ライフサイエンスコーパス: gibberellin

1 and the phytohormones auxin, cytokinin, and gibberellin.

2 by antagonizing the phytohormones auxin and gibberellin.

3 s flowering downstream from the phytohormone gibberellin.

4 egulated by sugar starvation and the hormone gibberellin.

5 nd mediated by hormones such as auxin and/or gibberellin.

6 ng overshoots after the removal of exogenous gibberellin.

7 esocotyl appears predominantly controlled by gibberellin.

8 nts exhibit reduced growth responsiveness to gibberellin.

9 the foolish-seedling disease of rice, makes gibberellin.

10 by MeJA but less responsive to promotion by gibberellin.

11 t the juvenile phase and have high levels of gibberellin.

12 production of the diterpenoid plant hormone gibberellin.

13 s mutants and in the presence of suppressive gibberellin.

14 teractions among glucose, abscisic acid, and gibberellins.

15 ids and to contribute to the biosynthesis of gibberellins.

16 oducing ent-kaurene, which is a precursor of gibberellins.

17 sed levels of chlorophylls, carotenoids, and gibberellins.

18 f ga1-3 (RGA), and have altered responses to gibberellins.

19 IS, the regulation of trichome initiation by gibberellins.

20 ormones such as auxin, brassinosteroids, and gibberellins.

21 hormones, including auxins, jasmonates, and gibberellins.

22 ed operon that may lead to the production of gibberellins.

23 ctors to control plant growth in response to gibberellin (1) .

24 ly regulate the acetylation level of the C19-GIBBERELLIN 2-OXIDASE2 (GA2ox2) locus and repress the ex

25 strate that the gibberellin-degrading enzyme GIBBERELLIN 2-OXIDASE6 is transcriptionally induced by E

26 ed significantly increased levels of ABA and gibberellin, 2- and 5-fold, respectively.

27 genome-wide transcriptome data and show that GIBBERELLIN 20 OXIDASE 2, which encodes an enzyme requir

28 mutations at GA locus 5 (GA5), which encodes gibberellin 20-oxidase 1 (GA20ox1) involved in the last

29 genes have low expression there is enhanced GIBBERELLIN 3 BETA-HYDROXYLASE 1 (GA3ox1) expression, ex

30 Gibberellin 3-oxidase (GA3ox) catalyzes the final step i

31 Gibberellin 3-oxidase in Arabidopsis is encoded by a mul

32 ranscriptional activation of GID1 and GA3ox (GIBBERELLIN 3-OXIDASE) genes controlling GA perception a

33 h direct repression of FLOWERING LOCUS T and GIBBERELLIN 3-OXIDASE1/2, encoding major components of t

34 FLOWERING LOCUS T (AcFT), LEAFY (AcLFY) and GIBBERELLIN-3 OXIDASE (GA3ox1) during the bulbing respon

35 degradation is promoted by the phytohormone gibberellin [4].

36 de pathways regulating phytohormones such as gibberellins, abscisic acid and jasmonic acid, but surpr

37 ns (calcium and MAPK), phytohormones (auxin, gibberellins, abscisic acid, JA and SA), and secondary m

38 ccurately predicts the response to exogenous gibberellin after a number of chemical and genetic pertu

39 gene interaction partners, and also modulate gibberellin and abscisic acid signaling to regulate dive

40 in seed dormancy, mediated by alteration of gibberellin and abscisic acid signalling.

41 several factors, including the phytohormones gibberellin and abscisic acid, through conserved cis-mot

42 sheath1, possibly correlated with changes in gibberellin and auxin signaling.

43 eased in the mutant, whereas the contents of gibberellin and brassinosteroid showed no difference bet

44 k between the growth-promoting plant hormone gibberellin and cortical microtubule organization.

45 s, we predict how these perturbations affect gibberellin and DELLA levels and thereby provide insight

46 ation and leaf growth by a process involving gibberellin and DELLA signaling.

47 Moreover, genes related to auxin, gibberellin and ethylene biosynthesis were significantly

48 n of genes encoding regulated enzymes in the gibberellin and ethylene biosynthetic pathways (LsGA3ox1

49 e in both modulating the level of endogenous gibberellin and generating overshoots after the removal

50 sponse element (RE), two heat shock REs, one gibberellin and two auxin REs, and five sugar REs.

51 e integration of photoperiod, vernalization, gibberellin and/or autonomous signaling pathways by regu

52 ranscript and selective hormone profiling of gibberellins and abscisic acid revealed changes only in

53 sis of unsaturated fatty acids, eicosanoids, gibberellins and carotenoids.

