AS 05

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



1 Aagaard J.E., Krutovskii 1997 RAPDs and allozymes exhibit similar Heredity 81: allozymes, DNA Thirty-six nuclear-encoded RAPD loci and

k.V., Straus S.H. levels of diversity and differentiation 69-79 markers, dominance 20 allozyme loci were studied to compare

among populations and races of Dougla- simulation, Douglas-fir, levels of diversity and differentiation

2 Aagaard J.E., Krutovskii 1998 fir

RAPD markers of mitochondrial origin Molecular RAPD diversity, RAPD,

geneticDNA markers, among populations and races of the

We developed a method of screening

k.V., Straus S.H. exibit lower population diversity and Ecology 7 (7): population RAPD markers for the presence of

higher differentiation than RAPDs of 801-812 differeniation, Douglas organelle DNA products using enriched

3 A'Hara, S.W.; Cottrell, Characterization Douglas of

2007 nucleus origin in of a suitefir 40 EST- Silvae fir, forest trees

EST, Sitka spruce, forest The paper describes 40 then used these

organelle DNA probes, novel, data-mined,

J.E. derived microsatellite markers for use in Genetica 56 (3- trees polymorphic microsatellite loci for use in

Sitka Spruce (Picea sitchensis (Bong.) 4): 138-141 a QTL association study in Sitka spruce.

4 Akerman, S., 1996 Carr)

Segregation of AFLP markers in Betula Forest AFLP, DNA markers, Publicly available EST sequences of Picea

-

Tammisola, J., Regina, pendula (Roth). Genetics 3 (2): PCR, Betula pendula ,

M., Kauppinen, V. and 117-123. DNA fingerprinting,

Akerman, S.

5 Lapinjoki, S., 1995 RAPD markers in Parentage Can. J. For. forest trees

Arbitrary primers, DNA, The general applicability of RAPDs

Tammisola, J., confirmation of a valuable breeding Res. 25 (7): PCR, molymorphism, , (random amplified polymorphic DNAs) as

Lapinjoki S.P., progeny of European white birch 1070-1076 forest trees genetic molecular markers for Betula

6 Soderlund H., Payton

Alba R., Fei Z., 2004 ESTs, cDNA microarrays, and gene The Plant expressed sequence tags, pendula Roth was evaluated. On average

Gene expression profiling holds

P., Liu Y., Moore S.L., expression profiling: tools for dissecting Journal 39, expression profiling, tremendous promise for dissecting the

Debbie P., Cohn J., plant physiology and development 697–714 transcriptome, digital regulatory mechanisms and transcriptional

Areškevičienė Gordon 2005 Miško medžių genetiniai tyrimai

7 D‘Ascenzo M.,R., Lietuvos expression analysis,

RAPD, genetic diversity, networks that underlie biological

Atsitiktinai pagausintos polimorfinės DNR

Žvingila D., Kuusienė atsitiktinai pagausintos polimorfinės biologinė genetic identity, forest metodas (APPD) plačiai taikomas augalų

S. DNR (APPD) metodu įvairovė: trees genetinės įvairovės tyrimams. Lietuvos

8 Areškevičienė, R., 2005 The Estimation of Genetic Diversity būklė, Forestry RAPD, Picea abies ,

Baltic miškų instituto Molekulinės genetikos ir

The genetic diversity and genetic

Žvingila, D., within and between Lithuanian 11 (2): 2-8 population, genetic differentiation of eight Lithuanian

Gabrilavičius, R. and Populations of Norway Spruce (Picea diversity, forest trees

QTL, wood quality, populations of Norway spruce (Picea abies

9 Kuusienė, S.

Arcade A., Faivre- 2002 abies (L.) Karst.) by using RAPD.

Localisation of genomic regions Ann. For. Sci. microdensitometry, The use of were studied using random

(L.) Karst.)wood quality components in

Rampant P., Paques controlling microdensitometric 59: 607-615 wood density, Larix, forest trees selection is hampered by long

L.E. and Prat D. parameters of wood characteristics in forest trees delays before phenotypic evaluation.

10 Arvai J.L. 2007 hybrid larches risk communication:

Rethinking of Tree Genetics Risk communication, Marker-assisted selection opens new

Risk communication involves three

lessons from the decision sciences & Genomes 3: Decision making, Risk primary elements: process, content and

173–185 management, GMO intent. Much has been written about the

first two. Much is known, for example,

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



11 Bacilierri R. , Ducousso 1995 Genetic, morphological, ecological and Silvae Quercus morphology, The sessile and pedunculate oaks are the

A. and Kremer A. phenological differentiation between phenology, gradient

Genetica 44, most common tree species in Europe. The

Quercus petraea (Matt.) Liebl. and 1: 1-10. ecology, allozymes, 2 taxons are closely related, and, in spite

12 Bacilieri, R, Ducousso, Comparison of L. in a mixed characters

1996 Quercus robur morphologicalstand of Ann Sci Fordifferentiation, forest

morphology; RAPD; of their ecological differences, they form

Interspecific hybridization is common in

A, Kremer, A and molecular markers for the analysis of hybridization; Quercus,

53 (1): 79-91 many plant groups, but the morphology of

hybridization in sessile and pedunculate forest trees hybrids has rarely been studied on an

13 Bacilieri, R., Roussel, 1993 oak

Hybridization and mating system in a Ann Sci For Allozymes, experimental basis. The sessile and the

Patterns of hybridization and of the mating

G. Ducousso, A. mixed stand of sessile and pedunculate 50, Suppl hybridizatlon, mating system of Quercus petraea and Quercus

oak. 1:122-127. system, pollen pool, robur have been inferred from

14 Bajaj,Y.P.S. 1986 Chapter I. Biotechnology of Tree Biotechnology Quercus robur , Quercus

forest trees examination of allozyme variation in 2

-

Improvement for Rapid Propagation and in Agriculture

Biomass Energy Production. and

15 Bastien D., Favre J.M., 2003 haracterization of a mosaic minisatellite Forestry.Trees minisatellite; VNTR;

Theor Appl A mosaic minisatellite region has been

Collignon A.M., locus in the mitochondrial DNA of Genet 107 (3): mtDNA; heteroplasmy; identified in the mitochondrial genome of

Sperisen C., Jeandroz S. Norway spruce [Picea abies (L.) Karst.] 574-580 Picea abies, forest trees Norway spruce (Picea abies). The array

16 Beavis, W.D. and Keim, 1996 Identification of quantitative trat loci that

Edited by forest trees was composed of three tandem repeats

-

P. are affected by environment. Kang, M.S.,

Gauch, H. G.,

17 Bedon, F., Grima- 2007 Conifer R2R3-MYB transcription Jr. Genotype- forest trees

BMC Plant BACKGROUND:Several members of the

Pettenati, J. and factors: sequence analyses and gene Biology 7(1): R2R3-MYB family of transcription factors

MacKay, J. expression in wood-forming tissues of 17 act as regulators of lignin and

18 Belahbib, N., Pemonge, 2001 white spruce (Picea glauca)

Frequent cytoplasmic exchanges Molecular cpDNA, geographical Chloroplast (cp) metabolism during wood

phenylpropanoidand mitochondrial (mt)

M.H., Ouassou, A., between oak species that are not closely Ecology 10 structure, hybridization, DNA variation were studied in 97

Sbay, H., Kremer, A., related: Quercus suber and Q-ilex in (8): 2003- introgression, mtDNA, populations of cork oak (Quercus suber) in

19 Petit, R.j. R. and

Bernatzky, 1992 Marocco.

Marker-aided selection in a backcross 2012.J. For.

Can. PCR-RELP, forest trees

MAS, DNA Morocco; in 31 of these populations, holm

Marker-assisted selection in backcross

Mulcahy, D.L. breeding program for resistance to Res. 22: 1033- fingerprinting, Castanea, breeding is discussed in general and with

chestnut blight in the American chestnut. 1037. forest trees specific reference to obtaining resistance

20 Binelli, G., Bucci, G. 1994 A genetic linkage map of Picea abies Theor Appl Picea abies , RAPD, to chestnut blight in American chestnut

Norway spruce (Picea abies Karst.) is a

Karst., based on RAPD markers, as a Genet 88: 283- Population genetics, most important species among European

tool in population genetics. 288. linkage map, forest trees forest trees for both economical and

ecological reasons. However, this species

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



21 Bordacs S., Popescu F., 2002 Chloroplast DNA variation of white oaks Forest Ecol Quercus spp.; A total of 1113 oak trees from 222

Slade D., Csaikl U.M., in northern Balkans and in the Manag 156: PCR–RFLP; Postglacial populations originating from eight

Lesur I., Borovics C, Carpathian Basin 197–209 recolonisation; Refugia; countries (Austria, Bosnia-Herzegovina,

22 Kezdy P., Konig A.O.,

Bouille, M. and 2005 Trans-species shared polymorphisms at Am J Bot Species distribution,

allele coalescence, Croatia, Hungary,nuclear Pile loci.

For each of three Romania, Slovakia,

Bousquet, J. orthologous nuclear gene loci among 92(1): 63-73. expressed sequence tag intraspecific- as well as trans-specific

distant species in the conifer Picea polymorphisms, EST, shared polymorphisms were detected in

23 Bousquet, J., Isabel, N., 2007 (Pinaceae):-Implications for the long-

Chapter 3 Spruce. In Genome historical demography,

forest trees UNA among three distantly related species

-

Pelgas, B., Cottrell, J., Mapping and

Rungis, D. and Ritland, Molecular

24 K.

Bradshaw, H.D., Ir., and 1992 Marker-aided selection and propagation Breeding in

Can. J. For. Genetic maps, MAS, Genetic maps with a high density of

Foster, G.S. systems in trees: advantages of cloning Res. 22: 1046- markers, forest trees markers have been used to locate discrete

for studying quantative inheritance. 1051 Mendelian components of quantitatively

25 Bradshaw H.D. Jr. and 1995 Molecular Genetics of Growth and Genetics 139: Molecular Genetics, We have traits in quantitative trait loci

inherited mapped a few crop plants. In

Stettled R.F. Development in Populus. IV. Mapping 963-973 growth, development, (QTLs) for commercially important traits

QTLs With Large Effects on Growth, Populus, mapping, QTL, (stem growth and form) and an adaptive

26 Bradshaw, H.D., and 1993 Form, and Phenology Traits inand

Molecular genetics of growth a Forest Theor Appl form, phenology, forest trait (spring leaf flushi)n a Populus F2

RFLP, polyploid, While constructing a genetic linkage map

Stettler, R.F. development in Populus I. Triploidy in Genet: nondisjunction, of a hybrid poplar genome (Populus

hybrid poplars. interspecific hybrid, trichocarpa x P. deltoides), we identified

27 Bradshaw, H.D., and 1994 Molecular-genetics of growth and Theor Appl cottonwood, forest trees several restriction fragment length

Cottonwood, inbreeding Distortion of expected Mendelian

Stettler, R.F. development in Populus 2: Segregation Genet 89 (5): depression, lethal segregation ratios, commonly observed in

distortion due to genetic load 551-558 equivalent, forest trees many plant taxa, has been detected in an

28 Bradshaw, H.D., Villar, 1994 Molecular genetics of growth and Theor Appl Cottonwood, experimental three-generation inbred

We have evaluated three DNA-based

M., Watson, B.D., Otto, development in Populus . III. A genetic Genet 89: 167- tacamahaca, aigeiros marker types for linkage map construction

K.G., Stewart,S., linkage map of a hybrid poplar 178. salix, genome, forest in Populus: RFLPs detected by Southern

29 Steeettler, R.F. and

Bradshaw, H.D., 1995 Molecular-genetics STS, and RAPD

composed of RFLP,of growth and Theor Appl trees

Cottonwood, MAS, blot have mapped quantitative traitby a

We hybridization, STSs detected loci

Stettler, R.F. development in Populus 4: Mapping Genet 139 (2): QTL, poplars, hybrids, (QTLs) for commercially important traits

QTLs with large effects on growth, form, 963-973 forest trees (stem growth and form) and an adaptive

30 Bradshaw H.D., 2000 and phenology traits in a forest tree

Emerging model systems in plant J Plant Growth forest genetics; tree Forest trees leaf tremendous economic

trait (spring haveflush) in a Populus F-2

Ceulemans R., Davis J., biology: Poplar (Populus ) as a model Regul 19 (3): physiology; genomics, and ecological value, as well as unique

Stettler R. forest tree 306-313 QTL, forest trees biological properties of basic scientific

interest. The inherent difficulties of

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



31 Brinker M., van Zyl L., 2004 Microarray Analyses of Gene Expression Plant Microarray, gene In order to investigate the gene expression

Liu W., Craig D., during Adventitious Root Development Physiology expression, root pattern during adventitious root

Sederoff R.R. in Pinus contorta 135: development, Pinus development, RNA of Pinus contorta

32 Brondani R.P.V., 2006 A microsatellite-based consensus linkage 1526–1539,

BMC Plant contorta, forest trees

SSR, microsatelites, hypocotyls, pulse-treated with the auxin

Background: Eucalypts are the most

Williams E.R., Brondani map for species of Eucalyptus and a Biology 6: 20 DNA markers, linkage widely planted hardwood trees in the

C., Grattapaglia D. novel set of 230 microsatellite markers map, Eucalyptus, forest world occupying globally more than 18

33 Brondani R.P.V., 2002 for the genus

owards a genus-wide reference linkage Mol Genet trees

microsatellite; simple million hectares as an important source of

A novel set of 50 highly polymorphic

Brondani C., map for Eucalyptus based exclusively on Genomics 267 sequence repeats (SSR); microsatellite markers were developed and

Grattapaglia D. highly informative microsatellite (3): 338-347 Eucalyptus; linkage map, mapped on existing RAPD framework

34 T

Brown G.R., Kadel III 2001 markers Reference Loci in Loblolly

Anchored Genetics 159: forest trees

EST polymorphism, maps of Eucalyptus grandis and E.

Anchored reference loci provide a

E.E., Bassoni D.L., Pine (Pinus taeda L.) for Integrating 799–809 Pinus taeda, genomics, framework for comparative mapping.

Kiehne K.L, Temesgen Pine Genomics forest trees They are landmarks to denote conserved

Brown Buijtenen J.P.,

35 B., van G.R., Bassoni 2003 Identification of Quantitative Trait Loci Genetics 164: QTL, wood property, chromosomal segments, allowing the map

A long-term series of experiments to

D.L., Gill G.P., Fontana Influencing Wood Property Traits in 1537–1546 Pinus taeda, forest trees QTL influencing wood property traits in

J.R., Wheeler N.C., Loblolly Pine (Pinus taeda L.). III. QTL loblolly pine has been completed. These

Brunner R.A., Li J.,

36 Megraw A.M., Davis 2007 Verification and Candidate Gene

Genetic containment of forest plantations Tree Genetics Populus, Pinus, Dispersal of were designed to identify and

experiments pollen, seeds, or vegetative

DiFazio S.P., & Genomes 3 Eucalyptus, Sterility, propagules from intensively bred, exotic,

Shevchenko O., (2): 75-100 Confinement, Ablation, or recombinant DNA modified forest

37 Montgomery B.E.,

Brunner A.M, Busov 2004 Poplar genome sequence: functional Trends in Excision, Genetic

Poplar, genome In addition may cause detrimental

plantations to their value for wood or

V.B., Strauss S.H. genomics in an ecologically dominant Plant Science sequence, genomics, products, members of the genus Populus

plant species Vol.9 No.1 forest trees (poplars) provide a range of ecological

38 Buckler E.S., 2002 Plant molecular diversity and Current Molecular diversity, services,of nucleotide diversity are

Surveys including carbon sequestration,

Thornsberry J.M. applications to genomics Opinion in forest trees beginning to show how genomes have

Plant Biology been shaped by evolution. Nucleotide

39 Bucci, G, Binelli, G, 1995 Identification of a new set of molecular 5:107–111

Population Molecular markers, diversity is also being used to discover the

-

Menozzi, P markers in Norway spruce as revealed by genetics and Spruce, forest trees

random amplification techniques genetic

40 K Burg, M Zechmeister- 1993 Oak chloroplast-DNA polymorphisms conservation

Ann. For. Sci. oak, chloroplast, Petunia hybrida chloroplast (cp) DNA

Machhart, J Glössl and J detected by restriction fragment length 50: 66-69 restriction fragment probes were used to find restriction

Schmidt polymorphism (RFLP) length polymorphism, fragment length polymorphisms (RFLPs)

RFLP, forest trees in the cp DNA of the oak species Quercus

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



41 Byrne, M., Murrell, 1997 Identification and mode of action of Theor Appl Eucalypts, height, leaf Regions of the genome influencing height

J.C., Owen, J. V., quantitative trait loci affecting seedling Genet 94: 674- area, genetic mapping, and leaf area in seedlings of a three-

Kriedemann, P., height and leaf area in Eucalyptus 681. pleiotropy, forest trees generation outbred pedigree of Eucalyptus

42 Williams E.R., Moran,

Byrne, M, Murrell, JC, 1997 nitens . of quantitative trait loci

Mapping Theor Appl Eucalypts, QTL, Frost nitens have the genome influencingQTLs

Regions of been identified. Three frost

Owen, JV, et al. influencing frost tolerance in Eucalyptus Genet 95 (5- tolerance, Genetic tolerance in an outbred family of

nitens 6): 975-979 mapping, forest trees Eucalyptus nitens have been identified.

43 Byrne M., Murrell J.C., 1995 An integrated genetic linkage map for Theor Appl Genetic map, linkage, An integrated genetic the same linkage

Two QTLs present on linkage map for E.

Allen B., Moran G.F. Eucalyptus using RFLP, RAPD and Genet 91 (6- Eucalypts, RFLP; nitens was constructed in an outbred three-

Isozyme markers 7): 869-875 RAPD, forest trees generation pedigree. Analysis of 210

44 Byrne M., Moran G.F., 1994 Detection and inheritance of RFLPs in NOV Appl

Theor RFLP, Eucalypts, RFLP, 125 RAPD and 4 isozyme loci

The level of polymorphism using genomic

Murrell J.C., Tibbits Eucalyptus nitens Genet 89 (4): inheritance, forest trees and cDNA probes with a number of

W.N. 397-402 OCT restriction enzymes and the inheritance of

45 Campbell M.M., 2003 ForestryÕs fertile crescent: the Plant domestication, genetic the RFLP loci was investigated in E.

Relative to crop plants, the domestication

Brunner A.M., Jones application of biotechnology to forest Biotechnology engineering, forestry, of forest trees is still in its infancy. For

H.M., Strauss S.H. trees Journal 1: forest trees, wood example, the domestication of many crop

46 Cato S.A., · Gardner 2001 A rapid PCR-based method for 141Ð154

Theor Appl Expressed sequence tag, plants wassemi-automatable procedure ago

A simple, initiated some 10 000 years

R.C.,· Kent J.,· genetically mapping ESTs Genet Polymerase chain was developed for converting expressed

Richardson T.E. 102:296–306 reaction, Fragment sequence tags (ESTs) into mappable

47 Cavers S, Degen B, 2005? Optimal sampling strategy for estimation Heredity 95? length polymorphism,

spatial genetic structure; genetic markers. The polymerase chain

Fine-scale spatial genetic structure (SGS)

Caron H, Lemes MR, of spatial genetic structure in tree (4): 281-289 trees; sampling; spatial in natural tree populations is largely a

Margis R, Salgueiro F, populations autocorrelation; result of restricted pollen and seed

48 Lowe AJM.T., Gusmao, 1996

Cervera, Indentification of AFLP molecular Theor Appl dominant; codominant,

Mer, AFLP markers, We have Understanding markers tightly

dispersal.identified AFLPthe link between

J. Steenackers, M., markers for resistance against Genet 93: 733- bulked segregant linked to the locus conferring resistance to

Peleman, J. Storme, V., Melampsora larici-populina in Populus. 737. analysis, Melampsora the leaf rust Melampsora a larici-populina

49 Vanden Brooeck, A.,

Cervera, MT, Gusmao, 1996 The use of bulked segregant analysis to For Sci. 49: larici-populina , Populus,

AFLP markers, in Populus. The study was carried out

We have identified three AFLP markers

J, Steenackers, M, et al. identify AFLP(TM) molecular markers 205-210 Melamsora, resistance, tightly linked to the locus conferring

T closely linked to Melampsora larici- populus, forest trees resistance to the leaf rust Melampsora

50 Cervera, MT, Gusmao, 1996 populina resistance in Populus

Application of AFLP(TM)-based Plant Growth AFLP, fingerprint, larici-populina in Populus by Bulked eased

Molecular marker technologies have

J, Steenackers M., Van molecular markers to breeding of Regul 20 (1): genome mapping, and potentiated genetic analysis of plants

Gysel A., Van Montagu Populus spp 47-52 molecular markers, and have become an extremely useful tool

M. and Boerjan W. poplar, QTL, forest trees in forest tree breeding. The information

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



51 Cervera M.T., Storme 2001 Dense Genetic Linkage Maps of Three Genetics 158: AFLP, SSR, Populus Populus deltoides, P. nigra, and P.

V., Ivens B., Gusma J., Populus Species (Populus deltoides, P. 787–809 deltoides, Populus nigra, trichocarpa are the most important species

Liu B.H., Hostyn V., nigra and P. trichocarpa) Based on AFLP Populus trichocarpa, for poplar breeding programs worldwide.

52 Van Slycken J., Van

Cervera M.T., 2000 and Microsatellite Markers tree species

Improved AFLP analysis of Can. J. For. forest trees peach,

AFLP, trees, Amplified fragment has become a model

In addition, Populus length polymorphism

Remington D., Frigerio Res. 30: 1608- eucalypt, oak, poplar, (AFLP) is a high-throughput, molecular-

J.M., Storme V., Ivens 1615 lobloly pine, forest trees marker technique that is used increasingly

53 B., Boerjan W., Plomion 2000 Molecular markers and genome mapping

Cervera M.T., Plomion Molecular genome mapping, woody in a variety of genetic analyses. Here, the

-

C., Malpica C. in woody plants Biology of plants, forest trees

Woody Plants,

54 Chaffey N., Cholewa E., 2002 Secondary xylem development in 1:375-394

Physiologia molecular, wood Our understanding of the molecular

Regan S. and Sundberg Arabidopsis: a model for wood Plantarum formation, forest trees controls regulating the identity of the

B. formation 114: 594–600. vascular cambium and the development of

55 Chagné, D., Lalanne, C., 2002 A high density genetic map of maritime Ann. For. Sci. Pinus pinaster, genetic secondary xylem and phloem have not yet

We constructed a high-density linkage

Madur, D., Kumar, S., pine based on AFLPs. 59 (5-6): linkage map, AFLP, map of maritime pine (Pinus pinaster Ait.)

Frigério, J.-M., Krier, 627–636. double pseudo-testcross, based on AFLP (Amplified Fragment

56 C., Decroocq, S.,

Chalupa V. 1993 Vegetative propagation of oak (Quercus Ann. For. Sci. physical size, forest trees

vegetative propagation, Length Polymorphism) markers using a

The potential of cuttings of Quercus robur

robur and Q petraea) by cutting and 50: 295-307 Quercus, cutting, tissue and Q petraea to form adventitious roots

tissue culture culture, somatic decreased rapidly with increasing plant

57 Chaparro J.X., Werner 1994 Targeted mapping and linkage analysis Theor Appl embryogenesis,segregant,

RAPD, bulked forest Nine different F2 families older plants

age. The rooting ability of of peach

D.J., O'Malley D., of morphological isozyme, and RAPD Genet 87: 805- genomic mapping, peach, [Prunus persica (L.) Batsch] were

Sederoff R.R. markers in peach. 815. Prunus persica , forest analyzed for linkage relationships between

58 Chua N.H. and 2000 Plant biotecnology the ins and outs of a Current trees trees

forest 14 morphological and two isozyme loci.

-

Sundaresan V. vew green revolution. opinion in

biotechnology,

59 Collignon A-M., Van de 2002 Geographical variation in random Vol.11:117- Picea abies, RPD, DNA,

Can. J. For. Quantitative traits and random amplified

Sype H., Favre J-M. amplified polymorphic DNA and Res. 32: quantitative traits, polymorphic DNA variations were

quantitative traits in Norway spruce 266–282 geographical variation, investigated on the whole natural range of

60 Collignon A.M., Favre 2000 Contribution to the postglacial history at Annals of forest abies, Norway

Picea trees Norway spruce (Picea abies (L.) Karst.).

RAPD analysis was used (1) to assess the

J.M. the western margin of Picea abies' Botany 85 (6): spruce, phylogeography, diversity of indigenous Picea abies within

natural area using RAPD markers. 713-722 phenotypic diversity, the French massifs (Alps, Jura and

Annals of Botany 85 (6): 713-722 correspondence analysis, Vosges) in comparison with the Hercyno-

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



61 Comps B., Gömöry D., 2001 Diverging trends between heterozygosity Genetics 157: DNA, forest trees Variation at 12 polymorphic isozyme loci

Letouzey J., Thiébaut B. and allelic richness during postglacial 389-397. was studied in the European beech on the

and Petit R.J. colonization in the European beech. basis of an extensive sample of 389

62 Corre V.L., Kremer A. 2003 Genetic Variability at Neutral Markers, Genetics 164: QTL, DNA markers, populations distributed subdivided the

Genetic variability in a throughout

Quantitative Trait Loci and Trait in a 1205–1219 forest trees population under stabilizing and

Subdivided Population Under Selection diversifying selection was investigated at

63 Cottrell J.E., Munro 2002 Distribution of chloroplast DNA Forest Ecol Chloroplast DNA three levels: the non-coding region coding

Variation in neutral markers, QTL of

R.C., Tabbener H.E., variation in British oaks (Quercus robur Manag 156: (cpDNA); Quercus chloroplast DNA (cpDNA) was studied to

Gillies A.C.M., Forrest and Q. petraea): the influence of 181–195 robur; Quercus petraea; determine the route and pattern of

64 G.I., Deans J.D., Lowe

Csaikl U.M., Glaz I., Chloroplast DNA variation human

2002 postglacial colonisation andof white oak Forest Ecol PCR–RFLP;DNA,

Chloroplast postglacial recolonisation of native oak

In this study we were interested how

Baliuckas V., Petit R.J., in the Baltic countries and Poland Manag 156: cpDNA, Quercus robur, recolonisation of oak in the Baltic region

Jensen J.S. 211-222 Quercus petraea, PCR- occurred after the last ice-age. To analyse

65 Csaikl U.M, Burg K., 2002 Chloroplast DNA variation of white oaks Forest Ecol RFLP, phylogeography,

Chloroplast DNA; After the last glacial (cpDNA) the Alps

the chloroplast DNA maximum variation

Fineschi S., Konig A.O., in the alpine region Manag 156: Quercus robur; Quercus have represented a major obstacle to the

Matyas G., Petit R.J. 131–145 petraea; Quercus recolonisation of central and northern

66 Dayanandan S., Rajora 1998 Isolation and characterization of Theor Appl pubescens; PCR–RFLP;

Poplars, Populus, simple We have identified, fauna surviving in

Europe by flora and isolated, and

O.P., Bawa K.S. microsatellites in trembling aspen Genet 96: 950-sequence repeats, characterized microsatellite/simple

(Populus tremuloides ). 956. microsatellite loci, sequence repeat (SSR) loci in trembling

67 Degen B., Caron H., 2001 Fine-scale spatial genetic structure of Heredity 87: polymorphism, clone

Genetic distance, The fine-scale tremuloides) structure of

aspen (Populusspatial geneticby screening

Bandou E., Maggia L., eight tropical tree species as analysed by 497-507. permutation test, RAPD, eight tropical tree species (Chrysophyllum

Chevallier M.H., RAPDs. spatial genetic structure, sanguinolentum, Carapa procera,

68 Leveau A., Kremer A.

Deguilloux M-F., 2002 Novel perspectives in wood certification woody trees, PCR;

Proc. R. Soc. tropicaltissues;forest treesDicorynia guianensis, Eperua grandiflora,

The importance of wood for human

Pemonge M.H., Petit and forensics: dry wood as a source of Lond. B 269: DNA retrieval; societies can hardly be understated. If dry

R.J. DNA 1039–1046 contaminations; wood were amenable to molecular genetic

69 Demesure, B., Comps, 1995 Chloroplast DNA phylogeography of the Evolution 50 genotyping, forest trees

Fagus sylvatica , investigations, this could lead to major

B., and Petit, R.J. common beech (Fagus sylvatica L.) in (6): 2515- intraspecific cp DNA

Europe. 2520. diversity,

70 Dong, J.and Wagner, 1994 Paternally inherited chloroplast Genetics 136: phylogeography, seed

forest trees We have surveyed a chloroplast DNA

D.B. polymorphism in Pinus: estimation of 1187-1194. restriction fragment length polymorphism

diversity and population subdivision, and in 745 individuals, distributed rangewide

tests of disequilibrium with a maternally in eight allopatric natural populations of

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



71 Doudrick, R.L., Heslop- 1995 Karyotype of slash Pine (Pinus elliottii Heredity forest trees

Harrison, J.S., Nelson, var. elliottii) using patterns of 66(4): 289-

C.D., Schmidt, T., fluorescence in situ hybridization and 296.

72 Nance, W.L. and

Ducousso A., Michaud 1993 fluorochrome banding. flow in the genus

Reproduction and gene Ann. For. Sci. floral biology, life cycle, In this paper we review the characteristics

H. and Lumaret R. Quercus L 50: 91-106 breeding system, gene of the floral biology, life cycle and

flow, oak, cpDNA, forest breeding system in the genus Quercus.

73 Dumolin-Lapègue, S., 1999 Are chloroplast and mitochondrial dna Evolution, trees

CpDNA, hybridization, The species of this genus are self-

Kremer, A. and Petit, variation species independent in oaks? 53(5): 1406- introgression, mtDNA,

R.J. 1413. Quercus, species co-

74 Egertsdotter, U., van 2004 Gene expression during formation of Plant Biology occurrence, white oaks,

forest trees The natural variability of wood formation

Zyl, L.M., MacKay, J., earlywood and latewood in loblolly pine: 6(6):654-663. in trees affords opportunities to correlate

Peter, G., Kirst, M., Expression profiles of 350 genes. transcript profiles with the resulting wood

75 Clark, C., Whetten, R.

FAO 2004 Preliminary review of biotechnology in Forest Genetic Forest biotechnology, properties. We have used cDNA

forestry, including genetic modification. Resources forest trees

Working

76 Farnum P., Lucier A. 2007 Ecological and population genetics PaperGenetics transgenic trees, gene

Tree Applied research that supplies requisite,

and Meilan R. research imperatives for transgenic trees & Genomes 3 flow, ecological effects, albeit incomplete, scientific knowledge is

(2): 119-133 GMO, forest trees necessary if we are to address the legal,

77 Fineschi,S., Gillet, E. 1990 Genetic of sweet chestnut( Castanea Silvae Electrophoresis, regulatory, and social/ethical issues the

Genetic analysis was performed on

and Malvolti, E. sativa Mill.). III. Genetic analysis of Genetica 39, 5- zymogram, genetic basis of four enzyme systems:

zymograms of single tree offspring . 6: 188-194. analysis, Castanea, phosphoglucose-isomerase (PGI),

78 Fineschi S. 1988 Short Note: Genetics of chestnut Silvae forest trees

Isozymes, grafting, isocitrate dehydrogenase (IDH), selected

A sample of 30 individuals was

(Castanea sativa Mill.). II. Uniformity Genetica 37, clone, Castanea , forest from a stand of grafted C. sativa trees in

of isozyme phenotypes in grafted 2: 82-83. trees Italy and examined for the following

79 Fineschi, S., Gillet, E. 1991 orchards. among fruits from single

Segregation Biochemical forest trees enzyme systems: LAP, GOT, SKDH, IDH,

and Malvolti, M. E. burrs of sweet chestnut Castanea sativa markers in the

Mill. population

80 Fineschi S., Taurchinia 2002 Chloroplast DNA variation of white oaks genetics of

Forest Ecol Chloroplast DNA; Polymorphism in non-coding regions of

D., Grossoni P., Petit in Italy Manag 156: Quercus petraea; Q. the chloroplast genome was studied in

R.J., Vendramin G.G. 103–114 robur; Q. pubescens; Q. four white oak species (Q. robur L., Q.

frainetto; petraea (Matt.) Liebl., Q. pubescens Willd.

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



81 Finkeldey, R. 2001 Genetic variation of oaks (Quercus spp .) Silvae Differentiation, diversity, Sessile oak (Quercus petraea) and

in in switzerland. 2. Genetic structures inGenetica 50, isozyme, homozygote, pedunculate oak (Q. robur) are two closely

''Pure'' and ''Mixed'' forests of 1: 22-30. excess, Quercus petraea , related, interfertile taxa. They are the most

82 Finstad K., Bonfils A- 2007 pedunculate oak (Q, robur L.) and

Trees with novel traits in Canada: Tree Genetics biosafety seed

Q. robur ,regulation, frequent oak species in Switzerland.

Straipsnis be abstrakto

C., Shearer W. and regulations and related scientific issues & Genomes 3 plants with novel traits,

Macdonald P. (2):135–139 forest trees

83 Fernardez-Manjarres 2006 Differential patterns of morphological Molecular France, Fraxinus, We examined large-scale patterns of

J.F., Gerar P.R., Dufor and molecular hybridization between Ecology 15: hybridization, morphology, genetic structure and

J., Raquin C., Frascaria- Fraxinus excelsior L. and Fraxinus 3245–3257 microsatellites, ecological correlates of Fraxinus excelsior

84 Lacoste N. J., Pereira,

Fernandez, 1993 angustifolia Vahl (Oleaceae) in eastern Biotechnology

Isozymes in the management of a morphology, Oleaceae,

Isozymes, chestnut, and the closely related species Fraxinus

S., Miranda, E. foundation stock of chestnut hybrid of trees;131- clonal forestry,

clones. 136. Edited Castanea sativa x C.

85 Frascaria N., Santi F., 1993 Genetic differentiation within and among Pardos, J.A.,

Heredity 70: asexual forest trees

crenata,and sexsual

Gouyon P.H. populations of chesnut (Castanea sativa 634-641 propagation, Castanea

Mill.) and wild cherry (Prunus avium L.) sativa, genetic

86 Frewen B.E., Chen 2000 Quantitative Trait Loci and Candidate Genetics 154: differentiation, QTL,

bud phenology, The genetic control of bud phenology in

T.H.H., Howe G.T., Gene Mapping of Bud Set and Bud Flush 837–845 candidate genes, forest hybrid poplar was studied by mapping

Davis J., Rohde A., in Populus trees quantitative trait loci (QTL) affecting the

87 Boerjan W., Bradshaw

Gaiotto, F.A., Bramucci, 1997 Estimation of outcrossing rate in a Theor Appl Mating system, AFLP, timing of autumn bud set and spring bud

Eucalyptus breeding is typically

M., Grattapaglia, D. breeding population of Eucalyptus Genet 95: 842- RAPD, Eucalyptus, conducted by selection in open-pollinated

urophylla with dominant RAPD and 849. forest trees progenies. As mating is controlled only on

88 Gartland K.M.A., 2002 AFLP markers.

Forest Biotechnology and Europe‘s A Challenge Forest biotechnology, Application of of the cross, knowledge of

the female sidebiotechnology to trees and

Kellison R.C., Fenning Forests of the Future Document for forest trees forests will have significant impacts

T.M. Presentation worldwide and particularly, by early

89 Gartland K.M.A. & 2007 Growing trees: risks and rewards for and Genetics

Tree Genetic modification, indications, in Europe. The forum meters

Forests provide 1.75 billion cubic Forest

Oliver C.D. society & Genomes 3: Tree improvement, of timber each year and a similar amount

169–172 Forest biotechnology, of fuel wood. Our understanding of forest

90 Gebhardt K., Frühwacht- 1993 Micropropagation and restricted-growth Ann. For. Sci. The winter is far from complete.

forest trees vitro culture, ecosystems buds of stump sprouts,

Quercus, in

Wilms U. and storage of adult oak genotypes 50: 323-329 bud, temperature, epicormic shoots and grafts from adult

Weisgerber H. conservation, forest trees pedunculate and sessile oak trees proved

to be valuable sources of shoot tips.

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



91 Gerard P.R., Fernandez- 2006 New insights in the recognition of the Ann. For. Sci. ashes, RAPD-SCAR, Common ash (Fraxinus excelsior L.) and

Manjarres J.F., European ash species Fraxinus excelsior 63: 733–738 dormancy, discriminant narrow-leaved ash (F. angustifolia Vahl)

Bertolino P., Dufour J., L. and Fraxinus angustifolia Vahl as markers, hybridization, are the most common ash species

92 Raquin C., Frascaria-M.

Gerber, S., Lascoux, 1997 useful tools for forest managementand

Relation between protein markers Silvae forest 2-dimensional

Pine , trees Eighteen maritime The (Pinus pinaster

inWestern Europe. pinesformer is

and Kremer, A. quantitative traits in maritime pine Genetica 46, electrophoresis, QTL, AIT.) were genotyped at 84 loci using 2-

(Pinus pinaster Ait.). 5: 286-290. growth, seed weight, dimensional electrophoresis of total

93 Gerber, S., Mariette, S., 2000 Comparison of microsatellites and Molecular megagemetophyte, forest

AFLP, LOD scores, protein contained in theirproperties of

This study compares the haploid

Streiff, S., Bodenes, C., amplified fragment length polymorphism Ecology 9 (8): markers, microsatellites, dominant markers, such as amplified

Kremer, A. markers for parentage analysis. 1037-1048. parentage, forest trees fragment length polymorphisms (AFLPs),

94 Glenn T. Howe, Sally 2003 From genotype to phenotype: unraveling Can. J. Bot. association genetics, cold with those of codominant multiallelic

N. Aitken, David B. the complexities of cold adaptation in 81: 1247–1266 hardiness, dormancy,

Neale, Kathleen D. forest trees genecology, bud

Godbout, Nicholas C.

95 Jermstad, J., Jaramillo- 2005 A mitochondrial DNA minisatellite Molecular phenology, quantitative

mtDNA, minisatellite, Jack pine (Pinus banksiana Lamb.) is a

Correa, J.P., Beaulieu, J. reveals the postglacial history of jack Ecology 14 pinus, forest trees broadly distributed North American

and Bousquet, J. pine (Pinus banksiana), a broad-range (11): 3497- conifer and its current range was covered

96 Gomory D., Yakovlev 2001 North American conifer. oak

Genetic differentiation of 3512

Heredity 86: di€rentiation, diversity,

e Genetic structure ice sheet during

by the Laurentian of 25 indigenous the last

I., Zhelev P., Jedinakova populations within the Quercus 557-563 isozymes, Quercus populations of sessile and pedunculate

J., Paule L. robur/Quercus petraea complex in petraea, Quercus robur, oaks (Quercus petraea and Q. robur),

97 Gomory D., Vysny J., 1992 Central and Eastern Europe

Geographical patterns of genetic Biologia 47 forest trees

Fagys sylvatica, Forty-eight European geographical

originating from threebeech populations

Comps B., Thiebaut B. differentiation and diversity in European (7): 571-579 isozymes, genetic from the territory of France have been

beech (fagus sylvatica L.) populations in differentiation, diversity, analyzed using twelve isozyme loci.

98 Goncharenko G., Kurm 2005 FranceBIOLOGIA 47 (7): 571-579 1992 Baltic Forestry clinal variation, forest

Norway spruce, genetic Practically in all loci the relation was in

Using isoenzymes as genetic markers

M., Birgelis J., Maaten 11 (2): 9-19 structure, diversity, studies of Norway spruce populations

T., Tamm U. and isoenzymes, situated in four natural stands in Estonia,

Gosselin I., L.

99 ShevchenkoZhou Y., 2002 Megagametophyte-derived linkage maps Theor Appl differentiation, forest

codominant markers; We in Latvia and six in Byelorussia, an

five have constructed linkage maps for two

Bousquet J., Isabel N. of white spruce (Picea glauca) based on Genet 104 (6- conifers; genetic linkage parents of white spruce [Picea glauca

RAPD, SCAR and ESTP markers 7): 987-997 map, RAPD, SCAR, (Moench) Voss]. Haploid

100 Grattapaglia, D. 2000 Molecular breeding of Eucalyptus . Jain, S.M. and forest trees

forest trees megagametophytes from 92 and 96 seeds

-

Minocha, S.C.

(eds.),

Molecular

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



101 Grattapaglia, D. Opportunities and challenges for the Conferencia forest trees -

incorporation of genomic analysis in IUFRO sobre

Eucalyptus breeding. Silvicultura e

102 Grattapaglia D., 1996 Genetic Mapping of Quantitative Trait Melhoramento QTL, growth, wood

Genetics 144: Quantitative trait loci (QTL) mapping of

Bertolucci F.L.G., Loci Controlling Growth and Wood 1205-1214 quality, forest trees forest productivity traits was performed

Penchel R., Sederofft Quality Traits in EucaZyptus grandis using an open pollinated half-sib family of

103 R.R.

Grattapaglia, D., 1994 Genetic mapping Half-sib Family and

Using a Maternal of quantitative trait loci Genetica 236- forest trees Eucalyptw grandis. For volume growth, a

-

Bertolucci, F.L., (QTLs) controlling growth and wood 278.

Penchel, R. and quality traits in Eucalyptus grandis using

104 Sederoff, R. D,

Grattapaglia, 2004 a half-sib family and RAPD markers.

Retrospective selection of elite parent Theor Appl Eucalyptus, MAS, The conventional way to drive

Ribeiro, VJ, Rezende, trees using paternity testing with Genet 109 (1): paternity, microsatellites, modifications in old forest tree seed

GDSP microsatellite markers: an alternative 192-199 forest trees orchards is to establish progeny trials

105 Gros-Louis, M.-C.,, 2005 short term breedingmarkers inEucalyptus

Species-diagnostic tactic for Larix spp. Tree Genetics ESTP, Hybrids, Larix, Genetic markers from the and then

involving each parent tree nuclear,

Bousquet, J.,, Paques, based on RAPDs and nuclear, cpDNA, & Genomes, Genetic identity, Genetic chloroplast, and mitochondrial genomes

L.E. and Isabel, N. and mtDNA gene sequences, and their V1(2):50-63. fingerprint, cpDNA, were developed to distinguish

106 Guillet-Claude C., 2004 phylogenetic implications.

The evolutionary implications of knox-I Mol Biol Evol mtDNA, Phylogeny,

conifer knox-I genes; unambiguously among four larch species

Class I knox genes code for transcription

Isabel N., Pelgas B., gene duplications in conifers: Correlated 21 (12): 2232- evolutionary rates; factors that play an essential role in plant

Bousquet J. evidence from phylogeny, gene mapping, 2245 functional divergence; growth and development as central

107 Gunter L.E., Kopp R.F., 2003 and analysissex-linked, sequence-

Analysis of of functional divergence Can. J. For. gene duplication;

Salix, SCAR markers, regulators of meristem, cell identity.

