ライフサイエンスコーパス: Populus

1 asmonic acid (JA)-induced gene regulation in Populus.

2 ironmental selection and local adaptation in Populus.

3 tative resistance to Melampsora in leaves of Populus.

4 prior to the salicoid genome duplication in Populus.

5 h sink provisioning and drought tolerance in Populus.

6 al responses to shade in the woody perennial Populus.

7 ling were induced under enriched FR light in Populus.

8 o both sink demand and plant water status in Populus.

9 es were expressed in secondary stem xylem of Populus.

10 iRNA family sizes were generally expanded in Populus.

11 many miRNAs still remain to be discovered in Populus.

12 those miRNAs that have only been observed in Populus.

13 se miRNAs were also found in Arabidopsis and Populus.

14 rom new and publically available datasets in Populus.

15 on wood development in the model angiosperm, Populus.

16 435 individuals from a natural population of Populus.

17 nkage-linkage disequilibrium (LD) mapping in Populus.

18 bium maintenance and cell differentiation in Populus.

19 to identify ARK1 binding loci genome-wide in Populus.

20 d we consequently named it Populus tremula x Populus alba (Pta) LBD1.

21 ts) to address this topic in hybrid zones of Populus alba and P. tremula, two widespread, ecologicall

22 No thylakoid isoforms could be identified in Populus alba or in Salix babylonica.

23 o water stress, transgenic Populus tremula x Populus alba plants characterized by the strong down-reg

24 following shoot removal in Populus tremula x Populus alba softwood cuttings in the absence of exogeno

25 abidopsis (Arabidopsis thaliana) and poplar (Populus alba x grandidentata), and a series of analytica

26 Populus alba x P. glandulosa is used widely in scientifi

27 n were modified in poplar (Populus tremula x Populus alba) by specifically down-regulating CINNAMYL A

28 Poplars (Populus tremula x Populus alba) down-regulated for cinnamoyl-CoA reductase

29 activation-tagged poplar (Populus tremula x Populus alba) mutant with enhanced woody growth and chan

30 wn-regulated poplar trees (Populus tremula x Populus alba) on the bacterial rhizosphere microbiome an

31 s as well as hybrid aspen (Populus tremula x Populus alba) overexpressing the MYB134 transcription fa

32 veloped transgenic poplar (Populus tremula x Populus alba) plants with greatly increased rates of met

33 n of CSE in hybrid poplar (Populus tremula x Populus alba) resulted in up to 25% reduced lignin depos

34 erized response of poplar (Populus tremula x Populus alba) roots to low nitrogen (LN), which involves

35 ence that, in gray poplar (Populus tremula x Populus alba), Suc enters the phloem through plasmodesma

36 Using hybrid poplar (Populus tremula x Populus alba), we applied this strategy and examined fie

37 y stands of hybrid poplar (Populus tremula x Populus alba).

38 od anatomy (Quercus robur, Populus tremula x Populus alba, and Pinus pinaster).

39 members, we searched the genome sequences of Populus and Arabidopsis, and identified, respectively, 9

40 chocarpa and 15 SSPs exhibiting expansion in Populus and closely related lineages.

41 small proportion of the apple genome to the Populus and possibly to the Arabidopsis genomes.

42 Focusing on Eucalyptus, Pinus, Populus and Pseudotsuga - genera that represent diverse

43 ully sequenced plant genomes of Arabidopsis, Populus and rice.

44 In contrast, we found a single ICS gene in Populus and six other sequenced plant genomes, pointing

45 s analysis between the woody perennial plant Populus and the herbaceous annual plants Arabidopsis and

46 oss of conifers and large increases of Acer, Populus, and Quercus in northern hardwoods, whereas to t

47 genetic variation in narrowleaf cottonwood, Populus angustifolia, a dominant riparian tree.

48 ied a riparian broadleaf angiosperm species, Populus angustifolia, growing on water with a constant d

49 son of the organization of miRNA families in Populus, Arabidopsis and rice showed that miRNA family s

50 phenotypic variation in freeze resistance of Populus balsamifera across latitude and the growing seas

51 Using balsam poplar (Populus balsamifera) as a case study, we demonstrate how

52 nes for adaptive phenology in balsam poplar, Populus balsamifera, a widespread forest tree whose rang

53 of a single widely distributed tree species, Populus balsamifera, with variation represented in globa

54 vergence of host species Populus tremula and Populus balsamifera/Populus trichocarpa at 5 Ma.

55 as observed, in varying degrees, in rice and Populus but not in Arabidopsis.