54 otype is associated with increased levels of gibberellins and certain flavonoid compounds in roots.

55 gnaling is highly integrated with the light, gibberellin, and auxin pathways through both direct inte

56 red the expression of genes involved in ABA, gibberellin, and ethylene biosynthesis and signaling pat

57 ndole acetic acid, active cytokinins, active gibberellin, and salicylic acid were detected in the roo

58 as chlorophylls, tocopherols, phylloquinone, gibberellins, and carotenoids.

59 nd response of phytohormones, such as auxin, gibberellins, and strigolactone, were differentially exp

60 We distinguished single and double bonds in gibberellins, and we enantioselectively crystallized rac

61 ient carbon metabolism and the plant hormone gibberellin are required to guarantee optimal plant grow

62 Gibberellins are a class of tetracyclic plant hormones t

63 apart from the circumstantial evidence that gibberellins are somehow involved in the expression of L

64 of seven hormones, including abscisic acid, gibberellin, auxin, ethylene, cytokinin, brassinosteroid

65 Gibberellin binds its receptor, GID1, to form a complex

66 served as a histidine in enzymes involved in gibberellin biosynthesis and as an arginine in those ded

67 Conversely, genes for gibberellin biosynthesis and inactivation using methyltr

68 heir Mg(2+) cofactor, with those involved in gibberellin biosynthesis being more sensitive to such in

69 nt of the pickle (pkl) mutant, inhibition of gibberellin biosynthesis during germination induces embr

70 prominent role than the embryo in auxin and gibberellin biosynthesis for fruit set.

71 lases and as a novel, selective inhibitor of gibberellin biosynthesis in plants.

72 erved after biotic stress treatments and the gibberellin biosynthesis inhibitor paclobutrazol.

73 , which encodes ent-kaurene oxidase 2 of the gibberellin biosynthesis pathway, is down-regulated in O

74 n which LsERF1 acts through the promotion of gibberellin biosynthesis to counter the inhibitory effec

75 te-dependent dioxygenase 2-ODD2, involved in gibberellin biosynthesis was significantly increased at

76 isic acid and paclobutrazol (an inhibitor of gibberellin biosynthesis) on seed germination.

77 se 1 (GA20ox1) involved in the last steps of gibberellin biosynthesis, are found in different populat

78 biochemical regulatory mechanism in limiting gibberellin biosynthesis, but the importance of its rele

79 -specific auxin transport, strigolactone and gibberellin biosynthesis, degradation of phospholipids a

80 ssinosteroid signaling, auxin transport, and gibberellin biosynthesis.

81 ys, which is transduced into a daily rate of gibberellin biosynthesis.

82 o changes in transcripts encoding enzymes of gibberellin biosynthesis.

83 rding ent-kaurenoic acid from ent-kaurene in gibberellin biosynthesis.

84 germinate on paclobutrazol, an inhibitor of gibberellin biosynthesis.

85 rosettes, probably through the activation of gibberellin biosynthetic genes.

86 genes associated with the abscisic acid and gibberellin biosynthetic pathways and results of biosynt

87 ic acid catabolic pathway (via CYP707A2) and gibberellins biosynthetic pathway (via GA20ox1) in seeds

88 ds and sterols are derived from FPP, whereas gibberellins, carotenoids, casbenes, taxenes, and others

89 Our study demonstrates that FIS1 mediates gibberellin catabolism and regulates fruit firmness, and

90 ription factor LEAFY induces expression of a gibberellin catabolism gene; consequently, increased LEA

91 complexity from methanol to plant hormones (gibberellins, containing eight stereocenters), were crys

92 ng pathway and was associated with increased gibberellin content and reduced abscisic acid sensitivit

93 nd its mutation leads to increased bioactive gibberellin content, enhanced cutin and wax biosynthesis

94 The signals auxin, cytokinin and gibberellin control the balance between cell division an

95 These bioregulators include auxins, gibberellins, cytokinins, abscisic acid, brassinosteroid

96 ed significantly increased amounts of active gibberellins, cytokinins, salicylic acid, and jasmonate

97 overexpression line, we demonstrate that the gibberellin-degrading enzyme GIBBERELLIN 2-OXIDASE6 is t

98 e oxygen species (ROS) associated with early gibberellin-dependent flowering and abscisic acid hypers

99 regulating tubulin subunit availability in a gibberellin-dependent manner.

