ライフサイエンスコーパス: vegetative

1 tified novel transcript isoforms at both the vegetative (14-day old seedlings, stage 1.04) and reprod

2 ing that ba2 also plays an essential role in vegetative AM development.

3 recipitation and heat stress during the late vegetative and early reproductive phases of crop growth

4 plex paleopolyploid genome and exhibits many vegetative and floral development complexities.

5 enes show that they are broadly expressed in vegetative and floral organs, but have relatively higher

6 ther with extensive transcriptomic data from vegetative and floral organs.

7 on and control plots and measured effects on vegetative and floral traits, pollinator visitation and

8 criptome analysis has been performed at both vegetative and flowering stages of a terminal drought to

9 by the chloroplast maturation status in both vegetative and fruit tissues.

10 temperature during flowering and had shorter vegetative and maturation period than TSW.

11 3K4me2 and H3K4me3 methylation levels during vegetative and pathogenic development, respectively.

12 rotein calcium indicators, we show that both vegetative and pheromone-treated yeast cells exhibit dis

13 how SPL13 plays a crucial role in regulating vegetative and reproductive development in Medicago sati

14 and organ shapes in transgenic plants during vegetative and reproductive development.

15 double-mutant plants show marked defects in vegetative and reproductive development.

16 LATE4, and describe their diverse effects on vegetative and reproductive development.

17 rogen movement in support of metabolism, and vegetative and reproductive growth are assessed.

18 We hypothesized that vegetative and reproductive growth of plants from ASP an

19 plants grew normally at 22 degrees C, their vegetative and reproductive growth was severely compromi

20 for ER-localized phospholipid metabolism in vegetative and reproductive growth.

21 roduction during their lifetime, alternating vegetative and reproductive meristems in the same indivi

22 ed compromised effects on most of the tested vegetative and reproductive parameters, particularly pla

23 (for example, flowering within a season), to vegetative and reproductive phases, to the total lifespa

24 es, and seed) collected during the juvenile, vegetative and reproductive phases.

25 ssive mutations in rel2 revealed an array of vegetative and reproductive phenotypes, many related to

26 Insights into root system dynamics during vegetative and reproductive stages of the chickpea life

27 DNA methylation of isolated rice SAMs in the vegetative and reproductive stages, we show that methyla

28 sis and immunodetection of two major Hsps in vegetative and reproductive tissues showed that HsfA2 re

29 TWS1 is also expressed in vegetative and reproductive tissues, where it is respons

30 ns of homeobox genes suggested roles in both vegetative and reproductive tissues.

31 We sampled vegetative and reproductive traits in the field at 20 si

32 BF has been shown to be inherited in both vegetative and sexual progeny, with exhibition related t

33 ERA control of AM formation during both the vegetative and the reproductive phase in snapdragon.

34 (BONCAT) to interrogate protein synthesis in vegetative Arabidopsis (Arabidopsis thaliana) seedlings.

35 e-formation (via aggregation) versus staying vegetative (as non-aggregated cells).

36 ection, which is associated with exposure to vegetative bacteria in infected meat (carnivores) or to

37 Photosynthesis contributed strongly to vegetative biomass and sugar content of fruits but had a

38 With plant height as a covariate, vegetative biomass of ASP and SSP did not differ.

39 is data, we proposed that recycling of Po in vegetative biomass residues is an important mechanism fo

40 traits such as stress resistance, longevity, vegetative biomass, and seed yield.

41 high ambient temperatures by adjusting their vegetative body plan to facilitate cooling.

42 in the axils of leaf primordia and generate vegetative branches and reproductive inflorescences.

43 Vegetative bud dormancy is an important adaptive process

44 n patterns of the GmExo70J genes not only in vegetative but also in reproductive organs including mat

45 rameters (individually or in combination) on vegetative carbon gain is relatively unexplored.

46 ap-based) analyses, including assessments of vegetative carbon stocks, evapotranspiration, crop produ

47 photosynthetic traits and to predict future vegetative carbon uptake through modeling.