Two DNA markers, sequence-

McCord R.P., Tuskan characterized amplified region markers Res. 33 (9): sex locus, forest trees characterized amplified region (SCAR)

G.A. in Salix eriocephala 1785-1790 AE08(780) and SCAR 354(520), known to

108 Gunter L.E., Roberts 2003 The development of two flanking SCAR Journal of Salix, SCAR markers, Most studies of flanking a putative sex

be linked to andsex determination systems

G.T., Lee K., Larimer markers linked to a sex determination Heredity 94 sex locus, forest trees in plants involve dioecious annuals that

F.W., Tuskan G.A. locus in Salix viminalis L. (2): 185-189 have known sex chromosomes. Despite

109 Gunter L.E., Tuskan 2000 Genetic variation and spatial structure in Global Change Gene flow, genetic the absence of such structures in the

G.A., Gunderson C.A. sugar maple (Acer saccharum Marsh.) Biology 6: 335- variation, global

and Norby R.J. and implications for predicted global- 344. warming, population

110 Gupta, AK, Kang, BY, 2005 scale environmental change.selectively

Large scale development of Mol Ecol structure, RAPDs, sugare

AFLP; SAMPL markers; The spruce (Picea) species are

Roy, JK, Rajora OP amplified microsatellite polymorphic Notes 5 (3): spruce, Picea, forest trees ecologically and economically important

L loci (SAMPL) markers in spruce (Picea) 481-483 in Canada. Highly informative markers

with high multiplex ratios are needed to

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



111 Gyllenstrand N., 2007 A Norway spruce flowering locus T Plant Spruce, picea abies, Growth in perennial plants possesses an

Clapham D., Källman homolog is implicated in control of Physiology flowering, growth annual cycle of active growth and

T., and Lagercrantz U. growth rhythm in conifers 144: 248-257 rhythm, forest trees dormancy that is controlled by

112 Halpin C., Thain S.C., 2007 Ecological impacts of trees with Tree Genetics Ecological impacts, GM environmental factors, yet been performed

Few experiments have mainly photoperiod

Tilston E.L., Guiney E., modified lignin & Genomes trees, Lignin, GMO, to explore the potential ecological impacts

Lapierre C., Hopkins 3:101–110 Forest trees of genetic modification in long-lifespan

113 D.W.

Hamrick, J.L., Godt, 1989 Distribution and sampling of genetic Correlations forest trees species such as trees. In this paper, we

M.J.W., Murawski, variation. Correlations between species between

D.A. and Loveless, traits and allozyme diversity. species traits

114 M.D.K-H., Gordon M.P,

Han 1996 High-frequency transformation of and allozyme

Can. J. For. poplar, genetic Many species of Populus, particularly

Strauss S.H. cottonwoods (genus Populus) by Res. 27: 464- enginering, cottonwoods of sections Aigeiros and

Agrobacterium rhizogenes 470 agrobacteium, forest Tacamahaca, remain recalcitrant to genetic

115 Hansen O.K., Kjær E.D. 2005 Chloroplast microsatellite variation in Tree Genetics trees

Chloroplast transformation. We of Abies

Fifteen populations demonstrate that

and Vendramin G.G. Abies nordmanniana and simulation of & Genomes 1 microsatellites, nordmanniana, originating from all main

causes for low differentiation among (3): 116-123 Differentiation, parts of its distributional area in the

116 Harry D. E., Temesgen 1998 populations PCR-based markers for

Codominant Theor Appl Nordmann fir, forest

STS, Codominant PCR Caucasian a strategy for genotyped for

We report region, were developing

B., Neale D.B. Pinus taeda developed from mapped Genet 97: 327- marker, RFLP, Loblolly codominant PCR-based genetic markers

cDNA clones 336 pine, Pinus taeda, by using sequenced cDNA clones from

117 Heckrodt, W.F. 1987 Close spaced short rotation poplar Poplar Comparative map, forest

forest trees loblolly pine (Pinus taeda L.). These

production using paper mill sludge as councils of the

mulch. United States

118 Hemmat, M., Weeden, 1994 Molecular marker linkage map for apple. and Canada

Journal of forest trees Linkage maps for two apple clones, White

N.F., Manganaris, A.G., Heredity 85 Angel and Rome Beauty, were constructed

and Lawson, D.M. (1) :4-11. using isozyme and DNA polymorphisms

119 Hertzberg M., Aspeborg 2001 A transcriptional roadmap to wood PNAS vol. 98 DNA micoarray, poplar, segregating in a population produced from

The large vascular meristem of poplar

H., Schrader J., formation no. 25: wood formation, forest trees with its highly organized secondary

Andersson A., 14732–14737 trees xylem enables the boundaries between

Heurtz M., R.,

120 Erlandsson Carnevale 2006 Chloroplast DNA phylogeography of Molecular cpNA, Fraxinus, forest different developmental zones to be easily

We investigated range-wide

S., Fineschi S., European ashes, Fraxinus sp. (Oleaceae): Ecology 15 trees phylogeographic variation in three

Sebastiani F., Hausman roles of hybridization and life history (8): European ash species (Fraxinus sp.,

J. F., Paule L., traits. 2131–2140 Oleaceae). Chloroplast DNA (cpDNA)

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



121 Heurtz M., Fineshi S., 2004 Chloroplast DNA variation and Molecular chloroplast DNA, We used chloroplast polymerase chain

Anzidei M., Pastorelli postglacial recolonization of common Ecology 13: chloroplast reaction-restriction-fragment length

R., Salivani D., Paule ash (Fraxinus excelsior L.) in Europe 3437–3452 microsatellite, Fraxinus polymorphism (PCR-RFLP) and

122 L., Frascaria-Lacoste J-

Heurtz M., Hausman 2004 Nuclear microsatellites reveal Evolution, excelsior, PCR-RFLP,

Admixture, Bayesian To determine extant patterns assess the

chloroplast microsatellites to of population

F., Hardy O.J., contrasting patterns of genetic structure 58(5): methods, microsatellites, genetic structure in common ash and gain

Vendramin G.G., between western and southeastern 976–988 population genetic insight into postglacial recolonization

123 Frascaria-Lacoste N., J-

Heurtz M., Hausman 2001 European populations of the Common

Assessment of genetic structure within Molecular structure,excelsior,

Fraxinus postglacial We analysed applied multilocus-based

processes, wegenetic variation within and

F., Tsvetkov I., and among Bulgarian populations of the Ecology 10: genetic structure, between populations of the common ash

Frascaria-Lacoste N., common ash (Fraxinus excelsior L.) 1615–1623 inbreeding, from Bulgaria in order to extract

124 Vekemans X.

Heuertz M., Vekemans 2003 Estimating seed vs. pollen dispersal from Molecular microsatellites,

Fraxinus excelsior, biological information useful analysed

Spatial genetic structure was in the

X., Hausman J.-F., spatial genetic structure in the common Ecology 12: microsatellites, with five highly polymorphic

Palado M., Hardy O.J. ash 2483–2495 neighbourhood size, microsatellite loci in a Romanian

125 Hewitt, G.M. 1999 Post glacial re colonization of European Molecular DNA dispersal, seed

pollensequence, range population of common ash (Fraxinus

biota. genetics in change, population

animal structure, refugia, genetic

126 Holtken A.M., Tahtinen 2003 Effects of Discontinuous Marginal ecology.

Silvae divergence, biodiversity,

Common ash, Fraxinus Common ash (Fraxinus excelsior L.) has,

J., Pappinen A. Habitats on the Genetic Structure of Genetica 52, 5- excelsior, species in comparison to other tree species such as

Common ash (Fraxinus excelsior L.) 6: 206-212 northern margins, spruce (Picea), beech (Fagus) and oak

127 Hong, Y.-P., Hipkins, 1993 Chloroplast DNA diversity among trees, Genetics 135: discontinuous habitats,

forest trees (Quercus), poor competitive ability and is

The amount, distribution and mutational

V.D. and Strauss, S.H. populations and species in the California 1187-1196. nature of chloroplast DNA polymorphisms

closed-cone Pines (Pinus radiata, Pinus were studied via analysis of restriction

128 Houston, D.B. and 2000 muricata and Pinus attenuata ).

Allozyme genetic diversity among Can. J. For. Allozyme, Fagus, disease fragment length polymorphisms in three

American beech (Fagus grandifolia Ehrh.)

Houston, D.R. Fagus grandifolia tree resistant or Res. 30: 778- resistance, forest trees trees resistant (R = 760) and susceptible (S

susceptible to beech bark disease in 789. = 681) to beech bark disease were located

129 Howe G.T., Aitken 2003 natural populations.

From genotype to phenotype: unraveling Can. J. Bot. association genetics, cold Adaptation in nine cold in temperate and

and mappedto winternatural stands in West

S.N., Neale D.B, the complexities of cold adaptation in 81: 1247–1266 hardiness, dormancy, boreal trees involves complex genetic,

Jermstad D.D., Wheeler forest trees genecology, bud physiological, and developmental

Janssens, Chen T.H.H

130 N.C., and G.A., Goderis, 1995 A molecular method for S-allele Theor Appl phenology, quantitative

Malus x domestica, processes. Genecological studiesto two

cDNA sequences corresponding

I.J., Broekaert, W.F., identification in apple based on allele- Genet 91: 691- apple, self- self-incompatibility alleles (S-alleles) of

Broothaerts, W. specific PCR. 698. incompatibility, S- the apple cv Golden Delicious have

alleles, PCR, forest trees previously been described, and now we

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



131 Jany, J.L., Bousquet, J., 2006 Simple sequence repeat (SSR) markers Mycological forest trees Simple sequence repeat (SSR) markers

Gagne, A. and Khasa, in the ectomycorrhizal fungus Laccaria Research, were developed from SSR-enriched

D.P. bicolor for environmental monitoring of 110:51-59. genome libraries for the ectomycorrhizal

132 Jaramillo-Correa, J.P., 2006 introduced strains and molecular ecology

Decoupled mitochondrial and Molecular cpDNA, mtDNA, Picea basidiomycete Laccaria bicolor. Seven

Chihuahua spruce (Picea chihuahuana

Beaulieu, J., Ledig, F.T. chloroplast DNA population structure Ecology 15 chihuahuana, Picea Martínez) is a montane subtropical conifer

and Bousquet, J. reveals Holocene collapse and (10): 2787- martinezii, postglacial endemic to the Sierra Madre Occidental in

133 Jaramillo-Correa, J.P., 2004 population isolation in a threatened

Variation in mitochondrial DNA reveals 2800.

Molecular history, forest trees

mtDNA, Picea, forest northwesterngenetic variation of black

Range-wide México. Range-wide

Beaulieu, J. and multiple distant glacial refugia in black Ecology 13 trees spruce (Picea mariana) was studied using

Bousquet, J. spruce (Picea mariana), a (9): 2735-2747 polymerase chain reaction-random

134 Jaramillo-Correa, J.P. Mitochondrial North recombination in

2005 transcontinentalgenomeAmerican conifer. Genetics forest trees fragment length polymorphism markers of

Variation in mitochondrial DNA was

and Bousquet, J. the zone of contact between two 171(4):1951- surveyed at four gene loci in and around

hybridizing conifers. 1962. the zone of contact between two naturally

135 Jeandroz S., Collignon 2004 RAPD and mtDNA variation among Forest Ecol RAPD; mtDNA; hybridizing conifers, black spruce (Picea

RAPD phenotypic analysis (AMOVA and

A.M., Favre J.M. autochthonous and planted populations Manag 197 (1- autochtony; seed FCA) allowed to determine three groups

of Picea abies from the Vosges 3): 225-229 transfer; Picea abies, among the Picea abies French genetic

136 Jensen J.S., Gillies A., Chloroplast DNA variation within other

2002 mountains (France) in reference to the Forest Ecol forest trees DNA;

Chloroplast Chloroplast DNA (cpDNA) variation and

resources: the Vosges (autochthonouswas

Csaikl U., Munro R., Nordic countries Manag 156: Quercus robur; Quercus studied in the white oak species, Quercus

Madsen S.F., Roulund 167–180 petraea; PCR–RFLP; robur and Quercus petraea, from

137 H., Low A.

Jermstad, K.D., 2001 Mapping of quantitative trait loci Theor Appl Phylogeography; Post-

QTL maping, RFLP, bud Denmark, Norway, Sweden and trait loci

Thirty three unique quantitative Finland.

Bassoni, D.L., Jech, controlling adaptive traits in coastal Genet 102: phenology, genotype x (QTLs) affecting the timing of spring bud

K.S., Wheeler, N.C., Douglas-fir I. Timing of vegetative bud 1142-1151. environment interaction, flush have been identified in an

138 Neale, D.B.

Jermstad K.D., 2006 flush. of a full-length CC–NBS–LRR Tree Genetics

Isolation forest trees gene analog,

Resistance intraspecific mapping population of

The nucleotide-binding-site and leucine-

Sheppard L.A., Kinloch resistance gene analog candidate from & Genomes 2 SNP, Haplotype, rich-repeat (NBS–LRR) class of R

B.B., Delfino-Mix A., sugar pine showing low nucleotide (2): 76-85 Nucleotide diversity, proteins is abundant and widely

139 Ersoz E.S., Krutovsky

Johnson G.R., Wheeler 2000 diversity feasibility of marker-aided

Financial Can. J. For. forest trees Douglas-fir,

MAS, QTL, distributed in plants. By using degenerate

The land area required for a marker-aided

N.C., Strauss S.H. selection in Res. 30: Pseudotsuga menziesii, selection (MAS) program to break-even

Douglas-fir 1942–1952 selection efficiency, (i.e., have equal costs and benefits) was

140 Jonsson A. and Eriksson 1989 A review of genetic studies of some Dept Forest forest trees , Fraxinus ,

Acer , Fagus estimated using computer simulation for

G. important traits in the genera Acer, Genetics, Prunus , Quercus ,

Fagus, Fraxinus, Prunus, Quercus and Research Ulmus , provenance,

Ulmus. Notes 44, survival, phenology,

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



141 Jörgensen J. 1993 Embryogenesis in Quercus petraea Ann. For. Sci. somatic embryogenesis, Embryogenesis in Quercus petraea was

50: 344-350 androgenesis, protoplast achieved by culture of zygotic embryos

culture, Quercus and anthers on modified woody plant

142 Junghans D.T., Alfenas 2003 Resistance to rust (Puccinia psidii Theor Appl petraea, forest trees

Eucalyptus, resistance, medium with benzylaminopurine and 2,4

Rust is one of the most-damaging eucalypt

A.C., Brommonschenkel Winter) in Eucalyptus: mode of Genet 108 (1): RAPD, forest trees diseases in Brazil and is considered a

S.H., Oda S., Mello E.J., inheritance and mapping of a major gene 175-180 potential threat to eucalypt plantations

143 Grattapaglia D.

Isabel N., Beaulieu J., 1999 with RAPD markersbiased gene diversity

Direct evidence for Molecular conifers; haploid The relevance determine the mode of

worldwide. Toof using dominant random

Theriault P., Bousquet estimates from dominant random Ecology 8 (3): megagametophytes; amplified polymorphic DNA (RAPD)

J. amplified polymorphic DNA (RAPD) 477-483 genetic diversity; genetic fingerprints for estimating population

144 Isabel N., Beaulieu J., 1995 fingerprints

Complete congruence between gene P Natl Acad markers; RAPD

Allozymes, fingerprints, differentiation was investigated when

Controversy still exists over the adaptive

Bousquet J. diversity estimates derived from Sci USA 92 genetic markers, nature of variation of enzyme loci. In

genotypic data at enzyme and Random (14): 6369- population genetics, conifers, random amplified polymorphic

145 Isabel N., Boivin R., Evidence Polymorphic variation in

1995 Amplifiedof somaclonal DNA lociin 6373 Plant Sci forest trees

Curr forest trees DNAs (RAPDs) represent a class of

-

Levasseur C., Charest somatic embryo-derived plantlets of Biot 22: 247-

P.M., Bousquet J., white spruce (Picea glauca (moench) 252

Isabel N., F.M.

146 Tremblay Boivin R., 1996 voss)

Occurrence of somaclonal variation Am J Bot 83 Somatic, somaclonal Four different variegata phenotypes were

Levasseur C., Charest among somatic embryo-derived white (9): 1121-1130 variation, Picea, spruce, identified among 2270 white spruce plants

P.M,. Bousquet J., spruces (Picea glauca, Pinaceae) forest trees [Picea glauca (Moench.) Voss.] produced

Isabel N., F.M.

147 Tremblay Tremblay L., 1993 RAPDS as an aid to evaluate the genetic Theor Appl RAPD; Picea mariana, over usefulness of random the time of

The a period of 2 yr from amplified

Michaud M., Tremblay integrity of somatic embryogenesis- Genet 86 (1): genetic markers, genetic polymorphic DNA (RAPD) in assessing

F.M., Bousquet J. derived populations of Picea mariana 81-87 stability; somatic the genetic stability of somatic

148 Islam-Faridi M.N., 2007 (Mill) BSPkaryotype and cytomolecular

Reference Genome embryogenesis, forest

FISH, loblolly pine, 18S- embryogenesis-derivedis presented for

A reference karyotype populations of

Nelson C.D., and map for loblolly pine (Pinus taeda L.) 50(2): 28S rDNA, A-type TRS, loblolly pine (Pinus taeda L., subgenus

Kubisiak T.L. 241–251 reference karyotype, Pinus, section Pinus, subsection

149 Karhu, A., Hurme, P., 1996 Do molecular markers reflect patterns of Theor Appl cytomolecular map,

Scots pine , molecular Australes), based on fluorescent in situ of

We have examined patterns of variation

Karjalainen, M., differentiation in adaptive traits of Genet 93: 215- markers, isozymes, several kinds of molecular markers

Karvonen, P., conifers? 221. population structure, (isozymes, RFLPs of ribosomal DNA and

150 Kärkkäinen, K., Neale,

Karp A., Kresovich S., 1997 Molecular tools in plant genetic IPGRI adaptive genetic

DNA marker anonymous low-copy number DNA,

The dramatic advances in molecular

Bhat K.V., Ayad W.G., resources conservation: a guide to the Technical technologies, AFLP, genetics over the last few years have

Hodgkin T. technologies Bulletin No. 2. RAPD, SSR, STMS, provided workers involved in the

International forest trees conservation of plant genetic resources

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



151 Kearsey, M.J. and 1998 QTL analysis in plants; where are we Heredity 80: Bias, mapping, We have briefly reviewed the methods

Farquhar, A.G.L. now? 137-142. overdominance, QTL, currently available for QTL analysis in

numbers, synteny, forest segregating populations and summarized

152 Kelleher C.T., 2005 Species Distinction in Irish Populations Annals of trees differentiation,

Species Background and Aims arising from such

some of the conclusions Populations of oak

Hodkinson T.R., of Quercus petraea and Q. robur: Botany 96: pedunculate oak, sessile (Quercus petraea and Q. robur) were

Douglas G.C., Kelly Morphological versus Molecular 1237–1246, oak, AFLP, Quercus investigated using morphological and

153 D.L. D.P., Jaramillo-

Khasa, 2006 Analyses

Contrasting microsatellite variation Molecular petraea, Quercus robur,

comparative population Subalpine larch (Larix lyallii assess

molecular (AFLP) analyses toParl.) and

Correa, J.P., Jaquish, B. between subalpine and western larch, Ecology 15 genetics, conservation western larch (Larix occidentalis Nutt.)

and Bousquet, J. two closely related species with different (13): 3907- genetics, larch, represent two closely related species with

154 Khasa, D.P., Pollefeys, 2005 distribution patterns.

Species-specific microsatellite markers 3918

Molecular microsatellites, forest

hybrid identification; contrasting abundance and distribution

Species-specific microsatellite markers

P., Navarro-Quezada, to monitor gene flow between exotic Ecology interspecific gene flow; were obtained for the unambiguous

A., Perinet, P. and poplars and their natural relatives in Notes, microsatellites; Populus; recognition of five poplar species of

155 Bousquet, J.

Kim, H., Ralph, J., Lu, 2003 eastern North America. in CAD-

NMR analysis of lignins 5(4):920-923. forest trees

Organic and species-specific markers, ecological and commercial importance to

Peroxidase/H2O2-mediated radical

F.C., Ralph, S.A., deficient plants. Part 1. Incorporation of Biomolecular coupling of 4-hydroxycinnamaldehydes

Boudet, A.M., MacKay, hydroxycinnamaldehydes and Chemistry, produces 8-0-4-, 8-5-, and 8-8-coupled

156 J., Sederoff, R.R., Ito,

Kim S.-H., Huh .K., Lee 2007 hydroxybenzaldehydes into lignins.

Genetic relationships among taxa of 1(2):268-281. forest trees

Miškininkystė dehydrodimers as has been documented

J-H. genus Sorbus based on ISSR marker [Forest

analysis. Sciences], 1

157 King R.A, and Ferris C. 2002 A variable minisatellite sequence in the (61): 69-75.

Genome 45: Sorbus, atpE, homoplasy, The chloroplast genome is now known to

chloroplast genome of Sorbus L. 570–576 microsatellite, rowan, be more variable than was once thought.

(Rosaceae: Maloideae) VNTR, forest trees Reports of RFLP (restriction fragment

158 Kirst M., Cordeiro 2005 Power of Microsatellite Markers for Journal of SSR, fingerprining, We report the genetic and sequence

length polymorphism)analysis of 192

C.M., Rezende Fingerprinting and Parentage Analysis in Heredity parentage analysis, unrelated individuals of an elite breeding

G.D.S.P., Grattapaglia Eucalyptus grandis Breeding Populations 96(2):161–166 Eucalyptus grandis, population of Eucalyptus grandis (Hill ex

159 D.

Kjaer, E.D., 1996 A multivariate study on genetic variation Silvae breeding, forest trees

Tectona grandis , Maiden)differentiation between highly

Genetic with a selected set of six

Siegismund, H.D. and in teak (Tectona grandis (L.)). Genetica 45, 5- provenance variation, populations of teak (Tectona grandis (L.))

Suangtho, V. 6: 361-368. multivariate analysis of was examined in 9 quantitative characters

160 Kleinschmit, J.R.G. 1995 Title of the paper: Comparison of Quercus allozymes,

Mitteilungen variance,robur , Quercus and 10 allozyme loci. Large differences

morphological and genetic der petraea , species

discrimination characteristics in Forstlichen identification, isozymes,

pedunculate oak (Quercus robur L.) and Versuchsansta DNA, morphology,

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



161 Kleinschmit, J.R.G., 1995 Comparison of morphological and Silvae Quercus robur , Quercus Morphological and genetic traits are

Bacilieri, R., Kremer, A. genetic traits of pedunculate oak Genetica 44, 5- petraea , hybridization, compared for pedunculate oak (Quercus

and Roloff, A. (Q.robur L.) and sessile oak (Q.petraea 6: 256-268. species identification, robur L.) and sessile oak (Quercus petraea

162 Kleinschmit, J.R.G., (Matt.) Liebl.)

Artificial hybridization between mophology, RAPDs,

Hybridization, (MATT.) LIEBL.) by means Of controlled

Kleinschmit, J. Quercus robur L. and Quercus petraea Q.petraea, Q,robur ,

(Matt.) Liebl. RAPD, Discriminant

163 Knott, S.A., Neale, 1997 Multiple marker mapping of quantitative Theor Appl analysis, forest trees

Quantitative trat loci, A multiple marker least squares approach

D.B., Sewell, M.M., trait loci in an outbred pedigree of Genet 94: 810- outcrossing, Pinus is presented for the analysis of a single

Haley, C.S. loblolly pine. 820. taeda , forest trees three-generation pedigree for quantitative

164 Konig A.O., 2002 Chloroplast DNA variation of oaks in Forest Ecol Quercus robur, Quercus trait locus (QTL) characterisation. It is an

Oak chloroplast DNA (cpDNA) variation

Ziegenhagen B., van western Central Europe and genetic Manag 156: petraea, PCR–RFLPs, was studied in a grid-based inventory in

Dam B.C., Csaikl U.M., consequences of human influences 147–166 Haplotypes, Spatial western Central Europe, including

165 Coart E., Degen B.,S.-

Kostia, S., Varvio, 1995 Microsatellite sequences in a conifer, Genome 38: genetic patterns, Genetic

forest trees Belgium, The Netherlands, Luxembourg,

L., Vakkari, P., and Pinus sylvestris . 1244-1248.

Pulkkinen, P.

166 Kremer A, Kleinschmit 2002 Is there a correlation between Forest Ecol Quercus; Provenance The aim of this work was to investigate

J, Cottrell J., et al chloroplastic and nuclear divergence, or Manag 156 (1- test; Chloroplast DNA; whether a correlation exists between

what are the roles of history and 3): 75-87 Genetic distance; Mantel maternal lineage, assessed by variation in

167 Kremer, A., Petit, R.J. 1993 selection on genetic diversity in

Gene diversity in natural populations of Ann Sci For test, forest trees gene

Quercus, nuclear maternally inherited chloroplast DNA

This contribution reviews studies of

oak species. 50, Suppl 1: diversity, organelle gene nuclear and organelle gene diversity in oak

186-202. diversity, gene species. Studies of allozymes were

168 Kremer, A., Petit, R., 1991 Nuclear and organelle gene diversity in Genetic differentiation, forest

forest trees reported for 33 species belonging to the

Zanetto, A., Fougére, Quercus robur and Q. petraea. variation in

V., Ducousso, A., European

Kremer D. and

169 Wagner,A., Kleinschmit 2000 Is there a correlation between populations of

Forest Ecol Quercus, provenance The aim of this work was to investigate

J., Cottrell J., Cundall chloroplastic and nuclear divergence, or Manag 156: test, chloroplast DNA, whether a correlation exists between

E.P., Deans J.D., what are the roles of history and 75–87 genetic distance, mantel maternal lineage, assessed by variation in

Kumar S., A., Konige

170 DucoussoaGarrick D.J. Genetic response to diversity in

2001 selection on genetic within-family Can. J. For. test, forest trees

MAS, QTL, within- maternally inherited chloroplast DNA

Marker-assisted selection (MAS) provides

selection using molecular markers in Res. 31: family selection, an opportunity to increase the efficiency

some radiata pine breeding schemes 779–785 simulation, forest trees of within-family selection in forest tree

breeding. Within-family MAS involves

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



171 Kuramoto N., Kondo T., 2000 Detection of quantitative trait loci for Can. J. For. RAPD, QTL, MOE, Cryptomeria japonica D. Don (sugi) is one

Fujisawa Y., Nakata R., wood strength in Cryptomeria japonica Res. 30: Cryptomeria japonica, of the most important forest tree species in

Hayashi E., Goto Y. 1525–1533 forest trees Japan. The progeny of a cross between the

172 D. Lachance, L.-P. 2007 Expression of a Bacillus thuringiensis Tree Genetics Bacillus thuringiensis, A synthetic version of the cry1Ab were

cultivars Iwao-sugi and Boka-sugi gene

Hamel, F. Pelletier, J. cry1Ab gene in transgenic white spruce & Genomes 3 White spruce, Budworm, from Bacillus thuringiensis (Bt) was

Valéro, M. Bernier- and its efficacy against the spruce (2): 153–167 Insect resistance, introduced into white spruce (Picea

Lande, K. Chapman,

173 Cardou,R. and 1990 budworm (Choristoneura fumiferana)

Efficiency of marker-assisted selection Genetics 124: Biotechnology, Conifers,

forest trees glauca) by genetics can be integrated with

Molecular microprojectile bombardment.

Thompson, R. in the improvement of quantitative traits. 743-756. traditional methods of artificial selection

on phenotypes by applying marker-

174 Lang, P. And Huang, H. 1999 Genetic variation and population Proc. 2nd Int C.mollissima Bl., assisted selection (MAS). We derive

structure of three endemic Castanea Symp. On C.seguinii Dode., C.

species in china. Chestnut henryi Rchhd.and Wils.,

175 Larsen, A.B. 1996 Genetic structure of populations of beech Ed.G. Salesses

Scand. J. For. population, allozyme,

Fagus sylvatica L.,

(Fagus sylvatica L.) in Denmark. Res. 11: 220- genetic variability,

232. isozymes, population

176 Larsen A.S., Asmussen 2006 Hybridization and genetic variation in Tree Genetics structure, forest trees

hybridization; The aim of the present study was to

C.B., Coart E., Olrik Danish populations of European crab & Genome 2 introgression; Malus investigate the genetic variation in Danish

D.C., Kjaer E.D. apple (Malus sylvestris) (2): 86-97 populations of the endangered European

sylvestris; microsatellite;

177 Latouche-Halle, C, 2003 Nuclear and chloroplast genetic structure Heredity 91 morphology, forest trees

dicorynia guianensis; crab apple guianensis is a canopy tree,

Dicorynia (Malus sylvestris). Special

Ramboer, A, Bandou, E, indicate fine-scale spatial dynamics in a (2): 181-190 microsatellites; spatial endemic to the tropical rain forest of

Caron H, Kremer A neotropical tree population analysis; genetic French Guiana. We compared generational

178 Le Corre V, Kremer A. 2003 Genetic variability at neutral markers, Genetics 164 differentiation; gene

forest trees and spatial genetic structure for maternally

Genetic variability in a subdivided

quantitative trait loci and trait in a (3): 1205-1219 population under stabilizing and

subdivided population under selection. diversifying selection was investigated at

179 Leibenguth F., Shoghi 1998 Analysis of Random Amplified Silvae Abies alba, Picea abies, three levels: neutral markers, QTL coding

From 40 arbitrary primers tested with one

F. polymorphic DNA Markers in Three Genetica 47, Pinus sylvestris, RAPDs, DNA from each species, two, three and

Conifer Species 2–3 polymorphism, forest four were chosen to generate RAPD

180 Lefort, F., Douglas, 2000 Microsatellite DNA profiling of Silvae trees

Fraxinus excelsior , profiles in Norway spruce, silver forest

Oak and ash are two of the main fir and

G.C. and Thompson, D. phenotypically selected clones of irish Genetica 49, microsatellite, Quercus species in Europe. Because of their

oak (Quercus spp .) and ash (Fraxinus 1: 21-28. petraea , Quercus robur , commercial importance, genetic

excelsior L.). single sequence repeats, improvement of such species is considered

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



181 Lefort, F., Edwards, K. 1997 Identification of microsatellite of ash Dendrome, forest trees

and Douglas, G. (Fraxinus excelsior L.). vol.4, 1: 4-5.



182 Lemes, MR, Brondani, 2002 Multiplexed systems of microsatellite Journal of Swetenia, Mahogany (Swietenia macrophylla King

RPV, Grattapaglia, D markers for genetic analysis of Heredity 93 microsatellites, DNA, [Meliaceae]) is the most valuable

mahogany, Swietenia macrophylla king (4): 287-291 heterozygosity, gene hardwood species in the neotropics. Its

183 Lescot M., Rombauts S., 2004 (Meliacelae), aathreatened neotropical

Annotation of 95-kb Populus deltoides Theor Appl flow, forest trees gene,

Populus deltoides, Poplar has become a model the subject

conservation status has been system for of

Zhang J., Aubourg S., genomic sequence reveals a disease Genet 109 (1): resistance, forest trees functional genomics in woody plants.

Mathe C., Jansson S., resistance gene cluster and novel class I 10-22 Here, we report the sequencing and

Lexer P. Heinze B.,

184 Rouze C., and Boerjan 2004 and class II transposable elements

Hybrid zones as a tool for identifying Forest Ecol Hybrid zones; annotation of the first large contiguous

The identification and study of adaptively

Alia R., Rieseberg L.H. adaptive genetic variation in outbreeding Manag 197: Admixture; important genes in forest trees represents a

forest trees: lessons from wild annual 49–64 Introgression; formidable challenge because of theirlong

185 Lexer, C., Heinze, B., Microsatellite analysis spp.)

2000 sunflowers (Helianthusof maternal half- Theor Appl Adaptation; QTL;

Oak, Quercus, We present an approach to or perennial

generation spans. In annualinfer the

Gerber, S., Macalka- sib families of Quercus robur, Genet 100: relatedness, linkage number of pollen donors directly from

Kampfer, S., pedunculate oak:II. Inferring the number 858-865. disequilibrium, genotype data of open- pollinated progeny

186 Steinkellner, H., B.,

Lexer, C., Heinze, Microsatellite analysis of offspring.

1999 of pollen donors from the maternal half- Theor Appl microsatellites,half-sibs, of Quercus robur (pedunculate oak), a

Oak, Quercus, forest Microsatellites were used for genetic

Steinkellner, H., sib families of Quercus robur, Genet 99: 185- microsatellites, simple- analysis of maternal half-sib families of

Kampfer, S., pedunculate oak: detection of seed 191. sequence repeats, forest Quercus robur, pedunculate oak, a highly

Advantages of and inference of the

187 Ziegenhagen, B., Glössl, 2001 contaminationsclonal propagation. seed

Lindgren, D. Draft for the trees

Breeding, tree Clones in forestry may be model half-sib

outcrossing tree species. Ainteresting for

proceedings improvement, production many reasons; three main purposes may be

from a population, clonal mentioned: To produce a more uniform

188 Lindqvist-Kreuze, H., 2003 Genetic diversity of arctic bramble meeting at

Can. J. Bot. AFLP, breeding,

forestryAMOVA, tree product; To improve theand genetic

The levels of genotypic forest by using a

Koponen, H. and (Rubus arcticus L. subsp. arcticus) as 81: 805–813. population, habitat variation were estimated in six natural

Valkonen, J.P.T. measured by amplified fragment length naturel, Rubus arcticus populations of arctic bramble (Rubus

189 Liu Z. and Furnier G.R. 1993 polymorphism. linkage of allozymes and

Inheritance and Journal of subsp. arcticus, Rubus

Populus, allozymes, Allozyme subsp. in leaf tissue of the

arcticus L.variantsarcticus) in Finland.

restriction fragment length Heredity 84 RFLP, forest trees parents and progeny of five full-sIb

polymorphisms in trembling aspen. (5): 419-424. families of trembling aspen (Populus

190 Lu, M.-Z., Szmidt, A.E. 1995 Iheritance of RAPD fragments in haploid Heridity 74: Controlled cross, diploid tremuloides; n = 19) were examined for

and Wang, X.-U. and diploid tissues of Pinus sylvestris 582-589. bud, haploid

(L.). macrogametophyte,

inheritance, Pinus

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



191 Lu, M.-Z., Wang, X.- 1997 Molecular properties of RAPs in Pinus Forest Pinus sylvestris , RAPD,

U.and Szmidt, A.E. sylvestris (L.) and their implications for sequence homology,

Genetics 4 (4):

genetic analysis. 227-234. repetitive sequence,

192 Lundkvist K. 1978 Allozymes in population genetic studies presence/absence

Allozyme, genetic,

Allozymes in

of Norway spruce (Picea abies K.). populationlinkage, Picea abies ,

Akademisk avandling. population, spruce, forest

genetic studies

193 Luoranen, J., Zhang, G. 2005 Production of even-sized hybrid aspen of Norway trees. height, hybrid

grading,

Baltic Forestry At present in Finnish nurseries, hybrid

and Smolander, H. plants from root cuttings: transplanting, aspen, planting, Populus,

11 (2): 20-28 aspens are reproduced from root cuttings

height grading and planting dates. root cutting, forest trees by transplanting the sprouted cuttings to

194 MacKay, J., Becwar, 2006 Genetic control of somatic Tree Genetics forest trees the large plugs (trays with 380-400 cm3

M.R., Park, Y.-S., & Genomes,

embryogenesis initiation in loblolly pine

Corderro, J.P. and and implications for breeding. V2(1):1-9.

195 Pullman, G.S.

MacKay, J., Berube, H., 2004 Functional genomics in forest trees: Plantation forest trees

Regan, S. and Seguin, A application to the investigation of Forest

defense mechanisms and wood Biotechnology

196 MacKay, J., Seguin, A. 1988 formation.

Genetic-Transformation of 9 Invitro for the 21st

Plant Cell forest trees

and Lalonde, M. Clones of Alnus and Betula by Reports,

Agrobacterium-Tumefaciens. 7(4):229-232.

197 Magri, D, Vendramin, 2006 A new scenario for the Quaternary New Phytol beech, Fagus sylvatica, Here, palaeobotanical and genetic data for

GG, Comps B., history of European beech populations: 171 (1): 199- chloroplast markers; common beech (Fagus sylvatica) in

Dupanloup I,. Geburek palaeobotanical evidence and genetic 221 fossil pollen; glacial Europe are used to evaluate the genetic

198 T., Gomory D., and

Malabadi, R. B. 2007 consequences

Influence of Triacontanol on Somatic Baltic Forestry refugia; nuclear markers;

Chir pine, Pinus This work highlights the influence in

consequences of long-term survivalof

Nataraja, K. Embryogenesis of Pinus roxburghii Sarg.13(1): 39-44 roxburghii, Somatic triacontanol on somatic embryogenesis

embryogenesis, Tissue and rooting of somatic seedlings in Pinus

199 Mariette, S., Chagne, 2001 Genetic diversity within and among Heredity 86 AFLP, ABA-Abscisic

culture genetic diversity, roxburghii. Mature zygotic embryos

-

D., Lezier, C., Pinus pinaster populations: comparison (4): 469-479. genetic differentiation,

Pastuszka, P., Baffin, between AFLP and microsatellite microsatellite, Pinus

Mariette S., , C.,

200 A., Plomion Cottrell J., 2002 markers.

Comparison of Levels of Genetic Silvae pinaster , forest trees

microsatellite, AFLP, The aim of this study was to compare

Csaikl U.M., Diversity Detected with AFLP and Genetica 51, genetic diversity, genetic genetic diversity within and among

Goikoechea P., Konig Microsatellite Markers within and 2–3: 72-79 differentiation, Quercus Quercus spp. populations based on two

A., Lowe A.J., Van among Mixed Q. petraea (MATT.) robur, Quercus petraea, contrasting types of nuclear markers.

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



201 Mariette, S., Lefranc, 1997 Genetic variability in wild cherry Theor Appl Gene diversity, genetic Isoenzymes were used to evaluate gene

M., Legrand, P., populations in France. Effects of Genet 94: 904- differentiation, founder diversity and genetic differentiation

Taneyhill, D., colonizing processes. 908. effect, isoenzymes, among six populations of wild cherry

202 Franscaria-Lacoste, N.,

Markussen, T.; Pakull, 2007 Positioning of sex-correlated markers for Silvae Prunum avium , forest

Populus, sex-related A preliminary L.) in France. of contrast

(Prunus aviumconsensus mapWe Populus

B.; Fladung, M. Populus in a AFLP- and SSR-marker Genetica 56 (3- marker, Linkage map, tremula x tremuloides has been

based genetic map of Populus tremula x 4): 180-184 AFLP, SCAR, forest constructed from an interspecific hybrid

203 Marques C.M., 2002 tremuloides and synteny of SSR loci and

onservation Theor Appl trees mapping; QTLs;

SSR; population of of microsatellitethe cross

Conservation 66 seedlings of loci,

Brondani R.P.V., QTLs for vegetative propagation in four Genet 105 (2- eucalyptus; synteny, heterozygous in Eucalyptus grandis,

Grattapaglia D., Eucalyptus species 3): 474-478 forest trees Eucalyptus urophylla, Eucalyptus

204 Sederoff R.

Marques C.M., Carocha 2005 T

Verification of QTL linked markers for Tree Genetics Eucalyptus, AFLP, QTL tereticornis and Eucalyptus globulus,

V.J., Pereira de Sa A.R. propagation traits in Eucalyptus & Genomes 1 verification, Vegetative

, Oliveira M.R., Pires (3): 103-108 propagation, Marker-

205 A.M., Sederoff R.and

Mattila, A., Pakkanen, 1994 Genetic variation in English oak Silva Fennica aided selection,, MAS,

Quercus robur Genetic variation in 5 natural stands of

A., Vakkari, P. and (Quercus robur ) in Finland. 28 (4): 251- allozymes, Quercus robur in Finland was analyzed

Raisio, J. 256. heterozygosity, genetic electrophoretically for 13 isozyme loci.

206 Mattila, A., Vakkari, P. 1996 Genetic variation of Quercus robur and differences, population,

Quercus robur , Ulmus Stands were on average polymorphic at

Ulmus laevis in Finland. laevis , allozymes,

heterozygosity, genetic

207 Meier-Dinkel A., 1993 Micropropagation and ex vitro rooting of Ann. For. Sci. differentation, forest

tissue culture, Green acorns from 11 selected late-

Becker B. and several clones of late-flushing Quercus 50: 319-322 micropropagation, in flushing Quercus robur trees were used as

Duckstein D. robur L vitro propagation, initial explants for micropropagation.

208 Metzler, B. and 1987 The in-vitro-mycorrhization of Pinus Sonderdruck Ouercus, ex vitro

forest trees From 60 acorns, 45 clones which

Oberwinkler, F. sylvestris L. and its deppendence on the aus European

pH-value. Journal of

209 Miranda, M.E. and 1993 Cost components analysis of Forest

Biotechnology Micropropagation, Costs

Fernandez, J. micropropagating chestnut plants. of trees.Edited analysis, chestnut,

Pardos, J.A., Castanea sativa x C.

210 Miranda, M.E. and 1992 The micropropagation of chestnut tree: Ahuja, M.R., crenata, forest trees

Symposium Chestnut, Castanea,

Fernandez, J. in vivo establishment and post- Bordeaux micropropagation,

propagation growth. France 1992. microcuttings, nursery,

Mass forest trees

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



211 Missiaggia A.A., 2005 Genetic mapping of Eef1, a major effect Tree Genet Eucalyptus grandis; early An early flowering mutant plant of

Piacezzi A.L., QTL for early flowering in Eucalyptus Genomes 1 flowering mutant; bulk Eucalyptus grandis with normal vegetative

Grattapaglia D. grandis (2): 79-84 segregant analysis, growth was found in a nursery in northern

212 Merila J, Crnokrak P 2001 Comparison of genetic differentiation at Journal of microsatelittes genetic

allozymes, FST, Brazil. This mutant the degree of at

The comparison of plant flowers

marker loci and quantitative traits. Evolutionary drift, geographical differentiation in neutral marker loci and

Biology 14 variation, meta-analysis, genes coding quantitative traits with

213 Merkle S.E., Andrade 2007 Restoration of threatened species: a (6): 892-903

Tree Genetics microsatellites, natural

American chestnut, Some of the and equivalent measures of

standardizedfirst applications of

G.M., Nairn C.J., noble cause for transgenic trees & Genomes 3 American elm, transgenic trees in North America may be

Powell W.A. and (2): 111-118 Transgenic trees, forest for the conservation or restoration of

214 Maynard C.A. R.,

Mockeliūnaitė 2005 Paprastojo uosio (Fraxinus excelsior L.) Lietuvos trees

Fraxinus excelsior, threatened forest (Fraxinus have beenL.)

Paprastojo uosio trees that excelsior

Kuusienė S. morfogenezės tyrimai in vitro ir DNR žemės ūkio morfogenezė, APPD, morfogenezės tyrimai atlikti su trimis

polimorfizmo įvertinimas universiteto motinmedžio palikuonių motinmedžių palikuonimis izoliuotų

215 Moran G.F., Thamarus 2002 Genomics of Eucalyptus wood traits doktorantų

Ann. For. Sci. įvairovė, forest trees

eucalypt, linkage maps, subrendusių gemalų kultūroje. has been on

A major focus of our research Didžiausią

K.A., Raymond C.A., 59 (5-6): QTL, candidate genes, using molecular technologies to guide

QiuaD., Uren T., 645–650 xylem, microarrays, breeding for high value wood and fibre

216 Southerton S.G.

Müller-Starck G., 1993 Intra- and interpopulational genetic Ann. For. Sci. forest trees

Quercus robur, Q traits in of 5 2-year-old populations ofbeen

In each eucalypts. One approach has

Herzog S. and Hattemer variation in juvenile populations of 50: 233-244 petraea, alloenzymes, Quercus robur and Q petraea (single and

H.H. Quercus robur L and Quercus petraea heterozygosity, diversity, multipopulation samples), genetic

217 Moreau, F., 1994 Liebl

Molecular differentiation between Q. Forest genetic distahce, genetic

RAPD, genetic variation was quantified with respect to 13

Kleinschmit, J. and petraea and Q. robur assessed by Genetics 1 (1):differentiation,

Kremer, A., random amplified DNA fragments. 51-64. similarity, Quercus

218 Morgante, M. and 2003 From plant genomics to breeding Current petraea , Quercus robur ,

genomics, breeding, New alleles are constantly accumulated

Salamini, F. practice. Opinion in QTL, SNP, MAS, forest during intentional crop selection. The

Biotechnology trees molecular understanding of these alleles

219 Müller-Strack, G. 1992 Genetic variation within European tree ,14: 214–219.

New Forets 6: Genetic markers, has stimulated new genomic approaches to

Baradat, Ph. and species. 23-47. isoenzymes, terpenes,

Bergmann, F. polyphenols,

220 Muona, O., Yazdani, R 1987 Analysis of linkage in Picea abies . Heriditas 106: heterozygosity,

forest trees

and Lindqvist, G. 31-36.

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



221 Murillo, O. and 1997 Inheritance of isozyme variants of Alnus Silvae Alnus acuminata , Inheritance of isozyme variants of Alnus

Hattemer, H.H. acuminata ssp.arguta (Schlectendal) Genetica 46: isozymes, inheritance acuminata ssp. arguta were determined on

Furlow. 51-54. analysis, forest trees the basis of horizontal starch gel

222 Namkoong G. and 2001 Application of Genetic Markers to Forest Draft report to Isozymes, DNA markers, electrophoresis procedures. Vegetative as

The application of genetic markers such

Koshy M.P. tree species IPGRI of the RAPD, microsatelites, allozymes and DNA (Deoxyribose Nucleic

project SSR, AFLP, RFLP, Acid) markers has shown to be useful in

223 Nance, W.L., Tuskan, 1992 Potential applications of molecular ―Developing VNTR, forest trees

Can. J. For. DNA markers, host- studying geneticmolecular in humans,

Applications of diversity markers for

G.A., Nelson, C.D. and markers for genetic analysis of host- Res. 22: 1038- pathogens, forest trees genetic analysis of host–pathogen systems

Doudric, R.L. pathogen systems in forest trees. 1045. are presented within the framework of the

224 Naugžemys D., Žvingila 2006 Comparison of DNA polymorphism in Biologija 1: 30-Pinus sylvestris, gene-for-gene model. The literature on

We used random amplified polymorphic

D., Aučina A., Rančelis seedlings of Pinus sylvestris L. from 35 comparison of DNA (RAPD) to examine genetic

V. different populations by RAPD markers populations, RAPD, differences among three populations of

225 Neale, D.B., Devey, 1992 Use of DNA markers in forest tree New Forests genetic diversity, mean

DNA markers, genetic Pinus sylvestris L. (Labanoras,

M.E., Jermstad, K.D., improvement research. 6: 391-407. maps, RFLPs, forest

Ahuja, M.R., Alosi, trees

226 M.C. and Marshall,

Neale D.B., Sewell 2002 Molecular dissection of the quantitative Ann. For. Sci. QTL, wood properties, Significant progress has been made toward

M.M. and Brown G.R. inheritance of wood property traits in 59: 595-605 SNP, marker-aided the molecular dissection of the

loblolly pine breeding, loblolly pine, quantitative inheritance of wood property

227 Nesbitt KA, Potts BM, 1997 Fingerprinting and pedigree analysis in Silvae MAS, Forest trees

Eucalyptus globulus; traits in were used to confirm clonal and

RAPDs loblolly pine (Pinus taeda L.)

Vaillancourt RE, Reid Eucalyptus globulus using RAPDs genetica 46 RAPD; fingerprinting; fidelity and distinguish individuals of

JB (1): 6-11 breeding system; varying degrees of relationship in

228 Nicole M-C., Hamel 2006 MAP-ping genomic organization and BMC Populus analysis;

pedigree trichocarpa, Eucalyptus globulus.other eukaryotes,was

Background: As in RAPD variation

L.P., Morency M-J., organ-specific expression profiles of Genomics 7: genome mapping, forest plant mitogen-activated protein kinase

Beaudoin N., Ellis B.E., poplar 223 trees (MAPK) cascades are composed of

229 Seguin A. L.M.,

O'Connell 2006 MAP kinases and MAP kinase kinases Heredity 97

mpacts of forest fragmentation on the conifer; forest three classes of hierarchically organized

We studied the mating system of white

Mosseler A., Rajora mating system and genetic diversity of (6): 418-426 fragmentation; genetic spruce (Picea glauca) in a landscape

O.P. white spruce (Picea glauca) at the diversity; mating system; fragmented by agriculture in northern

230 I

Oddou-Muratorio S., Real-time level

2006 landscape patterns of pollen flow in the Am J Bot 93 pollen pool; white

correlated paternity; Ontario, Canada. We sampled 23 stands as

Understanding the role of mother plants

Klein E.K., Demesure- wild-service tree, Sorbus torminalis (11): 1650- covariance analyses; pollen recipients in shaping mating

Musch B., Austerlitz F. (Rosaceae). III. Mating patterns and the 1659 flowering phenology; patterns is essential for understanding the

ecological maternal neighborhood insect pollination; pollen evolution of populations and in particular

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



231 Oddou-Muratorio S., 2004 Impacts of gene flow and logging history Molecular microsatellite; Ripley's K- Sorbus torminalis L. Crantz is a colonizing

Demesure-Musch B., on the local genetic structure of a Ecology 13 function; silviculture; tree species usually found at low density

Pelissier R., Gouyon scattered tree species, Sorbus torminalis (12): 3689- SPAGEDI; spatial auto- in managed European forests. Using six

232 P.H.

Oddou-Muratorio S., 2003 L. Crantz in the wildservice tree,

Pollen flow 3702

Molecular correlation;microsatellite; microsatellite markers, of polymorphic

CERVUS; spatial The joint development we investigated

Houot M.L., Demesure- Sorbus torminalis (L.) Crantz. I. Ecology 12 parentage assignment; molecular markers and paternity analysis

Musch B., Austerlitz F. Evaluating the paternity analysis (12): 3427- population size; scoring methods provides new approaches to

233 Olalde M., Herran A., 2002 procedure in continuous populations

White oaks phylogeography in the 3439 Ecol

Forest The geographic distribution of pollen flow

error; simulations, forest investigate ongoing patterns of maternally

Oaks; cpDNA;

Espinel S., Goicoechea Iberian Peninsula Manag 156: Phylogeography; Genetic inherited chloroplast DNA polymorphisms

P.G. 89–102 diversity; Glacial was studied to determine the

234 Ouinsavi, C., Sokpon, 2006 Novel microsatellite DNA markers for Molecular refugia, tree species;

African forest trees Eleven microsatellite primer white oaks

phylogeographic structure of pairs were in

N., Bousquet, J., the threatened African endemic tree Ecology enriched genomic developed for the tropical African tree

Newton, C.H. and species, Milicia excelsa (Moraceae), and Notes, library; microsatellites; Milicia excelsa. Genomic DNA was

Paglia, D.P.

