ライフサイエンスコーパス: seed germination

1 rosette vernalization persisted to influence seed germination.

2 sary for efficient WE mobilization following seed germination.

3 ts to oxidative and salinity stresses during seed germination.

4 iption factor plays a key role in regulating seed germination.

5 and the regulation of stomatal aperture and seed germination.

6 e and loss of ABA sensitivity rescues sly1-2 seed germination.

7 isplayed an ABA-insensitive phenotype during seed germination.

8 ith altered rates of abscisic acid-dependent seed germination.

9 but a positive regulator in light-regulated seed germination.

10 flower and silique development and decreased seed germination.

11 hyposensitive to a NaCl-induced blockage of seed germination.

12 rotein coordinating hormone responses during seed germination.

13 e than 20-fold and was sufficient to prevent seed germination.

14 ly described factors influencing Arabidopsis seed germination.

15 gibberellic acid biosynthesis inhibitor, on seed germination.

16 d are defective in lipid mobilization during seed germination.

17 n the negative regulation of ABA response in seed germination.

18 ng gibberellic acid-related processes during seed germination.

19 ka4.1-1, slightly enhanced ABA inhibition of seed germination.

20 repressed in darkness, and light-insensitive seed germination.

21 wers, or roots, and were undetectable during seed germination.

22 hyposensitive to both R and FR light-induced seed germination.

23 LA gene RGL2, suggesting that RGL2 represses seed germination.

24 egulating various plant processes, including seed germination.

25 lant in which the hormone GA is required for seed germination.

26 pathways involved in suppressing GA-induced seed germination.

27 tion times, fewer seeds per fruit and slower seed germination.

28 (ABA) antagonizes gibberellin (GA)-promoted seed germination.

29 entration that completely inhibits wild-type seed germination.

30 understanding of the molecular mechanisms of seed germination.

31 nc finger protein is a positive regulator of seed germination.

32 coregulated at single-cell resolution during seed germination.

33 s of GCR1 are less sensitive to GA and BR in seed germination.

34 in- (GA) and brassinosteroid- (BR) regulated seed germination.

35 sensitive regulation of stomatal closing and seed germination.

36 nstrated that RGL2 is the major repressor in seed germination.

37 evidence that RGL2 and possibly RGL1 control seed germination.

38 and ABA biosynthesis, which in turn controls seed germination.

39 and protein levels are induced by ABA during seed germination.

40 trations of Glc were more potent in delaying seed germination.

41 ly expressed genes for fiber development and seed germination.

42 regeneration and in planta for the timing of seed germination.

43 es to point to a role for NAE metabolites in seed germination.

44 tion during A. thaliana root development and seed germination.

45 sm were investigated during maize (Zea mays) seed germination.

46 velopmental transition from embryogenesis to seed germination.

47 g seed maturation and regained activity upon seed germination.

48 idation occurs in the same cell types during seed germination.

49 ith immature embryos, and mycorrhiza-induced seed germination.

50 levated radiation on the timing and rates of seed germination.

51 d passage through cougar guts did not affect seed germination.

52 roles for these sensor kinases in control of seed germination.

53 ght during seedling de-etiolation as well as seed germination.

54 mber, leaf area, dwarf phenotype and delayed seed germination.

55 aliana ARABIDILLOs function similarly during seed germination.

56 root meristem activation during Arabidopsis seed germination.

57 nalization flowering pathway also influenced seed germination.

58 ses fruit surface lesions and inhibits plant seed germination.

59 seed maturation and become deneddylated upon seed germination.

60 ents, determines the optimal temperature for seed germination.

61 l metabolisms and hormone regulations during seed germination.

62 box-containing genes and negatively affects seed germination.

63 se TAP46 transcript level transiently during seed germination.

64 an inhibitor of gibberellin biosynthesis) on seed germination.

65 RCAR7 and RCAR9 resulted in ABA-insensitive seed germination.

66 wth of secondary inflorescences, and promote seed germination.

