ライフサイエンスコーパス: seed germination

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

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

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

4 aliana ARABIDILLOs function similarly during seed germination.

5 root meristem activation during Arabidopsis seed germination.

6 ses fruit surface lesions and inhibits plant seed germination.

7 seed maturation and become deneddylated upon seed germination.

8 ents, determines the optimal temperature for seed germination.

9 box-containing genes and negatively affects seed germination.

10 se TAP46 transcript level transiently during seed germination.

11 an inhibitor of gibberellin biosynthesis) on seed germination.

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

13 nd whether they are indeed translated during seed germination.

14 wth of secondary inflorescences, and promote seed germination.

15 eostasis during stress/defense signaling and seed germination.

16 wering and abscisic acid hypersensitivity at seed germination.

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

18 sion play a crucial role during Brassicaceae seed germination.

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

20 tional activation of the XERICO inhibitor of seed germination.

21 temporal transcriptome changes that lead to seed germination.

22 inhibitor to investigate PME involvement in seed germination.

23 sary for efficient WE mobilization following seed germination.

24 ts to oxidative and salinity stresses during seed germination.

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

26 and the regulation of stomatal aperture and seed germination.

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

28 isplayed an ABA-insensitive phenotype during seed germination.

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

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

31 flower and silique development and decreased seed germination.

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

33 rotein coordinating hormone responses during seed germination.

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

35 ly described factors influencing Arabidopsis seed germination.

36 gibberellic acid biosynthesis inhibitor, on seed germination.

37 increase in free amino acids, a key event in seed germination.

38 d are defective in lipid mobilization during seed germination.

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

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

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

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

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

44 closure and are hypersensitive to ABA during seed germination.

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

46 egulating various plant processes, including seed germination.

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

48 pathways involved in suppressing GA-induced seed germination.

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

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

51 entration that completely inhibits wild-type seed germination.

52 understanding of the molecular mechanisms of seed germination.

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

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

55 ng the role of lipid homeostasis during rice seed germination.

56 ABA- and light-regulated pathways to control seed germination.

57 omes are translationally up-regulated during seed germination.

58 overexpressing plants show ABA-hyposensitive seed germination.

59 enes and highlight those that also influence seed germination.

60 ibberellin-mediated endosperm expansion, and seed germination.

61 ntribute to the switch from dormant stage to seed germination.

62 n from contaminated seeds, without affecting seed germination.

63 apical meristem, implying their function in seed germination.

64 nalization flowering pathway also influenced seed germination.

65 l metabolisms and hormone regulations during seed germination.

66 rosette vernalization persisted to influence seed germination.

67 ng gibberellic acid-related processes during seed germination.

68 coregulated at single-cell resolution during seed germination.

69 ly expressed genes for fiber development and seed germination.

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

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

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

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

74 ndividual phenolic compounds was found after seeds germination.

75 ironment are used to decide when to initiate seed germination, a process driven by the expansion of c

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

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

78 oss a wide climate range and scored each for seed germination across a range of 13 cold stratificatio

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

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

81 protected soybean plants, allowing 78.3% of seed germination and 56.6% of plant development.

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

83 5SAtPP2CA fusion caused ABA insensitivity in seed germination and ABA-induced stomatal closure respon

84 e synthesized from carotenoids, functions in seed germination and abiotic stress responses.

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

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

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

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

89 unter hypoxia or even anoxia leading to poor seed germination and crop establishment.

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

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

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

93 1 each negatively regulates ABA signaling in seed germination and early seedling development.

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

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

96 the seed, to supply the necessary energy for seed germination and early seedling establishment.

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

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

99 roles in regulation of seed dormancy during seed germination and early seedling growth.

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

101 Efficient seed germination and establishment are important traits

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

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

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

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

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

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

108 laden biochar significantly stimulated grass seed germination and growth.

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

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

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

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

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

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

115 se delivery of biofertilizers that can boost seed germination and mitigate abiotic stressors.

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

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

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

123 By inhibiting seed germination and post-germinative growth through the

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

125 er transcription factor whose level controls seed germination and postgerminative development.