48 are activated in the sperm companion cell - vegetative cell (VC) - of the flowering plant Arabidopsi

49 eemingly unrelated proteins expressed on the vegetative cell surface or spore coat of C. difficile Th

50 demonstrate that siRNAs produced from pollen vegetative cell transcripts can silence TE reporters in

51 Reduced cell size was observed for multiple vegetative cell types, suggesting a role for ALA4/5 in c

52 nality of the filament, as an association of vegetative cells and heterocysts, is postulated to depen

53 ally in the case of calcein transfer between vegetative cells and heterocysts.

54 of various chemical compounds, enzymes, and vegetative cells and spores of microorganisms in various

55 hesin system is not essential for mitosis in vegetative cells and suggests that plants may contain a

56 RY within the algal cell body varies between vegetative cells and the different cell types of gametog

57 loid nuclei (n + n), most Armillaria gallica vegetative cells are uninucleate.

58 Above 45 degrees C, concentrations of vegetative cells drop two orders of magnitude and endosp

59 able treatments and concomitant virulence of vegetative cells has made it imperative to develop newer

60 rogen-limiting conditions, a fraction of the vegetative cells in each filament terminally differentia

61 fusion protein localized to the periphery of vegetative cells in vivo, but lost this association foll

62 Rec8 expressed in vegetative cells localizes to chromosomal arms and to th

63 ns associated with Martian surface regolith, vegetative cells of Bacillus subtilis in Martian analogu

64 diates into crossovers or noncrossovers from vegetative cells or cells undergoing meiosis.

65 ular totipotency, where embryos develop from vegetative cells rather than from gamete fusion.

66 overexpressing SepJ made wider septa between vegetative cells than the wild type, which correlated wi

67 ill associated with components of the living vegetative cells that produced them, enabling the morpho

68 .g., eukaryotic cells, membranes of Bacillus vegetative cells).

69 els of CG methylation in wild-type sperm and vegetative cells, as well as in wild-type microspores fr

70 In vegetative cells, bursts are scarce but preferentially o

71 Cpd2 is also found in somatic nuclei in vegetative cells, but is dispensable for growth and nucl

72 The septa between heterocysts and vegetative cells, which are narrow in wild-type Anabaena

73 terior of the nucleus in both live and fixed vegetative cells.

74 c exchange reactions between heterocysts and vegetative cells.

75 tent (late night) enriched in the nucleus in vegetative cells.

76 te undergoes meiosis that gives rise to four vegetative cells.

77 independently of its reproductive context in vegetative cells.

78 with a pattern of one heterocyst every 10-12 vegetative cells.

79 come more than 6000 times more abundant than vegetative cells.

80 can trigger growth arrest and cell death in vegetative cells.

81 During a second stage, vegetative changes occurred independently of reproductiv

82 unknown is whether the variable physical and vegetative characteristics associated with vacant parcel

83 t summation operator26PFAS concentrations in vegetative compartments with up to 97 ng g(-1) wet weigh

84 vus communities composed of isolates in many vegetative compatibility groups (VCGs) with varying abil

85 uencing data from seven reproductive and two vegetative control tissues of the basal angiosperm Ambor

86 tors (0.42 versus 0.18%) were higher for low vegetative cover compared to adequate vegetative cover p

87 obility patterns to assess the extent of the vegetative cover in the desert.

88 or low vegetative cover compared to adequate vegetative cover pastures.

89 that under rainy season conditions, adequate vegetative cover through proper pasture management could

90 O) lost from soil under paired degraded (low vegetative cover) and non-degraded (adequate vegetative

91 vegetative cover) and non-degraded (adequate vegetative cover) pastures across five countries of the

92 razing cattle on degraded pastures, with low vegetative cover, is highly susceptible to losses.

93 vity is often associated with a reduction in vegetative cover.

94 In general, the last step in the vegetative cycle of bacterial viruses, or bacteriophages

95 percentages of trees vs. shrubs) at the same vegetative density shows a non-linear relationship betwe

96 ovide strong support for the hypothesis that vegetative desiccation tolerance arose by redirection of

97 n mechanisms induced by desiccation, and how vegetative desiccation tolerance circumvents destructive

98 Vegetative desiccation tolerance in X. viscosa was found

99 he molecular and genetic mechanisms enabling vegetative desiccation tolerance, we produced a high-qua

100 s, but only a few angiosperm species possess vegetative desiccation tolerance.

