ライフサイエンスコーパス: vegetative

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

2 Understanding the relationships between vegetative and environmental variables is important for

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

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

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

6 with the developmental stage; indeed, at the vegetative and fruiting stages, analysis revealed the pr

7 quantify expression and DNA methylation from vegetative and gametic cells of each mating type and fro

8 ears and tassels as well as greatly enlarged vegetative and inflorescence meristems.

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

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

11 at it functions in different pathways during vegetative and reproductive development.

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

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

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

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

16 elongation, and the axial growth of various vegetative and reproductive organs, as the loss of At KI

17 ing leaf and flowering stages led to shorter vegetative and reproductive phases, respectively, which

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

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

20 andscape, and enabled development of complex vegetative and reproductive plant morphologies.

21 le AL2 was able to reverse silencing in both vegetative and reproductive plants, L2 and ADK inhibitio

22 wo small RNA libraries from radish leaves at vegetative and reproductive stages were constructed and

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

24 gen content and biomass accumulation in both vegetative and reproductive tissues, and this beneficial

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

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

27 ic capacity, which may support the increased vegetative and reproductive yields of the F1 hybrids.

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

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

30 TMF, SlBOP gene expression is highest during vegetative and transitional stages of meristem maturatio

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

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

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

34 challenge, resulting in the establishment of vegetative bacteria in the distal GI tract.

35 ground allocation by stimulating season-long vegetative biomass and decreasing reproductive biomass a

36 ts for both phenomena and leads to increased vegetative biomass and enhanced pollinator visits to flo

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

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

39 ds can outperform their parents in yield and vegetative biomass, features of hybrid vigor that form t

40 Tillers are vegetative branches that develop from axillary buds loca

41 ing petunia (Petunia hybrida) as a model for vegetative branching, we manipulated both light quality

42 uction of fertilizer applications, employing vegetative buffers, and implementing widespread cover cr

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

44 Vegetative C. difficile, microinjected into the lumen of

45 pheric deposition due to the smaller-stature vegetative canopy; in contrast, no change was observed i

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

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

48 porting sperm during pollen tube growth, the vegetative cell also contributes transcripts to the sper

49 e is intercellular communication between the vegetative cell and the sperm cells.

50 sphatase, is specifically transcribed in the vegetative cell but predominantly translated in sperm ce

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

52 ument transport of AHG3 transcripts from the vegetative cell to sperm and showed that their transport

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

54 le gametophyte) consists of three cells: the vegetative cell, which forms the pollen tube, and two sp

55 ube, and two sperm cells enclosed within the vegetative cell.

56 present in the genome are expressed in both vegetative cells and heterocysts but do not seem to have

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

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

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

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

61 that functions under anaerobic conditions in vegetative cells are under the control of the promoter f

62 ysis showed katB to be expressed only in the vegetative cells but not in heterocysts.

63 In addition, photosynthetic, vegetative cells can form cytosolic LDs and much less in

64 in the surface architecture of C. difficile vegetative cells can play a significant role in disease.

65 ependent of additional sporulation proteins; vegetative cells engineered to divide near a pole seques

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

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

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

69 f nifB2:lacZ from A. variabilis in anaerobic vegetative cells of Anabaena sp. PCC 7120 depended on th

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

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

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

73 nd reciprocally, the transport of sugar from vegetative cells to heterocysts.

74 Reciprocally, vegetative cells transfer fixed carbon to heterocysts.

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

76 transport of amino acids from heterocysts to vegetative cells, and reciprocally, the transport of sug

77 ndency on these enzymes is similar in sperm, vegetative cells, and somatic tissues, although DRM acti

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

79 In vegetative cells, bursts are scarce but preferentially o

80 DRM activity extends into heterochromatin in vegetative cells, likely reflecting transcription of het

81 When produced ectopically in vegetative cells, Ndj1 caused SPB separation defects and

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

83 Nondividing Arabidopsis pollen vegetative cells, which transport engulfed sperm by exte

84 yzed purified Arabidopsis thaliana sperm and vegetative cells-the cell types that comprise pollen-wit

85 separate within minutes after duplication in vegetative cells.

