ライフサイエンスコーパス: brassinosteroid

1 factors, such as the phytohormones auxin and brassinosteroid.

2 auxin, strigolactone, gibberellic acid, and brassinosteroids.

3 of responses to the plant hormones auxin and brassinosteroids.

4 5, two defective transmembrane receptors for brassinosteroids.

5 and in alterations in response to auxin and brassinosteroids.

6 ptional pathway and can act independently of brassinosteroids.

7 NSTITUTIVE PHOTOMORPHOGENIC DWARF, DWF4, and BRASSINOSTEROID-6-OXIDASE 2 Phenotypic characterization

8 to three brassinosteroid-biosynthesis genes (BRASSINOSTEROID-6-OXIDASE, CONSTITUTIVE PHOTOMORPHOGENIC

9 esponse, thus illuminating one aspect of the brassinosteroid/abscisic acid antagonism.

10 Analysis of gene expression showed that brassinosteroid action is positively associated with gen

11 Similar to cytokinin, brassinosteroid acts post-transcriptionally by increasin

12 xplore the mechanism by which cytokinins and brassinosteroids affect ethylene biosynthesis.

13 uxin affected the expression of a few genes; brassinosteroid and gibberellin had only modest effects.

14 tly, TT8 affects stress response, along with brassinosteroid and jasmonic acid biosynthesis, by direc

15 mutant displayed reduced responses to GA and brassinosteroid and showed decreased expression of sever

16 The remainder appear to be unlinked to brassinosteroids and related to primary and secondary me

17 alyses also suggested an induction of auxin, brassinosteroid, and gibberellin signatures and the invo

18 growth was found to be independent of auxin, brassinosteroid, and reactive oxygen species signaling p

19 evel or signaling of hormones such as auxin, brassinosteroids, and gibberellins.

20 ontrolled temporally and spatially by auxin, brassinosteroids, and light to result in AM initiation o

21 ion of VUP1 represses the expression of many brassinosteroid- and auxin-responsive genes.

22 We observed that brassinosteroid application mimicked the auxin response,

23 Brassinosteroids are phytohormones involved in plant dev

24 Brassinosteroids are plant steroid hormones that control

25 Brassinosteroids are plant-derived polyhydroxylated deri

26 Nevertheless, brassinosteroids are ubiquitous in land plants, suggesti

27 fied a R2R3-MYB transcription factor, BRAVO (BRASSINOSTEROIDS AT VASCULAR AND ORGANIZING CENTER), act

28 ants, steroid hormone action occurs when the brassinosteroids bind a membrane tyrosine kinase recepto

29 id, carotenoid, oxylipin, glucosinolate, and brassinosteroid biosyntheses and have shown that both P4

30 ng sturdy culm, specific for deficiencies in brassinosteroid biosynthesis and signaling in semidwarf

31 The application of a brassinosteroid biosynthesis inhibitor could not revert

32 CYP90D2 gene, which encodes an enzyme in the brassinosteroid biosynthesis pathway.

33 igned more than 20 historic mutants to three brassinosteroid-biosynthesis genes (BRASSINOSTEROID-6-OX

34 e ubiquitous in land plants, suggesting that brassinosteroid biosynthetic pathways differ between ear

35 studies have demonstrated that cytokinin and brassinosteroid (BR) act as regulatory inputs to elevate

36 to investigate the relationship between the brassinosteroid (BR) and gibberellin (GA) hormones acros

37 A paradigmatic case is the concurrence of brassinosteroid (BR) and gibberellin (GA) signaling in t

38 Brassinosteroid (BR) and glucose (Glc) regulate many com

39 Brassinosteroid (BR) binding activates the receptor kina

40 e show here that noncoding variations of the brassinosteroid (BR) biosynthesis gene DWARF1 (DWF1) lea

41 At the macroscopic level, brassinosteroid (BR) biosynthetic and receptor mutants h

42 The brassinosteroid (BR) class of steroid hormones regulates

43 Brassinosteroid (BR) hormone is shown here to have oppos

44 coding sterol C-22 hydroxylases that control brassinosteroid (BR) hormone levels using a promoter tha

45 Brassinosteroid (BR) hormone signaling controls multiple

46 Brassinosteroid (BR) hormones are primarily perceived at

47 es accumulation of the plant steroid hormone brassinosteroid (BR) in organ boundaries.

