ライフサイエンスコーパス: vegetative growth

1 -fold lower frequency during asexual mitotic vegetative growth.

2 (Mud2, Nam8 and Tgs1) that are optional for vegetative growth.

3 primary and lateral root systems, and longer vegetative growth.

4 rated by pulvini may have an impact on plant vegetative growth.

5 minate meiotic messenger RNAs (mRNAs) during vegetative growth.

6 nt appears likely to allow the resumption of vegetative growth.

7 ans but is nearly restricted to roots during vegetative growth.

8 n of alpha-toxin and perfringolysin O during vegetative growth.

9 istinct, neither appears to be essential for vegetative growth.

10 that are required for virulence, but not for vegetative growth.

11 ited hormogonia differentiation and enhanced vegetative growth.

12 or proteins to its cell wall envelope during vegetative growth.

13 ly integrate into the host chromosome during vegetative growth.

14 the developmental phase of life than during vegetative growth.

15 promoter displayed luminescence only during vegetative growth.

16 thway during cell wall stress and unstressed vegetative growth.

17 o1 impaired sporulation, but does not affect vegetative growth.

18 t(s) of alpha-tomatine is not present during vegetative growth.

19 the germinated spores outgrew and initiated vegetative growth.

20 MXAN_5522 and MXAN_4569 are expressed during vegetative growth.

21 poIIIE is not required for separation during vegetative growth.

22 Macronuclear ASI2 is nonessential for vegetative growth.

23 ntaneous entry into competence and return to vegetative growth.

24 development as well as during the subsequent vegetative growth.

25 ndent on the actin cytoskeleton during yeast vegetative growth.

26 e expression patterns during development and vegetative growth.

27 Xyl-less and wild-type plants had similar vegetative growth.

28 d is important for cellular expansion during vegetative growth.

29 rmant K-state, distinct from sporulation and vegetative growth.

30 pC expression by phosphorylating MrpC during vegetative growth.

31 opment and eventually died, unable to resume vegetative growth.

32 trol and salinity-stressed conditions during vegetative growth.

33 sis I but also has specific functions during vegetative growth.

34 evelopment as well as social motility during vegetative growth.

35 cytosis and played a role in adhesion during vegetative growth.

36 ough an EVH1 domain at its N terminus during vegetative growth.

37 eus but is absent in the macronucleus during vegetative growth.

38 s of MrpC in Deltapkn8 and Deltapkn14 during vegetative growth.

39 nate the exit from dormancy and the start of vegetative growth.

40 , is deleterious when forced to occur during vegetative growth.

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

42 nic development, seedling establishment, and vegetative growth.

43 commitment sporulating cultures returning to vegetative growth.

44 of protein reserves during germination, and vegetative growth.

45 tical control point regulating initiation of vegetative growth.

46 skeleton in a highly polarized manner during vegetative growth.

47 educed apoplast acidification and suppressed vegetative growth.

48 ous fungi, somatic cell fusion occurs during vegetative growth.

49 sporulation but is apparently unimpaired in vegetative growth.

50 vironmental osmotic status before initiating vegetative growth.

51 responsible for basal gene expression during vegetative growth.

52 y fail to do so during sporulation or normal vegetative growth.

53 eproductive flowers after the adult phase of vegetative growth.

54 potential (psi w) of -2.0 megapascal during vegetative growth.

55 eedling establishment, as well as subsequent vegetative growth.

56 d division during sporulation but not during vegetative growth.

57 MYB112 may be involved in regulating alfalfa vegetative growth.

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

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

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

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

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

63 oduce a characteristic orange pigment during vegetative growth.

64 at enables stable plasmid maintenance during vegetative growth.

65 ring embryo morphogenesis and, later, during vegetative growth.

66 l mutant lines are viable and display normal vegetative growth.

67 231-amino acid Yhc1 polypeptide sufficed for vegetative growth.

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

69 trate that miR408 is a powerful modulator of vegetative growth.

70 o and unisexual mating compared with mitotic vegetative growth.

71 oxidase Erv1 (essential for respiration and vegetative growth 1) plays a central role in the biogene

72 of OXIDATIVE STRESS 2 (OXS2) in maintaining vegetative growth, activating stress tolerance, or enter

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

74 , individually or together, is essential for vegetative growth, although these mutants have altered m

75 t which retained the ability to support both vegetative growth and 50% sporulation efficiency.

76 tions in the LST8-1 gene resulted in reduced vegetative growth and apical dominance with abnormal dev

77 es, larger transcripts are detectable during vegetative growth and asexual development whereas smalle

78 larity establishment causes defects in later vegetative growth and asexual reproduction.