67 eostasis during stress/defense signaling and seed germination.

68 wering and abscisic acid hypersensitivity at seed germination.

69 eeds into water during the initial stages of seed germination.

70 sion play a crucial role during Brassicaceae seed germination.

71 ht-tolerant and hypersensitive to ABA during seed germination.

72 tional activation of the XERICO inhibitor of seed germination.

73 temporal transcriptome changes that lead to seed germination.

74 inhibitor to investigate PME involvement in seed germination.

75 hormonal networks that underpin dormancy and seed germination, a process that involves the action of

76 ered a subset of these mutants with abnormal seed germination, accumulation of oil bodies, and delaye

77 Regulation of spore- or seed-germination allows control over the timing of trans

78 PNet, we identified four novel regulators of seed germination (ALTERED SEED GERMINATION5, 6, 7, and 8

79 serves as a repressor of ABA response during seed germination and ABA- and stress-induced gene expres

80 alcium sensor, regulates ABA response during seed germination and ABA- and stress-induced gene expres

81 shows ABA insensitivity in ABA inhibition of seed germination and ABA-induced gene expression.

82 5SAtPP2CA fusion caused ABA insensitivity in seed germination and ABA-induced stomatal closure respon

83 tant showed hyposensitivity to light-induced seed germination and accumulation of chlorophyll and car

84 genes based on expression stabilities during seed germination and bud growth.

85 undance and phosphorylation of CDKF;1 during seed germination and bud growth.

86 Abscisic acid-induced blockage of seed germination and cotyledon greening is reduced in CK

87 xicity of anthraquinone and azo dyes on rice seed germination and decolorized industrial textile effl

88 ys an important role in Arabidopsis thaliana seed germination and deetiolation in response to environ

89 ates many key processes in plants, including seed germination and development and abiotic stress tole

90 cose and ABA signaling in Arabidopsis during seed germination and early seedling development.

91 cose and ABA signaling in Arabidopsis during seed germination and early seedling development.

92 1 each negatively regulates ABA signaling in seed germination and early seedling development.

93 immediately downstream of GPA1 in regulating seed germination and early seedling development.

94 negative regulator of salt tolerance during seed germination and early seedling growth by enhancing

95 e and abscisic acid (ABA) sensitivity during seed germination and early seedling growth.

96 be involved in the metabolic preparation for seed germination and efficient seedling establishment, r

97 more than 11% CPA exhibit strongly decreased seed germination and establishment, and no seeds with CP

98 PYR/PYLs plays a major role in regulation of seed germination and establishment, basal ABA signaling

99 lites necessary for growth are essential for seed germination and establishment.

100 However, seed germination and flower development defects were not

101 ockout mutants of CPRabA5e displayed delayed seed germination and growth arrest during oxidative stre

102 It also alters the seed germination and growth of plants.

103 ive regulators of ABA mediated inhibition of seed germination and growth.

104 forces the proteolytic control necessary for seed germination and growth.

105 laden biochar significantly stimulated grass seed germination and growth.

106 of these genes, bZIP16 functions to promote seed germination and hypocotyl elongation during the ear

107 AS inhibitor, 5-methyl-Trp, was found during seed germination and in suspension cultures of the trans

108 ducing the abscisic acid (ABA) signal during seed germination and in the stress responses of mature p

109 ires 10-fold less ABA than the inhibition of seed germination and is only slightly reduced in charact

110 erm provides nutrients for embryogenesis and seed germination and is the primary tissue where gene im

111 eases seed oil by as much as 48% but reduces seed germination and leaf growth in maize.

112 sensitive response to far-red light-mediated seed germination and light-regulated gene expression.