48 BES1 functions as a master regulator in the brassinosteroid (BR) pathway that promotes plant growth.

49 onic acid (JA) pathway was induced while the brassinosteroid (BR) pathway was suppressed in infected

50 In Arabidopsis (Arabidopsis thaliana), the brassinosteroid (BR) receptor BR INSENSITIVE1 (BRI1) und

51 nase that functions as a coreceptor with the brassinosteroid (BR) receptor BRI1 and the flagellin rec

52 urally defective yet biochemically competent brassinosteroid (BR) receptor BRI1, resulted in identifi

53 urally imperfect yet biochemically competent brassinosteroid (BR) receptor bri1-9, causing its increa

54 BAK1 is also a coreceptor for the plant brassinosteroid (BR) receptor, the LRR-RK BRI1.

55 In plants, the steroidal hormone brassinosteroid (BR) regulates numerous developmental pr

56 Brassinosteroid (BR) regulates plant development by acti

57 nome-wide screen for mutants showing altered brassinosteroid (BR) sensitivity or bri1-like phenotypes

58 Brassinosteroid (BR) signal transduction research has pr

59 show here that FKBP42/TWD1 is necessary for brassinosteroid (BR) signal transduction.

60 s GSK3-like kinase that negatively regulates brassinosteroid (BR) signaling by phosphorylating BES1 (

61 In this study, we found that brassinosteroid (BR) signaling converges with SUPPRESSOR

62 have been described as positive effectors of brassinosteroid (BR) signaling in plants.

63 Brassinosteroid (BR) signaling is essential for plant gr

64 The brassinosteroid (BR) signaling module is a central regul

65 The brassinosteroid (BR) signaling pathway includes two rece

66 Low R:FR light enhances brassinosteroid (BR) signaling through BRASSINOSTEROID S

67 In this study, we show that brassinosteroid (BR) signaling works downstream of Glc i

68 s in plant immunity, cell-death control, and brassinosteroid (BR) signaling, all four functional SERK

69 NSITIVE2 (BIN2), a key negative regulator of brassinosteroid (BR) signaling, can phosphorylate Arabid

70 e pattern; instead, the detailed analysis of brassinosteroid (BR) signaling, innate immunity, and sym

71 PRs of either the negative regulators of the brassinosteroid (BR) signaling, the glycogen synthase ki

72 in many plant signaling processes, including brassinosteroid (BR) signaling.

73 cated a negative regulatory role for BIN2 in brassinosteroid (BR) signaling.

74 nown mechanism upon receptor kinase-mediated brassinosteroid (BR) signaling.

75 hanced early seedling growth due to elevated brassinosteroid (BR) synthesis and/or signalling.

76 fferentially regulates genes associated with brassinosteroid (BR) synthesis during submergence.

77 we show that the activity of two homologous brassinosteroid (BR) transcriptional effectors, BRASSINA

78 enous signals, including light, temperature, brassinosteroid (BR), and gibberellin (GA), regulate cel

79 monal signals, involving light, temperature, brassinosteroid (BR), and gibberellin, that inhibit the

80 Interestingly, brassinosteroid (BR)-induced gene expression was inhibit

81 nstrating the role of BRAVO in counteracting Brassinosteroid (BR)-mediated cell division in the QC ce

82 pattern (PAMP)-triggered immunity (PTI) and brassinosteroid (BR)-mediated growth was recently report

83 gered immunity (PTI) and the LRR-RLK BRI1 in brassinosteroid (BR)-mediated growth.

84 through TOR controls the accumulation of the brassinosteroid (BR)-signaling transcription factor BZR1

85 controlled by hormones, including auxin and brassinosteroid (BR).

86 responses to two plant hormones, zeatin and brassinosteroid (BR).

87 uxin, gibberellic acid (GA), cytokinin (CK), brassinosteroids (BR) and peptide hormones are also impl

88 Auxin and brassinosteroids (BR) are crucial growth regulators and

89 cient for suppression of immune signaling by brassinosteroids (BR).

