mRNA at 17 wk, which 8928787     1996   0   0
                                                                          12500193
same interval, TRAIL-R1/DR4 and TRAIL-R2/DR5 mRNA expression increased 18-fold       2003   0   0
An 18-fold increase of UCP3 mRNA can be attained by                       14673524   2004   0   0
                                                                          11035776
7- to 30-fold induction of the mRNA encoding the putative cholesterol/phospholipid   2000   0   0
6 hours and a later increase in mRNA (18-fold at maximum)                 11054396   2000   0   0
                                                                           1315322
an approximately 18-fold increase in the steady-state mRNA levels for the Na+/H+     1992   0   0
in an 18-fold increase in the mRNA level. Mutant hepatoma cells            2869038   1986   0   0
in a 19.7-fold increase of alpha 2M mRNA already after                     2483766   1988   0   1
a approximately 19-fold increase in the calculated mRNA copy number from 9882620     1999   0   1
                                                                           9832422
induced a 19-fold increase in Fas antigen mRNA levels. Corresponding increases       1998   0   0
of 12 h. The glucokinase mRNA was increased 19.6-fold                      2037560   1991   0   0
                                                                          11406531
7.9- and 30.2-fold increase of hpa mRNA in chronic pancreatitis and pancreatic       2001   0   0
with a 19-fold increase in PAPP-A mRNA expression and an 8-fold           12744930   2003   0   0
had TGF-beta 1 mRNA levels which were increased 19-fold                    2169772   1990   0   0
that the TGF-beta 1 mRNA level was increased 19-fold                       8475255   1993   0   0
in a 19-fold increase in mRNA levels and a 3-fold increase                 3036872   1987   0   0
greater than 20-fold induction of a 2700-base mRNA that hybridized to a    3805014   1987   0   1
in a 20-fold increase in steady-state 4F2HC mRNA levels which was          3265471   1988   0   0
to a 20-fold increase in alpha 1-acid glycoprotein mRNA in the presence    2454192   1988   0   0
the constitutive alpha 1-acid glycoprotein-1 mRNA levels increased 20-fold 2054382   1991   0   0
                                                                           1400341
revealed a 20-fold increase in alpha 2 gene transcription upon megakaryocytic        1992   0   0
to a 20-fold increase in the endogenous ANF mRNA in the ventricle          1832775   1991   0   0
A 20-fold increase in placental apoB mRNA concentrations during the last 3464945     1986   0   0
the level of arylsulfatase A mRNA is increased 20-fold                     7916017   1994   0   0
                                                                           2628732
greater than 20-fold increase in beta-casein mRNA accumulation with an apparent      1989   0   0
                                                                           9050887
analysis revealed increases in abundance in calbindin mRNA (>20-fold for most        1997   0   1
during cell cycle re-entry. Calmodulin mRNA levels increased 20-fold       2199442   1990   0   0
TG induced 20-fold elevation of c-fos mRNA in WEHI7.2 and WEHI7.2-neo 9419976        1997   0   0
Treatment of cells with TPA increased c-fos mRNA 20-fold with only         8838143   1996   0   0
The CMP-NeuAc synthetase gene expression was increased 10-30-fold          2549035   1989   0   0
A 20-fold increase in c-myb mRNA and protein expression was                9815978   1995   0   0
The level of c-myc mRNA is transiently increased (20-fold                  2540002   1989   0   0
in a 20-fold increase in collagenase mRNA by 12 Transient                  7984435   1994   0   0
was > 20-fold induction of cyclin D1 mRNA and protein, beginning           7733934   1995   0   0
in a 20-fold increase of EPO mRNA in mouse brain as                        7731971   1995   0   0
if transient 20-fold increase in FasL mRNA and a threefold increase       11053034   2000   0   0
for the 20-fold increase in flagellar mRNA concentration during the        3405205   1988   0   0
in ovariectomized controls. Galanin mRNA levels were increased 20-fold     7694842   1993   0   0
an approximately 20-fold increase in GFAP mRNA content at 2 weeks;         7710688   1995   0   0
revealed a 20-fold increase of GGT mRNA between day 18 of gestation        1974921   1990   0   1
caused a 20-fold increase in brain HO-1 1.8-kb mRNA within 1               1737989   1992   0   0
least a 20-fold increase in HPRT mRNA levels resulting from approximately 6952245    1982   0   0
notably, the 20-fold induction of IL-6 mRNA and protein was completely        14764742 2004       0   0
that the level of kin1 mRNA is increased 20-fold                               2151730 1990       0   1
an approximately 20-fold increase in LDL receptor mRNA level, as determined    9392422 1997       0   0
two-fold whereas the level of legumin mRNA increased 20-fold                   2582360 1985       0   0
to a 20-fold increase in malic enzyme mRNA level when starved                  3541753 1986       0   0
to the 20-fold increase in malic enzyme mRNA caused by feeding                 2579951 1985       0   0
greater than 20-fold increase in mdr mRNA levels, there was little             1982215 1990       0   1
                                                                              12239237
an approximately 20-fold increase in mesangial MCP-1 mRNA and protein expression 2002             0   1
reaction and immunoassays, respectively. The MMP-1 mRNA increased 20-fold     13679308 2004       0   0
Mn-SOD activity was increased 3-fold and mRNA 20-fold after a 48-h             1850207 1991       0   0
The multidrug resistance-associated protein (MRP) mRNA was increased 20-fold  10856430 2000       0   0
cells a 20-fold increase in NPY mRNA levels was observed                       9533817 1998       0   0
                                                                               9346888 1997
exposure, a 20-fold induction of PAF-acetylhydrolase mRNA was detected. In cells                  0   1
produced a 20-fold increase in the gene expression of PAI-1 at                12014920 2002       0   0
analysis demonstrated that PB P-450 mRNA is increased 20-fold                  6689485 1983       0   0
PLRP-1 mRNA levels twofold and increased PLRP-2 mRNA 20-fold but had 8967484 1996                 0   0
using specific probes. mRNA levels of psaB increased 20-fold                   8292789 1993       0   0
caused a 20-fold increase in renin mRNA and a 10-fold increase                 9256163 1997       0   0
A 20-fold induction of serum amyloid A3 mRNA by O(3)                          12763052 2003       0   0
a 20 fold increase in u-PAR mRNA in rabbit jugular veins                       9684800 1998       0   1
of a 20-fold increase in a specific hepatic mRNA four hours                    6314118 1983       0   0
which specifies an mRNA whose level is increased 20-fold                       3017948 1986       0   0
                                                                               in THP-1
(CAT) reporter construct, live M. tuberculosis increased transcription 20-fold 7738195 1995       0   0
effect of the latter. Steady-state mRNA levels increased 20-fold               7557873 1995       0   0
20-fold increase of the mRNA was detected in the treated                       2895632 1988       0   0
a > 20-fold increase in reporter gene expression that was inhibited            8230418 1993       0   0
a 20 fold increase of beta-glucuronidase reporter gene expression in transgenic8219081 1993       0   0
approximately 20 fold increase in transcription (P < 0.005). This synergistic 12114445 2002       0   0
causes a 20-fold induction of the mRNA in the pre-pubertal                     3497926 1987       0   0
                                                                               8220480 1993
enhance a 20-fold increase of beta-glucuronidase reporter gene expression in transgenic           0   0
exhibits a 20-fold increase in mRNA levels after 16 wk                         7529396 1994       0   0
for the 20-fold increase in mRNA level. The level of malic                     2579951 1985       0   0
in a 20-fold increase of transcription from the tenascin reporter in NIH      11244566 2001       0   0
observed a 20-fold increase in reporter gene expression with plasmid DNA 12969505 2003            0   0
revealed a 20-fold increase in mRNA abundance, reaching a peak level           3872994 1985       0   0
                                                                               9109503 1997
seven- to 20-fold increase in reporter gene expression in catecholaminergic cell                  0   0
The expression of mRNA was induced 20-fold                                     8222045 1993       0   1
The observed 20-fold increase of mRNA for the isolated clone corresponding     9466813 1998       0   1
to 20 fold increase in transcription from the adenovirus major late            4075392 1985       0   0
with a 20-fold increase in the mRNA level during In                           11137704 2001       0   0
that the bGT 2.9 Kb mRNA was increased 21-fold                                 2302200 1990       0   1
showed a 21-fold increase in the hepatic Cyp2a-4/5 mRNA in the DBA/2           1417950 1992       0   1
and a 21-fold increase in erp72 and HO-1 mRNA levels; P                        9655603 1998       0   0
cells did not block induction of IL-1Ra mRNA (21.6-fold induction, P<0.02 14598021 2004           0   0
20 to 23-fold increase in ilv mRNA as compared to repressed                    1102933 1975       0   0
                                                                               8980166 1996
insulin significantly increased the expression of ob mRNA (21.4-fold compared to control).        0   0
(16- to 21-fold increase in tPA mRNA and 6- to 8-fold                          8119183 1994       0   1
                                                                              10644752 2000
a minimal promoter, co-expression of LBP-1b increased transcription 21-fold in a dose-dependent   0   0
induced a 21-fold increase in reporter gene expression in primary             10636896 2000       0   0
More strikingly, CYP2B1/2 mRNA levels were increased 22-fold                  11714877 2001       0   0
an approximately 22-fold increase in the mEH mRNA levels, demonstrating that   8043012 1994       0   1
of protooncogene mRNA levels; c-fos mRNA was induced 23-fold                   8436603 1993       0   0
A 23-fold increase in CYP2B1/2 mRNA in the SDR liver                          8667238 1996        0   0
Specifically, cytochrome P-450b gene transcription increased 23-fold          6408085 1983        0   0
A 23-fold up-regulation of ER mRNA expression coincided with the initiation 9528993 1998          0   1
data demonstrated that pyruvate carboxylase mRNA content increased 23-fold    6548474 1984        0   1
in a remarkable increase in AT(2) receptor mRNA (24-fold increase over 14749041 2004              0   0
in a remarkable increase in AT2 receptor mRNA (24-fold increase over         14749041 2004        0   0
was a 24.4-fold increase of Ckidelta mRNA in AD hippocampus compared 10814741 2000                0   0
differentiated adipocytes, the expression of CT mRNA increased 24-fold 12960010 2003              0   0
ulcerative colitis show elevated levels of ENA-78 mRNA (24-fold increase, P 9252512 1997          0   0
                                                                                dehydrogenase
and a 24-fold rise in GRP mRNA (normalized to glyceraldehyde-3-phosphate9614367 1998              0   1
                                                                               control
densitometry demonstrated a maximal increase in HO-1 mRNA 24-fold over 8160707 1994               0   0
relative content of liver ATP-citrate lyase mRNA increased 25-fold            6546379 1984        0   1
20- to 30-fold increase in calbindin-D28K mRNA peaking at 12-18 h,            1375904 1992        0   0
a 25 fold upregulation of eotaxin gene expression in the airway               9311484 1997        0   0
                                                                             10425197 1999
20- to 30-fold induction in hepatic FAS gene transcription observed in fasted-refed               0   0
                                                                             11279238
with the 20-30-fold induction in fatty-acid synthase gene transcription observed in fasted 2001   0   0
FSH beta mRNA levels were increased 25-fold                                   8504735 1993        0   0
showed a 25-fold increase in hTERT mRNA and a 300-fold increase              11943710 2002        0   0
                                                                              9573251 1998
a robust 25-fold increase of IkappaBalpha mRNA expression (the RelA:IkappaBalpha positive         0   0
                                                                              NF-kappaB
an approximately 25-fold increase in IL-6 mRNA levels. IL-1beta stimulated12676746 2003           0   0
to a 25-fold increase in the LDH-H mRNA and a 12-fold                        11878820 2002        0   0
10- to 40-fold increase in PBE mRNA levels by 24                              1533303 1992        0   1
in a 25-fold increase in RFP mRNA levels after 24 h                          12788653 2003        0   0
in a 25-fold increase in the mRNA level and, as a consequence,                9023927 1997        0   0
produced a 26-fold increase in P450cc24 mRNA which was detectable at 7681765 1993                 0   0
The 26-fold increase in TF mRNA levels induced by LPS                         9102164 1997        0   0
indicates a 26-fold increase in homologous mRNA in response to the feeding    6822548 1983        0   0
25- to 30-fold increase in c-myc mRNA at 3 weeks of age                       3479800 1987        0   0
induced a 27-fold increase in IL-12 p40 mRNA levels while killed              8606072 1996        0   0
with a 27-fold increase in mRNA content, and for kidney P(3)450               3785172 1986        0   0
and 28 fold induction of liver apo A-IV mRNA is observed                      4000948 1985        0   0
Our results show that MCP-1 mRNA levels increased 28-fold                     9301643 1997        0   1
After stimulation of differentiation, mRNA abundance increased 28-fold        9005979 1997        0   0
a 20-38 fold increase in COL1A1 and COL6A3 mRNA concentration at             11518275 2001        0   0
at 48 hr and CYP1A1 mRNA was increased 29-fold                                8432429 1993        0   0
The levels of ETA receptor mRNA were elevated 29.3-fold                       8575076 1996        0   0
induced a 29-fold increase in Krox-20 mRNA signal exclusively in the ischemic 1445346 1992        0   1
10- and 48-fold increase in PAI-1 mRNA in RME cells and RASMC,                7883982 1995        0   0
produced a 30-fold increase in the 24-hydroxylase mRNA level. This result 8506296 1993            0   1
In contrast, liver AT mRNA abundance increased 30-fold                        1723087 1991        0   0
10- to 50-fold increase in steady state mRNA for beta-myosin heavy            8781472 1996        0   1
kidney of mice. Intestinal CaT1 mRNA level increased 30-fold                 12933662 2003        0   0
more than 30-fold increase in CNTF mRNA and protein occurs in the             1824101 1991        0   1
                                                                              9394732
RESULTS: A 30-fold induction of collagenase mRNA and collagenase protein secretion 1997           0   0
An approximately 30-fold increase in COX-2 mRNA was seen after 24             9362331 1997        0   0
While a 30-fold increase in globin mRNA was detected in the spleen,          11286637 2001        0   0
                                                                              2891717 1987
an approximate 30-fold increase in glutamine synthetase mRNA after incubation of organ            0   0
to human GMP-r, and its mRNA is increased 30-fold                             9813009 1998        0   0
a dramatic, 30-fold induction of N/OFQ mRNA levels in these                   9681445 1998        0   0
The OPN mRNA in total ovine endometrium increased 30-fold                    12606367 2003        0   0
                                                                             30-fold
after bile duct ligation. Additionally, procollagen-alpha1(I) mRNA increased 12791596 2003        0   0
10- to 50-fold increase in RAR beta mRNA levels, whereas RAR                  2542014 1989        0   0
The 30-fold rise in TK mRNA levels in response to growth                     9776764 1998      0   0
was a 20-40-fold induction of TNF-alpha mRNA that persisted at lower         9540974 1998      0   0
greater than 30-fold increase in type I collagen mRNA relative to normal     2243137 1990      0   0
approximately a 30-fold induction of Ucp mRNA within 4 The                   1603085 1992      0   0
(A1251), a 20-40-fold increase in urokinase mRNA level is obtained after     3958045 1986      0   0
15- to 45-fold increase of the mRNA levels for the individual                8755862 1996      0   0
20- to 40-fold increase in transcription when compared with a corresponding 9811930 1998       0   1
                                                                            10926935 2000
increased expression of FOG increased reporter construct transcription 30-fold Unexpectedly,   0   0
causes a 30-fold increase in transcription of the malic enzyme gene          9624119 1998      0   0
expressed a 30-fold increase in mRNA but, due to a reading                   8473524 1993      0   0
provided a 30-fold increase in transcription from a SV40 viral promoter      8894694 1996      0   0
to a 30-fold increase in transcription of a stably transfected c-myc         2662014 1989      0   0
with a 30-fold increase in mRNA and a 21-fold increase in protein.           1539169 1992      0   0
gave a 31-fold induction of mRNA levels at 300 In                            8169528 1994      0   0
25- to 40-fold induction of endogenous mouse beta-casein mRNA was observed   2747652 1989      0   0
was a 32.4-fold increase in betaig-h3 mRNA levels in pancreatic cancers 12379307 2002          0   0
stimulated a 32-fold increase in collagenase-3 mRNA at 48 h after           10529279 1999      0   0
Specifically, a 33-fold increase in brain HO-1 mRNA was observed within      2052613 1991      0   0
was a 33-fold increase in the P450scc mRNA level. Both TNF-alpha             9397943 1994      0   0
                                                                            11063652 2000
with a 33-fold increase in mRNA expression from normal endometria to advanced                  0   1
with a 34-fold increase in the mRNA levels of betaFSH and a                 10570010 1999      0   0
The 34-fold increase in TF mRNA levels induced by TNF-alpha                  1330076 1992      0   0
MRC-5 CM also increased u-PA receptor mRNA 34.9-fold in MDCK                 1328201 1992      0   0
                                                                             7554451 1995
and a 34-fold increase in percentage area inflammation. mRNA analysis revealed                 0   0
various culture periods. The amount of mRNA increased 34-fold                3865226 1985      0   0
30- to 40-fold increase in the transcription rate of the CYP1A5              9705900 1998      0   0
progesterone, a 20-50-fold increase in hsp 108 mRNA is detected above        3571271 1987      0   0
to a 35-fold increase of HSP70 mRNA expression measured by Northern 10561481 1999              0   1
and a 35-fold increase in IL-1 beta mRNA within 2 h                          9378369 1997      0   1
of development, Na+/K+ ATPase alpha-subunit mRNA content increased 35-fold   2160296 1990      0   1
carcinoma (EC) cell lines. Pem mRNA is induced 35-fold                       1680379 1991      0   0
mediate the 20-50-fold induction of TK mRNA observed as cells traverse       7848915 1994      0   0
30- to 40-fold induction in CAT gene expression was observed in the          8911578 1996      0   1
a 30-40 fold increase of the CAT gene expression compared to the             1923810 1991      0   0
mdr genes and the mRNA levels were increased 30--40-fold                     1682162 1991      0   1
                                                                             3492677 1987
as a 35-fold increase in mRNA translational efficiency; moreover, the translational            0   0
lines, a 35-fold induction of mRNA accumulation, peptide synthesis, or CAT 2792562 1989        0   0
hours after injury, EGF-R mRNA levels were increased 36-fold                 8765213 1996      0   0
possess a 36-fold elevation of mdm-2 mRNA relative to A31 cells,            10365438 1999      0   0
By real-time quantitative RT-PCR, NK-1R mRNA was increased 36.7-fold 12746482 2003             0   0
                                                                            10525116
unprecedented approximately 37-fold increase in 1.8-kb HO-1 mRNA in PBN pretreated 1999        0   1
but a 37-fold increase in beta-casein mRNA accumulation. In contrast, whey 3062379 1988        0   0
gland P450IIE1 mRNA was found to be induced 25-50-fold                       8344939 1993      0   0
3.4-fold at 180 min, and PGHS-2 mRNA increased 38-fold                      10691023 1999      0   0
a polyadenylated 4.5 kb mRNA which is induced 30-50-fold                     1936242 1991      0   0
                                                                             1
caused a 40-fold increase in adrenomedullary ppEnk mRNA levels only in the 317492 1992         0   0
by a 40-fold increase in CD11a mRNA levels. Nuclear run-on transcription 1730867 1992          0   0
by a 40-fold increase in CD-RAP mRNA between days 7 and 10.                 12568962 2003      0   0
                                                                             a2
an approximately 40-fold increase of COX-2 mRNA in macrophages during10810453 2000             0   0
fasting, and diabetes. CPT-Ialpha mRNA abundance is increased 40-fold 10956641 2000            0   0
observed a 40-fold increase in prostatic IGF-I mRNA levels in response       9924191 1999      0   0
revealed a 40-fold increase in MRP mRNA levels (maximum at 4-6               8723762 1996      0   0
                                                                            10686076 2000
approximately a 40-fold increase in netrin-1 mRNA levels. Immunohistochemistry data show    0   1
The 40-fold increase in NGF mRNA elicited by 1,000 U/ml                      9282915 1997   0   0
northern blot analysis, p75NTR mRNA levels were increased 40-fold           12741461 2003   0   1
and transient 40-fold induction of the 3.2-kilobase PAI-1 mRNA and a 30-fold 8034668 1994   0   0
a transient 40-fold increase in PAI-1 gene transcription rate. The relative  1655729 1991   0   0
elicited a 40-fold increase in POMC mRNA levels. In vivo experiments         3769863 1986   0   1
A 40-fold induction of relaxin mRNA was observed in cells                   10770494 2000   0   0
At this time, rGAL-encoding mRNA was increased 40-fold                       7688905 1993   0   0
We show here that SOCS-3 mRNA is induced 40-fold                            11375418 2001   0   0
that ST6Gal I mRNA in W16 is elevated 40-fold                               10543981 1999   0   0
in a 40-fold increase in TGF-beta 1 mRNA after 4 days                        7757990 1995   0   0
expressed at high levels, and its transcription induced 40-fold              1964095 1990   0   0
A 40-fold increase in the steady-state mRNA level in the larval              9512531 1998   0   1
least a 40-fold increase in translatable mRNA in livers of induced           2414298 1985   0   1
                                                                             9008232 1997
showed a 40-fold increase in mRNA expression, whereas mitochondrial NAD5 and NAD6           0   1
showed a 40-fold induction of mRNA levels, comparable to wild type           2849256 1987   0   1
of steady-state immunoglobulin (Ig) mu mRNA is increased 23-60-fold          2119479 1990   0   1
stability of mRNA. CYP3A1 mRNA levels maximally increased ~42-fold          11181506 2001   0   0
IL-10 mRNA levels in lung were increased 43-fold                            10806208 2000   0   1
ATPase alpha-subunit mRNA content of mouse embryos increased 45-fold 1963318 1990           0   1
greater than 45-fold increase in cox2 mRNA levels after a 2-h                8132578 1994   0   0
In vivo, CYP3A1 mRNA levels increased 45-fold                               11020454 2000   0   1
                                                                            10745160 2000
a 40-50 fold increase in [(3)H]L-glutamate uptake. DipEAAT1 mRNA is expressed               0   0
of gestation, the GHBP-encoding mRNA (1.4 kb) increased 45-fold              7511151 1994   0   1
much as 40-50-fold induction of HSP-70A mRNA levels during the peak          8083107 1994   0   1
with a 45-fold increase of SCD1 mRNA and a 10-fold increase                  7961698 1994   0   0
step of heme biosynthesis. Its transcription is increased 40-50-fold         8593679 1995   0   0
45 +/- 19-fold increase in IFN-gamma gene expression over those in resting  10201989 1999   0   0
days after bupivacaine injection, IGF-II mRNA was increased 46-fold          9249571 1997   0   0
The 47-fold increase in c-fos mRNA caused by 100 nM                         11166731 2001   0   0
                                                                             477.4 copies
demonstrated approximately 48-fold increase in PDGF-B mRNA (7667.1 +/- 8708960 1996         0   1
by a 49-fold increase in mRNA levels after 1 Thus,                           8156927 1994   0   0
revealed a 49-fold increase in transcription rate of the FAS gene           10484571 1999   0   0
induced a 50-fold increase in 5'DI mRNA levels that preceded by              8404614 1993   0   0
in a 50-fold induction of cathepsin L mRNA and secretion of the              2180257 1990   0   0
Moreover, a 50-fold increase of the steady-state c-fgr mRNA concentration is 3003578 1986   0   0
about a 50-fold increase in amounts of COX-2 mRNA in normal-appearing 10070952 1999         0   0
a 50 fold increase in the transcription of gp30 in young                     7716403 1994   0   0
However, a 50-fold increase of IL--6 mRNA was found after stimulation       11406463 2001   0   0
by a >50-fold induction of inducible NO synthase mRNA and the release        9915771 1999   0   0
exhibited about 50-fold increase in LCB2 mRNA relative to the wild          12570999 2003   0   0
a 50 fold increase in PTHrP mRNA expression 30 min after                     9345287 1997   0   1
greater than 50-fold increase in rGH mRNA level was seen after               3371552 1988   0   0
showed that the amount of smc01944 mRNA increased 50-fold                   14993315 2004   1   1
was > 50-fold increase in TYRP2 mRNA with a moderate increase               11310793 2001   0   1
produced a 50-fold increase in its mRNA content at 3                         8912151 1996   0   0
in a 50-fold increase in steady state mRNA levels for the kinase             8049264 1994   0   1
an approximately 50-fold increase in transcription by 4 h, which was         2917991 1989   0   0
                                                                            polylysine
average of 50-fold increase in reporter gene expression in comparison with10541433 1999     0   0
conferred a 50-fold increase in luciferase reporter gene expression in      11024036 2001   0   0
least a 50-fold increase in mRNA levels, indicating that expression of HlyB 7536296 1995    0   0
producing a 50-fold induction of mRNA within 1 hour of                      10477716 1999   0   0
to 50 fold increase in the level of mRNA transcribed from                    6572107 1983       0      0
Up to 50-fold induction of gene expression in human tumor cell              12525840 2003       0      0
5- to 100-fold increase in IL-2 gene expression and secretion that           2543699 1989       0      0
A 52-fold increase in PDGF-B mRNA was seen at 12                             9546351 1998       0      1
intracellular infection, the intramonocyte 85B mRNA level increased 54-fold11169120 2001        0      0
37- to 71-fold increase in PGE2 accumulation. PGHS-1 mRNA levels were 8079657 1994              0      1
steady state levels of 4F2HC mRNA are induced 50-60-fold                     2789062 1989       0      0
stimulated a 55-fold increase in osteocalcin mRNA as early as 24            14745233 2004       1      0
10- to 100-fold increase in gene expression in numerous FGFR positive       10363982 1999       0      0
insertion of both GLUT1 mRNA cis-regulatory elements increased 59-fold 9878834 1999             0      0
in a 59-fold induction in gene expression under inducing As                 12000993 2002       0      0
in a 60-fold increase in 4F2HC mRNA levels. This induction was               3265471 1988       0      0
A 60-fold increase in alpha 1-acid glycoprotein mRNA levels was              3259230 1988       0      0
the severely anemic calf, Epo mRNA levels increased 60-fold                  8666286 1996       0      1
an over 60-fold increase in epsilon-globin mRNA level. Exposure to cytosine 2606728 1989        0      0
of the 20-100fold increase in cellular histone mRNA levels during S-phase 2480181 1989          0      0
with a 60-fold increase in expression of IGF-I mRNA in LAPC-9               11507082 2001       0      0
over 60 fold increase in metallothionein and its mRNA upon                   2959533 1987       0      0
gal, hepatic levels of MIP-2 mRNA were increased >60-fold                   10223730 1999       0      0
an approximately 60-fold increase in PRL-R mRNA levels. This effect by       2293027 1990       0      1
observed a 60-fold increase in reelin mRNA levels. The histone deacetylase  12087179 2002       0      0
identified a 60-fold induction of VEGFR-1 mRNA in retina from P3            12840058 2003       0      1
39+/-4 and 64+/-2-fold increase in leptin mRNA compared with 0 h            11934523 2002       0      1
human peripheral mononuclear cells (PMCs). TRAP mRNA increased 50-75-fold    8135751 1994       0      0
                                                                             3
a 30-100 fold induction of metallothionein mRNA levels. The level of induction125519 1988       0      0
to a 66-fold increase in translatable alpha 2-macroglobulin mRNA after 18 6197304 1983          0      0
while the levels of P450 2B1/2 mRNA increased 66-fold                        8489239 1993       0      0
60- to 75-fold induction of IGFBP-3 mRNA and protein This                   10077006 1999       0      0
to 0.54 fmol/lobe), while POMC mRNA levels increased 69-fold                 2233740 1990       0      0
was a 70-fold increase in the beta-MHC mRNA (P < 0.01),                     10072897 1997       0      1
40- to 100-fold increase in IGF-II mRNA was shown in 9/40                    3180092 1988       0      0
an over 70-fold increase in PGHS-2 mRNA by 1 h, and maximal                  8215426 1993       0      0
an approximately 70-fold increase in TP mRNA levels 4 days after            12481438 2002       0      1
                                                                             3062379 1988
the maximal 73-fold induction in mRNA accumulation. This posttranscriptional effect of hormones 0      0
in a 75-fold increase in CyP40 mRNA levels, but no corresponding            11525244 2001       0      0
(3) 70% O2. Total lung elastin mRNA increased 70-80-fold                    10761639 1999       0      0
50- to 100-fold increase in Epo mRNA which we have accurately                8318914 1993       0      0
5:718-724]. MGF gene expression was increased 77-fold                       12589681 2003       0      0
induced a 79-fold increase in Gs alpha mRNA and a 5-fold                     7703916 1994       0      0
Fourteen- and 80-fold induction of CYP1A1 and CYP1A2 mRNA were shown,       14514442 2003       0      0
with an 80-fold increase in GRP78 mRNA and a 10-fold increase                2511206 1989       0      0
caused a 80-fold induction of IL-6 mRNA level which was due                  9655919 1998       0      0
respectively while the mRNA level for knox-24 increased 80-fold              9042210 1996       0      0
greater than 80-fold increase in mdr gene expression over that in normal     2890168 1987       0      0
                                                                             8419313 1993
that the 70-100-fold induction of CYP1A2 mRNA by polycyclic aromatic compounds                  0      0
produced an 85-fold increase in CYP1A2 mRNA levels. Levels of CYP1A1 12396271 2002              0      0
75- to 100-fold increase in steady-state mRNA levels. Southern blot analysis 2428042 1986       0      0
                                                                             2547373 1989       0      0
caused a 90-fold increase in mRNA for 6-phosphofructo 2-kinase/fructose-2,6-bisphosphatase. Glucocorticoid administration
to a ninety-fold increase in transcription rate over the dark control        8842141 1996       0      0
                                                                             9066532 1997
73-fold and 110-fold increase in matrix metalloproteinase-9 mRNA signal, respectively, relative 0      0
AS alpha 1 steady-state mRNA levels are increased 100-fold                   7757119 1995       0      0
in a 100-fold increase in AVP mRNA in the BNST and a                         8818400 1996       0      0
caused a 100-fold increase in c-fos mRNA levels, an effect partially           8238298 1993   0   0
Nearly a 100-fold increase in amounts of COX-2 mRNA was detected              10668483 1999   0   0
more than 100-fold increase in constitutive CYP1A1 mRNA levels; this dramatic  9792830 1998   0   1
activity could be measured. HIOMT mRNA concentration increased 100-fold 8665667 1995          0   1
caused a 100-fold increase in steady-state endogenous hREN mRNA but no8760248 1996            0   0
led to 100-fold upregulation of IL-13 mRNA within 4 h and detectable           8879181 1996   0   1
to 4 ng/ml. LPS also increased IL-6 mRNA 100-fold in mouse                    12842862 2003   0   0
in a 100-fold increase in PGHS-2 mRNA and a 25-fold increase                   8660662 1996   0   0
                                                                                life
exhibited a 100-fold increase in PNMTase mRNA levels between embryonic 6956894 1982           0   0
MPA for 28 days, PRL mRNA gradually increased 100-fold                         1380842 1992   0   1
an approximately 100-fold increase in steady-state TF mRNA levels in HAEC,    10444399 1999   0   1
by a 100-fold increase in TS mRNA and a 100-fold amplification                 2932632 1985   0   0
                                                                               1633435 1992
domain (-153 to -87), it synergistically increases transcription 100-fold (Muscat and Kedes   0   0
laevis oocytes injected with hOAT1 mRNA is increased 100-fold                 10049739 1999   0   0
the approximately 100-fold elevation in steady-state mRNA specific for this 10945983 2000     0   0
Gene expression in tumor tissue was increased 100-fold                        10493523 1999   0   0
in a >100-fold increase in mRNA levels. This increase in mRNA                  9628914 1998   0   0
or = 100-fold induction of mRNA and protein. In addition to some               8660317 1996   0   0
to a 100-fold increase in the production of mRNA in these                      6306281 1983   0   0
treatment, with steady state levels of mRNA increased 100-fold                 2176215 1990   0   0
Up to 100-fold increase of apparent gene expression in the presence            9621086 1998   0   0
was over 100-fold increase in mRNA levels in the adenoma compared              9458096 1998   0   0
with a 100-fold increase in gene expression per infectious particle when      10779163 2000   0   0
in 32% post-treatment. Levels of afp- mRNA increased 3-210-fold               11369140 2001   0   0
displayed a 120-fold increase in AdoMetDC mRNA levels and failed to form 9731498 1998         0   0
induce a 120-fold increase in IL-2R alpha mRNA and a 14-fold                   8056031 1994   0   0
During rhIL-6 infusion, IL-6 mRNA increased 120-fold                          14521945 2003   0   0
                                                                               short
an approximately 120-fold up-regulation of reporter gene expression from a12511603 2003       0   0
EC and SMC. Membrane type-1-MMP (MT1-MMP) mRNA increased 121-fold             12231217 2002   0   0
to 0.159 fmol/lobe), while POMC mRNA levels increased 121-fold                 2233740 1990   0   0
                                                                              14568988
and a 125-fold increase in aortic IFN-gamma mRNA when compared with age-matched 2003          0   0
observed a 125-fold increase in TF mRNA levels. Our data demonstrate 10887118 2000            0   0
to the 130-fold increase in glutamine synthetase mRNA observed during terminal 1975588 1990   0   0
                                                                               1415807 1992
demonstrated that rat placental calbindin9K-to-beta-actin mRNA ratio increased 135-fold       0   1
showed a 140-fold increase in PDGF-A mRNA expression 4 hours after             9546351 1998   0   1
during sodium depletion, PRC and renin mRNA increased 144-fold                 2970225 1988   0   0
during sodium depletion, PRC and renin mRNA increased 144-fold                 2970225 1988   0   0
FIT2, and FIT3 mRNA transcript levels were increased 60-230-fold              11673473 2001   1   1
show a 150-fold increase in beta-tropomyosin mRNA expression in the heart,     8530495 1995   0   0
up to 150-fold induction of interleukin-6 (IL-6) mRNA was detected in the 12297145 2002       0   0
up to 150-fold increase in reporter gene expression in EGF receptor            9614577 1998   0   0
95- or 210-fold increase in CYP2C45 mRNA and a 140- or 290-fold               11867618 2002   0   0
found a 160-fold induction of mRNA encoding keratinocyte growth factor (KGF)   1379725 1992   0   0
displayed a 170-fold increase in AdoMetDC mRNA levels and formed vacuoles      9731498 1998   0   0
an approx 188-fold induction of c-fos mRNA at 30 min and an                    9657066 1997   0   0
was a 200-fold increase in AT2 mRNA levels in quiescent cells                  7580938 1995   0   0
more than 200-fold increase in c-sis mRNA level. DH at -8.6                    8375387 1993   0   0
more than 200-fold increase in the c-sis mRNA level. We have                   8375387 1993   0   0
treatment with PAHs, cytochrome P-450d mRNA levels increased 200-fold 3379039 1988            0   0
for four hours, right kidney Epo mRNA increased 200-fold                       8943479 1996   0   0
and a 200-fold increase in MTase mRNA levels compared with mucosa              8816806 1996   0   1
a 200 fold increase in osteocalcin gene expression occurs with mineralization  2605954 1989   0   0
of a 200-fold increase in its transcription rate. We have previously       10638709 1999           0       0
stimulated with IFN-gamma. This mRNA expression is induced >200-fold 9614071 1998                  0       0
                                                                             2432068 1987
inflammatory stimulation, rat alpha 2-macroglobulin mRNA levels increased 214-fold                 0       0
with a 218-fold increase in the mRNA levels of During                      10570010 1999           0       0
a significant 280-fold increase in MCP-1 mRNA expression in the muscularis,11751168 2002           0       0
as a 288-fold increase of cyclin D1 specific mRNA after a 24h              12921950 2003           0       1
a several hundredfold increase in glucoamylase mRNA in cells grown on        6440004 1984          0       0
                                                                              no
in a 300-fold increase in IE94-IFN-specific mRNA transcripts, compared with1316484 1992            0       0
a several hundred-fold increase in transcription of the adult mouse globin 6578416 1983            0       0
caused a 350-fold increase in lux mRNA levels. The results suggest           1385389 1992          0       0
270- to 430-fold increase in tetA mRNA and a 35- to 65-fold                  2995683 1985          0       0
in hyperosmolar environments. Transcription of proU is induced 400-fold      9081863 1996          0       0
                                                                           CCR5
We found up-regulation of endometrial CXCR1 mRNA (419-fold increase), 12651900 2003                0       0
100- to 1,000-fold increase in mRNA synthesis when it is located           11773405 2002           0       0
10- to 1200-fold increase in gene expression over the naked DNA            11059581 2000           0       0
                                                                           12651900
of endometrial CXCR1 mRNA (419-fold increase), CCR5 mRNA (612-fold increase) and2003      CCR2B 0          0
                                                                             6166321 1981
exhibited a 1000-fold increase in mRNA transport activity as compared to cytosol.                  0       0
                                                                           10201989 1999
1393 +/- 643-fold increase in IFN-gamma gene expression over those in resting                      0       0
obtain a 1500-fold induction of gene expression from GAL promoters in this 2512199 1989            0       0
limit among healthy controls, alphafp mRNA levels increased 23-3.4x103-fold10998444 2000           0       0
regulate the 2,000-fold increase in SAA mRNA after injection of endotoxin 3221863 1988             0       0
                                                                           transcription 200-5000-fold over0
side chain to generate 20-epi-1alpha,25(OH)(2)D(3) (20E-125D) increases 10893309 2000              0        125D
causes a 3,000-fold increase in the galanin mRNA content of the lactotroph. 9770544 1998           0       0
weeks after operation. Levels of afp mRNA increased 5-7600-fold            10632334 1999           0       1
white bass liver, hepcidin gene expression was induced 4500-fold           11985602 2002           0       0
PCR showed 2000-20,000-fold increase of ER mRNA transcript in all three 14620913 2003              0       1
5 x 10(4)-fold increase of iNOS gene expression was The                    12239095 2002           0       1
                                                                             9625760 1998
an approximately 400,000-fold increase in I-TAC mRNA expression, whereas stimulating monocytes     0       0
HCC and adenoma patients, alb mRNA levels increased 10-10(6)-fold          10632334 1999           0       1
Pattern#
    1       Microarray       27     0.8%                                                    mRNA     Protein    Total
    3       Validation      828    24.4%            Pattern 1                                  2310         782       3092
    1       Unique genes            1529            Pattern 2                                    933        326       1259
    1                                               Pattern 3                                    165         23        188
    1                                                                                          3408       1131        4539
    2      Fold change Reported Symmetrical
    1                          0
    1              >20       301
                                                                                                       800
    1                20       66
    1                19        9                                                                       700
    1                18       10




                                                           # of times reported in MEDLINE
    1                17       14
    1                16       12                                                                       600
    1                15       48
    1                14       17
    1                13       13                                                                       500
    1                12       43          Symmetrical
    2                11       22                  0                                                    400
    2                10      152      10      185
    1                 9       51        9       55
    1                 8       80        8       92                                                     300
    2                 7       87        7       96
    2                 6      134        6     151
    1                 5      267        5     308                                                      200
    1                 4      352        4     385
    1                 3      515        3     582                                                      100
    2                 2      725        2     784
    1              +/-1      155    +/-1      155
    1                -2       59      -2      784                                                                        0
    1                -3       67      -3      582                                                                            >20 20 19 18 17 16 15 14 13
    1                -4       33      -4      385
    2                -5       41      -5      308
    1                -6       17      -6      151
    1                -7        9      -7        96
                                                                                                                         900
                                                                             # times absolute fold-change was observed




    1                -8       12      -8        92
    1                -9        4      -9        55
    1               -10       33     -10      185                                                                        800
    1             <-10        60                  0
    1                          0                                                                                         700
    1                 0        3
    1                 1      150                                                                                         600
                                                                                            in MEDLINE




    1                -1        2
    1                                                                                                                    500
    2
    1                                                                                                                    400
    2
    3                                                                                                                    300
    1
    2                                                                                                                    200
    3
    1                                                                                                                    100
    # times absolute f
                         100
1
1
                          0
1
1
                               10 9 8 7 6 5
2
1
2
2
2
1
1
2
1
1
1
1
1
2
2
1
1
1
1
1
1
1
2
3
1
1
1
1
2
2
3
3
3
3
1
1
1
1
1
1
1
1
1
1
1
1
1
2
1
2
1
1
1
1
1
3
3
2
1
1
1
1
2
2
1
1
2
1
1
2
1
1
1
1
1
1
1
3
1
1
2
1
1
1
2
1
2
1
2
1
1
3
1
1
1
1
1
1
1
2
1
1
1
1
1
2
1
1
1
1
1
1
1
1
1
1
1
1
1
1
2
1
1
1
1
2
1
2
3
2
1
1
1
3
2
1
1
1
1
1
1
1
1
1
3
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
2
2
1
1
1
2
1
1
1
1
1
1
1
2
1
1
2
1
1
2
1
1
1
1
1
1
1
1
2
2
1
1
1
2
1
1
1
1
1
2
2
1
2
1
1
1
1
1
1
2
2
1
1
1
1
1
1
1
1
1
2
1
1
2
2
1
2
1
2
1
1
2
2
2
1
2
1
1
1
1
1
1
2
2
1
2
1
1
1
1
1
2
2
1
2
1
1
1
1
1
2
1
1
1
1
3
1
1
1
1
1
1
2
1
2
1
1
1
1
3
3
2
2
1
1
3
2
1
1
2
1
1
2
2
1
1
1
1
1
1
1
1
1
1
2
2
1
2
1
2
1
2
1
1
1
3
2
1
1
2
1
2
2
2
1
3
1
2
2
2
1
1
1
1
1
1
1
2
1
2
2
1
1
2
1
2
3
2
1
1
2
1
2
3
1
1
1
2
2
2
1
1
1
3
2
1
2
2
2
2
1
1
1
1
1
1
1
3
1
2
2
2
2
1
1
1
1
1
1
1
2
1
1
1
1
2
2
1
1
3
1
1
1
1
1
2
2
1
1
2
2
2
2
1
1
1
1
1
1
1
3
1
2
1
1
1
1
1
1
1
1
1
1
1
3
1
1
1
1
1
2
1
1
1
1
1
3
3
1
2
1
2
1
1
2
2
1
1
2
1
1
2
2
2
1
1
2
2
2
1
1
2
2
1
3
2
2
1
1
1
1
1
1
1
2
1
1
1
1
1
2
1
2
1
1
1
2
2
1
1
1
1
1
1
1
1
2
2
1
2
1
1
2
1
1
1
1
1
1
1
2
1
1
2
1
1
1
1
1
2
1
1
2
1
1
1
2
2
2
1
1
2
1
1
1
1
3
1
1
2
1
2
2
1
1
2
2
2
2
2
1
1
1
3
1
1
1
1
1
1
2
2
1
1
1
2
1
1
1
2
1
2
2
2
1
3
2
1
2
1
1
2
1
2
1
1
1
1
1
1
1
1
2
1
1
1
3
1
1
1
1
1
2
1
1
1
1
2
3
1
2
2
1
1
2
1
1
2
1
2
1
1
2
1
1
2
1
1
1
1
2
1
3
2
2
2
1
1
2
1
2
2
2
2
1
2
2
1
2
1
1
1
1
1
1
2
2
1
1
2
1
1
2
1
1
1
2
1
1
1
2
2
1
1
1
2
1
1
1
2
1
1
2
2
3
3
1
1
2
2
1
1
1
1
2
1
1
2
1
2
1
1
1
1
1
2
1
2
1
2
3
1
1
1
1
2
2
1
2
2
1
2
1
2
1
1
1
1
2
1
2
2
2
1
2
1
2
1
1
1
1
1
1
1
1
2
2
1
1
2
3
1
1
1
1
2
1
3
1
2
1
2
1
1
1
2
1
1
1
1
1
1
1
1
3
3
1
1
1
1
1
1
2
2
1
2
2
1
1
1
1
1
1
1
1
2
2
1
1
1
1
1
2
1
1
1
1
1
2
1
1
3
1
1
1
3
1
1
1
2
1
1
1
1
1
2
1
1
1
1
1
1
2
1
2
1
2
3
1
1
2
2
2
1
1
1
1
1
2
1
1
1
1
2
1
1
1
1
1
1
1
1
1
2
1
2
1
2
2
1
2
1
2
1
1
2
1
1
1
2
2
1
2
1
3
2
1
1
1
1
1
1
1
1
1
1
1
2
1
2
1
1
1
2
2
3
1
1
1
1
2
1
3
1
2
1
2
1
1
1
1
1
2
2
1
1
2
3
2
1
1
1
2
1
1
2
2
1
2
2
1
2
2
1
1
1
1
2
1
2
2
2
1
1
1
1
1
1
2
1
1
2
1
3
1
1
1
1
1
2
1
1
1
1
1
1
1
1
1
1
1
1
1
1
3
1
2
1
1
2
1
1
2
2
1
1
3
1
1
1
1
2
1
1
2
3
2
2
3
2
1
1
2
1
1
1
2
1
1
1
2
1
1
1
3
1
2
1
2
1
1
1
1
1
2
1
2
2
1
3
2
1
1
2
1
2
1
2
1
2
2
1
1
1
1
2
2
1
1
2
2
2
1
1
1
2
3
3
1
2
1
2
1
2
2
2
1
1
1
1
1
1
1
1
1
1
2
1
1
1
1
1
1
1
1
1
1
1
1
1
2
1
1
1
2
2
1
2
1
1
1
1
1
1
1
1
1
1
1
1
1
2
1
1
1
1
2
1
1
1
1
1
2
1
1
1
1
2
1
2
1
1
1
1
1
1
1
1
1
1
1
1
1
2
1
1
2
2
1
2
1
1
1
1
1
1
1
2
2
1
1
2
2
1
2
2
2
3
1
2
3
1
1
1
1
1
1
1
1
2
2
1
1
2
1
1
1
2
1
2
1
1
3
1
2
1
3
1
1
1
1
1
1
2
1
1
1
1
2
2
1
2
2
1
1
2
1
1
2
1
1
2
2
3
1
1
1
1
1
1
1
2
1
1
1
1
1
1
1
1
1
1
1
1
2
2
3
1
1
1
2
3
1
1
1
2
1
2
1
1
2
2
1
1
1
1
2
1
1
1
1
1
1
1
2
1
2
2
1
1
3
2
3
1
1
1
1
1
1
1
1
1
1
2
2
1
1
1
1
1
2
1
1
1
1
1
2
1
2
1
3
1
2
2
1
1
3
1
1
2
1
1
1
2
1
1
2
1
2
2
1
1
2
2
1
1
2
1
1
1
1
1
1
2
2
2
2
1
1
1
1
1
1
3
1
1
2
2
2
1
1
1
1
2
1
1
2
1
1
1
1
1
1
2
2
1
1
1
1
1
1
1
1
1
2
1
1
3
1
1
3
1
1
1
1
1
1
1
2
2
1
2
1
1
1
2
2
1
1
1
1
2
1
2
1
1
1
1
1
1
1
2
1
1
1
2
2
2
1
2
2
1
1
2
2
2
1
1
1
3
1
1
2
1
2
1
1
1
1
2
2
1
1
2
2
2
1
2
1
2
2
1
1
2
1
1
1
1
2
1
2
1
1
2
1
1
1
2
1
1
1
2
2
1
2
2
2
1
1
2
2
2
2
1
1
1
1
1
3
1
1
1
2
3
1
1
1
2
2
1
1
1
1
1
3
1
1
2
2
1
2
2
2
1
1
1
2
2
2
2
2
2
1
2
2
1
2
1
2
2
1
1
1
3
1
1
1
1
2
1
1
1
1
1
1
1
1
2
1
1
1
1
1
1
1
1
1
3
1
2
2
2
2
1
1
1
2
2
2
1
1
1
1
1
1
1
1
2
2
2
1
2
2
2
2
2
1
2
1
1
3
1
2
1
2
1
2
1
1
2
1
1
1
1
2
1
2
2
1
1
1
1
1
1
1
2
1
1
2
1
1
1
2
1
1
1
1
2
2
1
1
1
1
1
1
1
1
1
1
1
1
1
2
1
2
1
3
1
1
1
1
2
1
1
1
1
1
1
2
2
1
1
1
1
2
1
1
1
1
1
1
1
2
1
1
1
1
2
1
1
1
1
1
1
1
1
1
1
3
2
1
2
1
2
1
1
1
1
1
1
1
1
1
1
1
2
1
1
1
1
2
3
2
1
1
1
2
1
2
1
1
1
2
1
2
1
1
1
1
1
1
2
1
1
1
1
2
1
1
1
1
1
1
2
1
1
1
1
3
1
1
2
1
2
1
2
3
1
1
1
1
1
1
2
1
2
2
2
1
2
1
1
2
2
1
2
1
1
1
1
2
2
1
2
2
3
1
1
1
2
2
2
1
1
2
2
2
1
2
2
1
1
1
2
1
1
1
1
1
2
3
1
1
3
1
2
2
2
1
3
1
1
1
2
1
1
3
1
1
2
1
1
1
2
1
1
2
1
1
1
1
3
1
1
1
1
1
1
1
1
2
1
2
1
2
1
1
2
1
1
1
2
1
2
1
1
1
2
2
2
1
1
1
2
2
2
1
1
1
2
1
1
1
1
1
1
2
2
3
1
1
1
1
2
2
2
1
1
2
2
1
2
2
1
1
1
2
1
1
1
1
1
1
1
1
3
1
2
1
1
3
1
1
1
3
1
1
1
1
2
2
1
1
2
1
1
1
1
1
1
1
1
1
3
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
2
1
2
1
1
1
2
1
1
1
1
1
2
1
2
1
1
1
1
1
1
2
1
1
1
1
1
1
2
1
1
1
2
1
2
1
2
1
2
3
2
2
2
3
1
2
2
1
1
2
1
1
1
1
1
2
1
1
3
1
2
1
1
1
1
1
1
2
1
1
1
1
1
1
2
3
3
3
1
1
1
2
1
2
1
1
1
2
3
1
1
1
2
1
3
1
1
1
3
1
1
1
1
1
2
2
1
1
2
3
3
3
1
1
1
2
3
1
2
3
1
1
1
2
1
1
1
2
1
1
1
1
1
1
2
2
1
3
1
1
1
2
2
1
1
1
1
1
1
1
1
2
1
1
1
1
2
1
1
2
1
1
1
2
1
2
1
1
1
1
1
1
1
2
1
1
1
1
2
2
2
1
1
1
1
1
1
1
1
1
1
2
1
2
1
1
1
1
1
1
2
1
2
1
1
1
2
1
2
2
1
1
2
3
1
2
2
2
2
1
1
2
2
2
1
2
3
1
2
1
2
2
1
2
2
1
2
2
2
1
1
2
1
3
2
1
1
2
1
1
1
1
1
1
2
1
1
1
1
1
1
1
1
1
1
2
1
1
3
1
1
1
1
2
1
1
1
1
2
1
1
1
2
2
2
1
1
1
1
1
1
3
1
1
1
2
1
1
1
1
1
2
1
1
1
1
1
1
2
1
1
2
1
1
2
2
2
2
1
3
1
1
1
1
1
2
2
2
1
1
2
1
2
2
1
1
2
1
1
1
1
2
1
2
1
1
1
2
1
2
1
1
2
2
2
1
2
1
3
2
1
1
2
1
1
2
1
1
2
2
2
1
3
1
1
1
1
2
2
2
1
1
2
2
1
1
1
2
2
1
2
1
1
1
1
2
2
1
2
1
1
1
2
1
1
1
2
1
1
3
1
1
1
2
1
1
1
1
1
2
1
2
1
1
1
1
1
2
2
1
1
1
1
1
1
1
1
1
2
1
2
1
1
1
1
1
1
1
2
1
1
1
2
1
1
2
2
1
1
1
2
1
3
1
1
2
1
3
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
2
2
1
2
1
1
1
2
1
1
1
1
1
1
2
1
1
1
1
1
1
1
2
1
2
3
1
1
1
2
1
2
1
1
2
1
1
1
1
1
1
2
2
1
1
1
1
1
2
1
2
1
1
1
1
1
1
3
3
2
1
1
1
1
1
2
2
1
2
1
1
2
3
1
1
1
1
1
1
1
3
2
1
1
2
1
2
2
1
1
2
2
2
2
2
1
1
1
1
2
2
1
1
3
2
1
1
2
1
1
1
1
1
1
2
1
1
2
1
1
2
1
1
1
1
1
1
1
1
2
1
1
2
1
1
2
1
1
1
1
2
1
1
1
1
1
1
2
1
1
1
2
1
1
3
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
2
2
1
2
1
1
1
2
2
1
3
1
3
1
2
1
2
1
1
1
1
1
2
1
1
2
2
2
1
1
2
1
1
2
3
2
2
1
2
1
2
2
1
1
2
1
1
1
1
2
2
2
1
1
1
1
1
1
1
2
1
2
2
1
1
1
1
1
2
1
1
2
2
1
2
2
1
1
3
1
1
1
2
3
1
2
1
2
1
1
1
1
3
1
1
1
1
1
2
1
2
3
2
1
1
1
1
1
1
2
1
1
1
1
1
1
1
1
1
1
1
1
1
1
2
1
1
3
3
2
2
1
1
1
1
1
1
1
1
1
2
2
1
1
1
1
1
1
1
2
1
2
1
1
2
1
2
1
3
1
1
2
2
1
1
1
1
1
2
2
1
1
2
2
2
1
2
1
1
1
2
1
1
3
2
1
1
1
1
1
1
1
1
1
1
1
3
2
1
1
1
2
1
2
2
1
2
2
1
1
1
1
2
2
1
1
1
2
1
2
1
1
2
1
1
2
2
1
1
1
1
1
1
2
3
1
2
1
1
2
1
2
2
1
1
2
1
1
1
1
2
2
2
1
1
2
2
1
1
1
1
1
2
1
1
2
1
1
1
2
1
2
1
2
2
2
1
1
1
1
1
2
1
1
2
2
2
1
1
2
1
1
1
1
1
1
2
1
3
2
1
1
2
1
1
1
1
1
1
1
2
1
1
1
1
2
1
1
1
1
1
2
1
2
3
1
1
2
1
1
3
1
1
1
1
1
2
1
1
2
2
1
1
1
1
2
1
1
1
2
1
3
2
1
3
2
1
2
1
1
1
1
1
2
1
1
1
1
1
2
1
2
1
1
1
1
2
3
2
1
1
1
2
3
2
1
1
1
1
2
3
2
1
1
1
1
1
1
1
1
1
1
1
1
2
1
1
1
2
1
1
3
1
3
1
3
1
2
1
2
1
2
1
2
3
3
1
2
3
1
3
2
1
1
1
1
2
1
1
1
1
1
1
1
1
1
1
1
1
1
1
2
2
1
2
2
1
1
1
2
1
2
1
1
1
1
1
2
1
2
2
1
1
1
1
1
1
1
1
3
1
1
1
1
1
1
1
1
1
1
1
1
1
1
3
1
2
1
1
1
1
2
2
1
1
1
2
1
1
2
1
2
1
1
2
2
2
1
1
1
1
2
1
1
1
1
2
1
1
1
1
2
2
2
1
2
1
1
1
1
2
2
2
2
1
2
1
2
1
1
2
1
2
1
1
1
1
1
1
1
1
1
1
1
1
1
1
2
1
1
1
1
1
1
1
1
1
1
1
1
2
1
2
1
1
2
1
1
1
2
1
1
1
1
2
1
1
1
1
2
1
1
2
1
2
1
1
1
1
1
1
2
1
2
1
1
1
1
2
1
1
1
1
1
1
1
2
1
1
1
1
2
1
1
3
1
1
2
1
1
3
2
1
2
1
1
1
2
1
1
1
2
1
1
2
1
2
2
1
1
1
2
1
2
2
2
1
1
1
1
1
1
1
1
1
1
2
2
1
1
1
2
2
1
1
1
1
1
1
1
1
2
3
1
1
3
1
1
1
2
1
3
1
2
2
1
1
1
2
      68.1%
      27.7%
       4.1%
     100.0%




14 13 12 11 10 9   8   7   6   5   4   3   2 +/-1 -2 -3 -4 -5 -6 -7 -8 -9 -10<-10


         Fold change in mRNA
6 5 4 3 2 +/-1 -2 -3 -4 -5 -6 -7 -8 -9 -10

     Absolute fold-change
Reg. HighReg. LowReg. Avg    gene
 -10,000           -10,000
  -6,000            -6,000
   -1900       -4     -952
    -150              -150
      -65              -65
    -100       -6      -53
      -50              -50
      -39              -39
      -25              -25
      -20              -20
      -17              -17
      -16              -16   Pol
      -16              -16   SSG1
      -17     -14      -16   TS
      -15              -15
      -20     -10      -15
      -14              -14
      -10              -10   ATM
      -10              -10   coat
      -10              -10   mitochondrial
      -10              -10   NA-specific
      -10              -10   RB
      -10              -10   T24 transforming protein
      -10              -10   TIMP
      -10              -10   topoisomerase IIalpha
      -10              -10   VEGF121
      -10              -10   VirF
      -10              -10
      -10              -10
      -15      -5      -10
       -8               -8   FliC
       -8               -8   involucrin
       -8               -8
       -7               -7   AR
       -7               -7   c-Myc
       -6               -6   Int
       -6               -6   p53
       -6               -6
     -5.3               -6
       -5               -5   Bcl-XL
       -5               -5   COX-2
       -5               -5   CSF
       -5               -5   OGFr
       -5               -5   SMA
       -5               -5   topoisomerase IIalpha
       -5               -5
       -5               -5
       -5               -5
       -5               -5
      -30      20       -5
       -4               -4   20K
  -4          -4   bcl-X(L)
-3.3          -4   Cx43
  -4          -4   GFAP
  -4          -4   hMSH2
-3.8          -4   NaPi-2
  -4          -4   protein C
  -6   -1.5   -4   uidA
  -5     -3   -4   viral
  -4          -4
  -4          -4
  -4          -4
-2.4          -3   ADH
  -3          -3   AOX
-2.8          -3   BBM NaSi-1
 -10     5    -3   Chc
  -3          -3   cytochrome P4A1
  -3          -3   D1
  -3    -2    -3   gamma-zein
  -4    -2    -3   IL-6
  -3          -3   MMP-9
-2.5          -3   P45017 alpha
  -4    -2    -3   protein C
  -3          -3   PTPase
 -10     5    -3   RecA
  -3          -3   ribosomal protein L24
  -3          -3   Syk
  -3          -3   tau
  -3          -3
  -3          -3
  -3    -2    -3
  -2          -2   beta 2AR
  -2          -2   F
-1.4          -2   FMO1
  -2          -2   G-6-Pase
  -2          -2   heat shock protein
  -2          -2   mitochondrial
  -2          -2   OP-1
  -2          -2
  -2          -2
  -2          -2
  -2          -2
  -2          -2
  -2          -2
  -2          -2
-1.5          -2
-1.5          -2
  -3   1.5    -1
 1.8           1   39-kDa alpha
 1.8           1   56 kDa
 1.9           1   56-kDa
 1.5           1   BBM Na-Pi
 1.4           1   cAMP-dependent protein kinase II
 1.5         1   cotransport
 1.9         1   CYP2E1
 1.6         1   dehydrogenase 1 immunoreactive
 1.5         1   DENTT
 1.7         1   double-stranded RNA-dependent protein kinase
 1.9         1   endothelial NOS
 1.6         1   eNOS
 1.6         1   eNOS
 1.7         1   eNOS
 1.5         1   FN
 1.4         1   G(i)
 1.6         1   GAPDH
 1.6         1   GFAP
 1.6         1   glucose transporter
 1.5         1   GLUT1
 1.4         1   GLUT4
 1.4         1   Glut4
 1.7         1   Glut4
 1.6         1   GLUT-4
   2   1.5   1   gp63
 1.3         1   GRK5
 1.8         1   hsp70
 1.4         1   IGFBP-3
 1.8         1   IGFBP-3
1.93         1   KGF
 1.3   1.2   1   LDL-receptor
 1.9         1   LR11
1.62         1   mitochondrial
 1.4         1   MT-III
 1.8         1   NaPi-2
1.35         1   p53
 1.5         1   p53
 1.8         1   PDGF beta receptor
 1.2         1   PGP
 1.6         1   PKA
 1.6         1   Ras
 1.7         1   renal ET-1
 1.5         1   UCP3
 1.4         1   VAMP-2
   2   1.5   1   VDR
 1.8         1   VEGF
 1.7         1   VEGF
 1.7         1   VEGF
 1.4         1
 1.4         1
 1.7         1
 1.5         1
 1.5         1
 1.5         1
 1.5         1
 1.6         1
 1.6         1
 1.6         1
 1.6         1
 1.8         1
 1.8         1
 1.8         1
 1.8         1
 1.9         1
   2   1.7   1
   2         2   12/15-LO
   2         2   12/15-LO
   2         2   13.2 kDa SCP-2
 2.5         2   26 kDa
 2.7         2   26 kDa
   3    2    2   36-kDa
   3    2    2   36-kDa
   2         2   56-kDa
   2         2   56-kDa
   2         2   85-kDa PLA2
   3    2    2   ACLP
 2.4         2   actin
   2         2   alpha 1-subunit
   2         2   alpha 1-subunit
 2.4         2   alpha 1-subunit
2.23         2   alpha1a-AR
   2         2   alpha1C subunit
 2.2         2   alpha2
 2.9   1.5   2   alpha3
 2.6         2   alpha-tubulin
 2.5         2   ANT
 2.2         2   AR
   2         2   Bak
   2         2   Bax
 2.5         2   BBM Npt2c
   2         2   BCKD kinase
   3    2    2   Bcl-2
2.61         2   Bcl-x(L)
   2         2   BDNF
 2.8         2   beta-adrenergic receptor kinase-1
   2         2   beta-catenin
   2         2   BGP
 2.5         2   BSC-BLA fusion
   2         2   BvgA
   2         2   C protein
 2.7         2   Ca(v)1.2
   2         2   calmodulin-to-tubulin
   3    2    2   calpain
 2.5         2   cAMP-dependent
   2         2   Cap G
   2         2   Cardiac calsequestrin
   2         2   cardiac phospholamban
 2.2         2   Cat L
   2         2   catalase
2.5         2   CDC48
  3    2    2   Cdc5
  2         2   c-fos
  2         2   CFTR
  2         2   ChAT
  2         2   c-jun
2.5         2   cMoat
2.8         2   cNOS
2.3         2   Collaged
  2         2   collagen
  3    2    2   collagen
2.4         2   COX-1
  2         2   Cox-2
  2         2   CT-1
  2         2   Cx43
  3    2    2   cyclic AMP-dependent
2.6         2   cyclin A
  2         2   CYP2E1
  2         2   CYP2E1
2.2         2   CYP2E1
  3    2    2   cyp3A
  3    2    2   CYP3A4
  2         2   CYP4A
  2         2   DGAT1
  2         2   DGAT1
2.5         2   dihydrofolate reductase
  2         2   DOR
  2         2   EGFR
2.5         2   endogenous
  3    2    2   eNOS
  2         2   eNOS
2.1         2   eNOS
2.5         2   eNOS
  2         2   EP4
  2         2   ferritin heavy chain
2.5         2   fibronectin
2.5         2   FOS
  2         2   G
  2         2   G protein
  2         2   GFAP
  2         2   GLCLC
  2         2   GLUT1
  2         2   Glut4
  2         2   GLUT4
  2         2   GLUT4
  2         2   GLUT4
  2         2   Glut4
3.5    2    2   GLUT5
2.5         2   Gplb alpha
3.3   2.5   2   Grb2
  2         2   GRK6
  2         2   Grp75
  2         2   GS
  3     2   2   GSTP1
2.3   1.8   2   H
  2         2   HDL receptor SR-BI
2.4         2   hemeoxygenase-1
3.7   2.1   2   HIF-1alpha
2.2         2   HLA-DR
  2         2   HNF3beta
2.1         2   HO-1
  3    2    2   HO-1
  2         2   HSL
  2         2   HSL
2.7         2   Hsp25
  2         2   hsp70c
2.5         2   HSP72
  2         2   HSP90
  2         2   hTERT
2.1         2   Id2
  2         2   IGFBP-1
  2         2   IGFIIR
  2         2   IL-6
  2         2   iNOS
  2         2   insulin receptor
  2         2   insulin receptor substrate-1
  2         2   iron regulatory protein
  2         2   IRS2
2.6         2   IRS-2
  2         2   JAK2
2.4    2    2   KAP
  2         2   KFR1
  2         2   LDL-receptor
  2         2   LPL
2.5         2   LTP
  2         2   matrix gamma-carboxyglutamic acid
  3    2    2   MBP
  2         2   Mcl-1
  2         2   MCP-1
  2         2   MCP-1
2.2         2   MCP-1
  2         2   mEH
2.2         2   mitochondrial
3.9   1.7   2   mitogen-activated
  2         2   MnSOD
2.4   3.5   2   MnSOD
  2         2   MnSOD
  2         2   mPGES1
  3    2    2   MR
2.9         2   MT
2.5         2   MT1-MMP
2.4         2   MTP1
  2         2   Munc18c
  2         2   myofibrillar
  2         2   Na+/Ca2+ exchanger (NCX1)
2.1         2   Na+-K+-ATPase
2.4         2   NAG-1
2.8         2   NaPi-2
  2         2   natural resistance macrophage-associated
2.2         2   NHE3
2.5         2   NHE3 immunoreactive
2.3         2   NIS
  2         2   nitrate reductase
  2         2   non-collagen
  2         2   NQO1
  2         2   P-450(11) beta
  2         2   P450IIE1
  2         2   P450-IIEI
2.3         2   p85
  2         2   PAI-1
  2         2   PCNA
  2         2   PDE5
  2         2   PDGF-A
  2         2   phospholamban
  2         2   phosphorylated erk mitogen-activated
2.2         2   pIgR
  2         2   PKC
  2         2   PMCA4
  2         2   PP1alpha
  2         2   proapoptotic
  2         2   protein kinase C
  2         2   PrP
  2         2   PTK
  2         2   recA
  2         2   RecA
2.5         2   renal calbindin
  2         2   retinoblastoma
  3    2    2   RGS4
2.1         2   RhoA
  2         2   ribosomal
2.5    2    2   S-100
  2         2   sGC
  3   1.8   2   SNAP-25
  3     2   2   SR-BI
  2         2   tau
  3   2.5   2   TGF-beta
  2         2   TGF-beta 1
2.3         2   TGF-beta 1
  2         2   TGF-beta 1
2.5         2   TGF-beta 1
2.7         2   TGF-beta 1
  2         2   TGF-beta RII
  2         2   TGF-beta RII
  2         2   TH
2.5         2   thymidylate synthase
2.4         2   Tie2
2.3         2   TM
  2         2   topo II alpha
  2         2   TRACP
  2         2   UCP2
  2         2   UCP2
  3    2    2   UCP3
  2         2   VEGF
2.7   2.4   2   VEGF
  2         2   XDH/XO
  3    2    2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
  2         2
   2         2
   2         2
   2         2
   2         2
   2         2
   2         2
   2         2
   2         2
   2         2
   2         2
   2         2
   2         2
   2         2
 2.1         2
 2.2         2
2.28         2
 2.3         2
 2.3         2
 2.3         2
 2.3         2
 2.4         2
 2.4         2
 2.5   1.5   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
   3     2   2
 2.5         2
 2.5         2
 2.5         2
 2.5         2
 2.5         2
 2.5         2
 2.5         2
 2.5         2
 2.5         2
 2.6         2
 2.6         2
 2.6         2
 2.7         2
 2.7         2
 2.8         2
 2.8         2
 2.8         2
 2.8         2
   3   2.5   2
   2         2
 3.6         3   5-LO-activating
   3         3   ACAT2
   3         3   alpha subunit
 5.5   1.3   3   alpha2-Laminin mRNA expression and
   3         3   AQP6
   3         3   B2KR
   3         3   B2KR
   4    2    3   BAEC cotransporter
   3         3   BAL
   3         3   Bcl-2
 3.5         3   Bcl-2
   3         3   cAMP-dependent protein kinase regulatory subunit
 3.8         3   c-fos
 3.3         3   c-Jun
   3         3   c-Myc
   3         3   collagen
   3         3   collagen
   3         3   COX-1
 4.3   2.2   3   COX-2
3.79         3   COX-2
 3.2         3   CRBP
   3         3   cyclin D1
   3         3   cyclin D1
   3         3   cyclooxygenase-2
   3         3   c-yes
   4    3    3   CYP2E1
   3         3   CYP3A4
   3         3   CYP3A4
   3         3   cytidylyltransferase
   3         3   EGFP
 3.5         3   eNOS
 3.9         3   eNOS
   3         3   EP1
   3         3   Ep-CAM
   3         3   EPO
   3         3   ERK1/2
   3         3   ET-1
 3.6         3   ET-1
   4    2    3   Fas
   3         3   FasL
   3         3   FKBP51
   3         3   G alpha i-3
   3         3   G-6-Pase
  3         3   GDNF
  4    2    3   GFAP/mg
3.7         3   glial filamentous acidic
  4    2    3   Glut4
3.5         3   GS
  3         3   HB-EGF
  3         3   HLp
  3         3   HO-1
  3         3   HO-1
3.1         3   HO-2
  3         3   Hsp70
  3         3   HSP72
  3         3   I/R-induced
  3         3   IL-6
  3         3   iNOS
  5   2.5   3   IP-10