101 d is emerging as a model system for studying vegetative desiccation tolerance.

102 ewiring of seed desiccation pathways confers vegetative desiccation tolerance.

103 UPR) is activated by various stresses during vegetative development in Arabidopsis, but is constituti

104 ons to remove sodium from the cytosol during vegetative development preventing its accumulation to to

105 BR regulatory networks during soybean early vegetative development.

106 wer timing genes (SOC1 and SVP) may regulate vegetative development.

107 ated levels of Sr validate the assumed heavy vegetative diets of poor and enslaved Africans of the ti

108 erallelic interactions were also observed in vegetative diploid budding yeast, but their functional s

109 tion factor Mmi1 cause high levels of UPD in vegetative diploid cells.

110 bacter solanacearum' (CLso), associated with vegetative disorders in carrots, is transmitted by the c

111 a simple fire line and propagating through a vegetative environment where the midstory has been clear

112 e variation in the order of reproductive and vegetative events, or flower-leaf sequences (FLSs).

113 ether, these findings establish the untimely vegetative expression of gametogenic genes as a causativ

114 tracellular enzyme activity were assessed at vegetative, flowering and grain-filling stages of maize.

115 To understand the cellular basis for the vegetative functions of florigen, we explored the radial

116 haviour, social cognition, motor control and vegetative functions, including frontostriatal circuits,

117 eeds and spores but rare in leaves and other vegetative green tissues.

118 ffects versus climate in driving patterns of vegetative greening remain uncertain.

119 sequencing of plants collected during end of vegetative growth (August) yielded 48,411 unigenes.

120 not only in fumonisin biosynthesis but also vegetative growth and conidiation.

121 ctf7 plants exhibit major defects in vegetative growth and development and are completely ste

122 sis is the fundamental process fueling plant vegetative growth and development.

123 ggest that PpeGID1c serves a primary role in vegetative growth and elongation, whereas GID1b probably

124 r flowering allows for an extended period of vegetative growth and increased biomass production.

125 are mothbean, tepary bean and guar for their vegetative growth and physiological responses to four di

126 developmental repressor that acts to sustain vegetative growth and prevent entry into sporulation.

127 rassinosteroids play a crucial role in plant vegetative growth and reproductive development.

128 an important vegetable crop that carries on vegetative growth and reproductive growth simultaneously

129 g chromosome translocations exhibited normal vegetative growth but failed to undergo successful sexua

130 Despite maintaining higher A, rates of vegetative growth by guar and mothbean were lower than t

131 Herein, we show that nitrate regulates vegetative growth by modulating cell size and endoreplic

132 ranscripts are selectively eliminated during vegetative growth by the combined action of the YTH-fami

133 the fitness advantages of adult survival and vegetative growth in a mesic environment.

134 pact on stomatal function, gas exchange, and vegetative growth in Arabidopsis (Arabidopsis thaliana).

135 When compared with plants in vegetative growth in the chamber, we found that the ligh

136 evious work has shown that glacial Ca limits vegetative growth in the wild progenitors of both C3 and

137 ve as a logical osmostress escape route when vegetative growth is no longer possible.

138 zes Pxr against premature degradation during vegetative growth or positively regulates its transcript

139 Vegetative growth parameters were improved in both Cd-tr

140 photoperiod (conditions representing end of vegetative growth period).

141 bscisic acid sensitivity during germination, vegetative growth rate, and flowering time.

142 OX4 as the principal 13-LOXs responsible for vegetative growth restriction after repetitive wounding.

143 re Zn was retained in the basal stems at the vegetative growth stage.

144 sozyme contributing to shoot GS1 activity in vegetative growth stages and can be up-regulated to reli

145 m (SAM) is a hallmark of the transition from vegetative growth to flowering.

146 duced concomitantly with the transition from vegetative growth to sporulation in a complex developmen

147 dy, we first characterized how soybean early vegetative growth was specifically regulated by the BR b

148 s of unique genes, during multiple rounds of vegetative growth when sporulation is not required.