79 ethyl jasmonate, or mechanical damage during vegetative growth and assessed plant resistance in subse

80 that are bound by the Sum1 repressor during vegetative growth and by the Ndt80 activator during meio

81 ce to cationic antibacterial peptides during vegetative growth and cationic peptide, enzymatic, and c

82 nd is vital for septum site selection during vegetative growth and chromosome anchoring during sporul

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

84 us leads to severe abnormalities during both vegetative growth and conjugation.

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

86 sistent with a model in which Nla18 controls vegetative growth and development by activating the expr

87 t a subset of ethylene responses controlling vegetative growth and development may be constitutively

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

89 nthus has a complex life cycle that involves vegetative growth and development.

90 elevated in Deltapkn8 and Deltapkn14 during vegetative growth and development.

91 operon, and both genes are expressed during vegetative growth and development.

92 es different promoters for expression during vegetative growth and development.

93 y occur in flowers and have little effect on vegetative growth and development.

94 which showed defects in stress tolerance and vegetative growth and development.

95 is germinate during host infection and their vegetative growth and dissemination precipitate anthrax

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

97 the Giardia genome was measured during both vegetative growth and encystation.

98 ane protein preparations under conditions of vegetative growth and filamentation.

99 l alleles interact synergistically to rescue vegetative growth and floral initiation in ga1-3, indica

100 hese sucrose-rescued plants displayed normal vegetative growth and flowered, they set very few seeds.

101 al repair of double-strand DNA breaks during vegetative growth and for initiation of meiotic recombin

102 gresses from a juvenile to an adult phase of vegetative growth and from a reproductively incompetent

103 hibited for production of beta2 toxin during vegetative growth and in sporulating culture, providing

104 mutant that reduce CO(2) assimilation, slow vegetative growth and increase water use efficiency in t

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

106 in response to winter temperatures, whereas vegetative growth and inhibition of bud set are promoted

107 during seed germination and show defects in vegetative growth and lateral stem development.

108 Furthermore, SRM1 impacts vegetative growth and leaf shape.

109 etion (delta) of gpgA resulted in restricted vegetative growth and lowered asexual sporulation.

110 intenance of cell shape and integrity during vegetative growth and mating in Saccharomyces cerevisiae

111 maintenance of polarized growth sites during vegetative growth and mating.

112 e helicase (BLM), Sgs1 functions during both vegetative growth and meiosis.

113 um that exhibits a communal lifestyle during vegetative growth and multicellular development, forming

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

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

116 two successive divisions before reversion to vegetative growth and replication, necessarily yielding

117 coded virulence effectors (Yops and LcrV) or vegetative growth and repression of Yops and LcrV with >

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

119 o avoid the accumulation of mutations during vegetative growth and reproduction.

120 ealing a crucial function of PSI proteins in vegetative growth and reproduction.

121 ical role in stress tolerance, and in normal vegetative growth and reproductive development in plants

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

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

124 NENTS OF ABA RECEPTORS (RCAR) branch reduces vegetative growth and seed production and leads to a sev

125 unction as a general splicing factor in both vegetative growth and sexual differentiation.

126 (upland cotton) with a phenotype of impaired vegetative growth and short lint fibers.

127 segregation may differ significantly between vegetative growth and sporulation.

128 The strong role of RcoA in development, vegetative growth and ST production, compared with a rel

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

130 e show that only daytime temperatures affect vegetative growth and that SPT couples morning temperatu

131 rect expression of genes required for proper vegetative growth and the assembly of the conidiophore a

132 t role of PKA in trophozoite motility during vegetative growth and the cellular activation of excysta

133 Gene conversions continued throughout vegetative growth and were stimulated by further sexual

134 devA promoter was temporally associated with vegetative growth, and enhanced green fluorescent protei

135 irst crucial step in the return of spores to vegetative growth, and is induced by nutrients and a var

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

137 moters were found to be highly active during vegetative growth, and P limitation specifically induced

138 he augmented irradiance, and photosynthesis, vegetative growth, and reproduction increased significan

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

140 they are required for cell elongation during vegetative growth as herk1 the1 double and fer RNAi muta

141 s G gamma-subunit and is required for normal vegetative growth as well as proper asexual and sexual d

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

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

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

145 the sexual cycle and does not interfere with vegetative growth, asexual reproduction, differentiation

146 ssive mutation, resulted in gross defects in vegetative growth, asexual spore production and sterigma

147 , nullifying gprA and/or gprB did not affect vegetative growth, asexual sporulation, Hulle cell forma

148 In contrast, after successive years of vegetative growth at early ages, woody perennial shoot m

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

150 ting of DivIVA(R18C) is not essential during vegetative growth because the mutant can recognize the c

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

152 e gene At3g20570 shows minimal alteration in vegetative growth but a significant reduction in the ove

153 horylation sites to alanine had no effect on vegetative growth but a striking effect (>85% reduction)

154 31, caused defects in mismatch repair during vegetative growth but allowed nearly wild-type levels of

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

156 ochrome b5 reductase is not essential during vegetative growth but is required for correct pollen fun

157 opment, whereas ASK11 RNAi plants had normal vegetative growth but mild defects in flower development

158 Vegetative growth but not sporulation or sterigmatocysti

159 n yeast, SEPK and SNAD were not required for vegetative growth but only for timely septation.