100 bberellin signaling network, we simulate how gibberellin dilution affects the downstream components,

101 Gibberellin (GA) 3-oxidase, a class of 2-oxoglutarate-de

102 GAI) and Repressor of GAI-Like, which affect gibberellin (GA) action, and the GA catabolic gene, GA 2

103 The aim of this study was to investigate how gibberellin (GA) and abscisic acid (ABA) regulate conver

104 studying the regulation of transcription by gibberellin (GA) and abscisic acid (ABA).

105 analyses involving mutants in the long-day, gibberellin (GA) and phyB flowering pathways indicated t

106 oss talk with signaling pathways mediated by gibberellin (GA) and SPINDLY (SPY), a GA response inhibi

107 By contrast, the diterpene hormone gibberellin (GA) and the microRNA319-regulated TEOSINTE

108 We show here that exogenous gibberellin (GA) application accelerates spike developme

109 ntially sensitive to abscisic acid (ABA) and gibberellin (GA) at elevated temperatures.

110 The gibberellin (GA) biosynthesis inhibitor paclobutrazol ca

111 Gibberellin (GA) biosynthesis is necessary for normal pl

112 barley elf3 mutant are strongly dependent on gibberellin (GA) biosynthesis.

113 s transcriptional regulation of key genes of gibberellin (GA) biosynthesis.

114 on of GIBBERELLIC ACID3-OXIDASE2, encoding a gibberellin (GA) biosynthetic enzyme, and the levels of

115 The activity of the gibberellin (GA) biosynthetic enzymes GA 20-oxidases (GA

116 Transcripts of the gibberellin (GA) biosynthetic gene EaGA3ox1 and GA-respo

117 is induced not only by sugar starvation and gibberellin (GA) but also by O2 deficiency.

118 Conversely, the hormone gibberellin (GA) can antagonise the effects of KNOX over

119 in the biosynthesis or signaling pathways of gibberellin (GA) can cause dwarfing phenotypes in plants

120 The diterpenoid phytohormone gibberellin (GA) controls diverse developmental processe

121 gs were demonstrated to be non-responsive to gibberellin (GA) for cell elongation, hypersensitive to

122 Root elongation depends on the action of the gibberellin (GA) growth hormones, which promote cell pro

123 In particular, the growth-promoting hormone gibberellin (GA) has been shown to play a significant ro

124 The phytohormone gibberellin (GA) has long been known to regulate the gro

125 DELLA proteins are repressors of the gibberellin (GA) hormone signaling pathway that act main

126 e pathway or through proteolysis-independent gibberellin (GA) hormone signaling.

127 ionship between the brassinosteroid (BR) and gibberellin (GA) hormones across both stages of photomor

128 Involvement of the growth regulator gibberellin (GA) in the control of flowering by environm

129 Gibberellin (GA) involvement in the reproductive events

130 The phytohormone gibberellin (GA) is a key regulator of plant growth and

131 The hormone gibberellin (GA) is a key regulator of plant growth.

132 duced levels of the growth-promoting hormone gibberellin (GA) lead to increased tolerance to water de

133 is poorly understood, although a decrease in gibberellin (GA) levels is known to be required.

134 Gibberellin (GA) levels were investigated because it is

135 s rescued either by exogenous application of gibberellin (GA) or by introducing della quadruple mutan

136 ons enhance seed dormancy by suppressing the gibberellin (GA) pathway through de-represssion of the m

137 t cases the homologs must participate in non-gibberellin (GA) pathways.

138 P450 (CYP) 701 family member is required for gibberellin (GA) phytohormone biosynthesis.

139 The gibberellin (GA) phytohormones play important roles in p

140 the response of plants to application of the gibberellin (GA) precursors ent-kaurenoic acid and GA12

141 The phytohormone gibberellin (GA) promotes growth by inducing degradation

142 The phytohormone gibberellin (GA) promotes plant growth by stimulating ce

143 The hormone gibberellin (GA) regulates Arabidopsis root growth by co

144 Gibberellin (GA) regulates plant development primarily b

145 The pleiotropic and complex gibberellin (GA) response relies on targeted proteolysis

146 The application of bioactive gibberellin (GA) restored the runnering phenotype in the

147 oteins are the master negative regulators in gibberellin (GA) signaling acting in the nucleus as tran

148 ration of ethylene, abscisic acid (ABA), and gibberellin (GA) signaling during submergence.