3.2         3   IPF-1
  3         3   LBP
  3         3   LDL-receptor
  3         3   M1
  3         3   MAPK
  3         3   MAPK
  3         3   MCP-1
  3         3   mGlu5b
3.8         3   myocardial iNOS
  4    3    3   myofibrillar
  3         3   NCAM
  3         3   NCAM
  3         3   NHE3
3.1         3   NIS
  3         3   NOS2
  3         3   ODC
  3         3   ODC
  4    3    3   p27
3.1         3   p38 MAPK
3.8         3   p39 c-jun
  4    2    3   P-450 2E1
  3         3   P450coh
  2    5    3   p53
  3         3   PDK4
  3         3   PDX-1
  3         3   PEX1
  3         3   PGHS-1
  3         3   PGHS-2
3.3         3   PHAS-I
3.5         3   PI 3-kinase
  3         3   pim-1
  4   3.5   3   PKC delta
  3         3   PKCbetaII
  3         3   PrfA
  4    2    3   proline-rich
  3         3   proteoglycan
  3       3   Raf-1
  3       3   RAR beta
  3       3   recA
  3       3   renin
  3       3   RI alpha
  4   2   3   RI cAMP-binding
  3       3   RII beta
  3       3   SERCA
  4   2   3   SGP-2
  3       3   SR-A
3.7       3   StAR
  4   2   3   TGF-alpha
  4   2   3   TGF-beta 1
  3       3   TIMP-2
  4   3   3   TP/PD-ECGF
  4   2   3   TS
3.6       3   UCP2
3.8       3   UCP2
  3       3   UCP3
3.3       3   UCP3
  4   3   3   VCAM-1
3.5       3   VEE
  3       3   VEGF
  3       3   VPF
  4   2   3
  4   2   3
  5   2   3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3       3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
  3         3
3.1         3
3.2         3
3.4         3
  4     3   3
  4     3   3
  4     3   3
  4     3   3
  4     3   3
  5   2.5   3
3.5         3
3.7         3
  5    4    4 40s ribosomal
4.3         4   51-kDa
  4         4   67LR
  4         4   AhR
  4         4   alpha 1-subunit
  4         4   alpha6
  4         4   AQP5
  4         4   aromatase
  5    4    4   B(2)-receptor
  4         4   BAL
4.9         4   BBM NaPi-2
  4         4   BN51
  4         4   BRCA1
  4         4   calreticulin
  5    4    4   calreticulin
  4         4   calreticulun
  4         4   C-kinase
  4         4   collagenase
  5    4    4   cyclin D1
  4         4   ECP
4.5         4   ENA-78
  4         4   eNOS
  4         4   eNOS
  4         4   Epo
4.8         4   ERCC2
  4         4   EsMlp
4.5         4   fibroblast growth factor-2
  4         4   gas-mos
  5   4.5   4   Gi-2 alpha
  4     5   4   GLUT3
  4         4   heat shock protein
  4         4   HMGR
4.3         4   HSL
  5    4    4   ICAM-1
  4         4   IgG
  4         4   IL-1alpha
  5    3    4   KDR
  4         4   leucine binding
  4         4   LPL
  4         4   MBP
  4         4   mEH
  4         4   met
  4         4   Mi-CK
  4         4   MIF
4.5         4   mitochondria-associated Bax
4.5         4   MRP
  4         4   ODC
  4         4   P47
  5    3    4   p53
  4         4   p53
  4         4   PDH
  4         4   PDX-1
  4         4   P-gp
  4       4   photoreceptor
4.5       4   PP2A
  4       4   Rab5
  4       4   Rab7
  7   2   4   Rad51
  5   4   4   Ras
  5   3   4   rop
  4       4   Sgk1
4.4       4   TGF-alpha
  4       4   TGF-beta RI
  4       4   TRX-1
  4       4   UCP2
  4       4   UCP2
  4       4   utrophin
  4       4   VEGF
  4       4   VEGF
4.4       4   VEGF
  4       4   vimentin
  4       4   Vir90
  4       4   VLDL
  7   1   4
  6   2   4
  7   2   4
  6   3   4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4       4
  4         4
4.2         4
4.3         4
5.5         5   49-kD
5.2         5   99.8 kDa
  5         5   albumin
  5         5   albumin
  5         5   Bax
  5         5   Bcl-2
  5         5   Bcl-2
  5         5   beta1-subunit
  5         5   C/EBPalpha
  5         5   cAMP-dependent protein kinase
5.6         5   Cat B
  5         5   catalase
  5         5   CCTalpha
  5         5   Cdc2 kinase
  5         5   CDw150
  5         5   CETP
  5         5   c-myc
  5         5   COX-2
  5         5   COX-2
  5         5   creatine kinase
5.1         5   cyclin D1
5.1         5   cyclooxygenase-1
  5         5   CYP2B
  5         5   eNOS
  5         5   eotaxin
  5         5   FimE
  5         5   GFAP
  4    7    5   GLUT1
  6    5    5   GRO-1
  5         5   HO-1
  5         5   HsRAD51
  5         5   hTGF-alpha
  5         5   IAP
5.7         5   IL-6
  5         5   iNOS
  5         5   lipo I
  5         5   MARCKS
  5         5   Matrix metalloproteinase-8
  5         5   MnSOD
  5         5   non-cAMP-dependent
  5         5   p53
  6    4    5   PP-1G
  5         5   SAPK
  5         5   sIL-1 RA
  5         5   surfactant protein A
  5         5   topoIIalpha
  5         5   tPA
2.3   7.9   5
  5         5
  5       5
  5       5
  5       5
  5       5
  5       5
  5       5
  5       5
  5       5
  5       5
  5       5
  5       5
  5       5
  5       5
  5       5
  5       5
5.2       5
  6   5   5
  9   3   6   Ann-II
  6       6   B2
 10   3   6   BRCA1
  6       6   cdk inhibitor
6.5       6   c-Jun
  6       6   c-MYC
  6       6   COX-2
  6       6   EBNA-3
  6       6   Egr-1
  7   5   6   Ets-2
  6       6   globin
  6       6   HO-1
  6       6   HSP70
  6       6   IL-1 beta
  6       6   IL-6
  6       6   M-CSF
  7   5   6   osteoprotegerin
  6       6   P
  6       6   PD-ECGF
  6       6   PLTP
  6       6   PR
  6       6   procollagen
6.7       6   prostacyclin-synthase
  6       6   prothymosin alpha
  8   4   6   PSA
 10   2   6   SAP
  6       6   TNF
  8   4   6
  6       6
  6       6
  6       6
  6       6
  6       6
  6       6
  6       6
  6       6
  6       6
6.1       6
  7       7   bax
7.8       7   cyclin E
  7       7   GK
  7       7   H11 kinase
7.7       7   HSP70
7.7       7   IL-1 beta
  7       7   IL-6
7.5       7   KDR
 10   5   7   MAPK
  7       7   PAI-2
  7       7   PI-6
 10   5   7   Rb2/p130
 10   5   7   S6
  7       7   UCP1
 10   5   7
  7       7
  7       7
  7       7
  7       7
  8       8   72 kDa stress
  8       8   apo A-I
  8       8   beta GSase
  8       8   calmodulin-dependent
 10   7   8   catalase
  8       8   C-reactive
  8       8   EGF receptor
  8       8   GLUT5
8.2       8   Hsp70
  8       8   IGFBP-4
  8       8   PKCalpha
  8       8   Rb
 10   6   8   RI alpha
  8       8   SCP-2
  8       8   transferrin
8.1       8   UCP3
  8       8
  8       8
  8       8
  8       8
  8       8
  8       8
8.6       8
9.2       9   c-Jun
  9       9   Collagenase IV
  9       9   elastin
  9       9   HSP27
 15   4   9   p21(WAF1)
  9       9   PAI-1
 10   8   9   SERCA2b
   9          9   SP-D
   9          9   VEGF
  16   3.8    9
  12     7    9
   9          9
  10         10   ADAMTS-1
  10         10   alpha1AT
  10         10   CaBP9K
  10         10   cardiac AC(VI)
  10         10   CD40
  10         10   class 1 MHC
  10         10   C-reactive
  10         10   C-reactive
  10         10   Fas-associating death domain
  10         10   GFAP
  10         10   GFAP
  10         10   GST
10.7         10   hexokinase
  10         10   LAR
  10         10   LPL
  10         10   MAPK
  10         10   MAPK
  10         10   MCAF
  10         10   MCP-1
  10         10   MDR
  10         10   Mirk
  10         10   mitochondrial
10.2         10   NaPi-2
  12    8    10   OppA
  10         10   P450IIIA6
  10         10   p53
  10         10   PB2
  10         10   PKC alpha
  10         10   protein D
  10         10   protein kinase C
  10         10   RAD51
  10         10   Ran
  10         10   sigma(32)
  10         10   TGF-alpha
  10         10   TGF-beta 2
  10         10   TIMP-1
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
  10         10
10.9         10
  11         11   Bcl-xl
  11         11   p220
  11         11   SR-BI
  11         11
  11         11
  11         11
  12         12   fast-type Ca(2+)-ATPase
  12         12   NPTII
12.5         12   p53
  12         12   PKCtheta
  12         12   Raf-1
12.6         12   uPA receptor
  20    4    12
  15   10    12
  12         12
  12         12
12.2         12
  13         13   GK
  24    3    13   IL-8
  13         13   multidrug resistance-associated protein
13.5         13   ProCT
  21    8    14   c-jun
  14         14   c-Jun
   2    27   14   hsp27
  28   1.9   14
  15         15   androgen receptor
  15         15   beta-galactosidase
  15         15   CRABP-II
  20   10    15   cryIA(c)
  18   12    15   decorin
  20   10    15   HSP70
  20   10    15   MBP
  15         15   MT
  20   10    15
  16         16   30,000-Mr
  16         16   HEF1
  30    2    16   MnSOD
  20   12    16
  16         16
  16         16
17.6         17   Frd
  17        17   GLUT2
  17        17   PL
  18   16   17
  17        17
18.8        18   eNOS
  18        18   MTP1
  18        18   R2
  16   20   18
  18        18
19.8        19
  20        20   c-myb
  20        20   C-reactive
  20        20   CYP1A1/1A2
20.3        20   CYP3A4
  20        20   IGFBP-3
  20        20   IL-6
  20        20   thermal hysteresis
  20        20
  20        20
  20        20
  20        20
  20        20
  20        20
  21        21   beta-interferon
  23        23   GTPCH
23.7        23   MnSOD
  24        24
  25        25   CCT
  40   10   25   p185 erbB-2
  25        25   PGHS-2
  40   10   25
  37   14   25
  25        25
  25        25
  26        26
  27        27   p53
  28        28
  30        30   Cat-1
  30        30   CNTF
  30        30   Cox-2
  30        30   IGF binding protein
  30        30   P450 2B1/2-immunoreactive
  30        30
  34        34   translocase
  34        34   TS
  35        35   Cox-2
  49   22   35   MnSOD
  40   30   35
  36        36
  40        40   CYP3A4
12.3   70   41   HSP70
  46        46   CYP1A1
   50   45      47
   50           50   GM-CSF
   50           50
   50           50
   53           53
   54           54
 54.5           54
  100   10      55   cornifin-alpha/SPRR1
   55           55   iNOS
   56           56   TNF-alpha
   58           58
   75   60      67   IGFBP-3
   68           68   ENA-78
   70           70
  100   50      75
   80           80   cyclooxygenase 2
  150   30      90
  100          100   IL-6
  100          100
  100          100
  110          110
  127          127
  130          130   VPF
  160          160
  200          200
  300          300   ENA-78
  300          300   GCP-2
  300          300
  315          315
  400          400   ornithine decarboxylase
  500          500
  800          800
5000         5,000
9000         9,000   tnpA
sentence                                                                           PMID     Year   Pattern#
in a 10,000-fold reduction in the amount of protein in the purified                 6505639   1984     1
liver with 6,000-fold decrease in protein content and 840-fold increase in specific 8243125   1993     1
for S/D decreases the yield of expressed protein 4-1900-fold and the content        1396694   1992     3
showed a 150-fold reduction of protein when compared to crude viral                 2822746   1987     1
and a 65-fold decrease in translation efficiency. The latter was unaffected         2174744   1990     1
6- to 100-fold inhibition of translation compared to the same mRNA                 11243410   2000     1
and a 50-fold decrease of the protein content. Because more than                   14573891   2003     1
in a 39-fold reduction in the rate of translation relative to a                     8524291   1996     1
facing primarily away from the protein was reduced 25-fold                          2546586   1989     2
level of translation of recF-lacZ fusions is reduced 20-fold                        8021183   1994     2
indicated a 17-fold reduction in protein concentration when cells were grown       10048031   1999     1
an approximately 16-fold reduction in Pol protein levels, whereas the levels       10233929   1999     1
with SSG1 mRNA expression, SSG1 protein was decreased 16-fold                      11357054   2001     2
14- to 17-fold reduction in TS activity and protein levels (using                  11038143   2000     1
a phosphotyrosine-modified protein of 74 kilodaltons (kDa) decreased 15-fold        1705209   1990     2
10- to 20-fold decrease in translation from the transcribed This                    2038320   1991     1
with a 14-fold decrease in protein synthesis. In contrast, in confluent             7068770   1982     1
Intracellular levels of ATM protein were typically reduced 10-fold                 10373636   1999     2
stability a 10-fold reduction in coat protein was obtained. Destabilizations beyond 8013465   1994     1
percent of mitochondrial protein contamination in nuclei decreased 10-fold           184854   1976     2
an approximate 10-fold reduction of NA-specific mRNA and protein levels (Fodor10675411        2000     1
much as 10-fold decrease in total cellular RB protein occurs compared               1861863   1991     1
In contrast, the T24 transforming protein is reduced 10-fold                        6148703   1984     2
Concomitantly, a 10-fold reduction in TIMP protein and mRNA levels by               2174435   1990     1
In addition, topoisomerase IIalpha protein levels are decreased 10-fold             9371509   1997     2
tissue 24 h later. VEGF121 protein concentrations decreased 10-fold                11078823   2000     2
level of the virulence-associated protein VirF was reduced 10-fold                  9294434   1997     2
an approximate 10-fold decrease in protein and a significant loss of CEA             203387   1978     1
more than 10-fold reduction in protein production. For all three cytokines,         1551689   1992     1
5- to 15-fold decrease in the protein concentration at which the first             10692325   2000     1
and an eightfold decrease in FliC protein levels was observed by                   12775694   2003     1
Both involucrin mRNA and protein levels were decreased 8-fold                       1657375   1991     2
in a >8-fold reduction in the amount of protein but only                            9234695   1997     1
The content of penile AR protein decreased seven-fold                               9537291   1998     2
and a sevenfold decrease of basal c-Myc protein (P&#60; .05)                        8614006   1996     1
The six-fold decrease of Int protein concentration in the cell                      6265316   1980     1
because a sixfold decrease in p53 protein occurred within 3-24 h                   11108663   2000     1
A sixfold reduction of protein adsorption was obtained by adding                    7947476   1994     1
and 5.3 fold decrease in protein yield respectively, indicating that the PAP       10071866   1999     1
in a fivefold decrease in Bcl-XL protein levels, based on immunoblotting            9665822   1998     1
observed a 5-fold decrease in COX-2 protein in endotoxin-tolerant cells relative 10766854     2000     1
a marked 5-fold decrease in mean CSF protein in group A                             1856727   1991     1
The OGFr protein levels were reduced fivefold                                      12655527   2003     2
was a fivefold decrease in SMA protein content, SMA protein synthesis,             10595938   1999     1
                                                                                   11901227   2002
contained approximately 5-fold decrease in topoisomerase IIalpha protein level and approximately       1
and a 5-fold drop in extracellular protein compared to that obtained               11479027   2001     1
causing a 5-fold reduction in RNA and protein levels. Expression of neurofilament 9182797     1997     1
is a fivefold decrease in translation relative to wild-type-infected Transfection   1846205   1991     1
three- to fivefold decrease in the rate of translation of both                      1107598   1975     1
ARH-III to inhibit cell-free protein synthesis is decreased 20-30-fold              1692238   1990     2
treatment while 20K protein levels were only decreased 4-fold                       8600151   1996     2
in a fourfold downregulation of bcl-X(L) mRNA and protein levels followed                9141616 1997   1
detected a 3.3-fold decrease in Cx43 protein level in transgenic hypertensive            8222085 1993   1
                                                                                       12816277
a coincidental fourfold reduction in glial fibrillary acidic protein immunoreactivity at         2003   1
the cell cycle. Interestingly, hMSH2 protein expression decreased fourfold               8950986 1996   2
with a 3.8-fold decrease in NaPi-2 protein but no change in NaPi-2                       7977794 1994   1
two- to four-fold decrease in the quantity of protein C secreted,                        9112652 1996   1
1.5- to 6-fold reduction in uidA translation efficiency in all psbA                    12690442  2003   1
3 to 5-fold reduction of viral protein synthesis in wild-type VSV-infected               2984202 1985   1
in a 4-fold decrease in the affinity for protein In                                      8125945 1994   1
fraction of enzyme protein hydrolysates to be reduced fourfold                         11771330  2001   2
in a four-fold reduction in routine monitoring of protein nutrition in such               500984 1979   1
in a 2.4-fold drop in translation of ADH at the adult                                    1900921 1991   1
                                                                                       10751229
to a threefold reduction of mRNA and protein levels of acyl CoA oxidase (AOX) and cytochrome P4A12000   1
with a 2.8-fold decrease in BBM NaSi-1 protein abundance and a 2.2-fold                10362603  1999   1
the steady state protein levels of Chc decreased 5-10-fold                               8955161 1996   2
                                                                                       10751229
to a threefold reduction of mRNA and protein levels of acyl CoA oxidase (AOX) and cytochrome P4A12000   1
accumulation of the D1 protein and CP43 decreased three-fold                             8690097 1996   2
2- to 3-fold reduction in gamma-zein mRNA and protein synthesis and reduces 7892202              1995   1
with a 2-4-fold reduction of IL-6 receptor at protein and mRNA                         15087402  2004   1
At the protein level, MMP-9 is decreased 3-fold                                        11471571  2001   2
in a 2.5-fold decrease in P45017 alpha protein recovered with the microsomal             2005126 1991   1
caused a 2-4-fold decrease in the quantity of protein C secreted,                        7827066 1995   1
about a 3-fold decrease in the specific phosphotyrosine protein phosphatase (PTPase)     2169344 1990   1
Purified RecA protein from Escherichia coli inhibited 5-10-fold                          2668747 1989   2
from mutants lacking ribosomal protein L24 was decreased 3-fold                        11434779  2001   2
thymocyte subsets, expression of Syk protein is down-regulated threefold                 8176201 1994   2
was a threefold decrease in soluble tau protein in Alzheimer's disease                   8342603 1993   1
in a 3-fold decrease in urinary protein excretion. Glomerular filtration and electrolyte 9509560 1998   1
two- to threefold reduction in protein levels compared with wild-type                    9579828 1998   1
include a 2-3-fold decrease of total protein synthesis, 13 changes in the                3558495 1987   1
A 2-fold decrease in protein levels of the beta(2)-AR was                              14557486  2003   1
A similar two-fold decrease in F protein expression was noted after                      2277869 1990   1
that compared with controls, FMO1 protein was decreased 1.4-fold                       14744944  2004   2
and a 2-fold decrease in G-6-Pase protein compared with diabetic                       14617577  2004   1
presented a twofold decrease in heat shock protein mRNA, while no                        9881488 1998   1
label content in the mitochondrial protein was decreased 2-fold                          6626595 1983   2
and a twofold decrease in OP-1 protein content (p &#60; 0.007)                         12925612  2003   1
The protein content/1000 cells also dropped two-fold                                     7165791 1982   2
(i.e., a twofold decrease in total protein and total RNA content,                        1688860 1990   1
caused a 2-fold decrease of virus-specific protein synthesis in CEC infected             6127931 1982   1
an overall 2-fold decrease in protein synthesis in cells treated with ActD               6499763 1984   1
in a 2-fold decrease of protein coupling                                                 3360144 1988   1
in a twofold decrease of protein limiting adsorption on the lipid                        1138952 1975   1
macrophage chemoattractant protein (MCP)-1 in the cultures decreased twofold 12887346            2003   2
and a 1.5-fold decrease in the rate of protein synthesis, respectively,                   487327 1979   1
similar to controls. Concentration of protein was decreased 1.5-fold                     2200205 1990   2
rabbit reticulocyte lysate system. Protein synthesis was decreased 1.5-3-fold            6661426 1983   2
brain demonstrated that the 39-kDa alpha protein increased 1.8-fold                      3087984 1986   2
the abundance of the 56 kDa protein increased 1.8-fold                                 11463720  2001   2
rats, the abundance of the 56-kDa protein increased 1.9-fold                           11463720  2001   2
and a 1.5-fold increase in BBM Na-Pi protein abundance. Thus, dexamethasone-induced      7615789 1995   1
In contrast, cytosolic cAMP-dependent protein kinase II increased 1.4-fold               2821014 1987   2
but only 1.5-fold increase in expression of cotransport protein Sun,               8770003   1996       1
3 weeks) increased levels of hepatic CYP2E1 protein (1.9-fold that of untreated 8130774      1993       3
                                                                                   9101585
11 beta-hydroxysteroid dehydrogenase 1 immunoreactive protein was increased 1.6-fold         1997       2
than a 1.5-fold increase in DENTT protein occurred in GH3 or alphaT3-1            12112471   2002       1
and a 1.7-fold increase in the double-stranded RNA-dependent protein kinase 11248255         2001       1
revealed a 1.9-fold increase in endothelial NOS protein and a 37%                 12952847   2003       1
caused a 1.6-fold increase in eNOS protein levels (p &#60; 0.01                   11483869   2001       1
mRNA and protein for eNOS was significantly increased (1.6-fold                    8772540   1996       2
with a 1.7-fold increase in tissue eNOS protein level in mice                     11597990   2001       1
at both time points. FN protein also increased 1.5-fold                            9853252   1998       2
by RNAse protection. RESULTS: LPS induced G(i) protein 1.4-fold 72 h              11744024   2002       3
A 1.6-fold increase in GAPDH protein was detected in the uterine                   9408883   1997       1
or = 1.6-fold increase in glial fibrillary acidic protein (staining distribution   8780406   1996       1
1.6 +/- 0.2-fold increase in glucose transporter protein (GLUT4) in skeletal       8897005   1996       1
increased approximately 3-fold and LV GLUT-1 protein increased 1.5-fold            1415537   1992       2
and a 1.4-fold increase in skeletal muscle GLUT4 protein in SHRs                   9453263   1997       1
a 1.4 fold increase in Glut-4 protein content in DZ obese                         14976464   2004       1
by exercise training. GLUT-4 protein content was increased 1.7-fold                7506491   1993       2
with a 1.6-fold increase in vesicle GLUT-4 protein content. Glucose transport      8772493   1996       1
                                                                                   8033909
3-4-fold and 1.5-2-fold increase of gp63 protein in SF-resistant Leishmania donovani         1994       1
and a 1.3-fold increase in GRK5 protein levels. These changes were                11906480   2002       1
was a 1.8-fold increase in hsp70 protein induced by exposure of L.                 8644900   1996       1
was a 1.4-fold increase in IGF-binding protein 3. The subjects showed              7593445   1995       1
and a 1.8-fold increase in IGFBP-3 protein levels as compared to untreated        10199564   1999       1
showed a 1.93-fold increase in KGF protein in the androgen treated                 9783973   1998       1
low density lipoprotein (LDL) receptor protein was increased 1.2-1.3-fold          8774761   1996       2
Within 24 h, the LR11 protein rose 1.9-fold                                       10964672   2000       2
a 1.62 fold increase in mitochondrial protein synthesis in the young               7169093   1982       1
and a 1.4-fold elevation in cerebellum. Human MT-III protein was detected          7655346   1995       1
with a 1.8-fold increase in NaPi-2 protein but no change in NaPi-2                 7977794   1994       1
showed a 1.35-fold increase in p53 protein compared with that of SC-9             10631341   1999       1
showed a 1.5-fold increase in p53 protein level compared with that                10631341   1999       1
Expression of the PDGF beta receptor protein increased 1.8-fold                   10558917   1999       2
an approximately 1.2-fold elevation of PGP protein in these tissues in response 11640914     2001       1
by a 1.6-fold increase in protein kinase A (PKA) The                               9355746   1997       1
proteins, and aldosterone does increase both Ras protein 1.6-fold and Ras         10913010   2000       3
6 each group). Similarly, renal ET-1 protein increased 1.7-fold                   11078364   2000       2
and a 1.5-fold increase of UCP-3 protein compared with untreated                  10950831   2000       1
                                                                                   8772493
in a 1.4-fold increase in sarcolemmal vesicle-associated membrane protein (VAMP-2) content,1996         1
1.5- to 2-fold increase in VDR protein expression was observed in Western          9886836   1999       1
with a 1.8-fold increase in tissue VEGF protein level in IL-10(-/-)               10988235   2000       1
control astrocyte cultures and VEGF protein levels increased 1.7-fold              9174246   1997       2
approximately a 1.7-fold increase in VEGF protein expression, which was abolished  9073561   1997       1
                                                                                   2886640   1987
1.7-fold, calcium-calmodulin-dependent protein kinase (phosphorylase kinase) activity increased 1.4-fold2
per mg microsomal protein but was significantly increased 1.4-fold                 1567478   1992       2
an average 1.7-fold increase in protein from microvascular endothelium. Total mRNA10653602   2000       1
                                                                                   8508509
that both terpene diets increased GST affinity-purified protein 1.5-fold and the HPLC        1993       3
relative to total secreted protein levels, were increased 1.5-fold                 1325077   1992       2
induced a 1.5-fold increase in protein synthesis over 48 Prazosin                  8737063   1996       1
initial rate of protein kinase C was increased 1.5-fold                            2994997   1985       2
basal phosphorylation of Band 4.9 protein is increased 1.6-fold                    3169942   1988       2
to a 1.6-fold increase in the overall protein synthesis following 5                2469576   1989       1
approximately 1.6 fold increase in plasma protein C was accompanied by               3590078   1987   1
despite a 1.6-fold increase in secreted protein levels and a approximately           2558843   1989   1
by 168 hours. The total bladder protein increased 1.8-fold                         12031398    2002   2
&#60; .01) 1.8-fold increase in the protein expression of the ubiquitously         10381144    1999   1
and a 1.8-fold increase in protein within 6 h in each                              11373342    2001   1
Whereas protein kinase inhibitor levels were increased 1.8-fold                      2994997   1985   2
than the 1.9-fold increase in total protein (P less than 0.05);                      3971925   1985   1
1.7- and 2-fold increase in the total protein content, total soluble               15092103    1991   1
revealed a 2-fold elevation in 12/15LO protein compared with C57BLKS/J             12734208    2003   1
and a 2-fold increase in expression of 12/15-LO protein in                         14676201    2004   1
Surprisingly, the 13.2 kDa SCP-2 protein also increased 2-fold                     10191285    1999   2
cAMP, a 2.5-fold increase of the 26 kDa protein was noticed                          3032632   1987   1
of phosphorylation of the 26 kDa protein increased 2.7-fold                          3032632   1987   2
incorporation of [35S]methionine into the 36-kDa protein increased 2-3-fold          6190679   1983   2
Tyrosine phosphorylation of the 36-kDa protein is increased 2-3-fold                 3021742   1986   2
where the abundance of the 56-kDa protein increased 2-fold                         11463720    2001   2
the amount of a 56-kDa protein was increased 2-fold                                  8380054   1993   2
with a 2-fold increase in the 85-kDa PLA2 protein and activity                       7929310   1994   1
muscle cells, ACLP mRNA and protein were up-regulated 2-3-fold                       9624159   1998   2
to a 2.4-fold increase in net actin protein synthesis and a 3.3-fold                 9054856   1997   1
with a twofold increase in alpha 1-subunit protein accumulation and an               1330358   1992   1
with a twofold increase in the alpha 1-subunit protein Pretreatment                  8238401   1993   1
with a 2.4-fold increase in the alpha 1-subunit protein accumulation and a           8214095   1993   1
2.23 +/- 0.10-fold increase in the alpha(1A)-AR protein level (n =                 12784082    2003   1
                                                                                   10821427
an approximate 2-fold increase in alpha1C subunit protein in ventricular homogenates           2000   1
2.2 +/- 0.2-fold increase in alpha2 protein as compared to transplanted            11041452    2000   1
1.5- to 2.9-fold increase in the mRNA and protein levels of alpha3,                11742036    2001   1
                                                                                   10785506
vimentin, 1.7-fold (P&#60;0.05). Protein levels for alpha-tubulin increased 2.6-fold           2000   2
by a 2.5-fold increase in ANT protein (by Western blot), with no                     9362269   1997   1
and a 2.2-fold increase in AR protein levels after 96                              12692781    2003   1
whereas a 2-fold increase in Bak protein levels was An                             10411902    1999   1
associated with squamous differentiation. Bax protein was increased twofold        10193941    1999   2
elicited a 2.5-fold increase in BBM Npt2c protein abundance in Npt2+/+             12952859    2003   1
and a twofold increase in BCKD kinase protein levels. The response                 12217904    2002   1
demonstrated a 2-3-fold induction of Bcl-2 protein after 18-36 h of exposure         9582377   1998   1
at Ser 112. Downstream Bcl-x(L) protein was increased 2.61-fold                    11571784    2001   2
nerve injury, and BDNF protein was also increased twofold                            9592114   1998   2
                                                                                     9931136
a significant 2.8-fold increase in beta-adrenergic receptor kinase-1 protein levels, whereas   1999   1
an approximately two-fold increase in beta-catenin protein levels in the cortex 12460454       2002   1
A twofold increase of bone Gla protein (BGP) secretion was                           3001477   1986   1
the production of the BSC-BLA fusion protein increased 2.5-fold                      1368741   1991   2
with a two-fold increase in BvgA protein levels. Gene replacement experiments 11094274         2000   1
about a 2-fold increase in 32P-incorporation into C protein and the 15               1804635   1991   1
revealed a 2.7-fold increase of Ca(v)1.2 protein in transgenic myocytes, but       14741718    2004   1
is a 2-fold increase in the calmodulin-to-tubulin protein ratio relative to that     6262788   1981   1
On Western blot analysis, calpain protein was increased 2-3-fold                   12499268    2002   2
inhibitor of the cAMP-dependent protein kinase, and increased 2.5-fold               6245074   1980   2
A 2-fold increase of Cap G protein and a 5-fold                                    12754261    2003   1
                                                                                   12519072
suppressed until adulthood. Cardiac calsequestrin protein expression increased 2-fold          2003   2
indicated a 2-fold increase in the cardiac phospholamban protein levels compared9314829        1997   1
and a 2.2-fold increase in Cat L protein (P &#60;                                    9816204   1996   1
infection of 100, intracellular catalase protein was increased >2-fold             11071897    2001   2
for 25 days. CDC48 protein levels also increased 2.5-fold                         12914916        2003 2
a corresponding 2-3-fold increase in Cdc5 protein (105 kDa) levels at             11694351        2001 1
A two-fold induction of the protein levels of c-fos and c-jun                     14576975        2004 1
                                                                                     5-fold/cell) 1994
an approximately twofold increase in CFTR abundance/cell protein (approximately7524345 and intensified 1
Also, a 2-fold increase in ChAT protein as determined by western                    9795114       1998 1
A two-fold induction of the protein levels of c-fos and c-jun                     14576975        2004 1
and a 2.5-fold increase in cMoat protein content were observed in the             10377250        1999 1
2.8 +/- 0.3-fold elevation of cNOS protein levels in BAEC (n                        7544542       1995 1
and 1.8 time). Collaged protein synthesis was increased 2.3-fold                    9388374       1997 2
induced a twofold increase in collagen and total protein accumulation in fibroblast 2054930       1991 1
inducing a 2-3-fold increase in collagen and total protein production occurred      3493244       1987 1
revealed a 2.4-fold increase in Cox 1 protein and a slight                        12000807        2002 1
revealed a two-fold induction of Cox-2 protein by arsenite. This induction        11835400        2002 1
showed a twofold elevation of CT-1 protein in infected animals (P                   9657259       1998 1
cultured epithelial cells. The Cx43 protein content increased twofold             12701766        2003 2
produced a 2-3-fold increase in the cyclic AMP-dependent protein kinase             6651814       1983 1
micro M 5-FU, cyclin A protein level increased 2.6-fold                           14719102        2004 2
caused a 2-fold induction of CYP2E1 protein levels, which was inhibited           10215662        1999 1
A >/=2-fold increase in CYP2E1 protein levels was detected at                       9531527       1998 1
by a 2.2-fold increase in CYP2E1 protein and 2-fold increase in enzyme            11454726        2001 1
h) immediately after tumour excision increased cyp3A protein 2-3-fold over a 12 10834269          1999 3
2- to 3-fold increase in GSTP1 and CYP3A4 protein levels, 3                       15056853        2004 1
demonstrated a twofold increase in CYP4A protein levels and 20-HETE production    12388396        2003 1
a approximately 2-fold increase in DGAT1 protein caused by recombinant viral 12407108             2002 1
in approximately 2-fold increase in DGAT1 protein in mature adipocytes and little12407108         2002 1
than a 2.5-fold increase in the dihydrofolate reductase protein level in the        2967290       1988 1
or during mitosis. The DOR protein level increased twofold                        10931523        2000 2
                                                                                  1
greater than twofold increase in steady-state message and protein levels of EGFR0516208           1999 1
was a 2.5-fold increase in total endogenous protein phosphorylation at 2.0          1558536       1992 1
produced a 2-3-fold increase in eNOS mRNA and protein levels as                   10690351        1999 1
                                                                                  12595302
determined using radiotelemetry. Exercise training increased eNOS protein >2-fold in the aorta    2003 3
2.1 +/- 0.1-fold increase in eNOS protein content, but no change                  12663266        2003 1
caused a 2.5-fold increase in eNOS protein in BPAECs, inhibitable with an         10564099        1999 1
as a twofold increase in EP4 protein levels. Future studies will                  12888618        2003 1
demonstrated a twofold increase in ferritin heavy chain protein levels during     15010486        2004 1
was a 2.5-fold increase in fibronectin protein which by immunofluorescence appeared 1912395       1991 1
after whole-cell irradiation. FOS protein was transiently induced 2.5-fold        11025647        2000 2
in a 2-fold increase in DPDPE-stimulated G protein activation. The DPDPE            9547359       1998 1
and a 2-fold increase in both G protein (alpha(s)) and cyclooxygenase             10456856        1999 1
Glial fibrillary acidic protein RNA increased 2-fold                                1688656       1990 2
was a 2-fold induction in GLCLC: mRNA and protein in the gd                       10966520        2000 1
observed a 2-fold increase in GLUT-1 protein (P &#60; 0.01) in the                  1396328       1992 1
induces a 2-fold increase in Glut 4 protein content in the plasma                   8375502       1993 1
Furthermore, GLUT4 mRNA and protein increased twofold                             12827286        2003 2
in a twofold increase in GLUT4 protein and mRNA and a sixfold                       7869920       1995 1
After troglitazone treatment, GLUT4 protein expression was increased twofold 11756319             2002 2
with a twofold increase in GLUT-4 protein and mRNA in mixed                         1767839       1991 1
fructose exposure, GLUT5 mRNA and protein levels increased 2-3.5-fold               9606981       1998 2
Cell surface protein expression of GpIb alpha increased 2.5-fold                  10720423        1999 2
2.5- to 3.3-fold increase in Grb2 protein in infected livers (p                   10930041        2000 1
line HL-60, GRK6 protein levels and activity rose twofold                           8977246       1996 2
A 2-fold increase in the Grp75 protein content occurred over                        9202172       1997 1
and a twofold increase in GS protein level 8 h                                      9435573 1997     1
2- to 3-fold increase in GSTP1 and CYP3A4 protein levels, 3                        15056853 2004     1
than the original viruses. H protein expression increased 1.8-2.3-fold              2277869 1990     2
preceded a 2-fold induction of HDL receptor SR-BI protein To                       10579331 1999     1
                                                                                   11823716  with    3
17-beta-estradiol (460 ng/kg) increased levels of hemeoxygenase-1 protein 2.4-fold compared2002 ischemia
                                                                                   11356821
2.1- to 3.7-fold upregulation of HIF-1alpha protein expression in MLO-Y4 osteocyte-like     2001     1
2 d (HLA-DR). T4 increased IFN-gamma-induced HLA-DR protein 2.2-fold and HLA-DR     9670962 1998     3
progressively over 24 h. HNF3beta protein level increased twofold                  12124776 2002     2
exhibited a 2.1-fold increase in HO-1 protein level, which was associated          10409239 1999     1
in a 2-3-fold increase in HO-1 protein levels. Comet assay experiments             12489116 2002     1
HSL immunoreactive protein and HSL mRNA levels increased twofold                    8141275 1994     2
HSL activity to normal. HSL protein was increased twofold                           7476323 1995     2
microg/kg GA dose induced Hsp70 and Hsp25 protein 8.2-fold and 2.7-fold,           12064483 2002     3
showed a two-fold increase in hsp70c mRNA and protein These                         9515035 1998     1
Heat shock protein (HSP) 72 was increased 2.5-fold                                  9860887 1998     2
found approximately 2-fold increase in heat shock protein (HSP) 90, both           10454292 1999     1
provoked a 2-fold increase in hTERT mRNA and protein expression (P                 12843187 2003     1
loading in group 1. Id2 protein levels increased 2.1-fold                          12388448 2003     2
by a 2-fold increase in IGFBP-1 secretion. A protein synthesis inhibitor            1281991 1992     1
A twofold increase in IGFIIR protein expression was detected after                 10435587 1999     1
with a twofold increase in IL-6 protein release (P &#60;                           10362698 1999     1
was a twofold increase of iNOS protein in WT and eNOS(-/-)                         11435211 2001     1
induced a 2-fold increase of insulin receptor (IR) protein and aberrantly          11750072 2001     1
level of insulin receptor substrate-1 protein was increased 2-fold                 10747954 2000     2
a approximately 2-fold increase in iron regulatory protein activity. These indices 10571078 1999     1
revealed a 2-fold elevation in IRS2 protein levels in Tg(+) mice                   14978080 2004     1
1 day of exercise, IRS-2 protein expression increased 2.6-fold                     10618367 2000     2
by a 2-fold increase in JAK2 protein abundance. This was associated                10579313 1999     1
of PDH kinase activator protein (KAP) were increased 2-2.4-fold                     2539088 1989     2
and a 2-fold increase of KFR1 protein in the bloodstream form                       8126084 1994     1
in a twofold increase in LDL-receptor protein and of LDL binding                    2836199 1988     1
detected a 2-fold increase in LPL activity and protein level in brown               8864952 1996     1
Plasma lipid transfer protein (LTP) activity increased 2.5-fold                     2112388 1990     2
induced a 2-fold increase in matrix gamma-carboxyglutamic acid protein Warfarin,   11564701 2001     1
2- to 3-fold increase in myelin basic protein and proteolipid protein               2475873 1989     1
with a twofold upregulation of Mcl-1 protein levels in HL-60 and U937              11682609 2001     1
was a 2-fold increase in MCP-1 protein in the conditioned media                    12377739 2002     1
(IL-8) and monocyte chemotactic protein 1 (MCP-1) increased twofold                12535738 2003     2
the level of MCP-1 protein was also increased (2.2-fold                             9596963 1997     2
with a 2-fold increase in mEH protein detected. These results demonstrated          8043012 1994     1
A 2.2-fold increase in mitochondrial protein content was The                        8031314 1994     1
1.7- to 3.9-fold increase in basal mitogen-activated protein and S6 kinase          7593444 1995     1
treatment with 5-ASA. MnSOD protein levels were induced 2-fold                     11557525 2001     2
3.5-fold and 2.4-fold increase in MnSOD protein levels, respectively, that was      7958676 1994     1
The levels of Mn-SOD protein increased 2-fold                                       9671959 1998     2
in a twofold increase in mPGES1 mRNA, protein expression, and PGES                 12890577 2003     1
2- to 3-fold increase in MR protein that we have observed                          12399411 2002     1
with a 2.9-fold increase in MT protein levels (P&#60;0.02), and a 5.6-fold          9838151 1998     1
with a 2.5-fold increase in MT1-MMP protein in EC Ox-LDL                           10207013 1999     1
and a 2.4-fold increase in protein level of MTP1 were observed                     12376346 2002     1
vivo, a 2-fold increase in Munc18c protein was demonstrated in mice                12700337 2003     1
In response to fasting, myofibrillar protein degradation increased 2-fold           1417770 1992     2
a two fold increase in Na+/Ca2+ exchanger (NCX1) protein levels as                  9144401    1997     1
that the amount of Na+-K+-ATPase protein had increased 2.1-fold                     9950929    1999     2
In HCT-116 cells, NAG-1 protein expression was increased 2.4-fold                  11925476    2002     2
caused a 2.8-fold increase in NaPi-2 protein content, which was reduced             7733336    1995     1
                                                                                   12907459
hours, a 2-fold increase in natural resistance macrophage-associated protein 1 (Nramp1)        2003     1
NHE3 mRNA and NHE3 protein abundance were increased 2.2-fold                       10069999    1999     2
showed a 2.5-fold increase in NHE3 immunoreactive protein levels with MP            9435499    1997     1
a concentration-dependent manner, whereas NIS protein levels increased 2.3-fold    12865321    2003     2
and a twofold increase of nitrate reductase protein under conditions of nitrogen 2913954       1989     1
by a 2-fold increase in non-collagen protein production was noted when              2508503    1989     1
in a twofold increase in NQO1 protein levels and enzyme activity,                  11275421    2001     1
over a 2-fold increase in P-450(11) beta protein expression. The 12-lipoxygenase 1457080       1992     1
caused a 2-fold increase in hepatic P450IIE1 protein levels as determined           2116767    1990     1
caused a two-fold increase in microsomal P450-IIEI protein and a two-               2447892    1988     1
caused a 2.3-fold increase in immunoreactive p85 protein in these GLUT4-containing  8626583    1996     1
and 75%, respectively. Moreover, PAI-1 protein levels increased two-fold           14706215    2004     2
an over 2-fold increase in PCNA protein abundance (in proportion to total           9597779    1998     1
revealed a twofold increase in PDE5 protein in cytosolic extracts from             11260387    2001     1
an approximately 2-fold increase in PDGF-A protein in aortic and femoral           10362700    1999     1
revealed a twofold increase in the phospholamban protein levels in transgenic       8567978    1996     1
                                                                                   12925451
displayed a 2-fold increase in phosphorylated erk mitogen-activated protein kinase expression 2003      1
and a 2.2-fold increase in intracellular pIgR protein compared with water-loaded 9612336       1998     1
than a twofold increase in protein kinase C (PKC) In                                2715723    1989     1
in a 2-fold increase in total aortic PMCA4 protein expression and significant      12933703    2003     1
with pro-apoptotic cytosine arabinoside (araC), PP1alpha protein increased twofold 11593419    2001     2
relatively specific 2-fold up-regulation of the proapoptotic protein bak was        9815595    1997     1
of a two-fold increase in membrane (particulate) protein kinase C within            3046343    1988     1
showed a two-fold increase in PrP protein level 3 after heat                       12392052    2002     1
about a twofold increase in protein tyrosine kinase (PTK) activity in Day           1721842    1991     1
induced a two-fold increase in cellular recA protein content. In addition,          6814527    1982     1
The concentration of RecA protein increased twofold                                 8936329    1996     2
D-replete rats, renal calbindin protein and mRNA increased 2.5-fold                 2460748    1988     2
                                                                                   14592948
greater than twofold increase in retinoblastoma protein (Rb1). IGF-I elicited a time-dependent 2004     1
LV myocardium RGS4 mRNA and protein was upregulated 2-3-fold                       12176127    2002     2
analysis revealed that RhoA protein expression was induced 2.1-fold                14556075    2003     2
show that ribosomal protein mRNA levels are increased twofold                       8114723    1994     2
for 48 hr, the S-100 protein level increased 2-2.5-fold                             4038402    1985     2
more than twofold increase of sGC protein alpha(1)-subunit in rat lungs            10516227    1999     1
1.8- to 3-fold increase in SNAP-25 mRNA and protein as determined                  11277561    2001     1
2- to 3-fold increase in SR-BI mRNA and protein levels, in association             10508199    1999     1
promote a twofold increase in the tau protein levels in OLG,                       11460270    2001     1
                                                                                    9037198
revealed a 2.5-3-fold increase in cell-associated TGF-beta protein levels in adherent          1997     1
TGF beta 1 protein was increased twofold                                            7851468    1994     2
produced a 2.3-fold increase in TGF-beta 1 protein compared to pcDNA3               9334812    1997     1
cerulein (10 microg kg(-1) h(-1)). TGFbeta1 protein increased twofold              10576340    1999     2
                                                                                   12628581    2003     1
showed approximately 2.5-fold increase in cell-associated TGF-beta 1 protein expression in aniline-treated
by a 2.7-fold upregulation of TGF-beta1 protein expression in glomeruli of DSH 12771048        2003     1
to a twofold increase in glomerular TGF-beta RII protein expression, but           11012901    2000     1
an early twofold increase in TGF-beta RII protein expression and a fourfold        11012901    2000     1
21 DIV the concentration of TH protein increased 2-fold                             7820064    1994     2
TS, a 2.5-fold increase in total thymidylate synthase protein content, profound 11984070       2002     1
the left ventricular free wall. Tie2 protein increased 2.4-fold                    14966366    2004     2
a significant 2.3-fold increase in TM protein was observed in term                 9639321   1998   1
and a 2-fold increase in topo II alpha protein early in monocytic                 12467229   2001   1
normal, but median total TRACP protein was increased twofold                      11983200   2002   2
UCP2 mRNA and protein were increased twofold                                      11289045   2001   2
by a twofold increase in uncoupling protein (UCP)-2 levels in GK                  11872664   2002   1
despite a 2-3-fold increase in UCP3 mRNA and protein expression in skeletal 10995775         2000   1
induced a twofold increase in VEGF protein at the apical side                     12376368   2002   1
2.4- to 2.7-fold increase in endogenous VEGF protein level was measured,          12358602   2003   1
these values, respectively. XDH/XO protein expression was increased 2-fold         9655743   1998   2
revealed a approximately 90-kDa protein that was increased 2-3-fold                9030565   1997   2
in a two-fold increase in mRNA and protein expression. High glypican-1            15016071   2004   1
protein, while EC increased mRNA 3-fold and protein 2-fold over control            1539169   1992   3
than a 2-fold increase in both lipid and protein of                                3948172   1986   1
included a 2-fold increase in both total protein synthesis and lysosomal           3997816   1985   1
channel Cav1.2 by cAMP-dependent protein kinase is increased >2-fold              14665691   2003   2
with a 2-fold increase in cell protein content. The simultaneous increase         12856162   2003   1
was a 2-fold increase in core protein mRNAs while proteoglycan synthesis,          2307121   1990   1
with a twofold increase in dietary fat and protein caused a rapid                  9843740   1998   1
about a 2-fold rise in the enzyme protein concentration and a 4-fold               2055284   1991   1
While the enzyme protein concentration increased 2-fold                            6643479   1983   2
RNA (mRNA) expression and protein levels were increased twofold                   11419902   2001   2
about a twofold increase in granulosa cell protein synthesis as compared           8869597   1996   1
almost a two-fold increase in hepatic protein synthesis. The rate of 14C-leucine 2275024     1990   1
synthesis was unchanged, however, protein synthetic efficiency increased 2-fold 11588456     2001   2
protein responses in LC: protein levels are elevated twofold                      12653973   2003   2
By comparison, the intestinal protein was increased twofold                         884615   1977   2
hours after ischemia; 2) protein synthesis was increased 2-fold                    8558715   1996   2
more than twofold increase in Leydig cell protein synthesis compared with control 7836901    1994   1
an almost 2-fold increase in liver total protein within 66 hr,                     7452493   1980   1
basal rate of net protein loss was increased twofold                               3422801   1988   2
at 31.9 ng/100 micrograms protein and was increased 2-fold                         1693563   1990   2
hearts were negative. Overall protein ubiquitination was increased two-fold       12601813   2003   2
caused a 2-fold increase in pancreatic protein output and a >10-fold              10675361   2000   1
                                                                                   8039628
more than twofold increase in pancreatic protein secretion. Similar increases in plasma      1994   1
+/- 0.6 pg/mg protein in liver) were increased twofold                             3276964   1988   2
2-fold increase in protein/mg membrane protein with differentiation into           3466805   1986   1
Renal AT1 receptor protein expression was significantly elevated 2-fold           14610098   2003   2
A nearly two-fold increase in recombinant protein was detected in strains          8544862   1995   1
aspartate aminotransferase relative to total protein was increased 2-fold          3680262   1987   2
of net accumulation of right lung protein increased two-fold                       6500332   1984   2
only a twofold increase in expression. The protein fusion was expressed            8458856   1993   1
displayed a twofold increase in total protein mass released concomitant with the 3375439     1988   1
only a 2-fold increase in total protein synthesis, as judged by                    2822026   1987   1
other three metals. Total protein concentrations also increased twofold            3224301   1988   2
with the 2-fold increase in total cell protein content which included              3371543   1988   1
and rapid 2-fold increase in total cellular protein kinase C (PKC)                 8381656   1993   1
200 mg of testosterone enanthate. Protein synthesis increased twofold              9815007   1998   2
a concomitant 2-fold increase in the rate of protein synthesis and steady          2584230   1989   1
a nearly 2-fold increase in the protein concentration of the peroxisomal           9568359   1996   1
a rapid 2-fold increase in protein released following tobramycin A                 2515243   1989   1
A twofold increase in protein at constant levels of calcium                        3414594   1988   1
addition, a two-fold increase in protein level of PrP was found                   10757517   2000   1
an almost 2-fold increase in the rate of protein synthesis in the                10480312    1999   1
and a 2-fold increase in protein kinase activity, respectively. A kinetic         2166944    1990   1
and a twofold increase in protein levels vs. controls (P &#60;                   14675034    2004   1
                                                                                  3539321
approximately a 2-fold increase in protein sulfhydryl content compared to the SCC-25         1987   1
by a twofold increase in protein synthesis as well as the activation              3552785    1987   1
cyclic AMP-dependent protein kinase activities which also increased two-fold        200270   1977   2
                                                                                  3558182
high lymph-to-plasma protein concentration. Pulmonary arterial pressure increased twofold    1987   2
in a two-fold increase in protein synthesis at 6 and 12                           3645660    1986   1
in the twofold increase of protein content in the brain and its                     203887   1978   1
nearly a 2-fold increase in protein content at 24 h compared                      7929446    1994   1
only a 2-fold increase in protein expression. Thus, the fold-induction of CYP2E1 10215695    1999   1
Protein synthesis of CM-stimulated ARC increased twofold                         10362702    1999   2
to a 2-fold increase in protein synthesis per unit wet weight                     6840392    1983   1
stimulated a 2.1-fold increase in pancreatic protein and fluid The                1989876    1991   1
                                                                                  6665737
of phenytoin-treated mothers decreased 3-fold; protein synthesis increased 2.2-fold          1983   2
while the amount of the protein itself increased 2.28-fold                        9085267    1997   2
A 2.3-fold increase in protein kinase CK2 activity was measured                  12071839    2002   1
2.3 +/- 0.2-fold increase in total protein in AQP5 null mice                     11514581    2001   1
During hypertrophy, total protein synthesis was increased 2.3-fold               11952165    2002   2
and a 2.3-fold increase in their rate of protein All                              3559500    1987   1
and a 2.4-fold increase in protein relative to fed In                             2384600    1990   1
and a 2.4-fold increase in protein with insulin injection; and normal             2384600    1990   1
caused a 1.5-2.5-fold increase in the protein synthetic rate and a corresponding 3896785     1985   1
2- to 3-fold induction of a protein recognized by antibody against                7587963    1995   1
showing stem cell factor protein was significantly increased 2-3-fold            10365812    1999   2
2- to 3-fold increase in corresponding protein levels. The transcription rate     8187966    1994   1
activity of cytosolic protein kinase C was increased 2-3-fold                     2764885    1989   2
2- to 3-fold increase in nuclear protein content and cellular/nuclear volume      1659821    1991   1
2- to 3-fold increase in activity, on a protein basis, of FeSOD,                  8972606    1996   1
2- to 3-fold increase in particulate protein C kinase The                         3465431    1986   1
2- to 3-fold induction of this protein was produced in resistant                  6865929    1983   1
[3H]UTP into protein and RNA, respectively, was increased 2-3-fold                2461737    1988   2
2- and 3-fold increase in the rate of protein degradation, respectively,          2519713    1989   1
2- to 3-fold increase in protein carbonyls in serum samples taken                10569640    1999   1
2- to 3-fold increase in the protein after 24 and 48                              1317493    1992   1
2- to 3-fold increase in the protein content of the mitochondrial                 8018466    1994   1
2- to 3-fold increase in the protein levels within 24                             2475873    1989   1
2- to 3-fold increase in the rate of protein synthesis compared                   7691180    1993   1
a 2-3 fold increase in translation when compared to reporter expression           7979985    1994   1
results indicated that protein M1 levels were elevated 2-3-fold                   2827767    1987   2
to a 2-3-fold increase of the protein content in the                              4005317    1985   1
whereas a 2.5-fold increase in new protein synthesis was observed in normal       7510486    1994   1
maximal velocity (Vmax), normalized to protein concentration, increased 2.5-fold 6681601     1983   2
That the abundance of this protein increased 2.5-fold                             8742339    1996   2
about a 2.5-fold increase of the total protein urinary excretion during           1810261    1991   1
                                                                                  treated
demonstrated a 2.5-fold increase in total protein phosphorylation in macrophages 1847593     1991   1
(4 micrograms/kg), the protein leak index was elevated 2.5-fold                   3536835    1986   2
and a 2.5-fold increase in the amount of protein in the total                     9895282    1999   1
induced a 2.5-fold increase in protein content in SVs cultured for                1935767    1991   1
Protein synthesis after 2 days increased 2.5-fold                                12619864    2003   2
sodium pump activity per milligram membrane protein increased 2.6-fold            8928822    1996   2
the translation mixture. Total protein synthesis was increased 2.6-fold           2776768    1989   2
mRNA and protein expression in liver were increased 2.6-fold                       14684617    2004   2
of a 2.7-fold increase in protein with fasting. Fasted diabetics exhibited           2384600   1990   1
show a 2.7-fold increase in protein expression of the beta-secretase enzyme        12112088    2002   1
is a 2.8-fold increase in total protein and a 12.7-fold increase                     3755061   1986   1
&#60; 0.05) 2.8-fold increase in the amount of protein for 3                         8772608   1996   1
showed a 2.8-fold increase in the protein level and a 3.7-fold                     11420687    2001   1
with a 2.8-fold increase in protein of the isozyme hGST 5.8,                       10509662    1999   1
2.5- to 3-fold increase in total skeletal muscle protein synthesis, and this       11004243    2000   1
the amount of protein in interferon samples increased 11/2-2-fold                    6175106   1981   2
                                                                                   11865407
&#60;.05), and 5-LO-activating protein (FLAP)-positive cell counts increased 3.6-fold          2002   2
a significant 3-fold increase of ACAT2 protein mass in cynomolgus monkeys,         12080065    2002   1
exhibited a 3-fold increase in immunoreactive alpha subunit protein and a nearly 1713582       1991   1
alpha2-Laminin mRNA expression and protein increased 1.3-5.5-fold                  11038071    2000   2
had a threefold increase in both AQP6 protein and mRNA                             11097619    2000   1
A threefold increase in B2KR protein levels and a 40%                              11247764    2001   1
A threefold increase in B2KR protein levels was observed as                        14766673    2004   1
2- to 4-fold increase in BAEC cotransporter protein levels and a 1.5-              11121393    2001   1
mitigate the 3-fold increase in total BAL protein observed at 5                      8679228   1996   1
A 3-fold increase in full-length Bcl-2 protein conferred substantial resistance    12170773    2002   1
mediates a 3.5-fold increase in Bcl-2 protein expression, whereas the level        12095980    2002   1
I cAMP-dependent protein kinase regulatory subunit (RI) increased 3-fold             2445756   1987   2
brain (a 3.8-fold increase in c-fos protein level) and in spinal                     7717068   1994   1
5 wk post-AM treatment, c-Jun protein was increased 3.3-fold                       11597910    2001   2
showed a threefold increase in c-Myc protein in liver Hepatocytes                    7649406   1995   1
to a threefold increase in collagen and total protein synthesis per                  2556445   1989   1
a three fold increase in protein (collagen) synthesis by neointimal                  9614349   1998   1
caused a threefold increase in COX-1 protein expression and a threefold              9649571   1998   1
                                                                                   14654083
an approximately 2.2-4.3-fold increase in COX-2 protein expression relative to primary         2004   1
mRNA data, with COX-2 protein levels being upregulated 3.79-fold                   11571316    2001   2
Western analysis revealed that CRBP protein was elevated 3.2-fold                    7615982   1995   2
prevented the 3-fold increase in cyclin D1 protein expression induced by           12679459    2003   1
                                                                                   11470752
c-Jun protein (6.5-fold increase) and cyclin D1 protein (3-fold increase) in ethanol-fed       2001   3
iNOS and cyclooxygenase-2 protein expression increased threefold                   14757118    2004   2
two- to three-fold increase in the c-yes protein level over that                     3041345   1988   1
3- to 4-fold rise of the CYP2E1 protein in both liver                              11395987    2000   1
resulted in >/=3-fold induction of CYP3A4 mRNA and protein as assessed             12470639    2002   1
demonstrated a 3-fold increase in expression of CYP3A4 protein by 20               12920173    2003   1
                                                                                     8048539
Western blotting revealed that cytidylyltransferase protein content increased threefold        1994   2
two- to threefold increase in enhanced green fluorescent protein (EGFP) mean 12805432          2003   1
with a 3.5-fold increase in eNOS protein level in these aortas                     13129532    2003   1
indicated a 3.9-fold increase in eNOS protein in pulmonary artery tissue           11181626    2001   1
two- to three-fold increase in EP1 protein levels. IL-1 beta and IL-4                9352015   1997   1
two- to three-fold up-regulation of Ep-CAM protein expression. CONCLUSION: mAb 9C4 12063020    2002   1
approximately a 3-fold increase in plasma EPO protein concentration at 4           11115606    2001   1
Despite a >3-fold increase in the protein level for ERK1/2 in failing              12016632    2002   1
and a threefold increase in lung immunoreactive ET-1 protein We                      9575871   1998   1