56 de (programs and scripts) for processing the Populus ChIP-seq data are provided within a publically a

57 rt here the functional characterization of a Populus class III HD ZIP gene, popREVOLUTA (PRE), that d

58 cloning and functional characterization of a Populus class-I KNOX homeobox gene, ARBORKNOX2 (ARK2), w

59 Sequencing of 184 RT-PCR Populus clones revealed 37 alternative splice variants,

60 r of miRNA families previously identified in Populus, compared with the number of families identified

61 The genus Populus consists of dioecious woody species with largely

62 We found that the trunks of Populus davidiana emitted large quantities of CH4 during

63 Here, the Populus deltoides (Marsh.) RanBP gene (PdRanBP) was isol

64 also demonstrate neutral loss scanning on a Populus deltoides leaf and on a lignin sample, both sign

65 lion expressed sequence tag (EST) reads from Populus deltoides leaf transcriptome and reconstructed f

66 To aid in the investigation of the Populus deltoides microbiome, we generated draft genome

67 and 19 other diverse bacteria isolated from Populus deltoides roots.

68 ter availability on seedlings of two native (Populus deltoides spp. monilifera, Salix exigua) and thr

69 We pollinated Populus deltoides with gamma-irradiated Populus nigra po

70 In this study, poplars (Populus deltoides x nigra) and Arabidopsis thaliana were

71 In this study, poplar trees (Populus deltoides x nigra) were exposed hydroponically t

72 Poplar (Populus deltoides x nigra, DN34) was used to investigate

73 Poplars (Populus deltoides x nigra, DN34) were exposed to PCB3 wi

74 Poplars (Populus deltoides x nigra, DN34), a model plant with com

75 rifera) to the north vs. eastern cottonwood (Populus deltoides) and sweet gum (Liquidambar styraciflu

76 emission in oak (Quercus robur) and poplar (Populus deltoides) leaves in order to understand the reg

77 Here, we conducted the first GWAS in Populus deltoides, a genetically diverse keystone forest

78 s a plant-associated bacterium isolated from Populus deltoides, and its draft genome sequence is repo

79 ago truncatula, dicot, Leguminosae), poplar (Populus deltoides, dicot, Salicaceae), and switchgrass (

80 Here, we pair work in poplar (Populus) describing one of the smallest sex-determining

81 Foliar endophytes of Populus do not induce the hypersensitive response associ

82 Populus euphratica has been deemed to be a promising can

83 Populus euphratica Olivier, which has been considered as

84 a mapping experiment using Euphrates poplar (Populus euphratica), a so-called hero tree able to grow

85 x1) and GA-insensitive (35S:rgl1) transgenic Populus exhibited increased lateral root proliferation a

86 Transgenic Populus expressing a microRNA-resistant form of PRE pres

87 , comparison of genetic maps across multiple Populus families reveals consistently distorted segregat

88 formed ecological niche models (gENMs) using Populus fremontii (Salicaceae), a widespread tree specie

89 common garden with two native tree species, Populus fremontii and P. angustifolia, and their natural

90 crossing a naturally occurring F(1) hybrid (Populus fremontii x P. angustifolia) to a pure P. angust

91 ented or underrepresented in Arabidopsis and Populus gene pairs, while only two GO classes were under

92 Here, we identified a Populus gene, PsnSHN2, a counterpart of the Arabidopsis

93 idate sORF genes, 56 were new to the current Populus genome annotation.

94 ribution to the continued improvement of the Populus genome assembly, while demonstrating the feasibi

95 hIP-seq data have been integrated within the Populus Genome Integrative Explorer (PopGenIE) where the

96 romosome XIX that suggest this region of the Populus genome is in the process of developing character

97 , coupled with the recent publication of the Populus genome sequence, these maps present a unique opp

98 cation in Populus, the slow evolution of the Populus genome, or to differences in the selection press

99 istics, and evolution of ARK1 binding in the Populus genome.