86 suppressed the lethality of NDJ1-expressing vegetative cells.

87 and transfer the fixed nitrogen to adjacent vegetative cells.

88 transcript, inhibiting cum1(+) expression in vegetative cells.

89 tion of cum1(+) sense mRNA in copper-limited vegetative cells.

90 d by an antisense transcription mechanism in vegetative cells.

91 c exchange reactions between heterocysts and vegetative cells.

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

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

94 aic-like landscapes ideal for Cucurbita, and vegetative changes following the megafaunal extinctions

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

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

97 g/oil (1-6%), biomass combustion (4-13%) and vegetative debris (1-3%).

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

99 Vegetative desiccation tolerance in X. viscosa was found

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

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

102 d is emerging as a model system for studying 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 nscriptional coactivators, in the SAM during vegetative development, confers the late flowering of pn

106 While undergoing normal vegetative development, swp73a mutants display reduced e

107 ry pathways for the control of growth during vegetative development, there is little mechanistic unde

108 osmolarity glycerol pathways, and regulates vegetative differentiation, multiple stress responses an

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

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

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

112 Extensive clonal growth and vegetative dispersal can disrupt the functioning of thes

113 mpared to other regions, the topographic and vegetative diversity in the study area appear to provide

114 atory and signaling networks that controlled vegetative DT, which itself emerged as a crucial adaptiv

115 Limbs, hand grip strength, and evaluation of vegetative dysfunction, as well as electrophysiologic st

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

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

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

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

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

121 Furthermore, SRM1 impacts vegetative growth and leaf shape.

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

123 that AAPT1 and AAPT2 are essential to plant vegetative growth and reproduction and have overlapping

124 ng meiosis and gametogenesis, as compared to vegetative growth and starvation.

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

126 to decide between sporulation and continued vegetative growth during each cell cycle spent in starva

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

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

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

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

131 t of cell divisions in plant meristems where vegetative growth is primarily accomplished by expansion

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

133 rt of endogenous jasmonates across the plant vegetative growth phase.

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

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

136 al pathway that controls the transition from vegetative growth to asexual reproduction.

137 The phase transition from vegetative growth to flowering is crucial in the life cy

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

139 master regulator initiating the switch from vegetative growth to gametogenesis.

140 us fumigatus development, shifting from weak vegetative growth to induced asexual sporulation (conidi

141 nism when food is abundant and switches from vegetative growth to multicellular development upon star

142 onditions to the same moisture stress during vegetative growth to unravel the whole-plant (shoot and

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

144 calizes to the tips of growing hyphae during vegetative growth, ahead of the Spitzenkorper, and is re

145 that promotes C difficile spore germination, vegetative growth, and toxin production, leading to epit

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

147 terns at single-nucleotide resolution during vegetative growth, asexual reproduction, and infection-r

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

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

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

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

152 docytic and exocytic FgRabs are required for vegetative growth, conidiogenesis, sexual reproduction,

153 In vegetative growth, ethylene appears to have a dual role,

154 In contrast to vegetative growth, neither germination of B. anthracis s

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

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

157 of oriC placement, and also functions during vegetative growth.

158 is nearly independent of both life span and vegetative growth.

159 oduce a characteristic orange pigment during vegetative growth.

160 at enables stable plasmid maintenance during vegetative growth.

161 MYB112 may be involved in regulating alfalfa vegetative growth.

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

163 Feeding by Elysia suppresses the growth of vegetative Halimeda by approximately 50%.

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

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

166 diallelic virus-restricting allorecognition [vegetative incompatibility (vic)] loci were disrupted in

167 nisms required for the dynamic attainment of vegetative, inflorescence, and floral meristem (VM, IM,

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

169 time, supporting that TFL1 expression in the vegetative meristem controls flowering time.