90 well as intrinsic signals such as hormones (brassinosteroid [BR], auxin, cytokinin, ethylene) and nu

91 es have indicated that CYP734A1 binds active brassinosteroids, brassinolide and castasterone, as well

92 ponents of the signalling pathways of auxin, brassinosteroids (BRs) and cytokinins.

93 Brassinosteroids (BRs) are a group of polyhydroxylated p

94 Brassinosteroids (BRs) are a unique class of plant stero

95 Phytohormone brassinosteroids (BRs) are essential for plant growth an

96 Brassinosteroids (BRs) are essential growth-promoting ho

97 Brassinosteroids (BRs) are essential phytohormones regul

98 Brassinosteroids (BRs) are growth-promoting plant hormon

99 Brassinosteroids (BRs) are hormones that control many as

100 Brassinosteroids (BRs) are important regulators for plan

101 Brassinosteroids (BRs) are key regulators in plant growt

102 Brassinosteroids (BRs) are plant hormones involved in va

103 Brassinosteroids (BRs) are plant hormones that are perce

104 Brassinosteroids (BRs) are plant hormones that regulate

105 strong evidence that steroid hormones called brassinosteroids (BRs) are required to maintain position

106 Brassinosteroids (BRs) are steroid hormones that are ess

107 Brassinosteroids (BRs) are steroid hormones that coordin

108 Brassinosteroids (BRs) bind to the extracellular domain

109 Abscisic acid (ABA) and brassinosteroids (BRs) exhibit antagonistic interactions

110 ) is the main ligand-perceiving receptor for brassinosteroids (BRs) in Arabidopsis (Arabidopsis thali

111 to investigate a role for the phytohormones brassinosteroids (BRs) in specifying bristle identity an

112 The plant hormones brassinosteroids (BRs) participate in light-mediated reg

113 Notably, application of brassinosteroids (BRs) partly rescued the stomatal leaf

114 Here we show that brassinosteroids (BRs) play a key role in organ boundary

115 Brassinosteroids (BRs) play an essential role in plant g

116 Brassinosteroids (BRs) play crucial roles in plant devel

117 Brassinosteroids (BRs) play key roles in plant growth an

118 Here, we show that a phytohormone, the brassinosteroids (BRs) promotes pollen and seed developm

119 Brassinosteroids (BRs) regulate a wide range of developm

120 For instance, brassinosteroids (BRs) regulate cell elongation, vascula

121 Brassinosteroids (BRs) regulate plant development throug

122 Plant steroid hormones brassinosteroids (BRs) regulate plant growth and develop

123 Brassinosteroids (BRs) regulate plant growth and stress

124 Here we show that brassinosteroids (BRs), a class of natural plant hormone

125 Mutants in brassinosteroids (BRs), a class of plant hormones necess

126 at are coordinated by hormones including the brassinosteroids (BRs), a group of steroids with structu

127 Plant sterols and steroid hormones, the brassinosteroids (BRs), are compounds that exert a wide

128 Plant steroid hormones, brassinosteroids (BRs), are of great importance for plan

129 terplay of light and plant hormones, such as brassinosteroids (BRs), in the regulation of plant growt

130 Plant steroid hormones, brassinosteroids (BRs), play essential roles in modulati

131 Plant steroid hormones, brassinosteroids (BRs), play essential roles in plant gr

132 The plant steroid hormones, brassinosteroids (BRs), play important roles in plant gr

133 Plant steroid hormones, brassinosteroids (BRs), play important roles in plants.

134 Plant steroid hormones, brassinosteroids (BRs), regulate essential growth and de

135 regulators including plant steroid hormones, brassinosteroids (BRs).

136 3 double mutant roots are insensitive toward brassinosteroids but have a phenotype different from bri

137 the largely differing response to zeatin and brassinosteroid by the metabolic pathways in chloroplast

138 rom that of Primula, but both may inactivate brassinosteroids causing short styles.