100 nd associated putative target genes for four Populus homeodomain transcription factors expressed duri

101 Populus hopeiensis exhibits exceptional tolerance to wat

102 When expressed in Arabidopsis, Populus ICS again underwent alternative splicing, but di

103 The splice-site sequences of Populus ICS are unusual, suggesting a causal link betwee

104 The Populus ICS encodes a functional plastidic enzyme, and w

105 Populus ICS primarily functions in phylloquinone biosynt

106 Populus ICS underwent extensive alternative splicing tha

107 ICS evolved independently in Arabidopsis and Populus in accordance with their distinct defense strate

108 The SA response in Populus involved a reprogramming of carbon uptake and pa

109 othesize that duplicate gene preservation in Populus is driven by a combination of subfunctionalizati

110 0), even though the total number of genes in Populus is equivalent to that in Oryza and 1.5 times tha

111 ts) of potential QTLs for growth traits in a Populus linkage population (1200 progeny) and a natural

112 These results compared favorably with other Populus linkage studies, and addition of SSR loci from t

113 In Populus, low nitrogen (LN) elicits rapid and vigorous la

114 In poplar (genus Populus), MYB134 is known to regulate proanthocyanidin b

115 urements of isoprene emission from leaves of Populus nigra and hybrid aspen (Populus tremula x P. tre

116 ated Populus deltoides with gamma-irradiated Populus nigra pollen to produce >500 F1 seedlings contai

117 ranched and branched hybrid poplar saplings (Populus nigra x P. deltoides).

118 Black poplar (Populus nigra) is a potential feedstock for cellulosic e

119 e in trees constitutively emitting isoprene (Populus nigra) or monoterpenes (Quercus ilex), or that d

120 al activity of flavan-3-ols in black poplar (Populus nigra), which include both monomers, such as cat

121 o three real microarray datasets: one from a Populus nitrogen stress experiment with 3 biological rep

122 However, all members of the expanded Populus nucleoredoxin-1 family exhibited increased expre

123 nation and suggest that sex determination in Populus occurs through a ZW system in which the female i

124 All 26 Populus OMT genes were located in segmental duplication

125 ribes the development of transgenic poplars (Populus) overexpressing a mammalian cytochrome P450, a f

126 ates functional diversity and overlap of the Populus PHYB1 and PHYB2 in regulating shade responses.

127 Populus PHYB1 rescued Arabidopsis phyB mutant phenotypes

128 n initial attempt at deciphering the role of Populus PHYs by evaluating transcriptional reprogramming

129 e expression and subcellular localization of Populus PHYs was studied by quantitative real-time PCR (

130 Trees in the genus Populus (poplar) contain phenolic secondary metabolites

131 The number of F-box genes in Populus (Populus trichocarpa; approximately 320) is less

132 on in the number of most conserved miRNAs in Populus relative to Arabidopsis, may be linked to the re

133 es were identified in Arabidopsis, Oryza and Populus, respectively.

134 In several other species, including Populus, SA is derived primarily from the phenylpropanoi

135 tree genera such as Acer, Aesculus, Betula, Populus, Salix, and Ulmus.

136 Expression profiling of OMT genes in Populus showed that only PoptrOMT25 was differentially e

137 corn stover, sugar cane bagasse, and poplar (Populus sp.).

138 dimorphism using >1300 individuals from two Populus species and assessing 96 non-reproductive functi

139 interspecific hybrid family derived from two Populus species during the first 24 yr of ontogeny.

140 In several tree species, including Populus species, the majority of this carbon is derived

141 s Tricholoma populinum is host-specific with Populus species.

142 ecies (Populus trichocarpa), of which 11 are Populus specific.

143 The Populus-specific genes are candidates for carbon sequest

144 well as 48 new miRNA families that could be Populus-specific.

145 argeted by non-conserved miRNAs appear to be Populus-specific.

146 Elite poplar (Populus spp) varieties are created through interspecific

147 one of the most abundant proteins in poplar (Populus spp) xylem, but its biological role has remained

148 Field study of transgenic poplars (Populus spp.) for over 6 years showed that downregulatio

149 at IAMTs from Arabidopsis, rice, and poplar (Populus spp.) form a monophyletic group.

150 al properties of some representative poplar (Populus spp.) isoforms were investigated.

151 are highly susceptible to competition (e.g. Populus spp.) or to biotic disturbances (e.g. Abies bals

152 Isoprene emissions from poplar (Populus spp.) plantations can influence atmospheric chem

153 Specifically, in poplar (Populus spp.), the formation of xylem embolisms leads to

154 naling, and response are affected in poplar (Populus spp.)-Laccaria bicolor ECM roots.

155 productive growth in woody perennial poplar (Populus spp.).

156 naceae, additional cereal crops, and poplar (Populus spp.).