renal ET-1 protein levels in whole kidneys increased 3.6-fold                      11078364    2000   2
Fas mRNA and protein levels are increased two-to-fourfold                          10208933    1999   2
and a threefold increase in FasL protein levels. In contrast, Fas                  11053034    2000   1
FKBP51 mRNA and protein levels were increased 3-fold                               12746298    2003   2
but not G alpha i-3 protein is increased 3-fold                                      8227026   1993   2
and a 3-fold increase in G-6-Pase protein levels, consistent with a diabetic       14617577    2004   1
that GDNF mRNA and protein levels were elevated threefold                           11573987 2001    2
The concentration of GFAP/mg protein was induced 2-4-fold                            3900430 1985    2
The glial filamentous acidic protein complex increased 3.7-fold                       572941 1979    2
Skeletal muscle Glut4 protein levels were increased 2-4-fold                         7829503 1995    2
to a 3.5-fold increase in GS protein levels in lung tissue                           9733611 1998    1
                                                                                    12671899
in pancreatic beta cells, effectively elevating HB-EGF protein 3-fold over endogenous        2003    3
and a 3-fold induction of immunoreactive HLp protein as compared to the              3460094 1986    1
in a 3-fold increase in HO-1 protein compared with that the parental                14563492 2003    1
by Western blot. RESULTS: HO-1 protein was increased 3-fold                         12947311 2003    2
revealed a 3.1-fold increase in HO-2 protein which seemed to result                 10686338 2000    1
In addition, inducible Hsp70 protein levels were increased threefold                 7638752 1995    2
two- to threefold increase in HSP72 protein accumulation, but not antioxidant       11454553 2001    1
on this I/R-induced protein clearance. NF-kappaB activity increased three-fold 14572782      2003    2
IL-1 beta and IL-6 protein levels rapidly increased (3-fold                          9316474 1997    2
iNOS and cyclooxygenase-2 protein expression increased threefold                    14757118 2004    2
2.5- to 5-fold increase in inducible protein 10 (IP-10) levels was                  11756154 2002    1
culture, a 3.2-fold increase in IPF-1 protein was observed, corresponding to the 11016451    2000    1
was HDL phospholipid. Lipopolysaccharide binding protein (LBP) rose 3-fold          12754273 2003    2
                                                                                     2346673 as compared
an approximately threefold increase in the [35S]methionine-incorporated LDL-receptor protein 1990    1
in parental cells. The M1 protein was increased 3-fold                               7882331 1995    2
two to three-fold increase in activated mitogen-activated protein kinase (MAPK) as  12700627 2003    1
induces a threefold increase in mitogen-activated protein kinase (MAPK) activity, an 9038931 1997    1
and a threefold increase in medium MCP-1 protein accumulation in human              11317664 2001    1
is a three-fold increase of mGlu5b protein relative to at post-natal                12031354 2002    1
demonstrated a 3.8-fold increase in myocardial iNOS protein expression 24 h 12667952         2003    1
a 3-4 fold increase in myofibrillar protein breakdown in EDL muscles,                9852215 1998    1
two- to threefold increase in NCAM protein and mRNA abundance in both                2380247 1990    1
two- to threefold increase in NCAM protein and mRNA. Exposure of early-passage       2380247 1990    1
and a threefold increase in NHE3 protein abundance. NHE1 mRNA and protein 7771509            1995    1
The amount of NIS protein was also increased 3.1-fold                                9329364 1997    2
was a three-fold increase in NOS2 protein abundance detected by Western             10471353 1999    1
showed a 3-fold increase in thesynthesis of ODC protein after 4                     10816435 2000    1
the half-life of the ODC protein was increased three-fold                            2262070 1990    2
and a 3-4-fold increase in p27 protein levels, which correlated with decreased 12727827      2003    1
an average 3.1-fold increase in p38 MAPK protein throughout the study               11473637 2001    1
The p39 c-jun protein was also increased 3.8-fold                                    1448115 1992    2
P-450 2E1 protein and RNA levels were increased 2-4-fold                             9101732 1997    2
approximately a 3-fold increase of the P450coh protein in the liver                  1868078 1991    1
A 2-fold increase in p53 mRNA and protein amounts was                                8895543 1996    1
with summer-active levels. Similarly, PDK4 protein is increased threefold           11842126 2002    2
a paradoxical 3-fold increase in PDX-1 protein levels. To dissect the effect        10385428 1999    1
two- to threefold increase in PEX1 protein levels was observed, associated          11389485 2001    1
                                                                                     8079657
a corresponding 3-fold increase in immunoreactive PGHS-1 protein in response to combined 1994        1
h after treatment. PGHS-2 protein levels were elevated threefold                     8989914 1996    2
acquired sensitivity to insulin. Insulin increased PHAS-I protein (3.3-fold after 2 7629182  1995    3
was a 3.5-fold increase in PI 3-kinase protein [85 kilodalton (kDa)                  7520127 1994    1
twofold to threefold increase in pim-1 message and protein expression, correlating   7540064 1995    1
Both PKC delta protein and mRNA expression increased 3.5-4-fold                     10854711 2000    2
Mature PKCbetaII mRNA and protein rapidly increased >3-fold                          9422749 1998    2
                                                                                    10564496
demonstrate a threefold increase in PrfA protein synthesis during infection of mammalian     1999    1
A 2-4-fold increase in proline-rich protein mRNAs was observed in rat                3805012 1987    1
Synthesis of proteoglycan and non-collagen protein (NCP) increased threefold         2045977 1991    2
with a 3-fold increase in Raf-1 protein kinase activity. However, phosphoamino 2197271       1990   1
showed a 3-fold increase in the RAR beta protein expression over                  10929206   2000   1
induces a 3-fold increase of recA protein content, in comparison to the            6816801   1982   1
caused a 3-fold increase in renin mRNA and protein over 36                        11116131   2000   1
We found that RI alpha protein is induced threefold                               11722580   2001   2
2- to 4-fold increase in the RI cAMP-binding protein coincident with the           2837219   1988   1
and a 3-fold induction of RII beta protein was observed during                     8793051   1996   1
A maximal threefold increase of total SERCA protein expression over the level 10600859       1999   1
culture, SGP-2 protein and mRNA levels were increased 2-4-fold                     7974249   1994   2
a concomitant 3-fold increase in SR-A protein levels and increased cell           10679110   2000   1
more than 3.7-fold increase in StAR protein expression by 48                       8977433   1997   1
a 2-4 fold increase in TGFalpha protein concentrations in media conditioned        9605408   1998   1
a small, 2-4-fold increase in TGF beta1 protein levels in human                    9019169   1995   1
                                                                                  10679106
a approximately 3-fold increase of TIMP-2 protein levels. LXA4 inhibitory responses          2000   1
                                                                                   9815767
an average 3-4-fold increase of TP/PD-ECGF protein levels after treatment with either        1997   1
2- to 4-fold induction of TS protein following 5-fluorouracil (5-FU) treatment     9698077   1998   1
a 3.6 fold increase in muscle UCP2 protein levels compared to control             11244460   2001   1
found to increase the synthesis of uncoupling protein 3.8-fold in 4-5              3986309   1985   3
two- to threefold increase in both mRNA and protein levels of UCP3                12721157   2003   1
3.3 +/- 0.2-fold increase in UCP-3 protein content (P &#60;                       12813156   2003   1
vascular cell adhesion molecule-1 mRNA and protein increased 3-4-fold             10521464   1999   2
to a 3.5-fold increase in VEE protein production. Sera from mice                   9918402   1998   1
mRNA remained unchanged. VEGF mRNA and protein increased 3-fold                   10468530   1999   2
a corresponding 3-fold increase in VPF protein level by 12 h                       9342371   1997   1
a rapid 2-4-fold increase in the rate of protein synthesis within                  8243475   1993   1
is a 2-4-fold increase in the rate of protein synthesis per                        8243475   1993   1
2- to 5-fold increase in incorporation of 3H-thymidine, protein content, and cell  6315022   1983   1
greater than threefold increase in the mRNA and protein levels of the              8971097   1997   1
almost a threefold increase in protein elution from the Both                       7983083   1994   1
and a 3-fold increase in protein levels. In addition, luciferase activity         11861392   2002   1
A set of 25 protein spots increased >3-fold                                       12492832   2002   2
to a threefold upregulation of a single protein with a molecular                  10446315   1999   1
protein synthesis almost doubled and protein breakdown increased threefold         9790821   1998   2
and a 3-fold increase in bladder protein content compared with sham                8945952   1996   1
and whole body (L-[1-13C]leucine) protein synthesis were elevated threefold       11350780   2001   2
more than threefold increase in cellular protein synthesis which was inhibited     9846161   1998   1
that a three-fold increase in chromatin-bound protein cause only mild phenotypic 8534374     1995   1
Binding of cytosolic protein was increased 3-fold                                  2059215   1991   2
in a 3-fold increase in expressed inclusion body protein and producing            13129388   2003   1
The fractional protein synthesis rate was increased 3-fold                         9640347   1998   2
demonstrated a threefold increase in gastrointestinal protein loss, alpha 1-AT was6307792    1983   1
treatment with 17 Beta-estradiol. Hepatic protein synthesis increased threefold 8812375      1996   2
0.014) but intestinal total protein flux was increased 3-fold                      6627614   1983   2
rate of disappearance of intravascular radiolabeled protein increased threefold    8339433   1993   2
a three fold increase in its protein level. Folic acid suppressed                  9528665   1998   1
by a three-fold increase in mandibular organ protein content. Methyl transferase 11223394    2001   1
of phospholipid to milligrams of membrane protein increased three-fold               99426   1978   2
two- to threefold increase in optical density and protein content in 3            14617645   2003   1
Overall protein synthesis rates only increased threefold                           9715279   1998   2
in a threefold increase in pancreatic protein output and an increase               3953805   1986   1
is a 3-fold increase in the specific translation of transferrin receptor           6142046   1984   1
thiobarbituric acid test) and total protein content increased 3-fold               1566277   1992   2
duration of ischemia. The protein leak index increased threefold                     2180590   1990   2
increase after 16 days. The protein content increased 3-fold                         3030269   1986   2
The apparent binding of this protein is increased threefold                         10966482   2000   2
and a 3-fold increase in the total protein per platelet compared                     1751531   1991   1
and a 3-fold increase in total protein were observed in cells                        6966967   1980   1
                                                                                    10069269
and a three-fold increase in total protein concentration (P&#60;0.01). These returned          1999   1
and a threefold increase in total protein synthesis in the presence                  9534243   1998   1
bypass surgery, total protein in lavages was increased 3-fold                       10424996   1999   2
                                                                                     6
two- to threefold increase in total protein synthesis when exposed to progesterone. 383900     1984   1
experiments, the transcription rate and protein levels increased three-fold         11943172   2002   2
greater than three-fold increase in urinary protein excretion and histologic evidence7853790   1994   1
caused a threefold increase in urine protein in collections from 6                  10073606   1999   1
a mean 3-fold increase in protein expression was observed over the corresponding    11857399   2002   1
a nearly three-fold rise in the protein leak index (54.1 +/-                         2793711   1989   1
A threefold increase in protein concentration, from 0.5 to 1.5                       8683586   1996   1
A three-fold increase of protein synthesis by human platelets during                  989635   1976   1
activity of glutaminase per milligram of protein increased threefold                 7379773   1980   2
also a 3-fold increase in the protein content of lung lavage                         8933859   1996   1
although total protein determined in these homogenates increased 3-fold               198442   1977   2
and a 3-fold increase in the protein level. Transfection with pSVL17as,              3036872   1987   1
and a threefold increase in protein kinase A activity. The increase                  7518467   1994   1
and a threefold increase in protein levels. However, other parameters such           3840800   1985   1
and a three-fold increase in protein synthesis compared to enriched samples          6181350   1982   1
cell line (PC3-N). Protein levels of alpha(6)p increased 3-fold                     11359780   2001   2
fraction, a 3-fold increase in the amount of protein was measured                   10428962   1999   1
in a 3-fold increase in protein synthesis as compared to either                      2109158   1990   1
induced a three-fold increase in protein content of the culture after               12008070   2002   1
morphology, a threefold increase in protein content, and a three- to fourfold        1564396   1992   1
only a three-fold increase in enzyme activity, protein levels were increased        10630706   1999   1
preceded a 3-fold increase in protein synthesis. Moreover, TNF induced cell-cycle1700789       1990   1
produced a 3-fold increase in protein kinase C activity, small but                   3245226   1988   1
revealed a threefold increase in turnover of protein during hibernation compared 825685        1976   1
The three-fold increase of protein content in MCh was not                            6167036   1981   1
to three fold increase in protein synthesis. Second, the injection of globin         3831219   1985   1
two- to threefold increase in protein cysteinyl-dopamine in the striatum 2,          9952424   1999   1
two- to three-fold increase in protein level. Further, GRP78 is a gelatin-binding    2223014   1990   1
two- to threefold increase in protein synthesis and a twofold increase               6093541   1984   1
two- to threefold increase in the protein content of nuclei isolated                 8655591   1996   1
two- to threefold increase in the protein levels of proinflammatory cytokines        8163935   1994   1
two- to threefold increase in the protein synthetic rate. Progesterone-treated cells 6692987   1984   1
3.1 +/- 0.4 fold increase in protein content over control No                         8862131   1996   1
activity of 48 nmol/min/mg protein that gradually increased 3.2-fold                 7264640   1981   2
showed a 3.4-fold increase in protein 24 hours after heat shock                      8933757   1996   1
with a core protein of 43 kDa) increased 3-4-fold                                    1555588   1992   2
3) a four-fold increase in membrane-bound, or active, protein kinase C              10342815   1999   1
that against P-450c. This protein band was induced 3-4-fold                          2815823   1989   2
and a 3-4-fold increase in protein levels compared with Aurora-2                    15078988   2004   1
and a 3-4-fold increase in the protein level of the catalytic                        8626617   1996   1
was a 2.5--5-fold elevation of protein L11 level in the supernatant                  7024735   1981   1
and a 3.5-fold increase in total protein release (P &#60;                            8689401   1996   1
mRNA and 3.7-fold increase in protein content while in hyperthyroid aged             9630690   1998   1
4- to 5-fold increase in 40s ribosomal protein S-6 phosphorylation, and a            3559500   1987   1
protein increased 1.4-fold, and the 51-kDa protein increased 4.3-fold              11463720   2001   2
in a 4-fold increase in 67LR protein expression. Estrogen also induced              8472397   1993   1
greater than fourfold elevation of AhR mRNA and protein levels, whereas             9706865   1998   1
with a fourfold increase in alpha 1 subunit protein Transfection                    8408640   1993   1
by a fourfold increase in alpha6 protein level 6 h                                  9375663   1997   1
causes a 4-fold increase in AQP5 mRNA and protein levels and induces               12783871   2003   1
an approximately fourfold increase in aromatase protein in the cells 24            10731111   1999   1
                                                                                   11533702
with a 4-5-fold increase in B(2)-receptor protein levels. Expression of the AT(1)-B(2)        2001   1
BAL ACE activity increased 9-fold, BAL protein increased 4-fold                     6093659   1984   2
and a 4.9-fold increase in BBM NaPi-2 protein abundances. In contrast,              7977794   1994   1
a comparable 4-fold increase in BN51 protein synthesis following serum stimulation  7947392   1994   1
induced a 4-fold increase of BRCA1 protein expression in MCF-7 and a               10329379   1999   1
caused a 4-fold increase in calreticulin protein levels over a period               9425124   1998   1
A 5-fold increase in the immunoreactive calreticulin protein band was               1527030   1992   1
induced a fourfold increase in calreticulun protein levels. Importantly, we show    9245785   1997   1
                                                                                    2465349
transfer induced fourfold increase of particulate-associated protein kinase C (C-kinase)      1989   1
                                                                                     190326
manifested a 4-fold increase in collagenase protein in normal-appearing skin, and patients    1977   1
A 4-5-fold increase in cyclin D1 protein abundance was followed                     8867812   1996   1
levels of eosinophil cationic protein (ECP) were increased 4-fold                   1849409   1991   2
more than 4.5-fold increase in ENA-78 RNA and protein synthesis without            12882792   2003   1
endothelial cells and eNOS protein levels were increased fourfold                  10954898   2000   2
demonstrated a 4-fold increase in eNOS protein content in lambs treated            10879803   2000   1
tg21, a fourfold increase of Epo protein level was found in brain                  11435798   2001   1
ERCC2 (XPD) antibody-reactive protein levels were elevated 4.8-fold                 8033104   1994   2
three- to fourfold increase in EsMlp protein in midwinter larvae (January-February)11812047   2001   1
hours and fibroblast growth factor-2 protein levels increased 4.5-fold             14504515   2003   2
three- to fourfold increase in gas-mos protein kinase specific activity relative    2138725   1990   1
                                                                                   10435029
4.5- and 5.0-fold increase in immunoreactive Gi-2 alpha protein concentration occurs          1999   1
placental GLUT3 mRNA and protein levels were increased four-to-fivefold             7615800   1995   2
approximate four fold increase in heat shock protein antigen in the surrounding 7554781       1995   1
A 4-fold increase in HMGR protein levels due to restricting                         9237866   1997   1
Moreover, hormone-sensitive lipase (HSL) protein was increased 4.3-fold            11375348   2001   2
4- to 5-fold increase in ICAM-1 protein concentration in HSVECs stimulated         10712387   2000   1
equal to fourfold increase in IgG to F protein at 4                                 9269057   1997   1
almost a four-fold increase in IL-1alpha protein levels. Differences were most     11145356   2000   1
showed a 3-5-fold increase in total KDR protein following 4-day VEGF                9792718   1998   1
The leucine binding protein is increased fourfold                                    324970   1977   2
heparin, a 4-fold increase in LPL activity and protein mass was                    10364085   1999   1
two- to four-fold increase for myelin basic protein (MBP) and proteolipid           7522610   1994   1
an approximately 4-fold increase in hepatic mEH protein levels relative to controls8117322    1994   1
to a fourfold increase in met protein expression. We conclude that                  9188856   1997   1
an approximate 4-fold increase in Mi-CK protein and a concomitant 3-fold            8816948   1996   1
by a fourfold increase in MIF protein expression at day 1                          12704210   2003   1
with a 4.5-fold increase in mitochondria-associated Bax protein levels (p &#60; 9562975       1998   1
the MRP mRNA and protein levels were increased 4.5-fold                            11206006   2000   2
counteract a 4-fold increase of ODC protein in the The                              8088419   1994   1
response, a 4-fold increase in P47 protein after 7 days that                        3606573   1987   1
3- to 5-fold increase in nuclear p53 protein was observed in cells                 12869419   2003   1
blotting, we found that p53 protein levels increased fourfold                      10900468   2000   2
in lactate-infused animals. PDH protein was also increased (4-fold                 10329987   1999   2
specific antagonist of GLP-1. PDX-1 protein levels increased 4-fold                11108273   2000   2
with a 4-fold induction of P-gp protein was similar to that                         7945444   1994   1
the amount of the photoreceptor protein was increased 4-fold                        10347747   1998   2
anti-Fas antibody, protein phosphatase 2A (PP2A) activity increased 4.5-fold         9582351   1998   2
in a four-fold increase of Rab5 and Rab7 protein This                                9703948   1998   1
in a four-fold increase of Rab5 and Rab7 protein This                                9703948   1998   1
the net amount of Rad51 protein was increased 2-7-fold                              11782381   2002   2
ras mRNA was increased 8-17-fold and Ras protein 4-5-fold in white                   8626688   1996   3
3- to 5-fold induction of the rop protein causes a dramatic                          7946348   1994   1
an approximately 4-fold increase in Sgk1 protein levels after 7                     15007040   2004   1
as a 4.4-fold increase in TGF-alpha protein after 4 days of treatment.(ABSTRACT8398905         1993   1
and a fourfold increase in TGF-beta RI protein expression in the glomeruli          11012901   2000   1
revealed a fourfold increase of TRX-1 protein in the lens at                        10558869   1999   1
demonstrated a four-fold increase of UCP2 protein in spleens of Line                12664076   2003   1
to a 4-fold increase of uncoupling protein dependent proton conductance which 7903611          1993   1
We demonstrate that utrophin protein was increased 4-fold                           10923681   2000   2
an approximately fourfold increase in VEGF protein and mRNA expression, which       10444484   1999   1
two to fourfold increase in retinal VEGF protein gene expression (p                 11126403   2000   1
Additionally, astrocyte VEGF protein levels increased 4.4-fold                       9174246   1997   2
was a four-fold increase in vimentin protein levels in lactating tissue             11270122   2001   1
The accumulation of the Vir90 protein increased 4-fold                              12892851   2003   2
had a fourfold increase in VLDL triglyceride and protein The                         2770534   1989   1
of plasma protein advanced glycation endproduct residues increased 1-7-fold 12885296           2003   2
2- to 6-fold increase in the corresponding protein production was observed           1367240   1991   1
to new synthesis. Total new protein synthesis increased 2-7-fold                     6871465   1983   2
The present study revealed that protein phosphorylation increased 3-6-fold           2998842   1986   2
By 4 hr, biliary protein concentration was increased 4-fold                          1440618   1992   2
                                                                                     9832430
also a 4-fold increase in particulate protein tyrosine phosphatase activity of skeletal        1998   1
Incorporation of [3H]leucine into protein was increased fourfold                     6792927   1981   2
The fourfold increase in anterior translation of the tibia for                      11918313   2002   1
values for the bacterial control protein are increased 4-fold                        2542260   1989   2
two- to fourfold increase in both cartilage core protein and type                    3021549   1986   1
vesicles by exogenously added protein kinase was increased 4-fold                    6125508   1982   2
a 4 fold increase in the extravasated protein within 15 min                          7858896   1994   1
to four fold increase in in vivo protein phosphorylation at serine                   2441849   1987   1
stimulated a 4-fold elevation of membrane protein kinase C The                       3695811   1987   1
mRNA (24-fold increase, P &#60; 0.01) and protein (4-fold increase, P                9252512   1997   3
and the rate of receptor protein synthesis increased fourfold                        3208769   1988   2
approximately a fourfold elevation in total protein (41.3 versus 10.5 mg/dl),        1990940   1991   1
A four-fold increase in the total plasma protein concentration produced              9252530   1997   1
                                                                                     1465475
demonstrated a 4-fold increase in urinary protein excretion when compared to age-matched       1992   1
pustular psoriasis, (4-fold increase in urinary protein excretion rate in relapse   12056961   2002   1
produced a fourfold increase in vascular protein leakage. A 50-fold higher           1684268   1991   1
(three to fourfold increase of protein and mRNA) and in parallel                     9766518   1998   1
A fourfold increase in the protein to DNA ratio occurred                             3837806   1985   1
a nearly fourfold increase in the level of protein disulfide compared                2591503   1989   1
and a 4-fold increase in intensity for the protein adsorbed on                       2329148   1990   1
and a fourfold increase in the protein concentration (Western In                     9277376   1997   1
condition, 4 fold increase in protein content was obtained compared to the           8172690   1993   1
expressed a 4-fold increase in the protein and a 2-fold increase                    11375951   2001   1
greater than 4-fold induction of protein by hypoxia (1% The                          8995303   1997   1
on a 4-fold increase in the prevalence of protein C deficiency                       8211782   1993   1
three- to four-fold increase in protein levels, only a 1.5-fold increase             9513045   1998   1
was a fourfold increase in absolute amount of protein synthesized during            10352153   1999   1
whereas maximal 4-fold induction of the protein was attained with 16                8349038    1993   1
and a 4.2-fold increase in protein levels of the tumor suppressor                   9843914    1998   1
induced a 4.3-fold increase in protein content in cultured SVs and elicited         1935767    1991   1
The 49-kD protein was significantly increased 5.5-fold                             10505683    1999   2
The production of the 99.8 kDa protein increased 5.2-fold                           8464009    1993   2
of the negative acute-phase protein albumin were induced 5-fold                     2454192    1988   2
and a fivefold increase in resting plasma protein (albumin)                         6991462    1980   1
at least fivefold elevation of Bax protein together with decreased Bcl-2           11417611    2001   1
5-fold up-regulation of Bcl-2 protein during TNF-alpha Furthermore,                11080178    2000   1
                                                                                    9396780
displayed a 5-fold increase in Bcl-2 protein compared with empty-vector counter-parts          1997   1
to a fivefold increase in beta1-subunit protein abundance after DA stimulation, 11404249       2001   1
(i) a 5-fold increase in C/EBPalpha protein levels, (ii) increased electrophoretic 12668682    2003   1
                                                                                    3009250
an approximately 5-fold increase in total soluble cAMP-dependent protein kinase and a          1986   1
also a 5.6-fold increase in median Cat B protein (P &#60;                           9816204    1996   1
5-fold increase in catalase protein expression and a 2.3-fold                      10802226    2000   1
induced a 5-fold increase in the CCTalpha protein level. By means                  11892987    2002   1
(1) Cdc2 kinase protein levels increased fivefold                                   9166726    1997   2
                                                                                   12270725
an approximately fivefold increase in CDw150 at the protein level, and concomitantly,          2002   1
(ABCA1) and cholesteryl ester transfer protein (CETP) increased 5-fold             12897188    2003   2
induces a 5-fold increase in c-myc protein expression within 90 min                 1855215    1991   1
three- to fivefold induction of COX-2 mRNA and protein expression but              14988266    2004   1
inhibitor NS398, the amount of COX-2 protein increased 5-fold                      10027864    1999   2
a five fold increase in creatine kinase protein per mitochondrial                   9309701    1997   1
in NIH3T3 cells. ET-1 increased cyclin D1 protein (5.1+/-1.9-fold increase, 8      10082482    1999   3
in a 5.1-fold increase of cyclooxygenase-1 protein and a 6.7-fold increase         11823676    2002   1
5-fold increase in immunodetectable CYP 2B protein in microsomes                   11082426    2000   1
in a 5-fold increase in both eNOS protein and Endothelial                          10551875    1999   1
was a fivefold increase of eotaxin protein and a 25 fold                            9311484    1997   1
an approximately fivefold increase in FimE protein compared with phase OFF 12180928            2002   1
in a 5-fold increase in glial fibrillary acidic protein (GFAP) expression,          8000566    1994   1
7- and 4-fold increase in the GLUT1 protein content in these                        8323543    1993   1
5- to 6-fold increase in GRO-1 protein in the jp spinal                            10729341    2000   1
produced a 5-fold increase in HO-1 protein 24 h The                                12543450    2003   1
A five fold increase of HsRAD51 protein levels was observed in late                 8703992    1996   1
                                                                                    9010318
two- to five-fold induction of hTGF-alpha protein observed following estrogen treatment        1996   1
effected a fivefold induction of IAP protein synthesis in comparison to islets      3079815    1986   1
and 5.7+/-3.5 fold induction of IL-6 protein secretion. The increase in IL-6       10385244    1999   1
this gave five-fold induction of iNOS protein after a dose of 4                    10918479    2000   1
levels of lipo I mRNA and protein increased 5-fold                                  1827255    1991   2
less than fivefold increase in MARCKS protein level, the synthesis of PtdCho        8627336    1996   1
RESULTS: Matrix metalloproteinase-8 protein levels were increased 5-fold           15042023    2004   2
three- to five-fold increase in MnSOD protein in EIU rats as                       12076090    2002   1
                                                                                    3886452
three- to five-fold increase in non-cAMP-dependent protein phosphorylation has previously been 1985   1
marked, near fivefold increase in transformation-related protein 53 in I was       11960975    2002   1
4- to 6-fold increase in PP-1G protein expression compared to those                 9165028    1997   1
                                                                                    9740025
an approximate fivefold increase in SAPK protein levels. Paradoxically, in NGF-differentiated 1998    1
In contrast, sIL-1 RA protein increased 5-fold                                     10766854    2000   2
was a fivefold increase in surfactant protein A in alveolar lavage                  1907607    1991   1
                                                                                   10648639
contain approximately 5-fold increase in topoIIalpha protein levels and approximately 2.2-fold 2000   1
and a 5-fold increase in tPA protein which is not sufficient                        2157975    1990   1
7.9-fold and 2.3-fold increase in the protein A1 methylase activity after           1643091    1992   1
induced a 5-fold increase in mRNA and protein expression of                        10400916    1999   1
The -89 kD immunoreactive protein was also increased -5-fold                        8496666   1993   2
was a 5-fold increase in radioactivity bound to protein compared to nonoxidized 3102491       1987   1
levels of this oncogene related protein were increased five-fold                    2788950   1989   2
caused a fivefold increase in total protein per ISMC over control,                 10489904   1999   1
fourfold to fivefold increase in the total protein in AF obtained                   7350239   1980   1
in a fivefold increase in transgene protein product in lung tissue                 10834614   2000   1
in a 5-fold increase in protein binding to the region of the                        2308930   1990   1
in a 5-fold increase in protein production from a single transfection              12573000   2003   1
induced a five-fold increase in the amount of protein after 120                     9532237   1997   1
is a 5-fold increase in protein kinase C activity. Upon longer                      1301398   1992   1
produced a 5-fold up-regulation of protein levels with elevation of both           10908313   2000   1
threefold to fivefold increase in the labeling of protein and phospholipid          2413120   1985   1
to a 5-fold increase in protein expression. The seven mutants, H55N,                8155644   1994   1
two- to fivefold increase in protein and collagen synthesis. The same               6686270   1983   1
two- to five-fold increase in protein biosynthesis was observed in islets           9586965   1998   1
for the 5.2-fold increase in protein abundance, and was mediated by                11882670   2002   1
proteins were membrane associated. One protein (p27) increased 5-6-fold             2555364   1989   2
report a 3-9-fold increase in Ann-II protein and message levels in NGF-treated 11679580       2001   1
32P into the nuclear protein B2 is increased 6-fold                                 1627750   1992   2
3- to 10-fold induction of BRCA1 protein (230 kDa). Cell fractionation              9655254   1998   1
and the cdk inhibitor protein p21(Cip1/WAF1) was elevated 6-fold                   11710929   2001   2
                                                                                   11470752
associated with the induction of hepatic c-Jun protein (6.5-fold increase) and cyclin         2001   3
approximately six fold increase in measured c-MYC protein within 5 h                1316408   1992   1
showed a 6-fold increase in COX-2 protein which was evident at                      9635856   1998   1
revealed a sixfold increase in EBNA-3 protein expression from the genomic           9882321   1999   1
to a sixfold induction of Egr-1 protein on day 6 of disease.                       12631347   2003   1
to 7-) fold increase in Ets-2 protein level in DS tissues,                         11573964   2001   1
enabled a 6-fold elevation in globin protein to occur. Concurrently, the total      7794810   1995   1
about a sixfold increase in HO-1 protein levels as compared to the                 12593860   2003   1
a 6 fold increase in the heat shock protein HSP70 as                                9278266   1997   1
and a sixfold increase in IL-1beta protein in supernatant after 3                  12801886   2003   1
mRNA on day IL-6 protein was increased 6-fold                                       1544451   1992   2
and a 6-fold increase in M-CSF mRNA and protein levels after                        9278333   1997   1
contrast, osteoprotegerin mRNA and protein levels were induced 5-7-fold            10811631   2000   2
caused a sixfold increase in the P protein phosphorylation, solely at              11831729   1995   1
and in vivo. Levels of PD-ECGF protein increased 6-fold                             9044826   1997   2
demonstrated that phospholipid transfer protein (PLTP) was induced 6-fold          12454263   2002   2
changes were accompanied by increases in PR protein (6-fold increase by             8504742   1993   3
a approximately 6-fold increase in procollagen translation that is first observable 3972816   1985   1
and a 6.7-fold increase of prostacyclin-synthase protein in the cerebral           11823676   2002   1
by a 6-fold increase in prothymosin alpha protein content in ER-containing         11459795   2001   1
caused a 4-8-fold increase in secretion of PSA protein in culture                  11791186   2002   1
(SAP) is an acute-phase protein that is increased 2-10-fold                         6201557   1984   2
a near six-fold rise in liver TNF protein compared with controls                    9042866   1997   1
a 4-8 fold increase in protein kinase and 2-5A synthetase in cells.                 2461934   1988   1
increased five-fold, and overall protein degradation was elevated six-fold          3516349   1986   2
induced a 6-fold increase in the total protein level. The effect                   10810252   2000   1
of Dermacentor andersoni. Total protein and RNA increased sixfold                  12020839   2002   2
mg/day), a 6-fold increase in urinary protein excretion compared to age-matched 8807673       1996   1
a selective 6-fold increase in the rate of translation of protein                   8308006   1994   1
an approximate 6-fold increase in protein expression level during the cercaria      8051095   1994   1
binding sites per milligram of protein was increased 6-fold                         2600824   1989   2
in a 6-fold increase in the amount of protein produced and insertion               1373131    1992   1
Protein flux across the lung increased sixfold                                     2361918    1990   2
exhibited 6.1 fold increase in urinary protein excretion, 1.4 fold increase      10232838     1999   1
approximately a sevenfold increase in bax protein at seven days of infusion.     11168946     2001   1
low cyclin E protein levels which were increased 7.8-fold                        11737001     2001   2
leptin caused no further rise. GK protein rose 7-fold                              9751766    1998   2
an average 7-fold increase in H11 kinase protein expression. Transgenic hearts 12456486       2002   1
7.7 +/- 1.5-fold increase in HSP70 protein content, but did not                  12663266     2003   1
and a 7.7-fold increase in IL-1 beta protein in However,                           7622579    1995   1
and THP-1 cells. IL-6 protein production was increased sevenfold                   7526705    1994   2
after 24 h. KDR protein expression was increased 7.5-fold                        10331422     1999   2
                                                                                 14760102     2004
exhibited a 5-10-fold increase in activated phospho-mitogen-activated protein kinase and in the      1
7-fold increase in PAI-2 mRNA and protein levels in HT-1080                      10075998     1999   1
and a 7-fold increase in PI-6 protein upon differentiation, and indirect           9851866    1998   1
Levels of Rb2/p130 protein are increased 5-10-fold                               12915404     2003   2
5- to 10-fold increase in S6 protein kinase activity, the extracts                 3511851    1986   1
h, a 7-fold increase in the UCP1 protein content relative to levels                9618150    1998   1
a 5-10 fold increase in the protein level of the cyclin                          15040006     2004   1
                                                                                   2430565
and a 7-fold increase in protein phosphotyrosine phosphatase activity accompanied this        1986   1
five- to seven-fold increase in RNA and protein contents, over initial             6160192    1980   1
and a sevenfold rise in protein stability are responsible for the increase         8676376    1996   1
levels, receptor protein concentration in the parathyroid increased 7-fold         9203998    1997   2
of the 72 kDa stress protein was elevated eight-fold                               8283475    1993   2
for the 8-fold increase in secreted apo A-I protein level                          8003099    1994   1
GSase, confined O. beta GSase protein concentrations increased eightfold         10607541     2000   2
                                                                                 12660151
activity of the calmodulin-dependent protein kinase-II (CaMK-II) increased eightfold          2003   2
after infection, catalase protein and activity was increased 7-10-fold           12468545     2003   2
The mean serum C-reactive protein level increased eight-fold                       8792574    1996   2
to an eight-fold increase of EGF receptor protein expression on C4-I               2794520    1989   1
five- and eightfold increase in GLUT5 protein at 1 and 7                           8048533    1994   1
microg/kg GA dose induced Hsp70 and Hsp25 protein 8.2-fold and 2.7-fold,         12064483     2002   3
with an eightfold increase in IGF-binding protein (IGFBP)-4 and a fivefold       11739080     2002   1
sixfold to eightfold increase in protein kinase C (PKC)alpha RNA and protein.    12514310     2003   1
In T and B lymphocytes, Rb protein increased 8-fold                                2320588    1990   2
revealed a 6-10-fold increase in RI alpha protein by 5 h                           1321143    1992   1
in an 8-fold increase of SCP-2 protein levels and determined various             11113092     2000   1
in an 8-fold increase in transferrin protein synthesis, a 10-fold increase         1315521    1992   1
UCP3 mRNA and protein levels increased 8.1-fold                                  10823916     2000   2
six- to eightfold increase in normal aqueous humor protein concentration, which      91326    1979   1
hepatic polysomes (in a wheat-germ translation system) increased 8-fold            8375391    1993   2
detected an eightfold increase of green fluorescent protein (GFP)-expressing The 14984426     2004   1
(iii) an eight-fold increase in protein synthesis; and (iv) a three-fold           7799445    1994   1
a six-to eightfold increase in protein synthesis (P &#60; .01) with methionine     9535338    1998   1
cells, a 8-fold increase in protein production was measured. These results       10544911     1999   1
The lymphatic total protein clearance increased 8.6-fold                           6807946    1982   2
content, a 9.2-fold increase in c-Jun protein content, and a 2-fold              12007573     2002   1
Collagenase IV protein expression was induced 9-fold                               9018132    1997   2
of total protein synthesis), and elastin synthesis increased ninefold              2317897    1990   2
in a ninefold upregulation of HSP27 mRNA and protein in axotomized                 9671676    1998   1
A 4-15-fold induction of p21(WAF1) protein was observed in cells                 12243503     2002   1
by a 9-fold increase in PAI-1 protein from 6 hours (2.9                            7923681    1994   1
mRNA in transgenic hearts. SERCA2b protein was increased 8-10-fold               10816568     2000   2
was a 9-fold increase in SP-D protein levels in the 20,000                          11472974    2001   1
to a nine-fold increase in VEGF protein expression in macrophages, a 2.4-fold 12766200          2003   1
3.8- and 16-fold induction of protein seen in these tissues by                      11067848    2001   1
7- to 12-fold increase in total urinary protein excreted in 24                       3080763    1986   1
a approximately 9-fold increase in channel protein expression 24 h after            10842276    2000   1
Each form of ADAMTS-1 protein increased >10-fold                                    12907688    2003   2
least a 10-fold increase in measured human alpha1AT protein in culture               8600939    1996   1
and a 10-fold increase in CaBP9K protein content after 24                            1695565    1990   1
with a 10-fold increase in cardiac AC(VI) protein content. A similar                12393090    2002   1
induced a 10-fold increase in CD40 mRNA and protein Furthermore,                     7554483    1995   1
with a tenfold increase in class 1 MHC protein and mRNA                              2545735    1989   1
five- to tenfold increase in C-reactive protein was observed, as was                 9111579    1997   1
                                                                                    12094630
for a 10-fold increase in C-reactive protein concentration in cancer-specific survival          2001   1
                                                                                    12830053
at least 10-fold increase in Fas-associating death domain protein levels and decreased          2003   1
while a 10-fold increase in glial fibrillary acid protein (GFAP) mRNA                8622783    1995   1
and a 10-fold increase in glial fibrillary acidic protein (GFAP) level              12153475    2002   1
BHA caused 10-fold increase in GST activity and protein in livers                    8101791    1993   1
in a 10.7-fold increase in immunodetectable hexokinase protein and a similar         8063745    1994   1
greater than tenfold increase in LAR protein levels in breast cancer                10365916    1999   1
level thereafter; LPL protein and enzyme activity increased 10-fold                  1550225    1992   2
Mitogen-activated protein (MAP) kinase activity is increased 10-fold                 8631833    1996   2
a nearly 10-fold increase in mitogen-activated protein kinase activity; this effect 9230197     1997   1
induced a 10-fold increase in MCAF protein production and a 3-fold                   9620840    1998   1
addition, a 10-fold increase of MCP-1 protein in the supernatant was                 9848782    1998   1
showed a 10-fold increase in MDR protein and a 12-fold increase                     10411688    1999   1
Rho-induced differentiation gene, myogenin. Mirk protein levels increased 10-fold   12902328    2003   2
showed that mitochondrial protein recovered from WAT increased 10-fold              10942717    2000   2
accompanied by a large increase in NaPi-2 protein (10.2-fold in normal               8927512    1996   3
8- to 12-fold increase in OppA protein relative to the wild-type                    10692365    2000   1
greater than 10-fold increase in microsomal P450IIIA6 protein is detected by         2777787    1989   1
greater than 10-fold increase in p53 protein was measured with the PAb               7698234    1995   1
about a 10-fold increase in PB2 mRNA and protein The                                 2989815    1985   1
display a 10-fold increase in PKC alpha protein in their epidermis                  11259631    2001   1
cultures a 10-fold increase in the rate of protein D synthesis                         776971   1976   1
to a ten-fold increase in cytoskeletal protein kinase C and a corresponding          2226843    1990   1
analysis revealed that the RAD51 protein was elevated 10-fold                       12748186    2003   2
about a 10-fold increase in exogenous Ran protein compared with RanT/n              11521083    2001   1
While a >10-fold increase in sigma(32) protein level was found under                11010884    2000   1
and a 10-fold increase of TGFalpha protein expression were obtained 2-12            11989832    2002   1
nephritic rats, protein expression of TGF-beta(2) was upregulated tenfold           12545247    2003   2
shows a ten-fold increase in TIMP-1 protein secretion by SW620                      11113862    2000   1
1.14.16.2] activity increased 60-fold, while total protein rose 10-fold                 10572   1976   2
at 45 min, the aqueous protein concentration increased 10-fold                      10328973    1999   2
a synergistic 10-fold increase in enzyme protein as measured by kinase               8194665    1994   1
was a 10-fold increase in enzyme protein with unaltered affinity for                 1846175    1991   1
caused a 10-fold increase in jejunal protein loss over the controls                  2458986    1988   1
to a tenfold increase in secreted protein and carbohydrate. Among the proteins          15977   1977   1
normal colon and liver. This protein was increased 10-fold                           3005388    1986   2
to the V group. Urinary protein excretion increased >10-fold                         9676726    1998   2
excretion, a 10-fold increase in urine protein excretion and a 4-fold                4078735    1985   1
a maximal 10-fold increase in protein secretion. In contrast, the elemental          7933441    1994   1
activity and protein as assessed by immunoquantitation increased 10-fold             2001804    1991   2
by a 10-fold increase of protein expression. The size of message                     10733947   2000   1
by a tenfold increase in protein concentration. It is suggested that                  2268321   1990   1
equal to 10-fold increase in the efficiency of translation of the fusion              6387704   1984   1
in about 10-fold increase in the protein kinase activity. The activation              3848401   1985   1
In addition, protein levels were increased >10-fold                                   9058793   1997   2
requiring a tenfold increase in protein concentration. Despite its protective effect,10227419   1999   1
than a 10-fold increase in protein                                                     126234   1975   1
the lens protein preparations. Also, superoxide formation increased 10-fold          10433859   1999   2
thermal hysteresis protein message, but these levels increased 10-fold               11029589   2000   2
with a 10-fold increase in protein synthesis not seen in other                        6932042   1980   1
the concomitant 10.9-fold increase in translation of protein was heavily biased       2456525   1988   1
in an 11-fold increase in Bcl-xl protein in neonatal rat cardiac                     11922903   2002   1
shown an 11-fold increase of protein p220 of apparent MW 220,000                      3007243   1986   1
in an 11-fold increase in the SR-BI protein level in liver                           11108734   2000   1
increased 2-fold, and protein phosphotyrosine phosphatase activity increased 11-fold  2430565   1986   2
a reticulocyte cell-free translation assay was also increased 11-fold                 6086627   1984   2
                                                                                      the
an approximate 11-fold increase in hepatic microsomal protein between birth and 3572256         1987   1
by a 12-fold increase in the fast-type Ca(2+)-ATPase protein content of soleus        8093021   1994   1
up to 12-fold increase in NPTII protein levels, suggesting that methylation          10664454   2000   1
concentration of 300 nM, p53 protein was induced 12.5-fold                           11716435   2000   2
into myotubes, PKCtheta mRNA and protein were increased 12-fold                      10919262   2000   2
to a 12-fold increase in Raf-1 protein expression. TCR/CD3 activation did             1708096   1991   1
following Achilles tendon division, uPA receptor protein increased 12.6-fold         12919869   2003   2
less effective because the amount of protein increased 4-20-fold                      6175106   1981   2
10- to 15-fold increase in protein levels at 6 h following                            7936647   1994   1
the secretin-induced maximal output, whereas protein secretion increased 12-fold 3104127        1987   2
peak alveolitis (12-fold increase in protein in the lavage, 7-fold increase           9146704   1997   1
A 12.2-fold increase in protein yield was accompanied by a 4.3-fold                   8659895   1996   1
had a 13-fold increase in GK protein and a 2-fold decrease                           14617577   2004   1
3- to 24-fold increase in IL-8 protein expression of BEC, and a                      12792762   2003   1
EHR2, the multidrug resistance-associated protein mRNA was increased 13-fold10856431            2000   2
ProCT protein secretion into culture supernatant increased 13.5-fold                 12960010   2003   2
expression; the level of c-jun protein was elevated 8-21-fold                         9029170   1997   2
c-jun, a 14-fold increase in c-Jun protein phosphorylation, and an increase           9722577   1998   1
Levels of heat shock protein 27 increased 2-fold                                      9067284   1997   2
1.9- to 28-fold increase of the mRNA and protein levels of the                       12594236   2003   1
2.5-fold whereas the androgen receptor protein level increased 15-fold                7511045   1994   2
and a 15-fold increase of beta-galactosidase protein expression in the ELISA         11001372   2000   1
caused a 15-fold increase in transcript and protein concentration of CRABP-II, 12956703         2003   1
10-fold to 20-fold increase in cryIA(c) mRNA and protein levels compared              1515613   1992   1
In contrast, decorin protein expression is increased 12-18-fold                       1460033   1992   2
10- to 20-fold increase in HSP70 protein synthesis with little change                 3428602   1987   1
10- to 20-fold elevation of eosinophil major basic protein (MBP) immunoreactivity 6376683       1984   1
content increased fivefold and MT protein content increased 15-fold                   2429403   1986   2
10- to 20-fold increase in cell-bound protein A. As the serine                       11447146   2001   1
and a 16-fold increase in the 30,000-Mr protein after 120                             1697605   1990   1
in a 16-fold increase in HEF1 protein level. TGF-beta1 had no                        12189134   2002   1
A 2-30-fold increase of MnSOD protein and activity was observed                      11929863   2002   1
12- to 20-fold increase in p21/SDI-1 protein. Protein synthesis inhibition by         8846917   1996   1
encodes a cytoplasmic protein whose expression is induced 16-fold                     9151873   1997   2
and a 16-fold increase in protein product (luciferase activity, p =                   9607413   1998   1
transcription, a 17.6-fold increase in Frd protein translation, and a balancing       2456525   1988   1
transferred wild-type OB-R was functional. GLUT-2 protein rose 17-fold                 9751766     1998   2
more than 17-fold increase in lavage PL and protein levels and a                       8968411     1996   1
of beta-glucuronidase mRNA increased the efficiency of translation 16-fold to 18-fold  2535505     1989   3
alpha subunit (17-fold increase in protein concentration). The changes in pyruvate7487891          1995   1
in an 18.8-fold increase in cerebral microvessel eNOS protein CONCLUSIONS: 10512927                1999   1
as an 18-fold increase in the MTP1 protein level was detected                        12376346      2002   1
and an 18-fold increase in R2 protein as cells entered S                               9605773     1998   1
20- and 16-fold increase in phospholipid-, calcium-independent protein kinase To 8149484           1994   1
The translation capacity of embryo lysates increased 18-fold                         11508742      2001   2
dependence in their responses. Extracellular soluble protein increased 19.8-fold 3012822           1986   2
A 20-fold increase in c-myb mRNA and protein expression was                            9815978     1995   1
acute-phase response (20-fold increase in C-reactive protein and 12% decrease 10600658             2000
                                                                                      in pre-albumin      1
iron, CYP1A activity and CYP1A1/1A2 protein were elevated >20-fold                   10970442      2000   2
and a 20.3-fold increase in CYP3A4 activity, immunoreactive protein levels, and mRNA 14636322      2003   1
demonstrated a 20-fold increase in IGFBP-3 protein expression in NCI-H23 pOPI3/BP-3  10974650      2000   1
notably, the 20-fold induction of IL-6 mRNA and protein was completely               14764742      2004   1
                                                                                     11029589
an approximately 20-fold increase in thermal hysteresis protein concentration, well in excess 2000        1
messenger ribonucleic acid, and protein levels are increased 20-fold                   8550801     1996   2
the amount of immunoreactive protein expressed in increased 20-fold                    2188656     1990   2
only a 20-fold increase in membrane protein and a five- to sixfold                     2897955     1988   1
and a 20-fold increase in this protein at 6 h                                          9202209     1997   1
in a more-than-20-fold increase in the level of protein and                            7688350     1993   1
                                                                                     11595806
sixfold to 20-fold increase in protein accumulation. Naturally occurring variant amino             2001   1
                                                                                       2171189
greater than 21-fold increase in beta-interferon protein synthesis after viral infection           1990   1
a corresponding 23-fold increase in GTPCH protein levels. Northern blot analysis 8883940           1996   1
in a 23.7-fold induction of MnSOD protein after 48-h treatment with IL-1               9176234     1997   1
of [35S]methionine incorporation into acid-soluble total protein increased 24-fold 2536812         1989   2
lines, and CCT activity and protein were elevated 25-fold                              9442058     1998   2
10-fold to 40-fold increase in p185 erbB-2 protein levels compared with parental 1354442           1992   1
and a 25-fold increase in PGHS-2 protein levels by 4                                   8660662     1996   1
10- to 40-fold increase in protein content. The adherence of normal                    3674583     1987   1
14- to 37-fold increase in vascular protein flux. Local intra-arterial infusion        2301577     1990   1
protein in vitro, the protein synthesis rate increased 25-fold                         7539604     1995   2
Protein secretion by intercaruncular endometrium increased 25-fold                     6822778     1983   2
rats with anti-GBM disease, total protein excretion increased 26-fold                10692267      2000   2
The level of p53 protein was induced 27-fold                                         10753197      2000   2
 A 28-fold increase in secretory protein synthesis is associated with DNA              9283627     1997   1
mRNA, a 30-fold induction of Cat-1 protein levels, and a 4-fold                      11781318      2002   1
more than 30-fold increase in CNTF mRNA and protein occurs in the                      1824101     1991   1
was a 30-fold increase in Cox-2 content per protein extract between                    9369167     1997   1
a Mr 29,000 IGF binding protein is induced 30-fold                                     2474537     1989   2
16 beta-hydroxylation and P450 2B1/2-immunoreactive protein were elevated 30-fold      9056233     1997   2
in a 30-fold increase in nuclear protein at maximum induction and a                  10608861      1999   1
and a 34-fold increase in translocase protein as compared to the expression            9387243     1997   1
studies revealed 34-fold increase in TS protein levels in MCFTDX and a                 8787551     1996   1
and a 35-fold increase in protein for Cox-2 were In                                  12193735      2002   1
                                                                                       7657108
showed a 22-49-fold induction in MnSOD protein levels. Immunocytochemistry showed induction        1995   1
a thirty-to forty-fold increase in progesterone synthesis. Protein kinase activation was182451     1976   1
stimulated 2-fold and incorporation into secreted protein increased 36-fold            1117004     1975   2
of both inducers, CYP3A4 protein levels were increased 40-fold                       11587480      2001   2
Myocardial heat shock protein 70 (HSP 70) increased 12.3-fold                        11299231      2001   2
48 hr, respectively. Immunoreactive CYP1A1 protein was increased 46-fold               8432429     1993   2
induced a 45-50-fold increase in total urinary protein excretion, a 10-15-fold   7501960   1995   1
 A >50-fold increase in GM-CSF protein release in podocytes that                11752025   2002   1
50-fold increase in foreign protein production. Northern analysis suggested      8206381   1994   1
greater than 50-fold increase in protein accumulation. Thus, the same mutations 10758506   2000   1
was a 53-fold increase in protein from the early to late                         8464000   1993   1
3.8 +/- 0.6 ng/mg of protein and increased 54-fold                              10694406   2000   2
for factor B only: protein synthesis was increased 54.5-fold                     3121777   1988   2
                                                                                 8617999
10- and 100-fold increase in cornifin-alpha/SPRR1 protein and mRNA, and expression         1996   1
revealed that, after coculture, iNOS protein was up-regulated 55-fold           11103793   2000   2
indicated a 56-fold increase in TNF-alpha protein concentration after 4         11797114   2001   1
in a 58-fold increase in protein levels and increased arginine                  11114306   2001   1
60- to 75-fold induction of IGFBP-3 mRNA and protein This                       10077006   1999   1
                                                                                12882792
more than 68-fold increase in ENA-78 protein synthesis without significantly enhancing     2003   1
in a 70-fold increase in activity, while the protein remained                   10353852   1999   1
with a 50-100-fold increase in protein content in lung BAL fluid,               14607960   2003   1
up to 80-fold increase in cyclooxygenase 2 protein and a corresponding          10454683   1999   1
30- to 150-fold increase in reporter protein secretion, compared to simple      10985950   2000   1
reveal a 100-fold increase in IL-6 protein and enhance IL-6 and MMP-3           12517948   2003   1
induced a 100-fold increase in translation of a green fluorescent protein       12799445   2003   1
promoter, allowing 100-fold induction of protein expression. The vector pCQV2 has6302192   1983   1
was a 110-fold increase in the translation efficiency of the lacZ                2676996   1989   1
that the 127-fold increase in protein synthesis which occurs during Xenopus      4007263   1985   1
an average 130-fold increase in secreted VPF protein levels (CHO 0.13+/-0.12 8631593       1996   1
was a 160-fold increase in protein content from the expanded blastocyst          8882289   1996   1
ten- to 200-fold increase in protein synthesis depending on the recombinant      1347276   1992   1
more than 300-fold increase in ENA-78 and GCP-2 protein In                      12882792   2003   1
more than 300-fold increase in ENA-78 and GCP-2 protein In                      12882792   2003   1
in a 300-fold increase in the virus:total protein ratio in the supernatants     10466630   1999   1
activity per mg of enzyme protein was increased 315-fold                         6806291   1982   2
produced a 400-fold increase in ornithine decarboxylase protein in the kidney    6401734   1983   1
and a 500-fold increase in protein throughput was achieved without compromising2440579     1987   1
However, the 800-fold rise in protein levels between Days 5 and 15               1805986   1991   1
was a 5000-fold increase in total protein and a 1000-fold increase               1748554   1991   1
to a 9000-fold increase in tnpA protein production when combined with a          6277510   1982   1
Pattern#
            Pattern 1       777   69.1%
            Pattern 2       325   28.9%
            Pattern 3        23    2.0%
                           1125
            Unique genes            510

           Fold change Reported
                              0
                  >20        63                                            350