139 Treatment with auxin or brassinosteroids could enhance binding of either transcr

140 nt defense and growth such as jasmonic acid, brassinosteroids, cytokinins, auxin and synthesis of fla

141 ctivities of downstream MAPKs are reduced in brassinosteroid-deficient mutants but increased by treat

142 , and altered photomorphogenesis, resembling brassinosteroid-deficient mutants.

143 BAK1 is involved in brassinosteroid-dependent growth and development, innate

144 iption and integrate the auxin response to a brassinosteroid-dependent molecular circuit that promote

145 nthesis of structural sterols from signaling brassinosteroid derivatives and are highly regulated.

146 A15 (SAUR15), a well-characterized auxin and brassinosteroid early response gene in Arabidopsis (Arab

147 the mechanism by which another phytohormone, brassinosteroid, elevates ethylene biosynthesis in etiol

148 Overexpression of the HBI1-related bHLHs brassinosteroid enhanced expression2 (BEE2) and cryptoch

149 helix (bHLH) transcription factor homolog of brassinosteroid enhanced expression2 interacting with IB

150 binding of either transcription factor, and brassinosteroid enhancement of MP/ARF5 binding required

151 tive LRR-RK leads to strong gain-of-function brassinosteroid, floral abscission, and stomatal pattern

152 S lines revealed downregulation of auxin and brassinosteroid genes, and upregulation of cytokinin tra

153 growth-regulating signals, including auxin, brassinosteroid, gibberellin, light, and temperature.

154 Brassinosteroids have been implicated in the differentia

155 c activities shows that the enzyme regulates brassinosteroid homeostasis via mono- and diacetylation

156 tential to fine-tune the levels of different brassinosteroid hormones throughout plant growth and dev

157 date the putative cellular targets for plant brassinosteroids in mammals.

158 , abscisic acid (ABA), cytokinins (CKs), and brassinosteroids in molding plant-pathogen interactions.

159 and CYP72C1 in Arabidopsis diverge more than brassinosteroid inactivating P450s in other plants, this

160 YP734A1 and CYP72C1, have been identified as brassinosteroid-inactivating enzymes important for stero

161 rassinosteroid phytohormones and enzymes for brassinosteroid inactivation are present only in spermat

162 PAT inhibition by CMMC occurs in a brassinosteroid-independent manner.

163 ls to the hypocotyl, where it triggers local brassinosteroid-induced cell elongation in seedling stem

164 Our results indicate that brassinosteroid inhibits stomatal development by allevia

165 Recently, two Arabidopsis receptor kinases--BRASSINOSTEROID INSENSITIVE 1 (BRI1) and BRI1-ASSOCIATED

166 One of the best-studied receptors is BRASSINOSTEROID INSENSITIVE 1 (BRI1) in Arabidopsis (Ara

167 The brassinosteroid receptor brassinosteroid insensitive 1 (BRI1) is a member of the

168 ity of the dual-specificity receptor kinase, brassinosteroid insensitive 1 (BRI1), reflects the balan

169 ed in BR perception and signal transduction: brassinosteroid insensitive 1 (BRI1), which is the BR re

170 imp1 mutant is defective in the BR-receptor BRASSINOSTEROID INSENSITIVE 1 (BRI1).

171 using the membrane-integral receptor kinase BRASSINOSTEROID INSENSITIVE 1 (BRI1).

172 sphorylation of the Arabidopsis RD RLK BRI1 (brassinosteroid insensitive 1).

173 brane-resident RLKs, flagellin-sensing 2 and brassinosteroid insensitive 1-associated kinase 1 (BAK1)

174 phosphorylation on the plant protein kinase brassinosteroid insensitive 1-associated kinase 1 (BAK1)

175 atic embryogenesis receptor kinase 3 (SERK3)/brassinosteroid insensitive 1-associated kinase 1 (BAK1)

176 lagellin receptor FLAGELLIN SENSING 2 (FLS2)-BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED KINASE 1 (BAK1)

177 LLIN-SENSING 2 (FLS2) with their co-receptor BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED KINASE 1 (BAK1)

178 ll death was shown to require N. benthamiana Brassinosteroid insensitive 1-Associated Kinase 1 (NbBAK

179 However, in Brassinosteroid insensitive 1-Associated Kinase 1 (SERK3

180 Arabidopsis thaliana BRASSINOSTEROID INSENSITIVE 1-associated receptor kinase

181 ense responses required the known coreceptor BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED RECEPTOR KINASE

182 elopment, and immunity, Arabidopsis thaliana BRASSINOSTEROID INSENSITIVE 1-associated receptor kinase

183 ctivation of the Arabidopsis thaliana kinase BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED RECEPTOR-LIKE K

184 ired variant of the brassinosteroid receptor BRASSINOSTEROID INSENSITIVE 1.