157 In Populus spp., it has long been thought that one monolign

158 The Populus sucrose (Suc) transporter 4 (PtaSUT4), like its

159 sed network connectivity in SA-overproducing Populus, suggesting a previously undescribed role in SA-

160 a (Carica papaya; 139) is similar to that in Populus, supporting the hypothesis that the F-box gene f

161 In source leaves of Populus, SUT4 is the predominantly expressed gene family

162 framework was confirmed by simulation and a Populus szechuanica var.

163 framework was confirmed by simulation and a Populus szechuanica var. tibetica data set.

164 will reduce growth more for native Salix and Populus than for drought-tolerant exotic species.

165 pear to proceed substantially more slowly in Populus than in Arabidopsis.

166 sticated populations may be more feasible in Populus than previously assumed.

167 r degree of synteny with the closely related Populus than with the distantly related Arabidopsis.

168 e linked to the recent genome duplication in Populus, the slow evolution of the Populus genome, or to

169 s were compared among Arabidopsis, Oryza and Populus to identify differential gene (DG) sets that are

170 fore sought to investigate ICS regulation in Populus to learn the extent of ICS involvement in SA syn

171 ein-coding genes suggests that assignment of Populus to Malvidae, rather than Fabidae, is warranted.

172 ybrid population of the model hardwood plant Populus to uncover transcriptional networks in xylem, le

173 n 435 individuals of a natural population of Populus tomentosa.

174 Phenotypes of Populus transgenic lines and the expression of candidate

175 Here, we show, in Populus trees, that initial gravity perception and respo

176 e processes in a trispecific hybrid swarm of Populus trees.

177 ter the estimated divergence of host species Populus tremula and Populus balsamifera/Populus trichoca

178 ascular cambium, and wood-forming tissues of Populus tremula The transcriptome comprised 28,294 expre

179 Transgenic Populus tremula x alba (717-1B4) plants with reduced exp

180 re of the mature leaves of the model species Populus tremula x alba across all seven hierarchical ord

181 We report that transgenic Populus tremula x alba expressing a bacterial SA synthas

182 om leaves of Populus nigra and hybrid aspen (Populus tremula x P. tremuloides) in response to changes

183 opsis thaliana, and we consequently named it Populus tremula x Populus alba (Pta) LBD1.

184 poplar response to water stress, transgenic Populus tremula x Populus alba plants characterized by t

185 eling during 48 h following shoot removal in Populus tremula x Populus alba softwood cuttings in the

186 ent and composition were modified in poplar (Populus tremula x Populus alba) by specifically down-reg

187 Poplars (Populus tremula x Populus alba) down-regulated for cinna

188 y characterized an activation-tagged poplar (Populus tremula x Populus alba) mutant with enhanced woo

189 ield-grown, CCR-down-regulated poplar trees (Populus tremula x Populus alba) on the bacterial rhizosp

190 of catechin and PAs as well as hybrid aspen (Populus tremula x Populus alba) overexpressing the MYB13

191 We have developed transgenic poplar (Populus tremula x Populus alba) plants with greatly incr

192 hat down-regulation of CSE in hybrid poplar (Populus tremula x Populus alba) resulted in up to 25% re

193 sly poorly characterized response of poplar (Populus tremula x Populus alba) roots to low nitrogen (L

194 experimental evidence that, in gray poplar (Populus tremula x Populus alba), Suc enters the phloem t

195 Using hybrid poplar (Populus tremula x Populus alba), we applied this strateg

196 ar-old high-density stands of hybrid poplar (Populus tremula x Populus alba).

197 ith contrasting wood anatomy (Quercus robur, Populus tremula x Populus alba, and Pinus pinaster).

198 t evolved with Populus trichocarpa (Ptr) and Populus tremula x Populus tremuloides (Ptt) were studied

199 in the strong isoprene emitter hybrid aspen (Populus tremula x Populus tremuloides), and used rapid c

200 condary cell wall formation in hybrid aspen (Populus tremula x Populus tremuloides).

201 in the strong isoprene emitter hybrid aspen (Populus tremula x Populus tremuloides).

202 ension wood and normal wood of hybrid aspen (Populus tremula x Populus tremuloides).

203 nhibition in isoprene-emitting hybrid aspen (Populus tremula x Populus tremuloides).

204 rification, and functional reconstitution of Populus tremula x tremuloides CesA8 (PttCesA8), implicat

205 ambial development, we engineered transgenic Populus tremula x tremuloides trees with an elevated cyt

206 PECTIN METHYLESTERASE1 (PtxtPME1) in aspen (Populus tremula x tremuloides) triggers the formation of

207 poration to developing wood of hybrid aspen (Populus tremula x tremuloides).