160 Mx Hsp16.6 was not detected during normal vegetative growth but was immediately induced after heat

161 tion of Hho1 has proven to be elusive during vegetative growth, but here we demonstrate its requireme

162 (veg)) is present at a moderate level during vegetative growth, but is switched off within the first

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

164 leus (MIC) is transcriptionally inert during vegetative growth, but serves as the genetic blueprint f

165 le for the synthesis of bioactive GAs during vegetative growth, but that they are dispensable for rep

166 ate decreases in ambient temperature inhibit vegetative growth, but the mechanism is poorly understoo

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

168 at few nanocompartments are assembled during vegetative growth, but they increase fivefold upon starv

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

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

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

172 ts are primed for energy production early in vegetative growth by the developmental induction of phot

173 onoxylomannogalactan but was dispensable for vegetative growth, cell integrity, and virulence in a mo

174 During vegetative growth, Cik1 is expressed during mitosis and

175 genes, including whiG, ftsZ and ssgB, during vegetative growth, co-ordinating their expression during

176 pollen limitation persists for decades until vegetative growth coalesces plants into continuous meado

177 uole targeting pathway, which operates under vegetative growth conditions, and peroxisome degradation

178 sive growth upon overexpression under normal vegetative growth conditions.

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

180 ts deleted in GAS1 and GAS2 had no defect in vegetative growth, conidiation, or appressoria formation

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

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

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

184 tro to wild-type A. brassicicola in terms of vegetative growth, conidium production, and responses to

185 The artificial expression of RefZ during vegetative growth converts FtsZ rings into FtsZ spirals,

186 In addition, vegetative growth defects typical of brm mutants in the

187 s pleiotropic phenotypes, including retarded vegetative growth, delayed flowering time, dysfunctional

188 ozygous plants, while retaining their normal vegetative growth, displayed empty seed spaces as well a

189 In vegetative growth DivIVA attracts the bipartite cell div

190 de in the ERV (essential for respiration and vegetative growth) domain of TbQSOX is strongly reducing

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

192 life cycle, at relatively high levels during vegetative growth, early asexual and late sexual develop

193 hree generations exhibited vigorous root and vegetative growth, early-flowering, significantly improv

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

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

196 how only minor phenotypic alterations during vegetative growth, flowering stems are reduced in height

197 For example, Flo11p is required during vegetative growth for haploid invasion and diploid filam

198 or spore development and is important during vegetative growth for moving trapped chromosomal DNA awa

199 of the development-specific tps gene during vegetative growth, formation of fruiting bodies and spor

200 New vegetative growth from UABs of ACC-treated plants result

201 d that loss of pre-1 does not greatly affect vegetative growth, heterokaryon formation or male fertil

202 esses expression of sporulation genes during vegetative growth in a manner that depends on c-di-GMP-m

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

204 ivIVA(R18C) localized to the nucleoid during vegetative growth in a Spo0J/Soj-dependent manner and re

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

206 synchronize the transition from embryonic to vegetative growth in Arabidopsis.

207 pression of a subset of meiotic genes during vegetative growth in budding yeast.

208 t in DZF1, was present at high levels during vegetative growth in Deltapkn8 and Deltapkn14, thus MrpC

209 Nonself recognition during vegetative growth in filamentous fungi is mediated by he

210 f recognition mechanisms that operate during vegetative growth in filamentous fungi, and provides a m

211 n in wild-type and ume6Delta diploids during vegetative growth in glucose and acetate.

212 photoperiodic control of both generative and vegetative growth in strawberry.

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

214 to efficiently reprogram gene expression for vegetative growth in the light.

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

216 itin's 63 surface residues are essential for vegetative growth in yeast.

217 tress, OXS2 is cytoplasmic and is needed for vegetative growth; in its absence, the plant flowers ear

218 emporal separation of reproductive onset and vegetative growth into different seasons via FT1 and FT2

219 Second, the essentiality of Ser5 for vegetative growth is circumvented by covalently tetherin

220 the conclusion that a pathway essential for vegetative growth is largely dispensable for the special

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

222 letions are combined with a dynein deletion, vegetative growth is normal, but sexual reproduction fai

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

224 ed fungal genes occurs during infection, but vegetative growth is unaffected.