185 They include a BRASSINOSTEROID INSENSITIVE 2 (BIN2) interaction domain,

186 Brassinosteroids Insensitive 1 (BRI1) is required for BR

187 tion and ERAD of a brassinosteroid receptor, BRASSINOSTEROID-INSENSITIVE 1 (BR1).

188 Arabidopsis thaliana receptor-like kinases, brassinosteroid-insensitive 1 (BRI1) and BRI1-associated

189 gh plasma membrane-localized receptor kinase brassinosteroid-insensitive 1 (BRI1), BRI1-associated re

190 Brassinosteroid-INsensitive 2 (BIN2) is an Arabidopsis G

191 Y5 enhances the activity of GSK3-like kinase BRASSINOSTEROID-INSENSITIVE 2 (BIN2), a key repressor of

192 lycogen synthase kinase 3 (GSK3)-like kinase brassinosteroid-insensitive 2 (BIN2), which has been wel

193 LYCOGEN SYNTHASE KINASE 3)-like kinase BIN2 (BRASSINOSTEROID-INSENSITIVE 2), a well established negat

194 The cell surface receptor kinase BRASSINOSTEROID-INSENSITIVE-1 (BRI1) is the major recept

195 ifferent ligand-perceiving receptors such as BRASSINOSTEROID INSENSITIVE1 (BRI1) and FLAGELLIN-SENSIT

196 BRASSINOSTEROID INSENSITIVE1 (BRI1) is a BR receptor, an

197 Brassinosteroid insensitive1 (BRI1) is epistatic to HXK1

198 The BRASSINOSTEROID INSENSITIVE1 (BRI1) receptor kinase has

199 bidopsis thaliana), BRs are perceived by the BRASSINOSTEROID INSENSITIVE1 (BRI1) receptor.

200 plasma membrane through the receptor kinase BRASSINOSTEROID INSENSITIVE1 (BRI1) together with co-rec

201 of the leucine-rich repeat receptor kinase, brassinosteroid insensitive1 (BRI1), was shown to depend

202 tor in Arabidopsis (Arabidopsis thaliana) is BRASSINOSTEROID INSENSITIVE1 (BRI1).

203 the leucine-rich repeat receptor-like kinase brassinosteroid insensitive1 (BRI1).

204 surface by a membrane-bound receptor kinase, BRASSINOSTEROID INSENSITIVE1 (BRI1).

205 kinase domains of the SERK-dependent LRR-RKs BRASSINOSTEROID INSENSITIVE1, HAESA and ERECTA form tigh

206 avily glycosylated brassinosteroid receptor, BRASSINOSTEROID INSENSITIVE1, while MNS1 to MNS3 appear

207 IOS1 also associated with BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1 (BAK1) i

208 LecRK-VI.2 constitutively associates with BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1 (BAK1) i

209 exes between the membrane-localized IOS1 and BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1 (BAK1)-d

210 the leucine-rich repeat receptor-like kinase BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1 (BAK1)/S

211 flagellin sensing2 and its signaling partner brassinosteroid insensitive1-associated kinase1 is obser

212 production that was partially independent of BRASSINOSTEROID INSENSITIVE1-ASSOCIATED KINASE1.