208 the most abundantly expressed SUT isoform in Populus tremulaxalba, PtaSUT4, is a tonoplast (Group IV)

209 ase in the thermotolerance of hybrid poplar (Populus tremulaxPopulus alba) through overexpression of

210 (FTIRI) was developed that entailed growing Populus tremulodes seedlings on a thin, nutrient-enriche

211 ulus trichocarpa (Ptr) and Populus tremula x Populus tremuloides (Ptt) were studied from their ecolog

212 The scheme was upscaled to Populus tremuloides forests across Colorado, USA, using

213 tive MADS-box gene from quaking aspen trees, Populus tremuloides MADS-box 5 (PTM5).

214 -width chronologies from 40 trembling aspen (Populus tremuloides Michx.) sites along a latitudinal gr

215 ea increment series from 40 trembling aspen (Populus tremuloides Michx.) sites along a latitudinal gr

216 ent widespread mortality of trembling aspen (Populus tremuloides Michx.).

217 Arabidopsis (Arabidopsis thaliana) CAD5 and Populus tremuloides sinapyl alcohol dehydrogenase, respe

218 High concentrations of leaf tannins in Populus tremuloides were correlated with (15) N recovery

219 iyear widespread die-off of trembling aspen (Populus tremuloides) across much of western North Americ

220 enous auxin in stems of quaking aspen trees (Populus tremuloides) after wounding.

221 (Malacosoma disstria) and host trees aspen (Populus tremuloides) and birch (Betula papyrifera).

222 ies of four target species: trembling aspen (Populus tremuloides) and paper birch (Betula papyrifera)

223 espread and climate-induced trembling aspen (Populus tremuloides) forest mortality in western North A

224 e carbon stress in isolated trembling aspen (Populus tremuloides) ramets.

225 ponderosa) and angiosperm (trembling aspen - Populus tremuloides) tree species in the southwestern US

226 rene emitter hybrid aspen (Populus tremula x Populus tremuloides), and used rapid changes in ambient

227 formation in hybrid aspen (Populus tremula x Populus tremuloides).

228 rene emitter hybrid aspen (Populus tremula x Populus tremuloides).

229 rmal wood of hybrid aspen (Populus tremula x Populus tremuloides).

230 ene-emitting hybrid aspen (Populus tremula x Populus tremuloides).

231 two altitudinal transects in the model tree Populus trichocapra.

232 of the known miRNAs from various tissues of Populus trichocarpa (black cottonwood).

233 Using hydroponically grown Populus trichocarpa (clone Nisqually-1), we have establi

234 edon species Medicago truncatula (Medicago), Populus trichocarpa (poplar) and Arabidopsis thaliana (A

235 Populus trichocarpa (poplar) is distinguished from its h

236 small RNAs from abiotic stressed tissues of Populus trichocarpa (Ptc) and the identification of 68 p

237 Two nectary types that evolved with Populus trichocarpa (Ptr) and Populus tremula x Populus

238 Populus trichocarpa and Brachypodium distachyon are emer

239 We resequenced 16 genomes of the model tree Populus trichocarpa and genotyped 120 trees from 10 subp

240 eudo-backcross progeny of 154 individuals of Populus trichocarpa and P. deltoides analyzed with long-

241 ding SBEs in rice, Arabidopsis thaliana, and Populus trichocarpa are described.

242 cies Populus tremula and Populus balsamifera/Populus trichocarpa at 5 Ma.

243 By functionally screening a subset of Populus trichocarpa BAHD/HXXXD acyltransferases, we iden

244 liana), guar (Cyamopsis tetragonolobus), and Populus trichocarpa catalyze beta-1,4-mannan and glucoma

245 bundance and distribution of foliar fungi of Populus trichocarpa in wild populations across its nativ

246 Interestingly, phylogenetic analysis using Populus trichocarpa revealed evidence for small RNA-medi

247 Using RNA sequencing of Populus trichocarpa roots in mutualistic symbiosis with

248 procedure for isolation and transfection of Populus trichocarpa stem differentiating xylem protoplas

249 ns peak in the developing phloem tissue of a Populus trichocarpa stem.

250 ection scans and association analyses of 544 Populus trichocarpa trees to reveal genomic bases of ada

251 representing 1,100 individual undomesticated Populus trichocarpa trees, 47 extreme phenotypes were se

252 parenchyma cells after embolism formation in Populus trichocarpa trees.

253 ce (Oryza sativa), Arabidopsis thaliana, and Populus trichocarpa using the Plant Cis-acting Regulator

254 sence of quantitative trait loci (QTLs) in a Populus trichocarpa x P. deltoides F(2) population.