                   20        13
                   19         1
                   18         5                                            300
                   17         5


                                          # of times reported in MEDLINE
                   16         6
                   15         9                                            250
                   14         4
                   13         4
                   12        11
                   11         6
                                                                           200
                   10        58
                    9        12
                    8        23                                            150
                    7        19
                    6        38
                    5        66                                            100
                    4       108
                    3       198
                    2       313                                            50
                 +/-1        66   5.9%
                   -2        16
                   -3        19                                             0
                   -4        12                                                  >20 20 19 18 17 16 15 14 13 12 11 10 9   8
                   -5        11
                   -6         4                                                                               Fold change in translation
                   -7         2
                   -8         3
                   -9         0
                  -10        13
                 <-10        17

                     0        0
                     1       65
                    -1        1
        8   7   6   5   4   3   2 +/-1 -2 -3 -4 -5 -6 -7 -8 -9 -10<-10


Fold change in translation
Reg. Type              gene                sentence
post-transcriptional                        Analysis of post-transcriptional regulation operating on transcription products
post-transcriptional                        Autogenous and post-transcriptional regulation of RNA polymerase
post-transcriptional   inducible            Caveolin-1-mediated post-transcriptional regulation of inducible nitric oxide
post-transcriptional                        Chilling-sensitive, post-transcriptional regulation of a plant fatty
post-transcriptional   EGF-receptor         Complex post-transcriptional regulation of EGF-receptor expression by
post-transcriptional   ferritin             Coordinate post-transcriptional regulation of ferritin and transferrin
post-transcriptional   ornithine            Differential post-transcriptional control of ornithine decarboxylase and spermidine-
post-transcriptional   p21WAF1/Cip1         Differential post-transcriptional regulation of p21WAF1/Cip1 levels in the
post-transcriptional   yeast                Differential post-transcriptional regulation of yeast mRNAs in response
post-transcriptional   COX-2                Dysregulated post-transcriptional control of COX-2 gene expression
post-transcriptional                        Evidence for post-transcriptional control of the morphogenetic genes
post-transcriptional   cyclin               Evidence for post-transcriptional regulation of cyclin B1 mRNA
post-transcriptional   cytokeratin          Evidence for post-transcriptional regulation of cytokeratin gene expression
post-transcriptional   interleukin-5        Evidence for post-transcriptional regulation of interleukin-5 by
post-transcriptional                        Evidence for post-transcriptional regulation of the synthesis of the
post-transcriptional                        Evidence of post-transcriptional regulation in mammalian mitochondrial
post-transcriptional   L-selectin           Evidence of post-transcriptional regulation of L-selectin gene expression
post-transcriptional   U6                   Evidence of post-transcriptional regulation of U6 small nuclear
post-transcriptional   maize                Expression and post-transcriptional regulation of maize transposable element
post-transcriptional   ornithine            Expression and post-transcriptional regulation of ornithine decarboxylase during
post-transcriptional   chemokine            Importance of post-transcriptional regulation of chemokine genes by
post-transcriptional   hepatic              Insulin-mediated post-transcriptional regulation of hepatic malic enzyme
post-transcriptional   thyroid              Neuroserpin is post-transcriptionally regulated by thyroid Neuroserpin
post-transcriptional   insulin-like         Non-receptor mediated, post-transcriptional regulation of insulin-like growth factor
post-transcriptional   gene                 Nuclear post-transcriptional control of gene The
post-transcriptional   COX-2                Polyamine-mediated post-transcriptional regulation of COX-2. Polyamines are
post-transcriptional                    26 Post-transcriptional control of 26 k casein
post-transcriptional                        Post-transcriptional control of a sporulation regulatory
post-transcriptional   bacteriophage        Post-transcriptional control of bacteriophage T4 gene
post-transcriptional   catalase             Post-transcriptional control of catalase expression in garlic-treated
post-transcriptional                        Post-transcriptional control of cell type-specific gene
post-transcriptional   c-erb                Post-transcriptional control of c-erb B-2 overexpression
post-transcriptional   chloroplast          Post-transcriptional control of chloroplast gene
post-transcriptional   class                Post-transcriptional control of class I MHC
post-transcriptional   c-myc                Post-transcriptional control of c-myc proto-oncogene expression
post-transcriptional   c-myc                Post-transcriptional control of c-myc RNA during
post-transcriptional   cyclooxygenase-2     Post-transcriptional control of cyclooxygenase-2 gene
post-transcriptional   expression           Post-transcriptional control of expression of the repA
post-transcriptional   gene                 Post-transcriptional control of gene expression during
post-transcriptional   H3                   Post-transcriptional control of H3 histone variants
post-transcriptional   hsp70                Post-transcriptional control of hsp70 mRNA in Trypanosoma
post-transcriptional                        Post-transcriptional control of human cytomegalovirus gene
post-transcriptional                        Post-transcriptional control of human maxiK potassium
post-transcriptional   IL-1                 Post-transcriptional control of IL-1 gene expression
post-transcriptional   L-12-propanediol     Post-transcriptional control of L-1,2-propanediol oxidoreductase in the
post-transcriptional   messenger            Post-transcriptional control of messenger RNA diversity
post-transcriptional   myc                  Post-transcriptional control of myc and p53
post-transcriptional   negative             Post-transcriptional control of negative acute phase
post-transcriptional   plastid              Post-transcriptional control of plastid mRNA accumulation
post-transcriptional                        Post-transcriptional control of protein synthesis in Balb/c-3T3
post-transcriptional   Pseudomonas          Post-transcriptional control of Pseudomonas aeruginosa lasB
post-transcriptional                         Post-transcriptional control of the Arabidopsis auxin
post-transcriptional                         Post-transcriptional control of the differential expression
post-transcriptional                         Post-transcriptional control of the level of mRNA
post-transcriptional                         Post-transcriptional control of the onset of DNA
post-transcriptional                         Post-transcriptional regulation of 3-hydroxy-3-methylglutaryl coenzyme A
                       3-hydroxy-3-methylglutaryl
post-transcriptional                         Post-transcriptional regulation of 3-hydroxy-3-methylglutaryl-CoA reductase mRNA
                       3-hydroxy-3-methylglutaryl-CoA
post-transcriptional   5S                    Post-transcriptional regulation of 5S rRNA synthesis
post-transcriptional                         Post-transcriptional regulation of a milk membrane
post-transcriptional                         Post-transcriptional regulation of a murine homeobox
post-transcriptional                         Post-transcriptional regulation of a salt-inducible alfalfa
post-transcriptional   acetylcholinesterase Post-transcriptional regulation of acetylcholinesterase mRNAs in nerve
post-transcriptional   albumin               Post-transcriptional regulation of albumin gene expression
post-transcriptional   apolipoprotein        Post-transcriptional regulation of apolipoprotein E expression
post-transcriptional   bacterial             Post-transcriptional regulation of bacterial motility by
post-transcriptional   bcl-2                 Post-transcriptional regulation of bcl-2 in acute
post-transcriptional   bifunctional          Post-transcriptional regulation of bifunctional alpha-amylase/subtilisin inhibitor
post-transcriptional   bovine                Post-transcriptional regulation of bovine parathyroid hormone
post-transcriptional   bradykinin            Post-transcriptional regulation of bradykinin B1 and B2
post-transcriptional   cAMP-dependent        Post-transcriptional regulation of cAMP-dependent protein kinase
post-transcriptional   c-fms                 Post-transcriptional regulation of c-fms proto-oncogene expression
post-transcriptional   chloramphenicol       Post-transcriptional regulation of chloramphenicol acetyl
post-transcriptional   chloroplast           Post-transcriptional regulation of chloroplast gene expression
post-transcriptional   chymase               Post-transcriptional regulation of chymase expression in mast
post-transcriptional   collagen              Post-transcriptional regulation of collagen alpha 1(I)
post-transcriptional   collagenase           Post-transcriptional regulation of collagenase and stromelysin
post-transcriptional   complement            Post-transcriptional regulation of complement C4 in low
post-transcriptional   CspA                  Post-transcriptional regulation of CspA expression in Escherichia
post-transcriptional   cyclin                Post-transcriptional regulation of cyclin D1 expression
post-transcriptional   cysteine              Post-transcriptional regulation of cysteine dioxygenase in rat
post-transcriptional   cytoskeletal          Post-transcriptional regulation of cytoskeletal actin and T
post-transcriptional   E2A                   Post-transcriptional regulation of E2A proteins via
post-transcriptional   early                 Post-transcriptional regulation of early T cell
post-transcriptional   endothelial           Post-transcriptional regulation of endothelial cell plasminogen
post-transcriptional   endothelial           Post-transcriptional regulation of endothelial nitric oxide
post-transcriptional   erythropoietin        Post-transcriptional regulation of erythropoietin mRNA stability
post-transcriptional   expression            Post-transcriptional regulation of expression of plasminogen
post-transcriptional   expression            Post-transcriptional regulation of expression of the Bronze2
post-transcriptional   extracellular         Post-transcriptional regulation of extracellular matrix metalloproteinase
post-transcriptional   gene                  Post-transcriptional regulation of gene expression by
post-transcriptional   gene                  Post-transcriptional regulation of gene expression during
post-transcriptional   gene                  Post-transcriptional regulation of gene expression in compensatory
post-transcriptional   gene                  Post-transcriptional regulation of gene expression in guinea
post-transcriptional   gene                  Post-transcriptional regulation of gene expression in hippocampal
post-transcriptional   gene                  Post-transcriptional regulation of gene expression in the
post-transcriptional   glutamyl-prolyl-tRNA Post-transcriptional regulation of glutamyl-prolyl-tRNA synthetase in rat
post-transcriptional   glutathione           Post-transcriptional regulation of glutathione peroxidase gene
post-transcriptional                         Post-transcriptional regulation of glyceraldehyde-3-phosphate-dehydrogenase gen
                       glyceraldehyde-3-phosphate-dehydrogenase
post-transcriptional   granulocyte-macrophagePost-transcriptional regulation of granulocyte-macrophage colony-stimulating facto
post-transcriptional   gro                   Post-transcriptional regulation of gro alpha, beta,
post-transcriptional   gurken                Post-transcriptional regulation of gurken by encore
post-transcriptional   hepatic               Post-transcriptional regulation of hepatic NADPH-cytochrome P450
post-transcriptional   H-ferritin            Post-transcriptional regulation of H-ferritin gene expression
post-transcriptional   H-ferritin           Post-transcriptional regulation of H-ferritin Identification
post-transcriptional                        Post-transcriptional regulation of human interleukin-2 gene
post-transcriptional                        Post-transcriptional regulation of human iron metabolism
post-transcriptional                        Post-transcriptional regulation of human microsomal epoxide
post-transcriptional   IME1                 Post-transcriptional regulation of IME1 determines initiation
post-transcriptional   inducible            Post-transcriptional regulation of inducible nitric oxide
post-transcriptional   insulin-like         Post-transcriptional regulation of insulin-like growth factor
post-transcriptional   interferon-alpha     Post-transcriptional regulation of interferon-alpha 4 subtype
post-transcriptional   interleukin          Post-transcriptional regulation of interleukin 1 alpha
post-transcriptional   interleukin-6        Post-transcriptional regulation of interleukin-6 gene expression
post-transcriptional   loss                 Post-transcriptional regulation of loss of rat
post-transcriptional   LTC4                 Post-transcriptional regulation of LTC4 synthase activity
post-transcriptional   lung                 Post-transcriptional regulation of lung antioxidant enzyme
post-transcriptional   luteinizing          Post-transcriptional regulation of luteinizing hormone receptor
post-transcriptional   messenger            Post-transcriptional regulation of messenger abundance in rat
post-transcriptional   methionine           Post-transcriptional regulation of methionine content in maize
post-transcriptional   MHC                  Post-transcriptional regulation of MHC class II
post-transcriptional                        Post-transcriptional regulation of mouse kappa-opioid receptor
post-transcriptional                        Post-transcriptional regulation of mouse renal cytochrome
post-transcriptional   MyD118               Post-transcriptional regulation of MyD118 and GADD45
post-transcriptional   Na+/glucose          Post-transcriptional regulation of Na+/glucose cotransporter (SGTL1)
post-transcriptional   neurofibromin        Post-transcriptional regulation of neurofibromin level in cultured
post-transcriptional   nitrate              Post-transcriptional regulation of nitrate reductase by
post-transcriptional   opioid               Post-transcriptional regulation of opioid receptors in the
post-transcriptional   organ-specific       Post-transcriptional regulation of organ-specific expression of individual
post-transcriptional   ornithine            Post-transcriptional regulation of ornithine decarboxylase in Xenopus
post-transcriptional   phenylalanine        Post-transcriptional regulation of phenylalanine ammonia-lyase expression
post-transcriptional                        Post-transcriptional regulation of plant ferritin accumulation
post-transcriptional   pro-inflammatory     Post-transcriptional regulation of pro-inflammatory gene
post-transcriptional                        Post-transcriptional regulation of rat alpha cardiac
post-transcriptional                        Post-transcriptional regulation of rat carnitine
post-transcriptional                        Post-transcriptional regulation of rat CYP2E1 expression:
post-transcriptional                        Post-transcriptional regulation of rat liver gene
post-transcriptional   retroviral           Post-transcriptional regulation of retroviral vector-transduced low
post-transcriptional   ribosomal            Post-transcriptional regulation of ribosomal protein gene
post-transcriptional   ribosome             Post-transcriptional regulation of ribosome accumulation during
post-transcriptional   ribosome             Post-transcriptional regulation of ribosome formation in the
post-transcriptional                        Post-transcriptional regulation of RNA polymerase II
post-transcriptional   S-adenosylmethionine Post-transcriptional regulation of S-adenosylmethionine synthetase from
post-transcriptional   secretory            Post-transcriptional regulation of secretory protein production
post-transcriptional   sex                  Post-transcriptional regulation of sex determination in Caenorhabditis
post-transcriptional   soluble              Post-transcriptional regulation of soluble guanylyl cyclase
post-transcriptional   synaptic             Post-transcriptional regulation of synaptic vesicle protein
post-transcriptional   syndecan-1           Post-transcriptional regulation of syndecan-1 expression by
post-transcriptional                        Post-transcriptional regulation of the abundance of mRNAs
post-transcriptional                        Post-transcriptional regulation of the arginine transporter
post-transcriptional                        Post-transcriptional regulation of the Bacillus subtilis
post-transcriptional                        Post-transcriptional regulation of the bacteriophage Mu
post-transcriptional                        Post-transcriptional regulation of the cell surface
post-transcriptional                        Post-transcriptional regulation of the chicken thymidine
post-transcriptional                        Post-transcriptional regulation of the content of spermidine/spermine
post-transcriptional                        Post-transcriptional regulation of the DNA damage-inducible
post-transcriptional                           Post-transcriptional regulation of the E/Daughterless ortholog
post-transcriptional                           Post-transcriptional regulation of the GAP-43 gene
post-transcriptional                           Post-transcriptional regulation of the gli1 oncogene
post-transcriptional                           Post-transcriptional regulation of the gonadotropin-releasing hormone
post-transcriptional                           Post-transcriptional regulation of the groEL1 gene
post-transcriptional                           Post-transcriptional regulation of the human liver/bone/kidney
post-transcriptional                           Post-transcriptional regulation of the human transforming
post-transcriptional                           Post-transcriptional regulation of the meiotic Cdc25
post-transcriptional                           Post-transcriptional regulation of the Na+/Ca2+ exchanger
post-transcriptional                           Post-transcriptional regulation of the p53 tumor
post-transcriptional                           Post-transcriptional regulation of the parathyroid hormone
post-transcriptional                           Post-transcriptional regulation of the peripheral myelin
post-transcriptional                           Post-transcriptional regulation of the pro alpha
post-transcriptional                           Post-transcriptional regulation of the Pseudomonas aeruginosa
post-transcriptional                           Post-transcriptional regulation of the sodium/iodide symporter
post-transcriptional                           Post-transcriptional regulation of the stanniocalcin gene
post-transcriptional                           Post-transcriptional regulation of the steady-state levels
post-transcriptional                           Post-transcriptional regulation of the str operon
post-transcriptional                           Post-transcriptional regulation of the Streptomyces coelicolor
post-transcriptional                           Post-transcriptional regulation of the transferrin receptor
post-transcriptional   thromboxane             Post-transcriptional regulation of thromboxane A2 synthase
post-transcriptional   thymidine               Post-transcriptional regulation of thymidine kinase gene
post-transcriptional   thyroid                 Post-transcriptional regulation of thyroid hormone receptor
post-transcriptional   tissue-specific         Post-transcriptional regulation of tissue-specific A
post-transcriptional   TNF-alpha               Post-transcriptional regulation of TNF-alpha during in vitro
post-transcriptional   transferrin             Post-transcriptional regulation of transferrin receptor mRNA
post-transcriptional   tubulin                 Post-transcriptional regulation of tubulin mRNA in developing
post-transcriptional   tyrosine                Post-transcriptional regulation of tyrosine hydroxylase gene
post-transcriptional   ura4+                   Post-transcriptional regulation of ura4+ gene expression
post-transcriptional   urokinase               Post-transcriptional regulation of urokinase Identification
post-transcriptional   urokinase               Post-transcriptional regulation of urokinase plasminogen activator
post-transcriptional   UV                      Post-transcriptional regulation of UV induced TNF-alpha
post-transcriptional   vascular                Post-transcriptional regulation of vascular endothelial growth
post-transcriptional   VEGF                    Post-transcriptional regulation of VEGF expression by
post-transcriptional   Xwnt-8                  Post-transcriptional regulation of Xwnt-8 expression is
post-transcriptional   zenk                    Post-transcriptional regulation of zenk expression associated
post-transcriptional   c-myc                   Tissue-specific post-transcriptional regulation of c-myc expression in normal
post-transcriptional   avian                   Transcription and post-transcriptional regulation of avian HSP70 gene
post-transcriptional   luteotropin/chorionic   Transcription and post-transcriptional regulation of luteotropin/chorionic gonadotro
post-transcriptional   apolipoprotein          Transcriptional and post-transcriptional control of apolipoprotein E gene
post-transcriptional   beta-galactosidase      Transcriptional and post-transcriptional control of beta-galactosidase lac
post-transcriptional   cold-shock              Transcriptional and post-transcriptional control of cold-shock A
post-transcriptional   lysyl                   Transcriptional and post-transcriptional control of lysyl oxidase expression
post-transcriptional   PHO8                    Transcriptional and post-transcriptional control of PHO8 expression by
post-transcriptional   polynucleotide          Transcriptional and post-transcriptional control of polynucleotide phosphorylase du
post-transcriptional   ribosomal               Transcriptional and post-transcriptional control of ribosomal protein and ribonuclei
post-transcriptional   rRNA                    Transcriptional and post-transcriptional control of rRNA synthesis in human
post-transcriptional                           Transcriptional and post-transcriptional control of specific messenger RNAs
post-transcriptional   tubulin                 Transcriptional and post-transcriptional control of tubulin gene expression
post-transcriptional   72-kDa                  Transcriptional and post-transcriptional regulation of 72-kDa gelatinase/type IV
post-transcriptional                           Transcriptional and post-transcriptional regulation of a brain growth
post-transcriptional   c-fos                   Transcriptional and post-transcriptional regulation of c-fos expression by
post-transcriptional   c-jun                 Transcriptional and post-transcriptional regulation of c-jun expression during
post-transcriptional   c-myc                 Transcriptional and post-transcriptional regulation of c-myc expression during
post-transcriptional   c-myc                 Transcriptional and post-transcriptional regulation of c-myc, c-myb, and p53
post-transcriptional   complement            Transcriptional and post-transcriptional regulation of complement factor I
post-transcriptional   FSH                   Transcriptional and post-transcriptional regulation of FSH receptor in rat
post-transcriptional   globin                Transcriptional and post-transcriptional regulation of globin gene accumulation
post-transcriptional   GM-CSF-induced        Transcriptional and post-transcriptional regulation of GM-CSF-induced IL-1 beta
post-transcriptional   granulocyte-macrophageTranscriptional and post-transcriptional regulation of granulocyte-macrophage colo
post-transcriptional                         Transcriptional and post-transcriptional regulation of human MHC class
post-transcriptional   IL-1                  Transcriptional and post-transcriptional regulation of IL-1 beta, IL-6
post-transcriptional   interleukin-8         Transcriptional and post-transcriptional regulation of interleukin-8. Steady-state m
post-transcriptional   kappaB-controlled     Transcriptional and post-transcriptional regulation of kappaB-controlled genes by
post-transcriptional   LDL                   Transcriptional and post-transcriptional regulation of LDL receptor gene
post-transcriptional   L-type                Transcriptional and post-transcriptional regulation of L-type pyruvate kinase
post-transcriptional   maternal              Transcriptional and post-transcriptional regulation of maternal and zygotic
post-transcriptional   monocyte              Transcriptional and post-transcriptional regulation of monocyte chemoattractant p
post-transcriptional   Na+K(+)-ATPase        Transcriptional and post-transcriptional regulation of Na+,K(+)-ATPase alpha isofo
post-transcriptional   pr22                  Transcriptional and post-transcriptional regulation of pr22 (Op18) with proliferation
post-transcriptional   prolactin             Transcriptional and post-transcriptional regulation of prolactin during the turkey
post-transcriptional   PTH                   Transcriptional and post-transcriptional regulation of PTH gene expression
post-transcriptional   rainbow               Transcriptional and post-transcriptional regulation of rainbow trout estrogen
post-transcriptional   ribulose              Transcriptional and post-transcriptional regulation of ribulose 1,5-bisphosphate ca
post-transcriptional   storage               Transcriptional and post-transcriptional regulation of storage protein gene
post-transcriptional   TcR                   Transcriptional and post-transcriptional regulation of TcR, CD4 and CD8
post-transcriptional                         Transcriptional and post-transcriptional regulation of the asialoglycoprotein recept
post-transcriptional                         Transcriptional and post-transcriptional regulation of the genes encoding
post-transcriptional                         Transcriptional and post-transcriptional regulation of the human IGF-II
post-transcriptional                         Transcriptional and post-transcriptional regulation of the receptor for
post-transcriptional   transforming          Transcriptional and post-transcriptional regulation of transforming growth factor
post-transcriptional   tyrosine              Transcriptional and post-transcriptional regulation of tyrosine hydroxylase gene
post-transcriptional   tyrosine              Transcriptional and post-transcriptional regulation of tyrosine hydroxylase messen
post-transcriptional   vitamin               Transcriptional and post-transcriptional regulation of vitamin D-dependent calcium
post-transcriptional   expression           (cyp7) mRNA in post-transcriptional regulation of expression of the cyp7
post-transcriptional                        (GM-CSF) mRNA levels are controlled post-transcriptionally by the 3'-untranslated
post-transcriptional                        (PTH) gene expression is regulated post-transcriptionally by hypocalcemia and hyp
post-transcriptional                        (SERCA2) gene products are regulated post-transcriptionally during rat cardiac
post-transcriptional                        (TfR) and ferritin is regulated post-transcriptionally by This
post-transcriptional   Rex                  1 (HIV-1) is post-transcriptionally regulated by Rex and Rev,
post-transcriptional                        1(I) collagen mRNA. Post-transcriptional regulation of the expression of the
post-transcriptional                        1,25(OH)2D3 and the post-transcriptional regulation of the PTH
post-transcriptional                        1,4-galactosyltransferase gene is post-transcriptionally regulated during differentia
post-transcriptional   r-protein            169:271-278, 1979) before post-transcriptional regulation of r-protein synthesis wa
post-transcriptional                        2 mRNA is post-transcriptionally controlled by a unique destabilizing
post-transcriptional   p53                  24 h, the post-transcriptional regulation of p53 occurs at
post-transcriptional                        3'-untranslated sequences mediate post-transcriptional regulation of 3-hydroxy-3-m
                       3-hydroxy-3-methylglutaryl-CoA
post-transcriptional   receptor             3'UTR contribute to post-transcriptional regulation of receptor expression, and prov
post-transcriptional                        3'UTRs in the post-transcriptional regulation of the interleukin-5
post-transcriptional   beta                 a differentiation-dependent and post-transcriptional regulation of beta 3-adrenocep
post-transcriptional                        a lack of post-transcriptional control in this copper-responsive
post-transcriptional   interferon           a mechanism of post-transcriptional regulation of interferon synthesis is
post-transcriptional   Ig                   a mode of post-transcriptional control of Ig gene expression
post-transcriptional   c-myc                a model of post-transcriptional regulation of c-myc expression at
post-transcriptional   gene             A post-transcriptional control of gene expression was
post-transcriptional   expression       a potential for post-transcriptional control of expression. In support
post-transcriptional                    a result of post-transcriptional regulation of mRNA The
post-transcriptional                    a result of post-transcriptional regulation of the Dzs10 gene,
post-transcriptional   A-SAA            a role for post-transcriptional control of A-SAA biosynthesis during
post-transcriptional   gene             a role for post-transcriptional control of gene expression during
post-transcriptional   zygotic          a role for post-transcriptional regulation of zygotic gene expression
post-transcriptional   expression       a role in post-transcriptional regulation of
post-transcriptional   GS               a role in post-transcriptional regulation of GS in
post-transcriptional   heart            a role in post-transcriptional regulation of heart
post-transcriptional   SR-BI            a role in post-transcriptional regulation of SR-BI Factors
post-transcriptional   Rab              a role of post-transcriptional regulation of Rab GGTase beta
post-transcriptional   ARE-containing   a site of post-transcriptional regulation of ARE-containing
post-transcriptional                    abnormality in the post-transcriptional regulation of the type I
post-transcriptional   molecular        acid-based techniques for post-transcriptional regulation of molecular PURPOSE
post-transcriptional   ribosomal        action involves the post-transcriptional control of ribosomal gene
post-transcriptional   serum            action of additional post-transcriptional control of serum apo(a)
post-transcriptional                    activity levels may be regulated post-transcriptionally during
post-transcriptional                    additional layers of post-transcriptional regulation have been imposed to modulate
post-transcriptional   Sh1              affects transcriptional and post-transcriptional regulation of Sh1 Insertion
post-transcriptional                    After fertilisation a post-transcriptional regulation of the gene is
post-transcriptional   gene             agents for the post-transcriptional control of gene 2-5A
post-transcriptional                    alter transcriptional and/or post-transcriptional regulation of the Genotypes
post-transcriptional                    although mechanisms of post-transcriptional regulation have also been
post-transcriptional   CNPase           although transcriptional or post-transcriptional regulation of CNPase gene express
post-transcriptional                    an impairment in post-transcriptional regulation of the synthesis of tyrosine
post-transcriptional   L-myc            analysing transcriptional and post-transcriptional control of L-myc gene
post-transcriptional   c-fos            analyze transcriptional and post-transcriptional control of c-fos expression by
post-transcriptional   gidA             and asnC and post-transcriptional control of gidA. The gidA
post-transcriptional   gene             and demonstrate that post-transcriptional control of gene expression can
post-transcriptional   REH              and differences in post-transcriptional regulation of REH
post-transcriptional   MAK3             and evidence for post-transcriptional regulation of MAK3. A putative
post-transcriptional   gene             and evidence that post-transcriptional control of gene IA2 does
post-transcriptional   telomerase       and for the post-transcriptional control of telomerase enzyme activity
post-transcriptional                    and mechanisms of post-transcriptional regulation (cf. 39,
post-transcriptional                    and mspSs is post-transcriptionally controlled by different
post-transcriptional   sodA             and oxidative stress: post-transcriptional regulation of sodA Escherichia
post-transcriptional                    and PDEbeta suggested post-transcriptional regulation of their We
post-transcriptional   COX-2            and post-transcriptional events. Post-transcriptional regulation of COX-2 is depend
post-transcriptional                    and protein level was regulated post-transcriptionally as supported by
post-transcriptional                    and recovery suggests post-transcriptional regulation of the production of this
post-transcriptional   ribosomal        and suggest that post-transcriptional regulation of ribosomal protein synthesis
post-transcriptional   gene             and that the post-transcriptional regulation of gene expression by
post-transcriptional                    And this lymphokine-mediated post-transcriptional control of the TNF-alpha gene
post-transcriptional   receptor         and/or protein expression, post-transcriptional regulation of receptor activity has
post-transcriptional                    antioncogenes and the post-transcriptional regulation of the proteins for
post-transcriptional                    appear to be post-transcriptionally regulated in these Thus,
post-transcriptional   gene             approaches, suggesting that post-transcriptional regulation of gene expression is
post-transcriptional                    are capable of post-transcriptional regulation of protein synthesis and are
post-transcriptional   TRAIL-R2         are consistent with post-transcriptional regulation of TRAIL-R2 expression by
post-transcriptional   gene             as in directing post-transcriptional regulation of gene expression or in
post-transcriptional   VEGF             as well as post-transcriptional control of VEGF, in macaque
post-transcriptional                      ascorbate peroxidase expression was regulated post-transcriptionally at the level
post-transcriptional   caspase-1          astrocytoma cells, and post-transcriptional regulation of caspase-1 may determine
post-transcriptional                      at least partially be controlled post-transcriptionally by its inductors
post-transcriptional   MnSOD              basal and stimulus-dependent post-transcriptional regulation of
post-transcriptional   expression         be due to post-transcriptional control of
post-transcriptional   TGF-beta1          be due to post-transcriptional regulation of
post-transcriptional   StAR               be important in post-transcriptional regulation of StAR activity and production
post-transcriptional                      be important in post-transcriptional regulation of this gene in rodents,
post-transcriptional   gene               be involved in post-transcriptional regulation of gene
post-transcriptional   gene               be involved in post-transcriptional regulation of gene expression after
post-transcriptional   gene               be involved in post-transcriptional regulation of gene expression as
post-transcriptional   rRNA               be involved in post-transcriptional regulation of rRNA The
post-transcriptional                      Because c-myc is regulated post-transcriptionally in various mouse
post-transcriptional                      because c-myc mRNA is regulated post-transcriptionally in both
post-transcriptional   cytokine           been implicated in post-transcriptional control of cytokine gene
post-transcriptional   gene               been implicated in post-transcriptional regulation of gene expression by
post-transcriptional                      beta transcripts and post-transcriptional regulation of protein levels (beta
post-transcriptional   IRP2               between the hypoxia-induced post-transcriptional regulation of IRP2 and
post-transcriptional   Cyp2a5             between transcriptional and post-transcriptional regulation of Cyp2a5 The
post-transcriptional   gene               both transcriptional and post-transcriptional control of gene
post-transcriptional                      both transcriptional and post-transcriptional regulation of certain cellular
post-transcriptional   COX-2              Both transcriptional and post-transcriptional regulation of COX-2 involved the MAP
post-transcriptional   delta-crystallin   both transcriptional and post-transcriptional regulation of delta-crystallin Current
post-transcriptional   Pit-1              both transcriptional and post-transcriptional regulation of Pit-1 gene expression
post-transcriptional                      both transcriptional and post-transcriptional regulation of the expression of 5
post-transcriptional   mEH                but may alter post-transcriptional regulation of mEH. To identify
post-transcriptional                      but possible different post-transcriptional regulation of the mt-GrpE#1 and #2
post-transcriptional   TGF-beta1          by clenbuterol, suggesting post-transcriptional regulation of TGF-beta1 protein afte
post-transcriptional   PRL-R              by modifying the post-transcriptional regulation of
post-transcriptional   ci                 By stage 11, post-transcriptional regulation of ci is
post-transcriptional   genes              by transcriptional and post-transcriptional regulation of genes which result
post-transcriptional   acute-phase        by turpentine injection. Post-transcriptional control of acute-phase protein genes
post-transcriptional   gene               caused by defective post-transcriptional control of gene Here
post-transcriptional   annexin            Cell cycle and post-transcriptional regulation of annexin expression in IMR-90
post-transcriptional                      cell may also be regulated post-transcriptionally by glycosylation of p67
post-transcriptional   SCG10              cells, indicating that post-transcriptional regulation of SCG10 expression during
post-transcriptional   Matrigel           cells, SMC is post-transcriptionally regulated by Matrigel by inhibition
post-transcriptional   APP                cell-specific transcriptional and post-transcriptional regulation of APP gene express
post-transcriptional                      certain condition(s), but post-transcriptional regulation of their activity is
post-transcriptional                      cervical carcinomas is post-transcriptionally controlled and independent from c-my
post-transcriptional   gene               changes in the post-transcriptional control of gene Cells
post-transcriptional   COX-2              chronic inflammatory diseases. Post-transcriptional regulation of COX-2 mRNA is
post-transcriptional   gene               cis-acting elements affecting post-transcriptional control of gene expression in Sac
post-transcriptional   gene               Cis-acting elements in post-transcriptional regulation of gene expression are
post-transcriptional   ribosomal          c-Myc oncoproteins in post-transcriptional regulation of ribosomal Overexpression
post-transcriptional                      common mechanism of post-transcriptional regulation affects cytoplasmic mRNA
post-transcriptional   gene               common mechanism of post-transcriptional regulation of gene In
post-transcriptional                      Comparison of the post-transcriptional regulation of the mRNAs for
post-transcriptional   IGFBP              complex transcriptional and post-transcriptional regulation of IGFBP metabolism d
post-transcriptional                      complex transcriptional and post-transcriptional regulation of the Xenopus liver-typ
post-transcriptional   GLUT5              conclude that the post-transcriptional regulation of GLUT5 by fructose
post-transcriptional                      concomitant activation of post-transcriptional control and of cell-mediated
post-transcriptional                      Concomitant transcriptional and post-transcriptional control of mRNA abundance d
post-transcriptional   gene               configurations), 3) imaging post-transcriptional regulation of gene expression, 4)
post-transcriptional   K7                 consistent with the post-transcriptional regulation of K7, K8, and K18
post-transcriptional   CHS                content and that post-transcriptional regulation of CHS gene expression
post-transcriptional   TR                 contribute to cell-specific post-transcriptional regulation of TR gene expression
post-transcriptional                      contribute to the post-transcriptional regulation of specific
post-transcriptional   BP                 contribute to this post-transcriptional regulation of BP mRNA
post-transcriptional   gene               contributes to the post-transcriptional regulation of gene Degradation
post-transcriptional                      cooperate in the post-transcriptional regulation of human immunodeficiency virus
post-transcriptional   variable           correlated with the post-transcriptional regulation of variable alternative spliced
post-transcriptional   wheat              could affect the post-transcriptional regulation of wheat mitochondrial cox2
post-transcriptional   gene               could disturb the post-transcriptional regulation of gene
post-transcriptional                      could result from post-transcriptional regulation of the Similarly,
post-transcriptional   ferritin           critical for the post-transcriptional regulation of ferritin synthesis by
post-transcriptional   gene               crucial role in post-transcriptional regulation of gene expression modulating
post-transcriptional   IGF-I              cultures, suggesting a post-transcriptional regulation of IGF-I receptor and the
post-transcriptional   cyclin             cycle progression via post-transcriptional control of cyclin A
post-transcriptional   chloroplast        cycle-dependent transcriptional and post-transcriptional regulation of chloroplast g
post-transcriptional                      Cyclin D expression is controlled post-transcriptionally via a phosphatidylinositol
post-transcriptional   cyclin             damage checkpoint involving post-transcriptional regulation of cyclin A
post-transcriptional   NR                 data imply that post-transcriptional control of NR expression is
post-transcriptional   TK                 data indicate that post-transcriptional regulation of TK is tightly
post-transcriptional   RP                 data strongly suggest post-transcriptional regulation of RP gene expression,
post-transcriptional                      data suggest a post-transcriptional regulation of the L-FABP during
post-transcriptional                      data suggest a post-transcriptional regulation of this
post-transcriptional   gene               data suggest that post-transcriptional regulation of gene expression may
post-transcriptional   mu-RNA             data suggest that post-transcriptional regulation of mu-RNA processing might
post-transcriptional   two                decision relies on post-transcriptional regulation of two key mRNAs,
post-transcriptional                      defensin genes are post-transcriptionally regulated and that their function
post-transcriptional   ferritin           deficiency the inverse post-transcriptional regulation of ferritin and transferrin
post-transcriptional                      depend upon the post-transcriptional regulation of a single gene
post-transcriptional   Otx2               dependent on the post-transcriptional control of Otx2 mRNA, we
post-transcriptional   H19                describe a novel post-transcriptional regulation of H19 gene expression
post-transcriptional                      detected, suggesting a post-transcriptional regulation of the inhibitor in these
post-transcriptional                      development and can be regulated post-transcriptionally by glycerol or hypoxia.
post-transcriptional                      developmentally controlled by post-transcriptional regulation of the R2
post-transcriptional                      development-dependent appearance of post-transcriptional regulation
post-transcriptional                      differences in the post-transcriptional regulation of rat metallothionein
post-transcriptional   TH                 differences in the post-transcriptional regulation of TH permits neuronal
post-transcriptional                      different mechanisms of post-transcriptional regulation in young and old
post-transcriptional   TNF-alpha          differentially affect the post-transcriptional control of TNF-alpha gene
post-transcriptional   cyclooxygenase-2   differentiation factor 88-dependent post-transcriptional regulation of cyclooxygenas
post-transcriptional   expression         displays the same post-transcriptional control of expression of proliferation-related
post-transcriptional   gene               distinct roles in post-transcriptional regulation of gene expression in both
post-transcriptional                      diverse set of post-transcriptional control pathways. Their additional putative
post-transcriptional                      E2A protein induction is regulated post-transcriptionally since E2A mRNA
post-transcriptional                      E2-induced transcriptional and post-transcriptional regulation of the chicken ovalbu
post-transcriptional   blood              early trypsin is post-transcriptionally regulated by blood Early
post-transcriptional   HrcA               effect in the post-transcriptional control of HrcA. When expression
post-transcriptional                      effects on the post-transcriptional control of the H4
post-transcriptional   genes              element binding protein. Post-transcriptional regulation of genes important in iron
post-transcriptional   E(spl)-C           element in the post-transcriptional regulation of E(spl)-C First,
post-transcriptional   gene                    elements in the post-transcriptional regulation of gene The
post-transcriptional   syndecan-1              embryoid bodies, suggesting post-transcriptional regulation of syndecan-1 express
post-transcriptional   rpsA                    endonuclease mapping and post-transcriptional regulation of rpsA, the structural
post-transcriptional   proliferation-related   epithelial cells display post-transcriptional regulation of proliferation-related To
post-transcriptional                           erbB-2 protein is post-transcriptionally regulated in mammary epithelial cells
post-transcriptional   inducible               ethanol (ETOH) on post-transcriptional regulation of inducible nitric oxide
post-transcriptional   ethylene                ethylene production by post-transcriptional regulation of ethylene biosynthetic gene
post-transcriptional   collagen                evidence for a post-transcriptional control of collagen synthesis in fibroblasts.
post-transcriptional   G-protein               evidence for extensive post-transcriptional regulation of G-protein subunit accumu
post-transcriptional   testis-specific         Evidence for post-transcriptional regulation of testis-specific calcineurin
post-transcriptional                           Evidence of post-transcriptional regulation of the quinone
post-transcriptional   NRF-2                   Evidence of tissue-specific, post-transcriptional regulation of NRF-2 Mitochondrial
post-transcriptional   FSH                     Evidence suggested significant post-transcriptional regulation of FSH
post-transcriptional   chalcone                evolved, developmentally controlled post-transcriptional regulation of chalcone syn
post-transcriptional   LH                      examine transcriptional and post-transcriptional regulation of LH and FSH
post-transcriptional   PHA-induced             existence of a post-transcriptional regulation of PHA-induced cytokine release
post-transcriptional   uPAR                    experiments indicate that post-transcriptional regulation of uPAR expression requir
post-transcriptional   GLCLC                   explore transcriptional and post-transcriptional regulation of GLCLC and GLCLR
post-transcriptional   MBP                     expression and for post-transcriptional regulation of
post-transcriptional                           expression may be post-transcriptionally regulated by cellular This
post-transcriptional                           Expression of fst is regulated post-transcriptionally by RNA
post-transcriptional                           Expression of fst is regulated post-transcriptionally by RNAII
post-transcriptional                           Expression of hok is regulated post-transcriptionally by Sok antisense
post-transcriptional                           expression of hok is regulated post-transcriptionally by the sok
post-transcriptional   guidance                extensive transcriptional and post-transcriptional regulation of guidance cues and t
post-transcriptional   sodB                    factor of three. Post-transcriptional regulation of sodB was investigated
post-transcriptional   its                     factor X is post-transcriptionally regulated by its partner protein
post-transcriptional                           Fertilization triggers a post-transcriptional control of the gene and the
post-transcriptional                           FeSOD mRNA, indicating post-transcriptional regulation of the As
post-transcriptional                           fibroblasts and is post-transcriptionally regulated in response to growth
post-transcriptional   CYP2A6                  findings to the post-transcriptional control of
post-transcriptional   c-myc                   finished, suggesting a post-transcriptional regulation of c-myc gene expression;
post-transcriptional   its                     FMRP in the post-transcriptional control of its own gene
post-transcriptional   gene                    focused on the post-transcriptional regulation of gene expression of all
post-transcriptional   transgene               for a striking post-transcriptional regulation of transgene expression by
post-transcriptional                           for investigations of post-transcriptional control is the atp operon,
post-transcriptional   gene                    for schemes of post-transcriptional regulation of gene expression and viral
post-transcriptional   Sxl                     for the early post-transcriptional regulation of Sxl in XX
post-transcriptional                           for transcriptional and post-transcriptional control of the cellular thymidine
post-transcriptional                           from rat brain. Post-transcriptional regulation of mRNA metabolism is
post-transcriptional                           function in the post-transcriptional regulation of numerous germ-line RNAs,
post-transcriptional                           functional analysis and post-transcriptional regulation of a type II
post-transcriptional                           functional organization of post-transcriptional control elements, using the HIV-1
post-transcriptional   organellar              functioning in the post-transcriptional regulation of organellar gene
post-transcriptional   ACIX                    functions, and (c) post-transcriptional regulation of ACIX gene expression
post-transcriptional   FeSOD                   Fur-mediated transcriptional and post-transcriptional regulation of FeSOD express
post-transcriptional   defensin                further evidence for post-transcriptional regulation of defensin. Clearance assays
post-transcriptional   ICAM-1                  further point of post-transcriptional regulation of ICAM-1 occurs and may
post-transcriptional   p21(cip1)               GATA-6, suggesting a post-transcriptional regulation of p21(cip1) Northern
post-transcriptional                           gene could be post-transcriptionally regulated in certain species as
post-transcriptional                           gene expression through post-transcriptional regulation of mRNA The
post-transcriptional   expression              gene family shares post-transcriptional regulation of expression, albeit by
post-transcriptional                    gene may be post-transcriptionally regulated and/or the IDO co-factor
post-transcriptional                    gene, indicating differential post-transcriptional regulation of this storage protein
post-transcriptional                    general aspect of post-transcriptional control which, in the past,
post-transcriptional                    genes by influencing post-transcriptional control of mRNA stability or mRNA
post-transcriptional                    glucose cotransporter SGLT1 is regulated post-transcriptionally at the level
post-transcriptional                    governing the largely post-transcriptional regulation of the intermediate steps
post-transcriptional                    G-protein coupled receptors, are regulated post-transcriptionally at the level
post-transcriptional   gene             granules may affect post-transcriptional regulation of gene expression via
post-transcriptional   4E-BP2           granulocytic maturation, whereas post-transcriptional regulation of 4E-BP2 express
post-transcriptional                    greater contribution of post-transcriptional regulation accounts for changes in expr
post-transcriptional   tryptophan       Green, Post-transcriptional control of tryptophan hydroxylase gene
post-transcriptional                    growth factor (VEGF) are regulated post-transcriptionally by proteins binding
post-transcriptional                    H1 appears to be regulated post-transcriptionally by a mechanism
post-transcriptional                    have investigated the post-transcriptional regulation of three of these
post-transcriptional   p53              have localized the post-transcriptional regulation of p53 mRNA in the
post-transcriptional                    have roles in post-transcriptional regulation of the expression of specific
post-transcriptional   HIV              helicase A in post-transcriptional regulation of HIV type
post-transcriptional                    HGRG-14 seems to be regulated post-transcriptionally and encodes a small
post-transcriptional                    high level of post-transcriptional regulation of RNA abundance during
post-transcriptional   interaction      higher eukaryotes is post-transcriptionally regulated by interaction of iron-responsiv
post-transcriptional   uMtCK            highly regulated, and post-transcriptional regulation of uMtCK and BCK
post-transcriptional   enzyme           hydroxymethyltransferase in the post-transcriptional regulation of enzyme Eliminat
post-transcriptional                    IGFBP4 may also be regulated post-transcriptionally by a protease
post-transcriptional   IGF-IRs          IGF-IR mRNA implies post-transcriptional regulation of IGF-IRs. Our results
post-transcriptional   gene             implicated in the post-transcriptional regulation of gene In
post-transcriptional                    important form of post-transcriptional control that is expected to act
post-transcriptional   TNF-alpha        important in the post-transcriptional regulation of TNF-alpha
post-transcriptional                    important mechanism of post-transcriptional regulation of nuclear CK-2 in relation
post-transcriptional   gene             important role in post-transcriptional regulation of gene expression, including
post-transcriptional   TGF-beta         important role in post-transcriptional regulation of TGF-beta 1 gene
post-transcriptional                    important to the post-transcriptional regulation of these key components
post-transcriptional                    in Caenorhabditis elegans. Post-transcriptional regulation of the sex-determining tr
post-transcriptional                    in favor of post-transcriptional regulation of protein The
post-transcriptional   histone          in G1-arrested cells. Post-transcriptional regulation of histone gene expression
post-transcriptional                    in iron metabolism is regulated post-transcriptionally by the binding
post-transcriptional   gene             in part by post-transcriptional control of gene expression, and has
post-transcriptional                    in part, by post-transcriptional control of mRNA
post-transcriptional                    in Schizosaccharomyces pombe: post-transcriptional regulation of mRNA stability
post-transcriptional                    in stamens, suggesting post-transcriptional regulation of the fbp1 gene
post-transcriptional   gene             in the virally-induced post-transcriptional control of gene Us11
post-transcriptional   ferritin         in transcription and post-transcriptional regulation of ferritin expression in Parkinso
post-transcriptional   MOK2             in transcription and post-transcriptional regulation of MOK2 target
post-transcriptional   apolipoprotein   in transcriptional and post-transcriptional regulation of apolipoprotein A-I by
post-transcriptional   gene             in transcriptional and post-transcriptional regulation of gene expression were
post-transcriptional                    include transcriptional and post-transcriptional regulation of the genes encoding
post-transcriptional   AflR             independent but RasA post-transcriptional control of AflR is partially
post-transcriptional   gene             indicated a massive post-transcriptional regulation of gene expression, the latter
post-transcriptional   bcl-2            indirect evidence of post-transcriptional control of bcl-2 and bax
post-transcriptional   IL-2             individuals could involve post-transcriptional regulation of IL-2
post-transcriptional   D(3)R            induces changes in post-transcriptional regulation of D(3)R expression in remainin
post-transcriptional   nonsense         influence on the post-transcriptional control of nonsense mutated beta-globin
post-transcriptional                    influence on the post-transcriptional regulation of the GLUT4 transporter
post-transcriptional   MyoD               inhibits myogenesis by post-transcriptional regulation of MyoD function: COUP-TF
post-transcriptional   gene               interactions in the post-transcriptional regulation of gene In
post-transcriptional   gene               intercistronic region in post-transcriptional control of gene expression in the
post-transcriptional   c-myb              Interestingly, the post-transcriptional regulation of c-myb by DMSO
post-transcriptional   transferrin        Interleukin-2-dependent transcriptional and post-transcriptional regulation of transf
post-transcriptional                      involved in a post-transcriptional control of the RHBP
post-transcriptional   arginine           involved in the post-transcriptional control of arginine metabolism in Saccharomyce
post-transcriptional                      involved in the post-transcriptional control of the citQRP operon
post-transcriptional   Eg                 involved in the post-transcriptional regulation of Eg mRNAs, gel-shift
post-transcriptional   GAP-43             involved in the post-transcriptional regulation of GAP-43 gene expression
post-transcriptional                      involved in the post-transcriptional regulation of mRNA expression for
post-transcriptional                      involved in the post-transcriptional regulation of the expression and function
post-transcriptional                      involved in the post-transcriptional regulation of the IL-8
post-transcriptional                      involved in the post-transcriptional regulation of the mouse catalase
post-transcriptional                      involved in the post-transcriptional regulation of the SV2B
post-transcriptional   type-I             involved in the post-transcriptional regulation of type-I 15-PGDH gene
post-transcriptional   ferritin           involves the coordinate post-transcriptional regulation of ferritin mRNA translation
post-transcriptional                      IRF-1 activity is post-transcriptionally regulated in addition to transcriptional
post-transcriptional                      iron levels by post-transcriptional regulation of the ferritin and transferrin
post-transcriptional                      iron regulatory protein-1. Post-transcriptional regulation of mRNA translation and s
post-transcriptional   HTH                is also a post-transcriptional control of HTH by exd:
post-transcriptional   rbcS               is also significant post-transcriptional control of rbcS gene expression
post-transcriptional   preapocytochrome   is attributed to post-transcriptional regulation of preapocytochrome f synthesis
post-transcriptional   gene               is critical to post-transcriptional regulation of gene expression, yet
post-transcriptional   TNF-alpha          is implicated in post-transcriptional control of TNF-alpha. In this
post-transcriptional   nitrate            is involved in post-transcriptional control of nitrate
post-transcriptional   ferritin           is involved in post-transcriptional regulation of ferritin
post-transcriptional   gene               is involved in post-transcriptional regulation of gene expression either
post-transcriptional   H-ferritin         is involved in post-transcriptional regulation of H-ferritin gene expression
post-transcriptional   SV2Bb              is involved in post-transcriptional regulation of SV2Bb When
post-transcriptional   TNF-alpha          is involved in post-transcriptional regulation of TNF-alpha production at
post-transcriptional   gene               is known for post-transcriptional control of gene In
post-transcriptional   immediate-early    is mediated by post-transcriptional regulation of immediate-early gene
post-transcriptional   viral              is mediated by post-transcriptional regulation of viral immediate-early gene
post-transcriptional   rpsB               is necessary for post-transcriptional control of rpsB The
post-transcriptional                      is presented for post-transcriptional regulation of the two responses
post-transcriptional   either             it known whether post-transcriptional regulation of either gene product
post-transcriptional   MeCP2              its function in post-transcriptional regulation of MeCP2
post-transcriptional   histone            key element for post-transcriptional regulation of histone gene expression
post-transcriptional   gene               key for understanding post-transcriptional regulation of gene expression? The
post-transcriptional   gene               key step in post-transcriptional control of gene Therefore,
post-transcriptional   ikappabalpha       kinase calpha in post-transcriptional regulation of ikappabalpha The
post-transcriptional   VEGF               kinases in the post-transcriptional regulation of
post-transcriptional   gene               LDH in the post-transcriptional regulation of gene
post-transcriptional   4E-BP2             level suggesting a post-transcriptional regulation of 4E-BP2 In
post-transcriptional                      level, mechanisms of post-transcriptional control such as glucose-regulated stabilit
post-transcriptional                      lic in a post-transcriptional regulation of the grk
post-transcriptional                      likely due to post-transcriptional regulation of the COXII subunit
post-transcriptional   CPG-1              lipid modification in post-transcriptional regulation of CPG-1
post-transcriptional                      LP mRNAs increased. Post-transcriptional regulation of the expression of the
post-transcriptional   trfA               maintenance, possibley through post-transcriptional regulation of trfA product level
post-transcriptional                      maize r1 gene is regulated post-transcriptionally by differential splicing
post-transcriptional                      mammalian cells is post-transcriptionally regulated by the interaction of iron-respon
post-transcriptional                      markers by glucocorticoids: post-transcriptional regulation of both proteolipid prote
post-transcriptional   MMP-9              may mediate the post-transcriptional regulation of
post-transcriptional   genes              may modulate the post-transcriptional regulation of genes involved in iron
post-transcriptional   GS-2               may reflect a post-transcriptional control of GS-2 protein
post-transcriptional                      may reflect the post-transcriptional regulation of cell-specific gene expression
post-transcriptional   phenotype          meaning part) denotes post-transcriptional regulation of phenotype of restricted
post-transcriptional   gene               mechanism for the post-transcriptional regulation of gene expression in mammals.