149 We explore the roles of gibberellin (GA) signaling genes SLEEPY1 (SLY1) and RGA-

150 (SLY1) F-box gene is a positive regulator of gibberellin (GA) signaling in Arabidopsis (Arabidopsis t

151 ressors in plants by inhibiting phytohormone gibberellin (GA) signaling in response to developmental

152 the concurrence of brassinosteroid (BR) and gibberellin (GA) signaling in the control of cell expans

153 ate the crosstalk of abscisic acid (ABA) and gibberellin (GA) signaling in wheat (Triticum aestivum),

154 e presents evidence that DELLA repression of gibberellin (GA) signaling is relieved both by proteolys

155 he gene encoding SlDELLA, a repressor in the gibberellin (GA) signaling pathway.

156 INDLY (SPY) protein negatively regulates the gibberellin (GA) signaling pathway.

157 Specifically, we show how GI modulates gibberellin (GA) signaling through the stabilization of

158 reviously been established in both light and gibberellin (GA) signaling, through interactions with ph

159 Here we show that gibberellin (GA) signalling mediated by DELLA proteins i

160 Abscisic acid (ABA) and gibberellin (GA) signalling responds rapidly following b

161 Excessive gibberellin (GA) signalling, mediated through the DELLA

162 KN1 negatively modulates the accumulation of gibberellin (GA) through the control of ga2ox1, which co

163 eurone cells responded to nitric oxide (NO), gibberellin (GA), and abscisic acid, with NO being upstr

164 cence downstream from auxin, cytokinin (CK), gibberellin (GA), and light signaling.

165 red for biosynthesis of the growth regulator gibberellin (GA), is upregulated in svp mutants.

166 ight, temperature, brassinosteroid (BR), and gibberellin (GA), regulate cell elongation largely by in

167 ed by a limited response to the phytohormone gibberellin (GA), resulting in improved resistance to st

168 cap enzyme endo-beta-mannanase is induced by gibberellin (GA), which is thought to be the major hormo

169 oss-talk between the phytohormones auxin and gibberellin (GA), which partly control overlapping proce

170 a quiescence survival strategy that inhibits gibberellin (GA)-induced carbohydrate consumption and el

171 l known that abscisic acid (ABA) antagonizes gibberellin (GA)-promoted seed germination.

172 e found that DOG1 inhibits the expression of gibberellin (GA)-regulated genes encoding cell-wall remo

173 nes encoding the DELLAs, a family of nuclear gibberellin (GA)-regulated growth-repressing proteins.

174 LLA, GhSLR1, repressor of the growth hormone gibberellin (GA).

175 phenotype is suppressed by the phytohormone gibberellin (GA).

176 pkl seedlings by the plant growth regulator gibberellin (GA).

177 ally acting hormones abscisic acid (ABA) and gibberellin (GA).

178 es and flavonoid accumulation; (2) increased gibberellin (GA)2-oxidase expression, diminished GA1 lev

179 Gibberellins (GA) and cytokinins act antagonistically in

180 To study the role of abscisic acid (ABA) and gibberellins (GA) in pre-maturity alpha-amylase (PMA) fo

181 Gibberellins (GA) promote while abscisic acid (ABA) inhi

182 GA19, the immediate precursor of the active gibberellin, GA1, by UV-B in this zone, which is regulat

183 growth was partially restored by the active gibberellin GA3 or the functional analog of jasmonoyl-is

184 Recently, we have shown that gibberellins (GAs) also play an important role in ovule

185 Light and gibberellins (GAs) antagonistically regulate hypocotyl e

186 The gibberellins (GAs) are a group of endogenous compounds t

187 Bioactive gibberellins (GAs) are central regulators of plant growt

188 Bioactive gibberellins (GAs) are diterpene phytohormones that modu

189 Gibberellins (GAs) are key modulators of plant growth an

190 Bioactive gibberellins (GAs) are phytohormones that regulate growt

191 Gibberellins (GAs) are plant hormones involved in the re

192 Gibberellins (GAs) are plant hormones that affect plant

193 Gibberellins (GAs) are plant hormones that promote a wid

194 Gibberellins (GAs) are plant hormones that regulate most

195 Previous work has shown that 13-hydroxylated gibberellins (GAs) are predominant in the long-day (LD)

196 actor for the induction of dormancy, whereas gibberellins (GAs) are required for germination.

197 Abscisic acid (ABA) and gibberellins (GAs) control several developmental process

198 trichome formation, a process controlled by gibberellins (GAs) in Arabidopsis rosette leaves.