255 studies of approximately 400 natural poplar (Populus trichocarpa) accessions phenotyped for 60 ecolog

256 Arabidopsis (Arabidopsis thaliana), poplar (Populus trichocarpa) and rice (Oryza sativa).

257 tuberosum), Medicago truncatula, and poplar (Populus trichocarpa) revealed conserved ratios of the AS

258 rect evidence demonstrating that the poplar (Populus trichocarpa) wood-associated NAC domain transcri

259 d from the genome of the model tree species (Populus trichocarpa), of which 11 are Populus specific.

260 on a screen of natural accessions of poplar (Populus trichocarpa), revealing that the leaf cuticular

261 er 40% had up-regulated orthologs in poplar (Populus trichocarpa), rice (Oryza sativa), or Chlamydomo

262 abidopsis (Arabidopsis thaliana) and poplar (Populus trichocarpa), two near-complete rosid genome seq

263 unction endoglucanase from black cottonwood (Populus trichocarpa), which reveals a small, newly recog

264 aldoxime formation in western balsam poplar (Populus trichocarpa).

265 spruce, grape (Vitis vinifera), and poplar (Populus trichocarpa).

266 abidopsis (Arabidopsis thaliana) and poplar (Populus trichocarpa).

267 ous root formation in the model tree poplar (Populus trichocarpa).

268 acetylesterase (PAE1) from black cottonwood (Populus trichocarpa).

269 ally expressed in developing wood of poplar (Populus trichocarpa).

270 Arabidopsis thaliana), and black cottonwood (Populus trichocarpa).

271 omosome, was applied to the chromosome 19 of Populus trichocarpa, an incipient sex chromosome, deciph

272 sphate synthase (DXS) enzyme was cloned from Populus trichocarpa, and the recombinant protein (PtDXS)

273 In stem differentiating xylem (SDX) of Populus trichocarpa, two cinnamic acid 4-hydroxylases (P

274 ) biosynthesis during stem wood formation in Populus trichocarpa, two enzymes, Ptr4CL3 and Ptr4CL5, c

275 two reference plant species, A. thaliana and Populus trichocarpa, with annotations based on UniProt,

276 iating xylem (SDX), in the model woody plant Populus trichocarpa.

277 wood-forming tissue of the model woody plant Populus trichocarpa.

278 two monolignol 4CLs, Ptr4CL3 and Ptr4CL5, in Populus trichocarpa.

279 ive of SND1 transcriptional network genes in Populus trichocarpa.

280 ly duplicated genes in the model forest tree Populus trichocarpa.

281 arCyc, from the recently sequenced genome of Populus trichocarpa.

282 ly contrasting populations of the model tree Populus trichocarpa.

283 nsferases (COMTs) from the black cottonwood, Populus trichocarpa.

284 apaya, Medicago truncatula, Oryza sativa and Populus trichocarpa.

285 ion of D14 homologs in the model woody plant Populus trichocarpa.

286 evealed homology with a predicted protein of Populus trichocarpa.

287 The number of F-box genes in Populus (Populus trichocarpa; approximately 320) is less than hal

288 boring chromosome regions of A. thaliana and Populus trichocarpa; whereas, no pairs are mapped to the

289 is thaliana, papaya [Carica papaya], poplar [Populus trichocarpa], and grape [Vitis vinifera]), we de

290 pressing a constitutively active form of the Populus type-B cytokinin response regulator PtRR13 (Delt

291 mall RNAs from leaves and vegetative buds of Populus using high throughput pyrosequencing.

292 or goal for bioenergy crops, such as poplar (Populus), which will be grown on marginal lands with lit

293 lower than expected from previous studies in Populus, with r(2) dropping below 0.2 within 3-6 kb.

294 The MALDI-LIT-MS images of young Populus wood stem showed even distribution of both cellu

295 and non-isoprene-emitting (NE) gray poplar (Populus x canescens) after acute ozone fumigation.

296 Knockdown lines of CYP79D6/7 in gray poplar (Populus x canescens) exhibited a decreased emission of a

297 Rays from wood samples of poplar (Populus x canescens) were enriched by laser microdissect

298 In this study, poplar plants (Populus x canescens) were exposed to water stress to inv

299 es and physiological performance in poplars (Populus x canescens) with either wild-type or RNAi-suppr

300 g (IE) and nonisoprene-emitting (NE) poplar (Populus x canescens).