ライフサイエンスコーパス: vegetative growth

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

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

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

4 ited hormogonia differentiation and enhanced vegetative growth.

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

6 ly integrate into the host chromosome during vegetative growth.

7 the developmental phase of life than during vegetative growth.

8 promoter displayed luminescence only during vegetative growth.

9 thway during cell wall stress and unstressed vegetative growth.

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

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

12 the germinated spores outgrew and initiated vegetative growth.

13 MXAN_5522 and MXAN_4569 are expressed during vegetative growth.

14 poIIIE is not required for separation during vegetative growth.

15 Macronuclear ASI2 is nonessential for vegetative growth.

16 ntaneous entry into competence and return to vegetative growth.

17 ndent on the actin cytoskeleton during yeast vegetative growth.

18 e expression patterns during development and vegetative growth.

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

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

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

22 pC expression by phosphorylating MrpC during vegetative growth.

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

24 trol and salinity-stressed conditions during vegetative growth.

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

26 evelopment as well as social motility during vegetative growth.

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

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

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

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

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

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

33 nic development, seedling establishment, and vegetative growth.

34 commitment sporulating cultures returning to vegetative growth.

35 of protein reserves during germination, and vegetative growth.

36 tical control point regulating initiation of vegetative growth.

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

38 skeleton in a highly polarized manner during vegetative growth.

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

40 sporulation but is apparently unimpaired in vegetative growth.

41 vironmental osmotic status before initiating vegetative growth.

42 responsible for basal gene expression during vegetative growth.

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

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

45 eproductive flowers after the adult phase of vegetative growth.

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

47 eedling establishment, as well as subsequent vegetative growth.

48 d division during sporulation but not during vegetative growth.

49 ng the transition of the new diploid cell to vegetative growth.

50 ts requiring the phosphatase calcineurin for vegetative growth.

51 e sporulation phenotype and severely reduced vegetative growth.

52 ositioning these bisected chromosomes during vegetative growth.

53 sensors for cell integrity signaling during vegetative growth.

54 e and inflorescence meristems that revert to vegetative growth.

55 es through the nucleus constitutively during vegetative growth.

56 nents function under the basal conditions of vegetative growth.

57 e genetically distinguished from its role in vegetative growth.

58 oduce a characteristic orange pigment during vegetative growth.

59 MYB112 may be involved in regulating alfalfa vegetative growth.

60 at enables stable plasmid maintenance during vegetative growth.

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

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

63 231-amino acid Yhc1 polypeptide sufficed for vegetative growth.

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

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

66 o and unisexual mating compared with mitotic vegetative growth.

67 -fold lower frequency during asexual mitotic vegetative growth.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

108 sides exclusively in the macronucleus during vegetative growth and is asymmetrically distributed to d

109 , functions in a third pathway that promotes vegetative growth and is essential in an och1 mutant tha

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

111 Furthermore, SRM1 impacts vegetative growth and leaf shape.

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

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

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

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

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

117 all stress induced by wall remodeling during vegetative growth and pheromone-induced morphogenesis.

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

119 at POG1 may regulate additional genes during vegetative growth and recovery.

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

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

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

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

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

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

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

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

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

129 segregation may differ significantly between vegetative growth and sporulation.

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

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

132 s does not induce chromosome breakage during vegetative growth and that excess copies of this germlin

133 dicated to signaling cell wall stress during vegetative growth and that Mid2 participates in this sig

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

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

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

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

138 thin a region of the genome expressed during vegetative growth and/or sporulation.

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

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

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

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

143 uld express CPE during either sporulation or vegetative growth, and that this lack of CPE expression

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

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

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

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

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

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

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

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

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

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

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

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

156 31, caused defects in mismatch repair during vegetative growth but allowed nearly wild-type levels of

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

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

159 Vegetative growth but not sporulation or sterigmatocysti

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

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

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

163 Expression of asgD was undetected during vegetative growth, but increased dramatically within 1 h

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

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

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

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

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

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

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

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, cells prey on other bacteria in large

175 During vegetative growth, Cik1 is expressed during mitosis and

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

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

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

179 sive growth upon overexpression under normal vegetative growth conditions.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

210 s demonstrates that top3 (+)is essential for vegetative growth in fission yeast.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

228 ot essential in Tetrahymena spp., and during vegetative growth no clear phenotype is observed in cell

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 that the actin promoter was expressed during vegetative growth on yeast extract-peptone-dextrose medi

237 pmental conditions and does not occur during vegetative growth or during glycerol-induced sporulation

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

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

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

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

242 sion of MCK1 does not suppress the yvh1 slow-vegetative-growth phenotype.

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

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

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

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

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

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

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

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

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

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

263 accharomyces cerevisiae exhibits alternative vegetative growth states referred to as the yeast form a

264 During vegetative growth, Ste5p is basally phosphorylated throu

265 We term this pathway the STE vegetative growth (SVG) pathway.

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

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

268 During vegetative growth, the SVG pathway is inhibited by the m

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

270 1, is required for proper cytokinesis during vegetative growth, timely exit from the mound stage duri

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

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

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

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

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

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

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

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

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

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

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

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

283 The transition from vegetative growth to reproductive development in Arabido

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

285 photoreceptors regulate the transition from vegetative growth to reproductive development, we examin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

300 The Cvt pathway functions during vegetative growth, while autophagy is induced during sta