235 Khasa, G.P., Olivieri, 1998 cross-species amplification in Milicia

Towards second generation STS 6(2):480-483.

Mol Gen Milicia, forest trees

Picea abies , Linkage enriched for dinucleotide (TCn and

-

A.M., Morgante, M. (sequuence- tagged sites) linkage maps Genet 258: map, sequence-tagged

in conifers : a genetic map of Norway 466-478. sites, AFLP, SAMPL,

236 Palme, A. Evolutionary history K.)

2003 spruce ( Picea abies and chloroplast Dissertation, forest trees DNA,

Chloroplast -

DNA variation in three plant genera: Uppsala phylogeography,

Betula, Corylus and Salix. The impact of University, 59 hybridization,

237 Palme, A.E., Su,Q., 2004 post-glacial colonization and

Extensive sharing of chloroplast p.

Molecular phylogeny, Salix caprea, Extensive sharing of chloroplast

Betula pendula, Betula

Palsson, S., Lascoux, M. haplotypes among European birches Ecology 13: pubescens, Betula nana, haplotypes among the silver birch, Betula

indicates hybridization among Betula 167 –178. chloroplast, pendula Roth., the downy birch, B.

238 Pandey M. 2005 pendula , B.pubescens and B.nana .

Development of microsatellites in Dissertation, hybridization,

Microsatellites, pubescens Ehrh., and the dwarf birch, B.

-

sycamore maple (Acer pseudoplatanus Georg-August sycamore maple, Acer

L.) and their application in population University of pseudoplatanus,

239 Pandey M., Gailing O., 2004 genetics

haracterization of microsatellite markers Gottingem,

Mol Ecol population genetics,

Acer pseudoplatanus; Sycamore (Acer pseudoplatanus L.) is a

Fischer D., Hattemer in sycamore (Acer pseudoplatanus L.) Notes 4 (2): cross-species tetraploid European hardwood tree

H.H., Finkeldey R. 253-255 amplification; maple; species. The reproduction system of the

240 C

Panetsos, K.P., 1998 Genetic variation of Pinus brutia from Silvae Pinus brutia, isoenzymes, insect-pollinated trees and patterns Pinus

microsatellite; The present study concentrated on of

Aravanopoulos, F.A., Islands of the Northeastern Aegean Sea. Genetica 47, Aegean, population brutia TEN. one of the main forest species

Scaltsoyiannes, A. 2–3:115-120. genetics, forest trees of the Aegean islands and one of the most

important low-elevation Mediterranean

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



241 Park Y-S. 2002 Implementation of conifer somatic Ann. For. Sci. somatic embryogenesis, Cloning of trees using somatic

embryogenesis in clonal forestry: 59: 651-656 cryopreservation, genetic embryogenesis (SE) could have a major

technical requirements and deployment stability, clonal forestry, impact on tree breeding and commercial

242 Patamsytė J., Žvingila Assessement of p. 651

2005 considerations ecological impact on Biologija 4: tree improvement, forest

RAPD, population The genetic diversity conjunction with

plantation forestry. Inof Rubus idaeus L.

D., Mažonytė I., genetic diversity among populations of 24–28 differentiation, rubus both within and among the populations in

Kleizaitė V., Baliuckas Rubus idaeus L. idaeus , forest trees different ecological conditions was

Paterson, A.H., L.,

243 V., Balčiūnienė Lander, 1988 Resolution of quantitative traits into Nature, vol forest trees compared. The diversity of RAPD markers

-

E.S., Hewitt§, J.D., Mendelian factors by using a complete 335: 721-726.

Peterson, S., Lincoln, E. linkage map of restriction fragment

244 and Tanksley, S.D. J.,

Pavy, N., Laroche, 2005 length polymorphisms.

Large-scale statistical analysis of Plant forest trees A computational analysis of pine

Bousquet, J. and secondary xylem ESTs in pine. Molecular transcripts was conducted to contribute to

MacKay, J. Biology, the functional annotation of conifer

245 Pavy, N., Parsons, L.S., 2006 Automated SNP detection from a large 57(2):203-224.

BMC forest trees Background: statistical analysis of

sequences. A High-throughput genotyping

Paule, C., MacKay, J. collection of white spruce expressed Genomics 7: technologies represent a highly efficient

and Bousquet, J. sequences: contributing factors and 174 way to accelerate genetic mapping and

246 Pavy, N., Paule, C., 2005 approaches for the categorizationand

Generation, annotation, analysis of BMC forest trees enable associationsequencing and analysis

Background: The studies. As a first step

Parsons, L., Crow, J.A., database integration of 16,500 white Genomics 6: of ESTs is for now the only practical

Morency, M.J., Cooke, spruce EST clusters. 144. approach for large-scale gene discovery

247 J., Johnson, J.E.,

Pelgas B., Beauseigle 2006 Comparative genome mapping among Theor Appl EST, Pinus taeda, QTL, and annotation in conifers because their

A composite linkage map was constructed

S., Achere V., Jeandroz Picea glauca, P-mariana x P-rubens and Genet genetic linkage maps, from four individual maps for the conifer

S., Bousquet J. and P-abies, and correspondence with other 113(8):1371- microsatellite markers, Picea glauca (Moench) Voss, from

248 Isabel N. Bousquet, J.,

Pelgas, B., 2005 Pinaceae.

A composite linkage map from two 1393 Appl

Theor Lobloly-pine, Black

Codominant markers, anonymous and linkage maps were

Four individual gene-specific markfers

Beauseigle, S. and crosses for the species complex Picea Genet colinearity,comparative constructed from two crosses for the

Isabel, N. mariana x Picea rubens and analysis of 111(8):1466- mapping,consensus map, species complex Picea mariana (Mill.)

249 Pelgas, B, Isabel, N, 2004 synteny with other Pinaceae.

Efficient screening for expressed 1488Breeding

Mol Pinaceae, synteny, forest B.S.P. is an urgent need to accelerate the

Codominant markers, There × Picea rubens Sarg in order to

Bousquet, J sequence tag polymorphisms (ESTPs) by 13 (3): 263- conifers, consensus development of informative codominant

DNA pool sequencing and denaturing 279 mapping, insertion- markers of coding regions such as ESTPs

250 Pereira-Lorenzo, S., 1996 gradient geland grouping of northwestern J. Amer. Soc.

Variability electrophoresis (DGGE) in Castanea sativa , genetic (expressed sequence tag polymorphisms)

deletion, Picea, single -

Fernández- López, J., spanish chestnut cultivars.II. Isoenzyme Hort.Sci. 121 variation, numerical

Moreno-González, J. traits. (2): xxx-xxx. taxonomy, markers,

forest trees

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



251 Perry, DJ, Isabel, N, 1999 Sequence-tagged-site (STS) markers of Heredity 83: allelic sequence We examined the amount and nature of

Bousquet, J arbitrary genes: the amount and nature of 239-248 Part 3 variation; codominant variation revealed by cDNA-based

variation revealed in Norway spruce PCR-based markers; sequence-tagged-site (STS) markers in

252 Petit, RJ, Aguinagalde, 2003 Glacial refugia: Hotspots but not melting Science 300 conifer genes; multiplex

cpDNA, refugia, genetic Norwayrefuge areas are expectedKarst.)

Glacial spruce (Picea abies (L.) to harbor

I, de Beaulieu, JL, pots of genetic diversity (5625): 1563- diversity, forest trees a large fraction of the intraspecific

Bittkau C, Brewer S, 1565 biodiversity of the temperate biota. To test

253 Cheddadi R, Ennos R,

Petit R.J., Csaikl U.M., 2002 Chloroplast DNA variation in European Forest Ecol Admixture genetic this hypothesis, we studied chloroplast

A consortium of 16 laboratories have

Bordacs S., Burg K., white oaks Phylogeography and patterns Manag 156: diversity, genetic studied chloroplast DNA (cpDNA)

Coart E., Cottrelle J., of diversity based on data from over 5–26 differentiation, variation in European white oaks. A

254 van Dam B., Deans J.D.,

Petit R.J., Brewer S., 2002 2600 populationsrefugia and post-glacial

Identification of Forest Ecol introgression, Glacial

Fossil pollen; phylogeny, common strategy for molecular screening,

The geographic distribution throughout

Bordacs S., Burg K., colonisation routes of European white Manag 156: period refugia; Europe of each of 32 chloroplast

Cheddadi R., Coart E., oaks based on chloroplast 49–74 Phylogeography; DNAvariants belonging to eight white oak

Petit R.J., Csaikl U.M.,

255 Cottrell J.,Latouche- 2002 DNA and fossil pollen evidence in

Chloroplast DNA variation of oaks Forest Ecol Quercus, forest trees

Genetic differentiation; Chloroplast DNA variation populations in

species sampled from 2613 was studied is

Halle C., Pemonge France and the influence of forest Manag 156: Interspecific gene flow; a total of 878 French oak populations from

M.H., Kremer A. fragmentation on genetic diversity 115–129 Landscape structure; four different species. Three main cpDNA

256 Petit J.R., Wagner D.B. 1993 Ribosomal DNA and chloroplast DNA Ann. For. Sci. Postglacial

Quercus petraea, More than 70 found, which have well-

lineages were trees belonging to the

and Kremer A. polymorphisms in a mixed stand of 50: 41-47 Quercus robur, gene morphologically distinguishable species

Quercus robur and Q petraea flow, diversity, Quercus robur L and Quercus petraea

257 Pfeiffer, A., Olivieri, 1997 Identification and characterization of Genome 40: sympatry, forest trees

Microsatellite, repetitive (Matt) Liebl were sampled in a mixed

A.M., and Morgante, M. microsatellites in Norway spruce (Picea 411-419. DNA, hypervariability,

abies K.) Picea abies , genome

258 Pigliucci, M., Villani, 1990 Geographic and climatic factors J. Genet 69 complexity, forest trees

Castanea ,

F.and Benedetteli, S. associated with the spatial structure of (3): 141-149. autocorrelation, Mantel´s

gene frequencies in Castanea sativa test, isozymes, spatial

259 Plomion, C., Durel, C.- 1996 Mill. From Turkey.of height in maritime

Genetic dissection Theor Appl structure, forest, trees

Pinus pinaster Random Amplified Polymorphic DNAs

E., O'Malley.D.M. pine seedlings raised under accelerated Genet 93: 849- muration, height, (RAPDs) were used to investigate

growth conditions. 858. RAPD, OTL, quantitative trait loci (QTL) for traits

260 Plomion C., Hurme P., 1999 Developing SSCP markers in two Pinus Molecular megagametophyte, forest

SSCP, Pinus pinaster, related to height growth on 126 F2

This study demonstrates the feasibility of

Frigerio J-M., Ridolfi species Breeding 5: Pinus sylvestris, linkage generating sequence-based markers in

M., Pot D., Pionneau C., 21–31, map, forest trees Pinus species, from data available in

Avila C., Gallardo F., electronic databases. Nucleotide

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



261 Plomion C., Bahrman 2000 Proteomics for genetic and physiological Proteomics, genetic The significant advances in proteomics

N., Costa P., Dubos C., studies in forest trees: application in mapping, genome during the last decade, attested two-

Frigerio J.M., Gion J.- maritime pine. expression analysis, dimensional gel electrophoresis coupled

Plomion C., C., Madur

262 M., Lalanne LeProvost 2001 Pollen contamination in a maritime pine Can. J. For. QTL, forest trees

Pinus pinaster, cpSSR, A new concept of seed (2DE-MS)

with mass-spectrometryorchard was as a

G., Pot D., Vendramin polycross seed orchard and certification Res. 31: forest trees developed by Institut National de la

G., Gerber S., Decroocq of improved seeds using chloroplast 1816–1825 Recherche Agronomique for the maritime

Plomion, J.,

263 C., Brach C., Raffin A., 2005 microsatellites

Advances in forest tree - Genomics New forest trees pine (Pinus pinaster Ait.) breeding

Richardson, T. and Forest Trees Workshop, Plant and Phytologist,

MacKay, J. Animal Genome XIII Conference, San 166(3):713-

264 Pollefeys, P. and Molecular USA, diversity of the

2003 diego, CA, geneticJanuary 2005. 717.

Genome 46: French–American French–American hybrid grapevines are

Bousquet, J. French–American grapevine hybrids 1037–1048. hybrids, genetic most popular in eastern and mid-western

cultivated in North America. diversity, RAPD, SSR, North America: they are hardy cultivars

265 Premoli A.C. 2003 Isozyme polymorphisms provide Journal of Vitis, forest trees

Isozymes, clinal Variable physical conditions the

derived from crosses betweenalong

evidence of clinal variation with Heredity variation, forest trees elevational gradients strongly influence

elevation in nothofagus pumilio. 94(3): patterns of genetic differentiation in tree

266 Rahman, M.H., 2000 Microsatellite DNA markers in Populus 218–226.43: Poplar, microsatellites, species.Here, the hypothesis is testedDNA

Genome Markers for eight new microsatellite that

Dayanandan, S. and tremuloides. 293–297. genetic mapping, simple or simple sequence repeat (SSR) loci were

Rajora, O.P. sequence repeat (SSR) developed and characterized in trembling

267 Rahman, M.H. and 2002 Microsatellite DNA fingerprinting, Genome 45: markers, DNA

Populus, simple aspen (Populus tremuloides) from a partial

Accurate identification of Populus clones

Rajora, O.P. differentiation, and genetic relationships 1083–1094. sequence repeat markers, and cultivars is essential for effective

of clones, cultivars, and varieties of six clonal identification, selection, breeding, and genetic resource

268 Rajora O.P. and Dancik 2000 Population genetic three sections of the

poplar species fromvariation, structure, Can. J. Bot. genetic fingerprinting,

Picea glauca, Picea management programs. The unit evolution

Genetic variation, structure, and of

B.P. and evolution in Engelmann spruce, 78: 768–780 engelmannii, of 12 populations of putative Engelmann

white spruce, and their natural hybrid biosystematics, natural spruce (Picea engelmanii Parry), white

269 Rajora, O.P., DeVerno, 1998 complexdiversity and population

Genetic in Alberta Can. J. Bot. hybridization, species The dramatic glauca of eastern white and

Pinus strobus, allozymes, spruce (Picea decline(Moench) Voss), pine

L., Alex Mosseler, A., structure of disjunct Newfoundland and 76: 500-508. gene conservation, (Pinus strobus L.) populations in

and Innes, D.J. central Ontario populations of eastern genetic diversity and Newfoundland over the past 100 years

270 Rajora, OP, Pluhar, SA 2003 Genetic diversity impacts ).

white pine ( Pinus strobusof forest fires, Theor Appl population structure,

forest management presents an opportunity to determine and

Benchmarks were established for genetic

forest harvesting, and alternative Genet 106 (7): practices; conservation diversity inherent in natural mature

reforestation practices in black spruce 1203-1212 of forest genetic populations, and genetic diversity impacts

(Picea mariana) resources; genetic of forest fires, clearcut harvesting and

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



271 Rajora, OP, Rahman, 2003 Microsatellite DNA and RAPD Theor Appl poplars; simple sequence Microsatellite DNA markers of ten SSR

MH fingerprinting, identification and genetic Genet 106 (3): repeats; DNA loci and 248 RAPD loci (resolved by 26

relationships of hybrid poplar (Populus x 470-477 fingerprinting; RAPD primers) were used for DNA

272 Raspé, O., Jacquemart, 1998 canadensis) cultivars

Isozymes in Sorbus aucuparia Int. J. Plant clone/cultivar

forest trees fingerprinting and differentiation of 17

A.-L. and Sloover, J. (Rosaceae: Maloideae): genetic analysis Sci. 159 (4):

and evolutionary significance of 627-636.

273 Ribeiro M.M., 2002 zymograms.

Origin identification of maritime pine Ann. For. Sci. cpSSR, microsatellites, Maritime pine seed-lots from north-

LeProvost G., Gerber S., stands in France using chloroplast simple- 59 (1): 53–62 terpene, origin western Iberian regions (Portugal and

Vendramin G.G., sequence repeats identification, Pinus Galicia) were introduced in the 1950s to

274 Anzidei M., Decroocq

Rishi, A.A., Nelson, 2001 Improvement of Populus through genetic Indian J.Plant Genetic forest trees

pinaster,engineering, the southwest of France (Aquitaine

Genetic engineering has provided tools to

N.D. and Goyal, A.. engineering, Physiol.,Vol.6, Populus, transformation, improve Populus through introducing

No.2, pp.119- forest trees genes from heterologous sources and also

275 Rishi, A.S., Nelson, 2001 Genetic modification for improvement of 126.

Physiol.Mol.B forest trees Species down-regulating metabolic

through of the genus Populus (poplars and

N.D. and Goyal, A. Populus. iol.Plants 7: 7- aspens) are widely grown in the temperate

21. regions of the Northern Hemisphere.

276 Rohde A., Prinsen E., 2002 PtABI3 Impinges on the Growth and The Plant Poplar, protein Hybridization of Populus through

The Arabidopsis ABSCISIC

De Rycke R., Engler G., Differentiation of Embryonic Leaves Cell, Vol. 14, expression, forest trees ACID–INSENSITIVE3 (ABI3) protein

Van Montagu M., and during Bud Set in Poplar 1885–1901, plays a crucial role during late seed

Roy A., W.

277 Boerjan Frascaria N., 1992 Segregating Random Amplified Theor Appl forest trees development and has an additional

Molecular markers are currently being

MacKay J. and Polymorphic Dnas (Rapds) in Betula- Genet 85(2- developed for Betula alleghaniensis

Bousquet J. Alleghaniensis. 3):173-180 Britton using random amplified

278 Rudin, D., Eriksson, G. 1974 Studies of allele frequencies and Silvae forest trees polymorphic DNA (RAPD). Arbitrarily

-

Ekberg, I., and Inbreeding in Scots pine populations by Genetica 23

Rasmuson, M. the aid of the isozyme technique. Heft 1-3, 1-98:

279 Rusanen, M., Vakkari, 2003 Genetic structure of Acer platanoides 10-13. For.

Can. J. Acer platanoides, Betula Marker variation was measured in 12 Acer

P. and Blom, A. and Betula pendula in northern Europe. Res. 33: pendula, genetic platanoides L. and 9 Betula pendula Roth

1110–1115. differentiation, isozymes, populations using 11 and 18 allozyme loci,

280 Samuel, R., Pinsker, W. 1995 Electrophoretic analysis of genetic Bot. Acta 108: forest trees

Quercus , allozyme respectively. Both species grow instudied

Allozyme variation at 14 loci was the

and Ehrendorfer, F. variation within and between populations 290-299. variation, heterozygosity, electrophoretically in 19 population

of Quercus cerris, Q pubescens, Q. genetic relationships, samples of Quercus cerris, Q. pubescens,

petraea and Q. robur (Fagaceae) from hybridization, forest Q. petraea, and Q. robur. Genetic

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



281 Sanchez, N., Grau, J.M., 1998 RAPD Markers for the iIdentification of Silvae Populus, RAPD DNA, Twenty five poplar clones, namely, 5 of

Manzanera, J.A. and Populus Species. Genetica 47, fingerprinting, species Populus nigra, 5 of P.deltoides, 5 of P.

Bueno, M.A. 2–3: 67-71 identification, forest alba, 5 of P. tremula, 1 of P. trichocarpa, 3

282 Sander T., König S., 2000 Genetic variation of European beech Molecular trees frequencies,

Allele Allelic and genotypic variation ―Platero‖

of P.x canescens and 1 of clone at 13

Rothe G.M., Janßen A. (Fagus sylvatica L.) along an altitudinal Ecology 9 (9): beech, Fagus silvatica , different enzyme loci of autochthonous

and Weisgerber H. transect at mount Vogelsberg in Hesse, 1349-1361. genetic variation, European beech (Fagus sylvatica L.) was

283 Savolainen, O. and 1992 Germany.forest management on gene

Effect of For Sci 6??: genotype frequencies,

Allozymes, forest investigated in six 110-160-year-old

-

Kärkkäinen, K. pools. 329-345?? management, genetic

markers, natural

284 Schubert R., Mueller- 2001 Development of EST-PCR markers and Theor Appl regeneration, seed EST-

cDNA sequencing, Fifteen cDNA sequences are reported for

Starck G., Riegel R. monitoring their intrapopulational Genet PCR markers, Isoenzyme the European coniferous forest tree

genetic variation in Picea abies (L.) 103:1223–123 gene markers, species Norway spruce [Picea abies (L.)

285 Scotti I., Magni F., Fink 2000 Microsatellite repeats are not randomly 1

Karst. Genome Intrapopulational

Picea abies, Karst.], including (Picea abies K.) cDNA

A Norway spruce the results of similarity

R., Powell W., Binelli distributed within Norway spruce (Picea 43(1): 41–46 microsatellites, SSRs, library obtained from vegetative bud tissue

G., and Hedley P.E. abies K.) expressed sequences ESTs, population was screened for the presence of (AG)n

286 Scotti-Saintagne C., 2004 Genome Scanning for Interspecific Genetics 168: genetics, forest trees

isozymes, AFLPs, and (AC)n microsatellite repeats. Ten

Interspecific differentiation values (GST)

Mariette S., Porth I., Differentiation Between Two Closely 1615–1626 SCARs, microsatellites, between two closely related oak species

Goicoechea P.G., Related Oak Species [Quercus robur L. SNPs, interspecific (Quercus petraea and Q. robur) were

Segura V., T., Bodenes

287 BarrenecheDenancé C., 2007 and Q. petraea (Matt.) Liebl.] complex

Wide range QTL analysis for Genome 50 differentiation, forest

Malus × domestica The present study aimed studies with the

compiled across differentat investigating

Durel C-E., and Costes architectural traits in a 1-year-old apple (2):159-171 Borkh., tree architecture, the genetic determinisms of architectural

E. progeny branching, growth, QTL traits in a 1-year-old apple (Malus ×

288 Senneville, S., Beaulieu, 2001 Evidence for low genetic diversity and J For Res 31: mapping, forest trees

forest trees domestica Borkh.). F1 progeny. Marsh.) is

Canada yew (Taxus canadensis A precise

J., Daoust, G., metapopulation structure in Canada yew 110–116 a gymnosperm that grows in the

Deslauriers, M., and (Taxus canadensis ): considerations for understory of mixed and deciduous forests

289 Bousquet, J. Neale B.

Sewell M.M., 2000 conservation.

Mapping quantitative traits in forest trees Molecular QTL, MAS, forest trees of northeastern North America. This shrub

Biology of

Woody Plants

290 Shepherd M., Cross M., 2003 Genetics of physical wood properties and 1: 407-423

Can. J. For. QTL, Hybrid Pinus Quantitative trait locus (QTL) detection

Dieters M.J., Harding early growth in a tropical pine hybrid Res. 33: elliottii x Pinus caribaea, was carried out for physical wood

K., Kain D.,and Henry 1923–1932 forest trees properties and early growth traits in an

R. interspecific hybrid between Pinus elliottii

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



291 Shepherd M., Cross M., 2002 Branch architecture QTL for Pinus Ann. For. Sci. genetic mapping, branch Putative quantitative trait loci (QTL) of

Dieters M.J. and Henry elliottii var. elliottii Pinus caribaea var. 59: 617-625 angle, branch diameter, moderate, additive effect were identified

R. hondurensis hybrids whorl spacing, whorl for branch diameter, average number of

292 Siegismund, H.R. and 2001 Intrapopulation and interpopulation Scand. J. For. regularity, Pinus, forest

Gene conservation, branches per whorlstands areaverage whorl

Native Danish oak per tree, fragmented

Jensen, J.S. genetic variation of Quercus in Res. 16: 103- genetic differentiation, and decreasing because of the extensive

Denmark. 116. isozyme, population use of foreign seed sources. Therefore, the

293 Smouse P.E., Robledo- 2007 Implications of natural propagule flow Tree Genetics structure, Quercus flow,

Forest trees, Gene Propagule structure of natural Danish oak

populationflow in populations of virtually

Arnuncio J.J and for containment of genetically modified & Genomes 3: GMO escapes, all organisms has importance for both the

González-Martínez S.C. forest trees 141–152 Monitoring, Transgenic genetic cohesion of the species and for its

294 Sosinski, B., 2000 Characterization of microsatellite Theor Appl risks

Rosaceae, peach, prunus, Microsatellites natural selection. It‘s

interaction withhave emerged as an

Gannavarapu, M., markers in peach [Prunus persica (L.) Genet 101: Microsatellite, simple important system of molecular markers.

Hager, L.D., Beck,L.E., Batsch]. 421-428. sequence repeats, SSR, We evaluated the potential of

295 King, G.J., Ryder, C.D.,

Spooner D., R. van 2005 Molecular markers for genebank IPGRI forest markers,

DNA trees In the last decade, use in of DNA

microsatellites for the usegenetic studies of

Treuren and M.C. de management. Technical Allozymes, RFLP, markers for the study of crop genetic

Vicente. Bulletin No. VNTR, DNA diversity has become routine, and has

296 Staniulytė R., Žvingila 2004 Paprastosios eglės (Picea Abies (L.) Miškininkystė sequencing, SSR,clones,

10. IPGRI, RAPD, plus tree STR, revolutionized biology. Increasingly,

The RAPD (random amplified

D., Kuusienė S. Karst.) pliusinių medžių klonų genetinės 1(55): 5-12 genetic diversity, clonal polymorphic DNA) was used to assess

įvairovės ir tapatumo įvertinimas APPD identity, Picea abies, genetic diversity and to identify genotype

297 Stelzer H.E and 1997 metodu

Implementing clonal forestry in the Can. J. For. forest trees

Clones, clonal forestry, specific markers in Norway genetics

Fifty people from the forest spruce (Picea

Goldfarb B. southeastern United States: SRIEG Res. 27: 442- forest trees community participated in a 2-day

satellite workshop summary remarks 446 workshop to identify and discuss issues

298 Sterky F., Regan S., 1998 Gene discovery in the wood-forming Proc. Natl. cambium, forestry, concerning the implementation of clonal

A rapidly growing area of genome

Karlsson J., Hertzberg tissues of poplar: Analysis of 5,692 Acad. Sci. functional genomics, research is the generation of expressed

M,. Rohde A., expressed sequence tags USA Vol. 95: xylem, xylogenesis, sequence tags (ESTs) in which large

299 Holmberg A., Amini B., 2003 Comparative sequence analysis between

Stirling, B, Yang, ZK, 13330–13335, forest sequence, Populus,

Can. J. For. DNA trees numbers of300 kb of DNA sequence from

More than randomly selected cDNA

Gunter, LE, Tuskan GA, orthologous regions of the Arabidopsis Res. 33 (11): forest trees five Populus bacterial artificial

Bradshaw HD and Populus genomes reveals substantial 2245-2251 chromosome (BAC) clones was compared

300 Soehr M.U. and Newton 2002 synteny and microcollinearity in a

Evaluation of mating dynamics Can. J. For. cpDN, Pinus contorta, with the complete (cpDNA) of the were

Chloroplast DNA sequence markers

C.H. lodgepole pine seed orchard using Res. 32(3): selfing, contamination, used to evaluate pollen dynamics in an

chloroplast DNA markers 469–476 seed orchard, forest trees operational lodgepole pine (Pinus contorta

Dougl. ex Loud. var. latifolia Engelm.)

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



301 Strauss, S.H.and 2002 Tree biotechnology in the 21 st century: Department Of Genetic enginiering,

Brunner, A.M. Transforming trees in the light of Forest GMO, forest trees

comparative genomics. Science,

302 Strauss, S.H., Hong, Y.- 1993 High levels of population differentiation Oregon State

Theor Appl Organelle, pine, We analyzed mitochondrial (mt) DNA

P., Hipkins, V.D. for mitochondrial DNA haplotypes in Genet 86: 605- mitochondrial DNA, restriction fragment length polymorphisms

Pinus radiata , muricata, and attenuata. 611. chloroplast DNA, (RFLPs) associated with cytochrome

303 Strauss, S.H., Lande, R. 1992 Limitations of molecular-marker-aided Can. J. For. phylogeny, forest trees

MAS, forest trees The advances to I (coxI)-related gene

oxidase, subunit date with quantitative

and Namkoong, G. selection in forest tree breeding. Res. 22: 1052- trait locus identification in agronomic

1063. crops, which have mostly been with

304 Streiff, R, Labbe, T, 1998 Within-population genetic structure in Molecular forest trees studies of inter- and intra-specific hybrids,

-

Bacilieri, R, et al Quercus robur L. and Quercus petraea Ecology 7 (3):

(Matt.) Liebl. assessed with isozymes 317-328

305 Takahashi, M., 2000 and microsatellites

Differences in genetic structure between Heredity 84: Fagus crenata , founder To examine the effects of forest cutting on

Mukouda, M. and two Japanese beech (Fagus crenata 103-115. effect, isozyme within-population genetic structure, the

Koono, K. Blume) stands. variability, linkage genetic structure and variability of two

306 Tammisola J., Akerman 1994 Strategies of pooling for parentage Biometrics in disequilibrium, self-

forest trees Japanese beech (Fagus crenata Blume)

S., Regina M., Lapinjoki analyses applying DNA markers plant breeding:

S., Kaupinev V. applications of

307 Tarca, A.L., Cooke, 2005 A robust neural networks approach for molecular

Bioinformatics forest trees Motivation: Microarray experiments are

J.E.K. and MacKay, J. spatial and intensity-dependent , 21(11):2674- affected by numerous sources of non-

normalization of cDNA microarray data. 2683. biological variation that contribute

308 Tauer, C.G., Hallgren, 1992 Using marker-aided selection to improve Can. J. For. MAS, stress, forest trees systematic bias to the resulting data. In a

The ability to locate quantitative trait loci

S.W. and Martin, B. tree growth response to abiotic stress. Res. 22: 1020- (QTL) on a restriction fragment length

1032. polymorphism (RFLP) genetic linkage

309 Thamarus, KA, Groom, 2002 A genetic linkage map for Eucalyptus Theor Appl Linkage map, Candidate map will provide tree breeders the means

A genetic linkage map containing

K, Murrell, J, et al. globulas with candidate loci for wood, Genet 104 (2- gene, EST, potential candidate loci for wood, fibre

fibre, and floral traits 3): 379-387 Microsatellite, Lignin, and floral traits has been constructed for

310 Triest, L., Greef, B., 1998 Variation and inheritance of isozyme loci Silvae Salix trees

forestalba, Salix fragilis, Eucalyptus globulus (Labill.) based on the

The expression of polymorphism in

D'Haeseleer, M., in controlled crosses of Salix alba and Genetica 47, willow, isozymes, gene different enzyme systems was investigated

Echchgadda, G., Salix fragilis . 2–3: 88-94 diversity, progeny in clones of Salix alba and Salix fragilis.

Slycken, J., and Coart, testing, hybridization, Dormant buds and sprouting leaves were

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



311 Troggio, M. 1998 Looking for QTL for adaptive and Climatic forest trees

economic traits in Norway spruce using adaptation of

molecular markers. boreal tree

312 Trontin J-F., 1999 Two highly divergent 5S rDNA unit size species -Tree

Genome 42: 5S rRNA genes, spacer The 5S ribosomal DNA unit structure and

Grandemange C., and classes occur in composite tandem array 837–848 variations, cluster organization have been investigated in

Favre J-M. in European larch (Larix decidua Mill.) organization, sequence Larix decidua and Larix kaempferi using

313 Troupin D., Nathan R., Analysis of spatial (Larix structure

2006 and Japanese larch genetickaempferi in an Molecular comparison,

microenvironmental We analysed the change of spatial spacer,

selective amplification of gene andgenetic

Vendramin G. G. expanding Pinus halepensis population Ecology 15 heterogeneity; structure (SGS) of reproductive

reveals development of fine-scale genetic (12): 3617- microsatellites; Pinus individuals over time in an expanding

314 Tyson, M, Vaillancourt, Determination time

1998 clustering over of clone size and age in a Aust J Bot 46 halepensis; population

3630 Eucalyptus, RAPD, Pinus halepensis population. To our

Fragmentation of lignotubers and the

RE, Reid, JB mallee eucalypt using RAPDs (2): 161-172 clones, forest trees consequent problems in genotype

identification make demographic studies

315 Tulsieram L.K., 1992 Single tree genetic linkage mapping in Biotehnology forest trees of mallee eucalypts unreliable. DNA

-

Glaubitz J.C., Kiss G. coniffers using haploid DNA from 10: 686-690.

and Carlson J.H. megagametophytes.

316 Tuskan G.A., DiFazio 2006 The genome of black cottonwood, Science 313 Genome, Populus, We report the draft genome of the black

S., Jansson S., Populus trichocarpa (Torr. & Gray) (5793): 1596- cottonwood, forest trees cottonwood tree, Populus trichocarpa.

Bohlmann J., Grigoriev 1604 Integration of shotgun sequence assembly

317 I., Hellsten U., Putnam

Unneberg P., Strömberg 2005 Analysis of 70,000 EST sequences to Tree Genetics EST, SNP, Assembly, The genetic genus has evolved

with Populus mapping enabled as the

M., Lundeberg J., study divergence between two closely & Genomes 1 cDNA library analysis, model organism for forest tree genomics,

Jansson S. and Sterky F. related Populus species (3): 109-115 Ortholog, forest trees which has been further emphasised with

318 Vaillancourt, R.E., 1995 Using RAPDs to, detect QTLs in an CRC for forest trees the sequencing of the Populus trichocarpa

-

Potts, B.M., Manson, interspecific F 2 hybrid of Eucalyptus. Temperate

A., Eldridge, T. and Hardwood

319 Reid, J.B.

Valbuena-Carabana M., 2007 Fine-scale spatial genetic structure in Forestry -

Molecular fine-scale spatial genetic Oaks are model species for the study of

Gonzalez-Martinez S.C., mixed oak stands with different levels of Ecology 16 structure; historical gene natural introgressive hybridization. High

Hardy O.J., Gil L. hybridization (6): 1207-1219 dispersal; hybrid zones; interfertility among oak taxa might result

320 Van Berloo, R., Stam, P. 1998 Marker-assisted selection in autogamous Theor Appl introgression;

Marker-assisted in collective evolution, through plant

Molecular markers may enable

RIL populations: a simulation study.. Genet 96: 147- selection, MAS, breeders to select indirectly for genes

154. simulation, quantitative affecting quantitative traits by selecting

trait loci, for molecular markers closely linked to

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



321 Van Berloo, R., Stam, P. 2001 Simultaneous marker-assisted selection Theor Appl Computer simulation, -

for multiple traits in autogamous crops. Genet 102: marker-assisted

1107-1112. selection, quantitative

322 van Buijtenen. J.P. 2001 Genomics and quantitative genetics. Can. J. For. trait loci, forest trees

forest trees The interaction between genomics and

Res. 31: quantitative genetics has been a two-way

617–622. street. Genomics contributed genetic

323 van Frankenhuyzen, K. 2004 Current status and environmental impact Can. J. For. forest trees markers and genetic maps making it

Advances in technology for in vitro

and Beardmore, T. of transgenic forest trees. Res. 34: propagation and genetic transformation

1163–1180. have accelerated the development of

324 Vaughan S.P., Cottrell 2007 Distribution and fine-scale spatial- Heredity 98 clonality; Prunus; sexual Insights into the within-population the

genetically engineered trees during spatial-

J.E., Moodley D.J., genetic structure in British wild cherry (5): 274-283 reproduction; SGS; SSR, genetic structure (SGS) of forest tree

Connolly T., Russell K. (Prunus avium L.) forest trees species, where little is known regarding

325 Vendramin G.G., 2000 Chloroplast microsatellite analysis Genome 43: haplotypic diversity, seed and pollen dispersal patterns,

Three chloroplast microsatellites

Anzidei M., Madaghiele reveals the presence of population 68–78 phylogeography, (cpSSRs), previously sequence

A., Sperisen C., and subdivision in Norway spruce (Picea chloroplast characterized and for which paternal

326 Bucci G. R., Ford-

Verbylaitė 2006 abies K.)

The phylogeny of woody Maloideae Biologija 1: 60-microsatellites,

Phylogeny, maloideae, In this study, the most and confirmed,

inheritance was tested suitable DNA

Lloyd B., Newbury J. (Rosaceae) using chloroplast trnL-trnF 63 TrnL-trnF, sequencing, extraction protocols for Maloideae

sequence data forest trees subfamily species were determined. Also,

327 Villani, F., Benedettelli, 1991 Genetic variation and differentiation Biochemical forest trees it was shown that the most suitable

S., Paciucci, M., between natural populations of chestnut markers in the

Cherubini, M and (Castanea sativa Mill.) from Italy. population

328 Pigliucci, M.

Villani, F., Lauteri, M., 1999 Genetic structure and quantitative traits genetics of

nd

Proc. 2 Int Genetic variability,

Sansotta, A.,Cherubini, variation in F1 full-sibs progenies of Symp. On isozymes, RAPDs,

M., Monteverdi, M.C., Castanea sativa Mill. Chestnut quantitative genetics,

329 Mattioni, C. and

Villani, F., Pigliucci, 1991 Genetic differentiation among Turkish Ed.G. Salesses morphometrics, water

Heredity 66: Castanea sativa , centre

M., Benedettelli, S. and chestnut (Castanea sativa Mill.) 131-136. of origin, cline,

Cherubini, M. populations. isozymes, forest trees

330 Villani, F., Pigliucci, 1992 Congruence between genetic, Genome 35: Castanae sativa ,

M., Lauteri, M. and morphometric, and physiological data on 251-256. isozymes,

Cherubini, M. differentiation of Turkish chestnut morphometrics, carbon

(Castanea sativa ). isotype discrimination,

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



331 Villan F., Sansott A., 199.. Genetic structure of natural populations Journal of Castanea sativa ,

Cherubini M., Cesaroni of Castanea sativa in Turkey: eidence of Evolutionary allozymes, hybrid zone,

D., Sbordoni V. a hybrid zone. Biology (in genetic structure, gene

332 Vysny, J, Shvadchak, I, 1995 Genetic diversity and differentiation of Genetika 233-

press);12:31 flow, forest treesgenetic

Fagus sylvatica, Two sets of European beech populations

Comps, B, et al. beech populations (Fagus sylvatica L) in (11): 1540- differentiation, forest from the western Ukraine, consisting of

western Ukraine 1551 trees eight and twelve populations, were

333 Ye T.Z., Yang R-C., and 2002 Population structure of a lodgepole pine Genome 45: introgression, RAPD analyzed using thirteen andstructure of a

We studied the population twelve

Yeh F.C. (Pinus contorta) and jack pine (P. 530–540 DNA, lodgepole–jack lodgepole (Pinus contorta Dougl.) and

banksiana) complex as revealed by pine complex, natural jack pine (Pinus banksiana Lamb.)

Supplemental mass pollination DNA

334 Yazdani, R., Hadders G. 1986 random amplified polymorphic in a seed Scand. J. For. hybridization, forest

Pinus sylvestris , seed complex in west central Alberta and

and Szmidt, A. E. orchard of Pinus sylvestris L. Res. 1: 309- orchard, pollination,

investigated by isozyme analyses. 315. isozymes, forest trees

335 Yazdani, R., Lindgren, 1989 Gene dispersion within a population of Scand. J. For. Natural population,

D. and Stewart, S. Pinus sylvestris . Res. 4: 295- isozymes, gene

306. dispersion, pollen

336 Yazdani, R., Yeh, 1995 Genomic mapping of Pinus sylvestris Forest dispersal, selfing,RAPDs,

Pinus sylvestris , forest

F.C.and Rimsha, J. (L.) using random amplified Genetics 2(2): linkage, forest trees

polymorphic dna markers. 109-116.

337 Yeh, F.C. Chong, 1995 RAPD variation within and among Journal of RAPD, Populus, forest This article described the population

D.K.X. and Yang, R.-C. natural populations of trembling aspen Heredity 86: trees structure of trembling aspen (Populus

(Populus tremuloides Michx.) from 454-460 tremuloides Michx.) in Alberta, a

338 Yin T., Zhang X., 2002 alberta. linkage maps of the Populus Genome 45: AFLP, Genetic map,

Molecular dioecious tree with continuous and wide

We report molecular genetic linkage maps

Huang M., Wang M., genome 541–555 poplar, RAPD, SSR, for an interspecific hybrid population of

Zhuge Q, Tu S., Zhu L- forest trees Populus, a model system in forest-tree

Yu Q., R.

339 H., WuLi B., Nelson 2006 Association of the cad-n1 allele with TREE Cinnamyl alcohol biology. The hybrids were produced by

Stem growth and wood density associated

C.D., McKeand S.E., increased stem growth and wood density GENETICS & dehydrogenase, half- with a mutant null (cad-n1) allele were

Batista V.B. and Mullin in full-sib families of loblolly pine GENOMES 2 diallel mating, null examined in three 15-year-old loblolly

340 J.T.

Wadenbäck J., Clapham 2005 Comparison of standard exponential and (2): 98-108

BMC mutation, heterozygotes,

Pinus taeda, cDNA pine half-diallel tests established on two

Background: The need to perform

D.H., Craig D., Sederoff linear techniques to amplify small cDNA Genomics 6: microarrays, forest trees microarray experiments with small

R., Peter G.F., von samples for microarrays 61 amounts of tissue has led to the

Arnold S., and development of several protocols for

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



341 Valbuena-Caraba M., 2007 Fine-scale spatial genetic structure in Molecular fine-scale spatial genetic Oaks are model species for the study of

Gonzales-Martines S.C., mixed oak stands with different levels of Ecology 16 structure, historical gene natural introgressive hybridization. High

Hardy O.J.. hybridization. (6): dispersal, hybrid zones, interfertility among oak taxa might result

342 Welling A., Moritz T., 2002 Independent Activation of Cold 1207–1219

Plant introgression,

transgenic hybrid aspen, in collective evolution, through

Temperate zone woody plants cold

Palva .T., and Junttila Acclimation by Low Temperature and Physiology cold aclimation, GMO, acclimate in response to both short

O. Short Photoperiod in Hybrid Aspen 129: forest trees daylength (SD) and low temperature (LT).

343 Whetten R., Sun Y-H., 2001 Functional genomics and cell wall 1633–1641

Plant EST sequencing, We were pine (Pinus taeda L.) is twomost

Loblolly able to show that these the

Zhang Y. and Sederoff biosynthesis in loblolly pine Molecular microarrays, Pinus taeda, widely planted tree species in the USA

R. Biology 47: xylogenesis, wood and an important tree in commercial

344 Whetten R., Chaparro J, 1993 Somatic mutation in woody plant 275–291

J Cell formation, forest trees

forest trees forestry world-wide. The large genome

-

Werner D. Omalley D., development and evolution Biochem : 47-

Sederof R. 47 Suppl. 17B

345 Whiteley R.E. 2004 Quantitative and molecular genetic JAN 26

Doctoral Adaptive, conservation, Genetic diversity is a prerequisite for

variation in Ulmus laevis Pall. thesis. microsatellite, evolutionary change. The conservation of

Swedish phenotypic plasticity, genetic diversity within species is

346 Wilcox P.L., Carson 2001 Benefit–cost analysis of DNA marker- University of

Can. J. For. QTL, MAS, Ulmus

quantitative, Pinus therefore important in order to ensure the

The financial viability of DNA marker-

S.D., Richardson T.E., based selection in progenies of Pinus Res. 31: radiata, forest trees based within-family selection (MBS)

Ball R.D., Horgan G.P. radiata seed orchard parents 2213–2224 compared with full-sib family forestry was

Williams, P.

347 and CarterC.G., 1995 Genetic diversity levels in an advanced- Forest Genetic forest trees evaluated for Pinus radiata Donn. ex D.