post-transcriptional   gene               mechanism in the post-transcriptional regulation of gene expression, which
post-transcriptional   ER                 mechanisms involved in post-transcriptional regulation of ER mRNA showed
post-transcriptional   huntingtin         Mechanisms involving the post-transcriptional regulation of huntingtin are not
post-transcriptional                      Mechanisms of post-transcriptional control of the hsp 70
post-transcriptional   gene               mechanisms of the post-transcriptional control of gene expression, a feature
post-transcriptional                      mechanisms that include post-transcriptional regulation of the 91 kDa
post-transcriptional   DAZ                mechanisms underlying the post-transcriptional regulation of DAZ family proteins
post-transcriptional   key                mediate the coordinate post-transcriptional regulation of key proteins in iron
post-transcriptional   cyclooxygenase-2   mediates transcriptional and post-transcriptional control of cyclooxygenase-2 (COX
post-transcriptional   transforming       milk, which is post-transcriptionally regulated by transforming growth factor
post-transcriptional   proteolytic        MMP activity is post-transcriptionally regulated by proteolytic activation of the
post-transcriptional                      model for the post-transcriptional regulation of the human c-myc
post-transcriptional   mom                models for the post-transcriptional regulation of mom gene expression
post-transcriptional   enzyme             modifications allowing a post-transcriptional regulation of enzyme activities or rece
post-transcriptional   ME1                Molecular characterization and post-transcriptional regulation of ME1, a type-I
post-transcriptional   glucocorticoids    most examples of post-transcriptional regulation by glucocorticoids, acts in the
post-transcriptional   Bearded            motif, mediates negative post-transcriptional regulation of Bearded and Enhancer
post-transcriptional                      mRNA abundance is post-transcriptionally regulated during development of Leishm
post-transcriptional                      mRNA in the post-transcriptional regulation of this A
post-transcriptional                      mRNA level is post-transcriptionally regulated and that the presence
post-transcriptional   A-SAA              mRNA levels and post-transcriptional regulation of A-SAA and C-SAA
post-transcriptional                      mRNA message stability. Post-transcriptional regulation of mRNA turnover plays
post-transcriptional   its                mRNA on the post-transcriptional control of its expression was
post-transcriptional   IL-1               mRNA, transcriptional and post-transcriptional regulation of IL-1 beta mRNA
post-transcriptional   NGF                mRNAs that are post-transcriptionally regulated by NGF. In PC12
post-transcriptional                      multiple layers of post-transcriptional control are executed by these
post-transcriptional   collagenase        Multiple levels of post-transcriptional regulation of collagenase (matrix metalloprote
post-transcriptional                      murine orthologue Cyp2a5 is regulated post-transcriptionally by mRNA
post-transcriptional   SOS1               NaCl treatment, suggesting post-transcriptional control of SOS1 transcript
post-transcriptional                      necessary for the post-transcriptional regulation of these mRNAs by
post-transcriptional   RNA-binding        neuropsychopharmacological understanding of post-transcriptional regulation by R
post-transcriptional   T3                 neuroserpin expression is post-transcriptionally regulated by T3 at the level
post-transcriptional   neuronal           NGF signaling and post-transcriptional control of neuronal gene
post-transcriptional                      nitrate assimilation pathway, is regulated post-transcriptionally in response to light
post-transcriptional                      nmt55/p54nrb protein is post-transcriptionally regulated in human breast tumors
post-transcriptional   albumin            No evidence for post-transcriptional control of albumin and alpha-fetoprotein
post-transcriptional                      no evidence for post-transcriptional control of the Cx43 gene
post-transcriptional   vitellogenin       nonylphenol on the post-transcriptional regulation of vitellogenin gene
post-transcriptional                      not required for post-transcriptional control of the irr
post-transcriptional                      novel form of post-transcriptional control is described. The 5'
post-transcriptional   gene               novel mechanism for post-transcriptional control of gene expression, although
post-transcriptional                      novel mechanism for post-transcriptional regulation of a multigene family
post-transcriptional                      novel mode of post-transcriptional regulation applies to Brd and many
post-transcriptional                      nuclear) involved in post-transcriptional regulation of this RNA during
post-transcriptional                       number of genes are regulated post-transcriptionally via the interaction
post-transcriptional                       of a demonstrated post-transcriptional control of the bcl-2 gene,
post-transcriptional   FGF-2               of a multilevel post-transcriptional control of FGF-2 expression; such
post-transcriptional                       of a well-demonstrated post-transcriptional control of the gene, the authors
post-transcriptional                       of both proteins is regulated post-transcriptionally by the interaction
post-transcriptional   elastin             of elastin mRNA. Post-transcriptional control of elastin expression appears
post-transcriptional   catalase            of MnSOD and post-transcriptional regulation of catalase gene expression
post-transcriptional                       of NO may be regulated post-transcriptionally by other factors
post-transcriptional   Id4                 of polyadenylation and/or post-transcriptional regulation of Id4 However,
post-transcriptional                       of ribulose-1,5-bisphosphate carboxylase) is regulated post-transcriptionally during
post-transcriptional   EGF                 of T3 in post-transcriptional control of EGF receptor expression,
post-transcriptional   transferrin         of the mRNA. Post-transcriptional regulation of transferrin receptor mRNA
post-transcriptional                       of this protein is controlled post-transcriptionally by a small
post-transcriptional                       of Tra is post-transcriptionally controlled and thus is not
post-transcriptional   beta-F1-ATPase      of transcriptional and post-transcriptional control of beta-F1-ATPase gene express
post-transcriptional   liver-specific      of transcriptional and post-transcriptional control of liver-specific gene expression
post-transcriptional   gamma-zein          of transcriptional and post-transcriptional regulation of gamma-zein gene expressio
post-transcriptional                       of transcriptional and post-transcriptional regulation of mRNAs to the increase
post-transcriptional   its                 of transcriptional or post-transcriptional regulation of its Results
post-transcriptional                       of TuKv2 is post-transcriptionally controlled through a mechanism that
post-transcriptional   maternal            often relies on post-transcriptional control of maternal Although
post-transcriptional   acetyl-CoA          on transcriptional and post-transcriptional regulation of acetyl-CoA carboxylase in r
post-transcriptional   fatty               on transcriptional and post-transcriptional regulation of fatty acid synthase
post-transcriptional   fibronectin         on transcriptional and post-transcriptional regulation of fibronectin in human
post-transcriptional   glucose-6-phosphate on transcriptional and post-transcriptional regulation of glucose-6-phosphate dehyd
post-transcriptional   malic               on transcriptional and post-transcriptional regulation of malic enzyme and glucose-
post-transcriptional   malic               on transcriptional and post-transcriptional regulation of malic enzyme synthesis
post-transcriptional                       on transcriptional and post-transcriptional regulation of protein production, the tran
post-transcriptional   IL-6                on transcriptional or post-transcriptional regulation of IL-6 gene expression
post-transcriptional                       only limited homology. Post-transcriptional control of the differential expression
post-transcriptional                       oocytes bFGF mRNA is regulated post-transcriptionally by interaction with an
post-transcriptional   micF                osmolarity, OmpF is post-transcriptionally regulated by micF mRNA, and that
post-transcriptional   glutaminyl-tRNA     our results suggest post-transcriptional regulation of glutaminyl-tRNA
post-transcriptional                       overexpressed, suggestive of post-transcriptional regulation (Lipschutz, J. H., Guo
post-transcriptional                       oxide and the post-transcriptional control of cellular iron
post-transcriptional   cAMP                P450scc activity, is post-transcriptionally regulated by
post-transcriptional                       PAI-2 mRNA could be regulated post-transcriptionally by PAI-2
post-transcriptional   maternal            part of the post-transcriptional regulation of maternal mRNAs in embryos.
post-transcriptional   APP                 participate in the post-transcriptional regulation of APP mRNA through
post-transcriptional   gene                participate in the post-transcriptional regulation of gene expression during
post-transcriptional   IGF-II              participate in the post-transcriptional regulation of IGF-II
post-transcriptional   pro-inflammatory    pathway in the post-transcriptional regulation of pro-inflammatory gene
post-transcriptional   expression          Pbs21 confirmed that post-transcriptional control of expression occurred in the
post-transcriptional   Kit                 period, suggesting that post-transcriptional regulation of Kit production is
post-transcriptional                       phosphorylase gene expression is regulated post-transcriptionally in late gestation
post-transcriptional   TNFalpha            pivotal role in post-transcriptional control of TNFalpha Certain
post-transcriptional                       plasmid R1 is post-transcriptionally controlled by an antisense RNA,
post-transcriptional   gene                players in the post-transcriptional control of gene We
post-transcriptional   gene                polyadenylation in the post-transcriptional control of gene
post-transcriptional   TGF-beta2           polyadenylation sites, indicating post-transcriptional regulation of TGF-beta2 The
post-transcriptional   gene                polycistronic transcription and post-transcriptional regulation of gene The
post-transcriptional                       population in cells is controlled post-transcriptionally by ribonucleases (RNases)
post-transcriptional                   possibility that the post-transcriptional control of the alpha-smooth muscle
post-transcriptional   receptor        Possible involvement in post-transcriptional regulation of receptor Numerous
post-transcriptional                   possible involvement of post-transcriptional regulation of mRNAs associated with t
post-transcriptional   which           possible mechanism of post-transcriptional control by which these genes
post-transcriptional   E74A            possible mechanisms for post-transcriptional regulation of E74A expression and su
post-transcriptional   BRCA1           possible transcriptional or post-transcriptional regulation of BRCA1 and BRCA2
post-transcriptional   c-myc           potential importance of post-transcriptional regulation of c-myc gene
post-transcriptional   gene            potential involvement in post-transcriptional regulation of gene Comparison
post-transcriptional                   presented and the post-transcriptional regulation of specific genes of nutritional
post-transcriptional   gene            processing and in post-transcriptional regulation of gene By
post-transcriptional   gene            production mechanisms and post-transcriptional regulation of gene Our
post-transcriptional   casein          Prolactin-mediated transcriptional and post-transcriptional control of casein gene
post-transcriptional   MHC             promoter activity, suggesting post-transcriptional control of MHC class I
post-transcriptional   p21             proteasome pathway in post-transcriptional regulation of p21. By the addition
post-transcriptional                   protein in the post-transcriptional regulation of a competence specific
post-transcriptional   LH              protein in the post-transcriptional regulation of LH receptor expression
post-transcriptional                   protein may mediate post-transcriptional control of specific RNA transcripts
post-transcriptional   expression      protein responsible for post-transcriptional regulation of expression of several
post-transcriptional                   protein that is post-transcriptionally regulated in vitro. Studies reported
post-transcriptional                   protein whose synthesis is regulated post-transcriptionally by a mechanism
post-transcriptional   AR              proteins in the post-transcriptional regulation of AR expression in cancer
post-transcriptional   HIV             proteins) in the post-transcriptional regulation of HIV Overexpression
post-transcriptional   rotavirus       provide evidence for post-transcriptional control of rotavirus gene expression
post-transcriptional   psbA            provide evidence for post-transcriptional regulation of psbA gene expression,
post-transcriptional                   ptsG levels are post-transcriptionally regulated by the glycolytic
post-transcriptional                   receptor expression is post-transcriptionally regulated by a conserved mRNA
post-transcriptional                   receptor function via post-transcriptional regulation of the NMDAR1 subunit
post-transcriptional                   receptor protein suggests post-transcriptional control in PC12 Expression
post-transcriptional   5-HT2C          receptor, and that post-transcriptional control of 5-HT2C receptor expression
post-transcriptional   extracellular   receptor-related protein is post-transcriptionally regulated by extracellular The
post-transcriptional                   recombination either by post-transcriptional regulation of the RAG genes
post-transcriptional   CD40L           regarding transcriptional and post-transcriptional regulation of CD40L expression in
post-transcriptional   expression      regenerating liver, indicating post-transcriptional regulation of expression of this
post-transcriptional   messengers      regions, suggesting the post-transcriptional regulation of messengers by iron
post-transcriptional   antisense       related bacteria is post-transcriptionally regulated by antisense micF
post-transcriptional                   related to the post-transcriptional regulation of the waxy
post-transcriptional   ferritin        relies on the post-transcriptional control of ferritin and transferrin
post-transcriptional   apoA-I          remain unaltered, suggesting post-transcriptional regulation of apoA-I production in
post-transcriptional                   report a novel post-transcriptional control of the ptsG gene
post-transcriptional   ferritin        reports describing a post-transcriptional control of ferritin amounts during
post-transcriptional   telomerase      required for the post-transcriptional control of telomerase enzyme activity
post-transcriptional   serum           requires transcriptional and post-transcriptional control of serum response
post-transcriptional                   response to copper, post-transcriptional regulation of these proteins is
post-transcriptional   c-Jun           responsible for the post-transcriptional control of c-Jun proto-oncogene mRNA
post-transcriptional   apoB            responsible for the post-transcriptional regulation of apoB
post-transcriptional                   resulted in additional post-transcriptional control of the PsbS transcript
post-transcriptional   message         results demonstrate that post-transcriptional regulation of message stability plays
post-transcriptional   myoD            results demonstrate that post-transcriptional regulation of myoD family members
post-transcriptional   cPLA2           results indicate predominant post-transcriptional regulation of cPLA2 mRNA
post-transcriptional   myogenin        results indicate that post-transcriptional regulation of myogenin may occur
post-transcriptional   gene            results indicated a post-transcriptional regulation of gene expression during
post-transcriptional                   results suggest that post-transcriptional control of mRNAs in trypanosomatids
post-transcriptional   gp185erbB-2     results suggest that post-transcriptional regulation of gp185erbB-2 expression may
post-transcriptional   IkappaB-alpha   results suggest that post-transcriptional regulation of IkappaB-alpha expression mi
post-transcriptional                   results suggest that post-transcriptional regulation of mRNA stability is
post-transcriptional   keratin         Retinoic acid mediates post-transcriptional regulation of keratin 19 mRNA
post-transcriptional   interleukin     Review: transcriptional and post-transcriptional regulation of interleukin 1 gene
post-transcriptional                   Rex protein in post-transcriptional control of human T-cell leukemia/lymphoma
post-transcriptional                   RFPL3S is a post-transcriptional regulation of the sense RFPL
post-transcriptional   tubulin         RNA structure and post-transcriptional control of tubulin gene
post-transcriptional   parathyroid     RNA-Protein binding and post-transcriptional regulation of parathyroid hormone ge
post-transcriptional   chloroplast     RNPs in the post-transcriptional regulation of chloroplast gene expression
post-transcriptional   VEGF            role in hypoxia-induced post-transcriptional regulation of VEGF mRNA
post-transcriptional   TRAP100         role in male-specific post-transcriptional regulation of TRAP100 in the D.
post-transcriptional   HIV             role in the post-transcriptional regulation of
post-transcriptional   all             role in the post-transcriptional regulation of all complex
post-transcriptional   Cas-1           role in the post-transcriptional regulation of Cas-1. Although the observed
post-transcriptional   CD40L           role in the post-transcriptional regulation of CD40L gene
post-transcriptional   FGF-2           role in the post-transcriptional regulation of FGF-2, but this
post-transcriptional   gene            role in the post-transcriptional regulation of gene expression in macrophages
post-transcriptional   gene            role in the post-transcriptional regulation of gene They
post-transcriptional   IL-1beta        role in the post-transcriptional regulation of IL-1beta To
post-transcriptional                   role in the post-transcriptional regulation of the 5-HT2C receptor,
post-transcriptional                   role in the post-transcriptional regulation of these Known
post-transcriptional   gene            roles in the post-transcriptional regulation of gene expression but
post-transcriptional   gene            roles in the post-transcriptional regulation of gene Here
post-transcriptional   ABI8            roots, suggesting substantial post-transcriptional regulation of ABI8 This
post-transcriptional                   R-PIA, suggesting a post-transcriptional regulation of this receptor during
post-transcriptional                   rtPCR suggested a post-transcriptional regulation of this molecule by
post-transcriptional   proline         salt stress, suggesting post-transcriptional control of proline biosynthesis in respon
post-transcriptional   gene            scaffolds for the post-transcriptional control of gene Most
post-transcriptional   IL1-alpha       secretion reflected primarily post-transcriptional regulation of IL1-alpha mRNA, tran
post-transcriptional                   segregation, indicating that post-transcriptional regulation of mRNA levels takes
post-transcriptional                   sequence that mediates post-transcriptional regulation of rat CYP2E1 by
post-transcriptional   IGF-IR          sequence to the post-transcriptional regulation of IGF-IR expression would
post-transcriptional   ATM             sequences suggests complex post-transcriptional regulation of ATM gene
post-transcriptional                   shape and is post-transcriptionally regulated by the dbl-1
post-transcriptional                   shock likely via post-transcriptional regulation of the Hsp47
post-transcriptional                   showed that fem-3 is regulated post-transcriptionally to achieve the sperm/oocyte
post-transcriptional   aflR            shows that FlbA post-transcriptional regulation of aflR is PkaA
post-transcriptional                   significantly different suggesting post-transcriptional regulation of the receptor play
post-transcriptional                   silencing process is post-transcriptionally regulated and subject to developmental
post-transcriptional                   similar pattern of post-transcriptional regulation was observed for a transfected
post-transcriptional   c-myc           smooth muscle cells. Post-transcriptional control of c-myc Proliferation
post-transcriptional                   some effect on post-transcriptional regulation of the stability of mRNA
post-transcriptional   either          some form of post-transcriptional regulation of either P5CS or P5CR.
post-transcriptional   salt            SOS1 mRNA are post-transcriptionally regulated by salt In
post-transcriptional   gene            spliceosomes and the post-transcriptional regulation of gene Among
post-transcriptional   gene            SSD1 functions in post-transcriptional regulation of gene The
post-transcriptional   selected        state coincides with post-transcriptional regulation of selected cytokine
post-transcriptional   GnRH            step for the post-transcriptional regulation of GnRH
post-transcriptional   ohrR            steps in the post-transcriptional regulation of ohrR, namely differential
post-transcriptional   At-HSP176A      stress, suggesting stress-induced post-transcriptional regulation of At-HSP17.6A O
post-transcriptional                   subunit in soybean. Post-transcriptional regulation of the genes encoding
post-transcriptional   Arabidopsis     suggest a complex post-transcriptional regulation of Arabidopsis U1-70K gene
post-transcriptional   myc             suggest that the post-transcriptional control of myc gene expression
post-transcriptional   viral           suggest that the post-transcriptional regulation of viral structural gene
post-transcriptional   rPRL            suggesting a cell-specific post-transcriptional control of rPRL During
post-transcriptional                   suggesting that expression is controlled post-transcriptionally during Inhibition
post-transcriptional   Karma           suggesting that the post-transcriptional regulation of Karma retrotransposition is
post-transcriptional   gene            suggests that additional post-transcriptional regulation of gene expression occurs
post-transcriptional   expression      suggests that the post-transcriptional regulation of expression of histone
post-transcriptional                   synthesis may be post-transcriptionally controlled under these
post-transcriptional                   system of oxygen-dependent post-transcriptional regulation of the quinone biosynt
post-transcriptional   gene            target in the post-transcriptional regulation of gene
post-transcriptional   COX-2           Tau-Cl affects the post-transcriptional regulation of COX-2 expression and suppor
post-transcriptional   SCG10           temporal and spatial post-transcriptional regulation of SCG10 expression which
post-transcriptional   gene            terms of the post-transcriptional regulation of gene expression in the
post-transcriptional   intracellular   TfR mRNA is post-transcriptionally regulated by intracellular Low
post-transcriptional                   that elav is post-transcriptionally regulated and we demonstrate that
post-transcriptional                   that gene expression is controlled post-transcriptionally as well as
post-transcriptional   fetal           that modulate the post-transcriptional regulation of fetal human small
post-transcriptional                   that modulates the post-transcriptional regulation of the PAI-2
post-transcriptional                   that subunit stoichiometry is controlled post-transcriptionally in var1 and var2,
post-transcriptional   iNOS            that the Gö6976-mediated post-transcriptional regulation of iNOS gene expressio
post-transcriptional                   that the latter is regulated post-transcriptionally by enterocyte iron
post-transcriptional                   that there is post-transcriptional control of the level of rpoH
post-transcriptional                   that there is post-transcriptional control of the three selenoenzymes,
post-transcriptional   beta2m          that there is post-transcriptional regulation of beta2m generation and/or
post-transcriptional   EAAT2           the 3'-UTR in post-transcriptional regulation of EAAT2 gene
post-transcriptional                   the asialoglycoprotein receptor. Post-transcriptional regulation of the asialoglyco-p
post-transcriptional                   the beta 2-receptor is regulated post-transcriptionally by agonist and cAMP.
post-transcriptional   ERF             The effect of post-transcriptional regulation of ERF activity, especially
post-transcriptional                   the elucidation of post-transcriptional control mechanisms of interferon synthesis
post-transcriptional                   the existence of post-transcriptional control mechanisms that govern sigma
post-transcriptional   GLUT4           the existence of post-transcriptional regulation of GLUT4 expression which
post-transcriptional                   The factors-regulators of post-transcriptional regulation of the rate of catalase
post-transcriptional   p38             the field of post-transcriptional regulation by
post-transcriptional                   the genes can be regulated post-transcriptionally in T
post-transcriptional   gene            the importance of post-transcriptional control of gene expression in prokaryotes
post-transcriptional                   the importance of post-transcriptional regulation and the role of the
post-transcriptional                   the importance of post-transcriptional regulation in antizyme
post-transcriptional   antioxidant     the importance of post-transcriptional regulation of antioxidant enzyme gene
post-transcriptional                   the importance of post-transcriptional regulation to the control of SSAT
post-transcriptional                   the iNOS/NO system, post-transcriptional control of this system may
post-transcriptional                   the involvement of post-transcriptional regulation as a mechanism of cyclin
post-transcriptional                   the involvement of post-transcriptional regulation mechanisms. Finally, we found
post-transcriptional   gene            the long term post-transcriptional regulation of gene expression during
post-transcriptional   HLA-G           the mechanisms controlling post-transcriptional regulation of HLA-G molecule asso
post-transcriptional   slow            the possibility of post-transcriptional control of slow troponin C
post-transcriptional                   the possibility of post-transcriptional regulation at the level of processing
post-transcriptional   ABCA1           the possibility of post-transcriptional regulation of ABCA1 expression in selected
post-transcriptional   histone         the possibility of post-transcriptional regulation of histone gene expression
post-transcriptional                   the possibility of post-transcriptional regulation of the expression mt
post-transcriptional                   the possibility of post-transcriptional regulation of the With
post-transcriptional                   The post-transcriptional control of the mRNA-S11 and its
post-transcriptional   caspase-3             The post-transcriptional regulation of caspase-3 might serve
post-transcriptional   factors               The post-transcriptional regulation of factors involved in the
post-transcriptional   gene                  The post-transcriptional regulation of gene expression by
post-transcriptional   gene                  The post-transcriptional regulation of gene expression underlies
post-transcriptional   genes                 The post-transcriptional regulation of genes of iron
post-transcriptional   histone               The post-transcriptional regulation of histone mRNA abundance
post-transcriptional   NR                    The post-transcriptional regulation of NR by light
post-transcriptional                         The post-transcriptional regulation of other rapidly degraded
post-transcriptional   RESP18                The post-transcriptional regulation of RESP18 expression and localization
post-transcriptional                         The post-transcriptional regulation of the BBB-GLUT1 gene
post-transcriptional                         the potential for post-transcriptional regulation of the avian MT
post-transcriptional                         the presence of post-transcriptional regulation events: an upstream ORF,
post-transcriptional                         the role of post-transcriptional regulation in cardiac myosin gene
post-transcriptional                         the role of post-transcriptional regulation in development by studying
post-transcriptional                         the TATA box is controlled post-transcriptionally by Induction
post-transcriptional                         the transcription and post-transcriptional regulation of the chicken HSP70
post-transcriptional   embryonic             The transcriptional and post-transcriptional control of embryonic globin gene
post-transcriptional   AMPA                  the transcriptional and post-transcriptional regulation of AMPA and kainate
post-transcriptional   expression            the transcriptional and post-transcriptional regulation of expression of the NMDA
post-transcriptional   Giardia               the transcriptional and post-transcriptional regulation of Giardia genes, including
post-transcriptional   glucose-6-phosphate The transcriptional and post-transcriptional regulation of glucose-6-phosphate deh
post-transcriptional   iNOS                  the transcriptional and post-transcriptional regulation of iNOS and TNFalpha
post-transcriptional   malic                 the transcriptional and post-transcriptional regulation of malic enzyme induction
post-transcriptional   MMP-1                 the transcriptional and post-transcriptional regulation of MMP-1 gene expression
post-transcriptional   MnSOD                 the transcriptional and post-transcriptional regulation of MnSOD gene (sodA)
post-transcriptional   prolactin             the transcriptional and post-transcriptional regulation of prolactin (PRL) by
post-transcriptional                         The transcriptional and post-transcriptional regulation of specific genes and metab
post-transcriptional                         the transcriptional and post-transcriptional regulation of the human laminin
post-transcriptional                         the transcriptional and post-transcriptional regulation of the Porcellio scaber
post-transcriptional                         the transcriptional and post-transcriptional regulation of this This
post-transcriptional                         the ureIEFGH operon is regulated post-transcriptionally by mRNA decay
post-transcriptional                         their steady-state abundance is regulated post-transcriptionally with increased mR
post-transcriptional   CD8A                  there is also post-transcriptional regulation of CD8A expression in a
post-transcriptional                         there is considerable post-transcriptional regulation of the expression of this
post-transcriptional                         there may be post-transcriptional control of mRNA The
post-transcriptional                         therefore involved in post-transcriptional regulation of the methionine-rich 10
post-transcriptional   N-myc                 Therefore, post-transcriptional control of N-myc gene expression
post-transcriptional   Epo                   Therefore, the post-transcriptional regulation of Epo expression in response
post-transcriptional                         these interactions and post-transcriptional regulation of the MyHC genes
post-transcriptional                         These proteins are regulated post-transcriptionally by interaction of specific
post-transcriptional   PTH                   These results demonstrate post-transcriptional regulation of PTH synthesis in cultu
post-transcriptional                         this enzyme in post-transcriptional regulation of lipopolysaccharide-induced expres
                       lipopolysaccharide-induced
post-transcriptional   TNF-alpha             This indicates differential post-transcriptional control of TNF-alpha in activated
post-transcriptional                         This indicates post-transcriptional regulation which, due to the similarity
post-transcriptional   histone               This indicates that post-transcriptional control of histone mRNA levels
post-transcriptional   INFgamma              this may represent post-transcriptional regulation of INFgamma expression in CFA
post-transcriptional   tobacco               This post-transcriptional regulation of tobacco leaf NiR1
post-transcriptional                         This process is regulated post-transcriptionally by the viral-encoded
post-transcriptional   hepatic               This reveals another post-transcriptional control of hepatic albumin
post-transcriptional   MAK3                  This suggests a post-transcriptional control of MAK3 expression by
post-transcriptional   Ac                    This suggests that post-transcriptional regulation of Ac activity occurs
post-transcriptional   cytoplasmic           This suggests that post-transcriptional regulation of cytoplasmic 70 kDa
post-transcriptional   MT                     This suggests the post-transcriptional control of MT protein levels
post-transcriptional   T3                     thought to be post-transcriptionally regulated by T3. Here we
post-transcriptional                          three aspects of post-transcriptional regulation in Dictyostelium discoideum: 1)
post-transcriptional                          Three human mRNAs are regulated post-transcriptionally by iron via
post-transcriptional   hnRNP                  thus suggesting a post-transcriptional regulation of hnRNP M and 2H9
post-transcriptional                          thus suggesting a post-transcriptional regulation of the This
post-transcriptional   iron                   Thus, IRP2 dominates post-transcriptional regulation of iron metabolism in mamm
post-transcriptional   Cim1                   Thus, post-transcriptional regulation of Cim1 by cytokinin
post-transcriptional   prepro                 Thus, post-transcriptional regulation of prepro ET gene
post-transcriptional                          Thus, post-transcriptional regulation of the genes for
post-transcriptional   mKv14                  Thus, transcriptional and post-transcriptional regulation of mKv1.4, coupled with se
post-transcriptional                          time with antisense. Post-transcriptional regulation of the heterochronic gene
post-transcriptional   5'DI                   tissue suggesting significant post-transcriptional regulation of 5'DI expression by
post-transcriptional   YB-1                   To address possible post-transcriptional regulation of YB-1 gene expression,
post-transcriptional                          to affect the
                       1-aminocyclopropane-1-carboxylic post-transcriptional regulation of 1-aminocyclopropane-1-carboxylic ac
post-transcriptional   rpsA                   to characterize the post-transcriptional regulation of rpsA, we constructed
post-transcriptional   ER                     To determine whether post-transcriptional regulation of ER gene expression
post-transcriptional   VEGF                   to examine the post-transcriptional regulation of VEGF Actinomycin
post-transcriptional   LAT1                   To further explore post-transcriptional regulation of LAT1 gene expression,
post-transcriptional                          To investigate post-transcriptional regulation of mRNA abundance, a cell-free
post-transcriptional   Period1                to investigate the post-transcriptional regulation of Period1 (Per1), the 3(')-untransl
post-transcriptional   genes                  to mediate the post-transcriptional regulation of genes in many
post-transcriptional                          to modify the post-transcriptional regulation of cellular gene expression
post-transcriptional   TK                     To study post-transcriptional regulation of TK expression, Ltk-
post-transcriptional   NiR                    to study the post-transcriptional regulation of NiR, Nicotiana plumbaginifolia
post-transcriptional   calbindin-D            to support significant post-transcriptional regulation of calbindin-D by
post-transcriptional   gene                   to transcriptional and post-transcriptional control of gene Related
post-transcriptional                          to transcriptional and/or post-transcriptional regulation of this Many
post-transcriptional                          TP protein would be regulated post-transcriptionally by another factor
post-transcriptional                          transcript expression and post-transcriptional regulation of human ADAM33, a rece
post-transcriptional   c-fms                  transcript half-life confirmed post-transcriptional regulation of c-fms transcript level
post-transcriptional                          transcription factors are post-transcriptionally regulated by their assembly with a
post-transcriptional                          transcription, rather than post-transcriptional regulation of mRNA processing or sta
post-transcriptional   CFTR                   Transcriptional and post-transcriptional regulation of CFTR (cystic fibrosis
post-transcriptional   gltX                   Transcriptional and post-transcriptional regulation of gltX, valU and alaW.
post-transcriptional   hepatic                Transcriptional and post-transcriptional regulation of hepatic expression of the
post-transcriptional                          Transcriptional and post-transcriptional regulation of human immunodeficiency viru
post-transcriptional   neuronal               Transcriptional and post-transcriptional regulation of neuronal and endothelial
post-transcriptional   PEPT1                  Transcriptional and post-transcriptional regulation of PEPT1 occurs in response
post-transcriptional                          T
                       proliferation-associated ranscriptional and post-transcriptional regulation of proliferation-associated nucle
post-transcriptional                          Transcriptional and post-transcriptional regulation of the rat
post-transcriptional                          Transcriptional and post-transcriptional regulation of this gene was
post-transcriptional                          transcripts can be post-transcriptionally regulated at the level of mRNA
post-transcriptional   pros                   transcripts, suggesting a post-transcriptional control of pros Our
post-transcriptional   HSA                    transgenic mice, suggesting post-transcriptional control of HSA The
post-transcriptional   tissue-specific        translation may be post-transcriptionally regulated by tissue-specific The
post-transcriptional                          Trypanosome alternative oxidase is regulated post-transcriptionally at the level
post-transcriptional   Ig                     tumor cells regarding post-transcriptional control of Ig gene expression
post-transcriptional   RNR                    tumours, suggesting possible post-transcriptional regulation of RNR. Moreover, RN
post-transcriptional                          Two forms of post-transcriptional control direct differential expression of the
post-transcriptional                          two genes may be regulated post-transcriptionally and they may
post-transcriptional                          two mechanisms of post-transcriptional control were identified. First, translation
post-transcriptional   p27                 U2OS cells through post-transcriptional regulation of p27. Many lines
post-transcriptional                       ubiquitous occurrence of post-transcriptional regulation makes mRNA an imperfec
post-transcriptional   gene                unaligned RNA sequences. Post-transcriptional regulation of gene expression is
post-transcriptional                       unchanged, suggesting a post-transcriptional control of the expression of GDH
post-transcriptional                       understand further the post-transcriptional control of the globin gene
post-transcriptional                       unknown means of post-transcriptional regulation of a gene
post-transcriptional                       vaccinia virus promoter is regulated post-transcriptionally in interferon-treated chic
post-transcriptional                       was detected, suggesting post-transcriptional regulation of the In
post-transcriptional                       was detected, suggesting post-transcriptional regulation of this These
post-transcriptional   LTC4                was determined by post-transcriptional regulation of LTC4
post-transcriptional   sigD                was due to post-transcriptional regulation of sigD, the gene
post-transcriptional   hIL-1ra             was to evaluate post-transcriptional regulation of hIL-1ra with specific
post-transcriptional   clp                 We demonstrate that post-transcriptional regulation of clp mRNA in the
post-transcriptional                       We describe post-transcriptional regulation of the chromosomal gene,
post-transcriptional   reductase           We hypothesize a post-transcriptional regulation of reductase mRNA by
post-transcriptional   psbA                we hypothesize that post-transcriptional regulation of psbA gene expression
post-transcriptional   CPR                 we propose that post-transcriptional regulation of CPR expression underlies
post-transcriptional   Grk                 we show that post-transcriptional regulation of Grk protein levels
post-transcriptional   rbcS                were consistent with post-transcriptional regulation of rbcS A
post-transcriptional                       which c-myc could be regulated post-transcriptionally in IFN-beta-treated cells
post-transcriptional                       which gene expression is regulated post-transcriptionally in the ever-increasing
post-transcriptional   amino               which include the post-transcriptional regulation of amino acid transporter
post-transcriptional                       which mediate the post-transcriptional regulation of a variety of genes
post-transcriptional                       which mediate the post-transcriptional regulation of many genes of iron
post-transcriptional   AQP5                which transcriptional and post-transcriptional regulation of AQP5 is
post-transcriptional                       which VIP is post-transcriptionally regulated through specific sequences in its
post-transcriptional                       whilst three are post-transcriptionally regulated (blt 14, blt 411,
post-transcriptional   MCP-1               with LPS, indicating post-transcriptional regulation of MCP-1 The
post-transcriptional   TfR                 with the well-characterized post-transcriptional control of TfR expression to expand
post-translational     tumor                Endotoxin-macrophage interaction: post-translational regulation of tumor necrosis
post-translational     P-glycoprotein       Evidence of post-translational regulation of P-glycoprotein associated with the
post-translational     Vitis                Indications for post-translational regulation of Vitis vinifera
post-translational     TCR                  Novel post-translational regulation of TCR expression in CD4+CD8+
post-translational     insulin-like         Post-transcriptional and post-translational regulation of insulin-like growth factor
post-translational     alcohol              Post-translational control of alcohol dehydrogenase levels
post-translational     collagen             Post-translational control of collagen fibrillogenesis in mineralizing
post-translational     endothelial          Post-translational control of endothelial nitric oxide
post-translational                          Post-translational control of human hemoglobin synthesis:
post-translational     occludin             Post-translational control of occludin membrane assembly
post-translational     ribosomal            Post-translational control of ribosomal protein L1
post-translational                          Post-translational control of the MEF2A transcriptional
post-translational     Adr1                 Post-translational regulation of Adr1 activity is
post-translational     AP-1                 Post-translational regulation of AP-1 transcription factor
post-translational     cytosolic            Post-translational regulation of cytosolic glutamine synthetase
post-translational     glucose-6-phosphate Post-translational regulation of glucose-6-phosphate dehydrogenase activity
post-translational     IgM                  Post-translational regulation of IgM expression in B
post-translational     interleukin          Post-translational regulation of interleukin 1 beta
post-translational     Lcr                  Post-translational regulation of Lcr plasmid-mediated peptides
post-translational     lipoprotein          Post-translational regulation of lipoprotein lipase activity
post-translational     macrophage           Post-translational regulation of macrophage apoprotein E
post-translational     mevalonate           Post-translational regulation of mevalonate kinase by
post-translational     neuronal             Post-translational regulation of neuronal acetylcholine receptors
post-translational   nitrate              Post-translational regulation of nitrate reductase: mechanism,
post-translational   perilipin            Post-translational regulation of perilipin Stabilization
post-translational   Saccharomyces        Post-translational regulation of Saccharomyces cerevisiae proteins
post-translational   steroidogenic        Post-translational regulation of steroidogenic acute regulatory
post-translational                        Post-translational regulation of the 54K cellular
post-translational   type                 Post-translational regulation of type I collagen
post-translational   aromatase            Pre- and post-translational regulation of aromatase by steroidal
post-translational   lysyl                Pre- and post-translational regulation of lysyl oxidase by
post-translational   renal                Pre- and post-translational regulation of renal insulin-like growth
post-translational   TSH                  Pre-translational and post-translational regulation of TSH synthesis in normal
post-translational   TSH:                 Pre-translational and post-translational regulation of TSH: relationship to bioactivit
post-translational   renal                Reciprocal post-translational regulation of renal 1 alpha-
post-translational                        Transcriptional and post-translational control of the plant plasma
post-translational   beta                 Transcriptional and post-translational regulation of beta 1 integrin
post-translational   CYP1A1               Transcriptional and post-translational regulation of CYP1A1 by
post-translational   insulin-like         Transcriptional and post-translational regulation of insulin-like growth factor-bindin
post-translational                        Transcriptional and post-translational regulation of S-adenosyl-L-methionine: salic
                     S-adenosyl-L-methionine:
post-translational   Escherichia         23S ribosomal RNA. Post-translational control of Escherichia coli ribosome
post-translational   MIS                 a form of post-translational regulation of MIS and shows
post-translational                       a level of post-translational control within the tissue which
post-translational                       a lysine residue. Post-translational regulation of the flight muscles/tergal
post-translational                       a mechanism of post-translational control that governs the activity
post-translational   Rad52               a mode of post-translational regulation of Rad52 mediated by
post-translational   GK                  a model for post-translational regulation of GK whereby insulin
post-translational   AIB                 a model of post-translational control of AIB transport by
post-translational   ORF239              a model of post-translational regulation of ORF239 expression based
post-translational                       a posttranscriptional or post-translational regulation of these The
post-translational                       a translational or post-translational regulation of these genes as
post-translational                       a translational or post-translational regulation of this polypeptide, or rapid
post-translational                       a type of post-translational regulation is
post-translational   JA                  active JAs, the post-translational control of JA responses leading
post-translational   iron                activity and is post-translationally regulated by iron. Although GEI-22/ACO-1
post-translational   sucrose             activity and the post-translational control of sucrose synthase stability
post-translational                       activity of IRP1 is regulated post-translationally by the insertion
post-translational                       activity of sigmaR is controlled post-translationally by an anti-sigma
post-translational   sucrase             activity, suggests a post-translational control of sucrase
post-translational   MT1-MMP             additional mechanism for post-translational control of MT1-MMP activity and sugge
post-translational                       affected, indicating a post-translational regulation of overall AChE
post-translational   its                 Although post-translational regulation of its subunits by
post-translational   GlnK                Analysis of the post-translational regulation of GlnK in vivo
post-translational   gp-1                and post-transcriptional events. Post-translational control of gp-1 activity, in effect,
post-translational   nitrogenase         and Rhodopseudomonas capsulatus post-translational regulation of nitrogenase is
post-translational                       and to investigate post-translational regulation of the
post-translational                       appear to be post-translationally regulated in zoospores and during
post-translational                       appeared to be post-translationally regulated as
post-translational                       approach to the post-translational regulation of protein function in Saccharomyces
post-translational   MCT1                are poorly understood. Post-translational regulation of MCT1 and MCT4
post-translational   neural              are related to post-translational control of neural cell adhesion
post-translational                       are required for post-translational regulation of both the molybdenum
post-translational   parvalbumin         as an important post-translational control of parvalbumin The
post-translational                       as part of post-translational regulation mechanisms. An overview is
post-translational   Pax6                at elucidating a post-translational regulation of Pax6 following activation
post-translational   RAD51                bacteria to humans. Post-translational regulation of RAD51 is
post-translational                        binding activity is post-translationally regulated during hypoxia and
post-translational   its                  biological activity is post-translationally regulated by its assembly with various
post-translational                        both transcriptional and post-translational regulation of the proteins that
post-translational   rbcL                 BSD2 in the post-translational regulation of rbcL in
post-translational   NOS-I                by both a post-translational regulation of NOS-I activity and an
post-translational   Bad                  by C5b-9 through post-translational regulation of Bad. This mechanism
post-translational   SUS                  by proteasome inhibition. Post-translational control of SUS protein level
post-translational                        by translational and post-translational regulation of the cell cycle
post-translational   secretion            calcium-mediated mechanism of post-translational regulation of secretion for interl
post-translational                        carboxylase (PEPC (Ppc)) are controlled post-translationally by an intricate
post-translational                        cells: evidence for post-translational regulation of a beta-galactoside alpha
post-translational                        certain circumstances of post-translational control of the activity levels
post-translational                        ClpX in the post-translational regulation of a sigma subunit
post-translational   spo0H                concentration of sigmaH. Post-translational control of spo0H is responsible
post-translational   N2                   conditions, transcriptional and post-translational regulation of N2 fixation was
post-translational   Gs                   data suggest a post-translational regulation of Gs expression by
post-translational   hydrogenase          degradation) or in post-translational regulation of hydrogenase The
post-translational                        degraded and can be regulated post-translationally by polyamines, indicating
post-translational   ABA                  dephosphorylation events are post-translationally regulated by ABA or whether
post-translational                        Developmental and light-regulated post-translational control of 3-hydroxy-3-methyl
                     3-hydroxy-3-methylglutaryl-CoA
post-translational   Myc                  differentiation suggest that post-translational regulation of Myc and Max
post-translational   myogenic             discussing upstream and post-translational regulation of myogenic regulatory facto
post-translational                        dramatic level of post-translational regulation on the expression of surface
post-translational                        due to a post-translational regulation of the tetrameric
post-translational                        E2 synthesis, which is regulated post-translationally by protein tyrosine
post-translational   isotype              embryogenesis: evidence for post-translational regulation of isotype Two
post-translational   light                enzyme PrK was post-translationally regulated by light, probably through
post-translational                        enzyme, but the post-translational regulation of this enzyme is
post-translational                        epileptic hippocampus, suggesting post-translational regulation of the PIMT
post-translational   turnover             estrogen receptor beta: post-translational regulation of turnover and transactivation
post-translational   Cdc2/cyclin          evidence for the post-translational control of Cdc2/cyclin B activation
post-translational                        Evidence of post-translational control of cell Using
post-translational   transmembrane        Examples of post-translational control of transmembrane signalling elements
post-translational                        exd activity is regulated post-translationally by a mechanism
post-translational                        extended to the post-translational control of the activity of short-chain
post-translational                        factors whose function is regulated post-translationally by selective nuclear
post-translational                        findings point to post-translational regulation of this enzyme and favor
post-translational   G-protein-linked     for mRNA stability. Post-translational regulation of G-protein-linked receptors is
post-translational   NO                   for transcriptional and post-translational regulation of NO Evidence
post-translational   sigmaH               function in the post-translational control of sigmaH. Mutations in lonA
post-translational   GLUT4                GLUT4 mRNA suggesting post-translational control of GLUT4
post-translational   adenylylation        GS enzyme is post-translationally regulated by adenylylation. Nitrogen regulation
post-translational                        GS(1) is regulated post-translationally by reversible phosphorylation
post-translational   telomerase           have suggested a post-translational regulation of telomerase Here
post-translational   beta-catenin         heart, suggesting the post-translational regulation of beta-catenin by APC
post-translational   nitrogenase          However, the post-translational regulation of nitrogenase activity by
post-translational   TDC                  However, the putative post-translational regulation of TDC via the ubiquitin
post-translational                        HSL activity is regulated post-translationally by phosphorylation and also
post-translational                        I collagen is post-translationally regulated in corneal endothelial cells
post-translational   IFN-gamma-R          IFN-gamma-R, indicating a post-translational control of IFN-gamma-R by
post-translational                        Immunological evidences for post-translational control of the parathyroid function
post-translational   SUS                  implicated in the post-translational regulation of SUS protein
post-translational   gene                 important level of post-translational control of gene Stem
post-translational   IRE-BP               In addition, post-translational regulation of IRE-BP activity via
post-translational                        in Streptomyces coelicolor is controlled post-translationally by the adenylyltransfera
post-translational   PTHrP                In studying the post-translational regulation of PTHrP, we observed
post-translational   nitrogen             in transcriptional and post-translational regulation of nitrogen Increase
post-translational   Gro/TLE              including the possible post-translational regulation of Gro/TLE activity as
post-translational   oxidants             indicate Cap1p is post-translationally regulated by oxidants. Green fluorescent
post-translational                        indicating post-transcriptional and/or post-translational regulation of these Due
post-translational   carotenoid           indicating translational or post-translational control of carotenoid gene
post-translational   alpha                indicating translational or post-translational regulation of alpha 2 protein
post-translational   inducible            induced to the post-translational control of inducible transcription factors
post-translational                        initiating role for post-translational control of 3-hydroxy-3-methylglutaryl coenzyme
                     3-hydroxy-3-methylglutaryl
post-translational   ABCA1                insight into the post-translational regulation of ABCA1 and the pathobiology
post-translational   Bim(EL)              insights into the post-translational regulation of Bim(EL) and the role
post-translational                        involve pre- and post-translational regulation of multiple transcription
post-translational                        involved in the post-translational control of a yeast
post-translational   glutamate            involved in the post-translational regulation of glutamate
post-translational   myogenin             involved in the post-translational regulation of myogenin as well
post-translational   Muc4                 involvement in the post-translational regulation of Muc4 via the transforming
post-translational   cPLA2                is consistent with post-translational regulation of cPLA2 C5b-9
post-translational   E-cadherin           is involved in post-translational regulation of E-cadherin Changes
post-translational   Pmc1p                is known about post-translational regulation of Pmc1p. In a genetic
post-translational   GABAA                is possible that post-translational regulation of GABAA receptors by
post-translational                        is required for post-translational regulation of both the molybdenum
post-translational   outer                is required for post-translational regulation of outer membrane but
post-translational   enzyme               isoproterenol evidence for post-translational control of enzyme activity? The
post-translational                        its activity may be regulated post-translationally or by the presence
post-translational   proteolytic          kinase, Axl, is post-translationally regulated by proteolytic Several
post-translational                        kinases can mediate post-translational regulation of the uptake of compatible
post-translational                        laboratory concerning the post-translational regulation of the angiotensin receptor
post-translational                        LDL (apo B100). Post-translational regulation of the assembly of apo
post-translational                        leash: transcriptional and post-translational control of the pro-apoptotic activity
post-translational   COX                  levels, indicating a post-translational regulation of COX by vitamin
post-translational   GnRH                 levels, suggesting a post-translational regulation of GnRH It
post-translational   nutrient             Loss of the post-translational control of nutrient transport in vitro
post-translational   p53                  major pathway for post-translational regulation of p53 comprises its
post-translational   enzyme               maturation steps in post-translational regulation of enzyme Indirect
post-translational                        may in part be controlled post-translationally at the level
post-translational   IGF-induced          may provide important post-translational regulation of IGF-induced mitogenesis du
post-translational                        mechanism for the post-translational control of protein function has
post-translational   p53                  mechanism underlying this post-translational regulation of p53. Specifically, we
post-translational                        mechanisms, and the post-translational control of the activity of both
post-translational   potato               meristematic tissue, suggesting post-translational regulation of potato HMGR affec
post-translational   hexose               metabolites to the post-translational regulation of hexose transport and GLUT-1
post-translational                        mexicana, LmmCRK1, is post-translationally regulated during the life
post-translational   Bim's                mice and the post-translational regulation of Bim's pro-apoptotic
post-translational                        mRNA, suggesting a post-translational regulation of the Conversely,
post-translational                        Muc4/SMC expression is post-translationally regulated through inhibition of Muc4/S
post-translational   MTG8                 new light on post-translational regulation of MTG8, perturbation of which,
post-translational                        notable for effective post-translational control of their endonuclease
post-translational   MMR                  novel type of post-translational regulation of MMR which might
post-translational   AP-1               novo synthesis and post-translational regulation of AP-1 This
post-translational   Swe1               nuclear division through post-translational regulation of Swe1 and that
post-translational                      ODC activity may be controlled post-translationally by macromolecules that
post-translational                      of beta-catenin is post-translationally regulated by an increased Wnt
post-translational                      of enzyme activation is regulated post-translationally by differential delivery
post-translational   NaCl               of gp26 is post-translationally controlled by
post-translational                      of hGHR may be regulated post-translationally by the two
post-translational                      of neurofibromin can be regulated post-translationally through the alteration
post-translational   LH                 of pre- and post-translational regulation of LH biosynthesis was
post-translational   DHFR               of translational or post-translational control of DHFR In
post-translational   c-myc              of translational or post-translational regulation of c-myc Further,
post-translational                      of UGPase for post-translational regulation of the enzyme are
post-translational   alpha              on a possible post-translational regulation of alpha 1(I) collagen
post-translational   ornithine          participate in the post-translational regulation of ornithine decarboxylase, the rate-l
post-translational   UDG1A              participate in the post-translational regulation of UDG1A protein
post-translational                      pigmentation genes and post-translational control of the melanin biosynthetic
post-translational   pigments           plastid membranes is post-translationally regulated by pigments, reconstitution stu
post-translational   GPI-PLC            possible mechanism for post-translational regulation of GPI-PLC An
post-translational   ornithine          possibly involved in post-translational regulation of ornithine decarboxylase
post-translational   calmodulin         post-transcriptional or a post-translational regulation of calmodulin
post-translational   MyHC               post-transcriptional, translational or post-translational regulation of MyHC isoforms
post-translational   NCED               potential means of post-translational regulation of NCED
post-translational   pre-existing       primarily by a post-translational regulation of pre-existing enzyme and not
post-translational   viral              processing in the post-translational regulation of viral gene expression
post-translational   D2                 proteasomes in the post-translational regulation of D2
post-translational   Bcl-2              protein can be post-translationally regulated by Bcl-2, probably in a
post-translational   heterodimer        protein expression and post-translational regulation of heterodimer
post-translational                      protein in the post-translational regulation of the sialyltransferase activity
post-translational                      protein kinase may be regulated post-translationally following DNA damage,
post-translational                      protein p34cdc2 is post-translationally regulated in a variety of cell
post-translational                      protein phosphorylation in post-translational regulation of protein B23 during
post-translational                      protein required for post-translational regulation of the rbcL gene
post-translational                      proteins that are post-translationally regulated in an identical manner)
post-translational                      proton transport and is regulated post-translationally in response to glucose
post-translational   phosphorylation    reductase (NR) is post-translationally regulated by phosphorylation and binding
post-translational                      reflecting translational of post-translational control mechanisms. Upregulation of E
post-translational                      relation to the post-translational regulation of the net production
post-translational                      results demonstrate a post-translational regulation of the 54K cellular
post-translational   5alpha-reductase   role in the post-translational regulation of 5alpha-reductase activity in the
post-translational   expression         role in the post-translational regulation of expression of soluble
post-translational   Smf1p              role in the post-translational regulation of Smf1p. The depletion
post-translational   dCK                sensitivity, suggesting a post-translational regulation of dCK. In conclusion,
post-translational   enzyme             SH reagents mirrors post-translational regulation of enzyme The
post-translational                      shown to be post-translationally regulated in response to the availability
post-translational                      sigma B activity is regulated post-translationally by a multi-component
post-translational                      study analyzed the post-translational regulation of the transcription factor
post-translational   apoE               study post-transcriptional and post-translational control of apoE production in macr
post-translational   macrophage         Such post-translational regulation of macrophage apo E
post-translational   CDK                suggest a strong post-translational regulation of CDK at the temporal
post-translational   activity           suggesting a potential post-translational regulation of activity. This study
post-translational   GABA               suggesting a tight post-translational regulation of GABA We
post-translational                      switches for the post-translational regulation of a wide variety
post-translational   enzyme              synthesis and temporary post-translational control of enzyme activity determine
post-translational   Egr-1               synthesis but on post-translational regulation of Egr-1. Egr-1 efficiently
post-translational                       synthetase I (GSI) is regulated post-translationally by reversible adenylylation
post-translational                       that myo-inositol accumulation is regulated post-translationally by wortmannin and
post-translational   gene                that translational or post-translational control of gene expression may
post-translational                       that translational or post-translational control of protein levels occurs
post-translational                       that wild-type mZip4 is regulated post-translationally in response to zinc
post-translational                       the absence of post-translational regulation via residues encoded by
post-translational   LDL                 The herein described post-translational regulation of LDL internalisation may
post-translational                       The induction or post-translational regulation of several proteins is
post-translational   NR                  the mechanism of post-translational regulation of NR is summarized
post-translational                       the mitotic trigger: post-translational regulation of the Cdc25C
post-translational   tubulin             the post-transcriptional and post-translational regulation of tubulin synthesis in plan
post-translational   picornavirus        The post-translational regulation of picornavirus gene expression
post-translational   cytosolic           The role of post-translational regulation of cytosolic GS and interactions
post-translational   processes           the transcriptional and post-translational regulation of processes that increase
post-translational   MyHC                the translational or post-translational regulation of MyHC
post-translational                       there may be post-translational regulation of the light-intermediate
post-translational                       thetaiotaomicron, suggesting a post-translational regulation of these Our
post-translational                       this mode of post-translational regulation as inducible gene expression
post-translational   CopZ                This post-translational control of CopZ expression presumably
post-translational                       This ratio is regulated post-translationally by at least
post-translational   glycosyltransferase This type of post-translational regulation of glycosyltransferase activities deserves
post-translational                       Thus post-translational control of both c-myc and RB
post-translational                       Thus, the unusual post-translational regulation of the CHL I2
post-translational                       time-delimited fashion, suggesting post-translational control of protein-DNA We
post-translational   gene                to determine if post-translational regulation of gene expression was
post-translational                       to explain the post-translational regulation of the
post-translational   HSL                 to involve either post-translational control of HSL or the regulation
post-translational                       to translational and/or post-translational regulation of the endogenous sam-s
post-translational                       transcriptional, allosteric and post-translational control of this enzyme's
post-translational   metallothionein     transcriptional, translational and post-translational control of metallothionein gene e
post-translational                       two levels of post-translational regulation and is enhanced by
post-translational   survivin            ubiquitin-proteasome pathway in post-translational regulation of survivin. Survivin i
post-translational   OPN                 We now show post-translational regulation of OPN production by
post-translational                       well-known mechanisms of post-translational regulation of the glycolytic
post-translational                       were examined for post-translational regulation of the molybdenum and the
post-translational                       which suggests a post-translational control of this Thus,
post-translational   translation         While the stress-induced post-translational regulation of translation initiation factor
post-translational   Hsp70               wholly, determined by post-translational regulation of Hsp70
post-translational                       would suggest a post-translational regulation of the 1 alpha-
transcriptional                           [Demonstration of transcriptional regulation of protein kinase C
transcriptional      neural               [Second messenger-mediated transcriptional regulation of neural genes and poss
transcriptional                           [The transcriptional regulation of the human gastrin
transcriptional                           [The transcriptional regulation of the TCA1 elements
transcriptional                           Activation-dependent transcriptional regulation of the human Fas
transcriptional                           Allele-dependent transcriptional regulation of the human integrin
transcriptional      proinflammatory      Alterations in transcriptional regulation of proinflammatory and immunoregulatory
transcriptional                           Altered transcriptional regulation of human interstitial collagenase
transcriptional      phosphoenolpyruvate Altered transcriptional regulation of phosphoenolpyruvate carboxykinase in rats
transcriptional                           Altered transcriptional regulation of the insulin-like growth
transcriptional                           Analysis of transcriptional control elements in the 5'-upstream
transcriptional                          Analysis of transcriptional control mechanisms of capsule expression
transcriptional                          Analysis of transcriptional control of the gerD spore
transcriptional                          Analysis of transcriptional control regions in the Streptomyces
transcriptional                          Analysis of transcriptional regulation of human breast aromatase
transcriptional                          Analysis of transcriptional regulation of the s38 chorion
transcriptional                          Androgen-Dependent transcriptional regulation of the prostate-specific antigen
transcriptional                          Antagonistic transcriptional regulation of the putrescine biosynthetic
transcriptional   measles                Antibody-dependent transcriptional regulation of measles virus in persistently
transcriptional                          Basal level transcriptional regulation of the human angiotensin
transcriptional                          Basal transcriptional regulation of human damage-specific DNA-binding
transcriptional                          Basal transcriptional regulation of rat AT1 angiotensin
transcriptional                          Biphasic transcriptional regulation of the interferon regulatory
transcriptional   small                  Burn-induced transcriptional regulation of small intestinal ornithine
transcriptional                          Carbon source-dependent transcriptional regulation of the mitochondrial glycerol-3
transcriptional                          Carbon source-dependent transcriptional regulation of the QCR8 gene
transcriptional                          CD40-mediated transcriptional regulation of the IL-6 gene
transcriptional                          Cell type-specific transcriptional regulation of the Drosophila FMRFamide
transcriptional                          Cell type-specific transcriptional regulation of the human adenosine
transcriptional   ribonucleotide         Cell-cycle associated transcriptional regulation of ribonucleotide reductase in L121
transcriptional                          Cell-specific transcriptional control of the mouse DNA-binding
transcriptional   follicle-stimulating   Cell-specific transcriptional regulation of follicle-stimulating hormone-beta by
transcriptional                          Cell-specific transcriptional regulation of human leukotriene B(4)
transcriptional                          Characterization and transcriptional regulation of rat glutamine tRNA-encoding
transcriptional                          Characterization and transcriptional regulation of the 2'-N-acetyltransferase gene
transcriptional                          Characterization and transcriptional regulation of the modABCD genes
transcriptional                          Characterization and transcriptional regulation of the Synechocystis PCC
transcriptional                          Characterization of transcriptional regulation during negative selection in vivo.