149 osaccharomyces pombe, TORC1 is essential for vegetative growth, and its activity is regulated in resp

150 on of the MoVRP1 gene resulted in defects in vegetative growth, asexual development, and infection of

151 ediated vesicle trafficking is important for vegetative growth, asexual development, conidial morphol

152 During vegetative growth, biennial sugar beet (Beta vulgaris) m

153 mplicated in meiotic mRNA elimination during vegetative growth, but its function is poorly understood

154 nventional mode of cell division and resumes vegetative growth, but the requirements for spore germin

155 d early infection stages and is required for vegetative growth, conidial production and sexual develo

156 s PDE1 and PDE2 had overlapping functions in vegetative growth, conidiation, sexual reproduction and

157 olVam7-mediated vesicle trafficking promotes vegetative growth, conidiogenesis and pathogenicity of F

158 Although none were required for vegetative growth, five GPCR genes (GIV1-GIV5) significa

159 genes are constitutively transcribed during vegetative growth, their effects are suppressed by stron

160 iverse proteins in the cytoplasm to regulate vegetative growth, virulence, fumonisin biosynthesis and

161 control and water-deficit conditions during vegetative growth, we phenotyped 35 traits, mostly relat

162 d is important for cellular expansion during vegetative growth.

163 ediated 'trade-off' between regenerative and vegetative growth.

164 drial fission do not show obvious defects in vegetative growth.

165 educed apoplast acidification and suppressed vegetative growth.

166 MYB112 may be involved in regulating alfalfa vegetative growth.

167 Mei2 to preserve the activity of Mmi1 during vegetative growth.

168 how prolific flowering, and do not return to vegetative growth.

169 ld and seed size relative to their decreased vegetative growth.

170 development as well as during the subsequent vegetative growth.

171 asting adult heat tolerance, measured as the vegetative heat tolerance of adult rice plants through v

172 both genetic and phenotypic variation within vegetative hyphae suggests that fungal individuals have

173 eria encompasses three developmental stages: vegetative hyphae, aerial hyphae and spores.

174 multicellular mycelial bacteria that grow as vegetative hyphae, which are compartmentalized via cross

175 , for their ability to adopt a non-branching vegetative hyphal conformation and rapidly transverse so

176 ntroduced transgenic corn that produces a Bt vegetative insecticidal protein (Vip).

177 ar pathways utilized by the virus during its vegetative life cycle and offers insights into the host-

178 fection, in which lambda chooses between the vegetative lytic fate and the dormant lysogenic fate.

179 high-resolution gene expression atlas of the vegetative maize shoot apex, we show here that distinct

180 primordia at the shoot apex, but not in the vegetative meristem or stem.

181 nd no significant difference in viability or vegetative morphology between XY and YY males.

182 ticle appressoria development as compared to vegetative (mycelia) growth or during in vivo growth in

183 tumors derived from the glomus cells of the vegetative nervous system.

184 As vegetative nuclei are produced by fusions of paired hapl

185 Here we report finding haploid vegetative nuclei in A. gallica at multiple sites in sou

186 tor which is constitutively expressed in the vegetative nucleus but dynamically accumulates in the ge

187 osis but also the movement of siRNA from the vegetative nucleus to the male germline, resulting in th

188 ments (TEs) are reactivated in the companion vegetative nucleus, resulting in siRNA production and th

189 because the terminally differentiated pollen vegetative nurse cell surrounding the sperm cells underg

190 ven by various promoters can severely impair vegetative or reproductive development, reflecting the s

191 is derived from amino acids remobilized from vegetative organs.

192 material developed from fungal mycelium, the vegetative part and the root structure of fungi.

193 Herein, vegetative parts of Fragaria vesca L.

194 = 0.94) with flowering time over an extended vegetative period.

195 In this study, we describe seven vegetative phage genomes homologous to the historic phag

196 mperatures suppress FT at dusk through SHORT VEGETATIVE PHASE (SVP) function, perhaps to suppress pre

197 k suppression, which was alleviated in short vegetative phase (svp) mutants, occurred particularly in

198 sis, the MADS-box transcription factor SHORT VEGETATIVE PHASE (SVP) plays a key role in the progressi

199 consistent with PP TC development reflecting vegetative phase change (VPC) in Arabidopsis.