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

171 in which parental genotypes (genets) produce vegetative modules (ramets) that are capable of independ

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

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

174 en tubes to deliver SCs, in which the pollen vegetative nucleus (VN) and the SCs migrate as a unit to

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

176 est complementary strategies for engineering vegetative oil accumulation.

177 ded on whether experiments were conducted in vegetative or reproductive Nicotiana benthamiana plants

178 sability) or unfavorable (severe disability, vegetative, or dead) at 6 months postinjury.

179 for multiple transgene expression in seeds, vegetative organs, or both simultaneously, while also pr

180 is derived from amino acids remobilized from vegetative organs.

181 d properties greatly differing from those on vegetative organs.

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

183 overcoming Zn translocation barriers between vegetative parts and grains, and achieving grain Zn biof

184 Herein, vegetative parts of Fragaria vesca L.

185 = 0.94) with flowering time over an extended vegetative period.

186 ductive daylengths during the early juvenile vegetative phase (JVP).

187 ON OF CO 1 (SOC1), SEPALLATA (SEP) and SHORT VEGETATIVE PHASE (SVP) Arabidopsis thaliana homologs.

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

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

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

191 the flowering negative regulator gene SHORT VEGETATIVE PHASE (SVP) was up-regulated in PnWB-infected

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

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

194 Vegetative phase change in flowering plants is regulated

195 hanism for the initiation and maintenance of vegetative phase change in plants.

196 hat the downregulation of these genes during vegetative phase change is associated with an increase i

197 e two developmental states and may influence vegetative phase change.

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

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

200 how QTLs regulate the timing and pattern of vegetative phase transition between independently regula

201 During the vegetative phase transition, which accompanies a reducti

202 by loss of FLOWERING LOCUS C (FLC) and SHORT VEGETATIVE PHASE, which both delay flowering and promote

203 pivotal role in AM determination during the vegetative phase.

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

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

206 L2 and ADK inhibition were effective only in vegetative plants.

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

208 cies-specific differences in growth rate and vegetative plasticity, indicating that these traits may

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

210 y a 2.5-fold decrease in the level of ATP in vegetative ppk1.

211 a, by tracking 4-hydroxybenzoic acid to find vegetative prey and the defensive metabolite halimedatet

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

213 e upper part, which plays a critical role in vegetative propagation based on headsets, contained high

214 arous leaf somatic embryos and thus enhances vegetative propagation in K. daigremontiana.

215 notypes by seed without the disadvantages of vegetative propagation or the expense and complexity of

216 pe of asexual reproduction is clonal growth (vegetative propagation) in which parental genotypes (gen

217 nts of potential economic interest with fast vegetative propagation, comprising 37 species with varia

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

219 Moreover, the clonal dispersal of vegetative propagules can assist "mate finding," particu

220 sociated with mussels function as nuclei for vegetative re-growth and, despite covering only 0.1-12%

221 size has been widely used to understand how vegetative resources are allocated in plants.

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

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

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

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

226 environmental stresses such as flooding and vegetative shade.

227 of altered source-sink relationships between vegetative shoot and reproductive tissues.

228 region necessary for TFL1 expression in the vegetative shoot and required for a wild-type flowering

229 was expressed in the peripheral zone of the vegetative shoot apical meristem and in the vasculature

230 HASE, which both delay flowering and promote vegetative shoot identity.

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

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

233 thanol extracts of aerial parts harvested at vegetative stage were the most toxic for lettuce germina

234 ogen peroxide (H2O2) in plant tissues at the vegetative stage, CeO2NPs led to significantly higher H2

235 to salt stress during germination and at the vegetative stage.

236 t on yield than high temperatures during the vegetative stage.

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

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

239 minimally conscious state [MCS] and 43 in a vegetative state [VS]).