113 mine the upper temperature limit for lettuce seed germination and may indirectly influence other regu

114 te that miR163 targets PXMT1 mRNA to promote seed germination and modulate root architecture during e

115 lipase D (PLDalpha1) in Arabidopsis enhanced seed germination and oil stability after storage or expo

116 is an important plant hormone that modulates seed germination and plant growth and stress responses,

117 bs (brown seed) -1, -2, or -4, which impair seed germination and possess dark testae.

118 mobilization of seed storage reserves during seed germination and post germination growth.

119 of ARF10 by miR160 plays a critical role in seed germination and post-embryonic developmental progra

120 ins BRIZ1 and BRIZ2 are essential for normal seed germination and post-germination growth.

121 ) promote while abscisic acid (ABA) inhibits seed germination and post-germination growth.

122 in the early developmental stages, including seed germination and post-germination seedling growth.

123 of ARF10 by miR160 plays important roles in seed germination and post-germination.

124 Seed germination and postembryonic development of fry1 a

125 ey regulator of abscisic acid (ABA)-mediated seed germination and postgermination seedling growth.

126 ABA inhibition of seed germination and root elongation are impaired in atr

127 BR1 led to hypersensitive response to ABA in seed germination and root growth assays.

128 showed strong ABA-insensitive phenotypes in seed germination and root growth inhibition.

129 psis phytochrome A (phyA) regulates not only seed germination and seedling de-etiolation but also cir

130 x3, and max4, did not display any defects in seed germination and seedling de-etiolation compared to

131 acids stored in oil bodies is essential for seed germination and seedling development in Arabidopsis

132 ytohormone abscisic acid (ABA) both regulate seed germination and seedling development, although how

133 tigate the role of this regulatory factor in seed germination and seedling establishment by comparing

134 nditions of salt stress, the ratios of their seed germination and seedling establishment were 50% hig

135 es involved in the metabolic preparation for seed germination and seedling establishment, respectivel

136 portant component of KAR/SL signaling during seed germination and seedling growth but is not necessar

137 Although stomatal regulation of snrk2.6 and seed germination and seedling growth of the snrk2.2/2.3

138 in kinases required for ABA signaling during seed germination and seedling growth remain elusive.

139 anced response to abscisic acid (ABA) in the seed germination and seedling growth stages, while mybs2

140 d in cotyledons, axis, and hypocotyls during seed germination and seedling growth, but was not expres

141 and FAAH catalytic activity increased during seed germination and seedling growth, consistent with th

142 TIVE5 (ABI5), hypersensitivity to ABA during seed germination and seedling growth, enhanced stomatal

143 d expression of GA biosynthesis genes during seed germination and seedling growth, indicating that SC

144 e to the phytohormone abscisic acid (ABA) in seed germination and seedling growth, whereas silencing

145 n to promoting seed maturation, ABA inhibits seed germination and seedling growth.

146 ad2-1 also exhibited ABA hypersensitivity in seed germination and seedling growth.

147 berellin (GA)-responsive genes essential for seed germination and seedling growth.

148 aliana, including ABA-mediated inhibition of seed germination and seedling growth.

149 smax1 restores the seed germination and seedling photomorphogenesis phenoty

150 In addition, the phytochromes control seed germination and shade-avoidance responses.

151 hypersensitive to abscisic acid (ABA) during seed germination and show defects in vegetative growth a

152 era1 mutant is hypersensitive to ABA during seed germination and shows a more closed stomata phenoty

153 ormone in two other ABA-dependent processes: seed germination and stomatal closure.

154 tors and signalling components that regulate seed germination and stomatal closure.

155 e used to study changes in endosperms during seed germination and suggest a role for mannan degradati

156 scisic acid (ABA) sensitivity of abi3 during seed germination and suppresses the early flowering phen

157 otein expression patterns over the course of seed germination and under diurnal and circadian light c

158 derstanding of growth and development during seed germination and vegetative propagation, a leafy spu

159 cisic acid (ABA) levels were depleted during seed germination, and both metabolites inhibited the gro

160 PONSE TO DROUGHT21A-LIKE1 in beta-oxidation, seed germination, and growth.

161 branching, root epithelial cell morphology, seed germination, and leaf conductance.