Hamrick, J.L. generation Pinus taeda L. program Resources No.

measured using molecular markers. 23: 45-

348 Williams, C.G., and 1992 Conifer wood quality and marker- aided 50.FAO,

Can. J. For. forest trees Using marker-aided selection for

Neale, D.B. selection: a case study. Res. 22: 1011- improving wood specific gravity in

1019 loblolly pine (Pinustaeda L.) could shorten

349 Wu, R., Ma, Ch.-X., 2002 Mapping epigenetic quantitative trait loci Genome 45: Genetic variation in a and improve

Epigenetic modification, the generation intervalquantitative trait

Zhu, J., and Casella, G. (QTL) altering a developmental 28–33. development, marker, that changes with age is important to both

trajectory. poplar, QTL, forest trees evolutionary biologists and breeders. A

350 Wu, J., Krutovskii, 1999 Nuclear DNA diversity, population Genome 41, We studied nuclear gene dynamics of

Allozymes, dominance, traditional analysis of thediversity and

K.V., and Strauss, S.H. differentiation, and phylogenetic 893-908. gene diversity, Pinus population dif9fe0r8entiation using 91–98

relationships in the California closed- attenuata, Pinus randomly amplifiedpolymorphic DNA

cone pines based on RAPD and allozyme muricata, Pinus radiata, (RAPD) loci in the California closed-cone

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



351 Wu, R, Bradshaw, HD, 1997 Molecular genetics of growth and Am J Bot 84 growth; leaf trait; linkage We examined the genetic variation of leaf

Stettler, RF development in Populus (Salicaceae) .5. (2): 143-153 map; Populus; morphology and development in the 2-yr-

Mapping quantitative trait loci affecting quantitative trait loci old replicated plantation of an

352 Wu, R, Bradshaw, HD, 1998 leaf variation quantitative genetics of

Developmental Theor Appl (QTL) mapping;

Genetic correlation, interspecific hybrid pedigree of were

Nursery growth and dry weight Populus

Stettler, RF growth in Populus Genet 97 (7): growth, Populus, analyzed for F2 genotypes derived from

1110-1119 Quantitative trait locus, Populus trichocarpa2P. deltoides that have

353 Wunsch A. and 2002 Molecular characterisation of sweet Heredity 89: QTL, seedling, forest

cultivar identification; been field 76 sweet cherry genotypes were

A total of tested with clonal replicates in

Hormaza J cherry (Prunus avium L.) genotypes 56–63 fingerprinting; SSR screened with 34 microsatellite primer

using peach [Prunus persica (L.) Batsch] transferability; molecular pairs previously developed in peach.

354 Zanetto, A., Roussel, 1994 SSR sequences

Geographic variation of inter-specific Forest Quercus microsatellites,

markers; petraea , Amplification of SSR loci was obtained

G.and Kremer, A. differentiation between Quercus robur Genetics 1(2): Quercus robur ,

L. and Quercus petraea (Matt.) Liebl. 111-123. aallozymes, genetic

355 Zhang, D.-X., Hewitt, 2003 Nuclear DNA analyses in genetic studies Molecular differentiation, forest

DHPLC, mitochondrial, Population-genetic studies have been

G. of populations: practice, problems and Ecology 12: microsatellite, nuclear remarkably productive and successful in

prospects. 563 -584. SNP, rate of evolution, the last decade following the invention of

356 Žiauka, J. and Kuusienė, 2006 Changes in Development of European Baltic Forestry recombination, forest

larch, bud development, PCR technology and the introduction of

Effects of exogenously applied auxins and

S. Larch (Larix decidua Mill.) Vegetative 12 (2): 141- cytokinins, auxins, cytokinins on morphogenesis of European

Buds Induced by Plant Hormones. 150 gibberellin, phase larch vegetative buds collected from 40-

357 Žvingila, D., Verbylaitė, 2005 Genetic diversity (RAPD) in natural Biologija 3: change, diversity, RAPD

genetic forest trees year-old tree were investigated using plant

Randomly amplified polymorphic DNA

R., Baliuckas, V., Lithuanian populations of common ash 46–53. markers, Fraxinus (RAPD) analysis was used to examine the

Pliūra, A., Kuusienė, S. (Fraxinus excelsior L.). excelsior, population genetic diversity and structure of ten

358 Žiauka J., Kuusienė S. 2007 Illumination-dependent effects of Biologija 1: structure, forest trees

Gibberellin, Larch, bud natural Lithuanian common ash (Fraxinus

Some morphological differences were

gibberellin on in vitro developing 69–74 explant, photoperiod, observed between European larch shoots

European larch shoots forest trees developing from isolated axillary buds

359 Vettori C., Vendramin 2004 Geographic distribution of chloroplast Theor Appl Fagus sylvatica, beech, The distribution of chloroplast decade

(buds were collected in the firstDNA of

G.G., Anzidei M., variation in Italian populations of beech Genet 109 (1): cpDNA, forest trees (cpDNA) variation in Italian beech (Fagus

Pastorelli C., Paffetti D. (Fagus sylvatica L.) 1-9 sylvatica L.) populations was studied

360 and Giannini R

Sari-Gorla M., 1999 Genetic analysis of drought tolerance in Theoretical Zea mays L · Maize · using PCR-RFLP and microsatellite

Drought is a serious agronomic problem,

Krajewski P., Di Fonzo maize by molecular markers. II. Plant and Applied Drought Molecular and one of the most important factors

N., Villa M., Frova C. height and flowering Genetics 99: markers · Flowering · contributing to crop yield loss. In maize

289-295 Linkage analysis grown in temperate areas, drought stress

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



361 Messmer M. M., 2000 Genetic analysis of durable leaf rust Theoretical Triticum aestivum · QTL Quantitative resistance that delays the

Seyfarth R., Keller M., resistance in winter wheat and Applied · Leaf rust · Durable epidemic development of leaf rust in

Schachermayr G., Genetics 100resistance · Leaf-tip wheat is an important source for durable

362 Winzeler M., Zanetti

Korzun V., Röder M. 1998 Genetic analysis of the dwarfing gene Theoretical Microsatellites - Marker resistanceof single chromosomewinter

necrosis Two sets breeding. The Swiss

S., Ganal M. W., (Rht8) in wheat. Part I. Molecular and Applied assisted breeding - recombinant lines comparing 2D

Worland A. J., Law C. mapping of Rht8 on the short arm of Genetics 96 Dwarfing gene (Rht8) - chromosomes from the wheat varieties

363 N. M., Sasaki T.

Yano 1997 Genetic and 2D of bread wheat

chromosomemolecular dissection of Plant Wheat traits - linkage - ‗Ciano 67‘ and ‗Mara‘ generation of a

Recent progress in the with the common

complex

quantitative traits in rice Molecular molecular marker - molecular genetic map and markers for

Biology 35: Oryza sativa - positional rice has made possible a new phase of

364 Feuillet C., Messmer 1995 Genetic and physical characterization of 145-153 and

Molecular cloning - QTL analysis mapping individual genes associated with

Leaf rust - RFLP - The objective of this study was to

M., Schachermayr G., theLR1 leaf rust resistance locus in General Sequence-tagged-site characterize the leaf rust resistance

Keller B. wheat (Triticum aestivum L.) (STS) - Wheat -

Genetics 248: locusLr1 in wheat. Restriction fragment

365 Louie R., Findley W. R., 1991 Genetic basis of resistance in maize to 553-562

Crop ScienceResistance disease

; genetics; gene length dwarf mosaic (MDM) is a

Maize polymorphism (RELP) analysis was

Knoke J. K., McMullen five maize dwarf mosaic virus strains. 31: 14-18. resistance; {Q2}; maize widespread viral disease of maize (Zea

M. D. dwarf mosaic virus; Zea mays L.) in the southern U.S. Corn Belt.

366 Xiao J., Li J., Yuan L., 1996 Genetic diversity and its relationship to TAG mays- Heterosis -

Rice An understanding of the genetics for six

Ten elite inbred lines (four japonica,

McCouch S. R., hybrid performance and heterosis in rice Theoretical RAPDs - Microsatellites - indica), chosen from those widely used in

Tanksley S. D. as revealed by PCR-based markers and Applied Genetic distance the hybrid rice breeding program at

367 Marsan P. A., The challenge Rice Research Center

1998 Genetic diversity and its relationship to Genetics 92: DNA polymorphisms · Human Hybridto maize breeders is to in

Theoretical

Castiglioni P., Fusari hybrid performance in maize as revealed and Applied Genetic distances · identify inbred lines that produce highly

F., Kuiper M., Motto by RFLP and AFLP markers Genetics 96: Molecular markers · heterotic hybrids. In the present study we

368 M.

Baum B. R., Nevo E., 1997 Genetic diversity in wild barley 219-227

Genetic Genetic polymorphism We analyzed the divergence among 88

Yield prediction · Zea - surveyed genetic genetic diversity in13

Johnson D. A., Beiles (Hordeum spontaneum C. Koch) in the Resources and wild barley - Hordeum genotypes from 20 populations of wild

A. Near East: a molecular analysis using Crop spontaneum barley (Hordeum spontaneum C. Koch)

369 Rani V., Raina S. N. Genetic Amplified Polymorphic DNA Evolution

Randomfidelity of organized meristem- In Vitro 44: enhanced axillary The Israel, Turkey and Iran, by randomly

fromcommercial multiplication of a large

derived micropropagated plants: A Cellular & branching - genetic number of diverse plant species represents

critical reappraisal Developmenta analysis - one of the major success stories of

370 Marhic A., Antoine- 1998 Genetic improvement of anther culture l Biology -

Theoretical Anther culture - Maize - urilizing tissueandrogenetic in vitro

micropropagation - Two cycles of culture technology

Michard S., Bordes J., response in maize: relationships with and Applied Breeding - Molecular doubled haploid (DH) plant production

Pollacsek M., molecular, Mendelian and agronomic Genetics 97: markers - Agronomic and intermating were implemented in an

Murigneux A., Beckert traits 520-525 traits experimental synthetic population of

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



371 Kumar V., Davey M. 1991 Genetic improvement of legumes using Euphytica 55: gene transfer - genetic The merits and limitations of somatic cell

R. somatic cell and molecular techniques 157-169 manipulation - chimaeric techniques involving Agrobacterium-

genes - legumes - mediated transformation, direct gene

372 Harding K. 2004 Genetic integrity of cryopreserved plant Cryoletters 25: transformation - somatic transfer and protoplast fusion, are for

Conservation, Cryopreservation techniques exist

cells: A review 3-22(20) cryobionomics, some 100 plant species. Cryopreservation

cryopreservation, enetic for the long-term conservation of in vitro

373 Jacobs J. M. E., Van 1995 genetic map of potato (Solanum TAG A genetic map of in the exposure

stability, plants markers - germplasm resultspotato (Solanum of

Morphological

Eck H. J., Arens P., tuberosum ) integrating molecular Theoretical Isozymes - Non-inbred tuberosum L.) integrating molecular

Verkerk-Bakker B., Te markers, including transposons, and and Applied species - Combined map - markers with morphological and isozyme

374 Lintel Hekkert B.,

Bolibok H., Rakoczy- Genetic markers

2006 classicalMapping of QTLs for Tissue- Plant regeneration from using a tissues

Genetics 91: JoinMap marker - QTL markers was constructedcultured backcross

Euphytica molecular

Trojanowska M. Culture Response in Plants Volume 149, analysis - regeneration has been shown to be under genetic

Numbers 1-2: ability - tissue culture control in a number of plant species.

375 Bohn M., Utz H. F., 1999 Genetic similarities among winter wheat 73-83Sci

Crop response

winter wheat, RFLPs, Using quantitative trait lociprograms could

The efficiency of breeding (QTL)

Melchinger A. E. cultivars determined on the basis of 39:228-237 AFLPs, SSRs, Genetic be increased by predicting the prospects of

RFLPs, AFLPs, and SSRs and their use similarities crosses for line development before

376 Desgagnés R., Laberge 1995 for predicting progeny variance

Genetic transformation of commercial Plant Cell, Agrobacterium producing and testing lines derived from

Bio-engineering technologies are now

S., Allard G., Khoudi breeding lines of alfalfa (Medicago Tissue and tumefaciens - genetic routinely used for the genetic

H., Castonguay Y., sativa ) Organ Culture transformation - improvement of many agricultural crops.

Zhang S., Michaud

377 Lapointe J.,Cho M.-J., 1999 Genetic transformation of commercial 42: 129-140

Plant Cell Medicago sativa - PCR However, breeding lines of Medicago

Barley ( Hordeum Genetic transformation using shoot

Koprek T., Yun R., cultivars of oat (Avena sativa L.) and Reports 18: vulgare L.) · Oat ( Avena meristematic cultures (SMCs) derived

Bregitzer P., Lemaux P. barley (Hordeum vulgare L.) using in 959-966 sativa L.) · Shoot from germinated seedlings is established

378 G.

Franklin C. I., Trieu T. Genetic transformation of green derived

1993 vitro shoot meristematic culturesbean Plant Cell Green bean - Phaseolus in commercial varieties of oat cv 'Garry'

meristematic culture · Kanamycin resistant callus was produced

N., Cassidy B. G., callus via Agrobacterium mediated DNA Reports 12 : vulgaris L - Genetic from leaf disc or hypocotyl expiants of

Dixon R. A., Nelson R. transfer 74-79 transformation - Stable green bean (Phaseolus vulgaris L.) when

379 S.

Kuchuk N., 1990 Genetic transformation of Medicago Plant Cell integration - chalcone

Medicago, cultured on a defined medium containing

Shoot and leaf segments of a non-

Komarnitski I., species by Agrobacterium tumefaciens Reports 8: Agrobacterium regenerable Medicago sativa L. genotype

Shakhovsky A., Gleba and electroporation of protoplasts 660-663 tumefaciens, were cocultivated with the shooty mutant

380 Y.

Guerche P., Jouanin L., 1987 Genetic transformation of oilseed rape Molecular and electroporation of

Brassica napus - of Agrobacterium tumefaciens carrying

transformed repeseed (Brassica napus )

Tepfer D., Pelletier G. (Brassica napus ) by the Ri T-DNA of General Agrobacterium roots were obtained by in vitro inoculation

Agrobacterium rhizogenes and analysis Genetics 206: rhizogenes - Genetic of excised stem segments with

of inheritance of the transformed 382-386 transformation - Genetic Agrobacterium rhizogenes. Axenic root

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



381 Lecardonnel A., Prévost 1999 Genetic transformation of potato with Molecular transgenic potato; Little is known about the effect of

G., Beaujean A., nptII-gus marker genes enhances foliage Breeding 5: Colorado potato beetle; transgenic plants containing commonly

Sangwan R. S., consumption by Colorado potato beetle 441-451 marker gene; foliage used marker genes, such as aph(3)II (nptII

Yamada T., Forster S.

382 Sangwan-Norreel B.J. 2005 larvae and molecular breeding in

Genetics Grassland consumption

Lolium, Festuce, encoding neomycinphosphotransferase)

Perennial ryegrass (Lolium perenne ) and

W., Humphreys M. W., Lolium/Festuca grass species complex Science Molecular breeding Italian ryegrass (L. multiflorum) are

Takamizo T. 51: 89-106 regarded as ideal grass species for use as

383 Drossou A., Katsiotis 2004 Genome and species relationships in TAG Avena, Genome, species, animal forage in temperate grassland

Species and genome relationships among

A., Leggett J. M., genus Avena based on RAPD and AFLP Theoretical relationship, RAPD, 11 diploid (A and C genomes), five

Loukas M.,Tsakas S. molecular markers and Applied AFLP tetraploid (AB and AC genomes) and two

384 Chen X. M., Line R. F., 1998 Genome scanning for resistance-gene Genetics 109:

Theoretical Candidate genes - hexaploid (ACD genome) Avena taxa

Genes cloned from diverse plants for

Leung H. analogs in rice, barley, and wheat by and Applied Disease resistance genes - resistance to different pathogens have

high-resolution electrophoresis Genetics 97: Germplasm diversity - sequence similarities in domains

385 Berrios E.F., Sarrafi A., 2000 Genotypic variation and chromosomal 345-355

Theoretical Host-pathogen

AFLP - Recombinant presumably involved in pathogen to

The present study was conducted

Fabre F., Alibert G., location of QTLs for somatic and Applied inbred lines - Somatic identify the genetic factors controlling

Gentzbittel L. embryogenesis revealed by epidermal Genetics 101: embryogenesis - somatic embryogenesis in the sunflower.

386 Campion B., Bohanec 1995 Gynogenic lines of onion (Allium cepa 1307-1312

layers culture of recombinant inbred Theoretical Sunflower - QTL Haploid induction via of embryogenic

Gynogenesis - Isozyme - Two traits, the numbergynogenesis offers

B., Javornik B. L.): evidence of their homozygosity and Applied RAPD - Agronomic the possibility of using doubled haploid

Genetics 91: evaluation - (DH) inbred lines in onion breeding. A

387 Snape J. W. 1998 Golden calves or white elephants? 598-602

Euphytica Wheat, biotechnologies, The 1990s have originated from the in

Gametoclonal variation - first DH line thatseen an acceleration open-

Biotechnologies for wheat improvement 100: 207-217 improvement,molecular the development of new biotechnologies

marker systems which can increase the efficiency of wheat

388 Maluszynski M., 2001 Heterosis in crop mutant crosses and Euphytica Heterosis appearing in crosses novel

mutant heterosis - barley - breeding by providing new andbetween

Szarejko I., Barriga P., production of high yielding lines using 120: 387-398 deleterious mutations - mutants derived from the same parent

Balcerzyk A. doubled haploid systems semidwarfness - doubled variety and crosses of mutants with parent

389 Tanksley D., Ganal J. 1992 Tomato, - anther

High Density Molecular Linkage Maps Genetics 132: haploids Potato, culture - varieties has been observed by many

High density molecular linkage maps,

V., Prince J. P., De- of the Tomato and Potato Genomes 1141-1160 geneomes, molecular comprised of more than 1000 markers

Vicente M. C., linkage maps with an average spacing between markers

390 Bonierbale M. W.,R. P.

Bush A. L., Wise 1998 High-resolution mapping adjacent to the Molecular bacterial artificial of approximately 1.2 cM (ca. 900 kb), of

The D526-derived BC1F2 population

Pc71 crown-rust resistance locus in Breeding 4: 13- chromosome (BAC) - hexaploid oat segregates for resistance to

hexaploid oat 21 Gramineae - oat crown crown rust isolate 345. A mapping

rust - Puccinia coronata - population consisting of 440 F2

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



391 Ahn S., Anderson J. A., 1993 Homoeologous relationships of rice, Molecular and Comparative maps - A set of cDNA clones, which had

Sorrells M. E., wheat and maize chromosomes General Dysploidy decrease - previously been mapped onto wheat

Tanksley S. D. Genetics 241: Translocation chromosomes, was genetically mapped

392 Kolb F. L., Baib G. H., 2001 Host Plant Resistance Genes for 483-490

Crop Science Wheat, barley, onto the chromosomes of rice. The by

Fusarium head blight (FHB), caused

Muehlbauerc G. J., Fusarium Head Blight 41:611-619 Resistance Genes, Fusarium graminearum Schwabe

Andersonc J. A., Fusarium Head Blight [teleomorph Gibberella zeae (Schwein.)],

Sledge K. K., Bouton J.

393 Smithc M. P., Fedakd G. 2002 Identification and Confirmation of Crop Sci. Medicago sativa, or scab, causes severeto liming is in yield

1986). An alternative reductions the

H., Dall‘Agnoll M., Aluminum Tolerance QTL in Diploid 42:1121–1128 Aluminum Tolerance, breeding of plants The acid, aluminum

Parrott W. A., Kochert Medicago sativa subsp. Coerulea QTL (Al) toxic soils found throughout the USA

394 G.

Schachermayr G., 1994 Identification and localization of Theoretical Leaf rust, RAPD, RFLP - are

Near-isogenic lines (NILs) for the leaf rust

Siedler H., Gale M. D., molecular markers linked to the Lr9 leaf and Applied Triticum aestivum, resistance gene Lr9 were screened for

Winzeler H., Winzeler rust resistance gene of wheat Genetics Triticum spelta polymorphisms at the molecular level.

Mago R., B.

395 M., KellerSpielmeyer 2002 Identification and mapping of molecular 88:110-115

Theoretical 1RS, AFLP, Gabo RAPD (random amplified polymorphic

The short arm of rye (Secale cereale)

W., Lawrence G., markers linked to rust resistance genes and Applied 1BL·1RS, Gabo chromosome 1 has been widely used in

Lagudah E., Ellis J., located on chromosome 1RS of rye using Genetics 104, 1DL·1RS, Imperial rye, breeding programs to incorporate new

396 Pryor A. Henry R. J.

Holton., 2002 wheat-rye translocation lines

Identification and mapping of Molecular Expressed Resistance

Petkus rye,sequence tag - disease resistance genes into wheat. Using

The growing availability of EST

polymorphic SSR markers from Breeding 9: 63- Marker - Microsatellite - sequences from a range of crop

expressed gene sequences of barley and 71 Simple sequence repeat plantsprovides a potentially valuable

397 Cherukuri D. P., Gupta 2003 wheat

Identification of a molecular marker Plant Breeding Agropyron elongatum, source ofrust resistance gene Lr19,

The leaf new DNA markers. We have

S. K., Charpe A., Koul linked to an Agropyron elongatum- 122 (3): wheat, Lr19, leaf rust transferred from Agropyron elongatum

S., Prabhu K. V., Singh derived gene Lr19 for leaf rust resistance 204–208. into wheat (Triticum aestivum L.) imparts

Yu K., Pauls M. R.,

398 R. B., Haq Q.K. P. 1993 in wheat

Identification of a RAPD marker Plant The current all pathotypes of leaf rust

alfalfa - linked random resistance tostudy was conducted to

associated with somatic embryogenesis Molecular amplified polymorphic identify random amplified polymorphic

in alfalfa Biology 22: DNA marker - somatic DNA (RAPD) markers linked to genes

399 Penner G. A., Chong J., 1993 Identification of a RAPD marker linked 269-277

Theoretical embryogenesis

Polymerase chain controlling somatic embryogenesis in

The feasibility of identifying molecular

Lévesque-Lemay M., to the oat stem rust gene Pg3 and Applied reaction - Disease markers linked to disease resistance genes

Molnar S. J., Fedak G. Genetics 85: resistance loci - Oat in oats was investigated utilizing random

400 Naik S., Gill K. S., 1998 Identification of a STS marker linked to 702-705

Theoretical RAPD RAPD primers

DNA - - STS marker - - primers in conjunction with polymerase

A sequence-tagged-site (STS) marker is

Prakasa Rao V. S., the Aegilops speltoides-derived leaf rust and Applied Leaf rust resistance gene - reported linked to Lr28, a leaf rust

Gupta V. S., Tamhankar resistance gene Lr28 in wheat Genetics Lr28 - Wheat resistance gene in wheat. RAPD (random

S. A., Pujar S., Gill B. 97:535-540 amplified polymorphic DNA) analysis of

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



401 Hartl L., Mohler V., 1999 Identification of AFLP markers closely Genome 42: Triticum aestivum, A total of 7654 DNA fragments were

Zeller F. J., Hsam S. L. linked to the powdery mildew resistance 322–329 powdery mildew, disease screened for linkage to wheat powdery

K., Schweizer G. genes Pm1c and Pm4a in common wheat resistance, AFLP, bulked mildew resistance gene Pm1c

402 Stuber C. W., Lincoln 1992 (Triticum aestivum L.) Factors

Identification of Genetic Genetics 132: segregant analysis

maize, genetic factors, employing molecular markers to identify

The use of fluorescently based AFLP

S. E., Wolf D. W., Contributing to Heterosis in a Hybrid 823-839 hybrid, imbred lines quantitative trait loci (QTLs) affecting

Helentjaris T., Lander From Two Elite Maize Inbred Lines agriculturally important traits has become

403 E. S.

Ivic-Haymesa S.D., Using Molecularhighly regenerative

Identification of Markers In Vitro Beta vulgaris, a key approach in plant genetics-both for

Development of an efficient

Smigockia A.C. plants with sugar beet (Beta vulgaris L.) Cellular and embryogenesis, genetic transformation method for recalcitrant

breeding lines for molecular breeding Developmenta variability, regeneration crops such as sugar beet (Beta vulgaris L.)

404 Chen Y., Hausner G., 1998 Identification of microspore-derived l Biology -

Plant Cell capacity

Anther culture · Flax · The microspore origin of of germplasm

depends on identification anther-culture-

Kenaschuk E., plants in anther culture of flax (Linum Reports 18: ISSRs · Linum derived plants of flax was determined

Procunier D., Dribnenki usitatissimum L.) using molecular 44-48 usitatissimum · RAPDs using inter-simple sequence repeat (ISSR)

405 P., Penner G. C. A.,

Liub S., Griffey 2001 markers

Identification of Molecular Markers Crop Science Wheat, powdery and randomly amplified polymorphic

Powdery mildew, caused by Blumeria

Maroofa M. A. S. Associated with Adult Plant Resistance 41:1268-1275 mildewm adult plant graminis (DC.) E.O. Speer f. sp. tritici Em.

to Powdery Mildew in Common Wheat ressitance, molecular Marchal (syn. Erysiphe graminis f. sp.

406 Wight C. P., Kibite S., 2006 Cultivar Massey molecular markers for

Identification of TAG The degree of aluminium diseases of

markers oat, aluminum, tritici), is one of the majortolerance varies

Diploid

Tinker N. A., Molnar S. aluminium tolerance in diploid oat Theoretical tolerence, molecular widely across cereal species, with oats

J. through comparative mapping and QTL and Applied markers (Avena spp.) being among the most

407 Robert O., Abelard C., 1999 analysis

Identification of molecular markers for Genetics 112: DNA markers, yellow

Molecular The Yr17 gene, which of this study was

tolerant. The objective is present in manyto

Dedryver F. the detection of the yellow rust Breeding rust resistance, Yr17 European wheat cultivars, displays yellow

resistance gene Yr17 in wheat 5:167-175 rust resistance at the seedling stage. The

408 Lin J. J., Kuo J., Ma J., Identification of molecular markers in Plant DNA fingerprinting - gene introducedDNAchromosome 2A

Three different into mapping

Saunders J. A., Beard H. soybean comparing RFLP, RAPD and Molecular Glycine max - PCR techniques—RFLP, RAPD and

S., MacDonald M. H., AFLP DNA mapping techniques Biology AFLP—were used on identical soybean

409 Cenci A., D'Ovidio G.

Kenworthy W., UdeR., 1999 Identification of molecular markers Reporter

Theoretical Triticum aestivum · germplasm to compare their ability to

RFLP, RAPD, STS and DDRT-PCR

Tanzarella O. A., linked to Pm13, an Aegilops longissima and Applied Aegilops longissima · techniques were applied to find molecular

Ceoloni C., Porceddu E. gene conferring resistance to powdery Genetics 98: Erisiphe graminis f.sp. markers linked to Pm13, an Aegilops

410 Schachermayr G. M., 1995 mildew in wheat molecular markers

Identification of 448-454

Theoretical Leaf · Resistance gene · The objective of this study resistance to

triticirust, RFLP, RAPD, longissima gene conferring was to identify

Messmer M. M., linked to the Agropyron elongatum- and Applied Wheat, Agropyron molecular markers linked to the wheat leaf

Feuillet C., Winzeler derived leaf rust resistance gene Lr24 in Genetics 90: elongatum rust resistance gene Lr24 derived from

H., Winzeler M., Keller wheat 982-990 Agropyron elongatum (3DL/3Ag

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



411 Sun G. L., Fahima T., 1997 Identification of molecular markers Theoretical Gene mapping - RAPD, The Yr15 gene of wheat confers resistance

Korol A. B, Turpeinen linked to the Yr15 stripe rust resistance and Applied RFLP, Stripe rust, to the stripe rust pathogen Puccinia

T., Grama A., Ronin Y. gene of wheat originated in wild emmer Genetics Triticum dicoccoides, striiformis West., which is one of the most

Endera E.

412 I., NevoM., Kellyb J. D. 2005 wheat, Triticum dicoccoides

Identification of QTL Associated with 95:622-628

Crop Sci Triticum durum White

Common Bean, devastating diseases by wheat throughout

White mold, caused of the necrotrophic

White Mold Resistance in Common 45:2482-2490 Mold Resistance, QTL fungus Sclerotinia sclerotiorum (Lib.) de

Bean Bary, is a serious disease of common bean

413 Xiao J., Li J., Yuan L., 1996 Identification of QTLs affecting traits of TAG Rice - Subspecies - To detect QTLs controlling use of

(Phaseolus vulgaris L.). Thetraitsof

Tanksley S. D. agronomic importance in a recombinant Theoretical Recombinant inbred agronomic importance in rice, two elite

inbred population derived from a and Applied population - Molecular homozygous lines 9024 and LH422, which

414 Jin H., Domier L. L., 1998 subspecific rice cross

Identification of Quantitative Loci for Genetics 92:

Phytopatholog markers - QTLs

Oat, QTL, tolerance, represent the indicalinked to quantitative

Molecular markers and japonica

Kolb F. L., Brown C. Tolerance to Barley Yellow Dwarf Virus y 88: 410-415 BYDV trait loci conditioning tolerance to barley

M. in Oat yellow dwarf virus (BYDV) were

415 Zhu S., Kaeppler H. F. 2003 Identification of Quantitative Trait Loci Crop Science Oat, resistance, QTL, identified in caused by the fungus Puccinia

Crown rust, oat (Avena sativa) using

for Resistance to Crown Rust in Oat Line 43:358-366 crown rust coronata Cda. f. sp. avenae Eriksson, is the

MAM17-5 most damaging disease of oat (Avena

416 Beavis W.D., Smith 1994 Identification of quantitative trait loci Crop science QTL, maize, topcross, sativabreeders have an interest in the

Plant L.). Breeding for resistance to

O.S., Grant D., Fincher using a small sample of topcrossed and 34: 882-896 per se evaluation identification of genomic regions

R. F[4] progeny from maize associated with the expression of

417 Araujo L.G., Prabhu 2002 IDENTIFICATION OF RAPD Fitopatol. 27 molecular markers, quantitative traits because they recognize

The gene Pi-ar confers resistance to

A.S., Filippi M. C. MARKER LINKED TO BLAST disease resistance, Pyricularia grisea race IB-45 in a

RESISTANCE GENE IN A somaclonal variation, somaclone derived from immature

418 Rokka V-M., Xu Y-S., Identification of somatic CULTIVAR

1994 SOMACLONE OF RICEhybrids of Euphytica 80: Pyricularia grisea subsp

Erwinia carotovora Symmetric the susceptible were produced

panicles of somatic hybridsrice (Oryza

Kankila J., Kuusela A., dihaploid Solanum tuberosum lines and 207-217 - atroseptica - by electrofusion of protoplasts of two

Pulli S., Pehu E. S. brevidens by species specific RAPD Phytophthora infestans - dihaploid tuber-bearing potato (Solanum

419 Armstrong C. L., Improved tissue culture of disease

1992 patterns and assessment response of an Theoretical PVY - RAPD - Solanum

Zea mays L. - Restriction tuberosum L.) lines and Solanum

The frequency of initiation of friable,

Romero-Severson J., elite maize inbred through backcross and Applied fragment length embryogenic callus from immature

Hodges T. K. breeding, and identification of Genetics 84: polymorphisms - Tissue embryos of the elite maize inbred line B73

420 Friedt W., Bickert C., 1995 chromosomal regions important for

In vitro breeding of high-linolenic, 755-762 Linum - Plant

Plant Breeding culture usitatissimum,In was increasedof a breeding programme for

In the course dramatically by

Schaub H. doubled-haploid lines of linseed (Linum 114: 322-326 vitro breeding, high-linolenic-acid linseed (oilflax, Linum

usitatissimum L.) via androgenesis androgenesis usitatissimum L.) doubled-haploid lines

(DH-lines) of three F1 hybrids were

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



421 Liu S., Wang H., 2005 In vitro mutation and selection of Plant Cell Brassica napus - Haploid This paper describes a new protocol to

Zhang J., Fitt B. D. L., Reports 24:

doubled-haploid Brassica napus lines somatic mutation and develop doubled-haploid (DH) Brassica

Xu Z., Evans N., Liu 133-144

with improved resistance to Sclerotinia selection - Resistance - napus lines with improved resistance to

Ozias-Akins Guo X.

422 Y.,Yang W.,P., Vasil I. 1988 sclerotiorum

In vitro regeneration and genetic Physiologia Sclerotinia sclerotiorum -

Grasses, invitro, Sclerotinia sclerotiorum. In this protocol,

Regeneration of plants from cultured cells

K. manipulation of grasses Plantarum 73: regeneration is an important and essential component of

565-569 plant biotechnology. Advances in the

423 Takahashi W., Fujimori 2005 Increased resistance to crown rust Plant Cell Disease resistance - We introduced the rice cultured (Cht-2;

recovery of plants fromchitinase cells and

M., Miura Y., Komatsu disease in transgenic Italian ryegrass Reports 23: Puccinia coronata - RCC2) gene into calli of Italian ryegrass

T., Nishizawa Y., Hibi (Lolium multiflorum Lam.) expressing 811-818 Particle bombardment - (Lolium multiflorum Lam.), with a

T., Takamizo T.

424 Ahloowalia B.S., 2001 the rice chitinase gene new paradigm in Euphytica

Induced mutations – A Pathogenesis-related in

induced mutations - The use of phosphotransferase (HPT)

hygromycinionizing radiation, such as X-

Maluszynski M. plant breeding 118: 167-173 vitro culture - molecular rays, gamma rays and neutrons and

markers - developmental chemical mutagens for inducing variation,

425 Christou P., Swain W. 1989 Inheritance and Expression of Foreign PNAS 86 : mutants Foreign

Syoybean, is well established. Inducedwere

DNA-coated gold particles mutations

F., Yang N-S., McCabe Genes in Transgenic Soybean Plants 7500-7504 Genes, Transgenic introduced into meristems of immature

D.E. Soybean soybean seeds using electric discharge

426 Puonti-Kaerlas J., 1992 Inheritance of a bacterial hygromycin Theoretical Transformation - Pisum particle acceleration to produce transgenic

An analysis of the progeny of primary

Eriksson T., Engström phosphotransferase gene in the progeny and Applied sativum - transgenic pea plants in terms of

P. of primary transgenic pea plants Genetics 84: Agrobacterium transmission of the transferred DNA,

427 Zhang F. L., Takahata 2001 Inheritance of microspore embryogenic 443-450

Theoretical tumefaciens - -

Diallel analysis fertility and of microspore embryogenic

Inheritance morphology is presented. A

Y. ability in Brassica crops and Applied Heritability - Microspore ability in oilseed rape (Brassica napus L.)

Genetics 103: embryogenesis - Oilseed and Chinese cabbage (Brassica

428 Amberger L. A., 1992 254-258

Inheritance of two independent isozyme Theoretical rape (Brassicanapus L.) -

Somaclonal variation - campestris L. ssp.max (L.) Merr.] plants

Soybean [Glycine pekinensis) was

Shoemaker R. C., variants in soybean plants derived from and Applied Tissue culture - Glycine were regenerated via somatic

Palmer R. G. tissue culture Genetics 84: max (L.) Merr. - embryogenesis from nine soybean

429 Polzin K. M., Lohnes 1994 The Journal of Isozymes Molecular

Integration of Rps2, Rmd, and Rj2 Into 600-607 Soybean, cultivars. Our objective was to identify

To correlate the classical soybean linkage

D. G., Nickell C. D., Linkage Group J of the Soybean Heredity Map, Linkage Group map with the USDA-ARS molecular map,

Shoemaker R. C. Molecular Map 85(4): 300-303 genes from the classical map must be

430 Pelletier G., Primard Intergeneric cytoplasmic hybridization in Molecular and Rapeseed, protoplasts, located relative to molecular markers. The

Rapeseed plants have been regenerated

C., Vedel F., Chetrit cruciferae by protoplast fusion General cytoplasmic after fusion between protoplasts bearing

P., Remy R., M. Genetics hybridization cytoplasms of different genera. Cybrids

Renard. combine, in a first experiment Brassica

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



431 Hu Q., Hansen L., 2002 Intergeneric hybrids between Brassica Theoretical Brassica napus, Fatty Protoplast fusions between Brassica napus

Laursen J., Dixelius C., napus and Orychophragmus violaceus and Applied acid composition, Male and Orychophragmus violaceus for

Andersen S. containing traits of agronomic Genetics 105: sterility, transfer of valuable traits to oilseed rape

432 Crossa J., Vargas M., 1999 importance for oilseed×rape breeding

Interpreting genotype environment 834-840

Theoretical Orychophragmus

Biplot · Factorial resulted in 257 somatic hybrid plants.

An understanding of the genetic and

Van Eeuwijk F. A., interaction in tropical maize using linked and Applied regression · Genetic environmental basis of

Jiang C., Edmeades G. molecular markers and environmental Genetics 99: marker · genotype2environment interaction (GEI)

433 O., Hoisington D. M.

Muñoza L. C., Blair 2004 covariables in Common Bean x Tepary

Introgression 611-625

Crop Sci. Genotype×environment is of fundamental importance in plant

Common Bean , Tepary Congruity and recurrent backcross

W., Duquea M. C, Bean Interspecific Congruity-Backcross 44:637-645 Bean, Introgression, interspecific hybrids between common

Tohmea J., Rocab W. Lines as Measured by AFLP Markers AFLP Markers bean (Phaseolus vulgaris L.) and tepary

434 Pestsova E., Ganal 2000 Isolation and mapping of microsatellite Genome 43: Aegilops tauschii, wheat, bean (P. acutifolius A. Gray) were

Abstract: The potential of Aegilops

M.W, Röder M.S. markers 689–697 molecular markers, tauschii, the diploid progenitor of the D

specific for the D genome of bread wheat genetic map, simple genome of wheat, as a source of

435 Wu S-C., Bögre L., 1988 Isolation of an alfalfa histone H3 gene: Plant sequence repeats.

codon usage - gene microsatellite gene wasfor hexaploid bread

A histone H3 markers isolated from a

Vincze É, Kiss G. B., structure and expression Molecular expression - histone H3 dicotyledonous plant, alfalfa (Medicago

Dudits D. Biology 11: gene - Medicago sativa - sativa). The sequence analysis of this gene

436 Doan D. N. P., 1996 Isolation of molecular markers from the 41-649

Plant barley - embryos

somatic endosperm The cereal obvious GC preference in

revealed noendosperm develops from aits

Linnestad C., Olsen O- barley endosperm coenocyte and the Molecular coenocyte - differential coenocyte to a cellular storage organ

A. surrounding nucellus cell layers Biology 31: screening - modified through formation of nucleo-cytoplasmic

437 Milbourne D., Meyer 1998 Isolation, characterisation and mapping 877-886 and

Molecular aleurone cells - nucellus- domains and cell wall deposition in the

Simple sequence repeat Solanum tuberosum L. DNA sequences

R. C., Collins A. J., of simple sequence repeat loci in potato General Linkage map - Single- containing simple sequence repeat (SSR)

Ramsay L. D., Genetics 259: strand hybridisation - motifs were extracted from the EMBL

Fransz P. C., Waugh R.

438 Gebhardt F., De Ruijter 1989 Isozymes as biochemical and 233-245

Plant Cell Triplex affinity capture - database,analysesand selectively enriched

Zea mays, embryogenic Isozyme cDNA were carried out on

N. C. A., Schel J. H. N. cytochemical markers in embryogenic Reports 8: 67- callus cultures, protein extracts of non-embryogenic and

callus cultures of maize (Zea mays L.) 70 embryogenic callus fromZea mays L.,

439 Tai G. C. C., Seabrook 2000 Linkage analysis of anther-derived Theoretical Gene mapping - Potato - using polyacrylamide gel electrophoresis.

Monoploids can be obtained from several

J. E. A., A. Aziz A. N. monoploids showing distorted and Applied Segregation ratio - diploid plant species by anther culture.

segregation of molecular markers Genetics 101: Solanum tuberosum L. Mapping of molecular markers using

440 Sourdille P., Perretant 1996 Linkage between RFLP markers and 126-130

Theoretical Kernel hardness - Wheat - monoploids is greatly facilitated by the

A molecular-marker linkage map of wheat

M. R., Charmet G., genes affecting kernel hardness in wheat and Applied RFLP - QTL - (Triticum aestivum L. em. Thell) provides

Leroy P, Gautier M. F., Genetics 93: Puroindoline a powerful tool for identifying genomic

Joudrier P., Nelson J. 580-586 regions influencing breadmaking quality.

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



441 Sourdille P., Charmet 1998 Linkage Between RFLP Molecular Hereditas 128: wheat, dwarfing genes, Identifying genotypes carrying the

G., Trottet M., Tixier Markers and the Dwarfing Genes Rht-B1 41-46, isozymes, markers dwarfing genes Rht-B1 and Rht-D1 would

M. H., Boeuf C., and Rht-D1 in Wheat be of great interest for wheat (Triticum

442 Barloy N. D., Bernard

Larson S. R., Young 1998 Linkage mapping of two mutations that Theoretical Barley - Mutations - aestivum L. em Thell) breeding. Two

This study describes the inheritance and

K. A., Cook A., Blake reduce phytic acid content of barley and Applied Phytic acid linkage map positions of two low phytic

T. K., Raboy V. grain Genetics 97 acid barley (Hordeum vulgare ) mutations,

443 O'DONOUGHUE L. S., 1996 Localization of stem rust resistance Phytopatholog oat, stem rust, resistance lpa1-1 and markersthat dramatically reduce

Molecular lpa2-1, have been identified in

CHONG J., WIGHT C. genes and associated molecular markers y 86: 719-727 genes, molecular markers cultivated oat for the Pg9 and Pg13 loci

P., FEDAK G., in cultivated oat conferring resistance to different races of

Giese H., S. J.

444 MOLNARHolm-Jensen 1993 Localization of the Laevigatum powdery Theoretical Barley leaf stripe - the stem rust pathogen, Puccinia graminis

The powdery mildew disease resistance

A. G., Jensen H. P., mildew resistance gene to barley and Applied Erysiphe graminis f.sp gene Ml(La) was found to belong to a

Jensen J. chromosome 2 by the use of RFLP Genetics 85: hordei - Heterodera locus on barely chromosome 2. We

445 Hayano-Saito Y., Tsuji 1998 markers

Localization of the rice stripe disease 897-900

TAG avena sativa - Stripe -

Oryza - Linkage map suggest that this locus be designated

We used graphical genotyping and linkage

T., Fujii K., Saito K., resistance gene, Stv-bi, by graphical Theoretical resistance gene - Genetic analyses with molecular markers to

Iwasaki M., Saito A. genotyping and linkage analyses with and Applied map - Molecular markers determine the chromosomal location of the

446 Champoux M. C., Locating markers

1995 moleculargenes associated with root Genetics 96:

Theoretical Drought, Rice - QTL rice stripe disease resistance gene, Stv-b i .

This research was undertaken to identify

Wang G., Sarkarung S., morphology and drought avoidance in and Applied analysis - Root and map quantitative trait loci (QTLs)

Mackill D. J., O'Toole rice via linkage to molecular markers Genetics 90: morphology - Molecular associated with five parameters of rice

447 J. C., Huang N., P.,

Sourdille P., Robe 1999 Location of Pm3g, a powdery mildew 969-981

Euphytica markers graminis -

Blumeria root morphology and to determine if these

A segregating population of doubled-

Tixier M., Doussinault resistance allele in wheat, by using a 110: 193-198 powdery mildew - QTL - haploid lines issued from the cross

G., Pavoine M., monosomic analysis and by identifying RFLPs - Triticum between the wheat (Triticum aestivum L.

Huanga M.

448 Bernard L., Brooksa S. Map-Based Cloning markers

2003 associated molecularof Leaf Rust leaf rust, - wheat

Genetics 164: aestivum wheat, Lr21, em. report the map-based cloning of the

We Thell) cultivars Courtot, resistant to

A., Lia W., Fellersb J. Resistance Gene Lr21 From the Large 655-664 molecular cloning leaf rust resistance gene Lr21, previously

P., Tricka H. N., Gilla and Polyploid Genome of Bread Wheat mapped to a gene-rich region at the distal

449 B. S. C., Travella S.,

Feuillet 2003 Map-based isolation of the leaf rust PNAS wheat, genome, leaf rust, More chromosome arm 1DS of (Lr)

end ofthan 50 leaf rust resistancebread

Stein N., Albar L., disease resistance gene Lr10 from the 100:15253- Lr10, genes against the fungal pathogen

Nublat A., Keller B. hexaploid wheat (Triticum aestivum L.) 15258 Puccinia triticina have been identified in

450 Nelso J.C., Sigh R.P., 1997 genome genes conferring and

Mapping Crop science wheat, leaf rust the wheat caused by Puccinia recondita

Leaf rust, gene pool, and a large number

Autrique J.E., Sorrells suppressing leaf rust resistance in wheat 37:1928-1935 resistance, mapping Roberge ex Desmaz. f. sp. tritici Eriks. &

M.E. genes E. Henn., is a serious disease of wheat

(Triticum aestivum L.) worldwide. We

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



451 Hirata M. M., Fujimori 2007 Mapping of EST-derived CAPS markers Plant Breeding lolium multiflorum, New molecular markers derived from

M. in Italian ryegrass (Lolium multiflorum 126: 353-360 CAPS markers expressed sequence tag (EST) sequences

Lam.) were mapped on linkage maps of Italian

452 Hsam S.L. K., Mohler 2000 Mapping of powdery mildew and leaf Plant breeding wheat, translocation, ryegrass by a two-way pseudo-testcross

Powdery mildew and leaf rust resistance

V., Hartl L., Wenzel rust resistance genes on the wheat-rye 119: 87-89 powdery mildew genes on the 1RS arm of the T1BL.1RS

G., Zeller F.J. translocated chromosome T1BL.1RS translocated chromosome were mapped in

453 Parka O. S.,. Coyne D. 2001 using molecular and biochemicalto White

Mapping of QTL for Resistance Crop Science Common Bean, White relation to the Sec-1incitedand Sclerotinia

White mold (WM), locus by AFLP and

P., Steadmanb J. R., Mold Disease in Common Bean 41:1253-1262 Mold Disease, QTL, sclerotiorum (Lib.) de Bary, is a serious

Skrochc P. W. mapping disease of common bean (Phaseolus

454 Börner A., Schumann 2002 Mapping of quantitative trait loci Theoretical Agronomic traits, A set of L.). recombinant inbred lines of

vulgaris 114 However, plant breeders have

E., Fürste A., Cöster determining agronomic important and Applied Genetic mapping, QTL, the 'International Triticeae Mapping

H., Leithold B., Röder characters in hexaploid wheat (Triticum Genetics 105: Disease resistance, Initiative' mapping population was grown

455 M., Weber W. E.Y.,

Sacco F., Suárez 1998 aestivum of the leaf rust resistance gene 921-936 41: MorphologicalLr3 gene, during the seasons 1997, 1998,race 66 of

Mapping L.) Genome wheat, RFLP, traits, The Lr3 gene for resistance to 1999 and

Naranjo T. Lr3 686–690 chromosome 6B, C- Puccinia recondita present in hexaploid

on chromosome 6B of Sinvalocho MA banding. wheat cv. Sinvalocho MA

456 Mckenzie N., Dale P. J. 2004 wheat of transposable element

Mapping Theoretical To mapped on chromosome

Brassica oleracea, plant wasinvestigate the potential of6B, using

Dissociation inserts in Brassica oleracea and Applied regeneration, heterologous transposons as a gene-

following plant regeneration from Genetics 109: streptomycin selection, tagging system in broccoli (Brassica

457 Taguchi-Shiobara F., 1997 Mapping quantitative of loci associated Theoretical

streptomycin selectiontraitcallus 333-341 callus

Regeneration ability - oleracea var. trait loci we have introduced a

Quantitative italica), (QTL) controlling

Lin S. Y., Tanno K., with regeneration ability of seed callus in and Applied QTL - Rice - Oryza the regeneration ability of rice seed callus

Komatsuda T., Yano rice, Oryza sativa L. Genetics 95: sativa L. - Seed callus were detected using 245 RFLP markers

458 M., Sasaki T., Oka S.

Ballvora A., Hesselbach 1995 Marker enrichment and high-resolution 828-833 and Potato - Solanum

Molecular The dominant lines Gro1 confers on

and 98 BC1F5allele derived from two

J., Niewöhner J., map of the segment of potato General tuberosum - Nematode potato resistance to the root cyst nematode

Leister D., Salamini F., chromosome VII harbouring the Genetics 249: resistance - Map-based Globodera rostochiensis. The Gro1 locus

Ghislain C.