225 expression was at a low level in DZF1 during vegetative growth, it was highly elevated in Deltapkn8 a

226 The transition from embryonic to vegetative growth marks an important developmental stage

227 We have now determined that during vegetative growth Mdm30p mediates ubiquitylation of Fzo1

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

229 lobal regulatory changes during steady-state vegetative growth occurring after shift from 26 to 37 de

230 lin-binding proteins (PBPs) expressed during vegetative growth of Bacillus subtilis.

231 Vegetative growth of cbr1-2 plants was relatively normal

232 perimentally identify genes expressed during vegetative growth of S. coelicolor cultures, we used DNA

233 lated to compensate for GA deficiency during vegetative growth of the double mutant.

234 me encodes 'core' functions expressed during vegetative growth of this species, while 1.5 Mb and 2.3

235 hat contains nutrients sufficient to sustain vegetative growth of wild-type cells.

236 ed no obvious morphological defects in yeast vegetative growth or in ability to carry out polymorphic

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

238 the cell's decision whether to continue with vegetative growth or to initiate the differentiation pro

239 Vegetative growth parameters were improved in both Cd-tr

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

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

242 We show that the early flowering and vegetative growth phenotypes of the barley elf3 mutant a

243 ctive for early developmental events and for vegetative growth, phenotypes that are consistent with a

244 nla18 also causes a dramatic decrease in the vegetative growth rate of M. xanthus cells.

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

246 of day and temperature signaling to control vegetative growth rate.

247 eduction in virulence and a 25% reduction in vegetative growth rates in vitro.

248 itivity to osmotic stress, and no changes in vegetative growth rates in vitro.

249 confirmed that ySAG is essential for normal vegetative growth, rather than being required for sporul

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

251 kn14) induce untimely FruA production during vegetative growth resulting in significantly faster frui

252 of published ChIP-chip data obtained during vegetative growth reveals a high binding correlation of

253 , but not gneY, is required for B. anthracis vegetative growth, rod cell shape, S-layer assembly, and

254 During vegetative growth, Saccharomyces cerevisiae cells divide

255 ich spatially regulates cell division during vegetative growth, serves as a forespore-specific inhibi

256 Vegetative growth signaling in the filamentous fungus As

257 protein negatively controlling FadA-mediated vegetative growth signaling were suppressed by delta gpg

258 ng that GpgA functions in FadA-SfaD-mediated vegetative growth signaling.

259 The inactivation of sleL does not affect vegetative growth, spore viability, or the initial stage

260 Leaves formed during the vegetative growth stage did not show a significant ozone

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

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

263 genes appeared to reflect a switch back to a vegetative growth state.

264 During vegetative growth, Ste5p is basally phosphorylated throu

265 pph1 null mutant showed defects during late vegetative growth, swarming and glycerol spore formation

266 mutant also displayed a mutator phenotype in vegetative growth that was similar to mlh3Delta.

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

268 e bonds become reduced in RBs to accommodate vegetative growth, thereby linking the redox status of c

269 1, is required for proper cytokinesis during vegetative growth, timely exit from the mound stage duri

270 ationalized by the fact that transition from vegetative growth to aerial mycelium production, the fir

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

272 he mechanisms underlying the transition from vegetative growth to development remain obscure.

273 The transition from vegetative growth to flower formation is critical for th

274 onditioned accelerated phase transition from vegetative growth to flowering and resulted in misregula

275 dramatically accelerates the transition from vegetative growth to flowering in Arabidopsis: The effec

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

277 of the photoperiod-dependent transition from vegetative growth to flowering.

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

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

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

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

282 The transition from vegetative growth to reproductive development in Arabido

283 Floral transition, the turning point from vegetative growth to reproductive development, is achiev

284 and (3) CnAIP2 promoted the transition from vegetative growth to reproductive initiation (i.e. flowe

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

286 d it regulates the developmental switch from vegetative growth to sporulation.

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

288 cluding delayed flowering time and increased vegetative growth under standard growing conditions.

289 PK and RNase domains are required for normal vegetative growth under unstressed conditions.

290 myces pombe, microtubules regulate polarized vegetative growth via a landmark involving the protein T

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

292 Remarkably, in meiosis, Cdc10 made during vegetative growth was reutilized to build sporulation-sp

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

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

295 opmental stages, and no differences in plant vegetative growth were observed.

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

297 Quelling targets transgenes during vegetative growth, whereas meiotic silencing by unpaired

298 richa, the somatic genome is responsible for vegetative growth, whereas the germline contributes DNA

299 re subject to antisense transcription during vegetative growth, which suggests a mechanism for their

300 ronucleus is transcriptionally active during vegetative growth while there is no expression in the mi