162 Stomatal closure, seed germination, and primary root growth are well-known

163 uding cell differentiation, cell elongation, seed germination, and response to abiotic stress.

164 hypersensitivity affecting gene regulation, seed germination, and stomatal closure.

165 ulates another major life-history transition-seed germination, and that natural variation at the FLC

166 action of ABA in developing seeds and during seed germination, and the TAP46 transcript reaches to th

167 A-induced cytosolic calcium increases and in seed germination, and the wild-type RCN1 genomic DNA com

168 functions of these hydrolases during tomato seed germination are discussed.

169 in, plant growth and development, as well as seed germination, are normal, demonstrating that Hsp101

170 eater ABA hypersensitivity (gene expression, seed germination arrest and primary root growth inhibiti

171 -3 mutations caused ABA hypersensitivity for seed germination arrest and seedling primary root growth

172 it ABA insensitivity in stomatal closure and seed germination assays, establishing ICMT as a negative

173 nts isolated here respond normally to ABA in seed germination assays, root growth inhibition, and gen

174 ABA hypersensitivity in stomatal closure and seed germination assays.

175 enhanced response to abscisic acid (ABA) in seed germination assays.

176 ressing lines for ABA-insensitive mutants in seed germination assays.

177 had reduced toxicity on shoot growth in rice seed germination assays.

178 p lines is an efficient tool for identifying seed germination-associated genes.

179 f plants overexpressing AtGA2ox6 in terms of seed germination attributes and effects on somatic embry

180 e to salt stress and to abscisic acid during seed germination but are more sensitive to freezing dama

181 yposensitivity to abscisic acid (ABA) during seed germination but not in other related assays.

182 SPY construct possess reduced GA response at seed germination, but also possess phenotypes consistent

183 Addition of 2-deoxyglucose inhibited seed germination, but did so less in lines overexpressin

184 ant did not show a phenotype at the level of seed germination, but it did at a cellular level with re

185 lopment, particularly in hormonal control of seed germination, but it is not yet clear which of these

186 rsensitive to methyl methanosulfonate during seed germination, but lose this sensitivity in seedlings

187 w that IMB1 plays a role in the promotion of seed germination by both negatively and positively regul

188 that LeEXP4 is involved in the regulation of seed germination by contributing to cell wall disassembl

189 Phytochrome B (PHYB) promotes seed germination by increasing GA biosynthesis, but inhi

190 e the mechanisms governing the regulation of seed germination by temperature.

191 ession of Arabidopsis (Arabidopsis thaliana) seed germination can be lifted either through DELLA prot

192 mally expressed simultaneously during tomato seed germination, Chi9 and GluB genes are regulated dist

193 RGL2 protein disappears before wild-type seed germination, consistent with the model that GA stim

194 in dry seed, consistent with its function in seed germination control.

195 Analysis of ABA responses in seed germination, cotyledon greening, and root growth as

196 ltiple photomorphogenic processes, including seed germination, cotyledon opening and expansion, chlor

197 xpression of OsbHLH068 in Arabidopsis delays seed germination, decreases salt-induced H2O2 accumulati

198 .2) and SnRK2.3, control responses to ABA in seed germination, dormancy, and seedling growth in Arabi

199 alization of the receptors in the control of seed germination during salt stress.

200 ltiplicative inbreeding depression (based on seed germination, early and late survival, seed mass and

201 Seed germination, early seedling development, stomatal g

202 component HY5 also mediates ABA response in seed germination, early seedling growth, and root develo

203 s in plant growth and development, promoting seed germination, elongation growth and reproductive dev

204 Seed germination failure in the GA biosynthesis mutant g

205 rpn10-1 plants displayed reduced seed germination, growth rate, stamen number, genetic tr

206 were assessed for thermotolerance defects in seed germination, hypocotyl elongation, root growth, and

207 Our study shows that SA blocks barley seed germination in a dosage dependent manner.

208 s a negative regulator of ABA suppression of seed germination in Arabidopsis (Arabidopsis thaliana).