transcriptional   gamma-glutamyl         Characterization of transcriptional regulation of gamma-glutamyl transpeptidase in
transcriptional   Shewanella             Characterization of transcriptional regulation of Shewanella frigidimarina Fe(III)-ind
transcriptional                          Characterization of transcriptional regulation of the kdp operon
transcriptional                          Cloning and transcriptional control of a eucaryotic permease
transcriptional                          Cloning and transcriptional regulation of a novel adipocyte-specific
transcriptional                          Cloning and transcriptional regulation of the elastase lasA
transcriptional                          Cloning and transcriptional regulation of the gene encoding
transcriptional   CAH1                   CO(2)-responsive transcriptional regulation of CAH1 encoding carbonic
transcriptional                          Complex transcriptional control of the sigma s-dependent
transcriptional                          Complex transcriptional control of the streptokinase gene
transcriptional   myc                    Complex transcriptional regulation of myc family gene
transcriptional                          Complex transcriptional regulation of the Saccharomyces cerevisiae
transcriptional                          Complexity of transcriptional control in neuropeptide gene expression;
transcriptional                          Considerations of transcriptional control mechanisms: do TFIID-core promoter
transcriptional                          Coordinate transcriptional control of murine endogenous retrovirus
transcriptional   alpha                  Coordinate transcriptional regulation of alpha and delta
transcriptional   dopamine               Co-ordinate transcriptional regulation of dopamine synthesis genes
transcriptional                          Coordinate transcriptional regulation of the three fibrinogen
transcriptional   type                   Coordinate transcriptional regulation of type I procollagen
transcriptional                          Coordinated transcriptional regulation of the unc-25 glutamic
transcriptional   methane                Copper-dependent reciprocal transcriptional regulation of methane monooxygena
transcriptional                          Delineation of transcriptional control signals within the Moloney
transcriptional                          Deranged transcriptional regulation of cell-volume-sensitive kinase hSGK
transcriptional   Gi                     Differential gene transcriptional regulation of Gi isoforms and Gs
transcriptional                          Differential transcriptional control of the H-2K and H-2D
transcriptional                          Differential transcriptional control of the two tRNA(fMet)
transcriptional   CD161                  Differential transcriptional regulation of CD161 and a novel
transcriptional   c-myc                  Differential transcriptional regulation of c-myc promoter through
transcriptional   endothelin-1           Differential transcriptional regulation of endothelin-1 by immunosuppressants
transcriptional   individual             Differential transcriptional regulation of individual TCR V
transcriptional                          Differential transcriptional regulation of rat vasopressin gene
transcriptional   silencer               Differential transcriptional regulation of silencer of death
transcriptional   sulfur                 Differential transcriptional regulation of sulfur assimilation gene
transcriptional                          Differential transcriptional regulation of the apoAI gene
transcriptional                          Differential transcriptional regulation of the human squalene
transcriptional                          Differential transcriptional regulation of the human thrombin
transcriptional                          Differential transcriptional regulation of the monocyte-chemoattractant protein-1
transcriptional                          Differential transcriptional regulation of the two vascular
transcriptional   two                    Differential transcriptional regulation of two distinct S-adenosylmethionine
transcriptional   apolipoprotein         Differential, tissue-specific, transcriptional regulation of apolipoprotein B secretion
transcriptional                          Differentiation-specific transcriptional regulation of the hepatitis B
transcriptional                          Direct transcriptional control of the chloroplast genes
transcriptional                          Direct transcriptional control of the Dpp target
transcriptional   RelB                   Direct transcriptional regulation of RelB by 1alpha,25-dihydroxyvitamin
transcriptional                          Direct transcriptional regulation of the progesterone receptor
transcriptional   ICSBP                  Disabled-2 is transcriptionally regulated by ICSBP and augments
transcriptional                          Distinct transcriptional regulation of a gene coding
transcriptional   multidrug              Divergent transcriptional control of multidrug resistance genes
transcriptional                          Dual transcriptional regulation of the Escherichia coli
transcriptional                          Enzymatic and transcriptional regulation of human ecto-ATPase/E-NTPDase
transcriptional                          Epithelial specific transcriptional regulation of the bovine papillomavirus
transcriptional                          Epithelial-cell-specific transcriptional regulation of human Galbeta1,3GalNAc/Galb
transcriptional                          Evidence for transcriptional control of human mdr1 gene
transcriptional   orotidine-5'-phosphate Evidence for transcriptional regulation of orotidine-5'-phosphate decarboxylase in
transcriptional   plastid                Evidence for transcriptional regulation of plastid photosynthesis genes
transcriptional                          Evidence for transcriptional regulation of the myosin heavy
transcriptional   prokaryotic            Evolution of transcriptional control from prokaryotic beginnings to eukaryotic
transcriptional                          Evolution of transcriptional regulation system through promiscuous coupling
transcriptional                          Expression and transcriptional control of the Salmonella typhimurium
transcriptional   caspase-14             Expression and transcriptional regulation of caspase-14 in simple
transcriptional   functionally           Expression and transcriptional regulation of functionally distinct Bmf
transcriptional                          Expression and transcriptional regulation of the human alpha1,
transcriptional                          Expression and transcriptional regulation of the human alpha3
transcriptional                          Expression and transcriptional regulation of the PD-Ialpha/autotaxin gene
transcriptional                          Factors affecting transcriptional regulation of the formate-hydrogen-lyase pathway
transcriptional   Bim                    FoxO3a transcriptional regulation of Bim controls apoptosis
transcriptional   PAH-inducible          Functions and transcriptional regulation of PAH-inducible human
transcriptional   15-lipoxygenase-1      GATA-6 transcriptional regulation of 15-lipoxygenase-1 during NSAID-induced
transcriptional   NO                     Gender and transcriptional regulation of NO synthase and ET-1
transcriptional                          Genetics of transcriptional regulation in yeast: connections to the
transcriptional   PAI-1                  Genotype-specific transcriptional regulation of PAI-1 expression by
transcriptional   PAI-1                  Genotype-specific transcriptional regulation of PAI-1 gene by
transcriptional                          Glucose-dependent transcriptional regulation of the human sucrase-isomaltase
transcriptional                          Glutamate-dependent transcriptional regulation of the chkbp gene:
transcriptional                          Growth-phase-dependent transcriptional regulation of the pcm and surE
transcriptional                          Helicobacter pylori-mediated transcriptional regulation of the human beta-defensin
transcriptional   HLA-G                  Here, the transcriptional control of HLA-G and classical
transcriptional                   Identical transcriptional control of the divergently transcribed
transcriptional                   Identification and transcriptional control of the genes encoding
transcriptional                   Identification and transcriptional regulation of the baculovirus lef-6
transcriptional                   IFN-gamma-mediated coordinated transcriptional regulation of the human TAP-1
transcriptional   p53-dependent   Imaging transcriptional regulation of p53-dependent genes with positron
transcriptional                   Impacts of transcriptional regulation on aging and
transcriptional                   In vivo transcriptional regulation of the human immunodeficiency
transcriptional                   Independent transcriptional regulation of a single VL30
transcriptional                   Inference of transcriptional regulation relationships from gene expression
transcriptional                   Influence of transcriptional regulation and mRNA stability on
transcriptional   phospholipid    Injury-elicited differential transcriptional regulation of phospholipid growth factor
transcriptional                   Interferon action: transcriptional control of a gene specifying
transcriptional   xpsR            Joint transcriptional control of xpsR, the unusual
transcriptional   connexin32      Liver cell-specific transcriptional regulation of connexin32. Gap junctional
transcriptional   utrophin        Local transcriptional control of utrophin expression at
transcriptional                   Location of transcriptional control signals and transfer RNA
transcriptional   HLA             Locus-specific transcriptional control of HLA One
transcriptional   genes           lon transcriptional regulation of genes necessary for
transcriptional   cytokine        Long-range transcriptional regulation of cytokine gene
transcriptional                   Mast cell-/basophil-specific transcriptional regulation of human L-histidine decarbo
transcriptional   methyl-CpG      Mechanism of transcriptional regulation by methyl-CpG binding protein
transcriptional                   Mechanisms of transcriptional regulation and neural gene
transcriptional   Rb-E2F          Mechanisms of transcriptional regulation by Rb-E2F segregate by
transcriptional   Runt            Mechanisms of transcriptional regulation by Runt domain
transcriptional                   Mechanisms of transcriptional regulation of cellular genes by
transcriptional                   Mechanisms of transcriptional regulation of the human beta(3)-adrenergic
transcriptional   xak-c           Metamorphosis-dependent transcriptional regulation of xak-c, a novel
transcriptional   osteoblast      Minireview: transcriptional control of osteoblast The
transcriptional                   MluI site-dependent transcriptional regulation of the Candida albicans
transcriptional   adipogenesis    Modulating the transcriptional control of adipogenesis. Current evidence
transcriptional   LEF-1           Modulation of transcriptional regulation by LEF-1 in response
transcriptional   megakaryocyte   Molecular and transcriptional regulation of megakaryocyte Megakaryocytes,
transcriptional                   Molybdenum-sensitive transcriptional regulation of the chlD locus
transcriptional                   Multiple transcriptional control of the Lactococcus lactis
transcriptional                   Muscle-specific transcriptional regulation of the slowpoke Ca(2+)-activated
transcriptional                   Myometrial transcriptional regulation of the gap junction
transcriptional   iron            Negative transcriptional control of iron transport in Erwinia
transcriptional                   Negative transcriptional regulation of a positive regulator:
transcriptional   connexin        Negative transcriptional regulation of connexin 43 by
transcriptional                   Negative transcriptional regulation of human interleukin 2
transcriptional   PH081           Negative transcriptional regulation of PH081 expression in Saccharomyces
transcriptional                   Negative transcriptional regulation of the chicken Na+/K(+)-ATPase
transcriptional                   Negative transcriptional regulation of the interferon-gamma promoter
transcriptional                   Negative transcriptional regulation of the mce3 operon
transcriptional                   Negative transcriptional regulation of the VCAM-1 gene
transcriptional   virulence       Negative transcriptional regulation of virulence and oncogenes
transcriptional                   Networks of transcriptional regulation encoded in a grammatical
transcriptional                   NF-kappa B-mediated transcriptional regulation of human beta-defensin-2 gene
transcriptional                   Novel transcriptional control of the pyruvate formate-lyase
transcriptional                   Novel transcriptional regulation of the human CYP3A7
transcriptional   Methicillin     On the Transcriptional Regulation of Methicillin Resistance: MecI
transcriptional   neuronal        On the transcriptional regulation of neuronal nAChR
transcriptional                    Organization and transcriptional regulation of Drosophila Na(+), K(+)-ATPase
transcriptional                    Organization and transcriptional regulation of the Escherichia coli
transcriptional   cytochrome       Oxygen-dependent transcriptional regulation of cytochrome aa3 in Bradyrhizobium
transcriptional                    p53-dependent transcriptional regulation of the APC promoter
transcriptional   DNA              p73 is transcriptionally regulated by DNA damage, p53,
transcriptional                    Position-dependent transcriptional regulation of the murine dihydrofolate
transcriptional   mry              Positive transcriptional control of mry regulates virulence
transcriptional                    Positive transcriptional regulation of an iron-regulated virulence
transcriptional                    Positive transcriptional regulation of the human gamma-globin
transcriptional   gene             Post transcriptional control of gene expression in Leishmania.
transcriptional   metabotropic     Postlesional transcriptional regulation of metabotropic glutamate receptors:
transcriptional   collagen         Post-transcriptional and transcriptional control of collagen gene expression
transcriptional   polyamine        Post-translational and transcriptional regulation of polyamine biosynthesis in Esch
transcriptional                    Pre-B lymphocyte-specific transcriptional control of the mouse VpreB
transcriptional                    Principles of transcriptional control in the metabolic network
transcriptional   nif              Reciprocal light-dark transcriptional control of nif and rbc
transcriptional   TATA-binding     Reevaluation of transcriptional regulation by TATA-binding protein oligomerization
transcriptional   keratin          Retinoid-mediated transcriptional regulation of keratin genes in human
transcriptional                    Role of transcriptional regulation and enzyme inactivation in the
transcriptional                    Role of transcriptional regulation in controlling fluxes in central
transcriptional   sprE:            RpoS-dependent transcriptional control of sprE: regulatory feedback
transcriptional   transforming     Secretion and transcriptional regulation of transforming growth factor-beta
transcriptional   com101A          Sequence and transcriptional regulation of com101A, a locus
transcriptional                    Sex-specific transcriptional regulation of the elegans
transcriptional   Fas              Signaling and transcriptional control of Fas ligand gene
transcriptional   pancreatic       Signaling and transcriptional control of pancreatic The
transcriptional   pituitary        Signaling and transcriptional control of pituitary Many
transcriptional   gamma-glutamyl   Stability and transcriptional regulation of gamma-glutamyl transpeptidase mRNA
transcriptional                    Steroid-involved transcriptional regulation of human genes encoding
transcriptional   sterol           Sterol-dependent transcriptional regulation of sterol regulatory element-binding
transcriptional                    Stromal cell-mediated transcriptional regulation of the CD13/aminopeptidase N
transcriptional                    Structure and transcriptional control of the flagellar master
transcriptional                    Structure and transcriptional control of the Saccharomyces cerevisiae
transcriptional   BKJ              Structure and transcriptional regulation of BKJ, a novel
transcriptional                    Structure and transcriptional regulation of human alpha-mannosidase IIX
transcriptional                    Structure and transcriptional regulation of protein phosphatase 2A
transcriptional                    Structure and transcriptional regulation of the Escherichia coli
transcriptional                    Structure and transcriptional regulation of the gene encoding
transcriptional                    Structure and transcriptional regulation of the GFAP
transcriptional                    Structure and transcriptional regulation of the human cystatin
transcriptional                    Structure and transcriptional regulation of the human mammaglobin
transcriptional                    Structure and transcriptional regulation of the mouse ferrochelatase
transcriptional                    Structure and transcriptional regulation of the Nat2 gene
transcriptional                    Structure and transcriptional regulation of the ovine placental
transcriptional                    Studies of transcriptional regulation of the Bacillus subtilis
transcriptional   Cyp3a16          Studies on transcriptional regulation of Cyp3a16 gene in mouse
transcriptional                    Studies on transcriptional regulation of the mucosal T-cell
transcriptional   sucrose          Sucrose-mediated transcriptional regulation of sucrose symporter activity
transcriptional   transforming     Targets of transcriptional regulation by transforming growth factor-beta:
transcriptional   two              Targets of transcriptional regulation by two distinct type
transcriptional   expression       Temperature-dependent transcriptional regulation of expression of fimbriae
transcriptional                    The tissue-specific transcriptional regulation of the megakaryocytic glycoprotein
transcriptional                       The transcriptional control of plant responses to phosphate
transcriptional   TGF-beta            The transcriptional control of TGF-beta in human
transcriptional   heat                The transcriptional regulation of heat shock genes:
transcriptional                       The transcriptional regulation of human aldehyde dehydrogenase
transcriptional                       The transcriptional regulation of human arachidonate 12-lipoxygenase
transcriptional   phosphoenolpyruvate The transcriptional regulation of phosphoenolpyruvate carboxykinase gene
transcriptional                       The transcriptional regulation of the growth hormone
transcriptional                       The transcriptional regulation of the Streptococcus mutans
transcriptional   Xenopus             The transcriptional regulation of Xenopus 5s RNA
transcriptional   exogenous           Thyroid hormone-dependent transcriptional regulation of exogenous genes transfe
transcriptional                       Tight transcriptional control of the ETS domain
transcriptional   alpha-              Tissue-specific transcriptional control of alpha- and beta-tropomyosins
transcriptional                       Tissue-specific transcriptional regulation of human leukosialin (CD43)
transcriptional                       Tissue-specific transcriptional regulation of the cholesterol biosynthetic
transcriptional                       Trans-acting transcriptional regulation of human T-cell leukemia
transcriptional                       Transcriptional control of a nuclear gene
transcriptional                       Transcriptional control of a rRNA promoter
transcriptional   AAC3                Transcriptional control of AAC3 gene encoding
transcriptional   ADH                 Transcriptional control of ADH genes in the
transcriptional   adipogenesis        Transcriptional control of adipogenesis. Adipocyte differentiation
transcriptional   adipogenesis        Transcriptional control of adipogenesis. The major
transcriptional   adrenal             Transcriptional control of adrenal catecholamine and opiate
transcriptional   adrenomedullin      Transcriptional control of adrenomedullin induction by
transcriptional   apolipoprotein      Transcriptional control of apolipoprotein A-I gene
transcriptional   B                   Transcriptional control of B cell development
transcriptional   Bacillus            Transcriptional control of Bacillus subtilis hemN
transcriptional   B-cell              Transcriptional control of B-cell Significant
transcriptional   Borna               Transcriptional control of Borna disease virus
transcriptional   Ca(2+)-activated    Transcriptional control of Ca(2+)-activated K(+) channel
transcriptional   cardiac             Transcriptional control of cardiac allograft vasculopathy
transcriptional                       Transcriptional control of cell cycle progression:
transcriptional                       Transcriptional control of cell phenotypes in the
transcriptional                       Transcriptional control of cell type and morphogenesis
transcriptional   circadian           Transcriptional control of circadian hormone synthesis
transcriptional   c-jun               Transcriptional control of c-jun by retinoic
transcriptional   c-myc               Transcriptional control of c-myc gene expression
transcriptional   CYP2E1              Transcriptional control of CYP2E1 in the perivenous
transcriptional   cytokine            Transcriptional control of cytokine With
transcriptional   dacB                Transcriptional control of dacB, which encodes
transcriptional   deformation-induced Transcriptional control of deformation-induced preproendothelin-1 gene
transcriptional   delta-crystallin    Transcriptional control of delta-crystallin gene expression
transcriptional   development         Transcriptional control of development, protein synthesis,
transcriptional   dimorphism          Transcriptional control of dimorphism in Candida
transcriptional   dopamine            Transcriptional control of dopamine neuron
transcriptional                       Transcriptional control of Drosophila bicoid by
transcriptional                       Transcriptional control of Drosophila fushi tarazu
transcriptional   early               Transcriptional control of early B cell
transcriptional   endogenous          Transcriptional control of endogenous virus genes
transcriptional   epidermal           Transcriptional control of epidermal growth factor
transcriptional   erythropoiesis      Transcriptional control of erythropoiesis. Over the past
transcriptional   estrogen            Transcriptional control of estrogen receptor in estrogen
transcriptional   expression          Transcriptional control of expression of fungal
transcriptional   expression          Transcriptional control of expression of genes
transcriptional   flagellar           Transcriptional control of flagellar genes in Escherichia
transcriptional   gene                Transcriptional control of gene expression during
transcriptional   genes               Transcriptional control of genes encoding CS1
transcriptional   glial               Transcriptional control of glial and blood
transcriptional   glial               Transcriptional control of glial fibrillary acidic
transcriptional   glucoamylase        Transcriptional control of glucoamylase synthesis in vegetatively
transcriptional   glutathione         Transcriptional control of glutathione S-transferase gene
transcriptional   gonococcal          Transcriptional control of gonococcal pilE expression:
transcriptional   hepatitis           Transcriptional control of hepatitis B
transcriptional   hepatocanalicular   Transcriptional control of hepatocanalicular transporter gene
transcriptional   herpesvirus         Transcriptional control of herpesvirus gene expression:
transcriptional   high                Transcriptional control of high molecular weight
transcriptional   HLA-ABC             Transcriptional control of HLA-A,B,C antigen in human
transcriptional   Hox                 Transcriptional control of Hox genes in the
transcriptional                       Transcriptional control of human cytochrome P1-450
transcriptional                       Transcriptional control of human diploid fibroblast
transcriptional                       Transcriptional control of human papillomavirus (HPV)
transcriptional                       Transcriptional control of human papillomavirus type
transcriptional                       Transcriptional control of human Tenon's capsule
transcriptional   IL-2                Transcriptional control of IL-2 and IL-4
transcriptional   intestinal          Transcriptional control of intestinal cytochrome P-4503A
transcriptional   IS1                 Transcriptional control of IS1 transposition in Escherichia
transcriptional   K5                  Transcriptional control of K5, K6, K14,
transcriptional   lignin              Transcriptional control of lignin biosynthesis by
transcriptional   matrix              Transcriptional control of matrix metalloproteinases and the
transcriptional   metabolic           Transcriptional control of metabolic regulation genes
transcriptional   MHC                 Transcriptional control of MHC class I
transcriptional   MHC                 Transcriptional control of MHC class II
transcriptional   MHC                 Transcriptional control of MHC genes and T
transcriptional   MHC                 Transcriptional control of MHC genes in fetal
transcriptional   monolignol          Transcriptional control of monolignol biosynthesis in Pinus
transcriptional   mu-                 Transcriptional control of mu- and kappa-gene
transcriptional   multidrug           Transcriptional control of multidrug resistance in the
transcriptional                       Transcriptional control of murine CD94 gene:
transcriptional                       Transcriptional control of muscle development by
transcriptional                       Transcriptional control of muscle plasticity: differential
transcriptional   myocardial          Transcriptional control of myocardial Rapid
transcriptional   neuronal            Transcriptional control of neuronal diversification in the
transcriptional   neuropeptide        Transcriptional control of neuropeptide gene expression
transcriptional   neurotransmitter    Transcriptional control of neurotransmitter The
transcriptional   nitric              Transcriptional control of nitric oxide reductase
transcriptional   nonfermentative     Transcriptional control of nonfermentative metabolism in the
transcriptional                       Transcriptional control of nuclear genes for
transcriptional   orf224/atp6         Transcriptional control of orf224/atp6 by the pol
transcriptional   ornithine           Transcriptional control of ornithine aminotransferase synthesis
transcriptional   osteoblast          Transcriptional control of osteoblast growth and differentiation.
transcriptional   pancreatic          Transcriptional control of pancreatic islet hormones
transcriptional   peptidoglycan       Transcriptional control of peptidoglycan precursor synthesis
transcriptional                       Transcriptional control of plant genes responsive
transcriptional                       Transcriptional control of plant storage protein
transcriptional   polarity            Transcriptional control of polarity in Escherichia
transcriptional                       Transcriptional control of rat heme oxygenase
transcriptional                       Transcriptional control of rat hepatic glutaminase
transcriptional   ribosome            Transcriptional control of ribosome production in regenerating
transcriptional                       Transcriptional control of several aerobically induced
transcriptional                       Transcriptional control of sex-pheromone-inducible genes on
                  sex-pheromone-inducible
transcriptional   SPARC               Transcriptional control of SPARC by v-Jun
transcriptional   SSL1                Transcriptional control of SSL1, a gene
transcriptional   steroid-regulated   Transcriptional control of steroid-regulated apoptosis in murine
transcriptional   synthesis           Transcriptional control of synthesis of acid-soluble
transcriptional   T                   Transcriptional control of T cell
transcriptional   t                   Transcriptional control of t lymphocyte
transcriptional   T4                  Transcriptional control of T4 coliphage-specific genes
transcriptional   tektin              Transcriptional control of tektin A mRNA
transcriptional                       Transcriptional control of the agr-dependent virulence
transcriptional                       Transcriptional control of the alpha 1(I)
transcriptional                       Transcriptional control of the arginine/lysine transporter,
transcriptional                       Transcriptional control of the Bacillus subtilis
transcriptional                       Transcriptional control of the bovine leukemia
transcriptional                       Transcriptional control of the cell
transcriptional                       Transcriptional control of the cell cycle
transcriptional                       Transcriptional control of the cellulase genes
transcriptional                       Transcriptional control of the chicken cardiac
transcriptional                       Transcriptional control of the citrate-inducible citMCDEFGRP
transcriptional                       Transcriptional control of the core cell-death
transcriptional                       Transcriptional control of the cysG gene
transcriptional                       Transcriptional control of the DNA methyltransferases
transcriptional                       Transcriptional control of the endogenous MYC
transcriptional                       Transcriptional control of the equine herpesvirus
transcriptional                       Transcriptional control of the expression of lipoprotein
transcriptional                       Transcriptional control of the expression of mouse
transcriptional                       Transcriptional control of the factor IX
transcriptional                       Transcriptional control of the fibronectin gene
transcriptional                       Transcriptional control of the forkhead thyroid
transcriptional                       Transcriptional control of the GAL/MEL regulon
transcriptional                       Transcriptional control of the galanin
transcriptional                       Transcriptional control of the glnD gene
transcriptional                       Transcriptional control of the heme oxygenase
transcriptional                       Transcriptional control of the Htf9-A/RanBP-1 gene
transcriptional                       Transcriptional control of the human aldehyde
transcriptional                       Transcriptional control of the human biliary
transcriptional                       Transcriptional control of the human Harvey
transcriptional                       Transcriptional control of the human MCP-2
transcriptional                       Transcriptional control of the human plasma
transcriptional                       Transcriptional control of the human pregnancy-specific
transcriptional                       Transcriptional control of the human sodium-coupled
transcriptional                       Transcriptional control of the human thromboxane
transcriptional                       Transcriptional control of the hydrogen cyanide
transcriptional                       Transcriptional control of the IL-5 gene
transcriptional                       Transcriptional control of the inducible nitrate
transcriptional                       Transcriptional control of the inflammatory response:
transcriptional                       Transcriptional control of the invariant chain
transcriptional                       Transcriptional control of the invasion regulatory
transcriptional                         Transcriptional control of the iron-responsive fxbA
transcriptional                         Transcriptional control of the isoleucine-valine messenger
transcriptional                         Transcriptional control of the low-temperature-inducible des
transcriptional                         Transcriptional control of the mouse alpha
transcriptional                         Transcriptional control of the mouse Col7a1
transcriptional                         Transcriptional control of the mouse prealbumin
transcriptional                         Transcriptional control of the mtr efflux
transcriptional                         Transcriptional control of the multiple catabolic
transcriptional                         Transcriptional control of the murine albumin/alpha-fetoprotein
transcriptional                         Transcriptional control of the murine polymeric
transcriptional                         Transcriptional control of the nah and sal
transcriptional                         Transcriptional control of the neuronal nicotinic
transcriptional                         Transcriptional control of the nuo operon
transcriptional                         Transcriptional control of the osteocalcin gene
transcriptional                         Transcriptional control of the platelet-derived growth
transcriptional                         Transcriptional control of the pref-1 gene
transcriptional                         Transcriptional control of the Pseudomonas putida
transcriptional                         Transcriptional control of the Pseudomonas TOL
transcriptional                         Transcriptional control of the rat alpha
transcriptional                         Transcriptional control of the rat heme
transcriptional                         Transcriptional control of the rat hepatic
transcriptional                         Transcriptional control of the rat serotonin-2
transcriptional                         Transcriptional control of the RECK metastasis/angiogenesis
transcriptional                         Transcriptional control of the RNA-dependent RNA
transcriptional                         Transcriptional control of the S10 ribosomal
transcriptional                         Transcriptional control of the Saccharomyces cerevisiae
transcriptional                         Transcriptional control of the sporulation-specific glucoamylase
transcriptional                         Transcriptional control of the stearoyl-CoA desaturase-1
transcriptional                         Transcriptional control of the sulfur-regulated cysH
transcriptional                         Transcriptional control of the testis-specific histone
transcriptional                         Transcriptional control of the tissue-specific, developmentally
transcriptional                         Transcriptional control of the uvrD gene
transcriptional                         Transcriptional control of the yeast acetyl-CoA
transcriptional                         Transcriptional control of the yeast PDR5
transcriptional   thymidine             Transcriptional control of thymidine kinase gene
transcriptional   thyroglobulin         Transcriptional control of thyroglobulin gene expression
transcriptional   toxT                  Transcriptional control of toxT, a regulatory
transcriptional   triglyceride          Transcriptional control of triglyceride metabolism: fibrates
transcriptional   two                   Transcriptional control of two gene subclusters
transcriptional   viral                 Transcriptional control of viral gene therapy
transcriptional   vitamin               Transcriptional control of vitamin D-regulated
transcriptional   yeast                 Transcriptional control of yeast phosphofructokinase gene
transcriptional   yeast                 Transcriptional control of yeast phosphoglycerate mutase-encoding
transcriptional   yeast                 Transcriptional control of yeast plasma membrane
transcriptional   yeast                 Transcriptional control of yeast ribosomal protein
transcriptional   2'3'-cyclic           Transcriptional regulation of 2',3'-cyclic nucleotide 3'-phosphodiesterase
transcriptional                         Transcriptional regulation of 3,4-dihydroxy-2-butanone 4-phosphate
                  34-dihydroxy-2-butanone
transcriptional                         Transcriptional regulation of 3-methylcholanthrene-inducible P-450 gene
                  3-methylcholanthrene-inducible
transcriptional   5-aminolevulinate     Transcriptional regulation of 5-aminolevulinate synthase by
transcriptional                         Transcriptional regulation of a Bacillus subtilis
transcriptional                         Transcriptional regulation of a BMP-6 promoter
transcriptional                         Transcriptional regulation of a contractile gene
transcriptional                         Transcriptional regulation of a gene encoding
transcriptional                         Transcriptional regulation of a hematopoietic proteoglycan
transcriptional                         Transcriptional regulation of a herpes simplex
transcriptional                         Transcriptional regulation of a mesangium-predominant gene,
transcriptional                         Transcriptional regulation of a mouse Clara
transcriptional                         Transcriptional regulation of a pair-rule stripe
transcriptional                         Transcriptional regulation of a patatin-1 gene
transcriptional                         Transcriptional regulation of a periodically controlled
transcriptional                         Transcriptional regulation of a plasminogen activator
transcriptional                         Transcriptional regulation of a promoter in the
transcriptional                         Transcriptional regulation of a Purkinje cell-specific
transcriptional                         Transcriptional regulation of a Ras nucleotide-exchange
transcriptional                         Transcriptional regulation of a rat hepatoma
transcriptional                         Transcriptional regulation of a rat liver
transcriptional                         Transcriptional regulation of a receptor protein
transcriptional                         Transcriptional regulation of a rice mitogen-activated
transcriptional                         Transcriptional regulation of a second flavodoxin
transcriptional                         Transcriptional regulation of a seed-specific carrot
transcriptional                         Transcriptional regulation of a sterol-biosynthetic enzyme
transcriptional                         Transcriptional regulation of a tumor promoter
transcriptional                         Transcriptional regulation of a Xenopus embryonic
transcriptional                         Transcriptional regulation of a yeast HSP70
transcriptional   A33                   Transcriptional regulation of A33 antigen expression
transcriptional   ABC                   Transcriptional regulation of ABC drug
transcriptional   acetyl                Transcriptional regulation of acetyl coenzyme A
transcriptional   actin                 Transcriptional regulation of actin and myosin
transcriptional   adipocyte             Transcriptional regulation of adipocyte hormone-sensitive lipase
transcriptional   adrenomedullin        Transcriptional regulation of adrenomedullin in rat
transcriptional   Alcaligenes           Transcriptional regulation of Alcaligenes eutrophus hydrogenase
transcriptional   alpha                 Transcriptional regulation of alpha 2(I) collagen
transcriptional   alpha                 Transcriptional regulation of alpha IIb integrin
transcriptional   alpha(1b)             Transcriptional regulation of alpha(1b) adrenergic receptors
transcriptional                         Transcriptional regulation of alpha1,3-galactosyltransferase in embryonal
                  alpha13-galactosyltransferase
transcriptional   alpha1-adrenoceptor Transcriptional regulation of alpha1-adrenoceptor gene in the
transcriptional   alpha-fetoprotein     Transcriptional regulation of alpha-fetoprotein expression by
transcriptional   ALV                   Transcriptional regulation of ALV bursal
transcriptional   Alzheimer's           Transcriptional regulation of Alzheimer's disease genes:
transcriptional   amyloid               Transcriptional regulation of amyloid precursor protein
transcriptional                         Transcriptional regulation of an aldolase gene
transcriptional                         Transcriptional regulation of an archaeal operon
transcriptional                         Transcriptional regulation of an endoglucanase and a
transcriptional                         Transcriptional regulation of an hsp70 heat
transcriptional                         Transcriptional regulation of an unusual trypsin-related
transcriptional   androgen              Transcriptional regulation of androgen receptor gene
transcriptional   angiogenesis-related Transcriptional regulation of angiogenesis-related puromycin-insensitive leucyl-sp
transcriptional   angiotensinogen       Transcriptional regulation of angiotensinogen gene
transcriptional   antigen               Transcriptional regulation of antigen MHC
transcriptional   apolipoprotein        Transcriptional regulation of apolipoprotein A-I expression
transcriptional   apolipoprotein        Transcriptional regulation of apolipoprotein A-I gene
transcriptional   apolipoprotein        Transcriptional regulation of apolipoprotein C-III gene
transcriptional   apolipoprotein        Transcriptional regulation of apolipoprotein E expression
transcriptional   aquaporin-2           Transcriptional regulation of aquaporin-2 water channel
transcriptional   Arabidopsis         Transcriptional regulation of Arabidopsis thaliana phytochelatin
transcriptional   aromatase           Transcriptional regulation of aromatase expression in human
transcriptional   atonal              Transcriptional regulation of atonal during development
transcriptional   atonal              Transcriptional regulation of atonal required for
transcriptional   BACE1               Transcriptional regulation of BACE1, the beta-amyloid
transcriptional   Bacillus            Transcriptional regulation of Bacillus subtilis citrate
transcriptional   Bacillus            Transcriptional regulation of Bacillus subtilis glucose
transcriptional   Bacillus            Transcriptional regulation of Bacillus thuringiensis
transcriptional   bacteriophage       Transcriptional regulation of bacteriophage SPO1 protein
transcriptional                       Transcriptional regulation of basal cyclooxygenase-2 expression
transcriptional                       Transcriptional regulation of basic fibroblast growth
transcriptional   B-cell              Transcriptional regulation of B-cell Transcription
transcriptional   bcl-2               Transcriptional regulation of bcl-2 by nuclear
transcriptional   bcl-2               Transcriptional regulation of bcl-2 mediated by
transcriptional   beta-defensin       Transcriptional regulation of beta-defensin gene expression
transcriptional   bialaphos           Transcriptional regulation of bialaphos biosynthesis in Streptomyces
transcriptional   bioluminesence      Transcriptional regulation of bioluminesence genes from
transcriptional   biomass-degrading   Transcriptional regulation of biomass-degrading enzymes in the
transcriptional   blood               Transcriptional regulation of blood formation during
transcriptional   BMP-2               Transcriptional regulation of BMP-2 activated genes
transcriptional   BMP-4               Transcriptional regulation of BMP-4 in the Xenopus
transcriptional   BMP4                Transcriptional regulation of BMP4 synexpression in transgenic
transcriptional   breathless          Transcriptional regulation of breathless FGF receptor
transcriptional   C/EBPdelta          Transcriptional regulation of C/EBPdelta in G(0)
transcriptional   carbonic            Transcriptional regulation of carbonic anhydrase II
transcriptional   cardiac             Transcriptional regulation of cardiac development: implications
transcriptional   carnitine           Transcriptional regulation of carnitine palmitoyltransferase synthesis
transcriptional   caspases            Transcriptional regulation of caspases in experimental
transcriptional   catalase            Transcriptional regulation of catalase gene in the
transcriptional   cathepsin           Transcriptional regulation of cathepsin B expression
transcriptional   CCSP                Transcriptional regulation of CCSP by interferon-gamma
transcriptional   CD28                Transcriptional regulation of CD28 expression by
transcriptional   CD6                 Transcriptional regulation of CD6 expression on
transcriptional                       Transcriptional regulation of cell division genes
transcriptional                       Transcriptional regulation of cell invasion: AP-1
transcriptional                       Transcriptional regulation of cell line-dependent, baculovirus-mediated
transcriptional                       Transcriptional regulation of cell type-specific expression
transcriptional                       Transcriptional regulation of cell-specific expression of the
transcriptional                       Transcriptional regulation of cellular ageing by
transcriptional                       Transcriptional regulation of cellular and viral
transcriptional                       Transcriptional regulation of cellular retinaldehyde-binding protein
transcriptional                       Transcriptional regulation of cellular retinol-binding protein,
transcriptional   ceruloplasmin       Transcriptional regulation of ceruloplasmin gene expression
transcriptional   c-Fes               Transcriptional regulation of c-Fes in myeloid
transcriptional   CHI3L1              Transcriptional regulation of CHI3L1, a marker
transcriptional   cholesterol         Transcriptional regulation of cholesterol 7 alpha-hydroxylase
transcriptional   choline             Transcriptional regulation of choline acetyltransferase gene
transcriptional   chorionic           Transcriptional regulation of chorionic gonadotropin alpha-
transcriptional   c-Jun               Transcriptional regulation of c-Jun expression during
transcriptional   c-jun               Transcriptional regulation of c-jun gene expression
transcriptional   class-I             Transcriptional regulation of class-I major histocompatibility
transcriptional   CLN3                Transcriptional regulation of CLN3 expression by
transcriptional   c-myc                   Transcriptional regulation of c-myc during chemically
transcriptional   c-myc                   Transcriptional regulation of c-myc oncogene expression
transcriptional   collagenase             Transcriptional regulation of collagenase (MMP-1, MMP-13)
transcriptional   collagenase-3           Transcriptional regulation of collagenase-3 by interleukin-1
transcriptional   comC:                   Transcriptional regulation of comC: evidence for
transcriptional   complement              Transcriptional regulation of complement Complement
transcriptional   connective              Transcriptional regulation of connective tissue growth
transcriptional   coordinate              Transcriptional regulation of coordinate changes in flagellar
transcriptional   cortical                Transcriptional regulation of cortical neuron migration
transcriptional   corticotropin-releasing Transcriptional regulation of corticotropin-releasing hormone-binding protein
transcriptional   CREB                    Transcriptional regulation of CREB (cyclic AMP
transcriptional   cruxrhodopsin           Transcriptional regulation of cruxrhodopsin gene from
transcriptional   cyclooxygenase          Transcriptional regulation of cyclooxygenase 2 by
transcriptional   cyclo-oxygenase         Transcriptional regulation of cyclo-oxygenase expression: three
transcriptional   cyclooxygenase-1        Transcriptional regulation of cyclooxygenase-1 by histone
transcriptional   cyclooxygenase-2        Transcriptional regulation of cyclooxygenase-2 gene expression:
transcriptional   cyclooxygenase-2        Transcriptional regulation of cyclooxygenase-2 gene in ovine
transcriptional   cyclooxygenase-2        Transcriptional regulation of cyclooxygenase-2 in mouse
transcriptional   cyclooxygenase-2        Transcriptional regulation of cyclooxygenase-2 in the human
transcriptional   CYP11A1                 Transcriptional regulation of CYP11A1. Steroid hormones
transcriptional   CYP19                   Transcriptional regulation of CYP19 gene (aromatase)
transcriptional   CYP2B1                  Transcriptional regulation of CYP2B1 induction in primary
transcriptional   CYP2C9                  Transcriptional regulation of CYP2C9 Role
transcriptional   cytochrome              Transcriptional regulation of cytochrome d in nitrogen-fixing
transcriptional   cytochrome              Transcriptional regulation of cytochrome p450 2B
transcriptional   cytochrome              Transcriptional regulation of cytochrome P4503A4 gene
transcriptional   cytokine                Transcriptional regulation of cytokine expression by
transcriptional   cytokine                Transcriptional regulation of cytokine genes in nontransformed
transcriptional   cytoskeletal            Transcriptional regulation of cytoskeletal functions and segmentation
transcriptional   cytosol                 Transcriptional regulation of cytosol and membrane
transcriptional   decorin                 Transcriptional regulation of decorin gene
transcriptional   decreased               Transcriptional regulation of decreased protein synthesis
transcriptional   delta-aminolevulinic Transcriptional regulation of delta-aminolevulinic acid dehydratase
transcriptional   dentin                  Transcriptional regulation of dentin matrix protein
transcriptional   DF3                     Transcriptional regulation of DF3 gene expression
transcriptional                           Transcriptional regulation of differentiation, selective toxicity
transcriptional                           Transcriptional regulation of divergent capsule biosynthesis
transcriptional   DNA                     Transcriptional regulation of DNA damage responsive
transcriptional   dog                     Transcriptional regulation of dog prostate arginine
transcriptional   drug                    Transcriptional regulation of drug efflux genes
transcriptional   E2F-1                   Transcriptional regulation of E2F-1 and eIF-2
transcriptional   early                   Transcriptional regulation of early B-lymphocyte
transcriptional   early                   Transcriptional regulation of early functions of bacteriophage
transcriptional   early                   Transcriptional regulation of early growth response
transcriptional   early-response          Transcriptional regulation of early-response genes during
transcriptional   endothelial             Transcriptional regulation of endothelial cell adhesion
transcriptional   endothelial             Transcriptional regulation of endothelial cell tissue
transcriptional   endothelial             Transcriptional regulation of endothelial constitutive PGHS-1
transcriptional   endothelial             Transcriptional regulation of endothelial nitric-oxide synthase
transcriptional   endothelin-1            Transcriptional regulation of endothelin-1 by erythropoietin
transcriptional   energy                  Transcriptional regulation of energy substrate metabolism
transcriptional   environmentally         Transcriptional regulation of environmentally inducible genes
transcriptional   erythropoiesis       Transcriptional regulation of erythropoiesis. Fine tuning
transcriptional   erythropoiesis:      Transcriptional regulation of erythropoiesis: an affair
transcriptional   Escherichia          Transcriptional regulation of Escherichia coli K-12
transcriptional   estrogen             Transcriptional regulation of estrogen receptor in breast
transcriptional   estrogen-responsive Transcriptional regulation of estrogen-responsive genes by
transcriptional   eukaryotic           Transcriptional regulation of eukaryotic gene expression
transcriptional   expression           Transcriptional regulation of expression of carbohydrate
transcriptional   expression           Transcriptional regulation of expression of the rainbow
transcriptional   F                    Transcriptional regulation of F plasmid gene
transcriptional   farnesyl             Transcriptional regulation of farnesyl pyrophosphate synthase
transcriptional   Fas                  Transcriptional regulation of Fas gene expression
transcriptional   fatty                Transcriptional regulation of fatty acid cyclooxygenases-1
transcriptional   fatty                Transcriptional regulation of fatty acid synthase
transcriptional   Fcgr2b               Transcriptional regulation of Fcgr2b gene by
transcriptional   ferric               Transcriptional regulation of ferric citrate transport
transcriptional   ferritin             Transcriptional regulation of ferritin H and L
transcriptional   ferritin             Transcriptional regulation of ferritin H messenger
transcriptional   ferritin             Transcriptional regulation of ferritin heavy chain
transcriptional   ferritin             Transcriptional regulation of ferritin messenger ribonucleic
transcriptional   fibroblast           Transcriptional regulation of fibroblast collagen synthesis
transcriptional   fibroblast           Transcriptional regulation of fibroblast growth factor-2
transcriptional   fibronectin          Transcriptional regulation of fibronectin gene by
transcriptional   fis                  Transcriptional regulation of fis operon involves
transcriptional   flocculation         Transcriptional regulation of flocculation genes in Saccharomyces
transcriptional   fosl-1               Transcriptional regulation of fosl-1 by licorice
transcriptional   furA                 Transcriptional regulation of furA and katG
transcriptional   GABAA                Transcriptional regulation of GABAA receptor gamma2
transcriptional   galectin-10          Transcriptional regulation of galectin-10 (eosinophil Charcot-Leyden
transcriptional                        Transcriptional regulation of gamma-glutamylcysteine synthetase-heavy subunit
                  gamma-glutamylcysteine
transcriptional   GATA-3               Transcriptional regulation of GATA-3 by an
transcriptional   gene                 Transcriptional regulation of gene expression by
transcriptional   gene                 Transcriptional regulation of gene expression during
transcriptional   gene                 Transcriptional regulation of gene expression in human
transcriptional   gene                 Transcriptional regulation of gene expression in Tetrahymena
transcriptional   gene                 Transcriptional regulation of gene expression of sec6,
transcriptional   gene                 Transcriptional regulation of gene expression: mechanisms
transcriptional   genes                Transcriptional regulation of genes encoding arabinan-degrading
transcriptional   genes                Transcriptional regulation of genes encoding glycolytic
transcriptional   genes                Transcriptional regulation of genes encoding insulin,
transcriptional   genes                Transcriptional regulation of genes encoding subunits
transcriptional   genes                Transcriptional regulation of genes encoding the acute-phase
transcriptional   genes                Transcriptional regulation of genes encoding the selenium-free
transcriptional   genes                Transcriptional regulation of genes for enzymes
transcriptional   genes                Transcriptional regulation of genes for plant-type
transcriptional   glial                Transcriptional regulation of glial cell
transcriptional   glial                Transcriptional regulation of glial fibrillary acidic
transcriptional   globin               Transcriptional regulation of globin gene expression
transcriptional   glutamine            Transcriptional regulation of glutamine synthetase gene
transcriptional   glutaredoxin         Transcriptional regulation of glutaredoxin and thioredoxin
transcriptional                        Transcriptional regulation of glyceraldehyde-3-phosphate dehydrogenase by
                  glyceraldehyde-3-phosphate
transcriptional   G-protein            Transcriptional regulation of G-protein alpha i
transcriptional   granulocyte          Transcriptional regulation of granulocyte and monocyte
transcriptional   growth          Transcriptional regulation of growth hormone gene
transcriptional   heat            Transcriptional regulation of heat shock
transcriptional   hematopoiesis   Transcriptional regulation of hematopoiesis in
transcriptional   heme            Transcriptional regulation of heme oxygenase-1 gene
transcriptional   heme            Transcriptional regulation of heme oxygenases by
transcriptional   hemoglobin      Transcriptional regulation of hemoglobin switching in chicken
transcriptional   hemopoiesis     Transcriptional regulation of hemopoiesis. The regulation
transcriptional   hepatic         Transcriptional regulation of hepatic angiotensinogen gene
transcriptional   hepatic         Transcriptional regulation of hepatic stellate cell
transcriptional   hepatic         Transcriptional regulation of hepatic sterol 27-hydroxylase
transcriptional   hepatitis       Transcriptional regulation of hepatitis B virus
transcriptional   herpes          Transcriptional regulation of herpes simplex virus
transcriptional   hexokinase      Transcriptional regulation of hexokinase I mRNA
transcriptional   hexokinase      Transcriptional regulation of hexokinase II in denervated
transcriptional   hippocampal     Transcriptional regulation of hippocampal 5-HT1a receptors
transcriptional   HIV-1           Transcriptional regulation of HIV-1 LTR during
transcriptional   HLA             Transcriptional regulation of HLA class II
transcriptional   HLA-A           Transcriptional regulation of HLA-A and -B:
transcriptional   HLA-DRA         Transcriptional regulation of HLA-DRA Transcriptional
transcriptional                   Transcriptional regulation of human 11beta-hydroxylase
transcriptional                   Transcriptional regulation of human 3'-phosphoadenosine 5'-phosphosulfate
transcriptional                   Transcriptional regulation of human 3'-phosphoadenosine 5'-phosphosulphate
transcriptional                   Transcriptional regulation of human adrenomedullin gene
transcriptional                   Transcriptional regulation of human and hamster
transcriptional                   Transcriptional regulation of human angiopoietin-2 by
transcriptional                   Transcriptional regulation of human apolipoprotein genes
transcriptional                   Transcriptional regulation of human beta-galactoside alpha2,
transcriptional                   Transcriptional regulation of human beta-galactoside alpha2,6-sialyltransferase
transcriptional                   Transcriptional regulation of human cardiac homeobox
transcriptional                   Transcriptional regulation of human corticotropin releasing
transcriptional                   Transcriptional regulation of human CYP2C genes:
transcriptional                   Transcriptional regulation of human CYP3A4 basal
transcriptional                   Transcriptional regulation of human excitatory amino
transcriptional                   Transcriptional regulation of human Galbeta1,3GalNAc/Galbeta1, 4GlcNAc
transcriptional                   Transcriptional regulation of human genes for
transcriptional                   Transcriptional regulation of human inducible nitric
transcriptional                   Transcriptional regulation of human insulin receptor
transcriptional                   Transcriptional regulation of human JC polyomavirus
transcriptional                   Transcriptional regulation of human mucin MUC4
transcriptional                   Transcriptional regulation of human osteopontin promoter
transcriptional                   Transcriptional regulation of human oxysterol [Formula:
transcriptional                   Transcriptional regulation of human oxysterol 7
transcriptional                   Transcriptional regulation of human oxysterol 7alpha-hydroxylase
transcriptional                   Transcriptional regulation of human papillomavirus type
transcriptional                   Transcriptional regulation of human placental corticotropin-releasing
transcriptional                   Transcriptional regulation of human placental leucine
transcriptional                   Transcriptional regulation of human polyomavirus JC:
transcriptional                   Transcriptional regulation of human prostaglandin-endoperoxide synthase-2
transcriptional                   Transcriptional regulation of human pulmonary surfactant
transcriptional                   Transcriptional regulation of human Rev-erbalpha gene
transcriptional                   Transcriptional regulation of human sodium/iodide symporter
transcriptional                   Transcriptional regulation of human SREBP-1c (sterol-regulatory-element-binding
transcriptional                         Transcriptional regulation of human thyroid hormone
transcriptional                         Transcriptional regulation of human transcription factor
transcriptional                         Transcriptional regulation of human transglutaminase1 gene
transcriptional                         Transcriptional regulation of human We
transcriptional                         Transcriptional regulation of human zeta and psi
transcriptional   hydrogenase           Transcriptional regulation of hydrogenase synthesis by
transcriptional   hydroxyindole         Transcriptional regulation of hydroxyindole O-methyltransferase in the
transcriptional   hydroxypyruvate       Transcriptional regulation of hydroxypyruvate reductase gene
transcriptional   IGF-I                 Transcriptional regulation of IGF-I expression in skeletal
transcriptional   IGF-I                 Transcriptional regulation of IGF-I receptor gene
transcriptional   IL-5                  Transcriptional regulation of IL-5 gene by
transcriptional   ILT                   Transcriptional regulation of ILT family
transcriptional   immunoglobulin        Transcriptional regulation of immunoglobulin expression in a
transcriptional   immunoglobulin        Transcriptional regulation of immunoglobulin gene expression
transcriptional   immunoglobulin        Transcriptional regulation of immunoglobulin heavy chain
transcriptional   immunoglobulin        Transcriptional regulation of immunoglobulin V
transcriptional   inducible             Transcriptional regulation of inducible nitric oxide
transcriptional   inflammatory          Transcriptional regulation of inflammatory secreted phospholipases
transcriptional   inhibin               Transcriptional regulation of inhibin beta B
transcriptional   iNOS                  Transcriptional regulation of iNOS by IL-1
transcriptional   insulin               Transcriptional regulation of insulin receptor gene
transcriptional   insulin               Transcriptional regulation of insulin receptor substrate
transcriptional   insulin-like          Transcriptional regulation of insulin-like growth factor
transcriptional   insulin-like          Transcriptional regulation of insulin-like growth factor-binding
transcriptional   insulin-like          Transcriptional regulation of insulin-like growth factor-I
transcriptional   insulin-like          Transcriptional regulation of insulin-like growth factor-II
transcriptional   intercellular         Transcriptional regulation of intercellular adhesion molecule
transcriptional   intercellular         Transcriptional regulation of intercellular adhesion molecule-1
transcriptional   intercellular         Transcriptional regulation of intercellular adhesion molecule-1:
transcriptional   interferon            Transcriptional regulation of interferon gamma gene
transcriptional   interferon-responsive Transcriptional regulation of interferon-responsive genes is
transcriptional   interferon-stimulated Transcriptional regulation of interferon-stimulated Interferons
transcriptional   interleukin           Transcriptional regulation of interleukin (IL)-8 by
transcriptional   interleukin           Transcriptional regulation of interleukin 3 (IL3)
transcriptional   interleukin           Transcriptional regulation of interleukin 3 gene
transcriptional   interleukin-1beta     Transcriptional regulation of interleukin-1beta gene by
transcriptional   interleukin-2         Transcriptional regulation of interleukin-2 gene expression
transcriptional   interleukin-3         Transcriptional regulation of interleukin-3 expression in megakaryocytes.
transcriptional   interleukin-6         Transcriptional regulation of interleukin-6 in pituitary
transcriptional   intestinal            Transcriptional regulation of intestinal hydrolase biosynthesis
transcriptional   intracellular         Transcriptional regulation of intracellular IL-1 receptor
transcriptional   iodothyronine         Transcriptional regulation of iodothyronine deiodinases during
transcriptional   Kaposi's              Transcriptional regulation of Kaposi's sarcoma-associated herpesvirus-encoded
transcriptional   katE                  Transcriptional regulation of katE in Escherichia
transcriptional   laccase               Transcriptional regulation of laccase and cellulase
transcriptional   laminin               Transcriptional regulation of laminin gene
transcriptional   LDL                   Transcriptional regulation of LDL receptor-related protein
transcriptional   left                  Transcriptional regulation of left ventricular beta-adrenergic
transcriptional   leptin                Transcriptional regulation of leptin gene promoter
transcriptional   limulus               Transcriptional regulation of limulus factor C:
transcriptional   lipoprotein           Transcriptional regulation of lipoprotein lipase in the
transcriptional   liver                 Transcriptional regulation of liver Over
transcriptional   liver                 Transcriptional regulation of liver phosphoenolpyruvate carboxykinase
transcriptional   liver-specific        Transcriptional regulation of liver-specific gene
transcriptional   L-type                Transcriptional regulation of L-type calcium channel
transcriptional   lung                  Transcriptional regulation of lung development: emergence
transcriptional   lux                   Transcriptional regulation of lux genes transferred
transcriptional   lymphocyte            Transcriptional regulation of lymphocyte lineage
transcriptional   lysosomal             Transcriptional regulation of lysosomal acid lipase
transcriptional   major                 Transcriptional regulation of major histocompatibility complex
transcriptional   mammalian             Transcriptional regulation of mammalian cytochrome c
transcriptional   matrix                Transcriptional regulation of matrix gla
transcriptional   meiosis               Transcriptional regulation of meiosis in
transcriptional   meiosis               Transcriptional regulation of meiosis in budding
transcriptional   Mesp1                 Transcriptional regulation of Mesp1 and Mesp2
transcriptional   messenger             Transcriptional regulation of messenger RNA for
transcriptional   metabolic             Transcriptional regulation of metabolic processes: implications
transcriptional   metacyclic            Transcriptional regulation of metacyclic variant surface
transcriptional   metastasis-related    Transcriptional regulation of metastasis-related genes in human
transcriptional   methionine            Transcriptional regulation of methionine synthase by
transcriptional   mexR                  Transcriptional regulation of mexR, the repressor
transcriptional   MHC                   Transcriptional regulation of MHC class I
transcriptional   MHC                   Transcriptional regulation of MHC class II
transcriptional   mitfa                 Transcriptional regulation of mitfa accounts for
transcriptional   mitochondrial         Transcriptional regulation of mitochondrial HMG-CoA synthase
transcriptional   mitotic               Transcriptional regulation of mitotic checkpoint gene
transcriptional   mitotic               Transcriptional regulation of mitotic genes by
transcriptional   MMP-9                 Transcriptional regulation of MMP-9 expression in stromal
transcriptional   MnSOD                 Transcriptional regulation of MnSOD by manganese
transcriptional   Mn-superoxide         Transcriptional regulation of Mn-superoxide dismutase gene
transcriptional   molybdoenzyme         Transcriptional regulation of molybdoenzyme synthesis in Escherichia
transcriptional                         Transcriptional regulation of mouse delta-opioid receptor
transcriptional                         Transcriptional regulation of mouse dihydrofolate reductase
transcriptional                         Transcriptional regulation of mouse granulocyte-macrophage colony-stimulating
transcriptional                         Transcriptional regulation of mouse MARCKS promoter
transcriptional                         Transcriptional regulation of mouse mu-opioid receptor
transcriptional                         Transcriptional regulation of mouse type 1
transcriptional   mu                    Transcriptional regulation of mu and delta
transcriptional   mu                    Transcriptional regulation of mu opioid receptor
transcriptional   multidrug             Transcriptional regulation of multidrug efflux pumps
transcriptional   multidrug             Transcriptional regulation of multidrug resistance in breast
transcriptional   multigene             Transcriptional regulation of multigene loci: multilevel
transcriptional                         Transcriptional regulation of murine beta1,4-galactosyltransferase in somatic
transcriptional                         Transcriptional regulation of murine NADP(+)-dependent methylenetetrahydrofola
transcriptional                         Transcriptional regulation of muscle fatty acid-binding
transcriptional   muscle-specific       Transcriptional regulation of muscle-specific genes during
transcriptional   myelin                Transcriptional regulation of myelin associated glycoprotein
transcriptional   myeloid               Transcriptional regulation of myeloid differentiation primary
transcriptional   myeloperoxidase       Transcriptional regulation of myeloperoxidase gene expression
transcriptional   myelopoiesis          Transcriptional regulation of myelopoiesis. A common
transcriptional   Na/K-ATPase           Transcriptional regulation of Na/K-ATPase by corticosteroids,
transcriptional   Na+/H+                Transcriptional regulation of Na+/H+ exchanger expression
transcriptional                         Transcriptional regulation of N-acetylglucosaminyltransferase V by
                  N-acetylglucosaminyltransferase
transcriptional   neu                   Transcriptional regulation of neu by RB
transcriptional   neurofilament         Transcriptional regulation of neurofilament expression by
transcriptional   neuromodulin          Transcriptional regulation of neuromodulin (GAP-43) in mouse
transcriptional   neuronal              Transcriptional regulation of neuronal nicotinic acetylcholine
transcriptional   NF-kappa              Transcriptional regulation of NF-kappa B2: evidence
transcriptional   nicotinamide          Transcriptional regulation of nicotinamide adenine dinucleotide
transcriptional   nicotinic             Transcriptional regulation of nicotinic acetylcholine receptor
transcriptional   nitrogen              Transcriptional regulation of nitrogen fixation by
transcriptional   Nostoc                Transcriptional regulation of Nostoc hydrogenases: effects
transcriptional   Nostoc                Transcriptional regulation of Nostoc uptake
transcriptional   Notch                 Transcriptional regulation of Notch and Delta:
transcriptional                         Transcriptional regulation of nuclear orphan receptor,
transcriptional   OCI-5/Glypican        Transcriptional regulation of OCI-5/Glypican 3: elongation
transcriptional   osteocalcin           Transcriptional regulation of osteocalcin production by
transcriptional   osteopontin           Transcriptional regulation of osteopontin and the metastatic
transcriptional   osteopontin           Transcriptional regulation of osteopontin gene in vivo
transcriptional   osteopontin           Transcriptional regulation of osteopontin production in rat
transcriptional   oxytocin              Transcriptional regulation of oxytocin receptor by
transcriptional   P450scc               Transcriptional regulation of P450scc gene expression
transcriptional   p90                   Transcriptional regulation of p90 with sequence
transcriptional   PDGF-A                Transcriptional regulation of PDGF-A and TGF-beta
transcriptional   pentose               Transcriptional regulation of pentose utilisation systems
transcriptional   phosphate-responsive Transcriptional regulation of phosphate-responsive genes in low-affinity
transcriptional   phospholamban         Transcriptional regulation of phospholamban gene and translational
transcriptional   phospholipase         Transcriptional regulation of phospholipase C-gamma 1
transcriptional   phosphoprotein        Transcriptional regulation of phosphoprotein p18 during
transcriptional   pig                   Transcriptional regulation of pig lactase-phlorizin hydrolase:
transcriptional   pilC2                 Transcriptional regulation of pilC2 in Neisseria
transcriptional   pim-1                 Transcriptional regulation of pim-1 by prolactin:
transcriptional   pituitary             Transcriptional regulation of pituitary gonadotrophin subunit
transcriptional   pituitary             Transcriptional regulation of pituitary synthesis and secretion
transcriptional                         Transcriptional regulation of plant phosphate
transcriptional   plasma                Transcriptional regulation of plasma protein synthesis
transcriptional   plasminogen           Transcriptional regulation of plasminogen activator inhibitor
transcriptional   plasminogen           Transcriptional regulation of plasminogen activator inhibitor-1
transcriptional   platelet-activating   Transcriptional regulation of platelet-activating factor receptor
transcriptional   podocyte              Transcriptional regulation of podocyte specification and differentiation.
transcriptional   porcine               Transcriptional regulation of porcine endogenous retroviruses
transcriptional   precore               Transcriptional regulation of precore and pregenomic
transcriptional   pre-pro-endothelin-1 Transcriptional regulation of pre-pro-endothelin-1 gene by
transcriptional   prfA                  Transcriptional regulation of prfA and PrfA-regulated
transcriptional   prolactin             Transcriptional regulation of prolactin gene expression
transcriptional   prolactin             Transcriptional regulation of prolactin receptor gene
transcriptional   proliferin            Transcriptional regulation of proliferin gene expression
transcriptional   prostaglandin         Transcriptional regulation of prostaglandin synthase 2
transcriptional   prostaglandin-H       Transcriptional regulation of prostaglandin-H synthase-2 gene
transcriptional                         Transcriptional regulation of prostaglandin-H-synthase-1 in the amnion-derived
                  prostaglandin-H-synthase-1
transcriptional   prostate              Transcriptional regulation of prostate kallikrein-like genes
transcriptional                         Transcriptional regulation of protein complexes and biological
transcriptional                         Transcriptional regulation of protein kinase C
transcriptional   proto-oncogene        Transcriptional regulation of proto-oncogene expression by
transcriptional   pseudobactin          Transcriptional regulation of pseudobactin synthesis in the
transcriptional   Pseudomonas           Transcriptional regulation of Pseudomonas aeruginosa rhlR,
transcriptional   PS-IAA4/5          Transcriptional regulation of PS-IAA4/5 and PS-IAA6
transcriptional   puc                Transcriptional regulation of puc operon expression
transcriptional   pulmonary          Transcriptional regulation of pulmonary elastin gene
transcriptional   RANTES             Transcriptional regulation of RANTES expression in T
transcriptional                      Transcriptional regulation of rat alpha 1-acid
transcriptional                      Transcriptional regulation of rat calbindin expression
transcriptional                      Transcriptional regulation of rat cyclin D1
transcriptional                      Transcriptional regulation of rat cytochrome P450c17
transcriptional                      Transcriptional regulation of rat hepatic aryl
transcriptional                      Transcriptional regulation of rat hepatic low-density
transcriptional                      Transcriptional regulation of rat insulin-like growth
transcriptional                      Transcriptional regulation of rat liver epoxide
transcriptional                      Transcriptional regulation of rat liver glutathione
transcriptional                      Transcriptional regulation of rat liver protein
transcriptional                      Transcriptional regulation of rat microsomal epoxide
transcriptional                      Transcriptional regulation of rat Na(+)/H(+) exchanger
transcriptional                      Transcriptional regulation of rat P-450 2C
transcriptional                      Transcriptional regulation of rat scavenger receptor
transcriptional   repressor          Transcriptional regulation of repressor synthesis in mycobacteriophage
transcriptional   retinoic           Transcriptional regulation of retinoic acid receptor
transcriptional   retinoic           Transcriptional regulation of retinoic acid responsive
transcriptional   ribosomal          Transcriptional regulation of ribosomal proteins during
transcriptional   ribosomal          Transcriptional regulation of ribosomal RNA synthesis
transcriptional   S100A1             Transcriptional regulation of S100A1 and expression
transcriptional   salivary           Transcriptional regulation of salivary proline-rich protein
transcriptional   Salmonella         Transcriptional regulation of Salmonella enterica virulence
transcriptional   Salmonella         Transcriptional regulation of Salmonella virulence: a PhoQ
transcriptional   Schistosoma        Transcriptional regulation of Schistosoma mansoni calreticulin:
transcriptional   secondary          Transcriptional regulation of secondary growth in Arabidopsis
transcriptional   secretin           Transcriptional regulation of secretin gene
transcriptional   secretogranin      Transcriptional regulation of secretogranin II and chromogranin
transcriptional   sertoli            Transcriptional regulation of sertoli cell differentiation
transcriptional   Sertoli            Transcriptional regulation of Sertoli cell immediate
transcriptional   serum              Transcriptional regulation of serum amyloid A
transcriptional   serum              Transcriptional regulation of serum amyloid A1
transcriptional                      Transcriptional regulation of several genes for
transcriptional   Smad2              Transcriptional regulation of Smad2 is required
transcriptional   smooth             Transcriptional regulation of smooth muscle contractile
transcriptional   smooth             Transcriptional regulation of smooth muscle phenotypic
transcriptional   sodium             Transcriptional regulation of sodium transport by
transcriptional   solventogenesis    Transcriptional regulation of solventogenesis in Clostridium
transcriptional   sorghum            Transcriptional regulation of sorghum defense determinants
transcriptional   spermiogenesis:    Transcriptional regulation of spermiogenesis: insights from
transcriptional   sporulation        Transcriptional regulation of sporulation genes in yeast.