213 seedling lethal and cell death phenotypes of BRASSINOSTEROID INSENSITIVE1-associated receptor kinase1

214 The membrane-bound Brassinosteroid insensitive1-associated receptor kinase1

215 d PM accumulation of FLS2 and its coreceptor BRASSINOSTEROID INSENSITIVE1-ASSOCIATED RECEPTOR KINASE1

216 dent on the regulatory receptor-like kinases brassinosteroid insensitive1-associated receptor kinase1

217 Fls3, independently of flg22/flgII-28 or of BRASSINOSTEROID INSENSITIVE1-ASSOCIATED RECEPTOR KINASE1

218 th these findings, the transcription factors BRASSINOSTEROID INSENSITIVE1-EMS SUPPESSOR1 and MONOPTER

219 A BRASSINOSTEROID INSENSITIVE1-ETHYL METHANESULFONATE-SUPP

220 ffectors, BRASSINAZOLE RESISTANT1 (BZR1) and BRASSINOSTEROID INSENSITIVE1-ETHYL METHANESULFONATE-SUPP

221 The leucine-rich repeat receptor-like kinase BRASSINOSTEROID-INSENSITIVE1 (BRI1) is the main ligand-p

222 UTO) and one brassinosteroid-signaling gene (BRASSINOSTEROID-INSENSITIVE1 [HvBRI1]).

223 al transduction cascade, as is the case with BRASSINOSTEROID-INSENSITIVE1 Associated Kinase1 and CPK5

224 The PEPR coreceptor BRASSINOSTEROID-INSENSITIVE1 Associated Kinase1 contribu

225 ologs in Arabidopsis (Arabidopsis thaliana), brassinosteroid-insensitive1 suppressor (BSU1).

226 ffect mutant variants of the receptor kinase BRASSINOSTEROID-INSENSITIVE1.

227 Here, we demonstrate that the protein kinase BRASSINOSTEROID INSENSITIVE2 (BIN2), a key negative regu

228 interact with and are phosphorylated by the BRASSINOSTEROID insensitive2 (BIN2).

229 of which carry gain-of-function mutations in BRASSINOSTEROID-INSENSITIVE2 (BIN2), one of the three me

230 In addition, auxin, cytokinin, ethylene, brassinosteroids, jasmonates, and salicylic acid also co

231 pression data, the SUB1A genotype had higher brassinosteroid levels after submergence compared to the

232 harmacologically and genetically manipulated brassinosteroid levels in poplar trees and assayed the e

233 Elevated brassinosteroid levels resulted in increases in secondar

234 tants but increased by treatment with either brassinosteroid or GSK3-kinase inhibitor.

235 These data indicate that the brassinosteroid pathway promotes high vein density in th

236 xin transcriptional response on a functional brassinosteroid pathway.

237 vity of the locally acting, growth-promoting brassinosteroid pathway.

238 haracterized roles in stamen development and brassinosteroid perception, SERK1 plays a unique role in

239 1) is tyrosine phosphorylated in response to brassinosteroid perception.

240 coding the complete biosynthetic pathway for brassinosteroid phytohormones and enzymes for brassinost

241 iterpenoids, which include membrane sterols, brassinosteroid phytohormones, and non-steroidal triterp

242 Brassinosteroids play a crucial role in plant vegetative

243 The results presented here show that brassinosteroids play a foundational role in the regulat

244 Brassinosteroids play important roles in regulating root

245 ns, gibberellins, cytokinins, abscisic acid, brassinosteroids, polyamines, strigolactones, and ascorb

246 erols but without significant alterations to brassinosteroid profiles.

247 The brassinosteroid receptor brassinosteroid insensitive 1 (

248 ns of a structurally impaired variant of the brassinosteroid receptor BRASSINOSTEROID INSENSITIVE 1.

249 he auxin translocators PIN2 and AUX1 and the brassinosteroid receptor BRI1 into distinct endomembrane

250 d cell-death control by interacting with the brassinosteroid receptor BRI1, immune receptors, such as

251 ession of phenotypes caused by the defective brassinosteroid receptor bri1-9 strongly suggest that th

252 tation also hampered vacuolar sorting of the brassinosteroid receptor BRI1.

253 t plants, which harbour mutated forms of the brassinosteroid receptor BRI1.

254 160, which turned out to be identical to the brassinosteroid receptor BRI1.

255 is mutant caused by retention of a defective brassinosteroid receptor in the ER.