209 (SLY1) and RGA-LIKE2 (RGL2) in regulation of seed germination in Arabidopsis thaliana, a plant in whi

210 ed trigger and hormone-mediated induction of seed germination in Arabidopsis.

211 Rosette vernalization increased seed germination in diverse ecotypes.

212 gests that salicylic acid (SA) also inhibits seed germination in maize and Arabidopsis.

213 egulates GA and ABA biosynthesis to optimize seed germination in response to light.

214 ively regulates chlorophyll biosynthesis and seed germination in the dark, and light-induced degradat

215 In addition, seed germination in the mutant also showed increased sen

216 and ATI2, respectively, stimulate or inhibit seed germination in the presence of the germination-inhi

217 RGL2 disappearance is not a prerequisite for seed germination in the sly1 background.

218 han previously cited could delay the rate of seed germination in wild-ecotype seeds.

219 ivity and ethylene hypersensitivity, whereas seed germination in xlg triple mutants was hypersensitiv

220 During soya seeds germination in FeSO(4) solutions their phytoferrit

221 All three alleles cause lethality prior to seed germination, indicating that AtPARN is an essential

222 WERING IN SHORT DAYS from this region affect seed germination, indicating that conserved mechanisms c

223 s regulate developmental transitions such as seed germination, induction of flowering, leaf senescenc

224 und that rop10-1 enhanced the sensitivity of seed germination inhibition to mannitol and sodium chlor

225 imilarly weak enhancement of ABA response in seed germination inhibition.

226 phytochrome responses, such as induction of seed germination, inhibition of hypocotyl elongation, in

227 Seed germination is a complex trait of key ecological an

228 Seed germination is a critical stage in the plant life c

229 The time of seed germination is a major decision point in the life o

230 Seed germination is a vital developmental transition for

231 Seed germination is an important life-cycle transition b

232 Seed germination is controlled by environmental signals,

233 It is possible that the RGL2 repressor of seed germination is inactivated by after-ripening of sly

234 hen phytochrome B is activated by red light, seed germination is promoted by epigenetic transcription

235 Seed germination is regulated by endogenous hormonal cue

236 Plant populations for which seed germination is site limited will not respond at the

237 A complex phenotype such as seed germination is the result of several genetic and en

238 eeds, but tortoise gut passage also improved seed germination, leading to the widespread, successful

239 n and exhibited GA-independent activation of seed germination, leaf expansion, flowering, stem elonga

240 For seed germination, length, and width, there were from two

241 29% for fruit number and from -5% to +4% for seed germination, length, and width.

242 During seed germination, miR163 and its target PXMT1 are predom

243 During wild-type seed germination, mRNAs encoding seed storage proteins (

244 morphological and abscisic acid-insensitive seed germination mutants were identified for amiRNAs tar

245 In addition to their defects during seed germination, mutations in the AAR1 and AAR2 genes a

246 onmental and genetic factors determines when seed germination occurs.

247 r role in the rhizosphere in stimulating the seed germination of parasitic weeds such as the Striga a

248 Additionally, the differences in seed germination on salt between the two mutants and the

249 hyperfunctionality to ETR1 in the context of seed germination on salt, but not for other traits, that

250 er, rga and gai in combination cannot rescue seed germination or floral development in ga1-3.

251 deoxyorobanchol was active in KAI2-dependent seed germination or hypocotyl elongation, but both were

252 y of fire-dependent ecosystems by inhibiting seed germination or increasing mortality of seedlings an

253 The presence of LeEXP4 mRNA during seed germination parallels endosperm cap weakening deter

254 In seeds, germination per se is not affected in seipin2 sei

255 The decreased seed germination phenotype is only observed for homozygo

256 To understand whether seed germination relies on the degradation of specific s

257 Seeding establishment following seed germination requires activation of the root meriste

258 The completion of seed germination requires cell wall extensibility change

259 ver, limited applications of these lines for seed germination research have been reported.