transcriptional   squalene           Transcriptional regulation of squalene epoxidase by
transcriptional   Src                Transcriptional regulation of Src homology 2
transcriptional   SSA3               Transcriptional regulation of SSA3, an HSP70
transcriptional   steroid            Transcriptional regulation of steroid hydroxylase genes
transcriptional   steroid            Transcriptional regulation of steroid receptor coactivator-1
transcriptional   Streptomyces       Transcriptional regulation of Streptomyces coelicolor pathway-specific
transcriptional   stress-inducible   Transcriptional regulation of stress-inducible genes in procaryotes.
transcriptional   string             Transcriptional regulation of string (cdc25): a link
transcriptional   stromelysin-1   Transcriptional regulation of stromelysin-1 gene expression
transcriptional   styrene         Transcriptional regulation of styrene degradation in Pseudomonas
transcriptional   SUP35           Transcriptional regulation of SUP35 and SUP45
transcriptional   surfactant      Transcriptional regulation of surfactant proteins SP-A
transcriptional   Syndecan-1      Transcriptional regulation of Syndecan-1 expression by
transcriptional   T               Transcriptional regulation of T cell receptor
transcriptional   T               Transcriptional regulation of T lymphocyte development
transcriptional   T-cell          Transcriptional regulation of T-cell genes during
transcriptional   th2             Transcriptional regulation of th2 differentiation by
transcriptional                   Transcriptional regulation of the 11p15 mucin
transcriptional                   Transcriptional regulation of the 3-hydroxy-3-methylglutaryl coenzyme
transcriptional                   Transcriptional regulation of the 5' proximal
transcriptional                   Transcriptional regulation of the 5-HT2A
transcriptional                   Transcriptional regulation of the A and B
transcriptional                   Transcriptional regulation of the aconitase genes
transcriptional                   Transcriptional regulation of the adipocyte fatty
transcriptional                   Transcriptional regulation of the AhR gene
transcriptional                   Transcriptional regulation of the albumin gene
transcriptional                   Transcriptional regulation of the alpha 4
transcriptional                   Transcriptional regulation of the androgen signaling
transcriptional                   Transcriptional regulation of the Antifungal Protein
transcriptional                   Transcriptional regulation of the antioxidant protein
transcriptional                   Transcriptional regulation of the antioxidant response
transcriptional                   Transcriptional regulation of the AP-2alpha promoter
transcriptional                   Transcriptional regulation of the apoAI gene
transcriptional                   Transcriptional regulation of the apoC-III gene
transcriptional                   Transcriptional regulation of the apolipoprotein AI
transcriptional                   Transcriptional regulation of the apolipoprotein A-I
transcriptional                   Transcriptional regulation of the apolipoprotein A-IV
transcriptional                   Transcriptional regulation of the apolipoprotein B100
transcriptional                   Transcriptional regulation of the apolipoprotein B-100
transcriptional                   Transcriptional regulation of the Arabidopsis thaliana
transcriptional                   Transcriptional regulation of the ATP citrate-lyase
transcriptional                   Transcriptional regulation of the Bacillus ohbensis
transcriptional                   Transcriptional regulation of the Bacillus subtilis
transcriptional                   Transcriptional regulation of the Bacillus thuringiensis
transcriptional                   Transcriptional regulation of the BCL-6 gene:
transcriptional                   Transcriptional regulation of the BCL-X gene
transcriptional                   Transcriptional regulation of the beta1C integrin
transcriptional                   Transcriptional regulation of the beta-casein gene
transcriptional                   Transcriptional regulation of the Bmp2
transcriptional                   Transcriptional regulation of the bovine CYP17
transcriptional                   Transcriptional regulation of the bovine oxytocin
transcriptional                   Transcriptional regulation of the C1 inhibitor
transcriptional                   Transcriptional regulation of the calcitonin receptor
transcriptional                   Transcriptional regulation of the carbon monoxide
transcriptional                   Transcriptional regulation of the carcinoembryonic antigen
transcriptional                   Transcriptional regulation of the cardiac-specific MLC2
transcriptional                   Transcriptional regulation of the CDK inhibitor
transcriptional                   Transcriptional regulation of the cell cycle-dependent
transcriptional                   Transcriptional regulation of the cellular retinoic
transcriptional                   Transcriptional regulation of the c-erbB-3 gene
transcriptional   Transcriptional regulation of the cerevisiae
transcriptional   Transcriptional regulation of the c-fms (CSF-1R)
transcriptional   Transcriptional regulation of the c-fms proto-oncogene
transcriptional   Transcriptional regulation of the channel catfish
transcriptional   Transcriptional regulation of the chicken caldesmon
transcriptional   Transcriptional regulation of the chicken CYP2H1
transcriptional   Transcriptional regulation of the chicken hydroxyindole-O-methyltransferase
transcriptional   Transcriptional regulation of the cholesteryl ester
transcriptional   Transcriptional regulation of the c-H-ras1 gene
transcriptional   Transcriptional regulation of the c-jun gene
transcriptional   Transcriptional regulation of the CLC-K1 promoter
transcriptional   Transcriptional regulation of the c-myc protooncogene
transcriptional   Transcriptional regulation of the collagenase gene
transcriptional   Transcriptional regulation of the complement receptor
transcriptional   Transcriptional regulation of the cpr gene
transcriptional   Transcriptional regulation of the CRLR gene
transcriptional   Transcriptional regulation of the cryIVD gene
transcriptional   Transcriptional regulation of the cyclin D1
transcriptional   Transcriptional regulation of the cyclooxygenase-2 gene
transcriptional   Transcriptional regulation of the cydDC operon,
transcriptional   Transcriptional regulation of the CYP11A1 and ferredoxin
transcriptional   Transcriptional regulation of the CYP2B1 and CYP2B2
transcriptional   Transcriptional regulation of the cystathionine-beta -synthase
transcriptional   Transcriptional regulation of the cytochrome b562-o
transcriptional   Transcriptional regulation of the cytosolic chaperonin
transcriptional   Transcriptional regulation of the cytR repressor
transcriptional   Transcriptional regulation of the DAL5 gene
transcriptional   Transcriptional regulation of the development of neurons
transcriptional   Transcriptional regulation of the differentiation-linked human
transcriptional   Transcriptional regulation of the dihydrofolate reductase
transcriptional   Transcriptional regulation of the dihydrofolate reductase/rep-3
transcriptional   Transcriptional regulation of the divergent paa
transcriptional   Transcriptional regulation of the Drosophila catalase
transcriptional   Transcriptional regulation of the Drosophila CycA
transcriptional   Transcriptional regulation of the Drosophila gene
transcriptional   Transcriptional regulation of the Drosophila homeotic
transcriptional   Transcriptional regulation of the Drosophila raf
transcriptional   Transcriptional regulation of the Drosophila segmentation
transcriptional   Transcriptional regulation of the Drosophila-raf proto-oncogene
transcriptional   Transcriptional regulation of the early growth
transcriptional   Transcriptional regulation of the EGF receptor
transcriptional   Transcriptional regulation of the elafin gene
transcriptional   Transcriptional regulation of the elastin gene
transcriptional   Transcriptional regulation of the endothelin-1 gene
transcriptional   Transcriptional regulation of the Enterobacter cloacae
transcriptional   Transcriptional regulation of the Enterococcus faecium
transcriptional   Transcriptional regulation of the epiregulin gene
transcriptional   Transcriptional regulation of the Escherichia coli
transcriptional   Transcriptional regulation of the esp genes
transcriptional   Transcriptional regulation of the estrogen-inducible pS2
transcriptional   Transcriptional regulation of the expression of macrophage
transcriptional   Transcriptional regulation of the ezrin gene
transcriptional   Transcriptional regulation of the ferritin heavy-chain
transcriptional   Transcriptional regulation of the four promoters
transcriptional   Transcriptional regulation of the gene coding
transcriptional   Transcriptional regulation of the gene encoding
transcriptional   Transcriptional regulation of the gene for
transcriptional   Transcriptional regulation of the generic promoter
transcriptional   Transcriptional regulation of the genes encoding
transcriptional   Transcriptional regulation of the germline immunoglobulin
transcriptional   Transcriptional regulation of the glial cell-specific
transcriptional   Transcriptional regulation of the gltA and TLC
transcriptional   Transcriptional regulation of the glucokinase gene
transcriptional   Transcriptional regulation of the GluR2 gene:
transcriptional   Transcriptional regulation of the glycoprotein hormone
transcriptional   Transcriptional regulation of the GnRH receptor
transcriptional   Transcriptional regulation of the gonadotropin-releasing hormone
transcriptional   Transcriptional regulation of the hamster Muc1
transcriptional   Transcriptional regulation of the heat shock
transcriptional   Transcriptional regulation of the heavy subunit
transcriptional   Transcriptional regulation of the Hedgehog effector
transcriptional   Transcriptional regulation of the heme oxygenase
transcriptional   Transcriptional regulation of the heme oxygenase-1
transcriptional   Transcriptional regulation of the hepatic glutaminase
transcriptional   Transcriptional regulation of the hepatocyte growth
transcriptional   Transcriptional regulation of the HIV-1 promoter
transcriptional   Transcriptional regulation of the HLA-DRA
transcriptional   Transcriptional regulation of the HO-1 gene
transcriptional   Transcriptional regulation of the HOX4C gene
transcriptional   Transcriptional regulation of the human acid
transcriptional   Transcriptional regulation of the human ADP-ribosylation
transcriptional   Transcriptional regulation of the human alpha1a-adrenergic
transcriptional   Transcriptional regulation of the human alpha2(I)
transcriptional   Transcriptional regulation of the human alpha5
transcriptional   Transcriptional regulation of the human apolipoprotein
transcriptional   Transcriptional regulation of the human aromatase
transcriptional   Transcriptional regulation of the human asparagine
transcriptional   Transcriptional regulation of the human biglycan
transcriptional   Transcriptional regulation of the human CAD
transcriptional   Transcriptional regulation of the human calcitonin
transcriptional   Transcriptional regulation of the human carboxyl
transcriptional   Transcriptional regulation of the human CD9
transcriptional   Transcriptional regulation of the human cholecystokinin
transcriptional   Transcriptional regulation of the human cholesterol
transcriptional   Transcriptional regulation of the human chorionic
transcriptional   Transcriptional regulation of the human chromogranin
transcriptional   Transcriptional regulation of the human c-myc
transcriptional   Transcriptional regulation of the human CYP1B1
transcriptional   Transcriptional regulation of the human CYP3A4
transcriptional   Transcriptional regulation of the human cystathionine
transcriptional   Transcriptional regulation of the human cytomegalovirus
transcriptional   Transcriptional regulation of the human DNA
transcriptional   Transcriptional regulation of the human E-cadherin
transcriptional   Transcriptional regulation of the human eosinophil
transcriptional   Transcriptional regulation of the human erythroid
transcriptional   Transcriptional regulation of the human factor
transcriptional   Transcriptional regulation of the human FasL
transcriptional   Transcriptional regulation of the human FTZ-F1
transcriptional   Transcriptional regulation of the human GLUT4
transcriptional   Transcriptional regulation of the human glycoprotein
transcriptional   Transcriptional regulation of the human GM3
transcriptional   Transcriptional regulation of the human GnRH
transcriptional   Transcriptional regulation of the human H
transcriptional   Transcriptional regulation of the human high
transcriptional   Transcriptional regulation of the human IgE
transcriptional   Transcriptional regulation of the human IL5
transcriptional   Transcriptional regulation of the human iNOS
transcriptional   Transcriptional regulation of the human insulin
transcriptional   Transcriptional regulation of the human intercellular
transcriptional   Transcriptional regulation of the human interleukin
transcriptional   Transcriptional regulation of the human interleukin-6
transcriptional   Transcriptional regulation of the human 'leukemia
transcriptional   Transcriptional regulation of the human LINE-1
transcriptional   Transcriptional regulation of the human lipoprotein
transcriptional   Transcriptional regulation of the human manganese
transcriptional   Transcriptional regulation of the human MDR1
transcriptional   Transcriptional regulation of the human MIP-1alpha
transcriptional   Transcriptional regulation of the human monocyte
transcriptional   Transcriptional regulation of the human mu
transcriptional   Transcriptional regulation of the human Na/K
transcriptional   Transcriptional regulation of the human NAD(P)H:quinone
transcriptional   Transcriptional regulation of the human NaPi-IIb
transcriptional   Transcriptional regulation of the human neuropeptide
transcriptional   Transcriptional regulation of the human nonmuscle
transcriptional   Transcriptional regulation of the human osteopontin
transcriptional   Transcriptional regulation of the human papillomavirus-16
transcriptional   Transcriptional regulation of the human PAX6
transcriptional   Transcriptional regulation of the human placental-like
transcriptional   Transcriptional regulation of the human polymeric
transcriptional   Transcriptional regulation of the human prepronociceptin
transcriptional   Transcriptional regulation of the human PRL-releasing
transcriptional   Transcriptional regulation of the human prointerleukin
transcriptional   Transcriptional regulation of the human quinone
transcriptional   Transcriptional regulation of the human replacement
transcriptional   Transcriptional regulation of the human Runx2/Cbfa1
transcriptional   Transcriptional regulation of the human S100
transcriptional   Transcriptional regulation of the human sodium/iodide
transcriptional   Transcriptional regulation of the human Sp1
transcriptional   Transcriptional regulation of the human sterol
transcriptional   Transcriptional regulation of the human T
transcriptional   Transcriptional regulation of the human TATA
transcriptional   Transcriptional regulation of the human toll-like
transcriptional   Transcriptional regulation of the human topoisomerase
transcriptional   Transcriptional regulation of the human transferrin
transcriptional   Transcriptional regulation of the human transforming
transcriptional   Transcriptional regulation of the human trefoil
transcriptional   Transcriptional regulation of the human tumor
transcriptional   Transcriptional regulation of the human type
transcriptional   Transcriptional regulation of the human UDP-GlcNAc:alpha-6-D-mannoside
transcriptional   Transcriptional regulation of the human Wilms'
transcriptional   Transcriptional regulation of the Icam-1 gene
transcriptional   Transcriptional regulation of the Ig kappa
transcriptional   Transcriptional regulation of the IL-2
transcriptional   Transcriptional regulation of the IL-5 gene
transcriptional   Transcriptional regulation of the ilv-leu operon
transcriptional   Transcriptional regulation of the insulin receptor
transcriptional   Transcriptional regulation of the insulin-like growth
transcriptional   Transcriptional regulation of the int-2 gene
transcriptional   Transcriptional regulation of the intercellular adhesion
transcriptional   Transcriptional regulation of the interferon-beta 2/B
transcriptional   Transcriptional regulation of the interferon-gamma-inducible tryptophanyl-tRNA
transcriptional   Transcriptional regulation of the interleukin 2
transcriptional   Transcriptional regulation of the interleukin-1beta promoter
transcriptional   Transcriptional regulation of the interleukin-2 gene
transcriptional   Transcriptional regulation of the interleukin-6 gene
transcriptional   Transcriptional regulation of the iron-responsive sigma
transcriptional   Transcriptional regulation of the isocitrate lyase
transcriptional   Transcriptional regulation of the junB gene
transcriptional   Transcriptional regulation of the junB promoter
transcriptional   Transcriptional regulation of the junB promoter:
transcriptional   Transcriptional regulation of the K1 gene
transcriptional   Transcriptional regulation of the Kaposi's sarcoma-associated
transcriptional   Transcriptional regulation of the KEL gene
transcriptional   Transcriptional regulation of the KlDLD gene,
transcriptional   Transcriptional regulation of the Kluyveromyces lactis
transcriptional   Transcriptional regulation of the lactase-phlorizin hydrolase
transcriptional   Transcriptional regulation of the lactate dehydrogenase
transcriptional   Transcriptional regulation of the leptin gene
transcriptional   Transcriptional regulation of the leptin promoter
transcriptional   Transcriptional regulation of the leukocyte adherence
transcriptional   Transcriptional regulation of the liver beta-galactoside
transcriptional   Transcriptional regulation of the lung fatty
transcriptional   Transcriptional regulation of the lutropin/human choriogonadotropin
transcriptional   Transcriptional regulation of the lysozyme gene
transcriptional   Transcriptional regulation of the macrophage-induced gene
transcriptional   Transcriptional regulation of the major histocompatibility
transcriptional   Transcriptional regulation of the major promoters
transcriptional   Transcriptional regulation of the mBMP-4 gene
transcriptional   Transcriptional regulation of the mdm2 oncogene
transcriptional   Transcriptional regulation of the MDR1 gene
transcriptional   Transcriptional regulation of the melanoma prognostic
transcriptional   Transcriptional regulation of the membrane-associated prostaglandin
transcriptional   Transcriptional regulation of the mercury-resistance genes
transcriptional   Transcriptional regulation of the MET3 gene
transcriptional   Transcriptional regulation of the MHC class
transcriptional   Transcriptional regulation of the MHC II
transcriptional   Transcriptional regulation of the mismatch repair
transcriptional   Transcriptional regulation of the mitochondrial genome
transcriptional   Transcriptional regulation of the MN/CA 9
transcriptional   Transcriptional regulation of the moe (molybdate
transcriptional   Transcriptional regulation of the mosquito vitellogenin
transcriptional   Transcriptional regulation of the mouse alpha
transcriptional   Transcriptional regulation of the mouse angiotensin
transcriptional   Transcriptional regulation of the mouse calbindin-D9k
transcriptional   Transcriptional regulation of the mouse CSF-1
transcriptional   Transcriptional regulation of the mouse cytosolic
transcriptional   Transcriptional regulation of the mouse fatty
transcriptional   Transcriptional regulation of the mouse ferritin
transcriptional   Transcriptional regulation of the mouse metallothionein-I
transcriptional   Transcriptional regulation of the mouse presenilin-1
transcriptional   Transcriptional regulation of the mouse steroid
transcriptional   Transcriptional regulation of the mouse steroidogenic
transcriptional   Transcriptional regulation of the mouse uncoupling
transcriptional   Transcriptional regulation of the mts1 gene
transcriptional   Transcriptional regulation of the MUC1 mucin
transcriptional   Transcriptional regulation of the mucosal IgA
transcriptional   Transcriptional regulation of the mucosal mast
transcriptional   Transcriptional regulation of the mu-delta heavy
transcriptional   Transcriptional regulation of the murine 3'
transcriptional   Transcriptional regulation of the murine acetyl-CoA
transcriptional   Transcriptional regulation of the murine brca2
transcriptional   Transcriptional regulation of the murine erythroid-specific
transcriptional   Transcriptional regulation of the murine k-FGF
transcriptional   Transcriptional regulation of the murine multidrug
transcriptional   Transcriptional regulation of the murine surfactant
transcriptional   Transcriptional regulation of the murine TCR
transcriptional   Transcriptional regulation of the murine TSH
transcriptional   Transcriptional regulation of the murine urokinase-type
transcriptional   Transcriptional regulation of the muscle creatine
transcriptional   Transcriptional regulation of the N-acetylglucosaminyltransferase V
transcriptional   Transcriptional regulation of the neuronal L-type
transcriptional   Transcriptional regulation of the neuropeptide Y
transcriptional   Transcriptional regulation of the Nia1 gene
transcriptional   Transcriptional regulation of the nitrate reductase
transcriptional   Transcriptional regulation of the N-myc gene:
transcriptional   Transcriptional regulation of the non-specific cross-reacting
transcriptional   Transcriptional regulation of the nos genes
transcriptional   Transcriptional regulation of the NPT2 gene
transcriptional   Transcriptional regulation of the nuclear gene
transcriptional   Transcriptional regulation of the orf19 gene
transcriptional   Transcriptional regulation of the ornithine decarboxylase
transcriptional   Transcriptional regulation of the ospAB and ospC
transcriptional   Transcriptional regulation of the ovine follicle-stimulating
transcriptional   Transcriptional regulation of the ovine intestinal
transcriptional   Transcriptional regulation of the p53 tumor
transcriptional   Transcriptional regulation of the p67phox gene:
transcriptional   Transcriptional regulation of the Papilio polyxenes
transcriptional   Transcriptional regulation of the parathyroid hormone-related
transcriptional   Transcriptional regulation of the pas gene
transcriptional   Transcriptional regulation of the PCNA promoter
transcriptional   Transcriptional regulation of the phoPR operon
transcriptional   Transcriptional regulation of the phosphoenolpyruvate carboxykinase
transcriptional   Transcriptional regulation of the phosphotransacetylase-encoding and acetate
transcriptional   Transcriptional regulation of the pituitary vasopressin
transcriptional   Transcriptional regulation of the plastocyanin and cytochrome
transcriptional   Transcriptional regulation of the platelet-derived growth
transcriptional   Transcriptional regulation of the POU gene
transcriptional   Transcriptional regulation of the Prevotella ruminicola
transcriptional   Transcriptional regulation of the proC gene
transcriptional   Transcriptional regulation of the production of the
transcriptional   Transcriptional regulation of the promoter of the
transcriptional   Transcriptional regulation of the protective antigen
transcriptional   Transcriptional regulation of the prothrombin gene
transcriptional   Transcriptional regulation of the proton translocating
transcriptional   Transcriptional regulation of the proton-translocating ATPase
transcriptional   Transcriptional regulation of the pyruvate kinase
transcriptional   Transcriptional regulation of the Ras-related protein
transcriptional   Transcriptional regulation of the rat bradykinin
transcriptional   Transcriptional regulation of the rat eIF4E
transcriptional   Transcriptional regulation of the rat fatty
transcriptional   Transcriptional regulation of the rat glutamine
transcriptional   Transcriptional regulation of the rat glutathione
transcriptional   Transcriptional regulation of the rat insulin-like
transcriptional   Transcriptional regulation of the rat Müllerian
transcriptional   Transcriptional regulation of the rat Mrp3
transcriptional   Transcriptional regulation of the rat NAD(P)H:quinone
transcriptional   Transcriptional regulation of the rat NHE3
transcriptional   Transcriptional regulation of the rat platelet
transcriptional   Transcriptional regulation of the rat PLP
transcriptional   Transcriptional regulation of the rat poly(ADP-ribose)
transcriptional   Transcriptional regulation of the rat prostaglandin
transcriptional   Transcriptional regulation of the rat renin
transcriptional   Transcriptional regulation of the rat steroidogenic
transcriptional   Transcriptional regulation of the rat tissue
transcriptional   Transcriptional regulation of the rat type
transcriptional   Transcriptional regulation of the rat vascular
transcriptional   Transcriptional regulation of the redD transcriptional
transcriptional   Transcriptional regulation of the Rhodococcus rhodochrous
transcriptional   Transcriptional regulation of the Saccharomyces cerevisiae
transcriptional   Transcriptional regulation of the Schizosaccharomyces pombe
transcriptional   Transcriptional regulation of the Sex-lethal gene
transcriptional   Transcriptional regulation of the SIS/PDGF-B gene
transcriptional   Transcriptional regulation of the small nuclear
transcriptional   Transcriptional regulation of the SMK1 mitogen-activated
transcriptional   Transcriptional regulation of the sodium-sulfate cotransporter
transcriptional   Transcriptional regulation of the spo0F gene
transcriptional   Transcriptional regulation of the squalene synthase
transcriptional   Transcriptional regulation of the Staphylococcus aureus
transcriptional   Transcriptional regulation of the StAR
transcriptional   Transcriptional regulation of the stem cell
transcriptional   Transcriptional regulation of the steroid receptor
transcriptional   Transcriptional regulation of the Streptococcus mutans
transcriptional                       Transcriptional regulation of the Streptococcus salivarius
transcriptional                       Transcriptional regulation of the sucrase gene
transcriptional                       Transcriptional regulation of the T cell
transcriptional                       Transcriptional regulation of the tartrate-resistant acid
transcriptional                       Transcriptional regulation of the TATA-binding protein
transcriptional                       Transcriptional regulation of the TATA-less NADPH
transcriptional                       Transcriptional regulation of the TCA3 gene
transcriptional                       Transcriptional regulation of the telomerase hTERT
transcriptional                       Transcriptional regulation of the TFIIH transcription
transcriptional                       Transcriptional regulation of the TGF-beta 2
transcriptional                       Transcriptional regulation of the thrombomodulin
transcriptional                       Transcriptional regulation of the thyroperoxydase gene
transcriptional                       Transcriptional regulation of the thyrotropin subunit
transcriptional                       Transcriptional regulation of the thyrotropin-releasing hormone
transcriptional                       Transcriptional regulation of the tissue factor
transcriptional                       Transcriptional regulation of the tissue-type plasminogen-activator
transcriptional                       Transcriptional regulation of the Tn5276-located Lactococcus
transcriptional                       Transcriptional regulation of the transferrin receptor
transcriptional                       Transcriptional regulation of the transforming growth
transcriptional                       Transcriptional regulation of the Trichoderma longibrachiatum
transcriptional                       Transcriptional regulation of the tryptophan oxygenase
transcriptional                       Transcriptional regulation of the two sterol
transcriptional                       Transcriptional regulation of the type I
transcriptional                       Transcriptional regulation of the tyrosine hydroxylase
transcriptional                       Transcriptional regulation of the urokinase receptor
transcriptional                       Transcriptional regulation of the vacuolar H(+)-ATPase
transcriptional                       Transcriptional regulation of the vimentin-encoding gene
transcriptional                       Transcriptional regulation of the virA and virG
transcriptional                       Transcriptional regulation of the vitamin D(3)
transcriptional                       Transcriptional regulation of the Xenopus laevis
transcriptional                       Transcriptional regulation of the Xlim-1 gene
transcriptional                       Transcriptional regulation of the yeast cytochrome
transcriptional                       Transcriptional regulation of the yeast DnaJ
transcriptional                       Transcriptional regulation of the yeast gmp
transcriptional                       Transcriptional regulation of the yeast PHO8
transcriptional                       Transcriptional regulation of the yeast vacuolar
transcriptional                       Transcriptional regulation of the Yersinia pseudotuberculosis
transcriptional                       Transcriptional regulation of three double-stranded RNA
transcriptional   thyrotropin         Transcriptional regulation of thyrotropin subunit genes
transcriptional   tissue-             Transcriptional regulation of tissue- and urokinase-type
transcriptional   tissue              Transcriptional regulation of tissue factor expression
transcriptional   TNF                 Transcriptional regulation of TNF family receptors
transcriptional   topoisomerase       Transcriptional regulation of topoisomerase II alpha
transcriptional   tracheo-bronchial   Transcriptional regulation of tracheo-bronchial mucin (TBM)
transcriptional   transferrin         Transcriptional regulation of transferrin and albumin
transcriptional   transferrin         Transcriptional regulation of transferrin receptor expression
transcriptional   transforming        Transcriptional regulation of transforming growth factor
transcriptional   transport           Transcriptional regulation of transport and utilization
transcriptional   tristetraprolin     Transcriptional regulation of tristetraprolin by transforming
transcriptional   tropoelastin        Transcriptional regulation of tropoelastin expression in rat
transcriptional   TSG6                Transcriptional regulation of TSG6, a tumor
transcriptional   TT                  Transcriptional regulation of TT virus: promoter
transcriptional   tubulin              Transcriptional regulation of tubulin gene expression
transcriptional   tumor                Transcriptional regulation of tumor necrosis factor-alpha
transcriptional   two                  Transcriptional regulation of two cytotoxic T
transcriptional   two                  Transcriptional regulation of two genes specifically
transcriptional   two                  Transcriptional regulation of two myeloid-specific genes,
transcriptional   two                  Transcriptional regulation of two serum-induced RNAs
transcriptional   type                 Transcriptional regulation of type 4 pilin
transcriptional   type                 Transcriptional regulation of type I collagen
transcriptional   type                 Transcriptional regulation of type I diabetes
transcriptional   type                 Transcriptional regulation of type I receptor
transcriptional   type                 Transcriptional regulation of type III secretion
transcriptional   type                 Transcriptional regulation of type X collagen
transcriptional   tyrosine             Transcriptional regulation of tyrosine phenol-lyase gene
transcriptional   uncoupling           Transcriptional regulation of uncoupling protein-2 gene
transcriptional   urokinase            Transcriptional regulation of urokinase (uPA) gene
transcriptional   urokinase-type       Transcriptional regulation of urokinase-type plasminogen activator
transcriptional   vascular             Transcriptional regulation of vascular endothelial growth
transcriptional   vascular             Transcriptional regulation of vascular smooth muscle
transcriptional   vascular             Transcriptional regulation of vascular Vascular
transcriptional   vav                  Transcriptional regulation of vav, a gene
transcriptional   vertebrate           Transcriptional regulation of vertebrate cardiac
transcriptional   vertebrate           Transcriptional regulation of vertebrate Hox genes
transcriptional   Xbr-1a/Xvent-2       Transcriptional regulation of Xbr-1a/Xvent-2 homeobox gene:
transcriptional   Xvent                Transcriptional regulation of Xvent homeobox
transcriptional   xyn2                 Transcriptional regulation of xyn2 in Hypocrea
transcriptional   yeast                Transcriptional regulation of yeast peroxiredoxin gene
transcriptional   YML083c              Transcriptional regulation of YML083c under aerobic
transcriptional   zwf                  Transcriptional regulation of zwf, encoding glucose-6-phosphate
transcriptional   N-acyl-homoserine    Two-component transcriptional regulation of N-acyl-homoserine lactone productio
transcriptional                        Variability of transcriptional regulation after gene transfer with the
transcriptional                        Vitamin-D-dependent transcriptional regulation of the intestinal plasma
transcriptional   preproET-1          &#60; 0.05), suggesting transcriptional regulation of preproET-1 mRNA-expression
transcriptional   P-selectin          (2 hours), reflecting transcriptional regulation of P-selectin expression in situ.
transcriptional   biosynthesis        (3) analysis of transcriptional control of biosynthesis of parathyroid
transcriptional   cytochrome          (7 days) on transcriptional regulation of cytochrome P-450 cholesterol
transcriptional   two                 (ABP) gene is transcriptionally regulated from two promoters: the P1
transcriptional   dexamethasone       (AGP) gene is transcriptionally regulated by dexamethasone, interleukin 1
transcriptional   AR                  (AR) gene is transcriptionally regulated by AR (autoregulation); however,
transcriptional   amino               (AS) gene is transcriptionally regulated by amino acid deprivation
transcriptional                       (BENT-6) involved in transcriptional regulation of this
transcriptional                       (beta-gal) under the transcriptional control of a CMV promoter
transcriptional                       (beta-gal), under the transcriptional control of the HSV1 immediate-early
transcriptional   phosphoenolpyruvate (bGH) under the transcriptional control of phosphoenolpyruvate carboxykinase pro
transcriptional                       (BLV) proteinase under transcriptional control of the phage T7
transcriptional                       (CAT) construct under transcriptional control of the HIV-1 long
transcriptional   histone             (CAT) reporter gene. Transcriptional control of histone gene expression,
transcriptional                       (CAT) under the transcriptional control of the HIV-1 long
transcriptional                       (cDNA) that is transcriptionally regulated by the HCC-associated alpha-fetoprotein
transcriptional   NF-kappaB           (cIAP-1), which is transcriptionally regulated by NF-kappaB and functions
transcriptional   CMV                 (Cihp27kip1) under the transcriptional control of CMV promoter was
transcriptional   p53                 (CKI) p21Cip1 is transcriptionally regulated by p53 and can
transcriptional                       (CP2) gene is transcriptionally regulated during multicellular development, and the
transcriptional                        (CYP) 3A23 is transcriptionally regulated in rat liver by
transcriptional                        (DT-A) placed under transcriptional control of a tetracycline-responsive promoter
transcriptional                        (ECFP) under the transcriptional control of the ventricular myosin
transcriptional                        (EGFP) under the transcriptional control of a human cytomegalovirus
transcriptional                        (EGFP) under the transcriptional regulation of the cytomegalovirus (CMV)
transcriptional                        (Egr-1) in the transcriptional regulation of the luteinizing hormone
transcriptional   fbpA                 (Fur-), indicating that transcriptional regulation of fbpA in response
transcriptional                        (G-CSF) gene under transcriptional control of different regulatory elements
transcriptional                        (GFP) under the transcriptional control of the thymidine kinase
transcriptional                        (GST) under the transcriptional control of the SV40 early
transcriptional                     25 (hGH-N) gene is transcriptionally controlled by 2.5 kb of mouse
transcriptional                        (HIV) under the transcriptional control of the human metallothionein
transcriptional                        (HLF), in mediating transcriptional regulation of the Factor VIII
transcriptional                        (HMG) affect the transcriptional regulation of certain mammalian
transcriptional   inducible            (HO) activity or transcriptional regulation of inducible Therefore,
transcriptional   heat                 (hsps), under the transcriptional control of heat shock transcription
transcriptional                        (HSS) gene is transcriptionally regulated in HepG-2 cells, up
transcriptional   proinflammatory      (i) inhibiting IL-1beta-induced transcriptional regulation of proinflammatory cytokine
transcriptional                        (IFN) induced genes are regulated transcriptionally via a 29
transcriptional                        (ii) expression and transcriptional regulation of the COX-2 gene
transcriptional                        (IL-2) gene expression is controlled transcriptionally by the cooperative
transcriptional                        (IL-8), that are transcriptionally regulated by nuclear factor kappaB
transcriptional   NF-kappaB            (iNOS), which is transcriptionally regulated by NF-kappaB, were also
transcriptional   IFN-alpha            (ISG), which is transcriptionally regulated by IFN-alpha and
transcriptional   PEBP2)               (known to be transcriptionally regulated by PEBP2) in
transcriptional                        (L.) Heynh., the transcriptional regulation of a cyclin-dependent kinase,
transcriptional                        (LH) requires coordinated transcriptional control of the alpha and LHbeta
transcriptional                        (luc)--placed under the transcriptional control of the Autographa californica
transcriptional                        (MIP-2), under the transcriptional control of the tyrosinase promoter/enhancer
transcriptional   glucocorticoid       (MMTV) proviruses is transcriptionally regulated by glucocorticoid We
transcriptional                        (MT) expression is transcriptionally regulated but recent evidence suggests
transcriptional   glucocorticoid       (N)] to the transcriptional regulation of glucocorticoid hormones by
transcriptional                        (neo) under the transcriptional control of the 5' long
transcriptional                        (Nrf-2) in the transcriptional regulation of the spermidine/spermine N1-acetyltransfe
transcriptional                        (phbB) genes under transcriptional control of the lac promoter-operator
transcriptional   POT1                 (PKA) in the transcriptional regulation of POT1. PKA exerts
transcriptional   c-fos                (PKC) in the transcriptional regulation of c-fos protooncogene expression
transcriptional                        (PKC) pathway in transcriptional regulation of the human insulin-like
transcriptional                        (pp60v-src) under the transcriptional control of the mouse metallothionine
transcriptional                        (rP450c17) gene is transcriptionally regulated in steroidogenic Previous
transcriptional                        (SS) gene is transcriptionally regulated via the cyclic AMP
transcriptional                        (SV40) under the transcriptional control of the whey acidic
transcriptional                        (T/t-antigen) under the transcriptional control of the WAP promoter
transcriptional                        (T7RNAP) under the transcriptional control of the light-regulated promoter
transcriptional                        (TAR) involved in transcriptional regulation of the HIV
transcriptional                        (tet) system of transcriptional regulation are an efficient strategy
transcriptional   constitutive         (tsA58) under the transcriptional control of constitutive and ubiquitously
transcriptional                        (under the direct transcriptional control of the strong simian
transcriptional                        (VEGFR2) gene is transcriptionally regulated during angiogenesis. The ability
transcriptional                        (WT1) in the transcriptional regulation of the Mullerian-inhibiting substance
transcriptional   all                  . Transcriptional regulation of all genes is
transcriptional   vitamin              [Gene structure and transcriptional regulation of vitamin A, D
transcriptional   gene         [Methods of studying transcriptional regulation of gene expression] Transcription
transcriptional                [WT1-mediated pathway of transcriptional regulation and leukemia] WT1 gene
transcriptional                = +0.82), suggesting transcriptional regulation of the These
transcriptional                1. Transcriptional control of the human beta(2)
transcriptional                10 under the transcriptional control of an inducible promoter
transcriptional                14- to 31-fold. Transcriptional regulation of the par gene
transcriptional   generation   18 (p18), implying transcriptional regulation of generation of the nonstructural
transcriptional                1887) implicated in transcriptional regulation of the human NPY
transcriptional                1alpha,25-Dihydroxyvitamin D3-mediated transcriptional control of the bone-specif
transcriptional                1-antitrypsin cDNA under transcriptional control of the cytomegalovirus
transcriptional                1beta in the transcriptional regulation of human dipeptidyl peptidase
transcriptional                25-hydroxycholesterol, suggesting that transcriptional control of the LDL receptor
transcriptional                3' gene under transcriptional control of the herpes simplex
transcriptional                4) in the transcriptional control of the hnf6 gene
transcriptional                5' gene under transcriptional control of the viral long
transcriptional                5. Transcriptional regulation of the human blood
transcriptional                5'-flanking region change transcriptional regulation of the human cytochrome
transcriptional                6, under the transcriptional control of a heterologous, retroviral
transcriptional                -60 in modulating transcriptional regulation of the apoB gene
transcriptional   interferon   A acid) induced transcriptional control of interferon The
transcriptional                A and B1 are regulated transcriptionally as well as
transcriptional                a cascade of transcriptional regulation initiated by ethylene
transcriptional   c-jun        a change in transcriptional regulation of c-jun. The stable
transcriptional                A class of transcriptional control proteins, typified by c-Myb,
transcriptional                a coactivator for transcriptional control of protein-encoding genes by
transcriptional                a combination of transcriptional regulation and inhibition of histone
transcriptional                A combination of transcriptional regulation and rapid protein degradation
transcriptional                a consequence of transcriptional regulation of the enzymes involved
transcriptional                a consequence of transcriptional regulation of the mRNA coding
transcriptional                a continuum of transcriptional control within the hematopoietic
transcriptional                a deregulation of transcriptional control may account for the clinical
transcriptional                a differential temperature-related transcriptional control of the different class-I
transcriptional                a form of transcriptional regulation was responsible for their
transcriptional                a form of transcriptional regulation widely used by prokaryotic
transcriptional                a guanylate-binding protein. Transcriptional regulation of the gene encoding
transcriptional                a measure of transcriptional regulation by the cloned nutL,
transcriptional                a mechanism for transcriptional regulation of the HTLV-I
transcriptional   ferritin     a mechanism of transcriptional control of ferritin synthesis, associated
transcriptional                a mechanism of transcriptional control regulating high frequency phase
transcriptional                a mechanism of transcriptional control regulating Vlp phase variation
transcriptional                a mechanism of transcriptional regulation in nonphotosynthetic plastids in plant
transcriptional                a mechanism of transcriptional regulation of the human insulin
transcriptional                a mechanism of transcriptional regulation of the rat arginine
transcriptional   epithelial   a model for transcriptional control of epithelial In
transcriptional   nqo1         a model for transcriptional control of nqo1 through the ARE
transcriptional   s36          a model for transcriptional regulation of s36 based on
transcriptional                a model for transcriptional regulation of the RAR beta
transcriptional                a model of transcriptional control for the action of 1,25-(OH)2D3
transcriptional                a model of transcriptional regulation in which the distal
transcriptional                a model of transcriptional regulation involving multiple overlapping glucocorticoid
transcriptional   HCN          a novel, activity-dependent transcriptional regulation of HCN molecules by
transcriptional                a parasitic stage-specific transcriptional regulation of this novel and potentially
transcriptional                   a part in transcriptional regulation of the Insulin
transcriptional                   a partially re-established transcriptional control of the osmostress-induced express
transcriptional                   a pathway of transcriptional regulation mediated by WT1, which
transcriptional                   a pattern of transcriptional regulation different from that observed
transcriptional                   a plasmid under transcriptional control of the inducible
transcriptional                   a plasmid under transcriptional control of the lambda PL
transcriptional                   a quantitatively differential transcriptional regulation of the two genes
transcriptional   PGDH            a recently proposed transcriptional control of PGDH by mineralocorticoid
transcriptional   hepatic         A reductase unmask transcriptional regulation of hepatic low-density lipoprotein
transcriptional   Notch           a requirement for transcriptional regulation of Notch and/or Delta
transcriptional                   a result of transcriptional control but cannot be due
transcriptional                   a result of transcriptional control mechanisms. Treatment of HUVECs
transcriptional                   a result of transcriptional regulation and/or a change in messenger
transcriptional                   a result of transcriptional regulation of downstream genes which
transcriptional   uPA             a role for transcriptional regulation of uPA activity because
transcriptional   gene            a role in transcriptional control of gene Analysis
transcriptional   gene            a role in transcriptional control of gene In
transcriptional   AIRE            a role in transcriptional regulation of AIRE, which was
transcriptional   cartilage-      a role in transcriptional regulation of cartilage- or bone-specific
transcriptional   eukaryotic      a role in transcriptional regulation of eukaryotic The
transcriptional   JCV             a role in transcriptional regulation of JCV gene expression
transcriptional                   a role in transcriptional regulation of murine CD46 gene
transcriptional                   a role in transcriptional regulation of the C/EBP alpha
transcriptional                   a role in transcriptional regulation of the host cell
transcriptional                   a role in transcriptional regulation of the prothymosin alpha
transcriptional   development     a separate niche. Transcriptional regulation of development is not
transcriptional   mu              a site for transcriptional control of mu gene
transcriptional                   a soluble factor. Transcriptional regulation of the MUC1 mucin
transcriptional   viral           a study of transcriptional regulation by viral proteins, we
transcriptional                   a study of transcriptional regulation of the pyruvate kinase
transcriptional                   a subtype-specific prolonged transcriptional regulation of a beta AR
transcriptional   its             a tissue specific transcriptional regulation of its To
transcriptional                   A transcriptional control of a plausible bile
transcriptional   bFGF            A transcriptional regulation of bFGF expression via
transcriptional                   A under the transcriptional control of a liver-restricted enhancer/promoter
transcriptional                   a vector under transcriptional control of a regulated promoter
transcriptional                   a vector under transcriptional control of the GAL 1,
transcriptional   transforming    Aberrant transcriptional regulation of transforming growth factor
transcriptional   alpha           about mechanisms underlying transcriptional regulation of alpha 1a-adrenergic rec
transcriptional   podocyte        about more global transcriptional regulation of podocyte
transcriptional   dexamethasone   ABP gene is transcriptionally regulated by dexamethasone in primary
transcriptional                   abundance but by transcriptional control of other as yet
transcriptional   auxin           abundance independent of transcriptional regulation by auxin. After 2
transcriptional                   Accordingly, the activity-linked transcriptional regulation of the AChE gene
transcriptional   BCK             Accordingly, the transcriptional regulation of BCK in the developing
transcriptional                   account for the transcriptional regulation of the dhfr gene
transcriptional   globin          account for tissue-specific transcriptional control of globin gene expression?
transcriptional   genes           Ace1/Amt1-like recognition sequence. Transcriptional regulation of genes encodin
transcriptional                   aceB to aceA. Transcriptional regulation of the aceBA operon
transcriptional                   acetylcholine receptor under transcriptional control of the Rous Sarcoma
transcriptional                   acetyltransferase (CAT), under transcriptional control of the 5' region
transcriptional   wheat           ACGTCA functions in transcriptional regulation of wheat histone
transcriptional                      acid formation through transcriptional regulation of the CYP7
transcriptional   two                acid metabolism is transcriptionally regulated by two reciprocal systems:
transcriptional                      acid phosphatase is transcriptionally regulated in human prostate carcinoma
transcriptional   bile               acid synthesis, is transcriptionally regulated by bile acids and hormones.
transcriptional   gastrin            across many species. Transcriptional regulation of gastrin mRNA synthesis
transcriptional   PPARbeta           ACS2 gene is transcriptionally regulated by PPARbeta, demonstrating a role
transcriptional   preprotachykinin   act on the transcriptional control of preprotachykinin
transcriptional   promoter           act via concerted transcriptional control of promoter To
transcriptional   GR                 actinomycin D, suggesting transcriptional control of GR. However, cortisol
transcriptional                      actions and suppresses transcriptional regulation of multiple proinflammatory
transcriptional   IL-6               activation in the transcriptional regulation of IL-6
transcriptional                      activation to the transcriptional regulation of the target genes
transcriptional                      activator protein-1 in transcriptional regulation of the human mu-opioid
transcriptional                      activities mostly through transcriptional regulation of the target
transcriptional                      activities ranging from transcriptional regulation of a wide variety
transcriptional                      activities, suggesting a transcriptional regulation of these However,
transcriptional   SW14               activity and the transcriptional regulation of SW14 are eliminated,
transcriptional                      activity in the transcriptional regulation of the ATF3
transcriptional                      activity of telomerase: transcriptional control of the hTERT gene
transcriptional                      activity substantiates estrogen-dependent transcriptional regulation of the hTERT
transcriptional   GS                 activity suggests a transcriptional regulation of GS expression by
transcriptional   Cart1              activity, in the transcriptional control of Cart1. METHODS: To
transcriptional   GLCLR              activity, indicating that transcriptional regulation of GLCLR is likely
transcriptional                      activity, suggesting a transcriptional regulation of this Adrenalectomy
transcriptional   respiratory        acts in the transcriptional regulation of respiratory The
transcriptional   iNOS               acutely rejecting allograft. Transcriptional regulation of iNOS may vary
transcriptional                      Ad4BP/SF-1 in the transcriptional regulation of the DAX-1 gene,
transcriptional                      ADA-coding sequences under transcriptional regulation of the Rous sarcoma
transcriptional   PPO                addition to a transcriptional control of PPO expression, other
transcriptional   gene               addition to the transcriptional control of gene expression, these
transcriptional                      addition to the transcriptional control of the hepatic S-adenosylmethionine
transcriptional   GR                 addition to the transcriptional regulation of GR gene expression,
transcriptional   SSAT               addition to the transcriptional regulation of SSAT, PMF-1 or similar
transcriptional                      addition, we analyzed transcriptional regulation of the rat EP4
transcriptional                      Additional insight into transcriptional regulation of a gene can
transcriptional                      additional layer of transcriptional regulation complexity is due to the
transcriptional                      additional level of transcriptional control beyond that which results
transcriptional                      additional level of transcriptional regulation and that this step
transcriptional                      additional mechanism of transcriptional regulation by the trp
transcriptional                      additional type of transcriptional regulation restricted to
transcriptional   GTP-cyclohydrolase adhesion), perhaps by transcriptional regulation of GTP-cyclohydrolase. The increa
transcriptional   glucose            adipocytic genes are transcriptionally controlled by glucose and
transcriptional   carbon             ADP1 pobA gene. Transcriptional control of carbon source preferences
transcriptional                      adrenal cortical cells is regulated transcriptionally in part by
transcriptional                      advances in the transcriptional regulation of the human apolipoprotein
transcriptional   antioxidant        advantage include the transcriptional regulation of antioxidant enzymes via
transcriptional   allene             affected in the transcriptional control of allene oxide synthase,
transcriptional                      affecting mechanisms of transcriptional control of the preproenkephalin gene
transcriptional   genes              affects on the transcriptional regulation of genes containing both
transcriptional   genes              affects S-adenosylmethionine (AdoMet)-mediated transcriptional control of genes i
transcriptional                      AFP expression is transcriptionally controlled by the 5'-flanking sequence
transcriptional   p21                after DNA damage. Transcriptional control of p21 by factors
transcriptional                       after stimulation, suggesting transcriptional regulation of this gene during
transcriptional                       Ag cDNA under transcriptional control of the human E
transcriptional   VEGF                again suggesting direct transcriptional regulation of VEGF expression by
transcriptional   apoptosis-related   agents involves the transcriptional regulation of apoptosis-related In
transcriptional   eukaryotic          all aspects of transcriptional control of eukaryotic The
transcriptional                       all under the transcriptional control of the complex IE68
transcriptional                       allele under the transcriptional control of the Gal1
transcriptional                       allowing assessment of transcriptional regulation in defined cell
transcriptional   nonessential        allows absolute off-to-on transcriptional control of nonessential Two
transcriptional                       alpha Amy3 induction is regulated transcriptionally by a signal
transcriptional                       alpha IIb may be controlled transcriptionally by both positive
transcriptional   PRPL                alpha under the transcriptional control of PRPL promoters regulated
transcriptional                       alpha1,3-fucosyltransferase VII is transcriptionally regulated directly by IL-12 and IL
transcriptional   PDGF-A              alpha-amanitin, suggesting a transcriptional regulation of PDGF-A IL-1
transcriptional                       alpha-chain gene expression. Transcriptional regulation of the alpha-chain gene
transcriptional                       alpha-hydroxylase/C17-20-lyase gene (Cyp17): transcriptional regulation of the gen
transcriptional                       also analyzed the transcriptional regulation of the The
transcriptional   ribosomal           also demonstrated that transcriptional regulation of ribosomal protein genes
transcriptional   cyclin              also discuss the transcriptional regulation of cyclin A
transcriptional   IFNs                also evidence of transcriptional regulation by IFNs. We have
transcriptional   angiotensinogen     also investigated the transcriptional control of angiotensinogen by
transcriptional   sodA                also investigated the transcriptional regulation of sodA by monitoring
transcriptional                       also involved in transcriptional regulation of certain genes in response
transcriptional   erythroid           also involved in transcriptional regulation of erythroid
transcriptional   genes               also involved in transcriptional regulation of genes essential for
transcriptional                       also involved in transcriptional regulation of the rat P450c17
transcriptional                       also involved in transcriptional regulation of various genes, and the
transcriptional                       also placed under transcriptional control of the cholerae
transcriptional   OmpF                also result in transcriptional regulation of OmpF, OmpC and LamB
transcriptional   OmpF                also result in transcriptional regulation of OmpF, OmpC, and LamB
transcriptional   invasion            also suggest that transcriptional control of invasion genes could
transcriptional                       alteration in the transcriptional control of this proteolytic enzyme
transcriptional                       alteration of the transcriptional regulation of the DRD4 gene,
transcriptional   mry                 alterations in atmosphere. Transcriptional control of mry, a positive-acting
transcriptional   gene                Altered transcriptional regulation of gene expression is
transcriptional   RARbeta             Altered transcriptional regulation of RARbeta may play
transcriptional   Cox-2               although luteinization changes transcriptional regulation of Cox-2 from PKA-
transcriptional   hTERT               although roles for transcriptional control of hTERT, alternative-splicing of hTERT
transcriptional                       Although spo0H is transcriptionally regulated by the key regulatory
transcriptional   adipocyte           Although the transcriptional regulation of adipocyte differentiation is
transcriptional   alpha               Although transcriptional control of alpha and TSH-beta
transcriptional   metabolic           Although transcriptional regulation of metabolic genes by
transcriptional                       Although transcriptional regulation of the prion protein
transcriptional                       Among these are transcriptionally regulated adenovirus variants that preferentially
transcriptional   high                an absence of transcriptional regulation by high Long-term
transcriptional                       an alpha-1,2-fucosyltransferase, through transcriptional regulation of the FTB
transcriptional                       an array of transcriptional control elements that direct viral
transcriptional                       an E-box dependent transcriptional regulation of the PDX-1
transcriptional                       an effect of transcriptional regulation of specific Localized
transcriptional   AP-1                an integrator of transcriptional regulation by AP-1, Ets and CREB
transcriptional   light-regulated     an involvement in transcriptional control of light-regulated Here,
transcriptional   sterol-responsive   analyses indicate that transcriptional regulation of sterol-responsive genes by
transcriptional                   analysis indicates is transcriptionally regulated by the growth medium
transcriptional                   analysis of heme-dependent transcriptional regulation of several respiration-related
transcriptional                   analysis of the transcriptional control of a retrotransposon population
transcriptional                   analysis of the transcriptional regulation of a G(1 )phase
transcriptional   ACTH            analysis of the transcriptional regulation of ACTH receptor in Y-1
transcriptional                   analysis of the transcriptional regulation of an SR gene
transcriptional   biglycan        Analysis of the transcriptional regulation of biglycan in individuals
transcriptional   gD              analysis of the transcriptional regulation of gD may lead
transcriptional   HIV             analysis of the transcriptional regulation of HIV and hCMV
transcriptional   pentose         analysis of the transcriptional regulation of pentose utilization systems
transcriptional                   analysis of the transcriptional regulation of the adrenocorticotropin (ACTH)
transcriptional                   analysis of the transcriptional regulation of the C1-INH gene
transcriptional                   analysis of the transcriptional regulation of the gene encoding
transcriptional                   analysis of the transcriptional regulation of the human beta
transcriptional                   analysis of the transcriptional regulation of the human IL-10
transcriptional                   analysis of the transcriptional regulation of the human prolactin
transcriptional                   analysis of the transcriptional regulation of the IAPP gene
transcriptional                   analysis of the transcriptional regulation of the murine CD8
transcriptional                   analysis of the transcriptional regulation of the neuropeptide gene
transcriptional                   Analysis of the transcriptional regulation of the nodO gene
transcriptional                   analysis of the transcriptional regulation of the oryzae
transcriptional                   Analysis of the transcriptional regulation of this MCSP gene
transcriptional                   Analysis of transcriptional regulation by the MH1 JC
transcriptional                   Analysis of transcriptional regulation of the alpha FR
transcriptional                   analysis revealed potential transcriptional regulation of the putative promoter
transcriptional                   analysis suggests that transcriptional control of the Flavobacterium
transcriptional   COL1A1          analysis, and the transcriptional regulation of COL1A1 was examined
transcriptional                   analysis, and the transcriptional regulation of the spvR gene
transcriptional   SeP             and 4 in transcriptional regulation of SeP by TGF-beta1
transcriptional   Escherichia     and absolute off-to-on transcriptional control of Escherichia coli
transcriptional   steroidogenic   and adrenodoxin (Adx). Transcriptional regulation of steroidogenic genes is
transcriptional   intermediary    and allosteric and transcriptional regulation of intermediary metabolic enzymes
transcriptional   trace           and analysis of transcriptional control by trace metal
transcriptional                   and analysis of transcriptional control elements. The genomic region
transcriptional                   and analysis of transcriptional regulation of the mouse zinc-fingers
transcriptional                   and analysis of transcriptional regulation of the structural gene
transcriptional                   and analysis of transcriptional regulation of the TGH
transcriptional   receptor        and analyzing the transcriptional regulation of receptor gene
transcriptional   p53             and apoptosis through transcriptional regulation of p53 and possibly
transcriptional                   and beta-ZOL on transcriptional regulation of these
transcriptional                   and by autoregulation. Transcriptional control of the himA and the
transcriptional                   and cascades of transcriptional regulation necessary for APL cell
transcriptional                   and c-Fos in transcriptional regulation of the human polyomavirus,
transcriptional                   and c-Fos in transcriptional regulation of the JC virus
transcriptional   stretch         and c-fos were transcriptionally regulated by stretch. New protein
transcriptional   genes           and c-jun in transcriptional regulation of genes acting in osmoregulation.
transcriptional   well-studied    and contrast the transcriptional regulation of well-studied B lymphoid
transcriptional                   and control subjects. Transcriptional regulation of the IL-5 gene
transcriptional                   and demonstrated the transcriptional regulation of human squalene epoxidase
transcriptional                   and demonstration of transcriptional control correlated with altered chromatin
transcriptional                   and demonstration of transcriptional regulation in response to oxidative
transcriptional   cyclin          and differentiation through transcriptional regulation of cyclin Accumulating
transcriptional   haematopoiesis     and disrupts critical transcriptional regulation of haematopoiesis. Current evidence
transcriptional   its                and examined the transcriptional regulation of its The
transcriptional   all                and factors for transcriptional regulation of all the MDR
transcriptional   iron               and fip1+ are transcriptionally regulated by iron need, and disruption
transcriptional   HDL                and function in transcriptional control of HDL PURPOSE
transcriptional                      and function in transcriptional regulation of a wide variety
transcriptional   8S-LOX             and further investigated transcriptional regulation of 8S-LOX expression by
transcriptional                      and GRP78 are transcriptionally regulated with similar kinetics under
transcriptional   IL-6               and H3 were transcriptionally regulated by IL-6 in a dose-
transcriptional                      and HTF4/HEB in transcriptional regulation of the neurospecific, neurotrophin-indu
transcriptional                      and Hxt9p are transcriptionally regulated by the transcription factors
transcriptional                      and ICAM-1 are transcriptionally regulated by nuclear factor kappaB
transcriptional   Myc                and in negative transcriptional control of Myc. Here we
transcriptional   ciaRH              and in the transcriptional control of ciaRH and
transcriptional   genes              and in the transcriptional control of genes exerted by
transcriptional                      and in the transcriptional control of several groups of genes
transcriptional                      and in the transcriptional regulation of diverse genes in Saccharomyces
transcriptional   podocyte           and in the transcriptional regulation of podocyte specification and differentiation.
transcriptional                      and in the transcriptional regulation of the myeloid-specific genes
transcriptional   thyroid-specific   and in the transcriptional regulation of thyroid-specific TTF-1,
transcriptional                      and in vitro transcriptional regulation of the E3 promoter,
transcriptional                      and indicates that transcriptional control of the TSH genes
transcriptional   IL-6               and inflammatory diseases. Transcriptional control of IL-6 gene expression
transcriptional                      and intravascular coagulation. Transcriptional regulation of the TF promoter
transcriptional                      and investigation of transcriptional control
transcriptional                      and involved in transcriptional regulation of a large number
transcriptional   irgA               and IrgB in transcriptional regulation of
transcriptional                      and it is transcriptionally regulated during the differentiation of myeloid
transcriptional                      and leukemia cell-specific transcriptional regulation of the FUT4
transcriptional   p21                and linked UV-responsive transcriptional regulation of p21 to two
transcriptional                      and lymphotactin are transcriptionally regulated in thymocytes, whereas cytoskelet
transcriptional   steroid            and may be transcriptionally regulated by steroid hormones and stress.