200 te the role of the developmental transition, vegetative phase change (VPC), on morphological and phot

201 he effect of meristem-deficient mutations on vegetative phase change and on the expression of key reg

202 These results suggest that AMP1 regulates vegetative phase change downstream of, or in parallel to

203 As maize (Zea mays) plants undergo vegetative phase change from juvenile to adult, they bot

204 Previous work suggests that vegetative phase change is regulated by signals intrinsi

205 ants that affect AM determination during the vegetative phase have been isolated in several model pla

206 han by the G-Box binding motif (Box1) in the vegetative phase of development.

207 In flowering plants, the transition from the vegetative phase to the reproductive phase entails the o

208 During the vegetative phase transition, which accompanies a reducti

209 pivotal role in AM determination during the vegetative phase.

210 e most studies have focused on remote-sensed vegetative phenologies or at local scales with relativel

211 its physiology and Fe protein composition in vegetative photosynthetic tissue during Fe deficiency.

212 nd found that the mutant is also impaired in vegetative plant growth under conditions without externa

213 owever, cellular succulence can occur in any vegetative plant organ, with the level of succulence in

214 Differential plant growth rates and vegetative plasticity were hypothesized to drive species

215 st their motility and are transported by the vegetative pollen tube cell for fertilization, but the e

216 rawberry, stolon production is essential for vegetative propagation at the expense of fruit yield, bu

217 ic (epi-)mutations occurred during prolonged vegetative propagation of Gransden, causing regulatory d

218 ot (AR) formation is critically important in vegetative propagation through cuttings in some plants,

219 he trade-off between sexual reproduction and vegetative propagation.

220 mechanism of transmission of BRRV is through vegetative propagation; however, the virus can remain la

221 ing expression system was stable in multiple vegetative propagations, demonstrating the feasibility o

222 Our analyses revealed a decline in vegetative regeneration of bamboo in recent years, which

223 ing that LTM functions to suppress SP in the vegetative SAM In agreement, SP-overexpressing wild-type

224 layed flowering and precocious doming of the vegetative SAM LTM encodes a kelch domain-containing pro

225 larly at transposable elements (TEs), in the vegetative SAM relative to the differentiated leaf, and

226 developmental transition from a leaf-forming vegetative SAM to an inflorescence- and flower-forming r

227 d-type plants exhibited precocious doming of vegetative SAMs combined with late flowering, as found i

228 A mutation in SP restored the structure of vegetative SAMs in ltm sp double mutants, and late flowe

229 wth and the mean temperature of the previous vegetative season.

230 press PIF-stimulated growth in the light and vegetative shade and that they repress the rapid PIF-ind

231 rainsular, clinical signs related to aura or vegetative signs.

232 Carbonyl sulfide (COS) has a dominant vegetative sink, and plant COS uptake is used to infer G

233 morphotypes have not been linked to specific vegetative species.

234 several thousand Aspergillus conidia (i.e., vegetative spores) daily and typically clear these in an

235 es measured in flag leaves at the end of the vegetative stage and lower aboveground biomass and grain

236 This is a plasmodial, vegetative stage of acellular slime mould.

237 Arabidopsis thaliana) rosette throughout the vegetative stage of growth.

238 ific translatome map covering representative vegetative stage SAM and leaf domains.

239 e Johnsongrass cultivars near the end of the vegetative stage.

240 d PRLT2/89-33 at flowering stage than at the vegetative stage.

241 ociated genes is precociously upregulated in vegetative stages of ltm SAMs, among them, the antiflori

242 ulse GHG fluxes mostly occurred in the early vegetative stages of the corn, prior to activation of th

243 rate helps recovering from drought stress at vegetative stages while there is no such reprieve under

244 eriments conducted on wheat crops at several vegetative stages, showed that the accessible traits cou

245 covery Scale-Revised indicated coma (n = 2), vegetative state (n = 3), minimally conscious state with

246 that enable the crucial distinction between vegetative state (VS)-also coined unresponsive wakefulne

247 ging (fMRI) to determine whether he was in a vegetative state or minimally conscious state.

248 t who may be misidentified as remaining in a vegetative state or one of the similar conditions formul

249 .9% among 188 patients in the medical group; vegetative state, 8.5% versus 2.1%; lower severe disabil

250 and disorders of consciousness such as coma, vegetative state, and minimally conscious state are clea

251 cedure (hybrid neurosurgery) the patient, in vegetative state, was transferred to the intensive care

252 hree whose behavioural diagnosis suggested a vegetative state.