260 a quantitative trait locus (QTL) analysis of seed germination responses to priming using a recombinan

261 sensitive to GA and hypersensitive to ABA in seed germination responses.

262 However, silencing of FPS after seed germination resulted in a slight developmental dela

263 mutant exhibits enhanced responses to ABA in seed germination, root elongation, and stomatal closure

264 plants display decreased ABA sensitivity in seed germination, root elongation, and stomatal movement

265 splaying enhanced ABA-mediated inhibition of seed germination, root elongation, and stomatal opening.

266 ant sensitivity to drought stress and ABA in seed germination, root growth, and the expression of som

267 INSENSITIVE2 (KAI2) is essential for normal seed germination, seedling development, and leaf morphog

268 lopmental responses, including inhibition of seed germination, seedling establishment, and root growt

269 SCaBP5 or PKS3 are hypersensitive to ABA in seed germination, seedling growth, stomatal closing, and

270 We expected that if RGL2 negatively controls seed germination, sly1 mutant seeds that germinate well

271 and exhibited hyposensitivity to ABA during seed germination, smaller stomatal apertures, a lower tr

272 gative regulators of GA responses, including seed germination, stem elongation, and fertility.

273 which shows ABA-hypersensitive regulation of seed germination, stomatal closing, and cytosolic calciu

274 of diverse NO-regulated processes, including seed germination, stomatal closure, and hypocotyl elonga

275 under a variety of inhibitory conditions for seed germination such as treatment with KCl, CuSO4, ZnSO

276 own mutants are less sensitive to ABA during seed germination, suggesting that TAP46 functions positi

277 imeric G-protein in at least some aspects of seed germination, suggesting that this alternative mode

278 suggest that the biosynthesis of GAs during seed germination takes place in two separate locations w

279 RGL1 plays a greater role in seed germination than do GAI and RGA.

280 ecrka4.1-1 showed stronger ABA inhibition of seed germination than lecrka4.1-1, while the response to

281 are then absorbed by the embryo, and during seed germination, the embryo-stored pyrethrins are recru

282 g a robust technology to suppress or promote seed germination through engineering pathways of hormone

283 expressed in every developmental stage from seed germination through flowering.

284 evolutionary trait that temporally prevents seed germination, thus allowing seedling growth at a fav

285 Over various developmental phases, from seed germination to fruit production, these GB-accumulat

286 rations of sugars altered the sensitivity of seed germination to inhibition by exogenous abscisic aci

287 n involves several developmental stages from seed germination to seedling establishment, i.e. between

288 transmission and in adjusting the timing of seed germination, two key adaptive traits of great impor

289 t or PXMT1 overexpression line shows delayed seed germination under continuous light, and seedlings d

290 y affects Arabidopsis (Arabidopsis thaliana) seed germination under saline conditions by regulating t

291 determine the role of individual isoforms in seed germination under salt stress.

292 ontribute to defects in mucilage release and seed germination under water-stress conditions.

293 However, Glc-delayed seed germination was not caused by increased cellular AB

294 l proteins that function specifically during seed germination, we performed proteomic analysis of per

295 lating the expression of the ADH gene during seed germination; we then characterized three recessive

296 Phosphorylation levels of OLE3 during seed germination were determined to be higher than in de

297 aspects of growth and development, including seed germination, were observed.

298 tive form of ROP10 reduces ABA inhibition of seed germination, whereas dominant-negative mutants of R

299 finger factors confers ABA insensitivity to seed germination, while the zfp3 zfp4 double mutant disp

300 esponses, including hypocotyl elongation and seed germination, with exposure to GB03.