transcriptional   heat               and mechanism of transcriptional control of heat shock genes
transcriptional                      and mechanism of transcriptional regulation in hematopoietic cells remain
transcriptional   heat               and mechanisms of transcriptional regulation of heat shock/stress protein
transcriptional                      and mechanisms of transcriptional regulation of these three bona
transcriptional   NF-kappaB-DNA      and MMP, and transcriptional regulation of NF-kappaB-DNA binding were
transcriptional                      and more distal transcriptional regulation of the 5' flanking
transcriptional   heat               and neither is transcriptionally regulated by heat However,
transcriptional   PTEN               and NF-kappaB via transcriptional regulation of PTEN and offer
transcriptional   nif                and NifI(2), while transcriptional regulation of nif and glnA
transcriptional                      and of the transcriptional regulation of the other steroid
transcriptional                      and p53 in transcriptional control of the IGF-IR gene,
transcriptional                      and p53 in transcriptional regulation of the IGF-IR
transcriptional                      and particularly in transcriptional regulation of the LH beta-subunit
transcriptional   two                and pattern of transcriptional regulation of two nitrite reductase
transcriptional                      and PDX-1 in transcriptional regulation of the pdx-1
transcriptional                      and permit flexible transcriptional regulation of this cationic AA
transcriptional                      and placed under transcriptional control of the Serratia marcesens
transcriptional                      and position of transcriptional control elements responsible for the expression
transcriptional   ADP-glucose        and post-transcriptional level. Transcriptional regulation of ADP-glucose phosphory
transcriptional                      and PR-B in transcriptional regulation of human GnRHR gene
transcriptional                        and protein secretion. Transcriptional regulation of some of the major
transcriptional                        and pseudooperator(s) in transcriptional regulation of the lac
transcriptional                        and put under transcriptional control of the leftward promoter
transcriptional   metabolic            and refeeding on transcriptional regulation of metabolic genes in human
transcriptional                        and role in transcriptional control of the proto-oncogene
transcriptional   calpains             and second, that transcriptional regulation of calpains I and II
transcriptional   MITF                 and SILV/PMEL17/GP100 are transcriptionally regulated by MITF in melanocytes
transcriptional                        and Sp4 in transcriptional regulation of the rod-specific minimal
transcriptional                        and specificity of transcriptional regulation by the STAT family
transcriptional                        and SRC-1 in transcriptional regulation of the pulmonary surfactant
transcriptional                        and stress responses. Transcriptional control of the expression of stress-responsiv
transcriptional                        and studied the transcriptional regulation of this gene in two
transcriptional                        and studies of transcriptional control have revealed the existence
transcriptional                        and studying the transcriptional regulation of the cysG gene
transcriptional   CCK                  and suggest a transcriptional control of CCK
transcriptional   SERCA                and suggest a transcriptional regulation of SERCA
transcriptional   u-PAR                and summarizes the transcriptional regulation of u-PAR. The urokinase
transcriptional   Egr-1                and that are transcriptionally regulated by Egr-1. To identify
transcriptional   loricrin             and that the transcriptional control of loricrin and filaggrin
transcriptional                        and that the transcriptional control of this adaptive response
transcriptional   HOX4C                and that the transcriptional regulation of HOX4C genes by
transcriptional   PRLR                 and that the transcriptional regulation of PRLR expression by
transcriptional                        and that the transcriptional regulation of the serotonin transporter
transcriptional                        and that the transcriptional regulation of this gene is
transcriptional   CLB5                 and the coincident transcriptional regulation of CLB5 and CLN2,
transcriptional                        and the coordinate transcriptional regulation of these genes is
transcriptional   microspore           and the post-meiotic transcriptional regulation of microspore development within
transcriptional                        and the stage-specific transcriptional regulation of a germ cell
transcriptional                        and to be transcriptionally controlled by the redox state
transcriptional                        and to be transcriptionally regulated in different rat
transcriptional   interleukin-2        and TRAF-6 in transcriptional regulation of interleukin-2 gene expression
transcriptional                        and under the transcriptional control of an internal heavy
transcriptional                        and under the transcriptional control of the cauliflower mosaic
transcriptional                        and under the transcriptional control of the human elongation
transcriptional                        and under the transcriptional control of the p7
transcriptional   glucocorticoids      and UT-A3 are transcriptionally regulated by glucocorticoids, we measured
transcriptional                        and verifies the transcriptional control of these VSG
transcriptional   IL-18                and Western blot. Transcriptional regulation of IL-18 gene expression
transcriptional   IL-8                 and whether this transcriptional regulation of IL-8 is inhibited
transcriptional                        and zif268/egr-1 in transcriptional regulation of the human synaptobrevin
transcriptional                        and, nonetheless, are transcriptionally regulated in completely different manners,
transcriptional                        and/or by direct transcriptional regulation of the
transcriptional                        and/or differentiation through transcriptional regulation of a specific subset
transcriptional   prostatic            androgen receptor in transcriptional regulation of prostatic Androgens
transcriptional   PSA                  androgen-mediated and estrogen-mediated transcriptional regulation of PSA, andr
transcriptional                        angiopoietins, is the transcriptional control of these genes by
transcriptional                        animals and humans. Transcriptional control of the expression of at
transcriptional                        animals and humans. Transcriptional control of the expression of these
transcriptional   developing-associatedanother example of transcriptional regulation of developing-associated genes betw
transcriptional   IFN-inducible        antagonist of IRF-1-mediated transcriptional regulation of IFN-inducible IRF-1(-/)-
transcriptional   PKC                  antibodies exert a transcriptional regulation of PKC in human
transcriptional                        antigen gene under transcriptional control of the bacteriophage lambda
transcriptional                      antigen under the transcriptional control of the glial fibrillary
transcriptional                      antigen under the transcriptional control of the Rous sarcoma
transcriptional                      antigenically related protein. Transcriptional regulation of the human major
transcriptional                      antiprogestins in vitro. Transcriptional regulation of the glycodelin gene
transcriptional                      antisense orientation under transcriptional control of dexamethasone-inducible MM
                  dexamethasone-inducible
transcriptional                      any indication of transcriptional regulation based on the use
transcriptional                      AP-1 in the transcriptional regulation of the h2B4
transcriptional                      AP-1 in the transcriptional regulation of the IL-2 gene
transcriptional                      AP-1 in the transcriptional regulation of the rat apical
transcriptional                      AP-2-like element in transcriptional regulation of mouse micro-opioid receptor
transcriptional   E2F-1              Apaf-1 is under transcriptional regulation of E2F-1. These data
transcriptional   p53                apoptosis and is transcriptionally regulated by p53. Moreover, the introduction
transcriptional   related            apoptosis through the transcriptional control of related
transcriptional                      apoptotic mechanisms involve transcriptional regulation of specific proteins or prot
transcriptional   negative           appear to be transcriptionally regulated by negative acting catabolite
transcriptional   NO                 appear to be transcriptionally regulated by NO since NOS
transcriptional   p53                appear to be transcriptionally regulated by p53. We have
transcriptional                      appear to be transcriptionally regulated in normal flies during
transcriptional   expI               appear to exhibit transcriptional regulation of expI, but the effect
transcriptional                      appeared to be transcriptionally controlled in both developing tubers
transcriptional                      appears to be transcriptionally regulated and is not dependent
transcriptional   sterols            appears to be transcriptionally regulated by
transcriptional                      appears to be transcriptionally regulated by a unique mechanism
transcriptional   class              appears to be transcriptionally regulated by class I and II
transcriptional   fasting            appears to be transcriptionally regulated by fasting in dams,
transcriptional                      appears to be transcriptionally regulated during sporulation, at least
transcriptional                      appears to be transcriptionally regulated during the cell
transcriptional                      appears to be transcriptionally regulated since mRNA levels are
transcriptional   cyclin             appears to mediate transcriptional regulation of cyclin D1, thereby
transcriptional                      Appropriate transcriptional control of the CD21 gene
transcriptional                      Appropriate transcriptional regulation of the CD34 gene
transcriptional                      Arabidopsis seeds under transcriptional control of the seed-specific napin
transcriptional                      Arabidopsis thaliana under transcriptional control of the CaMV 35S
transcriptional                      archetypal mechanism of transcriptional regulation has been conserved in their
transcriptional   gene               architecture may influence transcriptional control of gene This
transcriptional                      are achieved by transcriptional regulation of the hTERT
transcriptional                      are associated with transcriptional regulation of the Ig
transcriptional   GFAP               are candidates for transcriptional regulation of GFAP. We propose
transcriptional   expression         are controlled by transcriptional regulation of expression of the beta3
transcriptional                      are critical for transcriptional regulation of the gene in trophoblast
transcriptional                      are due to transcriptional regulation of the In
transcriptional                      are important for transcriptional control of the IP-10 gene
transcriptional   GM-CSF             are important for transcriptional regulation of GM-CSF in A549
transcriptional                      are important for transcriptional regulation of the rat ICAM-1
transcriptional   beta               are independent of transcriptional control of beta 1,4-GalTase
transcriptional   acyl-CoA           are investigating the transcriptional control of acyl-CoA oxidase, the first
transcriptional                      are investigating the transcriptional regulation of the Xenopus laevis
transcriptional   alpha              are involved in transcriptional control of alpha 1(I) collagen
transcriptional                      are involved in transcriptional control of the dTMP-synthesizing enzymes
transcriptional                      are involved in transcriptional control of the observed expression
transcriptional                      are involved in transcriptional control of the rat glucokinase
transcriptional                      are involved in transcriptional regulation of the BRCA1 gene,
transcriptional                     are involved in transcriptional regulation of the gene encoding
transcriptional   Ucp1              are involved in transcriptional regulation of Ucp1 in response
transcriptional   wheat             are involved in transcriptional regulation of wheat histone
transcriptional   yeast             are involved in transcriptional regulation of yeast sulfur amino
transcriptional                     are largely unknown. Transcriptional regulation of the alpha-chain distal
transcriptional                     are likely to be regulated transcriptionally at the level
transcriptional   phosphorylation   are modes of transcriptional regulation by phosphorylation, altered DNA
transcriptional                     are provided exogenously, transcriptional regulation of several genes involves
transcriptional                     are reminiscent of transcriptional regulation in promoter regions of DNA,
transcriptional   Cox-2             are required for transcriptional regulation of Cox-2 expression induced
transcriptional   most              are required for transcriptional regulation of most genes in yeast.
transcriptional   viral             are required for transcriptional regulation of viral and cellular
transcriptional                     are responsible for transcriptional control of the substance P
transcriptional   E74               are studying the transcriptional control of E74, an early
transcriptional   QR1               are studying the transcriptional control of QR1, a neuroretina
transcriptional   angiogenesis      are studying the transcriptional regulation of angiogenesis. We observed
transcriptional   da                are under the transcriptional control of
transcriptional                     are under the transcriptional control of an inducible
transcriptional                     are under the transcriptional control of distinct
transcriptional   QacR              are under the transcriptional control of QacR repressor from
transcriptional   T3                are under the transcriptional control of T3. Six of them,
transcriptional                     are under the transcriptional control of the mdr1 promoter
transcriptional                     are under the transcriptional control of the PhoPQ two-component
transcriptional                     are under the transcriptional control of the specific activator
transcriptional   VH-independent    are under the transcriptional control of VH-independent promoters and have
transcriptional                     are unknown, but transcriptional regulation of the PDGF alpha
transcriptional                     ARE/EpRE, respectively) in transcriptional regulation of the rat (r)GST-Ya
transcriptional                     area indicates that transcriptional regulation of the genes and a
transcriptional   its               areas, suggesting a transcriptional regulation of its expression, whereas
transcriptional   FSH               aromatase gene is transcriptionally regulated by FSH and steroids
transcriptional                     aromatase gene, and transcriptional regulation of their multiple promoters
transcriptional                     artificial networks of transcriptional control elements in living cells
transcriptional   genes             as in the transcriptional regulation of genes. The repair
transcriptional                     as in vivo transcriptional regulation of these two
transcriptional                     as on the transcriptional control of the genes encoding
transcriptional                     as Rb and transcriptional regulation of the E2F-1
transcriptional   all               As the complete transcriptional regulation of all 3 genes
transcriptional   mucin             As transcriptional regulation of mucin genes begins
transcriptional   mast              as well as transcriptional regulation of mast cell characteristic
transcriptional                     as well as transcriptional regulation of the Bacillus subtilis
transcriptional                     ASF/SF2 under the transcriptional control of a regulated
transcriptional                     ASF-1 in the transcriptional regulation of the ocs promoter
transcriptional   genes             aspects of the transcriptional regulation of
transcriptional   Hox-2             aspects of the transcriptional regulation of Hox-2 genes in transgenic
transcriptional   MHC               aspects of the transcriptional regulation of MHC genes and the
transcriptional   LNGFR             assays reveal complex transcriptional regulation of LNGFR in astrocytes;
transcriptional                     assays suggest that transcriptional regulation of the p68 gene
transcriptional                     assays to measure transcriptional regulation of the same set
transcriptional   alpha-tubulin     assays, we observed transcriptional regulation of alpha-tubulin, thiazole biosynthet
transcriptional   respiratory       associated with the transcriptional regulation of respiratory chain
transcriptional   respiratory       associated with the transcriptional regulation of respiratory genes were
transcriptional                     associated with the transcriptional regulation of the LPH
transcriptional                  asthma, and the transcriptional regulation of the IL-5 gene
transcriptional   regulatory     astrocytes under the transcriptional control of regulatory sequences from
transcriptional                  astrocytes under the transcriptional control of the glial fibrillary
transcriptional   K(G)           at understanding the transcriptional regulation of K(G) channels and their
transcriptional   VCAM-1         atherogenesis through its transcriptional control of VCAM-1 gene
transcriptional                  AtMCM3 gene is transcriptionally regulated at S The
transcriptional   Scl            attention on the transcriptional regulation of Scl Previous
transcriptional                  attention on the transcriptional regulation of the Drosophila Troponin
transcriptional                  attenuation model for transcriptional regulation of the Escherichia coli
transcriptional                  attributed to a transcriptional control of the synthesis of acetyl
transcriptional   genes          availability through coordinate transcriptional regulation of genes involved in riboso
transcriptional                  availability through RpoN-mediated transcriptional control of the rfaH
transcriptional   B              available on the transcriptional regulation of B utrophin, which
transcriptional                  axonemal components, is transcriptionally regulated during reciliation. Analyses of
transcriptional                  B gene is transcriptionally regulated in concert with changing
transcriptional                  B with Smads. Transcriptional regulation of the junB
transcriptional                  BACKGROUND: Transcriptional regulation of cellular functions is
transcriptional   respiratory    bacteria, we examined transcriptional control of respiratory genes during
transcriptional                  baculovirus genome under transcriptional regulation of the viral polyhedrin
transcriptional                  baculoviruses under the transcriptional control of the strong polyhedrin
transcriptional                  Barrett's epithelium, suggesting transcriptional regulation of the gene in the
transcriptional                  basal and E1A-induced transcriptional regulation of the E3 promoter,
transcriptional                  basal and/or cAMP-stimulated transcriptional regulation of this gene in Y-1
transcriptional                  basal gene expression. Transcriptional regulation of the prolactin gene
transcriptional                  basal laminae, suggesting transcriptional control of these alpha (IV)
transcriptional                  based on the transcriptional regulation of the expression of specific
transcriptional                  basic mechanism of transcriptional control and the role of a
transcriptional                  basic mechanism of transcriptional regulation of the enzymes involved
transcriptional   glycerol       basic protein and transcriptional regulation of glycerol phosphate
transcriptional   ALAS-E         basis for the transcriptional regulation of ALAS-E during erythropoiesis,
transcriptional   HIV            basis for the transcriptional regulation of HIV by
transcriptional   Kit            basis for the transcriptional regulation of Kit during development
transcriptional                  basis of the transcriptional control of the CAII gene
transcriptional   BSP            basis of the transcriptional regulation of BSP gene transcription
transcriptional                  basis of the transcriptional regulation of the NAIP gene,
transcriptional                  basis of the transcriptional regulation of the rat connexin32
transcriptional                  B-cells whereas the transcriptional regulation of the glucokinase gene
transcriptional                  Bcl-2 family that is regulated transcriptionally and post-transcriptionally, with expres
transcriptional                  bcl-2 gene is transcriptionally regulated by nuclear factor-kappa B
transcriptional                  bcl-2 is under transcriptional control of the WT-1
transcriptional                  BCL-2 under the transcriptional control of the cognate 5'-
transcriptional                  Bcl-2 under the transcriptional control of the simian cytomegalovirus
transcriptional   key            be based on transcriptional regulation of key downstream genes
transcriptional                  be caused by transcriptional regulation of the gene encoding
transcriptional   H2B            be correlated with transcriptional regulation of H2B histone gene
transcriptional   NaK-ATPase     be correlated with transcriptional regulation of Na,K-ATPase gene
transcriptional                  be due to transcriptional control of the genes encoding
transcriptional                  be due to transcriptional regulation of the CAR gene
transcriptional                  be explained by transcriptional regulation of the
transcriptional   polydnavirus   be important for transcriptional regulation of polydnavirus gene expression
transcriptional   individual     be involved in transcriptional control of individual In
transcriptional   intestinal     be involved in transcriptional control of intestinal SR-BI
transcriptional                    be involved in transcriptional control of many other glycolytic
transcriptional   Her2/neu         be involved in transcriptional regulation of Her2/neu in HBL-100
transcriptional   MMTV             be involved in transcriptional regulation of MMTV in mammary
transcriptional   neuronal         be involved in transcriptional regulation of neuronal
transcriptional                    be involved in transcriptional regulation of other genes expressed
transcriptional                    be involved in transcriptional regulation of the apoA-I gene,
transcriptional                    be involved in transcriptional regulation of the human proenkephalin
transcriptional                    be involved in transcriptional regulation of the IFN-stimulable genes
transcriptional                    be involved in transcriptional regulation of the major immediate-early
transcriptional                    be involved in transcriptional regulation of the rat heme
transcriptional                    be involved in transcriptional regulation of the tts gene
transcriptional                    be involved in transcriptional regulation of this set of genes.
transcriptional   genes            be involved the transcriptional regulation of genes in many
transcriptional   full-length      be mediated by transcriptional control of full-length tk
transcriptional   cdaR             be mediated by transcriptional regulation of cdaR (a gene
transcriptional   DBF4             be mediated by transcriptional regulation of DBF4 (Jackson et
transcriptional   fos              be on the transcriptional regulation of fos and does
transcriptional                    be required for transcriptional regulation of the prolactin
transcriptional   antioxidant      be under the transcriptional control of antioxidant response elements
transcriptional   either           be under the transcriptional control of either the astrocyte-specific,
transcriptional                    be under the transcriptional control of mouse PPAR
transcriptional   IFN-gamma        Because transcriptional regulation of IFN-gamma and the pituitary
transcriptional                    Because transcriptional regulation of the smooth muscle
transcriptional                    been associated with transcriptional regulation of several cytokine
transcriptional   dioxin-induced   been elucidated, the transcriptional regulation of dioxin-induced genes like
transcriptional   genes            been implicated in transcriptional control of genes involved in growth
transcriptional   glnA             been implicated in transcriptional control of glnA Gel
transcriptional   rDNA             been implicated in transcriptional regulation of rDNA and rRNA
transcriptional                    been implicated in transcriptional regulation of several rhythmic genes
transcriptional                    been implicated in transcriptional regulation of specific Human
transcriptional                    been implicated in transcriptional regulation of the c-myc
transcriptional                    been implicated in transcriptional regulation of the kappa light
transcriptional   NOS-2            been mediated through transcriptional regulation of NOS-2 and HO-1
transcriptional                    been placed under transcriptional control of the Vibrio cholerae
transcriptional                    been studying the transcriptional regulation of the mammalian F(1)F(0)
transcriptional                    been studying the transcriptional regulation of the nuclear gene
transcriptional                    been studying the transcriptional regulation of the rat P450c17
transcriptional   ecdysone         being under the transcriptional control of ecdysone and its
transcriptional                    being under the transcriptional control of human CD2, is
transcriptional                    believe that the transcriptional regulation of these metabolic genes
transcriptional                    believed to be transcriptionally regulated in many developmental
transcriptional   expression       Besides transcriptional regulation of expression also regulation
transcriptional                    best examples of transcriptional control through the targeted recruitment
transcriptional                    beta-cells, such as transcriptional regulation of the insulin gene
transcriptional                    beta-chemokine that is transcriptionally regulated in mast cells; the gene
transcriptional                    beta-galactosidase (beta-gal) under transcriptional control of the murine sarcoma
transcriptional   regulatory       beta-galactosidase (nls-LacZ) under transcriptional control of regulatory sequence
transcriptional                    beta-galactosidase (under the transcriptional control of the Troponin I
transcriptional   GAL4             beta-galactosidase under the transcriptional control of GAL4 promoter and TATA
transcriptional                    beta-galactosidase under the transcriptional regulation of an endothelial cell-specif
transcriptional   P(GAP)           beta-lactamase synthesized under transcriptional control of P(GAP) is correctly
transcriptional   either           beta-NGF cDNA under transcriptional control of either the human
transcriptional   signals               beta-pol promoter is transcriptionally regulated by signals acting through
transcriptional                         better investigate the transcriptional regulation of the NIS gene,
transcriptional   glucocorticoid-inducedbetter understand the transcriptional control of glucocorticoid-induced S49 cell
transcriptional                         better understand the transcriptional control of this protein, the 5'
transcriptional                         better understand the transcriptional regulation of human endometrial remodeling,
transcriptional                         better understand the transcriptional regulation of human T-lymphotropic viruses,
transcriptional                         better understand the transcriptional regulation of the CYP2A genes,
transcriptional                         better understand the transcriptional regulation of the HOX-11 gene
transcriptional                         better understanding of transcriptional regulation at this important stage
transcriptional   adhesion              Better understanding of transcriptional regulation of adhesion molecules in ECs
transcriptional                         between genotype and transcriptional regulation of the CYP1A1
transcriptional                         between the genes. Transcriptional regulation of the COL4A1/COL4A2 set
transcriptional   classic               bile acids is transcriptionally regulated by classic feedforward and feedback
transcriptional                         binding and in transcriptional regulation of the alc genes
transcriptional                         binding factors for transcriptional regulation of the mouse type
transcriptional   Ca(2+)-binding        binding motif in transcriptional regulation of Ca(2+)-binding protein regucalcin
transcriptional                         binding or the transcriptional control of one of the genes
transcriptional   CYP51                 binding protein (SREBP)-dependent transcriptional regulation of CYP51 contribute
transcriptional                         binding site in transcriptional regulation of the gamma
transcriptional                         binding sites in transcriptional control of the divergently transcribed
transcriptional   level                 biochemical analysis of transcriptional regulation of level III and IV
transcriptional                         biochemical mechanisms of transcriptional regulation and to accelerate the delinea
transcriptional                         biochemical mechanisms of transcriptional regulation is not apparent, a portion
transcriptional   mutant                biological mechanisms of transcriptional regulation by mutant RARs and their
transcriptional                         biological significance of transcriptional regulation in olfactory system is
transcriptional   phospholipid          biosynthesis on the transcriptional regulation of phospholipid biosynthetic
transcriptional                         biosynthetic genes are transcriptionally regulated in response to inositol
transcriptional   two                   biosynthetic operons is transcriptionally controlled by two main mechanisms
transcriptional                         BK2 receptor is transcriptionally regulated by the tumor suppressor
transcriptional                         B-like factor in transcriptional regulation of the M-CSF
transcriptional   CRF                   blockade and subsequent transcriptional regulation of CRF by immediate-early
transcriptional   PR                    blot analysis demonstrated transcriptional control of PR by steroid
transcriptional   CD7                   blot analysis, indicating transcriptional regulation of CD7 The
transcriptional                         Bordetella virulence regulon: transcriptional control of a Bvg-intermediate phase
transcriptional                         both in the transcriptional regulation of their own genes
transcriptional                         both modes of transcriptional regulation have similar DNA-binding
transcriptional                         Both transcriptional regulation of rate limiting enzymes
transcriptional   protamine             box-binding proteins in transcriptional regulation of protamine 2 using
transcriptional                         boxes in the transcriptional regulation of the dmsCBA operon
transcriptional   analogs               BPI expression is transcriptionally regulated by analogs of endogenously
transcriptional                         BPyV under the transcriptional control of the long terminal
transcriptional                         Br1) under the transcriptional control of the cytomegalovirus (CMV)
transcriptional   hormone-responsive brake that modulates transcriptional regulation of hormone-responsive target gene
transcriptional                         branchial NBC1 is transcriptionally regulated to match the requirements
transcriptional                         BRCA1-Sp1 interactions in transcriptional regulation of the IGF-IR
transcriptional                         breaks on the transcriptional control of this During
transcriptional                         breast cancer, the transcriptional regulation of the LIF gene
transcriptional                         brlA alpha is transcriptionally controlled and a large portion
transcriptional                         broad array of transcriptional regulation proteins and two new
transcriptional                         broader context of transcriptional regulation and how particular regulators
transcriptional                         BTEB2 mediates the transcriptional regulation of the SMemb/NMHC-B gene
transcriptional   Pax3                  but also deregulates transcriptional control of Pax3 by overriding
transcriptional                       but also the transcriptional control of the gene through
transcriptional                       but partly overlapping transcriptional regulation of cell cycle regulatory
transcriptional   gene                by a purely transcriptional control of gene The
transcriptional   Hox                 by altering the transcriptional regulation of Hox target genes
transcriptional   key                 by causing abnormal transcriptional regulation of key target
transcriptional   structural          by CCR through transcriptional control of structural CCR
transcriptional   fibrinogen-induced  by characterizing the transcriptional regulation of fibrinogen-induced IL-1beta
transcriptional                       by cilium amputation is regulated transcriptionally in the normal
transcriptional                       by defining the transcriptional control of the L7 gene
transcriptional   ERalpha             by E(2) is transcriptionally regulated by ERalpha as the antiestrogen,
transcriptional                       by impairing CRX-mediated transcriptional regulation of the photoreceptor
transcriptional   inflammatory        by inducing the transcriptional regulation of inflammatory genes in VSMCs
transcriptional   NF-kappaB           by Notch-1 via transcriptional control of
transcriptional   cyclin              by PC3 through transcriptional control of cyclin D1 and Math1,
transcriptional   bacterial           by protein phosphorylation. Transcriptional control of bacterial phosphorylases furt
transcriptional   progesterone        by R5020 was transcriptionally regulated by progesterone receptor (PR)
transcriptional   gene                by rhGM-CSF, indicating transcriptional regulation of gene expression for
transcriptional                       by the differential transcriptional control of the expression sites,
transcriptional                       by TNF-alpha is transcriptionally regulated via activation of
transcriptional   HOXD9               by Western blotting. Transcriptional regulation of HOXD9 was examined
transcriptional                       C (PKC) in transcriptional regulation of the c-fos gene
transcriptional   cyclin              C in the transcriptional control of cyclin D1 and related
transcriptional                       C in the transcriptional regulation of 12-O-tetradecanoylphorbol-13-acetate-inducib
                  12-O-tetradecanoylphorbol-13-acetate-inducible
transcriptional   ornithine           C in the transcriptional regulation of ornithine decarboxylase gene
transcriptional                       C/EBP alpha is transcriptionally regulated in regenerating C/EBP
transcriptional   genes               C/EBP in the transcriptional regulation of genes. The study
transcriptional                       C/EBP mRNA is transcriptional regulation of the We
transcriptional                       C/EBPepsilon in the transcriptional regulation of a subset of myeloid-specific
transcriptional                       C7 (beta) is transcriptionally regulated by the iron-dependent diphtheria
transcriptional   genes               Ca(2+) concentrations to transcriptional regulation of genes related to the
transcriptional   inducible           Ca2+ in the transcriptional regulation of inducible NO synthase
transcriptional                       CaARN1 is transcriptionally regulated in response to
transcriptional                       CaCTR1 is transcriptionally regulated in S. cerevisiae in response
transcriptional                       calbindin-D28K protein is transcriptionally controlled by the steroid hormone
transcriptional   NGFI-A              calcineurin involvement in transcriptional regulation of NGFI-A and
transcriptional                       calcium binding protein. Transcriptional regulation of the gene for
transcriptional                       cAMP on the transcriptional regulation of the serotonin
transcriptional                       cAMP on the transcriptional regulation of the TNF-alpha gene
transcriptional   eukaryotic          cAMP-responsive enhancer elements. Transcriptional regulation of eukaryotic gen
transcriptional   adjacent            can affect the transcriptional regulation of adjacent genes and result
transcriptional   PPARgamma           can alter the transcriptional regulation of PPARgamma target gene
transcriptional                       can directly affect transcriptional regulation of certain Alternatively,
transcriptional   COX-2               can influence the transcriptional regulation of COX-2 in colonic
transcriptional   pro-apoptotic       can occur through transcriptional regulation of pro-apoptotic bax)
transcriptional                       candidates for the transcriptional control of the transformed and invasive
transcriptional                       capable of specific transcriptional regulation of a reporter gene
transcriptional                       capacity and is transcriptionally regulated by a promoter located
transcriptional                       capsulatum cdc2 is transcriptionally regulated during the morphologic mycelium&#
transcriptional   phosphoenolpyruvate carboxykinase gene transcription. Transcriptional regulation of phosphoenolpyruva
transcriptional                       carcinogenesis due to transcriptional regulation of target genes through
transcriptional                       cascade eventuating in transcriptional regulation of multiple genes including
transcriptional                       cascades, through the transcriptional regulation of certain TRAF and IAP
transcriptional   apobec-1       cases related to transcriptional regulation of apobec-1 ApoB
transcriptional                  cases, suggest aberrant transcriptional regulation of some genes in AD.
transcriptional   ecdysone       caspase that is transcriptionally regulated by ecdysone during
transcriptional                  cat genes, under transcriptional control of the Rous sarcoma
transcriptional                  CbbR, in the transcriptional control of the eutropha
transcriptional                  Cbf1p, in yeast. Transcriptional regulation of the yeast cytochrome
transcriptional                  CCAAT/enhancer-binding protein in transcriptional regulation of the human IL-5
transcriptional                  CD18 expression is transcriptionally regulated during 12-O-tetradecanoylphorbol-1
transcriptional                  CD34 gene is transcriptionally regulated in hematopoietic cell
transcriptional                  CD34 gene is transcriptionally regulated in tissue culture
transcriptional   lipoproteins   CD36 mRNA was transcriptionally regulated by lipoproteins. To determine
transcriptional                  CD46 gene was transcriptionally regulated by a neuron-specific
transcriptional                  CD4epsilon10 under the transcriptional control of the HIV-1 long
transcriptional                  cdc2 gene is transcriptionally regulated during the morphologic
transcriptional                  cDNA cloning and transcriptional regulation of the murine mitochondrial
transcriptional                  cDNA cloning and transcriptional regulation of the vitellogenin receptor
transcriptional                  cDNA is under transcriptional control of the hormone-inducible mouse
transcriptional                  cDNA placed under transcriptional control of the mouse OTC
transcriptional                  cDNA sequence under transcriptional control of the constitutively active
transcriptional                  cDNA under the transcriptional control of a 2.2 kb
transcriptional                  cDNA under the transcriptional control of a cytomegalovirus
transcriptional                  cDNA under the transcriptional control of a human beta-actin
transcriptional                  cDNA under the transcriptional control of a human beta-globin
transcriptional                  cDNA under the transcriptional control of a short human
transcriptional   Autografa      cDNA under the transcriptional control of Autografa californica nuclear
transcriptional   either         cDNA under the transcriptional control of either the simian
transcriptional                  cDNA under the transcriptional control of the cellular elongation
transcriptional                  cDNA under the transcriptional control of the chicken beta-actin
transcriptional                  cDNA under the transcriptional control of the Cytomegalovirus enhancer/promoter
transcriptional                  cDNA under the transcriptional control of the cytomegalovirus immediate
transcriptional                  cDNA under the transcriptional control of the endogenous
transcriptional                  cDNA under the transcriptional control of the endothelial cell
transcriptional                  cDNA under the transcriptional control of the HSV immediate-early
transcriptional                  cDNA under the transcriptional control of the human CMV
transcriptional                  cDNA under the transcriptional control of the human metallothionein
transcriptional                  cDNA under the transcriptional control of the human polypeptide
transcriptional                  cDNA under the transcriptional control of the human polypeptide-chain-elongation
transcriptional                  cDNA under the transcriptional control of the L-type pyruvate
transcriptional                  cDNA under the transcriptional control of the mouse muscle
transcriptional                  cDNA under the transcriptional control of the murine cytomegalovirus
transcriptional                  cDNA under the transcriptional control of the phosphoglycerate kinase
transcriptional                  cDNA under the transcriptional control of the Rous sarcoma
transcriptional                  cDNA under the transcriptional control of the SR alpha
transcriptional                  cDNA was under transcriptional control of the SV40 promoter
transcriptional   elongation     cDNAs under the transcriptional control of elongation factor 1-alpha
transcriptional                  Cell cycle and transcriptional control of human myeloid leukemic
transcriptional                  cell death by transcriptional regulation of the apoptotic
transcriptional                  cell growth and transcriptional regulation of a subset of yeast
transcriptional                  cell growth and transcriptional regulation of these CONCLUSION:
transcriptional                  cell line Hep3B, were regulated transcriptionally by retinoic acid
transcriptional                  cell line is transcriptionally regulated and showed that protein
transcriptional   respiratory    cell lineage, the transcriptional control of respiratory neuronal development,
transcriptional   BOULE              cell loss, and transcriptional control of BOULE, DAZL, and DAZ
transcriptional   kappaB             cell nucleus and transcriptional regulation of kappaB DNA-containing
transcriptional   tumor              cells (HUVECs) was transcriptionally regulated by tumor necrosis factor-alpha
transcriptional   p53                cells and is transcriptionally regulated by p53. Nitric oxide
transcriptional   p21                cells and the transcriptional control of p21 by a cascade
transcriptional                      cells are under transcriptional control of various Gastrin
transcriptional                      cells includes antagonistic transcriptional control of a growth-arrest-associated
transcriptional                      cells suggests tight transcriptional control of this MHC class
transcriptional                      cells under the transcriptional control of a murine retroviral
transcriptional                      cells under the transcriptional control of a rhodopsin gene
transcriptional   taq                cells under the transcriptional control of taq promoter and purified
transcriptional                      cells under the transcriptional control of the human interphotoreceptor
transcriptional                      cells under the transcriptional control of the human polypeptide
transcriptional                      cells under the transcriptional control of the Rous sarcoma
transcriptional                      cells under the transcriptional control of the simian virus
transcriptional   MnSOD              cells, but the transcriptional regulation of MnSOD expression in these
transcriptional                      cells, by the transcriptional control of the blistered nuclear
transcriptional   phorbol            cells, hCNT3 is transcriptionally regulated by phorbol myristate
transcriptional   BiP                cells, suggesting that transcriptional control of BiP gene expression
transcriptional   RA                 cells, suggesting that transcriptional regulation of RA synovial cell
transcriptional                      cells, suggesting that transcriptional regulation of the toxin genes
transcriptional                      cells, under the transcriptional control of the rat CC10
transcriptional   T1alpha            cells, we analyzed transcriptional regulation of T1alpha, a gene
transcriptional                      cell-specific expression and transcriptional regulation of the FUT4
transcriptional                      cellular aspects of transcriptional regulation and they are capable
transcriptional                      cellular localization and transcriptional regulation of the LH/CG receptor
transcriptional   immunologically    cellular programs through transcriptional regulation of immunologically relevant
transcriptional                      cellular response involves transcriptional control of the AS
transcriptional                      cellular specificity of transcriptional regulation of the nuclear receptor
transcriptional                      cellulase and is transcriptionally regulated by the carbon
transcriptional   two                cellulase system, is transcriptionally controlled by two independent cis-acting
transcriptional                      central enigma of transcriptional regulation is how the normally
transcriptional                      central to the transcriptional control of cell-type specific genes
transcriptional   pathway-specific   cerevisiae are under transcriptional control of pathway-specific regulators of phosp
transcriptional                      cerevisiae under the transcriptional control of the 3-phosphoglycerate kinase
transcriptional   striatal           c-fos expression in transcriptional regulation of striatal preproenkephalin, prodynor
transcriptional                      c-fos in the transcriptional regulation of other genes suggests
transcriptional                      chain gene is transcriptionally controlled by a modularly organized
transcriptional   insulin            chain genes are transcriptionally regulated by insulin and influenced
transcriptional   induction          chain reaction and transcriptional regulation of induction. Intestinal cytochromes
transcriptional   Myc:Max            change in the transcriptional regulation of Myc:Max target genes
transcriptional   aromatase          changes in the transcriptional control of aromatase Whereas
transcriptional   aromatase          changes in the transcriptional control of aromatase While
transcriptional   genes              changes in the transcriptional regulation of
transcriptional   genes              changes in the transcriptional regulation of genes for myelin
transcriptional   known              Changes in the transcriptional regulation of known ER stress
transcriptional                      changes in the transcriptional regulation of the two adhesion
transcriptional   estrogen           channel that is transcriptionally regulated by estrogen. To examine
transcriptional                      characteristic of the transcriptional regulation of the CYC1
transcriptional   gene               characteristics of the transcriptional control of gene expression by
transcriptional                      characteristics via the transcriptional regulation of the FLO11, STA1,
transcriptional   prp                characterization is presented. Transcriptional regulation of prp was studied
transcriptional               characterization of the transcriptional regulation of the mouse UGT1A1
transcriptional               characterized by a transcriptional control of the expression of these
transcriptional   ornithine   chemopreventive activity through transcriptional regulation of ornithine For
transcriptional   phorbol     chemopreventive responses through transcriptional regulation of phorbol ester-ind
transcriptional               chimeric proteins under transcriptional control of the p54 promoter,
transcriptional               chloride channels, are transcriptionally regulated on a tissue-specific
transcriptional               chloride channels, is transcriptionally regulated on a tissue-specific
transcriptional   Cpx1        chloroplasts occurs via transcriptional regulation of Cpx1 mediated by
transcriptional               cholesterol metabolism is transcriptionally regulated by several classes of orphan
transcriptional               cholesterol transport, is transcriptionally regulated by several nuclear receptors
transcriptional               chorionic gonadotropin (CG) are regulated transcriptionally in placental cells
transcriptional               chose to characterize transcriptional regulation of the MMP-9 gene
transcriptional               c-H-ras under the transcriptional control of the mouse metallothionein-I
transcriptional               chromatin conformation and transcriptional regulation of this Using
transcriptional               chromatin modifying enzymes. Transcriptional regulation of the human histone
transcriptional   gene        Chromatin organization and transcriptional control of gene expression in Drosophil
transcriptional   cyclin      chromatin remodelers in transcriptional regulation of cyclin genes and the
transcriptional   cta3(+)     chromatin structure and transcriptional regulation of cta3(+) and
transcriptional               Chromatin structure and transcriptional regulation of human papillomavirus type
transcriptional               Chromatin structure and transcriptional regulation of human RAG-1
transcriptional               Chromatin structure and transcriptional regulation of the beta-globin
transcriptional               Chromatin structure and transcriptional regulation of the stem cell
transcriptional   MMTV        chromatin structure in transcriptional regulation of MMTV LTR hormone-dependen
transcriptional               chromogenic identification of transcriptional control signals in Streptomyces lividan
transcriptional               chromosomal location, and transcriptional regulation of the human galanin-1
transcriptional               Chromosomal organization and transcriptional regulation of human GEM and local
transcriptional               chromosome under the transcriptional control of the cyanobacterial nirA
transcriptional               chromosome-wide mechanisms of transcriptional regulation control development i
transcriptional   NF-kappaB   cIAP-1, which are transcriptionally regulated by NF-kappaB and function
transcriptional               CIb1 gene is transcriptionally regulated during development and is
transcriptional   CRH         circuit, allowing differential transcriptional regulation of CRH and AVP
transcriptional   visna       cis- and trans-acting transcriptional regulation of visna Visna
transcriptional               Cis elements for transcriptional regulation of the human endothelin-A
transcriptional               cis-acting elements for transcriptional regulation of the human nonmuscle
transcriptional               cis-acting elements of transcriptional control in MHC class II
transcriptional               cis-element for cAMP-mediated transcriptional regulation of this gene and may
transcriptional   HBV         cis-elements for the transcriptional regulation of HBV gene
transcriptional   immune      cis-elements involved in transcriptional regulation of immune cell-derived GH,
transcriptional               cis-elements involved in transcriptional regulation of the mouse perforin
transcriptional               cis-elements involved in transcriptional regulation of the promoter for
transcriptional               cis-elements required for transcriptional control of the Chinese hamster
transcriptional               citrate transport system. Transcriptional regulation of the ferric citrate
transcriptional   neuronal    c-Jun and the transcriptional control of neuronal There
transcriptional               c-Jun in the transcriptional control of the TH
transcriptional   DMP1        c-jun on the transcriptional regulation of DMP1
transcriptional               clarify the complex transcriptional regulation of the human GM-CSF
transcriptional   cyclin      classes of regulation. Transcriptional control of cyclin genes has
transcriptional               cloned under the transcriptional control of the Escherichia coli
transcriptional               cloned under the transcriptional control of the highly inducible
transcriptional   CD7         clones implicating a transcriptional regulation of CD7 Ag
transcriptional               clones under the transcriptional control of the cauliflower mosaic
transcriptional               Cloning, sequence, and transcriptional regulation of the operon encoding
transcriptional                 Cloning, sequencing and transcriptional control of the Schizosaccharomyces pomb
transcriptional                 Cloning, sequencing and transcriptional regulation of the draT and draG
transcriptional   htrP          cloning, sequencing, and transcriptional regulation of htrP. We identified
transcriptional                 Cloning, sequencing, and transcriptional regulation of the Vibrio cholerae
transcriptional   viuA          Cloning, sequencing, and transcriptional regulation of viuA, the gene
transcriptional                 closely investigate the transcriptional regulation of the human MXI1
transcriptional   MRP1          clue that the transcriptional control of MRP1 by p53
transcriptional                 cluster and is transcriptionally regulated by the However,
transcriptional                 c-met protooncogene, is transcriptionally regulated by a wide variety
transcriptional                 c-myc oncogene under transcriptional control of the myelin basic
transcriptional                 c-neu oncogene under transcriptional control of the MMTV promoter
transcriptional                 cocaine abuse on transcriptional regulation of human dopamine transporter
transcriptional                 coding region under transcriptional control of a mouse mammary
transcriptional                 coding region, under transcriptional control of an Aspergillus oryzae
transcriptional                 coding sequence under transcriptional control of the androgen responsive
transcriptional                 coding sequences under transcriptional regulation of the Moloney murine
transcriptional                 coelicolor retain transcriptional regulation of the chitinase 63
transcriptional   full-length   coli beta-glucuronidase), under transcriptional control of full-length rolB promoter
transcriptional                 coli K-12 are transcriptionally regulated by numerous Two
transcriptional                 coli rhaT gene. Transcriptional regulation of the rhaT gene,
transcriptional   arginine      coli strain K12, transcriptional control of arginine biosynthesis is
transcriptional                 coli under the transcriptional control of a T7 bacteriophage
transcriptional                 coli under the transcriptional control of the bacteriophage lambda
transcriptional                 coli under the transcriptional control of the coli
transcriptional                 coli under the transcriptional control of the lac
transcriptional                 coli under the transcriptional control of the lac and tac
transcriptional                 coli under the transcriptional control of the trp-lac (tac)
transcriptional   two           coli under the transcriptional control of two tac promoters
transcriptional   T5            coli under the transcriptional regulation of T5 promoter yielded
transcriptional                 coli under the transcriptional regulation of the T5 promoter
transcriptional                 coli under the transcriptional regulation of the T7 promoter
transcriptional   T5            coli under transcriptional regulation of T5 promoter yielded
transcriptional                 coli, removed ANR-dependent transcriptional control of the remaining pfl
transcriptional   RA;           collagen IV are transcriptionally regulated by RA; but2cAMP also
transcriptional                 collagenase gene expression is regulated transcriptionally and is inducible
transcriptional                 collagenase, induction was transcriptionally regulated as demonstrated by nuclear
transcriptional   XCRMP-2       commitment, and that transcriptional control of XCRMP-2 gene, is
transcriptional                 common feature of transcriptional control in both prokaryotes and eukaryotes.
transcriptional                 common mechanism of transcriptional control for the two cloned
transcriptional                 common pathways of transcriptional regulation exist in the two
transcriptional                 common to the transcriptional regulation of both the albumin
transcriptional   spv           communication explores the transcriptional regulation of spv genes within
transcriptional                 comparative analysis of transcriptional regulation in prokaryotes and phylogenetic
transcriptional   Hoxc8         compared expression and transcriptional regulation of Hoxc8 in chicken
transcriptional   classical     Comparison of the transcriptional regulation of classical and non-classical
transcriptional                 complementary DNA under transcriptional control of the cytomegalovirus
transcriptional                 complementary DNA under transcriptional control of the human beta-actin
transcriptional   IMPDH         complex cell type-specific transcriptional regulation of IMPDH type I
transcriptional   ODC           complex exerts negative transcriptional control of ODC synthesis as
transcriptional                 complex in the transcriptional regulation of the cardiac actin
transcriptional                 complex involved in transcriptional regulation of mouse mu-opioid receptor
transcriptional                 complex involved in transcriptional regulation of the rat insulin
transcriptional                     complex mechanism of transcriptional regulation which orchestrates the sequentia
transcriptional   PAH-inducible     complex modes of transcriptional regulation of PAH-inducible They
transcriptional                     complex pattern of transcriptional control throughout embryonic
transcriptional                     complex pattern of transcriptional control were determined using transgenic
transcriptional                     complex pattern of transcriptional regulation of the chicken TGF-beta
transcriptional                     complex pattern of transcriptional regulation of the mouse HGF
transcriptional                     complex pattern of transcriptional regulation that may reflect targeted
transcriptional                     complex profiles of transcriptional regulation associated with individual dystrophin
transcriptional                     complexity in the transcriptional control of the class II
transcriptional                     complexity in the transcriptional control of this coordinately regulated
transcriptional                     complexity in the transcriptional regulation of distinct human H4
transcriptional                     complexity of the transcriptional control of the PDGF-B gene
transcriptional   Myf5              complexity of the transcriptional regulation of Myf5. Both within
transcriptional                     component of the transcriptional control of this cell
transcriptional                     component of the transcriptional regulation of the proU
transcriptional   cyt               components in the transcriptional regulation of cyt The
transcriptional   phenylpropanoid   components involved in transcriptional regulation of phenylpropanoid genes have
transcriptional   hematopoiesis     components of the transcriptional regulation of hematopoiesis The
transcriptional   mitochondrial     components of the transcriptional regulation of mitochondrial biogenesis is
transcriptional                     comprehensive dissection of transcriptional regulation in budding yeast, giving
transcriptional   eNOS              comprehensive understanding of transcriptional regulation of eNOS is emerging
transcriptional                     concentration, suggesting a transcriptional regulation of these two genes,
transcriptional                     concept that the transcriptional regulation of the [Ah] battery
transcriptional   IL-8              conclude that stretch-induced transcriptional regulation of IL-8 mRNA and IL-8
transcriptional   insulin           conclude that the transcriptional regulation of insulin production using
transcriptional   PN-1              conclude that the transcriptional regulation of PN-1 is not
transcriptional                     conclude that the transcriptional regulation of the human Na/K
transcriptional   c-jun             CONCLUSIONS: Radiation-mediated transcriptional regulation of c-jun is prolonge
transcriptional   SWI4              conditions and of transcriptional regulation of SWI4, an activator
transcriptional                     conditions on the transcriptional regulation of both flagellin genes
transcriptional                     confirmed variation of transcriptional regulation as assessed by reverse
transcriptional                     confirming that ODC is regulated transcriptionally by However,
transcriptional   myogenesis        conjunction with the transcriptional control of
transcriptional   PPARalpha         consequences on the transcriptional control of PPARalpha target
transcriptional                     conserved mechanism of transcriptional regulation of the BMP-4 target
transcriptional                     consistent also with transcriptional regulation of the ovalbumin
transcriptional   MCPI              consistent with a transcriptional control of MCPI gene
transcriptional   CaBP              consistent with a transcriptional regulation of CaBP biosynthesis by
transcriptional   CEA               consistent with a transcriptional regulation of CEA A
transcriptional   channel           Consistent with a transcriptional regulation of channel expression, mRNA
transcriptional   expression        consistent with a transcriptional regulation of expression of these
transcriptional   sequential        consistent with coordinate transcriptional regulation of sequential steps of reverse
transcriptional   Xwnt8             consistent with direct transcriptional regulation of Xwnt8 by
transcriptional   BGP               consistent with primary transcriptional regulation of BGP production and suggest
transcriptional   glycophorin       consistent with the transcriptional regulation of glycophorin expression by
transcriptional                     constitutive transcriptional element. Transcriptional regulation of the BRCA1 proxim
transcriptional                     constitutively expressed under transcriptional control of the phosphoglycerate kina
transcriptional   PLSCR1            constructs showed that transcriptional control of PLSCR1 was entirely
transcriptional                     constructs under the transcriptional control of the highly inducible
transcriptional                     constructs under the transcriptional control of various subgenomic fragments
transcriptional                     constructs under the transcriptional regulation of the Rous sarcoma
transcriptional                     containing lacZ under transcriptional control of the mouse MLC3F
transcriptional   either                containing lacZ, under transcriptional control of either cytomegalovirus (CMV)
transcriptional                         containing MyoD under transcriptional control of the Rous sarcoma
transcriptional                         contains v-H-ras under transcriptional control of the glucocorticoid-sensitive mouse
transcriptional   metabolic             content on exercise-induced transcriptional regulation of metabolic Transcription
transcriptional   CAD                   contrast to the transcriptional regulation of CAD previously reported
transcriptional   GAPDH                 contrast to the transcriptional regulation of GAPDH that has
transcriptional                         contrasting patterns of transcriptional regulation in each Cooperativity
transcriptional                         Contrasting patterns of transcriptional regulation in these neurons may
transcriptional   hns                   contribute to the transcriptional control of
transcriptional                         contribute to the transcriptional control of cell growth and differentiation.
transcriptional   constitutive          contribute to the transcriptional control of constitutive and IFN-gamma-induced
transcriptional   jun                   contribute to the transcriptional control of jun, fos and krox
transcriptional                         contribute to the transcriptional control of the AChR alpha-subunit
transcriptional                         contribute to the transcriptional control of the interleukin 2
transcriptional                         contribute to the transcriptional regulation of a number of subunits
transcriptional   genes                 contribute to the transcriptional regulation of genes involved in differentiation
transcriptional   MMP-9                 contribute to the transcriptional regulation of MMP-9 in arterial
transcriptional                         contribute to the transcriptional regulation of several promoters by
transcriptional                         contribute to the transcriptional regulation of specific genes which
transcriptional                         contribute to the transcriptional regulation of the CD36
transcriptional                         contribute to the transcriptional regulation of the HNF-4
transcriptional   plastid               contributes to light-dependent transcriptional regulation of plastid
transcriptional   Sgs-4                 contributes to the transcriptional control of
transcriptional   type                  contributes to the transcriptional control of type I collagen
transcriptional   PRL                   contributes to the transcriptional regulation of PRL gene expression
transcriptional                         contributes to the transcriptional regulation of the IL-2 promoter,
transcriptional   mammalian             contributing to negative transcriptional control of mammalian gene
transcriptional   Tnf                   contribution of the transcriptional regulation of Tnf to susceptibility
transcriptional   type                  contribution to the transcriptional regulation of type III IF
transcriptional                         contributions to the transcriptional regulation of an individual gene
transcriptional   six                   contributions to the transcriptional regulation of six immediate early
transcriptional                         control of Dorsal. Transcriptional control of the Drosophila terminal
transcriptional   flaA                  control system mediates transcriptional control of flaA through a regulatory
transcriptional   string                controlled by the transcriptional regulation of string expression, which
transcriptional                         controlled through the transcriptional regulation of specific subsets of genes.
transcriptional                         controller for the transcriptional regulation of the gene expression
transcriptional   oligodendrocyte       controversial, and the transcriptional control of oligodendrocyte lineage specificatio
transcriptional   segmental             co-operate in the transcriptional control of segmental expression of Hoxb3
transcriptional                         cooperate in the transcriptional regulation of this We
transcriptional                         cooperating factors in transcriptional regulation of the GADD45a gene
transcriptional                         coordinate oPL transactivation. Transcriptional regulation of human and rodent
transcriptional   replication-dependent Coordinate transcriptional control of replication-dependent human H4,
transcriptional   yeast                 Coordinate transcriptional control of yeast genes involved
transcriptional                         cope with pathogens. Transcriptional regulation of this highly complex
transcriptional   carbon                CoQ synthesis, is transcriptionally regulated by carbon We
transcriptional   psbD                  core promoter motifs. Transcriptional regulation of psbD may be
transcriptional   viral                 correlated by glial-specific transcriptional regulation of viral gene
transcriptional                         correlated with a transcriptional regulation of the DHBP
transcriptional                         correlated with the transcriptional regulation of target genes by
transcriptional   ROX1                  correlations suggest that transcriptional regulation of ROX1 is an
transcriptional                         corresponding transporters is transcriptionally regulated by the ambient pH
transcriptional   ACTH                  cortex and is transcriptionally regulated by ACTH. We examined
transcriptional   corticotropin          cortex and is transcriptionally regulated by corticotropin In
transcriptional   pIgR                   corticosteroids alter the transcriptional regulation of pIgR expression has
transcriptional                          corticotrophs and melanotrophs. Transcriptional regulation of the rPOMC-LacZ fus
transcriptional   genes                  could potentially occur. Transcriptional regulation of genes by nutritionally
transcriptional                          coupled to the transcriptional regulation of the glnA gene
transcriptional   glutathione            Coupling of the transcriptional regulation of glutathione biosynthesis to the
transcriptional                          CRABP-II gene is transcriptionally regulated by a newly synthesized
transcriptional                          c-Raf in the transcriptional regulation of the hypertrophic chondrocyte-specific
transcriptional                          cre under the transcriptional control of the B lineage-restricted
transcriptional                          CRE1 in the transcriptional control of the CWDE encoding
transcriptional                          CREB in the transcriptional regulation of the human GM3
transcriptional                          CREB-1-mediated mechanism of transcriptional regulation of the GSTP1 gene
transcriptional                          CRH cDNA under transcriptional control of a cytomegalovirus promoter
transcriptional                          critical component of transcriptional regulation by the estrogen receptor
transcriptional                          critical for basal transcriptional regulation of the human mdr1
transcriptional                          critical for basal transcriptional regulation of the mouse sst5
transcriptional   p21                    critical in mediating transcriptional regulation of p21 in response
transcriptional   TNFalpha               critical in the transcriptional control of TNFalpha Evidence
transcriptional   NF-kappaB              critical role in transcriptional regulation of NF-kappaB through control
transcriptional                          critical role in transcriptional regulation of target genes involved
transcriptional                          critical roles in transcriptional regulation of the protein C
transcriptional   MHC                    critical to the transcriptional control of MHC class II
transcriptional   Escherichia            CRP and PAA. Transcriptional regulation of Escherichia coli ATCC11105
transcriptional                          crucial for the transcriptional regulation of many erythroid-specific
transcriptional   insulin                crucial role in transcriptional control of insulin 5'deletional
transcriptional                          crucial role in transcriptional control of the insulin genes
transcriptional                          crucial role in transcriptional control of the tissue specific
transcriptional                          crucial role in transcriptional regulation of the AFP gene
transcriptional                          crucial roles in transcriptional regulation of the
transcriptional                          c-src) dependent and was regulated transcriptionally through GT-box (-52),
transcriptional   copper                 cueAR operon was transcriptionally regulated by copper and
transcriptional   O                      cues in the transcriptional regulation of O polysaccharide
transcriptional                          cultures to analyze transcriptional control of the rat atrial
transcriptional                          current understanding of transcriptional control of the well-studied murine
transcriptional                          current understanding of transcriptional regulation in the brain comes
transcriptional                          current understanding of transcriptional regulation of one such human
transcriptional   plasma                 current understanding of transcriptional regulation of plasma membrane lipid
transcriptional                          current understanding of transcriptional regulation of the steroidogenic enzyme
transcriptional   sulfur                 cyanobacterial plasmid are transcriptionally regulated by sulfur availability and Cys
transcriptional                          cycle- and age-dependent transcriptional regulation of human thymidine kinase
transcriptional   DNA                    cycle expression and transcriptional regulation of DNA topoisomerase IV
transcriptional                          c
                  proliferation-associatedycle progression via transcriptional regulation of proliferation-associated
transcriptional                          cycle regulation are transcriptionally regulated in the residual small
transcriptional                          cyclin B expression is regulated transcriptionally and post-translationally during
transcriptional   cyclin                 cyclin-dependent kinase inhibitors; transcriptional regulation of cyclin gene express
transcriptional                          cyclin-dependent kinases and is regulated transcriptionally by p53, which
transcriptional   fatty                  cyclooxygenases-1 and -2. Transcriptional regulation of fatty acid cyclooxygenase
transcriptional   oxygen                 cyd operon is transcriptionally regulated by oxygen via both
transcriptional   NAM7                   Cyp1p influences the transcriptional regulation of NAM7. In addition,
transcriptional                          cytochrome c gene. Transcriptional regulation of the mouse testis-specific
transcriptional                          cytochrome
                  3-methylcholanthrene-dependent P-450c gene. Transcriptional control of 3-methylcholanthrene-depende
transcriptional   HIV                    cytokine secretion and transcriptional regulation of HIV replication, and they
transcriptional   rabbit               cytokines in the transcriptional regulation of rabbit CYP2E1 and CYP2E2.
transcriptional   ERV3                 cytokines on the transcriptional regulation of ERV3 in
transcriptional   ERV3                 cytokines on the transcriptional regulation of ERV3. Although the level
transcriptional   secretory            cytokines on the transcriptional regulation of secretory granule protease
transcriptional   primary              cytokinin perception to transcriptional regulation of primary cytokinin-responsive ge
transcriptional                        cytotoxic effector mechanisms. Transcriptional control of the expression of Fas
transcriptional                        D1 cDNA under transcriptional control of the cytomegalovirus promoter/enhancer
transcriptional                        D15 under the transcriptional control of the glyceraldehyde-6-phosphate dehydroge
transcriptional   type                 D3 in the transcriptional control of type I collagen
transcriptional   125-dihydroxyvitamin D-9k gene is transcriptionally regulated by 1,25-dihydroxyvitamin D3 in the
transcriptional   estrogen             D-9K gene is transcriptionally regulated by estrogen in the uterus
transcriptional                        damage under the transcriptional control of the p53 tumour
transcriptional                        data base of transcriptional regulation and operon organization in E.
transcriptional   genes                data clearly shows transcriptional regulation of genes in all
transcriptional                        data demonstrate that transcriptional control of the smooth muscle
transcriptional   egr-1                data demonstrate that transcriptional regulation of egr-1 by PIXY321
transcriptional                        data exist on transcriptional regulation of the NCX1
transcriptional                        data for the transcriptional regulation of these and of other
transcriptional   pTalpha              data illustrate that transcriptional regulation of pTalpha limits developmental
transcriptional   DAB2IP               data indicate that transcriptional regulation of DAB2IP is responsible
transcriptional   svb                  data indicate that transcriptional regulation of svb integrates inputs
transcriptional                        data indicate that transcriptional regulation of the fibronectin gene
transcriptional   TIMP-1               data indicate that transcriptional regulation of TIMP-1 gene expression
transcriptional   algC                 data on the transcriptional regulation of algC The
transcriptional   ID2                  data suggest that transcriptional regulation of ID2 by the MycN
transcriptional                        data suggest that transcriptional regulation of the AhR is
transcriptio