256 sfolded variants of the heavily glycosylated brassinosteroid receptor, BRASSINOSTEROID INSENSITIVE1,

257 ich are caused by ER retention and ERAD of a brassinosteroid receptor, BRASSINOSTEROID-INSENSITIVE 1

258 Here, we report that a mutated brassinosteroid receptor, bri1-5, that carries a Cys69Ty

259 rmation with a second receptor kinase termed brassinosteroid receptor1 associated kinase1 (BAK1).

260 Brassinosteroid receptors and auxin transporters, both o

261 o bacterial pathogens, but have no effect on brassinosteroid-regulated growth.

262 Genetic analysis demonstrated that brassinosteroid-regulated root epidermal cell patterning

263 Here we demonstrate in Arabidopsis that brassinosteroid regulates stomatal development by activa

264 tudy provides insights into the mechanism of brassinosteroid regulation of root hair patterning.

265 In silico mapping of brassinosteroid-related genes in the barley genome in co

266 barley plant architecture and sturdiness by brassinosteroid-related genes.

267 tematically examined root hair phenotypes in brassinosteroid-related mutants, and found that brassino

268 The expression of the brassinosteroid-related transcription factor BZR1/BES1 a

269 teroid signaling components to attenuate the brassinosteroid response, thus illuminating one aspect o

270 nation is an important control mechanism for brassinosteroid responses in plants.

271 Evidence points to the interplay of auxin, brassinosteroids, SHORTROOT/SCARECROW and INDETERMINATE

272 ant, whereas the contents of gibberellin and brassinosteroid showed no difference between the mutant

273 ein in rice directly interacts with critical brassinosteroid signaling components to attenuate the br

274 ssinosteroid-related mutants, and found that brassinosteroid signaling inhibits root hair formation t

275 iverged, Brassicaceae-specific member of the BRASSINOSTEROID SIGNALING KINASE (BSK) family.

276 phosphorylation of the downstream substrate brassinosteroid signaling kinase 1 (BSK1).

277 ances brassinosteroid (BR) signaling through BRASSINOSTEROID SIGNALING KINASE 5 (BSK5) and leads to t

278 Sterols are also the precursors to the brassinosteroid signaling molecules.

279 A brassinosteroid signaling pathway was predicted to be in

280 m of BES1, a transcriptional effector of the brassinosteroid signaling pathway.

281 crotubule organization and by modulating the brassinosteroid signaling pathway.

282 are key regulators in light, jasmonate, and brassinosteroid signaling pathways, respectively.

283 s associated with cell wall modification and brassinosteroid signaling were induced under enriched FR

284 and biomass accumulation and is regulated by brassinosteroid signaling, auxin transport, and gibberel

285 We found that with enhanced brassinosteroid signaling, GL2, a cell fate marker for n

286 olved in auxin, abscisic acid, ethylene, and brassinosteroid signaling, peroxisome function, disease

287 OID-INSENSITIVE 2 (BIN2), a key repressor of brassinosteroid signaling, to repress hypocotyl elongati

288 About half of these are related to brassinosteroid signaling.

289 , impaired BRI1 endocytosis and enhanced the brassinosteroid signaling.

290 HOTOMORPHOGENIC DWARF, and DIMINUTO) and one brassinosteroid-signaling gene (BRASSINOSTEROID-INSENSIT

291 e role of Arabidopsis (Arabidopsis thaliana) BRASSINOSTEROID-SIGNALING KINASE5 (BSK5), a member of th

292 regulated transcription factor PIF4, and the brassinosteroid-signaling transcription factor BZR1, int

293 lyses indicate that receptor kinase-mediated brassinosteroid signalling inhibits stomatal development

294 Application of auxin to the brassinosteroid synthesis mutant, diminuto1, induced tra

295 tension wood formation, while inhibition of brassinosteroid synthesis resulted in decreased growth a

296 members of the CYP734A subfamily inactivate brassinosteroids through C-26 hydroxylation, the biochem

297 ant MAPKKK to its upstream regulators and of brassinosteroid to a specific developmental output.

298 ide the nucleus occurs from plants that make brassinosteroids to higher metazoans (primates).

299 Reporter response to brassinosteroid treatment relied on the same two element

300 ASE1 (BAK1), the receptor and coreceptor for brassinosteroids--were shown to autophosphorylate on tyr