253 ths and 2 women who remained in a persistent vegetative state.

254 A cohort of 127 patients in vegetative state/unresponsive wakefulness syndrome (VS/U

255 ing disorders of consciousness (DoC) such as vegetative state/unresponsive wakefulness syndrome (VS/U

256 sing disorders of consciousness (e.g., coma, vegetative-state, locked-in syndrome), these theories ar

257 Plants vegetative status did not differ between the two fertili

258 ment has emphasized engineering practices or vegetative strategies centered on monocultural plantings

259 bal-scale increases in surface pollution and vegetative stress caused by increasing anthropogenic emi

260 re, but then the lateral meristems generated vegetative tillers subtended by leaves instead of spikel

261 ncreases grain yield, whereas application to vegetative tissue improves recovery and resurrection fro

262 of anthocyanins and other flavonoids in the vegetative tissue of Arabidopsis.

263 However, CaMYB31 also was expressed in vegetative tissues (leaves, roots, and stems).

264 long-distance transport, remobilization from vegetative tissues and accumulation in grain.

265 ocyanin formation was induced within 24 h in vegetative tissues and in undifferentiated cells.

266 LA4/5 and ALA6/7, are expressed primarily in vegetative tissues and pollen, respectively.

267 curs in a programmed manner to dismantle the vegetative tissues and redirect nutrients towards metabo

268 LRXs are involved in cell wall formation in vegetative tissues and required for plant growth.

269 o overcome transcriptional gene silencing in vegetative tissues contributing to the host's next gener

270 ion tolerance is an ancient trait, lost from vegetative tissues following the appearance of tracheids

271 umulation of triacylglycerol (TAG) or oil in vegetative tissues has emerged as a promising approach t

272 Engineering plants to accumulate oils in vegetative tissues is a novel strategy, because most pla

273 In vegetative tissues of Arabidopsis (Arabidopsis thaliana)

274 t abundance in comparison with other UGTs in vegetative tissues of Nicotiana benthamiana and peppermi

275 is tolerated by the majority of seeds and by vegetative tissues of only a small number of land plants

276 changeable, as transgenes expressing ALA6 in vegetative tissues partially rescued ala4/5 mutant pheno

277 a strong indicator of RdDM, were similar to vegetative tissues, although lower in magnitude.

278 e behavior of cells with adaxial identity in vegetative tissues, providing evidence of how cell proli

279 matin boundaries in both gametes relative to vegetative tissues, reminiscent of siRNA patterns in DDM

280 extractable tricin-type metabolites in rice vegetative tissues.

281 esis of LDs and neutral lipid homeostasis in vegetative tissues.

282 is are expected to affect both embryonic and vegetative tissues.

283 VP) plays a key role in the progression from vegetative to floral development, and in woody perennial

284 r dormancy for the meristem to change from a vegetative to floral state.

285 To shift from vegetative to generative growth, they require a chilling

286 ls require prolonged cold to transition from vegetative to reproductive development.

287 ss is required for a correct transition from vegetative to reproductive growth and influences inflore

288 are required to regulate the transition from vegetative to reproductive growth via a pathway called v

289 olved in plant developmental transition from vegetative to reproductive growth.

290 The transition from vegetative to the reproductive stage is the critical dev

291 The vegetative-to-reproductive phase change in tulip (Tulipa

292 ore, downregulation of both genes leads to a vegetative-to-reproductive reversion in the inflorescenc

293 hange in gene expression occurred during the vegetative-to-reproductive transition, suggesting that i

294 st, there was a slight genetic cline in some vegetative traits in the native but not the introduced r

295 s among floral traits and between floral and vegetative traits may influence the distribution of flor

296 while the low QTL overlap between floral and vegetative traits suggests that these trait suites are g

297 s (size and numbers of grains and ears) than vegetative traits.

298 eritabilities and genetic correlations among vegetative traits.

299 the sea is moderated by processes including vegetative trapping and particle flocculation, remains p

300 on due to adaptive plasticity in life-phase (vegetative vs sexual) and fruit morph (dehiscent [DEH] v