126 aths of signal integration that culminate in seed germination and provides a resource to uncover link

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 Seed germination and seedling establishment are importan

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

135 A signaling termination that is critical for seed germination and seedling establishment in Arabidops

136 own about how the ABA-mediated inhibition of seed germination and seedling establishment is thwarted.

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

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

139 ization and fatty acid beta-oxidation during seed germination and seedling establishment.

140 A together regulate lipid degradation during seed germination and seedling establishment.

141 itches off ABA signaling and is critical for seed germination and seedling establishment.

142 Salinity impairs seed germination and seedling establishment.

143 Overexpression of ABT promotes seed germination and seedling greening in the presence o

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

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

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

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

148 lants with ABA-insensitive phenotypes during seed germination and seedling growth, and decreased drou

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

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

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

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

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

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

155 smax1 restores the seed germination and seedling photomorphogenesis phenoty

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

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

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

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

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

161 Seed priming uses treatments to improve seed germination and thus potentially increase growth an

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

163 ic acid accumulation, which inhibits lettuce seed germination) and absence of trans-zeatin and trans-

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

165 suggests hormonal regulation, novel roles in seed germination, and functional conservation among dive

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

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

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

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

170 al phases during silique (seed) development, seed germination, and seedling establishment in Arabidop

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

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

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

174 However, how control of flowering and seed germination are regulated in moso bamboo is largely

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

176 -3 mutations caused ABA hypersensitivity for seed germination arrest and seedling primary root growth

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

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

179 ABA hypersensitivity in stomatal closure and seed germination assays.

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

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

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

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

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

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

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

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

188 SW and KAR(1) significantly promote lettuce seed germination by reducing levels of ABA and enhancing

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

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

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

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

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

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

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

196 The seasonal timing of seed germination determines a plant's realized environme

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

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

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

200 Seed germination, early seedling development, stomatal g

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

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

203 anslation of these mRNAs occurs during early seed germination, even before the requirement of transcr

204 urther, down-regulation of AtPAM16L affected seed germination, even in the presence of its seemingly

205 ective hardware and open-source software for seed germination experiments, automated seed imaging, an

206 Seed germination failure in the GA biosynthesis mutant g

207 ted that seed priming with AgNPs can enhance seed germination, growth, and yield while maintaining fr

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

209 regulate various light responses, including seed germination, hypocotyl gravitropism, and chlorophyl

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

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

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

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

214 s or graphene led to the activation of early seed germination in Catharanthus and overall higher germ

215 Rosette vernalization increased seed germination in diverse ecotypes.

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

217 portant roles as regulators of flowering and seed germination in moso bamboo and thereby are necessar

218 h smoke-water (SW), KAR(1), and TMB regulate seed germination in photosensitive 'Grand Rapids' lettuc

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

220 er Serine hydrolases (SHs), expressed during seed germination in rice (Oryza sativa).

221 phytochrome B photoreceptor, such as delayed seed germination in the dark and long hypocotyl growth.

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

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

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

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

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

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

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

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

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

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

232 Seed germination is a complex trait of key ecological an

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

234 Seed germination is a fundamental process in the plant l

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

236 Seed germination is a vital developmental transition for

237 Seed germination is affected by physical and chemical fa

238 Seed germination is an important life-cycle transition b

239 Seed germination is controlled by environmental signals,

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

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

242 Seed germination is regulated by endogenous hormonal cue

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

244 A key component of seed germination is the interplay of mechanical forces g

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

246 such as the embryonic root (radicle) during seed germination, is a fundamental question.

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

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

249 29% for fruit number and from -5% to +4% for seed germination, length, and width.

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

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

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

253 onmental and genetic factors determines when seed germination occurs.

254 wildfire smoke play a key role in regulating seed germination of many plant species.

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

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

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

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

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

260 the convergence, at the global level, of the seed germination patterns of alpine species.

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

262 The decreased seed germination phenotype is only observed for homozygo

263 ngly, the overexpression of PhFT1 suppressed seed germination rate in Arabidopsis.

264 dition, the overexpression of PhFT5 promotes seed germination rate.

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

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

267 The completion of seed germination requires cell wall extensibility change

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

288 of seeds in degraded environments, reducing seed germination time, and boosting crop yields.

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

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

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

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

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

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

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

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 Apical growth in plants initiates upon seed germination, whereas radial growth is primed only d

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.