199 The role of gibberellins (GAs) in regulation of lateral root develop

200 Because gibberellins (GAs) increase internode length by affectin

201 Light and gibberellins (GAs) mediate many essential and partially

202 Gibberellins (GAs) or gibberellic acids are ubiquitous d

203 Gibberellins (GAs) play a critical role in fruit-set and

204 Gibberellins (GAs) play a key role in these adaptive res

205 Gibberellins (GAs) regulate many aspects of plant develo

206 e show that BRs regulate the biosynthesis of gibberellins (GAs), another class of growth-promoting ho

207 by changes in the metabolism of the hormones gibberellins (GAs), which promote the degradation of DEL

208 sis of several hormones, including auxin and gibberellins (GAs), which stimulate fruit set.

209 thaliana) in relation to the availability of gibberellins (GAs).

210 the final step in the synthesis of bioactive gibberellins (GAs).

211 t catalyze formation of the methyl esters of gibberellins (GAs).

212 ant hormones, including cytokinins (CKs) and gibberellins (GAs).

213 r the induction of SAUR63 subfamily genes by gibberellins (GAs).

214 pression of a few genes; brassinosteroid and gibberellin had only modest effects.

215 ng, in addition, indicated a modification of gibberellin homeostasis and a strong disturbance of the

216 hylene and the upregulation of cytokinin and gibberellin hormonal responses were also characteristic

217 by regulating the synthesis of cytokinin and gibberellin hormones--mobile molecules more usually asso

218 investigate the distribution of the hormone gibberellin in the root elongation zone.

219 , TATCCA box, and CAREs box, implicating the gibberellins in regulation of many rhizome-specific gene

220 r, the role of abscisic acid and diterpenes (gibberellins) in germination assumed much greater import

221 ir DNA-binding activities are blocked by the gibberellin-inactivated repressor RGA.

222 lt stress but repressed by the plant hormone gibberellin, indicating a complex regulation of BOI gene

223 idopsis (Arabidopsis thaliana) DELLA protein GIBBERELLIN INSENSITIVE and screened a collection of con

224 f the gibberellin signal transduction [e.g., GIBBERELLIN INSENSITIVE DWARF 1 (GID1) and DELLA], biosy

225 NGR5 is a target of gibberellin receptor GIBBERELLIN INSENSITIVE DWARF1 (GID1)-promoted proteasom

226 s, three functionally redundant GA receptors GIBBERELLIN INSENSITIVE DWARF1 (GID1a, b, and c), and th

227 thesis and catabolism enzymes, GA receptors (GIBBERELLIN INSENSITIVE DWARF1, GID1) and early GA signa

228 pitation indicates that the interaction with GIBBERELLIN INSENSITIVE impairs the activity of RELATED

229 ELLA-dependent transcriptional activation of GIBBERELLIN-INSENSITIVE DWARF1 (GID1) GA receptor genes.

230 GA binding to the GIBBERELLIN-INSENSITIVE DWARF1 (GID1) GA receptors stimu

231 of DELLA proteins mediated by a GA-activated GIBBERELLIN-INSENSITIVE DWARF1 (GID1) receptor.

232 This response requires GIBBERELLIN-INSENSITIVE DWARF1-mediated GA perception an

233 Gibberellin is perceived by its nuclear receptors GA INS

234 changes in hormones including abscisic acid, gibberellin, jasmonic acid, indole-3-acetic acid, etc.

235 ther, we simulate perturbed systems in which gibberellin levels are reduced, considering both genetic

236 s response is absent in mutants with altered gibberellin levels or DELLA activity.

237 ose metabolism and altered abscisic acid and gibberellin levels.

238 o dilute, creating a significant gradient in gibberellin levels.

239 tly, increased LEAFY activity causes reduced gibberellin levels.

240 g signals, including auxin, brassinosteroid, gibberellin, light, and temperature.

241 The two opposing functions of gibberellin may facilitate evolutionary and environmenta

242 as upstream regulators of EXPA2 expression, gibberellin-mediated endosperm expansion, and seed germi

243 (five ERFs); and (3) negative regulation of gibberellin-mediated shoot elongation (four ERFs).

244 synthase activity relevant to the ancestral gibberellin metabolic function.

245 xpression of GA2ox2, HDT1/2 likely fine-tune gibberellin metabolism and they are crucial for regulati

246 Osmotic stress induces changes in gibberellin metabolism, resulting in the stabilization o

247 monofunctional enzymes (TPS-c and TPS-e) of gibberellin metabolism.

248 tially contribute to light regulation of the gibberellin metabolism.