459 GebhardtM., Zhang D., 1999 nematode resistance gene Gro1

Marker-assisted sampling of the 82-90

Genetic cloning

core collection - has been mapped to chromosome Andean

The potato crop originated in the VII on

Fajardo D., Huamán Z., cultivated Andean potato Solanum Resources and germplasm - molecular highlands where numerous farmer's

Hijmans R. J. phureja collection using RAPD markers Crop marker - potato - RAPD - varieties and non-cultivated wild species

460 Barker D. G., Bianchi 1990 Medicago truncatula , a model plant for Evolution 46: Solanum phureja

Plant symbiotic nitrogen exist. An Andean potato collection is held

Medicago truncatula has all the

S., Blondon F., Dattée studying the molecular genetics of the Molecular fixation - legume - characteristics required for a concerted

Y., Duc G., Essad S., Rhizobium -legume symbiosis Biology Medicago truncatula analysis of nitrogen-fixing symbiosis

Flament P., Gallusci P., Reporter 8: 40- withRhizobium using the tools of

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



461 McLean N.L., Nelke 1999 Meiotic Chromosome Pairing, Isozyme Annals of Trifolium pratenseL., red Red clover genotypes capable of

M., Nowak J., Wright Analyses and Ferritin Expression in a Botany 83: clover, ferritin, isozymes, regenerating plantletsin vitrofrom non-

J.M. Red Clover Mutant Capable of Somatic 315-323 meiosis, peroxidase, meristem-derived callus are rare. A

462 McCouch S. R., Chen 1997 Embryogenesis

Microsatellite marker development, Plant somatic embryogenesis

allelic diversity - previous study identified a tandemly

Microsatellites are simple, pair of near

X., Panaud O., mapping and applications in rice genetics Molecular microsatellite marker - repeated di- to tetra-nucleotide sequence

Temnykh S., Xu Y., and breeding Biology 35: 89- molecular mapping - motifs flanked by unique sequences. They

Suenaga K., Singh N.,

463 Cho Y. G., Huang R. P., 2003 Microsatellite Markers for Genes Phytopatholog polymerase chain

99 slow rusting, Triticum are valuable as genetic markers because

Huerta-Espino J., Lr34/Yr18 and Other Quantitative y 93:881-890. aestivum. Leaf rust and stripe rust, caused by

William H. M. Trait Loci for Leaf Rust and Stripe Rust Puccinia triticina and P. striiformis,

464 Peng J. H., Fahima T., 1999 Resistance in Bread Wheat stripe-rust

Microsatellite tagging of the Theoretical Genetic mapping · respectively, are important diseases of

Stripe rust caused by Puccinia striifomis

Röder M. S., Li Y. C., resistance gene YrH52 derived from wild and Applied Microsatellite marker · West. is one of the most devastating

Dahan A., Grama A., emmer wheat, Triticum dicoccoides, and Genetics Stripe-rust resistance · diseases relating to wheat production.

Hernández Korol A.

465 Ronin Y. I.,P., Dorado Microsatellites and crossover

2001 suggestive negative RFLP probes from 98:862-872

Theoretical Puccinia striiformis ·

Miscanthus · Wild emmerGramineae markers was

A survey of wheat, Triticum dicoccoides,

G., Laurie D. A., maize are efficient sources of molecular and Applied Microsatellite · RFLP · carried out with the aim of developing cost-

Martín A., Snape J. W. markers for the biomass energy Genetics 102: Maize · Biomass crop · effective methods for the molecular

466 Zhiponova M. K., 2006 Mitosis-Specific Promoter of the Alfalfa 616-622

Plant Diversity

Alfalfa, Mitosis-Specific analysis of Miscanthus species. Ten out of

Cyclin-dependent serine/threonine kinases

Pettkó-Szandtner A., Cyclin-Dependent Kinase Gene Physiology Promoter, Kinase Gene (CDKs) have pivotal roles in regulating

Stelkovics É., Neer Z., (Medsa;CDKB2;1) Is Activated by 140:693-703 the eukaryotic cell cycle. Plants possess a

Fedak S.,

467 BottkaG. Krenács T., Molecular and for integration of alien

1999 Wounding aids Ethylene in a Non-Cell Genome 42: Triticum aestivium, Abstract: Wide crosses in wheat have with

unique class of CDKs (B-type CDKs) now

chromatin through wide crosses 584–591 molecular markers, been performed for over 100 years. In that

disease resistance, gene time, approximately 100 genes

468 Guzy-Wróbelska, 2003 Molecular and agronomic evaluation of Plant Breeding introgression, haploid,

wheat, doubled Although transferred for numerous traits,

have beenmaize pollination (MP) and

Szarejko I. wheat doubled haploid lines obtained 122: 305-313 maize, pollination, anther culture (AC) are alternative

through maize pollination and anther anther culture techniques widely used for wheat doubled

469 Qureshi S. N., Saha S., 2004 culture methods and physiology EST- The Journal of Cotton, Molecular

Molecular biology haploidadvances in genomic technologies

Recent (DH) production, there is only

Kantety R. V., Jenkins SSR: A New Class of Genetic Markers Cotton biology, physiology, have

J. N. in Cotton Science Genetic Markers generated a large number of expressed

470 Zhu H., Briceño G., 1999 Molecular breeding for grain yield in 8:112–123

Theoretical Barley · Yield · Marker- sequence results from a breeding strategy

We report

Dovel R., Hayes P. M., barley: an evaluation of QTL effects in a and Applied assisted selection · QTL · designed to accumulate favorable QTL

Liu B. H., Liu C. T., spring barley cross Genetics 98: QTL×E alleles for grain yield identified in the

Ullrich S. E. 772-779 Steptoe2'Morex' (SM) barley germplasm.

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



471 Baird E., Cooper-Bland 1992 Molecular characterisation of inter and Molecular and Protoplasts - RAPDs - Protoplast fusion allows the transfer of

S., Waugh R., DeMaine intra-specific somatic hybrids of potato General Potato - Somatic hybrids - both mono- and polygenic traits between

M., Powell W. using randomly amplified polymorphic Genetics 233: Molecular markers species that are sexually incompatible.

472 Liu Z., Sun Q., Ni Z., 2002 DNA (RAPD) markers

Molecular characterization of a novel 469-475

Euphytica Powdery mildew caused by relevance

Erysiphe graminis f. sp. This approach has particularErysiphe for

Nevo E., Yang T. powdery mildew resistance gene Pm30 123: 21-29 tritici - Blumeria graminis f. sp. tritici is one of the most

in wheat originating from wild emmer graminis - Triticum important wheat diseases in many regions

473 Lukaszewski A .J., 1998 Molecular characterization of two Crop Sci dicoccoides -

Triticum speltoides, of theworld. A powdery mildew resistance

Resistance genes for leaf rust (Puccinia

Echaide M., Antonelli Triticum speltoides interstitial 38:1655-1660 Molecular recondita Rob. ex Desm.) and greenbug

E.F., Porter D.R. translocations carrying leaf rust and characterization, leaf rust (Schizaphis graminum Rondani) were

474 Binh L. T., Oono K. Molecular Cloning genes

1992 greenbug resistanceand Characterization Plant Polyadenylated chromosome 7S of

Rice, molecular cloning, transferred fromRNA was isolated and a

of Genes Related to Chilling Tolerance Physiology chiling tolerance cDNA library constructed from seedlings

in Rice 1 99:1146-1150 of a chilling-tolerant rice cultivar (Oryza

475 Feuillet C., 1997 Molecular cloning of a new receptor-like The Plant Wheat, leaf rust, sativa than 100 resistance cv Nipponbare).

More L. subsp. Japonica genes against

Schachermayr G., kinase gene encoded at the Lr10 disease Journal 11: 45- resistance locus, wheat rust pathogens have been described

Keller B. resistance locus of wheat 52 molecular cloning in wheat and its relatives. Although many

476 Spano A. J., He Z., 1992 Molecular cloning, nuclear gene Plant light-dependent pchlide of them have been extensively used in

Complementary DNA clones and a

Michel H., Hunt D. F., structure, and developmental expression Molecular reductase - lpcr - Pisum corresponding nuclear gene (lpcr)

Timko M. P. of NADPH: protochlorophyllide Biology 18: sativum - chlorophyll encoding the NADPH-dependent

477 Isenegger D. A., Taylor 2003 oxidoreductase in pea (Pisum sativum

Molecular detection of a bacterial 967-972

Plant Cell synthesis - marker,

Molecular chloroplast protochlorophyllide oxidoreductase

An aberrant random amplified

P. W. J., Mullins K., contaminant Bacillus pumilus in Reports 21: Diagnostic tool, polymorphic DNA (RAPD) marker in

McGregor, Barlass M., symptomless potato plant tissue cultures 814-820 Microbial contaminant genomic DNA of tissue culture plantlets

478 Hutchinson J. F. Rines

Milach S. C. K., 1997 Molecular genetic mapping of dwarfing TAG Avena sativa - Dwarfing was frequently observed during a

Restriction fragment length polymorphism

H. W., Phillips R. L. genes in oat Theoretical genes - RFLP - RFLP (RFLP) analysis provides a valuable tool

and Applied mapping - Bulked for characterizing and understanding

479 Hartl L., Weiss 1995 Molecular identification of powdery Genetics 95: Segregant Analysis-

Theoretical Mildew resistance relationships among genes for useful traits

RFLP markers for the wheat powdery

H.,Stephan U., Zeller mildew resistance genes in common and Applied Triticum aestivum Near- mildew resistance genes Pm1 and Pm2

F. J., Jahoor A. wheat (Triticum aestivum L.) Genetics 90: isogenic lines - Bulked were tagged by means of near-isogenic

480 Ma J., Zhou R., Dong 2001 Molecular mapping and detection of the 601-606

Euphytica Triticum analysis L. - Yellow rust (stripe rust), is located

segregantturgidum RFLP lines. The probe Whs178 caused by 3 cM

Y., Wang L., Wang X., yellow rust resistance gene Yr26 in 120: 219-226 wheat - yellow rust Puccinia striiformis Westend f. sp. tritici,

Jis J. wheat transferred from Triticum resistance - Yr26 is one of the most devastating diseases of

turgidum L. using microsatellite markers wheat throughout the world. Wheat-

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



481 Jin W., Palmer R.G., 1998 Molecular mapping of a male-sterile Crop Sci Soybean, Molecular A newly identified genic male-sterile

Horner H.T., Shoemaker gene in soybean 38:1681-1685 mapping, male-sterility mutant in soybean [Glycine max (L.)

R. C. Merr.] has high seed set under natural

482 Ivandic V., Walther U., 1998 Molecular mapping of a new gene in Theoretical CAPS · Disease field conditions and is potentially useful in

A dominant gene conferring resistance to

Graner A. wild barley conferring complete and Applied resistance · Hordeum all known races of Puccinia hordei Otth

resistance to leaf rust (Puccinia horde i Genetics 97: vulgare ssp. spontaneum was identified in two accessions of

483 Chetelat R. T., Meglic 2000 Otth)

Molecular mapping of chromosome 1235-1239

TAG · RFLP-mapping · STS-

Comparative mapping The wild nightshade spontaneum. Using

Hordeum vulgare ssp.Solanum

V. segments introgressed from Solanum Theoretical Homoeologous lycopersicoides (accessionLA2951) was

lycopersicoides into cultivated tomato ( and Applied recombination - backcrossed to the cultivated tomato

484 Shaha M.M., Gilla 1999 Lycopersicon esculentum ) for

Molecular Mapping of Loci Genetics 100:

Crop Sci Segregation distortion -

wheat, molecular Chromosome esculentum cv ‘VF36‘),

(Lycopersicon3A of bread wheat (Triticum

K.S., Baenzigera P.S., Agronomic Traits on Chromosome 3A of 39:1728-1732 mapping, agronomic aestivum L.) cultivar `Wichita' (WI) was

Yenb Y., Kaepplerc Bread Wheat traits previously found to differ from that of

Bauer Ariyarathned

485 S.M., E., Weyen J., 1997 Molecular mapping of novel resistance Theoretical Barley Mild Mosaic `Cheyenne' (CNN) for genes affecting a

In the present study three novel genes

Schiemann A., Graner genes against Barley Mild Mosaic Virus and Applied Virus (BaMMV) · from barley accessions 10247 (ym8),

A., Ordon F. (BaMMV) Genetics 95: Hordeum vulgare · Bulgarian 347 (ym9), and Russia 57

486 Brigneti G., Garcia-Mas 1997 Molecular mapping of the potato virus Y 1263-1269

TAG Molecular markers ·

Potato virus Y - Rysto Ry sto which confer resistance confers

(ym11),is a dominant gene whichto Barley

J., Baulcombe D. C. resistance gene Rysto in potato Theoretical extreme resistance - resistance to potato virus Y (PVY) in

and Applied Solanum tuberosum - potato. We have used bulked segregant

487 Brunner S., Keller B., 2000 Molecular mapping of the Rph7.g leaf Genetics 94: High-resolution map -

Theoretical Barley - Leaf rust - analysis of an F1 tetraploid potato

In many temperate areas of the world, leaf

Feuillet C. rust resistance gene in barley ( Hordeum and Applied Marker-assisted selection rust is becoming an important disease of

vulgare L.) Genetics 101 - Resistance gene - barley. In the last decade, new races of

488 Huang X. Q., Hsam S. 2000 Molecular mapping of the wheat Theoretical Single-nucleotide

AFLPs - Bulked Puccinia hordei G. Otth have emerged

Molecular markers were identified in

L. K., Zeller F. J., powdery mildew resistance gene Pm24 and Applied segregant analysis - common wheat for the Pm24 locus

Wenzel G., Mohler V. and marker validation for molecular Genetics 101 Marker-assisted selection conferring resistance to different isolates

489 Nelson J. C., Sorrells 1995 breeding Mapping of Wheat: Major

Molecular Genetics 141: - Microsatellites -

Molecular mapping, of molecular-marker linkage map of

A the powdery mildew pathogen,

M. E., Van-Deynze A. Genes and Rearrangements in 721-731 wheat, genes hexaploid wheat (Triticum aestivum L.

E., Lu Y. H., Atkinson Homoeologous Groups 4, 5, and 7 em. Thell) provides a framework for

490 M., Bernard M., Leroy 1995

Berry S. T., Leon A. J., Molecular marker analysis of Helianthus Theoretical Restriction fragment A detailed linkage classical genetic map

integration with themap of Helianthus

Hanfrey C. C., Challis annuus L. 2. Construction of an RFLP and Applied length polymorphism annuus was constructed based on

P., Burkholz A., linkage map for cultivated sunflower Genetics 91: (RFLP) - Linkage map - segregation at 234 RFLP loci, detected by

Barnes S. R., Rufener 195-199 Helianthus annuus - 213 probes, in an F2 population of 289

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



491 Kandemir N., Kudrna 2000 Molecular marker assisted genetic Theoretical Brittle rachis - Weak Head shattering in barley (Hordeum

D. A., Ullrich S. E., analysis of head shattering in six-rowed and Applied rachis - QTL - Spike vulgare L.) has two forms; brittle rachis

Kleinhofs A. barley Genetics 101: density - Peduncle and weak rachis. Brittle rachis is not

492 Lu H., Bernardo R. 2001 Molecular marker diversity among 203-210

Theoretical curvature

Genetic diversity · Maize observed in cultivated barley since all

Advanced-cycle pedigree breeding has

current and historical maize inbreds and Applied · SSR caused maize (Zea mays L.) inbreds to

Genetics 103: become more-elite but more-narrow

493 Zhang Q., Zhou Z. Q., 1996 Molecular marker heterozygosity and 613-617

Theoretical Oryza sativa - Hybrid genetically. Our objectives were to

An essential assumption underlying

Yang G. P., Xu C. G., hybrid performance in indica and and Applied rice - Predicting markerbased prediction of hybrid

Liu K. D., Saghai japonica rice Genetics 93: heterosis - Diallel cross - performance is a strong linear correlation

494 Maroof M. A.

William M., Singh R. 2003 Molecular Marker Mapping of Leaf Rust 1218-1224

Phytopatholog Wheat, leaf rust, yellow between molecular marker heterozygosity

Restriction fragment Leaf and stripe rusts, caused by Puccinia

P., Huerta-Espino J., Resistance Gene Lr46 y 93:153-159 rust, Lr46, Yr29 triticina and P. striiformis,

Ortiz Islas S., and Its Association with Stripe Rust respectively, are globally important fungal

Veldboom D.

495 HoisingtonL. R., Lee 1994 Molecular Gene Yr29 in Wheat

Resistance marker-facilitated studies in Theoretical Maize - Restriction diseases of wheat that cause

Restriction fragment length

M., Woodman W. L. an elite maize population: I. Linkage and Applied fragment length polymorphisms (RFLPs) and one

analysis and determination of QTL for Genetics 88 polymorphisms (RFLPs) - morphological marker were used to

496 DUDLEY J. W., 1991 morphological traits grouping of

Molecular markers and Crop science Qualitative and

Maize, breeding In maize (Zea mays L.) trait loci programs

investigate quantitative breeding (QTL)

SAGHAI MAROOF M. parents in maize breeding programs 31: 718-723 programmes, molecular identifying potentially high yielding

A., RUFENER G. K. markers hybrids, assigning new inbreds to heterotic

497 Burstin J., De Vienne 1994 Molecular markers and protein quantities Theoretical Zea mays L. - Genetic groups, and determiningmays L.) inbred

Twenty-one maize (Zea the parental line

D., Dubreuil P., as genetic descriptors in maize. I. and Applied distances - Protein lines were analysed using isozyme

Damerval C. Genetic diversity among 21 inbred lines Genetics 89: polymorphism - Two- electrophoresis, restriction fragment

498 Gupta P. K., Varshney 1999 943-950

Molecular markers and their applications Plant Breeding dimensional

Molecular markers, length polymorphism (RFLP), and two-

In recent years, considerable emphasis has

R. K., Sharma P. C., in wheat breeding 118: 369-390 applications, wheat been placed on the development of

Ramesh B. breeding molecular markers to be used for a variety

499 Cloutier S., Landry B. 1994 Molecular markers applied to plant In Vitro molecular markers - of objectives. This review attempts to give

The last decade has witnessed successful

S. tissue culture Cellular & somaclonal variation - applications of plant tissue culture

Developmenta doubled haploids - techniques in several crops. During that

500 Goldman I.L., 1994 Crop science molecular mapping -

Molecular markers associated with maize l Biology - maize, kernel oil, same period, studies in plant molecular

The Illinois Long Term Selection Strains

Rocheford T.R., Dudley kernel oil concentration in an Illinois 34: 908-915 molecular markers, offer a unique opportunity to investigate

J.W. High Protein × Illinois Low Protein cross the quantitative genetic basis of kernel

chemical traits. This study was conducted

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



501 Schachermayr G., 1997 Molecular markers for the detection of Molecular leaf rust - molecular We recently showed that the Lr10 wheat

Feuillet C., Keller B. the wheat leaf rust resistance gene Lr10 Breeding 3:65- marker - receptor-like leaf rust resistance gene cosegregated with

in diverse genetic backgrounds 74 kinase - resistance the candidate resistance gene Lrk10 which

502 Gupta P. K., Rustgi S. 2004 Molecular markers from the Functional & breeding - resistance

Functional markers encodes ayears, molecular marker

In recent putative receptor-like kinase.

transcribed/expressed region of the Integrative (FMs) - Gene targeted technology in higher plants has witnessed

genome in higher plants Genomics 4: markers (GTMs) - a shift from the so-called random DNA

503 Cadalen T., SourdilleP., 1998 Molecular markers linked to genes 139-162

Theoretical Transcript maps - eQTLs

Plant height - Molecularmarkers (RDMs), developed in the past

Plant height in wheat (Triticum aestivum

Charmet G., Tixier M. affecting plant height in wheat using a and Applied markers - QTL - Wheat - L. em Thell) is known to be under

H., Gay G., Boeuf C., doubled-haploid population Genetics 96: Doubled-haploid lines polygenic control. Crosses involving

504 Bernard S., Leroy P.,

Dedryver F., Jubier 1996 Molecular markers linked to the leaf rust 933-940

Genome Wheat, leaf rust, RAPD, genes Rht-B1 and Rht-D1,to find on

The aim of this study was located

M.F., Thouvenin J., resistance gene Lr24 in different wheat 39:830-835. SCAR molecular markers (RAPD and SCAR) for

Goyeau H. cultivars. the wheat leaf rust resistance gene Lr24. A

505 Craig Yencho G., 1996 Molecular markers locate genes for The wild line, RL potato, Solanum

Entomologia insect resistance - plant backcross Bolivian 6064, possessing a

Bonierbale M. W., resistance to the Colorado potato beetle, Experimentali breeding - restriction berthaultii Hawkes, has been used as a

Tingey W. M., Plaisted Leptinotarsa decemlineata, in hybrid s et Applicata fragment length source of resistance to the Colorado potato

506 R. L., Tanksley S. D.

Matthews B. F., Molecular markers × S. berthaultii

1998 Solanum tuberosumresiding close to the 81: 141-154

Theoretical polymorphisms (RFLPs) - beetle (CPB), Leptinotarsa decemlineata

Soybean cyst nematode The restriction fragment length

MacDonald M. H., Rhg4 locus conferring resistance to and Applied resistance - Molecular polymorphism (RFLP) clone pBLT65 is a

Gebhardt J. S., Devine soybean cyst nematode race 3 on linkage Genetics 97: markers - Polymerase 450-nt soybean cDNA encoding a portion

Molecular, soybean

507 T. E. F., Businelli S., 1995 group A of cytological and morpho-

Pupilli 1047-1052

Theoretical chain reaction

Medicago - Somatic of the bifunctional enzyme aspartokinase-

Somatic hybrid plants produced by

Caceres M. E., Damiani agronomical characterization of and Applied hybrids - RFLP analysis - protoplast fusion between tetraploid

F., Arcioni S. hexaploid somatic hybrids in Medicago Genetics 90: Meiotic analysis - Field Medicago sativa (2n= 4x=32) and the

508 Foisset N., Delourme 1996 Molecular-mapping analysis in Brassica 347-355

Theoretical evaluation

Brassica napus - L. diploid species Medicago coerulea (2n= a

We have undertaken the construction of

R., Barret P., Hubert napus using isozyme, RAPD and RFLP and Applied Genetic mapping - RFLP Brassica napus genetic map with isozyme

N., Landry B. S., markers on a doubled-haploid progeny Genetics 93: and RAPD markers - (4%), RFLP (26.5%) and RAPD (68%)

Renard M.

509 Freymark P. J., Lee 1994 Molecular-marker-facilitated 1017-1025

Theoretical RFLPs on a 152 to investigate

Segregation distortions - markerswere used lines of a doubled-

Breeding -

M., Martinson C. A., investigation of host-plant response to and Applied Helminthosporium components of host-plant response to

Woodman W. L. Exserohilum turcicum in maize (Zea Genetics 88: turcicum - RFLP - QTLs Exserohilum turcicum in 150 unselected

510 Wu P., Zhang G., 1995 mays L.): components of resistance

Molecular-marker-facilitated 305 -313

TAG Oryza sativa L. - Atom F23F2 population, consisting of 231

- Disease-resistance - An lines of a B52/Mo17 maize

Ladha J. K., McCouch investigation on the ability to stimulate Theoretical 15N% excess - N2 individuals derived from a cross between

S. R., Huang N. N2 fixation in the rhizosphere by and Applied fixation - Restriction rice cultivars with a similar growing

irrigated rice plants Genetics 91: fragment length duration, Palawan and IR42, was utilized

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



511 Edwards M. D., 1992 Molecular-marker-facilitated Theoretical Restriction fragment Restriction fragment length

Helentjaris T., Wright investigations of quantitative trait loci in and Applied length polymorphisms have become powerful

S., Stuber C. W. maize Genetics 83: polymorphisms(RFLPs) - tools for genetic investigations in plant

512 Edwards M. D., Stuber 1987 Molecular-Marker-Facilitated 765-774 116: Isozymes - Quantitative species. They allow a much greater degree

Genetics Maize, QTL, molecular Individual genetic factors which underlie

C. W., Wendel J. F. Investigations of Quantitative-Trait Loci 113-125 marker, gene action variation in quantitative traits of maize

in Maize. I. Numbers, Genomic were investigated

513 Veldboom L. R., Lee 1994 Distribution and Types of Gene Action Theoretical

Molecular-marker-facilitated studies of Restriction fragment in each of two F2 populations by

Genetic factors controlling quantitative

M. morphological traits in maize. II: and Applied length polymorphism inheritance of grain yield and its

Determination of QTLs for grain yield Genetics 89: (RFLP) - Quantitative components have not previously been

514 Ragot M., Sisco P.H., 1995 and yield components

Molecular-marker-mediated Crop science trait loci (QTLs) - Plant investigated by using replicated lines of an

451-458 maize, QTL, molecular Exotic maize (Zea mays L.) germplasm,

Hoisington D.A., Stuber characterization of favorable exotic 35: 1306-1315 marker, exotic alleles shown to be useful for developing

C.W. alleles at quantitative trait loci in maize improved temperate cultivars, has

515 Gao D., Guo D., Jung 2001 Monosomic addition lines of Beta TAG Beta vulgaris · remained little used partly because of

ttBeta corolliflora is a wild relative of

C. corolliflora Zoss in sugar beet: Theoretical Monosomic addition line sugar beet (Beta vulgaris) with 2n=4x=36

cytological and molecular-marker and Applied · Repetitive DNA · FISH chromosomes. Monosomic addition lines

516 Frugis G., Mele G., DnaJ-like B. corolliflora in B. vulgaris

1999 analysis alfalfa DnaJ-like gene, is tissue- Genetics 103: · Species-specific- heat (2n=19) ofproteins are molecular

MsJ1, an Plant cell cycle - DnaJ

Giannino D., Mariotti specific and transcriptionally regulated Molecular shock - Medicago sativa - chaperones that regulate Hsp70 ATPase

D. during cell cycle Biology 40: molecular chaperones - activity both in protein folding, assembly

517 Spielmeyer W., Huang 2000 NBS-LRR sequence family is associated 397-408Theoretical transcriptional regulation and disassembly of protein constructed of

Wheat - Rust resistance - A detailed RFLP map was complexes.

L., Bariana H., with leaf and stripe rust resistance on the and Applied RGA markers - Ae. the distal end of the short arm of

Laroche A., Gill B.S., end of homoeologous chromosome group Genetics 101: Tauschii chromosome 1D of Aegilops tauschii and

Carrillo E.S.

518 LagudahJ. C., Ojeda 2004 1S of wheat of a protocol for direct

Optimization A series of experiments were resistance-

2000 Res. 37 In vitro culture, meristem wheat. At least two unrelated carried out

Biol.

V.A., Campos-De organogenesis of culture, red clover, in order to optimize a protocol for the

Quiroz H.A., Ortega red clover (Trifolium pratense L.) Trifolium pratense L. direct organogenesis of Chilean red clover

519 F.M.

Rodrigues L. R., Terra Origin of for

2004 meristemsEmbryo-Like Structures in Plant Cell, androgenesis - anther germplasm. A range of cultivars were used

The Satt418 microsatellite locus was

T. D. F., Bered F., Soybean Anther Culture Investigated Tissue and culture - Glycine max - examined in order to investigate the origin

Bodanese-Zanettini M. Using SSR Marker Organ 77: 287-microsatellite - somatic of embryo-like structures (ELS) obtained

520 H.

Chabaud M., Passiatore 1988 Parameters affecting the frequency of 289 Cell

Plant embryogenesis Kanamycin resistant plants Four

Alfalfa, Agrobacterium from soybean anther culture.of Medicago

J. E., Cannon F., kanamycin resistant alfalfa obtained by Reports 7: 512- tumefaciens, kanamycin varia A2 were obtained by an optimized

Buchanan-Wollaston V. Agrobacterium tumefaciens mediated 516 resistant procedure for high frequency

transformation transformation using Agrobacterium

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



521 Morgante M., Olivieri 1993 PCR-amplified microsatellites as The Plant Plant, genetics, PCR, In order to assess the feasibility of using

A. M. markers in plant genetics Journal 3: 175- microsatelites microsatellites as markers in plant

182 genetics, a survey of published DNA

522 Paulus, Köllner B., 1993 Physiological and biochemical Planta 189: Auxin - Enzyme sequence data for presence, abundance

Using a strictly auxin-dependent soybean

Jacobsen H-J. characterization of glyoxalase I, a 561-566 induction - Glycine (cell(Glycine max (L.) Merr.) cell suspension,

general marker for cell proliferation, suspension) - Glyoxalase we studied the correlation of auxin-

523 Pan R-C., Gui H. Physiological basis suspension

1997 from a soybean cell of the synergistic Plant Growth I (purification

adventitious root dependent cell proliferation and the and

Mixtures of 1–3 × 20.32 mg L-1 IBA

effects of IBA and triadimefon on Regulation formation - gibberellin -1–3 × 289.5 µg L-1 triadimefon (TRI)

rooting of mung bean hypocotyls 22: 7-11 indole butyric acid - significantly increased the formation of

524 Muñoz J. A., Palomares 1996 Plant genes induced in the Rhizobium- gene expression - acid -

World Journal indole-3-yl acetic nodule adventitious roots in mung bean hypocotyl

Rhizobium, Bradyrhizobium and

A. J., Ratet P. legume symbiosis of development - nodulin Azorhizobium can elicit the formation of

Microbiology genes - Rhizobium- N2-fixing nodules on the roots or stems of

525 Kameswara R. N. 2004 Plant genetic resources: Advancing and

African legume symbiosis

Biotechnology, Conservation and sustainable use nodule

their leguminous host plants. The of

conservation and use through Journal of conservation, plant genetic resources is essential to meet the

biotechnology Biotechnology genetic resources demand for future food security. Advances

526 Samac D. A., Tesfaye 2003 Plant improvement for tolerance to 3: 136-145

Plant Cell, acid soil - aluminum in biotechnologyacid soils that limit crop

Development of have generated new

M. aluminum in acid soils – a review Tissue and toxicity - cell culture -production is an increasing problem

Organ Culture DNA markers - genetic worldwide. Many factors contribute to

527 MonteiroI M., 2003 Plant regeneration from proroplasts of 75: 189-207

Sci. agric.60 modification - organic

plant biotechnology, in phytotoxicity of these soils, however, in

Alfalfa is one of the most frequently

Appezzato-da-GlóriaII alfalfa (Medicago sativa ) via somatic vitro culture, studied species from the production of

B., ValariniIII M. J., embryogenesis morphogenesis, forage tissue culture-derived embryos point of

528 De OliveiraI C. A.,

Holland J.B., Helland 2001 Polymorphism of PCR-based markers Genome 44: legume Zea, genetic

Avena, view. In this study, five alfalfa cultivars

Sequence databases could be efficiently

S.J., Sharopova N., targeting 1065–1076 diversity, DNA exploited for development of DNA

Rhyne D.C. exons, introns, promoter regions, and sequence. markers if it were known which

529 Burkhamer R. L., 1998 SSRs in progeny variance from

Predicting Crop Sci spring wheat, progeny, Selection of reveal is most

gene regionsparents thean important first

Lanning S. P., Martens parental divergence in hard red spring 38:243-248 parental divergence step in any breeding program. The ability

R. J., Martin J.M., wheat to assess accurately genetic differences

Hu Q., L. E.

530 Talbert Andersen S., 2002 Production of fertile intergeneric somatic Plant Cell Blackleg resistance, Somatic parents between Brassica napus

between hybrids and subsequently to

Dixelius C., Hansen L. hybrids between Brassica napus and Reports 21: Intergeneric (oilseed rape) and its wild relative Sinapis

Sinapis arvensis for the enrichment of 147-152 hybridization, Protoplast arvensis (Xinjiang wild mustard) from

the rapeseed gene pool fusion, Xinjiang wild northwestern China were produced by

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



531 Puonti-Kaerlas J., 1990 Production of transgenic pea (Pisum Theoretical Transformation - Pea - A transformation system that allows

Eriksson T., Engström sativum L.) plants by Agrobacterium and Applied Pisum sativum - regeneration of transgenic pea plants from

P. tumefaciens — mediated gene transfer Genetics 80: Agrobacterium calli selected for antibiotic resistance was

532 Griga M., Horáček J., 2007 Protein patterns associated with Pisum 246-252

Biologia tumefaciens -

embryo development - developed. Explants from axenic shoot

Total protein patterns were studied in the

Klenotičová H. sativum somatic embryogenesis Plantarum 51: pea - seed proteins - course of development of pea somatic

201-211 storage substances - embryos using simple protocol of direct

533 Maksyutova N. N., 2005 Proteins as Morphogenetic Markers in Biology zygotic embryogenesis

Fagopyrum tataricum, regenerationof soluble proteinsmeristems

The content from shoot apical and

Galeeva E. I., Callus Cultures of Buckwheat Bulletin 32: Morphogenetic Markers, individual polypeptides was studied in

Rumyantseva N. I., Fagopyrum tataricum (L.) Gaertn with 250-253 Callus Cultures calluses of buckwheat Fagopyrum

Kwon Y.S., V.

534 Viktorova L. Eun 2002 Different Morphogenetic Potential

QTL mapping and associated marker Plant Breeding anther culture, rice, tataricum (L.) Gaertn with different

Anther culturability of rice is a

K.M.Y., Sohn J.K. selection for the efficacy of green plant 121: 10-16 QTL, mapping quantitative trait controlled by nuclear-

regeneration in anther culture of rice encoded genes. The identification of

535 Manifestoa M.M., 2001 Quantitative Evaluation of Genetic Crop Science Wheat, molecular, quantitative trait loci (QTL) and means

Characterization of germplasm by

Schlattera A.R., Hoppb Diversity in Wheat Germplasm Using 41:682-690 markers, Genetic of DNA fingerprinting techniques

H.E., Suáreza E.Y., Molecular Markers diversity provides a tool for precise germplasm

Haddon L. J.

536 DubcovskyE., 1975 Quantitative measurement of the course maintenance and a quantitative estimate

Journal of Cell Bean, callus, quantitative identificationmedium supplemented with 2

Northcote D. H. of bean callus differentiation Science 17: 11- measurements mg/l. 2:4-dichlorophenoxyacetic acid

26 (2:4D) and 2% sucrose. Root initiation

537 Schippers L., Gieffers 1994 Quantitative Resistance to Phytophthora Genetics 137: Potato, Phytophthora was observed infestans is the most

Phytophthora in one strain and formation

W., Schafer-Pregl R., infestans in Potato: A Case Study for 67-77 infestans, resistance important fungal pathogen in the

Ritter E., Knapp S. J., QTL Mapping in an Allogamous Plant QTL., cultivated potato (Solanum tuberosum).

538 Salamini F., Gebhardt

Narasimhamoorthy B., 2007 Species

Quantitative trait loci and candidate gene Theoretical Aluminum (Al) toxicity resistance alleles

diploid alflafa, aluminum Dominant, race-specific in acid soils is a

Bouton J. H., Olsen K. mapping of aluminum tolerance in and Applied tolerance, major limitation to the production of

M., Sledge M. K. diploid alfalfa Genetics 114: alfalfa (Medicago sativa subsp. sativa L.)

539 Beavis W. D., Grant D., 1991 Quantitative trait loci for plant height in 901-913

Theoretical Zea mays L. - Molecular in the USA. Developing Al-tolerant alfalfa

We report that plant height quantitative

Albertsen M., Fincher four maize populations and their and Applied markers - Restriction trait loci (QTLs) identified in a given

R. associations with qualitative genetic loci Genetics 83: fragment length small population are not consistent with

540 Hayes P. M., Liu B. H., 1993 Quantitative trait locus effects and 141-145

Theoretical polymorphisms (RFLPs) - QTLs identified in other small and QTL x

QTL - RFLP mapping - Quantitative trait locus (QTL)

Knapp S. J., Chen F., environmental interaction in a sample of and Applied marker-assisted selection environment (E) interaction effects for

Jones B., Blake T., North American barley germ plasm Genetics 87: - Barley agronomic and malting quality traits were

Franckowiak J., 392-401 measured using a 123-point linkage map

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



541 Visser R. G. F., 1989 ransformation of homozygous diploid Plant Agrobacterium Transformed potato (Solanum tuberosum)

Jacobsen E.,Hesseling- potato with an Agrobacterium Molecular tumefaciens - plants were obtained from homozygous

Meinders A., Schans tumefaciens binary vector system by Biology 12: adventitious shoot diploid potato by using a transformation

542 M. J., Witholt B.,

Osipova E. S., Kokaeva 2001 adventitious shoot regeneration on leaf

RAPD Analysis of Maize Somaclones 329-337

Russian regeneration -

Maize, somaclones, procedure indifference betweenan

The genetic combination with maize line

Z. G., Troitskij A. V., Journal of RAPD, analysis A188 and A188-derived somaclones was

Dolgikh Yu. I., Genetics 37: assessed via analysis of randomly

543 Shamina Z. B.,

Vitale M., Pupilli F., 1998 RAPD analysis reveals a low rate of 80-84

Genetic burr medic - genetic Although polymorphic DNA (RAPD). In

amplified burr medic (Medicago

Labombarda P., Arcioni outcrossing in burr medic (Medicago Resources and variability - Medicago - polymorpha L.) is commonly considered a

S. polymorpha L.) Crop outcrossing rate - RAPD - self-pollinating species, intrapopulational

544 Kuznetsova O. I., Ash 2005 RAPD and ISSR analyses of regenerated Evolution 45:

Russian selfingsativum, RAPD, variation for morphological, biochemical

Pisum Long-term pea callus cultures of different

O. A., Hartina G. A., pea Pisum sativum L. plants Journal of ISSR, callus culture, genotypes (mutants R-9 and W-1 and

Gostimskij S. A. Genetics 41: regenerants cultivar Viola) were used to regenerate

545 Trinh T. H., Ratet P., 1998 Rapid and efficient transformation of 60-65Cell

Plant M. truncatula - M. plants (generation R0). The regenerants

We describe a simple and efficient

Kondorosi E., Durand diploid Medicago truncatula and Reports 17: falcata - MsEnod12A - protocol for regeneration-transformation

P., Kamaté K., Bauer Medicago sativa ssp. falcata lines 345-355 MsEnod12B - Srglb3 of two diploid Medicago lines: the annual

Aulinger I. E., A.

546 P., Kondorosi Peter S. 2003 improved in somaticaembryogenesis

Rapid attainment of doubled haploid In Vitro androgenesis - M. truncatulastrategy for establishing a

We present a R108-1(c3) and the

O., Schmid J. E., line from transgenic maize ( Zea mays Cellular & homozygosity - SSR - transgenic doubled haploid maize line

Stamp P. L.) plants by means of anther culture Developmenta pat gene - herbicide from heterozygous transgenic material by

547 Hatamoto H., Boulter 1990 Recovery of morphologically normal l Biology -

Plant Cell resistance

Agrobacterium means of anther culture. Compared to

Co-transformation of tobacco (Nicotiana

M. E., Shirsat A. H., transgenic tobacco from hairy roots co- Reports 9: 88- rhizogenes, tobacco, tabacum) leaf explants with

Croy E. J., Ellis J. R. transformed with Agrobacterium 92 hairy roots, Recovery Agrobacterium rhizogenes harbouring

548 Christey M. C., Sinclair 1997 Regeneration of binary vector plasmid Plant Cell

rhizogenes and atransgenic vegetable Agrobacterium pRi1855 and for the productionpBin19 was

A procedure the binary vector of fertile

B. K., Braun R. H., brassicas (Brassica oleracea and B. Reports 16: rhizogenes · Brassica transgenic brassicas via Ri-mediated

Wyke L. campestris ) via Ri-mediated 587-593 oleracea · Brassica transformation is reported in this paper.

549 Bernardo R. 1992 transformation

Relationship between single-cross Theoretical campestris ·

Isozymes - RFLPs - Transgenic hairy root lines were selected

studies involving isozymes or restriction

performance and molecular marker and Applied Heterozygosity - Hybrid fragment length polymorphisms (RFLPs),

heterozygosity Genetics 83: performance - correlations of parental molecular marker

550 Harpster M. H., 1988 Relative strengths of the 35S califlower 628-634 and

Molecular Combining ability -

Promoter strength diversity promoter of cauliflower mosaic

The 35S with grain yield of maize (Zea

Townsend J. A., Jones mosaic virus, 1′, 2′, and nopaline General Transformed callus - virus and promoters from the nopaline

J. D. G., Bedbrook J., synthase promoters in transformed Genetics 212: Chitinase gene - synthase, 1 and 2 genes of Agrobacterium

Dunsmuir P. tobacco sugarbeet and oilseed rape callus 182-190 Octopine synthase gene - tumefaciens T-DNA were fused to the

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



551 Seah S., Spielmeyer W., 2000 Resistance Gene Analogs within an MPMI 13: genomic library, linked A resistance (R) gene-rich 2S

Jahier J., Introgressed 334–341. rust genes, wheat genetic chromosomal segment from

Sivasithamparam K., Chromosomal Segment Derived stocks. Triticum ventricosum contains a cereal

552 and Lagudah E.S. Line

Yan G., Chen X., 2003 from Triticum ventricosum That Confers

Resistance gene-analog polymorphism Theoretical Molecular markers, cyst Yr5 gene confers resistance to all

The nematode

R., Wellings C. markers co-segregating with the YR5 and Applied Puccinia striiformis, races of the stripe rust pathogen (Puccinia

gene for resistance to wheat stripe rust Genetics 106: Resistance gene-analog striiformis f. sp. tritici) of wheat in the

553 Rose R. J., Johnson L. 1986 Restriction endonuclease studies on the 636-643

Plant Alfalfa protoclones were molecular

polymorphism, Triticum United States. To developregenerated from

alfalfa - chloroplast

B., Kemble R. J. chloroplast and mitochondrial DNAs of Molecular DNA - Medicago sativa the mesophyll protoplasts of two cloned

alfalfa (Medicago sativa L.) protoclones Biology 6: 331- L. - mitochondrial DNA - source plants (parents), RS-K1 and RS-

554 Apuya N. R., Frazier B. 1988 Restriction fragment length 338

Theoretical protocloneRestriction

Soybean - - protoplast K2, initiated from Regen S seed. Because

Restriction Fragment Length

L., Keim P., Jill Roth polymorphisms as genetic markers in and Applied fragment length Polymorphisms (RFLP) have been

E., Lark K. G. soybean, Glycine max (L.) merrill Genetics 75: polymorphism - Genetics identified between widely distant cultivars

555 Queen R. A., Gribbon 2004 Retrotransposon-based molecular 889-901

Molecular - Allele - Variation

Retrotransposon - (Minsoy and Noir 1 ) ofmolecularGlycine

Retrotransposon-based soybean markers

B. M., James C., Jack markers for linkage and genetic diversity Genetics and Transposable element - have been developed to study bread wheat

P., Flavell A. J. analysis in wheat Genomics Triticum aestivum - ( Triticum aestivum) and its wild relatives.

556 Brown C. R., Yang C. 1996 RFLP analysis of resistance to Columbia 271: 91-97

Theoretical copia species -

Wild SSAP (Sequence-Specific Amplification

The mapping of resistance toMeloidogyne

P., Mojtahedi H., root-knot nematode derived from and Applied Introgression - chitwoodi derived from Solarium

Santo G. S., Masuelli Solanum bulbocastanum in a BC2 Genetics 92: Meloidogyne chitwoodi - bulbocastanum is reported. A population

557 R.

Schon C.C., 1994 population

RFLP mapping in maize : quantitative 572-576 maize, RFLP, - Potato The dissection of quantitative traits as

Crop science Gene mappingmapping, suitable for mapping was developedinto

Melchingera A.E., trait loci affecting testcross performance 34: 378-389 flint lines their underlying Mendelian factors has

Boppenmaier J., of elite european flint lines become possible with the aid of molecular

558 Brunklaus-Jung Moreno- 1999 RFLP mapping of QTL for fusarium

Waldron B. L., E., Published in wheat, fusarium head markers. In this study, we mapped and

Recent epidemics of fusarium head blight

Sevilla B., Anderson J. head blight resistance in wheat Crop Sci blight, resistance, QTL (FHB), caused by Fusarium graminearum

A., Stack R. W., 39:805-811 Schwabe (telomorph: Gibberella zeae), in

559 Frohberg R. C.

Ritter E., Debener T., 1991 RFLP mapping on potato chromosomes Molecular and Potato virus X - the USA chromosomal locations of major

different and Canada have caused severe

Barone A., Salamini F., of two genes controlling extreme General Resistance genes - RFLP genes controlling extreme resistance to

Gebhardt C. resistance to potato virus X (PVX) Genetics 227: - Solanum tuberosum - potato virus X (PVX) were found by

560 Moser H., Lee M. 1994 RFLP variation and genealogical 81-85

Theoretical Avena sativa L. - Genetic restriction fragment length polymorphism

Genetic introgression Patterns of restriction fragment length

distance, multivariate distance, heterosis, and Applied distance - RFLPs - polymorphisms (RFLPs) have been

and genetic variance in oats Genetics 87: Heterosis - Genetic proposed as estimators of genetic diversity

947-956 variance among breeding lines and as predictors of

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



561 Saghai-Maroof M. A., 1984 Ribosomal DNA Spacer-Length Population barley, ribosomal, DNA, Spacer-length (sl) variation in ribosomal

Soliman K. M., Polymorphisms in Barley: Mendelian Biology 81: Mendelian Inheritance, RNA gene clusters (rDNA) was surveyed

Jorgensen R. A., Allard Inheritance, Chromosomal Location, and 8014-8018 Chromosomal Location in 502 individual barley plants, including

562 R. W.

Nagamura Y., Antonio 1997 Population Dynamics map using RFLPs

Rice molecular genetic Plant RFLP marker - In the past decade, notable of cultivated

samples from 50 accessionsprogress has

B. A., Sasaki T. and its applications Molecular molecular genetic map - been made in rice molecular genetic

Biology 35: application - comparative mapping using genomic or cDNA clones.