240 d that a significant number of patients in a vegetative state are covertly aware and capable of follo

241 who fulfilled all clinical criteria for the vegetative state but produced repeated evidence of cover

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

243 hat AGL22 is involved in the transition from vegetative state to flowering but here we show that AGL2

244 ic electroencephalogram (EEG, attesting to a vegetative state) or were too ill to travel.

245 nts versus 52.0% among 179 medical patients; vegetative state, 6.2% versus 1.7%; lower severe disabil

246 .9% among 188 patients in the medical group; vegetative state, 8.5% versus 2.1%; lower severe disabil

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

248 When death, vegetative state, and severe disability at 6 months were

249 ulted in lower mortality and higher rates of vegetative state, lower severe disability, and upper sev

250 ers and patients, (2) clinical entities (eg, vegetative state, minimally conscious state), (3) clinic

251 hree whose behavioural diagnosis suggested a vegetative state.

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

253 We enrolled 119 consecutive patients: 72 vegetative state/unresponsive wakefulness state (VS/UWS)

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

255 om 73 patients in minimally conscious state, vegetative state/unresponsive wakefulness syndrome and c

256 nts in minimally conscious state compared to vegetative state/unresponsive wakefulness syndrome encom

257 ew York: five minimally conscious state, one vegetative state/unresponsive wakefulness syndrome, one

258 1 patients (26 minimally conscious state, 19 vegetative state/unresponsive wakefulness syndrome, six

259 ional MRI data acquired from 18 patients (11 vegetative state/unresponsive wakefulness syndrome, VS/U

260 patients in a minimally conscious state and vegetative state/unresponsive wakefulness syndrome.

261 en patients in minimally conscious state and vegetative state/unresponsive wakefulness syndrome.

262 Salzburg: 10 minimally conscious state, five vegetative state/unresponsive wakefulness syndrome; New

263 of abscisic acid biosynthetic genes and bark/vegetative storage proteins suggested altered metabolism

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

265 henotypic innovation: the production in both vegetative structure (thallus) and fruiting body (apothe

266 r, our results reveal a new role for TAGs in vegetative tissue and show that PHOT1 and PHOT2 are invo

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

268 a major role in controlling JA responses in vegetative tissue, but are not likely to play a role in

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

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

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

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

273 me data including Arabidopsis pollen, Lilium vegetative tissues and the Amborella trichopoda genome.

274 In vegetative tissues of Arabidopsis (Arabidopsis thaliana)

275 ic expression has led to TAG accumulation in vegetative tissues of different dicotyledonous plants.

276 that only HbXIP2;1 was expressed in all the vegetative tissues tested (leaves, stem, bark, xylem and

277 re sensitive to heat stress (HS) compared to vegetative tissues, but the basis of this phenomenon is

278 ompared these with transcriptomes of diverse vegetative tissues, including leaves, roots, and stems.

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

280 predominantly expressed in actively growing vegetative tissues, whereas GID1b was more highly expres

281 o accumulate in response to water deficit in vegetative tissues, which leads to a remarkable associat

282 of PLATZ1 in WT plants confers partial DT in vegetative tissues.

283 repressing the seed maturation programme in vegetative tissues.

284 tributes more than AAPT2 to PC production in vegetative tissues.

285 invariant (21%) by profiling across several vegetative tissues.

286 ssed between floral buds of either stage and vegetative tissues.

287 f the five Arabidopsis MT genes expressed in vegetative tissues.

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

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

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

291 The transition from vegetative to reproductive growth in woody perennials in

292 The switch from vegetative to reproductive growth is extremely stable ev

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

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

295 enthamiana plants (i.e., before or after the vegetative-to-reproductive transition).

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

297 a benthamiana plants that have undergone the vegetative-to-reproductive transition.

298 we characterized the genetic architecture of vegetative traits and onset of reproduction over ontogen

299 eritabilities and genetic correlations among vegetative traits.

300 are early flowering, but their flowers have vegetative traits.