249 icity indicates the ease with which primary (gibberellin) metabolism can be subverted to secondary bi

250 This suggests that bioactive gibberellins might be present in bryophytes, although th

251 e synthesis of ent-kaurene, the precursor of gibberellins, no other tomato TPS genes could be demonst

252 ce of exogenous auxin and sugars, but not by gibberellin or abscisic acid, and is antagonized by cyto

253 P3b is not involved in flowering promoted by gibberellin or vernalization.

254 he production of or sensitivity to ethylene, gibberellin, or cytokinin.

255 ssinolide but cannot be recovered by auxins, gibberellins, or cytokinins.

256 enes interact with the cytokinin, auxin, and gibberellin pathways.

257 ast, we engineered an optogenetic biosensor, GIBBERELLIN PERCEPTION SENSOR 1 (GPS1), that senses nano

258 of the diterpene synthase genes required for gibberellin phytohormone biosynthesis provided an early

259 ene synthases found in all higher plants for gibberellin phytohormone biosynthesis to the production

260 site presence of CPSs in all land plants for gibberellin phytohormone biosynthesis, such plasticity p

261 phate synthases found in all seed plants for gibberellin phytohormone metabolism, by a larger aromati

262 rpenoid as a virulence factor, potentially a gibberellin phytohormone, which is antagonistic to JA, c

263 ich presumably limits flux toward the potent gibberellin phytohormones.

264 to ent-kaurene, the olefin precursor to the gibberellin plant hormones.

265 tural products, which includes the important gibberellin plant hormones.

266 gi produce ent-kaurene as a precursor to the gibberellin plant hormones.

267 In contrast, similar diterpenes of gibberellin primary (i.e. general) metabolism are produc

268 moting cytokinin biosynthesis but repressing gibberellin production to condition a replication compet

269 modulate the jasmonate pathway to facilitate gibberellin-promoted stem growth during flowering.

270 Although gibberellin promotes termination of vegetative developme

271 Abscisic acid (ABA) inhibits, whereas gibberellin promotes, germination and early seedling dev

272 NGR5 is a target of gibberellin receptor GIBBERELLIN INSENSITIVE DWARF1 (GID

273 and cytokinin treatments, while darkness and gibberellin reduce expression.

274 sociated with stress, manganese binding, and gibberellin-regulated transcription factor were common i

275 However, gibberellin regulates expression of GID1, GA20ox, and GA

276 Control of abscisic acid- and gibberellin-related gene expression in seeds requires no

277 In this way, gibberellin relieves DELLA-dependent growth repression.

278 henotype seems to be a partial or incomplete gibberellin response emerging from a strongly altered ho

279 and in vivo data on the expression levels of gibberellin-responsive genes.

280 This allows accumulation of gibberellin-sensitive DELLA proteins.

281 Many of the components of the gibberellin signal transduction [e.g., GIBBERELLIN INSEN

282 c transferase (OGT) SPINDLY (SPY) suppresses gibberellin signaling and promotes cytokinin (CK) respon

283 While SPY has been shown to suppress gibberellin signaling and to promote cytokinin (CK) resp

284 We identified roles for auxin and gibberellin signaling in Suc-induced hypocotyl elongatio

285 By incorporating the gibberellin signaling network, we simulate how gibberell

286 Fourteen of them are up-regulated by the gibberellin signaling pathway during pollen development,

287 but hinted at a link with jasmonic acid and gibberellin signaling pathways.

288 how these feedback loops interact to control gibberellin signaling.

289 te the role of the various feedback loops in gibberellin signaling.

290 ay between symbiosis, nutrient, and hormone (gibberellin) signaling.

291 e we provide genetic evidence that the light/gibberellin-signaling pathway affects the properties of

292 smitted via CCaMK and CYCLOPS) and hormonal (gibberellin) signals.

293 an induction of auxin, brassinosteroid, and gibberellin signatures and the involvement of several ca

294 aurene synthase, a key regulatory enzyme for gibberellin synthesis, the following day.

295 the interplay between carbon metabolism and gibberellins that modulates plant growth.

296 ight, temperature, brassinosteroid (BR), and gibberellin, that inhibit the atypical basic helix-loop-

297 l quantifies how rapid cell expansion causes gibberellin to dilute, creating a significant gradient i

298 that dual opposite roles of the phytohormone gibberellin underpin this phenomenon in Arabidopsis.

299 ated diterpenoid, although the production of gibberellins was not observed.

300 owering and plant architecture, florigen and gibberellin, were the source of multiple revolutions tha