563 Sukhapinda K., Spivey 1987 Ri-plasmid as a helper for introducing 79-87

Plant mapping - gene transfer

hairy root A total of over 3000 of legumes and other

Genetic engineering DNA markers,

R., Shahin E. A. vector DNA into alfalfa plants Molecular important dicotyledonous plants is limited

Biology 8: 209- because of the difficulty of regenerating

564 Nieto-Lopez R.M., 1994 Russian wheat aphid resistance in Barley 216 science Barley, russian wheat

Crop plants via cell culture. Since aDiuraphis

Russian wheat aphid (RWA),

Blake T.K. : inheritance and linked molecular 34: 655-659 aphid, resistance, noxia (Mordvilko), is an important pest of

markers molecular markers small grains cereals in many areas

565 Causse A. , Fulton T. 1994 Saturated Molecular Map of the Rice Genetics 138: Rice, molecular map, throughout the world. been constructed for

A molecular map has This research was

M., Cho Y. G., Ahn S. Genome Based on an Interspecific 1251-1274 genome, backross the rice genome comprised of 726 markers

N., Chunwongse J. , Backcross Population population (mainly restriction fragment length

Kuai K. Wu. J.,

566 Xiao B., Morris P.Yu Z., 1996 Screening for stable transformants and Plant Cell Festuca arundinacea, β- polymorphisms; RFLPs). The mapping

By screening cell colonies derived from

stability of β-glucuronidase gene Reports 15: glucuronidase gene protoplasts of tall fescue (Festuca

expression in suspension cultured cells 804-808 expression, suspension arundinacea), transformed with a rice actin-

Segregation (Festuca at marker loci:

567 Dufour P., Johnsson C., 2001 of tall fescuedistortion arundinacea) Theoretical cultured cells

Microspore 1-promoter-ß-glucuronidase gene the

In the present study, we analyzed

Antoine-Michard S., variation during microspore and Applied embryogenesis - segregation distortions of markers during

Cheng R., Murigneux embryogenesis in maize Genetics 102: Regeneration - AFLP - in vitro androgenesis in maize. This was

568 A., Beckert M. T.,

Michael Spencer 1992 Segregation of transgenes in maize 993-1001

Plant maize - Segregation

Maize - transformation - based on recovered from backcrossed

Progeny four segregating populations

O'Brien J. V., Start W. Molecular inheritance - transgenic maize tissue culture regenerants

G., Adams T. R., Biology 18: phosphinothricin (R0) were analyzed to determine the

569 Gordon-Kamm W. J.,

Özcan S., Firek S., Bio/Technolog acetyltransferase - Plant

1993 Selectable Marker Genes Engineered for 201-210 Genes Engineered, A wound-induced promoter stability

segregation, expression, and(AoPRl) of

Draper J. Specific Expression in Target Cells for y 11: 218 - Transformation, isolated from Asparagus officinalis was

Plant Transformation 221 Asparagus officinalis shown by GUS reporter gene analysis to

570 Chen X., Yang W., 2005 Selective elimination of perennial Molecular argE - N-acetyl- be active during callus formation in tissue

Perennial ryegrass is widely used for

Sivamani E., Bruneau ryegrass by activation of a pro-herbicide Breeding 15: phosphinothricin - overseeding dormant bermudagrass on

A. H., Wang B., Qu R. through engineering E. coli argE gene 339-347 Perennial ryegrass - golf courses and sports fields in

Phosphinothricin - Southeastern United States to provide

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



571 Narasimhulu S. B., Kirti 1992 Shoot regeneration in stem expiants and Plant Cell Brassica carinata - Immature stem segments of seven

P. B., Mohapatra T., its amenability to Agrobacterium Reports 11: Agrobacterium different genotypes of Brassica carinata

Prakash S., Chopra V. tumefaciens mediated gene transfer in 359-362 tumefaciens - Shoot produced shoots with variable frequencies

572 L.

Smith O. S., Smith J. S. 1990 Brassica carinata a group of elite maize

Similarities among Theoretical regeneration - Gene

Zea Mays L. Restriction when cultured in MS medium withamong

Genetic distances were calculated BAP

C., Bowen S. L., inbreds as measured by pedigree, F1 and Applied fragment length 37 inbred lines representing a wide range

Tenborg R. A., Wall S. grain yield, grain yield, heterosis, and Genetics 80: polymorphisms - Nei's of related and unrelated elite Corn Belt

573 J.

SENIOR M. L., CHIN 1996 RFLPs sequence repeat markers

Simple 833-840

Crop science distance - Coefficient of

Maize, SSR, markers, germ plasm of maize (Zea Mays L.), using

Simple sequence repeats (SSRs) are

E. C. L., LEE M., developed from maize sequences found 36: 1676-1683 genbank rapidly becoming an important class of

SMITH J. S. C., in the GENBANK database : Map DNA markers that are being widely used

574 STUBER C. W.Frugis

Pouisen G. B., 1996 construction extracellular proteins in

Synthesis of Plant Cell, 2,4- to map both plant and animal genomes.

Extracellular proteins, released into the

G., Albrechtsen M., embryogenic and non-embryogenic cell Tissue and dichlorophenoxyacetic culture medium from alfalfa cells grown in

Mariotti D. cultures of alfalfa Organ Culture acid - Medicago sativa - embryogenic and non-embryogenic

575 Nenz E., Pupilli F., 1996 Somatic hybrid plants between the 44: 257-260

Theoretical somatic embryogenesis -

M. sativa - M. arborea conditions, were 35S-methionine labelled

Interspecific somatic hybrid plants were

Damiani F., Arcioni S. forage legumes Medicago sativa L. and and Applied Protoplast electrofusion - obtained by symmetrical electrofusion of

Medicago arborea L. Genetics 93: Somatic hybrids - mesophyll protoplasts of Medicago sativa

576 Dumsday L., Smith K. SSR-based genetic linkage analysis of 183-189

Plant Genome rearrangements

ryegrass, SSR, genetic Crown rust (caused by of Medicago

with callus protoplasts Puccinia coronata

F., Forster J. W., Jones resistance to crown rust (Puccinia Pathology 52 linkage, crown rust f. sp. lolii) is a serious foliar disease of the

E. S. coronata f. sp. lolii) in perennial (5): 628–637. pasture and turfgrass perennial ryegrass

577 Sidorov V. A., Kasten 1999 ryegrass (Lolium perenne )

Stable chloroplast transformation in The Plant potato, fluorescent (Lolium perenne).the development of a

We describe here Previous genetic studies

D., Sheng-Zhi P., potato: use of green fluorescent protein Journal 19: protein, chloroplast reproducible plastid transformation system

Hajdukiewicz P. T. J., as a plastid marker 209-216 transformation for potato and regeneration of plants with

578 Staub J. M., Nehra N..

Van Der Maas H. M., 1994 Stable transformation and long-term Plant Lolium perenne L. - uniformly transformedof perennial

Stable transformation plastids. Two

De Jong E. R., Rueb S., expression of the gusA reporter gene in Molecular transformation - rice ryegrass (Lolium perenne L.) was

Hensgens L. A. M., callus lines of perennial ryegrass Biology 24: gene GOS2 - long-term achieved by biolistic bombardment of a

Paiva F. A.

579 Krens N. L., Edwards Stress responses L.)

1991 (Lolium perenne in alfalfa (Medicago 401-405

Plant GUS expression

fungal elicitor - The major phytoalexin in alfalfa culture,

non embryogenic cell suspensionis the

R., Sun Y., Hrazdina sativa L.) 11. Molecular cloning and Molecular isoflavone reductase isoflavonoid (–)-medicarpin (or 6aR,

G., Dixon R. A. expression of alfalfa isoflavone Biology 17: mRNA - Medicago 11aR)-medicarpin. Isoflavone reductase

580 Blake T. K., STS-PCR a key enzyme of isoflavonoid

1996 reductase, markers appropriate for wheat- 653-667

Theoretical sativa - phytoalexin

STS-PCR markers - Introgression of chromosomal in

(IFR), the penultimate enzyme segments

Kadyrzhanova D., barley introgression and Applied Wheat-barley across large taxonomic distances has long

Shepherd K. W. , Islam Genetics 93: introgression been an objective of scientists interested

A. K. M. R., Langridge 826-832 in understanding the relationships between

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



581 Cloutier S., Cappadocia 1995 Study of microspore-culture Theoretical Microspore culture - RFLP segregation analyses were

M., Landry B. S. responsiveness in oilseed rape (Brassica and Applied Responsiveness genes - performed on a F2 population and two F1

napus L.) by comparative mapping of a Genetics 91: Comparative mapping - microspore-derived populations from the

582 Nadolska-Orczyk A., 2000 F2 population and two microspore-

Study of the factors influencing 841-847

Molecular Doubled haploid-

Agrobacterium same cross between the efficiency culture-

Factors influencing a microspore of

Orczyk W. Agrobacterium-mediated transformation Breeding 6: transformation - pea - Agrobacterium-mediated transformation

of pea (Pisum sativum L.) 185-194 Pisum sativum L. - PCR of pea were tested using highly efficient,

583 Al-Ahmad H., Galili S., 2004 Tandem constructs to mitigate transgene Molecular analysis transgene

Tabacco, direct transgenic crops can introgress

Some regeneration system. The virulence

Gressel J. persistence: tobacco as a model Ecology 13: persistence, model plant genes into other varieties of the crop, to

697-710 related weeds or themselves remain as

584 Bade J., Van Grinsven 2003 T-DNA tagging in Brassica napus as an Plant A simple strategy potentially enhancing

Brassica transformation - 'volunteer' weeds, to identify and isolate

E., Custers J., Hoekstra efficient tool for the isolation of new Molecular callus-specific promoter - new promoters suitable for driving the

S., Ponstein A. promoters for selectable marker genes Biology 52: gus::nptII fusion gene - expression of selectable marker genes is

585 Börner A., Röder M. S., 2000 The detection and molecular mapping of 53-68

Theoretical plasmid rescue -

Adult-plant disease described. By employing a Brassica napus

Unger O., Meinel A. a major gene for non-specific adult-plant and Applied resistance · Gene A major gene determining non-specific

disease resistance against stripe rust Genetics100: mapping · Microsatellites adult-plant disease resistance against

586 Forster B.P., Ellis R.P., 2000 (Puccinia striiformis) in wheat of

The development and application 1095-1099

Journal of · Puccinia striiformis ·

Molecular markers, This rust (Puccinia striiformis)

stripearticle represents some current

Thomas W.T.B., molecular markers for abiotic stress Experimental abiotic stress, molecular thinking and objectives in the use of

Newton A.C., tolerance in barley Botany 51: 19- breeding, cultivated molecular markers to abiotic stress

587 Tuberosa R., This D.,

Li C. D., Rossnagel B. 2000 The development of oat microsatellite 27

Theoretical Enriched-library SSR - Microsatellites have been chosen for

barley, Hordeum -vulgare, tolerance. Barley hasmany desirable

G., Scoles G. J. markers and their use in identifying and Applied Repetitive elements - marker properties. There has been no

relationships among Avena species and Genetics Allelic diversity - report of the development and utilization

588 Taylor C., Madsen K., 2001 oat cultivars

The development of sequence-tagged 101:1259-

Theoretical Evolution tagged sites · of microsatellite markers in oat. The

Sequence Genetic analysis, particularly the

Borg S., Møller M. C., sites (STSs) in Lolium perenne L.: the and Applied PCR · Homology · Wheat development of genetic linkage maps in

Boelt B., Holm P. H. application of primer sets derived from Genetics 103: · Barley · Lolium · forage grass species, lags well behind

589 Barta A., 1986 other genera of a nopaline synthase —

The expression 648-658

Plant Forage growth hormone other members of mammalian RNA

human grasses To study whether the Poaceae.

Sommergruber K., human growth hormone chimaeric gene Molecular gene - plant processing signals function in plants, we

Thompson D., in transformed tobacco and sunflower Biology 6: transformation - have constructed a chimaeric gene in

590 Hartmuth K., Matzke

Borovkova I.G., 1995 callus tissue in barley confers

The gene rpg4 347-357

Phytopatholog Barley, resistance, stem The gene complete human growth

polyadenylation signal - which therpg4 in barley confers resistance

Stefenson B.J., Jin Y., resistance to pathotype QCC of Puccinia y 85: 181-185 rust, pathotype to pathotype QCC of Puccinia graminis f.

Rasmussen J.B., Kilian graminis f. sp. tritici. To facilitate the sp. tritici. To facilitate the efficient

A., Kleinhofs A., efficient transfer of rpg4 into breeding transfer of rpg4 into breeding lines, an

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



591 Eck H. J. V., Van Der 1995 The inheritance and chromosomal Molecular AFLP marker - allelism - AFLPTM is a new technique to generate

Voort J. R., Draaistra J., localization of AFLP markers in a non- Breeding 1: allogamous - linkage large numbers of molecular markers for

Van Zandvoort P., Van inbred potato offspring 397-410 map - Solanum genetic mapping. The method involves the

Collins N. C., Segers

592 Enckevort E., Webb C. The Isolation and Mapping of Disease Molecular tuberosum

maize, disease resistance, selective the plant disease a limited genes

Many of amplification of resistance

A., Seah S., Ellis J. G., Resistance Gene Analogs in Maize Plant-Microbe gene mapping that have been isolated encode proteins

Hulbert S. H., Pryor A. Interactions with a putative nucleotide binding site and

593 Casa A. M., Brouwer 2000 The MITE family Heartbreaker (Hbr): 11: 968-978

PNAS Maize, Molecular leucine-rich repeats (NBS-LRR resistance

Transposable elements are ubiquitous in

C., Nagel A., Wang L., Molecular markers in maize 97:10083- markers, genomic DNA plant genomes, where they frequently

Zhang Q., Kresovich S., 10089 comprise the majority of genomic DNA.

Fernández R.¶

594 Wessler S.M., Figueiras 2002 The use of ISSR and RAPD markers for Theoretical RAPDs, ISSRs, Bulked The maize genome, which is believed to

The potential of bulk analyses of RAPD

A., Benito C. detecting DNA polymorphism, genotype and Applied analyses, Genetic and ISSR-PCR markers for fingerprinting

identification and genetic diversity Genetics 104: diversity, Barley purposes was evaluated using ten RAPD

595 Simcox K. D., 1993 among barley cultivars with known

The use of molecular markers to study 845-851

Phytopatholog resistance; markers; andfacilitate understanding phylogenetic

To ten ISSR primers. The of the

Bennetzen J. L. Setosphaeria turcica resistance in maize y 83: 1326- {Q2}; Setosphaeria molecular basis of Htn1 resistance in

1330 turcica; Zea mays maize to northern corn leaf blight, we

596 Varkonyi-Gasic E., 2002 The White Clover enod40 Gene Family. Plant Physiol white clover, Genes Enod40 the Htn1 locus by associated

mapped is one of the genesrestriction with

White D. W. R. Expression Patterns of Two Types of 129: 1107- Indicate, Vascular legume nodule development and has a

Genes Indicate a Role in Vascular 1118 Function putative role in general plant

597 Zacchini M., Marotta 1997 Function1 to salt stress in maize callus

Tolerance Plant Cell Polyamines · Maize · organogenesis. We have isolatedembryos

Four callus lines from immature a small

A., De Agazio M. lines with different polyamine content Reports 17: Callus culture · Salt of a self-crossed maize (Zea mays L.)

119-122 stress · RAPD hybrid cultivar were selected for "high"

598 Kilian A., Chen J., Han 1997 Towards map-based cloning of the Plant bacterial artificial The lines) and rust (two lines)

(twobarley stem"low"resistance genes

F., Steffenson B., barley stem rust resistance genes Rpg1 Molecular chromosome - cloning - Rpg1 and rpg4 were mapped in barley on

Kleinhofs A. and rpg4 using rice as an intergenomic Biology 35: disease resistance - chromosomes 1P and 7M, respectively and

599 Stark-Lorenzen P., 1997 cloning vehicle

Transfer of a grapevine stilbene synthase 187-195

Plant Cell mapping synteny

Oryza sativa · Pyricularia the syntenous rice chromosomes identified

A gene derived from grapevine (Vitis

Nelke B., Hänßler G., gene to rice (Oryza sativa L.) Reports 16: oryzae · Transformation · vinifera) coding for stilbene synthase has

Mühlbach H. P., 668-673 Stilbene synthase · been transferred into protoplasts of the

600 Thomzik J. E.Lee R. W. 2005 Transformation of alfalfa with a bacterial

Ziauddin A., Plant Cell, Phytoalexin

Agrobacterium-mediated commercially important japonica rice the

Alfalfa transformed with a portion of

H., Lo R., Shewen P., fusion gene, Mannheimia haemolyticaA1 Tissue and transformation - alfalfa - leukotoxin gene from Mannheimia

Strommer J. leukotoxin50-gfp: Response with Organ Culture C58 - somatic haemolytica was produced to test the

Agrobacterium tumefaciens strains 79: 271-278 embryogenesis - edible feasibility of developing an edible vaccine

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



601 Davies D. R., Hamilton 1993 Transformation of peas Plant Cell Peas - Seed - lateral cotyledonary meristems present in

J., Mullineaux P. Reports 12: Transformation - germinating seed were inoculated with a

180-183 Agrobacterium - non-oncogenic strain of A. tumefaciens

602 Cao M.X., Huang J.Q., 2006 Transformation of recalcitrant turfgrass Plant Cell, Meristems

Agrobacterium Tissue culture techniques, kanamycin

carrying a gene conferring medium

He Y.L., Liu S.J., cultivars through improvement of tissue Tissue and tumefaciens - pH value - composition, pH value and targeted

Wang C.L., Jiang W.Z., culture and selection regime Organ Culture selection procedure - tissues, agroinfection and co-culture

603 Wei Z.M.W. R.,

White D. 1987 Transformation of the forage legume 85: 307-316

Plant silicon element nutrition - conditions, selection process were

Agrobacterium A system was established for introducing

Greenwood D. Trifolium repens L. using binary Molecular tumefaciens - binary cloned genes into white clover (Trifolium

Agrobacterium vectors Biology 8: 461- vectors - gene transfer - repens L.). A high regeneration white

604 Ye X., Wang Z. Y., Wu 1997 Transgenic Italian ryegrass (Lolium 469 Cell

Plant kanamycin resistance - - clover genotype was transformed with

Forage and turf grasses Transgenic forage-type Italian ryegrass

X., Potrykus I., multiflorum ) plants from microprojectile Reports 16: Italian ryegrassLolium (Lolium multiflorum Lam.) plants have

Spangenberg G. bombardment of embryogenic 379-384 multiflorum - been obtained by microprojectile

605 Winicov I., Bastola D. 1999 suspension cells

Transgenic Overexpression of the Plant Physiol. Microprojectile

Alfalfa, salinity Alfin1 cDNA of embryogenic suspension

bombardment encodes a putative

R. Transcription Factor Alfin1 Enhances 120: 473-480 tolerance, transgenic transcription factor associated with NaCl

Expression of the Endogenous MsPRP2 tolerance in alfalfa (Medicago sativa L.).

606 Neuhaus G., 1987 Gene in Alfalfa and Improves Salinity

Transgenic rapeseed plants obtained by Theoretical A novel method protein binds DNA in

Embryoid microinjection The recombinantin the field of genetic a

Spangenberg G., Scheid the microinjection of DNA into and Applied - Neomycin engineering of higher plants is presented:

O. M., Schweiger H. G. microspore-derived embryoids Genetics 75: phosphotransferase II microinjection into multicellular structures

607 Sukhapinda K., Spivey Transgenic tomato (Lycopersicon Molecular and gene - root - Plant

30-36 Hairy Plant which have a high competence for plant

We transformed tomato (Lycopersicon

R., Simpson R. B., esculentum L.) transformed with a General transformatia esculentum L.) by using Agrobacterium

Shahin E. A. binary vector in Agrobacterium Genetics 206: rhizogenes containing two independent

608 Larkin P. J., Gibson J. Transgenic Non-chimeric origin with

1996 rhizogenes: white clover. Studies of 491-497

Transgenic Trifolium repens - plasmids: the improved method for white

We report an wild-type Ri-plasmid, and

M., Mathesius U., the auxin-responsive promoter, GH3, in Research 5: transformation - forage clover (Trifolium repens) transformation

Weinman J. J., Gartner root gravitropism and lateral root 325-335 legume - GUS promoter usingAgrobacterium tumefaciens. High

609 E., Hall E., Tanner G.

Hensgens L. A. M., De 1993 development stable expression ofgusA

Transient and Plant fusion - tropic response efficiencies of transgenic plant production

transformation - Transcriptional and translational fusions

Bakker E. P. H. M., fusions with rice genes in rice, barley Molecular promoters - introns - were made between the reading frame

Van Os-Ruygrok E. P., and perennial ryegrass Biology, 22: gene expression - Oryza coding for -D-glucuronidase and

610 Rueb S., Van De Mark

De Majnik J., Tanner 1998 Transient expression of maize 1101-1127

Australian sativa - HordeumB-

Anthocyanin, C1, Transient of either a constitutively

sequencesexpression of the maize

G.J., Joseph R.G., anthocyanin regulatory genes influences Journal of Peru, maize, pea, clover, anthocyanin regulatory genes, B-Peru and

Larkin P.J., Weinman anthocyanin production in white clover Plant biolistic bombardment C1, was examined in maize cell

J.J., Djordjevic M.A., and peas Physiology suspensions, and in pea and white clover

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



611 Sibov S. T., Gaspar M., 1999 Two genes control aluminum tolerance Genome 42: maize, aluminum We have identified two loci linked to

Silva M. J., Ottoboni L. in maize: 475–482 tolerance, molecular aluminum (Al) tolerance in the maize

M. M., Arruda P., Genetic and molecular mapping analyses mapping, somaclonal inbred line Cat-100-6 by means

612 Souza A. P. Kolmos E.,

Petersen K., 2006 Two MADS-box genes from perennial Physiologia variation. ryegrass,

Perennial Many plants fragment length

of restriction in temperate regions have a

Folling M., Salchert K., ryegrass are regulated by vernalization Plantarum vernalization, genes requirement for vernalization in order to

Storgaard M., Jensen and involved in the floral transition 126: 268-278 initiate the reproductive growth phase. In

613 C.S., Didion T.,

Yamada T., Tozawa Y., 2005 Use of a feedback-insensitive α subunit Molecular A selection requirement on been linked

Anthranilate synthase - 5- cereals, this system basedhas a mutant rice

Hasegawa H., Terakawa of anthranilate synthase as a selectable Breeding 14: methyltryptophan - gene for a feedback-insensitive subunit of

T., Ohkawa Y., Wakasa marker for transformation of rice and 363-373 Selectable marker - anthranilate synthase (OASA1D) was

614 K. X., Stam P.,

Qi 1998 potato locus-specific AFLP markers to

Use of Theoretical Transgenic potato --AFLP developed for the transformation of rice

Hordeum vulgare By using 25 primer combinations, 563

Lindhout P. construct a high-density molecular map and Applied markers - Genetic AFLP markers segregating in a

in barley Genetics 96: linkage map - recombinant inbred population (103 lines,

615 Xu Y., Clark M. S., 1993 Use of RAPD markers to screen somatic 376-384

Plant Cell Somatic hybrids - DNA F9) derived from L94/Vada were

Recombinant inbred The identification of somatic hybrids

Pehu E. hybrids between Solanum tuberosum and Reports 12: polymorphism - potato - between Solanum tuberosum and S.

S. brevidens 107-109 Solanum brevidens - brevidens can be carried out using

616 Carolan J. C.,Hook I. L. 2002 Using AFLP markers for species In Vitro AFLP - PCR

RAPDfingerprinting - polymerase chain reaction (PCR) and

Amplified fragment length polymorphism

I., Walsh J. J., differentiation and assessment of genetic Cellular & isothebaine - Oxytona - (AFLP) markers were employed to deteet

Hodkinson T. R. variability of in vitro-cultured Papaver Developmenta regeneration - Papaver genetic variation among species of

617 Swanston J. S., William 1999 bracteatum (section Oxytona)

Using molecular markers to determine l Biology -

Molecular Two barley quality characters assess

bracteatum - somaclonal Papever (section Oxytona) andof specific

Barley, molecular

T.B.T., Powell W., barleys most suitable for malt whisky Breeding markers, malt, distiling interest to whisky distillers are

Young G. R., Lawrence distilling 5:103-109 fermentability and production of the ethyl

618 P. E., Ramsay Murphy

Senior M. L., L., Utility of SSRs for determining genetic Crop Science, Genetic similarities, carbamate precursor, epi-heterodendrin.

Among maize (Zea maize L.) breeders,

J. P., Goodman M. M., similarities and relationships in maize 38: 1088- maize, genetic markers there is a heightened awareness of the

Stuber C. W. using an agarose gel system 1098, necessity for both maintaining genetic

619 Romagosa I., Han F., 1999 Verification of yield QTL through Molecular Hordeum vulgare - Verification crop improvement and

diversity for of putative quantitative trait

Ullrich S. E., Hayes P. realized molecular marker- assisted Breeding 5: molecular marker- loci (QTL) is an essential step towards

M., Wesenberg D. M. selection responses in a barley cross 143-152 assisted selection - implementing the use of marker-assisted

620 Polgár Zs., Preiszner J., 1993 Vigorous growth of fusion products Plant Cell hybrid vigor - potato -

quantitative trait loci - An early (MAS) in cultivar improvement.

selection identification of fusion products

Dudits D., Fehér A. allows highly efficient selection of Reports 12: Solanum - somatic was based on the presumed vigorous

interspecific potato somatic hybrids: 399-402 hybrids - species-specific growth of hybrid calluses after fusion

molecular proofs repetitive DNA between Solanum brevidens and S.

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



621 Patnaik D., Khurana P. 2001 Wheat biotechnology: A minireview EJB biotechnology, Due to the inherent difficulties associated

Electronic transgenic wheat, wheat with gene

Journal of improvement, wheat delivery into regenerable explants and

622 Downing, W.L., 1992 A Brassica napus transcript encoding a Biotechnology

Plant J 2, 685- transformation. water

Brassica napus, recovery of plantlets

A cDNA clone encoding a Brassica napus

Mauxion, F., Fauvarque, protein related to the Kunitz protease 693 stress, BnD22 drought-induced 22 kDa (BnD22) protein

M.O., Reviron, M.P., de inhibitor family accumulates upon water has been isolated and characterized. The

Weretilnyk, E., Orr, W., 1993 stress in leaves, not three related low-

623 Vienne, D., Vartanian, Characterization of in seeds. Plant Physiol Brassica napus, pBN115, BnD22 transcript accumulated in response

A cDNA clone, pBN115, encoding a low-

White, T.C., Iu, B., and temperature-regulated cDNAs from 101, 171-177. Low temperature, temperature-regulated transcript in winter

Singh, J. winter Brassica napus. Drought stress Brassica napus has been isolated. Northern

624 Murphy, D.J. 1994 Biogenesis, function, and biotechnology Prog Lipid Storage lipids, blotabstract available levels of

No analyses show that

of plant storage lipids. Res 33, 71-85. Biotechnology, Storage

lipids biogenesis

625 Krishna, P., Sacco, M., 1995 Cold-Induced Accumulation of hsp90 Plant Physiol hsp90, Brassica napus, Characterization of the expression of

Cherutti, J.F., and Hill, Transcripts in Brassica napus. 107, 915-923. mRNA, spinach hsp90 genes of Brassica napus by northern

S. blot analysis and immunoblotting showed

626 Boss, P.K., Davies, C., 1996 Expression of anthocyanin biosynthesis Plant Mol Anthocyanins, that the hsp90 mRNA and protein are

The expression of seven genes from the

and Robinson, S.P. pathway genes in red and white grapes. Biol 32, 565- Proanthocynidins, gene anthocyanin biosynthesis pathway was

569. expression regulation determined in different tissues of Shiraz

627 Boss, P.K., Davies, C., 1996 Analysis of the Expression of Plant Physiol Anthocyanin grapevines. All of the tissues contained L.

Anthocyanin synthesis in Vitis vinifera

and Robinson, S.P. Anthocyanin Pathway Genes in 111, 1059- biosynthesis Vitis cv Shiraz grape berries began 10 weeks

Developing Vitis vinifera L. cv Shiraz 1066. vinifera, Chalcone postflowering and continued throughout

628 Hincha, D.K., Meins Jr, 1997 [beta]-1,3-Glucanase Implications for

Grape Berries and the Is Cryoprotective Plant Physiol synthase ß-1,3-

Spinach, We have used Expression of seven genes

berry ripening.isolated spinach (Spinacea

F., and Schmitt, J.M. in Vitro and Is Accumulated in Leaves 114, 1077- glucanase, chitinase, oleracea L.) thylakoid membranes to

during Cold Acclimation. 1083. cryoprotection investigate the possible cryoprotective

629 Ishitani, M., Xiong, L., 1997 Genetic analysis of osmotic and cold Plant Cell 9, Arabidopsis, abiotic properties of class I [beta]-1,3-glucanase

To dissect genetically the complex

Stevenson, B., and Zhu, stress signal transduction in Arabidopsis: 1935-1949. stress, RD29A, luciferase network of osmotic and cold stress

J.K. interactions and convergence of abscisic signaling, we constructed lines of

630 Anderson, L.E., Li, 1998 The enolases of ice abscisic

acid-dependent and plant andacid- Phytochemistr Arabidopsis thaliana; Arabidopsis plants displaying enolases of

The simulated structures of the

A.D., and Stevens, F.J. Arabidopsis contain a potential y 47, 707-713. Brassicaceae; thale cress; Arabidopsis and the common ice plant

disulphide and are redox sensitive. Mesembryanthemum contain a pair of Cys residues in the

crystallinum; Aizoaceae; correct orientation to form a disulphide

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



631 Gilmour, S.J., Zarka, 1998 Low temperature regulation of the Plant J 16, CBF gene family, cold Cold-induced expression of the

D.G., Stockinger, E.J., Arabidopsis CBF family of AP2 433-442. response, COR, Arabidopsis COR (cold-regulated) genes

Salazar, M.P., transcriptional activators as an early step Arabidopsis is mediated by a DNA regulatory element

632 Houghton, J.M., and

Horvath, D.P., and 1998 in cold-induced COR gene expression.

Cloning and characterization of cold- Plant Mol Euphorbia esula,Freezing termedspurge (Euphorbia esula) is a

Leafy the CRT (C-repeat)/DRE

Olson, P.A. regulated glycine-rich RNA-binding Biol 38, 531- tolerance, COR20 perennial weed which is capable of

protein genes from leafy spurge 538. acclimating to sub-freezing temperatures.

633 Liu, Q., Kasuga, M., 1998 (Euphorbia esula L.) and comparison to

Two transcription factors, DREB1 and Plant Cell 10, Dehydration-responsive We have used the differential display

Plant growth is greatly affected by drought

Sakuma, Y., Abe, H., DREB2, with an EREBP/AP2 DNA 1391-1406. element, Low and low temperature. Expression of a

Miura, S., Yamaguchi- binding domain separate two cellular temperature stress, number of genes is induced by both

634 Shinozaki, K., and

Muhlbach, H.P. 1998 signal transduction pathways in drought-

Use of plant cell cultures in Biotechnol Cell culture, drought and low temperature, although

Plant cell cultures are being widely used

biotechnology. Annu Rev 4, Biotechnology, in scientific studies on the physiology,

113-176. Secondary metabolites, biochemistry and molecular biology of

635 Berna, A., and Bernier, 1999 Regulation by biotic and abiotic stress of Plant Mol Biol Pharmaceuticals

Cadmium, Copper, primary and secondary metabolism,

Germins and germin-like proteins (GLPs)

F. a wheat germin gene encoding oxalate 39, 539-549. Germin, Oxalate, constitute a ubiquitous family of plant

oxidase, a H2O2-producing enzyme. Oxidase,Stress, proteins that seem to be involved in many

636 Gao, Y.P., Young, L., 1999 Characterization and expression of Plant Mol Biol Response, Tobacco

Brassica napus, developmental and stress-related from a

Two aquaporin genes were isolated

Bonham-Smith, P., and plasma and tonoplast membrane 40, 635-644. Aquaporin, Water cDNA library of canola (Brassica napus

Gusta, L.V. ( aquaporins in primed seed of Brassica transportation L.). The first aquaporin, BnPIP1 of 1094

637 Medina, J., Bargues, M., 1999 napus during germination under stress

The Arabidopsis CBF gene family is Plant Physiol Transcriptional activator, bp, encoding a putative polypeptide of 287

We have identified two genes from

Terol, J., Perez-Alonso, composed of three genes encoding AP2 119, 463-470. AP2 domain, Arabidopsis that show high similarity with

M., and Salinas, J. domain-containing proteins whose Arabidopsis, CBF1 CBF1, a gene encoding an AP2 domain-

638 Smirnoff, N., and 1999 expression Isthe stress out of growing up. Nat

DREB takes regulated by low Transcription factor, containing transcriptional activator that

No abstract available

Bryant, J.A. Biotechnol 17, Abiotic stress, Gene

229-230. induction

639 Knight, H. 2000 Calcium signaling during abiotic stress Int Rev Cytol Intracellular calcium, Plants experience a wide array of

in plants. 195, 269-324. Abiotic stress, Plants environmental stimuli, not all of which are

favorable, and, unlike animals, are unable

640 Shinozaki, K., and 2000 Molecular responses to dehydration and Curr Opin Abscisic-acid- to move away from stressful system that

Recently, a major transcription

Yamaguchi-Shinozaki, low temperature: differences and cross- Plant Biol 3, independent gene controls abscisic-acid-independent gene

K. talk between two stress signaling 217-223. expression, Dehydration, expression in response to dehydration and

pathways. Low temperature stress, low temperature has been identified. The

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



641 Kizis, D., Lumbreras, 2001 Role of AP2/EREBP transcription FEBS Lett Drought, DRE cis- Crop plants are exposed to many types of

V., and Pages, M. factors in gene regulation during abiotic 498, 187-189. element, AP2/EREBP abiotic stress during their life cycle. Water

stress. transcription factor, deficit derived from drought, low

642 Knight, H., and Knight, 2001 Abiotic stress signalling pathways: Trends Plant Abscisic acid

Calcium, Signaling, temperature orahigh saltof responses toin

Plants exhibit variety concentration

M.R. specificity and cross-talk. Sci 6, 262- Kinase, Phosphatase, abiotic stresses that enable them to

267. Cross-talk, Specificity, tolerate and survive adverse conditions.

643 Savitch, L.V., Barker- 2001 Cold acclimation of Arabidopsis Planta 214, DREB, Oscillations

Arabidopsis (cold stress), The effects more about cold stress and

As we learnof short-termthe signalling

Astrom, J., Ivanov, thaliana results in incomplete recovery of 295-303. Cold acclimation, long-term cold acclimation on the light

A.G., Hurry, V., Oquist, photosynthetic capacity, associated with Photosystem I (II), reactions of photosynthesis were

644 G., Huner, N.P., and

Tolmay, V.L. 2001 an increased reduction of the chloroplast

Resistance to biotic and abiotic stress in Hereditas Reduction state of

Stress resistance, examined in vivo to assess their occur in

Poverty, hunger and malnutrition

the Triticeae. 135, 239-242. Triticaceae, Crops, many parts of the world despite the

Nutritional value enormous progress that has taken place in

645 Cattivell, L., Baldi, P., 2002 Chromosome regions and stress-related Plant Mol Biol Abiotic stress, crop, agriculture and food production in the last

Drought, low temperature and salinity are

Crosatti, C., Di Fonzo, sequences involved in resistance to 48, 649-665. QTL, gene expression the most important abiotic stress factors

N., Faccioli, P., Grossi, abiotic stress in Triticeae. limiting crop productivity. A genomic map

646 M., Mastrangelo, A.M.,

Chen, T.H., and Murata, 2002 Enhancement of tolerance of abiotic Curr Opin Betaines; Compatible The accumulation of compatible stress

of major loci and QTLs affectingsolutes,

N. stress by metabolic engineering of Plant Biol 5, solute; Environmental such as betaines, proline and sugar

betaines and other compatible solutes. 250-257. stress;Fructan; Mannitol; alcohols, is a widespread response that

647 Cheong, Y.H., Chang, 2002 Transcriptional profiling reveals novel Plant Physiol Image-ononitol; Proline;

Stress, wounding, Mechanical plants against environmental

may protect wounding not only damages

H.S., Gupta, R., Wang, interactions between wounding, 129, 661-677. Arabidopsis, plant tissues, but also provides pathways

X., Zhu, T., and Luan, pathogen, abiotic stress, and hormonal Transcriptional profiling for pathogen invasion. To understand

648 S.

Fowler, S., and Arabidopsis Arabidopsis.

2002 responses in transcriptome profiling Plant Cell 14, Freezing tolerance, CBF plant responses to wounding at a genomic

Many plants, including Arabidopsis,

Thomashow, M.F. indicates that multiple regulatory 1675-1690. regulon, Transcriptional increase in freezing tolerance in response

pathways are activated during cold profiling, Arabidopsis to low, nonfreezing temperatures, a

649 Frenette Charron, J.B., Molecular and structural the CBF cold

2002 acclimation in addition toanalyses of a FEBS Lett Wheat; Cold phenomenon corresponding to a novel

Two cDNAs known as cold acclimation.

Breton, G., Badawi, M., novel temperature stress-induced 517, 129-132. acclimation; Heat-shock; lipocalin were identified from wheat and

and Sarhan, F. lipocalin from wheat and Arabidopsis. Apolipoprotein D; Arabidopsis. The two cDNAs designated

650 Gao, M.J., Allard, G., 2002 Regulation and characterization of four Plant Mol Biol Lipocalin; Freezing

Brassica napus, BNCBF, Four for Triticum aestivum L. temperature-

Tatil orthologues of the Arabidopsis

Byass, L., Flanagan, CBF transcription factors from Brassica 49, 459-471. Transctiption factor CBF/Dreb transcriptional activator genes

A.M., and Singh, J. napus. were isolated from the winter Brassica

napus, cv. Jet neuf. All four BNCBF

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



651 Guo, Y., Xiong, L., 2002 An Arabidopsis mutation in translation Proc Natl Low temperature Low temperature regulates gene

Ishitani, M., and Zhu, elongation factor 2 causes Acad Sci U S response, arabidopsus, expression in bacteria, yeast, and animals

J.K. superinduction of CBF/DREB1 A 99, 7786- LOS1 as well as in plants. However, the signal

652 Haake, V., Cook, D., Transcription factor CBF4 is blocks the

2002 transcription factor genes but a regulator 7791. Physiol

Plant Cold, dehydration, transduction cascades mediating the low

In plants, low temperature and dehydration

Riechmann, J.L., of drought adaptation in Arabidopsis. 130, 639-648. arabidopsis, CBF4 activate a set of genes containing C-

Pineda, O., Thomashow, repeat/dehydration-responsive elements in

Hsieh, T.H., Lee, J.Z.

653 M.F., and Zhang, J.T.,( 2002 Heterology expression of the Plant Physiol Tomato, Arabidopsis, their promoter. It has been shown

In an attempt to improve stress tolerance

Yang, P.T., Chiu, L.H., Arabidopsis C-repeat/dehydration 129, 1086- CBF1, chilling stress of tomato (Lycopersicon esculentum)

Charng, Y.Y., Wang, response element binding factor 1 gene 1094. plants, an expression vector containing an

Yang, J., Chan, M.T.

654 Y.C., andand Yen, H.E. 2002 confers elevated tolerance to chilling and

Early salt stress effects on the changes Plant Physiol Ice plant, Arabidopsis, Arabidopsis C-repeat/dehydration

A technique based on Fourier transform

in chemical composition in leaves of ice 130, 1032- Fourier transform infrared (FT-IR) spectrometry was

plant and Arabidopsis. A Fourier 1042. infrered spectroscopy developed to detect the corresponding

655 Inatsugi, R., Nakamura, 2002 transform infrared spectroscopy study.

Phosphatidylcholine biosynthesis at low Plant Cell Arabidopsis, We cloned the gene composition

changes in chemical and a cDNA for a

M., and Nishida, I. temperature: differential expression of Physiol 43, phosphorylcholine second CTP: phosphorylcholine

CTP:phosphorylcholine 1342-1350. cytidylyltransferase , cytidylyltransferase (CCT, EC 2.7.7.15)

656 Jaakola, L., Maatta, K., 2002 cytidylyltransferase isogenes in

Expression of genes involved in Plant Physiol chilling

Vaccinium myrtillus, annotated in chromosome 4 by the fruit

The production of anthocyanins in

Pirttila, A.M., Torronen, anthocyanin biosynthesis in relation to 130, 729-739. Anthocyanin synthesis tissues is highly controlled at the

R., Karenlampi, S., and anthocyanin, proanthocyanidin, and developmental level. We have studied the

657 Hohtola, A.

Job, D. 2002 flavonol levels during bilberry fruit

Plant biotechnology in agriculture. Biochimie 84, Biotechnology, expression of flavonoid biosynthesis genes

Knowledge on plant genomes has

1105-1110. Transgenesis, Plants progressed during the past few years. Two

plant genomes, those of Arabidopsis

658 Knight, M.R. 2002 Signal transduction leading to low- Philos Trans R Apoaequorin, Calcium, thaliana and rice, have been sequenced.

Calcium is used by most cells to convert

temperature tolerance in Arabidopsis Soc Lond B Cytosol external signals into biochemical events

thaliana. Biol Sci 357, within the cytosol. To detect the effects of

659 Kobayashi, S., Ishimaru, 2002 Myb-related genes of the Kyoho grape ( 871-875.

Planta 215, Anthocyanin Partial cDNAs of encoding apoaequorin

cold stress, a genemyb-related regulatory

M., Hiraoka, K., and Vitis labruscana) regulate anthocyanin 924-933. biosynthesis, Fruit, myb, genes were isolated from the tetraploid

Honda, C. biosynthesis. Regulatory gene, Vitis Kyoho grape ( Vitis labruscana: V.

660 Koiwa, H., Barb, A.W., 2002 C-terminal domain phosphatase-like Proc Natl RD29A, Plant stress labrusca x V. vinifera) and the expression

Cold, hyperosmolarity, and abscisic acid

Xiong, L., Li, F., family members (AtCPLs) differentially Acad Sci U S adaptation, Arabidopsis (ABA) signaling induce RD29A

McCully, M.G., Lee, regulate Arabidopsis thaliana abiotic A 99, 10893- expression, which is an indicator of the

B.H., Sokolchik, I., Zhu, stress signaling, growth, and 10898. plant stress adaptation response. Two

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



661 Kreps, J.A., Wu, Y., 2002 Transcriptome changes for Arabidopsis Plant Physiol Global expression To identify genes of potential importance

Chang, H.S., Zhu, T., in response to salt, osmotic, and cold 130, 2129- profiling, Cold, to cold, salt, and drought tolerance, global

Wang, X., and Harper, stress. 2141. Arabidopsis expression profiling was performed on

662 J.F. J., Gilmour, S.J.,

Liu, 2002 Cold signalling associated with Physiol Plant Cold signaling, CBF1, In genotypes of Arabidopsis to stress

Arabidopsis plants subjectedthat exhibit a

Thomashow, M.F., and vernalization in Arabidopsis thaliana 114, 125-134. Abscisic acid, winter-annual flowering habit, floral

Van Nocker, S. does not involve CBF1 or abscisic acid. Arabidopsis induction in response to extended cold

663 Llorente, F., Lopez- 2002 A novel cold-inducible gene from Plant J 32, 13- Peroxidase, Abiotic exposure from Arabidopsis mediated by

A cDNA (vernalization) is corresponding

Cobollo, R.M., Catala, Arabidopsis, RCI3, encodes a peroxidase 24. stress, Arabidpsis, to a new cold-inducible gene, RCI3 (for

R., Martinez-Zapater, that constitutes a component for stress Dehydration telerance, Rare Cold Inducible gene 3), was isolated.

664 J.M., and Salinas, J.

Meyer, J.E., Pepin, 2002 tolerance. production from Vaccinium

Anthocyanin J Biotechnol Salt tolerance, Freezing

Agitation, Aggregation, Isoelectric focusing electrophoresis and

Physical microenvironmental parameters

M.F., and Smith, M.A. pahalae: limitations of the physical 93, 45-57. Bioreactor, Irradiance, conducive to production of flavonoids in

microenvironment. Flavonoids, Pigment vitro from continuous Vaccinium pahalae

665 Rapacz, M. 2002 Cold-deacclimation of oilseed rape Ann Bot Brassica napus var. The aim of cultures were to establish the

suspension this work was examined first in

(Brassica napus var. oleifera) in response (Lond) 89, 543-oleifera, cold role of factors that may trigger elongation

to fluctuating temperatures and 549. deacclimation, growth in the dehardening response,

666 Roberts, M.R., Salinas, 2002 photoperiod. and the response to

14-3-3 proteins Plant Mol Biol elongation growth,

14-3-3 protein, Abiotic namelyproteins function as regulators of a

14-3-3 temperature during daylight,

J., and Collinge, D.B. abiotic and biotic stress. 50, 1031- stress, Biotic stress, wide range of target proteins in all

1039. Defence Responses, eukaryotes by effecting direct protein-

667 Ruelland, E., Cantrel, 2002 Activation of phospholipases C and D is Plant Physiol Plant pathogen,

Phosphoinositide protein interactions. Primarily, by a cold

The signaling events generated

C., Gawer, M., Kader, an early response to a cold exposure in 130, 999- signaling pathway, cold exposure are poorly known in plants. We

J.C., and Zachowski, A. Arabidopsis suspension cells. 1007. stress, Phosphatidic acid, were interested in checking the possible

668 Sakuma, Y., Liu, Q., 2002 DNA-binding specificity of the Biochem Signaling cis-acting

DRE/CRT, activation of enzymes of the

DRE/CRT is a cis-acting element that is

Dubouzet, J.G., Abe, H., ERF/AP2 domain of Arabidopsis Biophys Res element, Gel mobility involved in gene expression responsive to

Shinozaki, K., and DREBs, transcription factors involved in Commun 290, shift assay drought and low-temperature stress in

669 Yamaguchi-Shinozaki,

Scholthof, K.B., Plant virus gene cold-inducible gene

2002 dehydration- andvectors: biotechnology 998-1009. (N Biotechnology, Plant

Genet Eng higher plants. DREB1A/CBF3 and

No abstract available

Mirkov, T.E., and applications in agriculture and medicine. Y) 24, 67-85. transformation, Plant

Scholthof, H.B. virus vectors

670 Stefanowska, M., Kuras, 2002 Low temperature-induced modifications Ann Bot Brassica napus var. Acclimation of winter oilseed plants in the

M., and Kacperska, A. in cell ultrastructure and localization of (Lond) 90, 637-oleifera, Cell cold (i.e. at temperatures >0 degrees C)

phenolics in winter oilseed rape 645. ultrastructure, Cold followed by short exposure to sub-lethal

(Brassica napus L. var. oleifera L.) acclimation, Phenolics, freezing temperatures resulted in

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



671 Stitt, M., and Hurry, V. 2002 A plant for all seasons: alterations in Curr Opin Arabidopsis; cold Low temperatures lead to the inhibition of

photosynthetic carbon metabolism Plant Biol 5, acclimation; sucrose synthesis and photosynthesis. The

during cold acclimation in Arabidopsis. 199-206. Photosynthesis; Sucrose biochemical and physiological adaptations

672 Taylor, N.J., and 2002 Microparticle bombardment as a tool in DNA Cell synthesis; Phosphate

Agricultural of plants to low temperaturestechnology

Microparticle bombardment include the

Fauquet, C.M. plant science and agricultural Biol 21, 963- biotechnology, has evolved as a method for delivering

biotechnology. 977. Microparticle exogenous nucleic acids into plant cells

673 Taji, T., Ohsumi, C., 2002 Important roles of drought- and cold- Plant J 29, 417- bombardment,

Drought stress, and is a commonly employed technique in

Raffinose family oligosaccharides (RFO)

Iuchi, S., Seki, M., 426.

inducible genes for galactinol synthase in Transgenic plants accumulating during seed development are

Kasuga, M., Kobayashi, stress tolerance in Arabidopsis thaliana. Galactonol synthase thought to play a role in the desiccation

674 M., Yamaguchi- Li,

Welti, R., Li, W., 2002 Profiling membrane lipids in plant stress Electrospray Galactinol,

J Biol Chem (GolS), RFO,ionization A sensitive seeds. However, the

tolerance ofapproach based on functions

M., Sang, Y., Biesiada, responses. Role of phospholipase D 277, 31994- tandem mass electrospray ionization tandem mass

H., Zhou, H.E., alpha in freezing-induced lipid changes 32002. spectrometry, membrane spectrometry has been employed to profile

675 Rajashekar, C.B., K.Y.

Wi, S.J., and Park, 2002 in Arabidopsis.

Antisense expression of carnation cDNA Polyamines, Cold

Mol Cells 13, lipid profile, Putrescinem membrane lipidpolyamines species in

The amount of molecular (such as

encoding ACC synthase or ACC oxidase 209-220. Spermidine, Spermine, putrescine, spermidine, and spermine)

enhances polyamine content and abiotic Senescence increased under environmental stress

676 Xiong, L., Lee, H., 2002 stress tolerance in transgenic tobacco by

Repression of stress-responsive genes Proc Natl FIERY2 (FRY2), Low temperature, drought, and technology

conditions. We used transgenic high

Ishitani, M., Tanaka, Y., FIERY2, a novel transcriptional Acad Sci U S Genetic screen, Abiotic salinity induce the expression of many

Stevenson, B., Koiwa, regulator in Arabidopsis. A 99, 10899- stress, Arabidopsis plant genes. To understand the

677 H., Bressan, R.A.,

Xiong, L., Schumaker, 2002 Cell signaling during cold, drought, and 10904. 14 Plant stress response,

Plant Cell mechanisms for the transcriptional

Low temperature, drought, and high

K.S., and Zhu, J.K. salt stress. Suppl, S165- Low temperature, salinity are common stress conditions that

183. Drought, High salinity adversely affect plant growth and crop

678 Xu, C., Hartel, H., 2002 The pgp1 mutant locus of Arabidopsis Plant Physiol Phosphatidylglycerol, production. The cellularaand molecular

Phosphatidylglycerol is ubiquitous

Wada, H., Hagio, M., encodes a 129, 594-604. Phospholipids, Cold phospholipid that is also present in the

Yu, B., Eakin, C., and phosphatidylglycerolphosphate synthase acclimation, photosynthetic membranes of plants.

679 Benning, C.

Zheng, B., Halperin, T., 2002 with impaired activity.

Characterization of Chloroplast Clp Physiol Plant Photosynthetic

Proteolysis, ATP- Multiple independent lines of evidence of

The ATP-dependent Clp protease is one

Hruskova- proteins in Arabidopsis: Localization, 114, 92-101. dependent Clp protease, the newly identified proteolytic systems in

Heidingsfeldova, O., tissue specificity and stress responses. Molecular chaperones plant organelles that incorporate the

Zhu, J., Gong, Clarke,

680 Adam, Z., and Z., 2002 OSM1/SYP61: a syntaxin protein in Plant Cell 14, T-DNA insertion, Salt activity of molecular chaperones to target

To identify the genetic loci that control

Zhang, C., Song, C.P., Arabidopsis controls abscisic acid- 3009-3028. tolerance, Genetic salt tolerance in higher plants, a large-

Damsz, B., Inan, G., mediated and non-abscisic acid-mediated screen, Arabidopsis, scale screen was conducted with a

Koiwa, H., Zhu, J.K., responses to abiotic stress. Syntaxin bialaphos marker-based T-DNA

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



681 Albrecht, V., Weinl, S., 2003 The calcium sensor CBL1 integrates Plant J 36, 457- CLB1, Stress response, Calcium ions represent both an integrative

Blazevic, D., D'Angelo, plant responses to abiotic stresses. 470. Drought stress, Cold signal and an important convergence point

C., Batistic, O., stress, Salt stress, of many disparate signaling pathways.

682 Kolukisaoglu, U., Bock,

Bae, M.S., Cho, E.J., 2003 Analysis of the Arabidopsis nuclear Plant J 36, 652- Calcium sgnaling

Proteomics, Arabidopsis, The nucleus is the subcellular calcineurin

Calcium-binding proteins, likeorganelle

Choi, E.Y., and Park, proteome and its response to cold stress. 663 Nuclear proteins, Cold that contains nearly all the genetic

O.K. stress, 2D gel information required for the regulated

683 Boyce, J.M., Knight, H., 2003 The sfr6 mutant of Arabidopsis is Plant J 34, 395- electrophoresis, MALDI-

Acclimation, sfr6, expression of cellular proteins. In this a

The sfr6 mutant of Arabidopsis displays

Deyholos, M., defective in transcriptional activation via 406. DREB, Cold, Drought, deficit in freezing tolerance after cold

Openshaw, M.R., CBF/DREB1 and DREB2 and shows Arabidopsis acclimation. We previously observed that

684 Galbraith, D.W.,

Breton, G., Danyluk, J., 2003 Expression profiling stress.

sensitivity to osmoticand bioinformatic Plant Physiol Cold acclimation, wheat, the transcripts of three cold-, ABA- and

Cold acclimation is a multigenic trait that

Charron, J.B., and analyses of a novel stress-regulated 132, 64-74. COR413 allows hardy plants to develop efficient

Sarhan, F. multispanning transmembrane protein tolerance mechanisms needed for winter

685 Catala, R., Santos, E., 2003 family from cereals and Arabidopsis.

Mutations in the Ca2+/H+ transporter Plant Cell 15, Calcium, Cold Transient increases in the genetic nature

survival. To determinecytosolic free

Alonso, J.M., Ecker, CAX1 increase CBF/DREB1 expression 2940-2951. acclimation, CBF/DREB calcium concentration ([Ca2+]cyt) are

J.R., Martinez-Zapater, and the cold-acclimation response in essential for plant responses to a variety of

Chinnusamy, V., J.

686 J.M., and Salinas,Ohta, 2003 Arabidopsis.

ICE1: a regulator of cold-induced Genes Dev 17, Cold signaling; freezing environmental stimuli, including low

Cold temperatures trigger the expression

M., Kanrar, S., Lee, transcriptome and freezing tolerance in 1043-1054. tolerance; bHLH protein; of the CBF family of transcription factors,

B.H., Hong, X., Arabidopsis. CBF regulation; which in turn activate many downstream

687 Agarwal, M., and Zhu,

Dubouzet, J.G., 2003 OsDREB genes in rice, Oryza sativa L., Plant J 33, 751- transcriptome factors,

Transcription The transcription factors and freezing

genes that confer chillingDREBs/CBFs

Sakuma, Y., Ito, Y., encode transcription activators that 763. DREB, DRE regulon, specifically interact with the dehydration-

Kasuga, M., Dubouzet, function in drought-, high-salt- and cold- rice, transgenic responsive element/C-repeat (DRE/CRT)

Gao, Miura, S., Seki,

688 E.G., M.J., Schafer, 2003 A novel protein expression.

responsive gene from Brassica napus has Plant J 33, Arabidopsis, abiotic

Histone deacetylase, To identify factors that motif:

cis-acting element (coreinteract with

U.A., Parkin, I.A., a putative KID domain and responds to 1073-1086. Brassica napus, Yeast histone deacetylase (HDAC) in Brassica

Hegedus, D.D., Lydiate, low temperature. two hybrid napus, a yeast two-hybrid library was

689 D.J., and Hannoufa, A.

Hazen, S.P., Wu, Y., 2003 Gene expression profiling of plant Funct Integr Abiotic stress, gene screened using the Arabidopsis HDA19 as

Expression profiling has become an

and Kreps, J.A. responses to abiotic stress. Genomics 3, expression profiling important tool to investigate how an

105-111. organism responds to environmental

690 Hegedus, D., Yu, M., 2003 Molecular characterization of Brassica Plant Mol Brassica napus, EST, changes. Plants, being sequence tag the

Subtractive expressed sessile, have

Baldwin, D., Gruber, napus NAC domain transcriptional Biol 53, 383- Wounding, Transcription analysis and screening of cDNA libraries

M., Sharpe, A., Parkin, activators induced in response to biotic 39 factors derived from Brassica napus leaves

I., Whitwill, S., and and abiotic stress subjected to mechanical wounding, flea

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



691 Yubero-Serrano, E.M., 2003 Identification of a strawberry gene cDNA and genomic clones encoding a

J Exp Bot 54, ABA, gene regulation,

Moyano, E., Medina- encoding a non-specific lipid transfer 1865-1877. strawberry (Fragariaxananassa cv.

LTPs, strawberry fruit,

Escobar, N., Munoz- protein that responds to ABA, wounding stress Chandler) non-specific lipid transfer

692 Blanco, J., and J.Y.,

Jung, S.H., Lee, 2003 and cold stress.

Use of SAGE technology to reveal protein (Fxaltp gene) withinisolated and

The genes expressed were an organism

Plant Mol Biol Serial analysis of gene

and Lee, D.H. changes in gene expression in determine its biological characteristics.

52, 553-567. expression, Cold stress,

Arabidopsis leaves undergoing cold Arabidopsis Various internal or external factors can

693 Li, R., Rimmer, R., Yu, 2003 stress.Brassica napus polygalacturonase

Two Planta 217, Polygalacturonase modulate these gene expression patterns,

Plants encode a distinct set of

M., Sharpe, A.G., inhibitory protein genes are expressed at 299-308. polygalacturonase inhibitory proteins

inhibitory proteins,

Seguin-Swartz, G., different levels in response to biotic and (PGIPs) that function to inhibit

Leucine-rich repeats,

694 Lydiate, D., and Yao, J., 2003 abiotic stresses.

Lu, Y., Sun, X., Isolation and expression of cold- DNA Seq 14, Brassica napus It has been established that produced

polygalacturonase enzymes changes inby

Brassica pekinensis,

Chai, Y., Zhao, X., regulated cDNA from Chinese cabbage 219-222. gene expression occur during cold

Arabidopsis, COR15,

Zhang, L., Song, J., (Brassica pekinensis). Cold stress acclimation in a wide range of plants.

695 Pang, Y.Z., Wu, W.,X., 2003 The BOTRYTIS SUSCEPTIBLE1 gene

Mengiste, T., Chen, and The we present a cellular mechanisms

Heremolecular andnovel cDNA encoding a

Plant Cell 15, Plant resistance, Botrytis

Salmeron, J., and encodes an R2R3MYB transcription 2551-2565. cinerea, T-DNA involved in plant resistance to the

Dietrich, R. factor protein that is required for biotic necrotrophic fungal pathogen Botrytis

insertional allele,

696 Mine, T., Hiyoshi, T., CIP353 encodes responses in

2003 and abiotic stressan AP2/ERF-domain Plant Cell Arabidopsis gene,

Cold inducible cinerea and theirCIP353 cDNA, which

We isolated the genetic control are

Kasaoka, K., and protein in potato (Solanum tuberosum Physiol 44, 10- Solanum tuberosum,encodes a novel cold-inducible protein,

Ohyama, A. L.) and responds slowly to cold stress. 15. from cold-stored tubers of potato

Transcription factor,

697 Morandini, P., and 2003 Plant biotechnology and breeding: allied Trends Plant Late-embryogenesis- (Solanum tuberosum L.). The level of

Plant metabolic engineering is lagging

Biotechnology, Plant

Salamini, F. for years to come. Sci 8, 70-75. metabolism, Breding behind other kinds of genetic manipulation

of plants. Creating metabolic pathways or

698 Provart, N.J., Gil, P., 2003 Gene expression phenotypes of Plant Physiol Arabidopsis improving their yieldsabiotic stress that

Chilling is a common requires a better

Chen, W., Han, B., Arabidopsis associated with sensitivity 132, 893-906. transcriptome, Chilling leads to economic losses in agriculture. By

Chang, H.S., Wang, X., to low temperatures. resistance, Gene comparing the transcriptome of

699 and Zhu, T.

Ratcliffe, O.J., 2003 Analysis of the Arabidopsis MADS Vernalization response, Arabidopsis under normal (22 degrees C)C

Plant Cell 15, expression patern The Arabidopsis FLOWERING LOCUS

Kumimoto, R.W., AFFECTING FLOWERING gene 1159-1169. Floral represor, (FLC) gene is a key floral repressor in the

Wong, B.J., and family: MAF2 prevents vernalization by FLOWERING LOCUS maintenance of a vernalization response.

700 Riechmann, J.L.

Segui-Simarro, J.M., 2003 short periods of cold.

Hsp70 and Hsp90 change their Brassica Arabidopsis

J Struct Biol C (FLC),napus; A vernalization-sensitive genetic

In stress treatment of 32 degrees C for at

Testillano, P.S., and expression and subcellular localization 142, 379-391. Microspore least 8h was able to change the

Risueno, M.C. after microspore embryogenesis embryogenesis; Hsp70; gametophytic program of the microspore,

induction in Brassica napus L. Hsp90; Immunoelectron switching it to embryogenesis in Brassica

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



701 Shen, Y.G., Zhang, 2003 An EREBP/AP2-type protein in Triticum Theor Appl DRE-binding protein, We characterize one transcription factor of

W.K., He, S.J., Zhang, aestivum was a DRE-binding Genet 106, One-hybrid, Abiotic DRE-binding proteins (TaDREB1) that

J.S., Liu, Q., and Chen, transcription factor induced by cold, 923-930. stresses, Triticum was isolated from a drought-induced

702 S.Y. Y.G., Zhang,

Shen, Characterization of a stress.

2003 dehydration and ABADRE-binding Theor Appl aestivumhortensis, DRE-

Atriplex L. cDNA library of wheat (Triticum aestivum

Environmental stresses, such as salinity,

W.K., Yan, D.Q., Du, transcription factor from a halophyte Genet 107, binding protein, drought and cold, can induce the

B.X., Zhang, J.S., Liu, Atriplex hortensis. 155-161. Transcription factor, Saltexpression of a large amount of genes.

703 Q., and Chen, S.Y.

Shinozaki, K., 2003 Regulatory network of gene expression Curr Opin stress, PEG

Drought stress, Cold Among these are many transcription

Molecular and genomic studies have

Yamaguchi-Shinozaki, in the drought and cold stress responses. Plant Biol 6, stress, Genetic studies, shown that several genes with various

K., and Seki, M. 410-417. Gene induction functions are induced by drought and cold

704 Streb, P., Aubert, S., 2003 Reversibility of cold- and light-stress J Exp Bot 54, Antioxidants, Cold- stresses, and that various transcription

Two high mountain plants Soldanella

Gout, E., and Bligny, R. tolerance and accompanying changes of 405-418. acclimation, Malate, alpina (L.) and Ranunculus glacialis (L.)

metabolite and antioxidant levels in the NMR-spectroscopy, were transferred from their natural

705 Takagi, T., Nakamura, 2003 two high mountain plant species

The leaf-order-dependent enhancement Plant Cell Photoinhibition,

Freezing tolerance, The central part of different growth

environment to twocold-acclimated

M., Hayashi, H., of freezing tolerance in cold-acclimated Physiol 44, Arabidopsis, Rosette rosettes of Arabidopsis thaliana L.

Inatsugi, R., Yano, R., Arabidopsis rosettes is not correlated 922-931. leaves, Transcription (ecotype Columbia) survived freezing at

Tyagi, A.K., I.

706 and Nishida, and 2003 Plant molecular biology of

with the transcript levelsandthe cold- Adv Biochem factor

Biotechnology, After temperatures of the recombinant

lower the beginning better than did those at

Khurana, J.P. biotechnology research in the post- Eng Transgenic plants, Plant DNA era in the mid-1970s, researchers in

recombinant DNA era. Biotechnol 84, transformation systems India started to make use of the new

707 Uemura, M., Warren, 2003 Freezing sensitivity in the sfr4 mutant of 91-121.

Plant Physiol technology to understand the structure of

Protoplasts were tested to determine

Freezing sensitivity, sfr4,

G., and Steponkus, P.L. Arabidopsis is due to low sugar content 131, 1800- Soluble sugars whether the freezing sensitivity of the sfr4

and is manifested by loss of osmotic 1807. (sensitive to freezing) mutant of

708 Vlachonasios, K.E., 2003 responsiveness.

Disruption mutations of ADA2b and Plant Cell 15, ADA, SAGA, Histone Arabidopsis was due to the mutant's

We previously identified Arabidopsis

Thomashow, M.F., and GCN5 transcriptional adaptor genes 626-638. acetyltransferase, CBF, genes homologous with the yeast ADA2

Triezenberg, S.J. dramatically affect Arabidopsis growth, Arabidpsis, Cold- and GCN5 genes that encode components

709 Wang, Y.J., Zhang, 2003 development, and gene expression. is Theor Appl

A rice transcription factor OsbHLH1 Oryza sativa, OsbHLH1, of thestress adversely affects plant growth

regulated genes Cold ADA and SAGA histone

Z.G., He, X.J., Zhou, involved in cold stress response. Genet 107, Transcription factor, and crop production. Some plants express

H.L., Wen, Y.X., Dai, 1402-1409. Cold stress a series of cold-responsive genes during

710 J.X., Zhang, J.S., and

Zarka, D.G., Vogel, 2003 Cold induction of Arabidopsis CBF Plant Physiol DREB, CBF, cold Arabidopsis to reduce and damage of

The acclimation CBF1, 2, the 3 genes

J.T., Cook, D., and genes involves multiple ICE (inducer of 133, 910-918. Arabidopsis, (also known as DREB1b, c, and a,

Thomashow, M.F. CBF expression) promoter elements and Transcriptional activator respectively) encode transcriptional

a cold-regulatory circuit that is activators that have a central role in cold

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



711 Beck, E.H., Heim, R., 2004 Plant resistance to cold stress: J Biosci 29, Cold acclimation of This introductory overview shows that

and Hansen, J. ( mechanisms and environmental signals 449-459. plants; environmental cold, in particular frost, stresses a plant in

triggering frost hardening and signals; frost hardening; manifold ways and that the plant's

712 Chinnusamy, V., 2004 dehardening.

Molecular genetic perspectives on cross- J Exp Bot 55, photoperiod; adaptive

Abiotic stress, The perception injurious stresses and

response, being of abiotic or adaptive, must

Schumaker, K., and talk and specificity in abiotic stress 225-236. response, expression signal transduction to switch on adaptive

Zhu, J.K. signalling in plants. profiling, genetic responses are critical steps in determining

713 Cook, D., Fowler, S., 2004 A prominent role for the CBF cold Proc Natl analysis, signal

Arabidopsis, cold the survival and reproduction of plants

The Arabidopsis CBF cold response

Fiehn, O., and response pathway in configuring the low- Acad Sci U S response, Cvi-1, CBF, pathway has a central role in cold

Thomashow, M.F. temperature metabolome of Arabidopsis. A 101, 15243- metabolome acclimation, the process whereby plants

714 Eastmond, P.J. 2004 Glycerol-insensitive Arabidopsis 15248. 37, 617- Glyycerol, Glycerol

Plant J The aim of this study was to in response

increase in freezing toleranceinvestigate

mutants: gli1 seedlings lack glycerol 625. kinase, Germination, the process of glycerol catabolism in

kinase, accumulate glycerol and are more Abiotic stress, germinating Arabidopsis seed. A genetic

715 Eliasova, A., Repcak, 2004 resistant to abiotic stress.

Quantitative changes of secondary Z Naturforsch Arabidopsis secondary

Abiotic stress, The responses of young isolate glycerol-

screen was performed toplants of diploid

M., and Pastirova, A. metabolites of Matricaria chamomilla by [C] 59, 543- metabolites, Matricaria and tetraploid Matricaria chamomilla

abiotic stress. 548. chamomilla cultivars to abiotic stress were studied.

716 Gimalov, F.R., 2004 Initial stages of low-temperature Biochemistry Calcium channels, The course of quantitative changes of

Some stages of low-temperature signal

Baymiev, A., induction of cabbage cold shock protein (Mosc) 69, calcium, membrane transduction causing appropriate cold

Matniyazov, R.T., gene csp5. 575-579. fluidity, cold regulation stress response in plants are considered.

Hund, A., A.V., and

717 Chemeris, Fracheboud, 2004 QTL controlling root and shoot traits of Theor Appl Maize, QTL, Cold- The effects of Ca2+ chelators, Ca2+crucial

The improvement of early vigour is

Y., Soldati, A., maize seedlings under cold stress. Genet 109, related trait for the adaptation of maize (Zea mays L.)

Frascaroli, E., Salvi, S., 618-629. to the climatic conditions of central

718 and Stamp, P. T.,

Imin, N., Kerim, 2004 Effect of early cold stress on the Proteomics 4, Rice, Cold stress, Europe and the northern Mediterranean,

Male reproductive development in rice

Rolfe, B.G., and maturation of rice anthers. 1873-1882. Proteomics (Oryza sativa Linnaeus is very sensitive to

Weinman, J.J. various forms of environmental stresses

719 Kaplan, F., Kopka, J., 2004 Exploring the temperature-stress Plant Physiol Metabolomic including low temperature. Here, we

Metabolic profiling analyses were

Haskell, D.W., Zhao, metabolome of Arabidopsis. 136, 4159- profiling,Heat shock, performed to determine metabolite

W., Schiller, K.C., 4168. Freezing tolerance temporal dynamics associated with the

720 Gatzke, N., Sung, D.Y.,

Kasuga, M., Miura, S., 2004 A combination of the Arabidopsis Plant Cell DREB1A/CBF3, induction of acquired thermotolerance in

The transcription factor DREB1A/CBF3

Shinozaki, K., and DREB1A gene and stress-inducible Physiol 45, Drought stress tolerance, specifically interacts with the dehydration

Yamaguchi-Shinozaki, rd29A promoter improved drought- and 346-350. Low temperature stress responsive element (DRE/CRT) and

K. low-temperature stress tolerance in tolerance induces expression of genes involved in

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



721 Kasukabe, Y., He, L., 2004 Overexpression of spermidine synthase Plant Cell Polyamines, Spermidine Polyamines play pivotal roles in plant

Nada, K., Misawa, S., enhances tolerance to multiple Physiol 45, synthase, Cucurbita defense to environmental stresses.

Ihara, I., and Tachibana, environmental stresses and up-regulates 712-722. ficifolia However, stress tolerance of genetically

722 S. H.J., Hyun, Y.,

Kim, A genetic link of various stress-regulated

2004 the expression between cold responses Nat Genet 36, C-repeat/ dehydration- engineered plants for polyamine

Cold induces expression of a number of

Park, J.Y., Park, M.J., and flowering time through FVE in 167-171. responsive element, genes that encode proteins that enhance

Park, M.K., Kim, M.D., Arabidopsis thaliana. freezing tolerance, tolerance to freezing temperatures in

Kitashiba, Moon, J.,

723 Lee, M.H.,H., Ishizaka, 2004 Expression of a sweet cherry Dehydration RD29A,

J Plant Physiol Arabidopsis, responsive plants. A cis-acting element responsive to

Dehydration responsive element binding

T., Isuzugawa, K., DREB1/CBF ortholog in Arabidopsis 161, 1171- element binding protein protein 1 (DREB1)/C-repeat binding

Nishimura, K., and confers salt and freezing tolerance. 1176. 1 (DREB1)/C-repeat factor (CBF) induces the expression of

724 Suzuki, T.K., Reski, R.,

Kroemer, 2004 Abiotic stress response in the moss Plant Cell Rep binding factor (CBF),

Physcomitrella patens, The mechanisms plants use in

many stress-inducible genesto adapt to

and Frank, W. Physcomitrella patens: evidence for an 22, 864-870. Gene regulation, abiotic stress have been widely studied in

evolutionary alteration in signaling Signaling pathway a number of seed plants. Major research

725 Lee, J., Finn, C.E., and 2004 pathways in land plants.

Comparison of anthocyanin pigment and J Agric Food Vaccinium; huckleberry; has been focused on the isolation of stress-

Two huckleberry species, Vaccinium

Wrolstad, R.E. other phenolic compounds of Vaccinium Chem 52, anthocyanins; phenolics; membranaceum and Vaccinium ovatum,

membranaceum and Vaccinium ovatum 7039-7044. antioxidant activity native to Pacific Northwestern North

726 Maestre, F.T., and Do positive Pacific Northwest of North

2004 native to theinteractions increase with Proc Biol Sci Semi-arid environment, America, were evaluated for their total,

Theoretical models predict that the

Cortina, J. abiotic stress? A test from a semi-arid 271 Suppl 5, Stipa tenacissima, relative importance of facilitation and

steppe. S331-333. Pistacia lentiscus, competition may vary inversely across

727 Maruyama, K., Sakuma, 2004 Identification of cold-inducible Plant J 38, 982- Competetive interactions

Abiotic stress, gradients of abiotic factor DREB/CBF

The transcriptional stress. However, these

Y., Kasuga, M., Ito, Y., downstream genes of the Arabidopsis 993. Transcription factor, (dehydration-responsive element/C-repeat-

Seki, M., Goda, H., DREB1A/CBF3 transcriptional factor Downstream genes, binding) specifically interacts with the

728 Shimada, Y., Yoshida,

McLaren, J.S., and Plant two microarray systems.

2004 using biotechnology and feedstock Appl Biochem Stress tolerance

Geneticaly modified dehydration-responsive element (DRE)/C-

No abstract available

Thomas, S.R. genomics. Biotechnol plants, Biotechnology,

113-116, 1163- Protein engineering

729 Mukhopadhyay, A., Vij, 2004 Overexpression of a zinc-finger protein 1165.Natl

Proc Zink-finger protein, Cold Stress perception and signal transduction

S., and Tyagi, A.K. gene from rice confers tolerance to cold, Acad Sci U S tolerance, Salt stress, leading to tolerance involve a complex

dehydration, and salt stress in transgenic A 101, 6309- Tobacco interplay of different gene products. We

730 Novillo, F., Alonso, CBF2/DREB1C is a negative regulator 6314.Natl

2004 tobacco. Proc CBF/DREB1, CBF/DREB1 the isolation and

describe here (C-repeat-binding

J.M., Ecker, J.R., and of CBF1/DREB1B and CBF3/DREB1A Acad Sci U S Arabidopsis thaliana, factor/dehydration responsive element-

Salinas, J. expression and plays a central role in A 101, 3985- Freezing tolerance binding factor 1) genes encode a small

stress tolerance in Arabidopsis. 3990. family of transcriptional activators that

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



731 Puhakainen, T., Hess, 2004 Overexpression of multiple dehydrin Plant Mol Biol Arabidopsis, Dehydrin, To elucidate the contribution of dehydrins

M.W., Makela, P., genes enhances tolerance to freezing 54, 743-753. Low temperature (DHNs) to freezing stress tolerance in

Svensson, J., Heino, P., stress in Arabidopsis. tolerance, Transgenic Arabidopsis, transgenic plants

732 and Palva, E.T.

Rohde, P., Hincha, 2004 Heterosis in the freezing tolerance of Plant J 38, 790- plants

Arabidopsis thaliana, overexpressing multiple DHN genes were

Heterosis is broadly defined as the

D.K., and Heyer, A.G. crosses between two Arabidopsis 799. Cold acclimation, increased vigour of hybrids in comparison

thaliana accessions (Columbia-0 and Compatible solutes, COR to their parents. In the model plant

733 Sakamoto, H., 2004 C24) that show differences in non-

Arabidopsis Cys2/His2-type zinc-finger Plant Physiol genes, Gene expression,

Cys-2/His-2-type zinc- Arabidopsis thaliana, athat have two

ZPT2-related proteins significant

Maruyama, K., Sakuma, proteins function as transcription 136, 2734- finger motif, canonical Cys-2/His-2-type zinc-finger

Y., Meshi, T., Iwabuchi, repressors under drought, cold, and high- 2746. Transcription factors, motifs in their molecules are members of a

734 M., Shinozaki, K., and

Seki, M., Satou, M., 2004 salinity stress conditions.

RIKEN Arabidopsis full-length (RAFL) cDNA localization

J Exp Bot 55, Proteinmicroarray, Cold family of plant transcription factors.the

Full-length cDNAs are essential for To

Sakurai, T., Akiyama, cDNA and its applications for expression 213-223. stress, Drought stress, correct annotation of genomic sequences

K., Iida, K., Ishida, J., profiling under abiotic stress conditions. Full-length cDNA, Gene and for the functional analysis of genes

735 Nakajima, M., Enju, A.,

Serrato, A.J., Perez- 2004 A novel NADPH thioredoxin reductase, J Biol Chem expression, High-salinity

Thioredoxin reductase, and their products. 155,144 RIKEN

Plants contain three thioredoxin systems.

Ruiz, J.M., Spinola, localized in the chloroplast, which 279, 43821- Chloroplast, Oryza sativa Chloroplast thioredoxins are reduced by

M.C., and Cejudo, F.J. deficiency causes hypersensitivity to 43827. ferredoxin-thioredoxin reductase, whereas

736 Sharma, P., and Deswal, 2004 abiotic stress in Arabidopsis thaliana.

Detection and characterization of Plant Physiol Brassica juncea; the cytosolic and mitochondrialdetecting

Here we describe a method for

R. calcineurin-like activity in Brassica Biochem 42, Calcineurin-like activity calcineurin-like activity in Brassica juncea

juncea and its activation by low 579-584. assay; Low temperature seedlings. The activity was standardized

737 Takezawa, D., and 2004 temperature.

Calmodulin-binding proteins in Biochem stress; R II

Abscisic acid; with respect to all the assay components.

Plant responses to environmental stresses

Minami, A. bryophytes: identification of abscisic Biophys Res Bryophytes; Ca2+; are mediated in part by signaling

acid-, cold-, and osmotic stress-induced Commun 317, Calmodulin; Freezing processes involving cytosolic Ca2+ and a

738 Tasseva, G., de Virville, Changes in the novel membrane-bound

2004 genes encodingendoplasmic reticulum 428-436.

Plant Physiol tolerance; Ion

Cold acclimation; Ca(2+)-binding protein, known to induce

Cold is an abiotic stress calmodulin.

J.D., Cantrel, C., lipid properties in response to low Biochem 42, Heterologous cDNA- changes in membrane lipid composition.

Moreau, F., and temperature in Brassica napus. 811-822. array; Lipid However, there is only limited information

Teige, M., A.

739 Zachowski,Scheikl, E., 2004 The MKK2 pathway mediates cold and Mol Cell 15, unsaturation; Membrane

Mitogen-activated on the differential reactivity to

The Arabidopsis mitogen-activated protein

Eulgem, T., Doczi, R., salt stress signaling in Arabidopsis. 141-152. protein kinase kinase, kinase (MAPK) kinase 2 (MKK2) and the

Ichimura, K., Shinozaki, Cold stress, Yeast two downstream MAPKs MPK4 and MPK6

740 K., Dangl, J.L., and

Vannini, C., Locatelli, 2004 Overexpression of the rice Osmyb4 gene Plant J 37, 115- hybrid, Arabidopsis

Myb transcription factor, wereexpression of the gene Osmyb4,

The isolated by functional

F., Bracale, M., increases chilling and freezing tolerance 127. Abiotic stress, Cold detected at low level in rice (Oryza sativa)

Magnani, E., Marsoni, of Arabidopsis thaliana plants. tolerance, Oryza sativa, coleoptiles grown for 3 days at 29 degrees

M., Osnato, M., Arabidopsis thaliana, C, is strongly induced by treatments at 4

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



741 Wang, W., Vinocur, B., 2004 Role of plant heat-shock proteins and Trends Plant Protein aggregation, Heat-Abiotic stresses usually cause protein

Shoseyov, O., and molecular chaperones in the abiotic Sci 9, 244- shock proteins dysfunction. Maintaining proteins in their

Altman, A. stress response. 252. (Hsps)/chaperones, functional conformations and preventing

742 Wiese, J., Kranz, T., and 2004 Induction of pathogen resistance in Plant Biol Abiotic stress

Hordeum vulgare, the aggregation of non-native proteins are

Enhanced resistance of barley (Hordeum

Schubert, S. barley by abiotic stress. (Stuttg) 6, 529- Powdery mildew, Plant vulgare L. cv. Ingrid) against barley

536. resistance powdery mildew (Blumeria graminis f. sp.

743 Zhang, X., Fowler, S.G., 2004 Freezing-sensitive tomato has a Plant J 39, 905- Arabidopsis, Tomato, Many race A6) was in freezing tolerance

hordeiplants increaseinduced by abiotic

Cheng, H., Lou, Y., functional CBF cold response pathway, 919. CBF/DREB1, Cold in response to low temperature, a process

Rhee, S.Y., Stockinger, but a CBF regulon that differs from that acvlimation, CBF known as cold acclimation. In

744 E.J., and Thomashow,

Zhu, J., Shi, H., Lee, 2004 of freezing-tolerant Arabidopsis.

An Arabidopsis homeodomain Proc Natl Stress-response screen, Arabidopsis, cold acclimation involves

regulon, Microarray To investigate essential components

B.H., Damsz, B., Cheng, transcription factor gene, HOS9, Acad Sci U S Arabidopsis, Stress mediating stress signaling in plants, we

S., Stirm, V., Zhu, J.K., mediates cold tolerance through a CBF- A 101, 9873- signaling, RD29A initiated a large-scale stress response

Zuther, E., P.M., and

745 Hasegawa, Buchel, K., The role of pathway.

2004 independentraffinose in the cold 9878. Lett

FEBS promoter

Cold acclimation; In many plants raffinose plants

screen using Arabidopsisfamily carrying

Hundertmark, M., Stitt, acclimation response of Arabidopsis 576, 169-173. Freezing tolerance; oligosaccharides are accumulated during

M., Hincha, D.K., and thaliana. Galactinol synthase; cold acclimation. The contribution of

746 Heyer, A.G.

Alonso-Blanco, C., 2005 Genetic and molecular analyses of Plant Physiol Raffinose family

Arabidopsis, raffinose accumulation to freezing

Natural variation for freezing tolerance is

Gomez-Mena, C., natural variation indicate CBF2 as a 139, 1304- Acclimatization, CBF, a major component of adaptation and

Llorente, F., Koornneef, candidate gene for underlying a freezing 1312. QTL geographic distribution of plant species.

Amtmann, A., and

747 M., Salinas, J.,Bohnert, 2005 tolerance quantitative trait locus in

Abiotic stress and plant genome Plant Physiol Abiotic stress, genome However, little is known about the genes

The remarkable ability of plants to adapt

H.J., and Bressan, R.A. evolution. Search for new models. 138, 127-130. evolution, Arabidopsis to many different adverse environments is

a fascinating process. Research into the

748 Bradford, K.J., Van 2005 Regulating transgenic crops sensibly: Nat Crops, Plant breeding, physiology and metabolism of so-called

The costs of meeting regulatory

Deynze, A., Gutterson, lessons from plant breeding, Biotechnol 23, Genetic ingineering, requirements and market restrictions

N., Parrott, W., and biotechnology and genomics. 439-444. Phenotype guided by regulatory criteria are

749 Strauss, S.H. Lindlof,

Brautigam, M., 2005 Generation and analysis of 9792 EST BMC Plant Oat, EST, Transcript substantial impediments to the

BACKGROUND: Oat is an important

A., Zakhrabekova, S., sequences from cold acclimated oat, Biol 5, 18. clustering, Transcription crop in North America and northern

Gharti-Chhetri, G., Avena sativa. factors, CBF Europe. In Scandinavia, yields are limited

750 Olsson, B., and Olsson,

Cao, S., Ye, M., and 2005 Involvement of GIGANTEA gene in the Plant Cell Rep Arabidopsis, Cold stress, by the fact that oat cannot be used as a

The Arabidopsis GIGANTEA (GI) gene

Jiang, S. regulation of the cold stress response in 24, 683-690. CBF, Flowering has been shown to regulate several

Arabidopsis. developmental processes, including

photoperiod-mediated flowering,

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



751 Criel, B., Panta, A., 2005 Cryopreservation and abiotic stress Commun Cryopreservation, potato, No abstract available

Carpentier, S., Renaut, tolerance in potato: a proteomic Agric Appl abiotic stress, proteomics

J., Swennen, R., Panis, approach. Biol Sci 70, 83-

752 B., and Hausman, J.F.

Cui, S., Huang, F., 2005 A proteomic analysis of cold stress 86.

Proteomics 5, Rice, cold adaptation, Using proteomic analysis, an investigation

Wang, J., Ma, X., responses in rice seedlings. 3162-3172. MALDI TOF MS aimed at a better understanding of the

Cheng, Y., and Liu, J. molecular adaptation mechanisms of cold

753 Das, S., Hussain, A., 2005 Cloning of Brassica napus phospholipase Planta 220, Brassica napus, stress was carried out in rice (Oryza

The cloning and identification of full-

Bock, C., Keller, W.A., C2 (BnPLC2), phosphatidylinositol 3- 777-784. phosphatidylinositol- length cDNA fragments coding for the

and Georges, F. kinase (BnVPS34) and specific phospholipase, Brassica napus phosphatidylinositol-

754 Davletova, S., Schlauch, 2005 phosphatidylinositol synthase1

The zinc-finger protein Zat12 plays a Plant Physiol phosphatidylinositol 3- specific phospholipase C2 (BnPLC2),

Zink fingers protein, Plant acclimation to environmental stress

K., Coutu, J., and central role in reactive oxygen and 139, 847-856. Arabidopsis, biotic and is controlled by a complex network of

Mittler, R. abiotic stress signaling in Arabidopsis. abiotic stress regulatory genes that compose distinct

755 Deng, Z., Pang, Y., 2005 A novel ABA-dependent dehydrin DNA Seq 16, ABA; Bndhn ERD10; A new dehydrin ERD10 In contrast to

stress-response regulons.gene was cloned

Kong, W., Chen, Z., ERD10 gene from Brassica napus. 28-35. Brassica napus; and characterized from Brassica napus

Wang, X., Liu, X., Pi, dehydrin; RACE (designated as Bndhn ERD10). The full-

756 Y., Sun, X., and Tang,

Dixon, R.A. 2005 Plant biotechnology kicks off into the Trends Plant Biotechnology, genetic length cDNA of Bndhn ERD10 was 1114

No abstract available

21st century. Sci 10, 560- engineering

561.

757 Fiorani, F., Umbach, 2005 The alternative oxidase of plant Plant Physiol Alternative oxidase, The alternative oxidase (AOX) pathway of

A.L., and Siedow, J.N. mitochondria is involved in the 139, 1795- mitochondria, plant mitochondria uncouples respiration

acclimation of shoot growth at low 1805. Arabidopsis from mitochondrial ATP production and

758 Gong, Z., Dong, C.H., 2005 temperature. A study of Arabidopsis

A DEAD box RNA helicase is essential Plant Cell 17, RNA helicase, Cold may ameliorate plant performance under

An Arabidopsis thaliana mutant,

Lee, H., Zhu, J., Xiong, for mRNA export and important for 256-267. tolerance, Cryophyte cryophyte, was isolated and found to have

L., Gong, D., Stevenson, development and stress responses in an enhanced cold stress-induction of the

759 B., and Zhu, J.K.

Hannah, M.A., Heyer, 2005 Arabidopsis.

A global survey of gene regulation Many regulator of cold tolerance, as

PLoS Genet 1, Freezing tolerence, Gene mastertemperate plant species suchC-

A.G., and Hincha, D.K. during cold acclimation in Arabidopsis e26 expression, Arabidopsis Arabidopsis thaliana are able to increase

thaliana. . thaliana their freezing tolerance when exposed to

760 Hong, J.P., and Kim, 2005 Isolation and functional characterization Planta 220, Capsicim annuum, Through the use temperatures

low, nonfreezingof subtractive in a process

W.T. of the Ca-DREBLP1 gene encoding a 875-888. Dehydration, pCa-DSRs hybridization analysis, we have identified

dehydration-responsive element binding- 14 partial cDNA clones (pCa-DSRs) that

factor-like protein 1 in hot pepper are rapidly induced by dehydration in hot

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



761 Hwang, E.W., Kim, 2005 Expression profiles of hot pepper J Biosci 30, Abiotic stresses; In an attempt to determine a cold defense

K.A., Park, S.C., Jeong, (Capsicum annum) genes under cold 657-667. Capsicum annuum; cold- mechanism in plants, we have attempted

M.J., Byun, M.O., and stress conditions. stress regulated genes; to characterize changes occurring in the

762 Kwon, H.B.

Yamaguchi-Shinozaki, 2005 Organization of cis-acting regulatory Trends Plant microarray

Transcriptional expression regulatory elements are

cis-Acting of cold-regulated transcript

K., and Shinozaki, K. elements in osmotic- and cold-stress- Sci 10, 88-94. regulation, ABRE, stress- important molecular switches involved in

responsive promoters. inducible genes the transcriptional regulation of a dynamic

763 Yano, R., Nakamura, 2005 Starch-related alpha-glucan/water Plant Physiol Starch degradation, network of gene activities controlling

Cold-induced soluble sugar accumulation

M., Yoneyama, T., and dikinase is involved in the cold-induced 138, 837-846. Freezing tolerance, enhances the degree of freezing tolerance

Nishida, I. development of freezing tolerance in Arabidopsis in various cold-hardy plants including

764 Yoshida, K. 2005 Arabidopsis.

Plant biotechnology--genetic engineering J Biosci Transgenic plant, Hyper- Arabidopsis (Arabidopsis thaliana), where

Plants not only provide food to humans

to enhance plant salt tolerance. Bioeng 94, osmotic stres, Ectoine; and animals, but also provide a large

585-590. Na+-ATPase; K+-Na+ number of non-food products of industrial

765 Young, L.W., Cross, 2005 A high- and low-temperature inducible Genome 48, co-transporter; K+ and and chemical importance. Moreover, they

Promoter function, Low Transcriptional activity of a 573-bp

R.H., Byun-McKay, Arabidopsis thaliana HSP101 promoter 547-555. temperature stress, High fragment of HSP101 (At1g74310)

S.A., Wilen, R.W., and located in a nonautonomous mutator-like temperature stress; incorporated into a Mutator-like element

Kaplan, F., and P.C.

766 Bonham-Smith, Guy, 2005 element.

RNA interference of Arabidopsis beta- Plant J 44, 730- Arabidopsis HSP101,

Biochemistry, (MULE) transposon was investigated in

It has been suggested that beta-amylase

C.L. amylase8 prevents maltose accumulation 743. Environmental stress, (BMY) induction during temperature

upon cold shock and increases sensitivity Metabolism, Starch, stress in Arabidopsis could lead to starch-

767 Kwak, K.J., Kim, Y.O., 2005 of PSII photochemical efficiency to

Characterization of transgenic Glycine-rich stress

J Exp Bot 56, Temperature RNA- dependent maltose accumulation, and that

A glycine-rich RNA-binding protein4 (GR-

and Kang, H. Arabidopsis plants overexpressing GR- 3007-3016. binding protein, RNA- RBP4), one of the eight GR-RBP family

RBP4 under high salinity, dehydration, binding protein, stress, members in Arabidopsis thaliana, was

768 Lee, S.C., Lee, M.Y., 2005 or cold stress. of an abiotic stress-

Characterization Mol Cells 19, transgenic Arabidopsis investigated for its stress-related

Oryza sativa, Dehydrin, A full-length 1.1 kb cDNA, designated

Kim, S.J., Jun, S.H., An, inducible dehydrin gene, OsDhn1, in rice 212-218. Drought, Cold stress Oryza sativa Dehydrin 1 (OsDhn1), was

G., and Kim, S.R. (Oryza sativa L.). isolated from the seed coat of rice. The

769 Massonneau, A., 2005 Maize cystatins respond to Biochim Comprehensive is hydrophilic and has

Cystatin; Kernel; Maize; deduced protein searches of maize EST

Condamine, P., developmental cues, cold stress and Biophys Acta Stress; Zea mays data allowed us to identify 8 novel Corn

Wisniewski, J.P., Zivy, drought. 1729, 186- Cystatin (CC) genes in addition to the

770 M., and Rogowsky, M., 2005 Cold acclimation in bryophytes: low-

Minami, A., Nagao, 199. 220,

Planta Physcomitrella patens, Bryophyte known growing in areas in

previously species genes CCI and CCII.

Ikegami, K., Koshiba, temperature-induced freezing tolerance 414-423. Freezing tolerance, which temperatures fall below zero in

T., Arakawa, K., in Physcomitrella patens is associated winter are likely to have tolerance to

Fujikawa, S., and with increases in expression levels of freezing stress. It is well established in

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



771 Moller, B.L. 2005 Plant biotechnology in Europe: a Trends Plant Biotechnology, No abstract available

changing environment and landscape. Sci 10, 562- Agriculture, Transgenic

564. crops

772 Moloney, M., and 2005 Plant biotechnology. Curr Opin Transgenic crops, No abstract available

Peacock, J. Plant Biol 8, Molecular biology,

163-164. Biotechnology

773 Montagu, M.V. 2005 Technological milestones from plant Trends Plant Agriculture, Transgenic No abstract available

science to agricultural biotechnology. Sci 10, 559- crops, Plant

560. transformation

774 Morsy, M.R., Almutairi, 2005 The OsLti6 genes encoding low- Gene 344, 171- Cold-regulated genes, Rice (Oryza sativa L.) is sensitive to

A.M., Gibbons, J., Yun, molecular-weight membrane proteins are 180. Membrane injury, chilling particularly at early stages of

S.J., and de Los Reyes, differentially expressed in rice cultivars Hydrophobic proteins, seedling establishment. Two closely

775 B.G. T., Pan, L.,

Ogawa, 2005 with contrasting sensitivity to low

Functional analysis of Arabidopsis Plant Physiol Cold tolerance, Genetic

Ethylene-responsive related genes(Arabidopsis thaliana)

Arabidopsis (OsLti6a, OsLti6b), which

Kawai-Yamada, M., Yu, ethylene-responsive element binding 138, 1436- element binding protein ethylene-responsive element binding

L.H., Yamamura, S., protein conferring resistance to Bax and 1445. (AtEBP), Arabidopsis, protein (AtEBP) gene was isolated as a

Oh, S.J., T., Kitajima,

776 Koyama, Song, S.I., 2005 abiotic stress-induced plant cell death.

Arabidopsis CBF3/DREB1A and ABF3 Plant Physiol Abiotic stress

CBF3/DREB1A, Oryza suppressor of Bax-induced cell death by

Rice (Oryza sativa), a monocotyledonous

Kim, Y.S., Jang, H.J., in transgenic rice increased tolerance to 138, 341-351. sativa, Arabidopsis plant that does not cold acclimate, has

Kim, S.Y., Kim, M., abiotic stress without stunting growth. thaliana, Cold evolved differently from Arabidopsis

777 Kim, Y.K., Nahm, B.H.,

Rensink, W., Hart, A., 2005 Analyzing the potato abiotic stress Genome 48, Acclimation

Potato, Solanaceae, (Arabidopsis thaliana), which cold

To further increase our understanding of

Liu, J., Ouyang, S., transcriptome using expressed sequence 598-605. Abiotic stress responses in potato to abiotic stress and

Zismann, V., and Buell, tags. the potato transcriptome in general, we

778 C.R.

Rensink, W.A., Iobst, 2005 Gene expression profiling of potato Funct Integr Potato, Gene expression generated 20 756 expressed sequence tags

In order to identify genes involved in

S., Hart, A., Stegalkina, responses to cold, heat, and salt stress. Genomics 5, profilig, Abiotic stress abiotic stress responses in potato,

S., Liu, J., and Buell, 201-207. seedlings were grown under controlled

779 C.R. J., Ainley, W.M.,

Rice, 2005 Plant-made vaccines: biotechnology and Anim Health Plant-made, Vaccine, The use of plants as production (4

conditions and subjected to coldsystems

and Shewen, P. immunology in animal health. Res Rev 6, Immunogenecity, Animal for vaccine antigens has been actively

199-209. health investigated over the last 15 years. The

780 Saidi, Y., Finka, A., 2005 Controlled expression of recombinant Plant Mol Biol Acetyl salicylivc acid, original research focused on the value of

The ability to express tightly controlled

Chakhporanian, M., proteins in Physcomitrella patens by a 59, 697-711. Actin cytosceleton, amounts of endogenous and recombinant

Zryd, J.P., Schaefer, conditional heat-shock promoter: a tool Benzyl alcohol, GFP- proteins in plant cells is an essential tool

D.G., and Goloubinoff, for plant research and biotechnology. talin, ß-glucuronidase, for research and biotechnology. Here, the

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



781 Savitch, L.V., Allard, 2005 The effect of overexpression of two Plant Cell CBF/DREB1, The effects of overexpression of two

G., Seki, M., Robert, Brassica CBF/DREB1-like transcription Physiol 46, Transcription factors, Brassica CBF/DREB1-like transcription

L.S., Tinker, N.A., factors on photosynthetic capacity and 1525-1539. Brassica napus factors (BNCBF5 and 17) in Brassica

Suzuki, M., Shinozaki,

782 Huner, N.P.,Ketterling, 2005 freezing tolerance in Brassica napus.

Quantitative statistical analysis of cis- Plant Physiol Cis-regulatory napus cv.developed a simple quantitative

We have Westar were studied. In addition

M.G., and McCarty, regulatory sequences in ABA/VP1- and 139, 437-447. sequences, MotifFinder, computational approach for objective

D.R. CBF/DREB1-regulated genes of Abiotic stress analysis of cis-regulatory sequences in

783 Vashisht, A.A., and 2005 Arabidopsis.

Cold stress-induced pea DNA helicase Arch Biochem Abiotic stress; DEAD- Helicases of ubiquitous genes. The

promoters are coregulatedmolecular motor

Tuteja, N. 47 is homologous to eIF4A and inhibited Biophys 440, box protein; DNA- proteins that play important role in

by DNA-interacting ligands. 79-90. dependent ATPase, maintaining the genome integrity and thus

784 Vashisht, A.A., 2005 Cold- and salinity stress-induced bipolar Abiotic stress, Plant

Plant J 44, 76- Pisum sativum;DEAD- involved in plant growth and development.

Helicases are involved in the metabolism

Pradhan, A., Tuteja, R., pea DNA helicase 47 is involved in 87. box protein, DNA- of nucleic acid; this is very sensitive to the

and Tuteja, N. protein synthesis and stimulated by dependent ATPase, abiotic stresses that reduce plant growth

785 Vergnolle, C., Vaultier, 2005 phosphorylation with protein kinase C.

The cold-induced early activation of Phospholipase plant

Plant Physiol Pisum sativum,D, and productivity. However, the molecular

In plants, a temperature downshift

M.N., Taconnat, L., phospholipase C and D pathways 139, 1217- Phospholipase C, Cold represents a major stress that will lead to

Renou, J.P., Kader, J.C., determines the response of two distinct 1233. signal, CBF pathway the induction or repression of many genes.

786 Zachowski, A., and P.,

Viljanen, K., Kylli, 2005 clusters of genes in Arabidopsis cell

Anthocyanin antioxidant activity and J Agric Food Protein oxidation; The antioxidant activities has to be

Therefore, the cold signal of anthocyanins

Hubbermann, E.M., partition behavior in whey protein Chem 53, Anthocyanins; and anthocyanin fractions isolated from

Schwarz, K., and emulsion. 2022-2027. Antioxidants; Partition; blackcurrants, raspberries, and

787 Heinonen, M.

Vinocur, B., and 2005 Recent advances in engineering plant Curr Opin Emulsion; Salinity,

Crop loss, Berries lingonberries were investigated in whey

Abiotic stresses, especially salinity and

Altman, A. tolerance to abiotic stress: achievements Biotechnol 16, Drought stress, Plant drought, are the primary causes of crop

and limitations. 123-132. adaptation loss worldwide. Plant adaptation to

788 Vogel, J.T., Zarka, 2005 Roles of the CBF2 and ZAT12 Plant J 41, 195- Arabidopsis, Cold Summary The stresses is dependent upon

environmental CBF cold response pathway

D.G., Van Buskirk, transcription factors in configuring the 211. acclimaiton, has a prominent role in cold acclimation.

H.A., Fowler, S.G., and low temperature transcriptome of CBF/DREB1, Freezing The pathway includes action of three

Wei, G., Pan, Y., Lei, J., 2005 Arabidopsis.

789 Thomashow, M.F. Molecular cloning, phylogenetic J Biochem tolerance, Low

ABA, DREB, One- A cDNA that was rapidly induced 3 (also

transcription factors, CBF1, 2 and upon

and Zhu, Y.X. analysis, expressional profiling and in Mol Biol 38, hybrid, Stress, abscisic acid, cold, drought, mechanical

vitro studies of TINY2 from Arabidopsis 440-446. Transcription factor wounding and to a lesser extent, by high

790 Wheeler, D.L., Smith- 2005 thaliana.

Plant genome resources at the national Plant Physiol Biological databases, salinity treatment, was isolated from

The National Center for Biotechnology

White, B., Chetvernin, center for biotechnology information. 138, 1280- National Center for Information (NCBI) integrates data from

V., Resenchuk, S., 1288. Biotechology more than 20 biological databases through

Dombrowski, S.M., Information, Plant a flexible search and retrieval system

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



791 Wong, C.E., Li, Y., 2005 Expressed sequence tags from the Yukon Plant Mol Biol Thellungiella salsuginea, Thellungiella salsuginea (also known as T.

Whitty, B.R., Diaz- ecotype of Thellungiella reveal that gene 58, 561-574. Drought stress, Salt halophila) is a close relative of

Camino, C., Akhter, expression in response to cold, drought stress, Cold stress Arabidopsis that is very tolerant of

792 S.R., Brandle, J.E.,

Agarwal, M. 2006 and salinity shows little overlap. factor

A R2R3 type MYB transcription J Biol Chem MYB, Transcription Cold temperatures trigger the and may be

drought, freezing, and salinityexpression

Hao, Y. is involved in the cold regulation of CBF 281: 37636-45 factors, CBF, Cold of the CBF family of transcription factors,

Kapoor, A. genes and in acquired freezing tolerance Regulation which in turn activate many downstream

793 Dong, C. H. Agarwal,

Agarwal, P.K., 2006 Role of DREB transcription factors in Plant Cell Rep DREB, CBF, Cold genes that confer freezing tolerance to

Abiotic and biotic stresses negatively

P., Reddy, M.K., and abiotic and biotic stress tolerance in 25, 1263- acclimation influence survival, biomass production

Sopory, S.K. . plants. 1274. and crop yield. Being multigenic as well

794 Alcazar, R., Marco, F., 2006 Involvement of polyamines in plant Biotechnol Abiotic stress, Gene Environmental stresses is challenge

as a quantitative trait, it areathe major to

Cuevas, J.C., Patron, response to abiotic stress. Lett 28, 1867- expression, Mutants, cause of crop loss worldwide. Polyamines

M., Ferrando, A., 1876. Polyamines, Transgenic are involved in plant stress responses.

795 Carrasco, P., Tiburcio,

Amme, S., Matros, A., 2-D DIGE, Arabidopsis, However, the precise role(s)2-Dpolyamine

2006 Proteome analysis of cold stress response J Exp Bot 57, plants A proteome study based on of gel

Schlesier, B., and Mock, in Arabidopsis thaliana using DIGE- 1537-1546. cold stress, differential in-electrophoresis was performed in order to

H.P. technology. gel electrophoresis, ESI- analyse the cold-stress response of

796 Armstrong, A.F., Logan, 2006 Heterogeneity of plant mitochondrial Plant Cell MS/MS, fluorescent

Confocal microscopy, Arabidopsis plants. The emphasis was to

In this study, we investigated whether

D.C., Tobin, A.K., responses underpinning respiratory Environ 29, Cytochrome oxidase, changes in mitochondrial abundance,

O'Toole, P., and Atkin, acclimation to the cold in Arabidopsis 940-949. Epidermic, Mesophyll, ultrastructure and activity are involved in

797 O.K. D., Roy, S.,

Bagchi, 2006 thaliana leaves.

Safety and whole-body antioxidant Mol Cell Respiration,

Berry, Anthocyanins, the respiratory cold acclimation response

Edible berry extracts rich in anthocyanins

Patel, V., He, G., potential of a novel anthocyanin-rich Biochem 281, Glutathione, Hyperbaric possess a broad spectrum of therapeutic,

Khanna, S., Ojha, N., formulation of edible berries. 197-209. oxygen, in vivo, pharmacologic and anti-carcinogenic

798 Phillips, C., Ghosh, S.,

Bohnert, H.J., Gong, Q., 2006 Unraveling abiotic stress tolerance Curr Opin OptiBerry, Oxidative

Abiotic stress, properties. Six berry extractsmetabolism

Homeostasis, a set-value for (wild

Li, P., and Ma, S. mechanisms--getting genomics going. Plant Biol 9, Transcription factor, cs, under optimal conditions, is rarely

180-188. Proteomics, achieved by plants because of the cost

799 Bonham-Smith, P.C., 2006 Non-lethal freezing effects on seed Planta 224, Transcriptomics seed,

Brassica, Green exerted by external stress factors: climatic,

The effects of a non-lethal freezing stress

Gilmer, S., Zhou, R., degreening in Brassica napus. 145-154. Freezing, ABA, on chlorophyll content, moisture level and

Galka, M., and Abrams, Chlorophyll distribution, and abscisic acid (ABA)

800 S.R.

Borner, A. 2006 Preservation of plant genetic resources Biotechnol J Speciment Bank, Thousands examined in siliques and seeds

levels were of years ago humans began

in the biotechnology era. 1, 1393-1404. Preservation, Genetic domesticating crops as a food source.

resources Among the wild germplasm available, they

selected those that were best adapted for

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



801 Cao, Y., Song, F., 2006 Molecular characterization of four rice J Plant PhysiolBiotic and abiotic stress; We isolated and identified four rice genes,

Goodman, R.M., and genes encoding ethylene-responsive 163, 1167- Disease resistance OsBIERF1 to OsBIERF4 (Oryza sativa

Zheng, Z. transcriptional factors and their 1178. response; ERF benzothiadiazole (BTH)-induced ethylene

802 Chen, F., Li, Q., Sun, The rice 14-3-3 gene family and and

2006 expressions in response to biotic its DNA Res 13, transcriptional factors;

Rice; 14-3-3 family; responsive transcriptional factors (ERF))

14-3-3 proteins function as major

L., and He, Z. involvement in responses to biotic and 53-63. Biotic and abiotic stress; regulators of primary metabolism and

abiotic stress. Expression regulation; cellular signal transduction in plants.

803 Compton, M.E. 2006 Use of statistics in plant biotechnology. Methods Mol Subcellular localization

Plant biotechnology, However,and experimental design are

Statistics their involvement in plant

Biol 318, 145- Plant tissue culture, important tools for the plant

163. Statistical analysis biotechnologist and should be used when

804 de las Mercedes Dana, 2006 Transgenic tobacco plants Plant Physiol Tobacco, resistance to planning and conducting experiments as

Genes encoding defense-related proteins

M., Pintor-Toro, J.A., overexpressing chitinases of fungal 142, 722-730. pathogens, chitinase have been used to alter the resistance of

and Cubero, B. origin show enhanced resistance to biotic plants to pathogens and other

805 Dong, C.H., Agarwal, 2006 and abiotic stress agents. plant cold

The negative regulator of Proc Natl Cold stress, RING finger environmental challenges, butare mediated

Plant responses to cold stress no single

M., Zhang, Y., Xie, Q., responses, HOS1, is a RING E3 ligase Acad Sci U S protein by a transcriptional cascade, in which the

and Zhu, J.K. that mediates the ubiquitination and A 103, 8281- transcription factor ICE1 and possibly

806 Egawa, C., Kobayashi, Differential of ICE1.

2006 degradation regulation of transcript 8286. Genet

Genes Abiotic stress, related proteins activate the expression of

A number of cold responsive (Cor)/late

F., Ishibashi, M., accumulation and alternative splicing of Syst 81, 77-91 Alternative splicing, embryogenesis abundant (Lea) genes are

Nakamura, T., a DREB2 homolog under abiotic stress Cor/Lea genes, DREB2 induced by both low temperature (LT) and

Fujita, M., C., and

807 Nakamura, Fujita, Y., Crosstalk in common wheat

2006 conditionsbetween abiotic and biotic Curr Opin transcription factor,

Biotic and Abiotic stress, dehydration.evolved a wide range of

Plants have To understand the molecular

Noutoshi, Y., stress responses: a current view from the Plant Biol 9, Signaling pathways mechanisms to cope with biotic and

Takahashi, F., points of convergence in the stress 436-44 abiotic stresses. To date, the molecular

808 Narusaka, Y.,

Goulas, E., Schubert, 2006 signaling networks. and stromal

The chloroplast lumen Plant J 47, 720- Difference gel mechanisms that are involved in eachby

Cold acclimation and over-wintering

M., Kieselbach, T., proteomes of Arabidopsis thaliana show 73 electrophoresis, herbaceous plants are energetically

Kleczkowski, L.A., differential sensitivity to short- and long- Proteomics, Matrix expensive and are dependent on functional

809 Gardestrom, P.,

Grennan, A.K. Abiotic stress to low An "omic"

2006 term exposure in rice. temperature. Abiotic laser desorption

Plant Physiol assisted stress, Rice, plastid metabolism. To understand how

Abiotic stress can impose limitations on

approach. 140, 1139- Environmental stress crop productivity and also limit land

1141. available for farming, often in regions that

810 Hannah, M.A., Wiese, 2006 Natural genetic variation of freezing Plant Physiol Arabidopsis, Cold can ill afford suchis a primary determinant

Low temperature constraints, thus

D., Freund, S., Fiehn, tolerance in Arabidopsis. 142, 98-112. tolerance, Meabolomics, of plant growth and survival. Using

O., Heyer, A.G., and Transcriptomics accessions of Arabidopsis (Arabidopsis

Hincha, D.K. thaliana) originating from Scandinavia to

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



811 Hendrickson, L., 2006 Cold acclimation of the Arabidopsis FEBS Lett Cold acclimation; We compared the thylakoid membrane

Vlckova, A., Selstam, dgd1 mutant results in recovery from 580, 4959- Digalactosyl–diacylglyce composition and photosynthetic properties

E., Huner, N., Oquist, photosystem I-limited photosynthesis. 4968. rol; Lipid; of non- and cold-acclimated leaves from

812 G., and Hurry, V. M.,

Houde, M., Belcaid, 2006 Wheat EST resources for functional BMC Monogalactosyl–diacylgl

Wheat, Freezing BACKGROUND: Wheat is an of

the dgd1 mutant (lacking >90%excellent

Ouellet, F., Danyluk, J., genomics of abiotic stress. Genomics 7, tolerance, EST species to study freezing tolerance and

Monroy, A.F., 149. other abiotic stresses. However, the

813 Dryanova, A., Gulick,

Langridge, P., Paltridge, 2006 Functional genomics of abiotic stress Brief Funct Cereals,Abiotic stress, sequence of the wheat genome has not

Abiotic stresses such as extreme

N., and Fincher, G. tolerance in cereals. Genomic Cold, Drought, Salinity temperatures, low water availability, high

Proteomic 4, salt and mineral deficiencies or toxicities

814 Loyola-Vargas, V.M. 2006 Plant biotechnology and tissue culture 343-354. Mol

Methods Biotechnology, Plant severely diminish productivity of cereal

No abstract available

resources on the internet. Biol 318, 379- tissue culture, Database

384. analysis

815 Mittler, R. 2006 Abiotic stress, the field environment and Trends Plant Abiotic stress, Farmers and breeders have long known

stress combination. Sci 11, 15-19. Transgenic corps, Stress that often it is the simultaneous occurrence

co-occurrence of several abiotic stresses, rather than a

816 Mittler, R., Kim, Y., 2006 Gain- and loss-of-function mutations in FEBS Lett Abiotic stress, C2H2- particular stress condition, that is most

C(2)H(2)-zinc finger proteins that contain

Song, L., Coutu, J., Zat10 enhance the tolerance of plants to 580, 6537- zinc finger; EAR motif, the EAR repressor domain are thought to

Coutu, A., Ciftci- abiotic stress. 6542. Stress tolerance, Zat10, play a key role in modulating the defense

Oono, Y., Seki, H.,

817 Yilmaz, S., Lee,M., 2006 Monitoring expression profiles of Funct Integr Arabidopsis thaliana

Deacclimation, Cold response of plants to abiotic stress.

A comparative analysis of gene expression

Satou, M., Iida, K., Arabidopsis genes during cold Genomics 6, acclimation, Recovery profiles during cold acclimation and

Akiyama, K., Sakurai, acclimation and deacclimation using 212-234. from cold stress, Cold deacclimation is necessary to elucidate the

Owttrim, M.,

818 T., Fujita,G.W. RNA microarrays.

2006 DNA helicases and abiotic stress. Nucleic Acids stress helicase, Abiotic

RNA molecular mechanisms of cold stress

RNA helicases function as molecular

Res 34, 3220- stress, Cold-induced motors that rearrange RNA secondary

3230. RNA helicase structure, potentially performing roles in

819 Rajashekar, C.B., Zhou, 2006 Suppression of phospholipase Dalpha1 J Plant Physiol Antisense suppression, any cellular process involving RNA plays

Phospholipase D (PLD; EC 3.1.4.4)

H.E., Zhang, Y., Li, W., induces freezing tolerance in 163, 916-926. Arabidopsis thaliana, an important role in membrane lipid

and Wang, X. Arabidopsis: response of cold-responsive Cold-responsive genes, hydrolysis and in mediation of plant

820 Reyes-Diaz, M., Ulloa, 2006 genes and osmolyte accumulation. by J Exp Bot 57,

Arabidopsis thaliana avoids freezing COR genes, Freezing

Apoplastic fluid, responses to thaliana (L.) Heynh. has been

Arabidopsis a wide range of stresses.

N., Zuniga-Feest, A., supercooling. 3687-3696. Arabidopsis thaliana, described as a freezing-tolerant species

Gutierrez, A., Gidekel, Chlorophyll based on freezing-resistance assays.

M., Alberdi, M., fluorescence, Cold Nonetheless, this type of experiment does

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



821 Rosso, D., Ivanov, A.G., 2006 IMMUTANS does not act as a stress- Plant Physiol Terminal oxidase, Stress- IMMUTANS (IM) encodes a thylakoid

Fu, A., Geisler-Lee, J., induced safety valve in the protection of 142, 574-585. induced mitochondrial membrane protein that has been

Hendrickson, L., the photosynthetic apparatus of alternative oxidase hypothesized to act as a terminal oxidase

822 Geisler, M., Stewart, G., 2006 Arabidopsis during steady-state case

Sandermann, H. Plant biotechnology: ecological Trends Plant (AOX), Arabidopsis

Roundup-Ready plants, that couples the reduction of O(2) to the

The emerging field of molecular ecology

studies on herbicide resistance. Sci 11, 324- Molecular ecology, aims to improve the ecological

328. Transgenic crop predictability of transgenic crop plants.

823 Swindell, W.R. 2006 The association among gene expression Genetics 174, Transcriptional profiling, The most widely cultivated lines are

The identification and analysis of genes

responses to nine abiotic stress 1811-1824. Gene expression, Stress exhibiting large expression responses to

treatments in Arabidopsis thaliana. tolerance several different types of stress may

824 Tondelli, A., Francia, 2006 Mapping regulatory genes as candidates Theor Appl Candidate genes, Stress Cereal insights into the functional in

providecrop yield is greatly affectedbasis

E., Barabaschi, D., for cold and drought stress tolerance in Genet 112, tolerance, CBF1, ICE1, many growing areas by abiotic stresses,

Aprile, A., Skinner, J.S., barley. 445-454. FRY1 mainly low temperature and drought. In

825 Stockinger, E.J., Stanca, 2006

Towill, L.E., Bonnart, Cryopreservation of Arabidopsis thaliana Cryo Letters Vitrification, Two-Step order to find candidates for the tolerance

Development of a successful shoot tip

R., and Volk, G.M. shoot tips. 27, 353-360. cooling, Cryoprotectant, cryopreservation method for Arabidopsis

Liquid nitrogen, Cold thaliana L. will enable researchers to use

826 Vollenweider, P., and 2006 Diagnosis of abiotic and biotic stress Environ Pollut acclimation

Foliage, Symptom Visible symptoms study foliage of

molecular tools to in the processes trees

Gunthardt-Goerg, M.S. factors using the visible symptoms in 140, 562-571. gradiens, Abiotic stress are recorded to monitor the effects of

foliage. abiotic and biotic stress. Difficulties are

827 Wenzel, G. 2006 Molecular plant breeding: achievements Appl Transgenic crop, reported in diagnosing transgenic of stress.

Since one decade ago, the origin crop

in green biotechnology and future Microbiol Herbicide tolerance, plants are globally grown; in 2004, it was

perspectives. Biotechnol 70, Insecticide tolerance, estimated to cover a total of 81 Mio ha in

828 Wong, C.E., Li, Y., 2006 Transcriptional profiling implicates Plant Physiol Green Biotechnology

642-650. Thellungiella, 17 countries. At present, four plant species

Thellungiella, an Arabidopsis

Labbe, A., Guevara, D., novel interactions between abiotic stress 140, 1437- Arabidopsis thaliana, (Arabidopsis thaliana)-related halophyte,

Nuin, P., Whitty, B., and hormonal responses in Thellungiella, 1450. Halophyte, Model is an emerging model species for studies

829 Diaz, C., Golding, G.B.,

Xiong, Y., and Fei, S.Z. 2006 a close relative phylogenetic analysis of Planta 224,

Functional and of Arabidopsis. species

DREB/CBF, Cold designed to elucidate molecular

The dehydration-responsive element

a DREB/CBF-like gene in perennial 878-888. acclimaiton, Freezing binding proteins (DREB1)/C-repeat (CRT)

ryegrass (Lolium perenne L.). tolerance, Lolium perene binding factors (CBF) function as

830 Zhang, Y., Wang, Z., 2006 Molecular cloning and stress-dependent J Plant Physiol L., Transgenic

Chinese cabbage transcription factors are important for

Potassium channels and bind to the

Zhang, L., Cao, Y., regulation of potassium channel gene in 163, 968-978. (Brassica rapa ssp. many physiological functions in plants,

Huang, D., and Tang, K. Chinese cabbage (Brassica rapa ssp. Pekinensis); Expression one of which is to regulate plant adaption

Pekinensis). patterns; KCT2; to stress conditions. In this study, KCT2,

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



831 Zhao, T.J., Sun, S., Liu, 2006 Regulating the drought-responsive J Biol Chem CBF, Transcription DREB1/C-repeat binding factor (CBF) is a

Y., Liu, J.M., Liu, Q., element (DRE)-mediated signaling 281, 10752- factor, Freezing plant-specific family of transcription

Yan, Y.B., and Zhou, pathway by synergic functions of trans- 10759. tolerance, Cis-acting factors and plays a crucial role in freeze

832 H.M.

Agarwal, P., Agarwal, 2007 active and trans-inactive DRE binding

Stress-inducible DREB2A transcription Mol Genet element

DRE, DREB2A, Abiotic stress-mediated work, two groups

tolerance. In the present gene expression is

P.K., Nair, S., Sopory, factor from Pennisetum glaucum is a Genomics 277, Pennisetum glaucum, regulated via different transcription

S.K. Reddy, M.K. phosphoprotein and its phosphorylation 189-198. Phosphorylation, factors of which drought-responsive

833 Blodner, C., Goebel, C., 2007 negatively regulates its DNA-binding

Warm and cold parental reproductive Plant Cell Transcription factors element-binding (DREB) proteins play an

Conditions in the parental environment

Chilling, Ecophysiology,

Feussner, I., Gatz, C., environments affect seed properties, Environ 30, Epigenetic effect, during reproduction can affect the

and Polle, A. fitness, and cold responsiveness in 165-175. Freezing, Transcriptionperformance of the progenies. The goals

834 Burdulis, D., Analysis of thaliana progenies.

2007 Arabidopsisanthocyanin content in Medicina factor

Anthocyanins, of this study were to investigate whether

Bilberry (Vaccinium myrtillus L.) is rich

Ivanauskas, L., Jakstas, bilberry (Vaccinium myrtillus L.) fruit (Kaunas) 43, Chromatography, fruits,in flavonoids (major part anthocyanins),

V., and Janulis, V. crude drugs by high-performance liquid 568-574. Bilberry, Pharmacopoeiatannins, phenolic and organic acids, and

835 Chawade, A., 2007 chromatography method. pathways in

Putative cold acclimation BMC other biologically active the advent of

BACKGROUND: With compounds.

Microarray, Arabidopsis,

Brautigam, M., Lindlof, Arabidopsis thaliana identified by a Genomics 8, Cold-related genes microarray technology, it has become

A., Olsson, O., and combined analysis of mRNA co- 304. feasible to identify virtually all genes in an

Cheng, B.

836 Olsson, C., Yun, K.Y., An early response regulatory motifs

2007 expression patterns, promotercluster and BMC Japonic rice, organism that are inducedrespond to low

BACKGROUND: Plants by a certain

Ressom, H.W., induced by low temperature and Genomics 8, transcriptional network, temperature through an intricately

Mohanty, B., Bajic, hydrogen peroxide in seedlings of 175. CBF/DREB, cold coordinated transcriptional network. The

837 V.B., Jia, Y., Yun, S.J.,

Choi, C.S., and Sano, H. 2007 chilling-tolerant japonica rice.

Abiotic-stress induces demethylation and Mol Genet resistanceGene

Tobacco, CBF/DREB-regulated network of genes

To examine the relationship between gene

transcriptional activation of a gene Genomics 277, expression, DNA expression and DNA methylation,

encoding a glycerophosphodiesterase- 589-600. methylation transcriptionally activated genes were

838 Cuming, A.C., Cho, 2007 like protein in tobacco plants.

Microarray analysis of transcriptional New Phytol. Physcomitrella patens, screened in hypomethylated transgenic

* Dehydration tolerance was an adaptive

S.H., Kamisugi, Y., responses to abscisic acid and osmotic, microarray, dehydration trait necessary for the colonization of land

Graham, H., and salt, and drought stress in the moss, tolerance by plants, and remains widespread among

Denslow, R.S.

839 Quatrano, S.A., 2007 Physcomitrella patens.

Regulation of the Arabidopsis thaliana Plant Physiol Antioxidant; Plant Vitamin B(6) (pyridoxine and relatives of

bryophytes: the nearest extant its vitamers)

Rueschhoff, E.E., and vitamin B6 biosynthesis genes by abiotic Biochem 45, abiotic stress; SNZ1; plays an essential role as a co-factor for

Daub, M.E. stress. 152-161. SNO; YaaD; YaaE enzymatic reactions and has also recently

840 Einsele, A. 2007 The gap between science and perception: Adv Biochem Biotech crops, GM food, been implicated in defense against cellular

Although the global area of biotech crops

the case of plant biotechnology in Eng agriculture continues to climb for the tenth

Europe. Biotechnol consecutive year at a sustainable double-

107, 1-11. digit growth rate, the acceptance of

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



841 Gamboa, M.C., 2007 Isolation and characterization of a Plant Physiol Eucalyptus; CBF; Cold- The transcription factors CBF/DREB play

Rasmussen-Poblete, S., cDNA encoding a CBF transcription Biochem 45, 1- tolerance; Acclimation; an important role during low temperature,

Valenzuela, P.D., and factor from E. globulus. 5. Abiotic stress; Forest drought and high-salt stress in higher

842 Krauskopf, E.

Griffith, M., Timonin, 2007 Thellungiella: an Arabidopsis-related Plant Cell biotechnology

Adaptation, Anti-freeze plants. In this salsuginea, a wild crucifer

Thellungiella work, we isolated one full-

M., Wong, A.C., Gray, model plant adapted to cold Environ 30, proteins, CBF1, Cold- that grows in subarctic Canada and is

G.R., Akhter, S.R., temperatures. 529-538. regulated genes, closely related to Arabidopsis thaliana,

843 Saldanha, M., Rogers,

Groppa, M.D., and 2007 Polyamines and abiotic stress: recent Amino Acids. COR15a, COR47,

Abiotic stres, was examined we willsuitability as inmodel

In this review for its concentrate a the

Benavides, M.P. advances polyamines, putrescinem results published the last years regarding

spermidine, spermine the involvement of polyamines in the plant

844 Hashimoto, M., and 2007 Proteomic analysis of rice seedlings Proteomics 7, Rice, Cold response, responses to abiotic one of the important

Low temperature is stresses, most

Komatsu, S. during cold stress. 1293-1302. Proteomics environmental changes that affect plant

growth and agricultural production. To

845 Hodkinson, T.R., 2007 DNA banking for plant breeding, J Plant Res Databases, DNA bank, investigate the responses of rice to cold

The manipulation of DNA is routine

Waldren, S., Parnell, biotechnology and biodiversity 120, 17-29. DNA extraction, practice in botanical research and has

J.A., Kelleher, C.T., evaluation. Exchange, Management, made a huge impact on plant breeding,

846 Salamin, K., and

Young Jang, J., Jin 2007 Molecular cloning of a cDNA encoding a J Plant Abiotic transfer

Materialstress; biotechnology and biodiversity evaluation.

A cDNA encoding a high mobility group

Kwak, K., and Kang, H. high mobility group protein in Cucumis Physiol 164, Cucumber; Cucumis B (HMGB) protein was isolated from

sativus and its expression by abiotic 205-208. sativus; High mobility Cucumis sativus and characterized with

847 James, V.A., Neibaur, 2007 stress treatments.

Stress inducible expression of the Transgenic group protein; HMG-box respect to its sequence, expression and

DREB1A, Transcription The dehydration-responsive element

I., and Altpeter, F. DREB1A transcription factor from xeric, Res. factor, Hordeum binding proteins (DREB1)/C-repeat (CRT)

Hordeum spontaneum L. in turf and spontaneum, Bahiagrass, binding factors (CBF) function as

848 Kagale, S., Divi, U.K., 2007 forage grass (Paspalum notatum Flugge) Planta 225,

Brassinosteroid confers tolerance in Turfgrass, Forage,

Brassinosteroids, transcription activators and bind to the

In addition to an essential role in plant

Krochko, J.E., Keller, Arabidopsis thaliana and Brassica napus 353-364. envinronmental stress, development, brassinosteroids (BRs)

W.A., and Krishna, P. to a range of abiotic stresses. Brassica napus, tomato appear to have the ability to protect plants

849 Kant, P., Kant, S., 2007 STRS1 and STRS2, Two DEAD-Box Plant Physiol. Functional genomics, against various environmental stresses.

Two genes encoding Arabidopsis DEAD-

Gordon, M., Shaked, R., RNA Helicases that Attenuate RNA helicases, Abiotic box RNA helicases were identified in a

and Barak, S. Arabidopsis Responses to Multiple stress functional genomics screen as being down-

850 Kaplan, F., Kopka, J., 2007 Abiotic Stresses.

Transcript and metabolite profiling Plant J 50, 967- Post-transcriptional Exposure of multiple abiotic stresses.

regulated by Arabidopsis to low

Sung, D.Y., Zhao, W., during cold acclimation of Arabidopsis 981. regulation, Low temperatures results in cold acclimation

Popp, M., Porat, R., and reveals an intricate relationship of cold- temperature, where freezing tolerance is enhanced. To

Guy, C.L. regulated gene expression with Metabolism, Sugars, achieve a wider view of the role of

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



851 Kim, J.Y., Park, S.J., 2007 Functional characterization of a glycine- Plant J 50, 439- Abiotic stress, Although glycine-rich RNA-binding

Jang, B., Jung, C.H., rich RNA-binding protein 2 in 451. Arabidpsis thaliana, protein 2 (GRP2) has been implicated in

Ahn, S.J., Goh, C.H., Arabidopsis thaliana under abiotic stress Glycine-rich RNA- plant responses to environmental stresses,

852 Cho, K., Han, O., and

Kim, J.S., Park, S.J., 2007 conditions. domain proteins and glycine-

Cold shock Nucleic Acids binding prozein, RNA

Glycine-rich RNA- the functionfact that cold shockGRP2 in

Despite the and importance of domain

Kwak, K.J., Kim, Y.O., rich RNA-binding proteins from Res 35, 506- binding proteins, cold proteins (CSDPs) and glycine-rich RNA-

Kim, J.Y., Song, J., Arabidopsis thaliana can promote the 516. acclimation binding proteins (GRPs) have been

Kim, B., Jung, C.H.,

853 Jang, M.J., Lim, G.H., 2007 cold adaptation process in Escherichia

Abiotic and biotic stress tolerance in Biochem Glucose insensitive, We conducted a genetic during the cold

implicated to play a role yeast screen to

Kim, E.S., Ko, C.B., Arabidopsis overexpressing the Biophys Res MBF1a, Pathogen identify salt tolerance (SAT) genes in a

Yang, K.Y., Jeong, J.A., multiprotein bridging factor 1a (MBF1a) Commun 354, defense, Salt stress maize kernel cDNA library. During the

Kim, S.H., and Kim,

854 Lee, M.C., Kim, J.Y., 2007 transcriptional coactivator gene. genes

Isolation of cold stress-responsive 440-446.

Plant Cell mRNA differential screening, we identified a stage, rice crops

During their reproductive maize clone

Kim, S.J., An, K.S., An, in the reproductive organs, and Rep 26, 1097- display, cold response often are exposed to cold stress, which

G., and Kim, S.R. characterization of the OsLti6b gene 1110. genes, Rice leads to sterility and reduced yields. To

855 Lee, H.E., Shin, D., Ethylene (Oryza sativa L.).

2007 from rice responsive element binding Biochem Ethylene responsive understand the cold response mechanism

To identify components of the plant stress

Park, S.R., Han, S.E., protein 1 (StEREBP1) from Solanum Biophys Res element binding protein; signal transduction cascade and response

Jeong, M.J., Kwon, tuberosum increases tolerance to abiotic Commun 353, Cold stress; GCC-box; mechanisms, we screened plant genes

856 T.R., Lee, S.K., Park,

Livingston, D.P., 3rd, 2007 stress in transgenic potato plants.model

Using Arabidopsis thaliana as a Cryobiology Solanum tuberosum L.;

863-868. Arabidopsis; Cold- using reverse Northern blot analysis,as a

The suitability of using Arabidopsis and

Van, K., Premakumar, to study subzero acclimation in small 54, 154-163. acclimation; Freezing model plant to investigate freezing

R., Tallury, S.P., and grains. tolerance; Winter tolerance was evaluated by observing

857 Herman, E.M.

Mano, H., Ogasawara, 2007 Isolation of a regulatory gene of Flavonoid Gene

Plant Physiol hardiness; biosynthesis, similarities to winter cereals in tissue the

Many transcriptional factors harboring

F., Sato, K., Higo, H., anthocyanin biosynthesis in tuberous 143, 1252- Regulatory elements, R2R3-MYB domain, basic helix-loop-

and Minobe, Y. roots of purple-fleshed sweet potato. 1268. Ipomoea batatas L. helix domain, or WD40 repeats have been

858 Muthukumar, B., 2007 Transcriptional activation and BMC Plant Brassica juncea, Metal identified in various plant species as

BACKGROUND: Metal

Yakubov, B., and Salt, localization of expression of Brassica Biol 7, 32. hyperaccumulation, hyperaccumulators, including various

D.E. juncea putative metal transport protein Metal transportedr, Thlaspi species, constitutively express the

859 Nakayama, K., Okawa, 2007 BjMTP1. Cor15am is a chloroplast

Arabidopsis Plant Physiol BjMTP1

Arabidopsis, Freezing putative metal transporter MTP1 to high

Many plants acquire increased freezing

K., Kakizaki, T., stromal protein that has cryoprotective 144, 513-523. tolerance, Cor15am, tolerance when they are exposed to

Honma, T., Itoh, H., and activity and forms oligomers. Chloroplast, Stromal nonfreezing temperatures of a certain

Peng, T.

860 Inaba, Y., Lin, W., Cai, 2007 Overexpression of a Panax ginseng Planta 226, protein

Aquaporins, Cold Water movement across known

duration. This process is cellular as cold

W., and Arora, R. tonoplast aquaporin alters salt tolerance, 729-740. acclimation ability, membranes is regulated largely by a

drought tolerance and cold acclimation Drought tolerance, Panax family of water channel proteins called

ability in transgenic Arabidopsis plants. ginseng, tonoplast aquaporins (AQPs). Since several abiotic

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



861 Phillips, J.R., Dalmay, 2007 The role of small RNAs in abiotic stress. FEBS Lett MicroRNAs, It was recently discovered that plants

T., and Bartels, D. 581, 3592- Dehydration stress, respond to environmental stress not only

3597. Oxidative stress, with a specific gene expression

862 Shao, H.B., Guo, Q.J., 2007 Understanding molecular mechanism of Colloids Surf Nutrient stress

Plant gene regulatory Higher plants the the most important role

programme at playmRNA and protein level

Chu, L.Y., Zhao, X.N., higher plant plasticity under abiotic B network system; Abiotic in keeping a stable environment on the

Su, Z.L., Hu, Y.C., and stress. Biointerfaces stress; Signal; earth, which regulate global circumstances

863 Cheng, J.F. Cram, D.,

Sharma, N., 2007 Exploiting the wild crucifer Thlaspi 54, 37-45. Biol Biointerfaces;

Plant Mol Cold stress, Cross in many arvense, terms of different levels

Thlaspi ways in a wild species from the

Huebert, T., Zhou, N., arvense to identify conserved and novel 63, 171-184. species microarray, S- Brassicaceae family, was shown to have a

and Parkin, I.A. genes expressed during a plant's response adenosyl-methionine, higher level of freezing tolerance than

864 Sreenivasulu, N., Abiotic arvense

2007 to cold stress.the regulatory mechanisms Gene 388, 1- Thlaspi stress tolerance;

Deciphering Environmental constraints the include

either of its close relatives,that model

Sopory, S.K., and Kavi of abiotic stress tolerance in plants by 13. Osmoregulation; abiotic stress factors such as salt, drought,

Kishor, P.B. genomic approaches. Regulators; Genomic cold and extreme temperatures severely

865 Sunkar, R., 2007 Small RNAs as big players in plant Trends Plant approaches; Transgenics

Crop, Abiotic stress, Abiotic stress is one of Improvement of

limit crop productivity. the primary causes

Chinnusamy, V., Zhu, abiotic stress responses and nutrient Sci 12, 301- MicroRNAs, Small of crop losses worldwide. Much progress

J., and Zhu, J.K. deprivation. 309. interfering RNA has been made in unraveling the complex

866 Swindell, W.R., 2007 Plastic and adaptive gene expression Heredity 99, Adaptation, Gene stress response mechanisms, particularly

Transcriptional profiling using DNA

Huebner, M., and patterns associated with temperature 143-150. expression, Microarray, microarrays has become a widely used

Weber, A.P. stress in Arabidopsis thaliana. Plasticity, Reaction norm approach for identifying genes with

867 Tardif, G., Kane, N.A., 2007 Interaction network of proteins Plant Mol Biol Abiotic stress, Stress importantthe most stress-regulatory

Wheat is roles in widely adapted crop to

Adam, H., Labrie, L., associated with abiotic stress response 63, 703-718. tolerance, Wheat, Protein abiotic stresses and considered an

Major, G., Gulick, P., and development in wheat. interaction excellent system to study stress tolerance

868 Sarhan, and and

Vij, S., F., Tyagi, A.K. 2007 Emerging trends in the functional Plant Abiotic stress, Stress Plants are its genetic different abiotic

in spite of exposed to complexity. Recent

genomics of the abiotic stress response Biotechnol J tolerance, Crop, Stress stresses, such as water deficit, high

in crop plants. 5, 361-380. response temperature, salinity, cold, heavy metals

869 Xin, Z., Mandaokar, A., 2007 Arabidopsis ESK1 encodes a novel Plant J 49, 786- Freezing tolerance, Cold and mechanical wounding, under field

The eskimo1 (esk1) mutation of

Chen, J., Last, R.L., and regulator of freezing tolerance. 799. acclimation, esk1 Arabidopsis resulted in a 5.5 degrees C

Browse, J. mutant, Microarray improvement in freezing tolerance in the

870 Zhang, J.Y., Broeckling, 2007 Heterologous expression of two Plant Mol Drought tolerance, absence of cold acclimation. Here we

Cuticular waxes are the major components

C.D., Sumner, L.W., Medicago truncatula putative ERF Biol 64, 265- Frezing tolerance, of plant cuticle and play an important role

and Wang, Z.Y. transcription factor genes, WXP1 and 278. Medicago truncatula, in protecting aerial organs from damage

WXP2, in Arabidopsis led to increased Transcription factor, caused by biotic and abiotic stresses. Here

Nr. Autorius Metai Pavadinimas Leidinys Raktažodžiai Abstraktas



871 Zhao, J., Ren, W., Zhi, 2007 Arabidopsis DREB1A/CBF3 bestowed Plant Cell Rep Agrobacterium In order to improve drought tolerance of

D., Wang, L., and Xia, transgenic tall fescue increased tolerance 26, 1521- tumefaciens, DREB1A tall fescue (Festuca arundinacea Schreb.),

G. to drought stress. 1528. gene, Festuca an important perennial cool-season grass,

arundinacea, Drought we introduced Arabidopsis