ライフサイエンスコーパス: abscisic acid

1 compounds as isorhamnetin-3-O-rutinoside and abscisic acid.

2 ehyde, which is oxidized to the phytohormone abscisic acid.

3 pathway and signalling by the plant hormone abscisic acid.

4 pression decreased after exposure to NaCl or abscisic acid.

5 and cellular stress responses downstream of abscisic acid.

6 is rapidly downregulated by the phytohormone abscisic acid.

7 correlated with increased responsiveness to abscisic acid.

8 mechanism involving the plant stress hormone abscisic acid.

9 We identified a further QTL, Reduced ABscisic Acid 1 (RABA1) that influenced ABA content and

10 smonic acid (200muM), menadione (120muM) and abscisic acid (3.026mM) treatments were applied to detac

11 One of the candidate genes, Abscisic acid 8'-hydroxylase, is verified to play a nega

12 regulate stomatal closure upon perception of abscisic acid-a plant hormone associated with abiotic st

13 n 20 transcription factor (DMG400000248) for abscisic acid; a SAUR gene (DMG400016561) induced in epi

14 In grape (Vitis vinifera), abscisic acid (ABA) accumulates during fruit ripening an

15 plication and coincide with pathogen-induced abscisic acid (ABA) accumulation.

16 ta6-5 mutants were more tolerant to NaCl and abscisic acid (ABA) and accumulated less Na(+) In contra

17 Abscisic acid (ABA) and brassinosteroids (BRs) exhibit a

18 ss response pathway initiated by the hormone abscisic acid (ABA) and executed by SnRK2 (Snf1-RELATED-

19 ance of the antagonistically acting hormones abscisic acid (ABA) and gibberellin (GA).

20 trations of the drought-induced phytohormone abscisic acid (ABA) and isoprene; and whether isoprene a

21 e fall might induce the accumulation of leaf abscisic acid (ABA) and jasmonic acid (JA) concentration

22 ted in seedlings after long-term exposure to abscisic acid (ABA) and polyethylene glycol, while treat

23 Furthermore, the endogenous levels of abscisic acid (ABA) and proline were also reduced in str

24 Here, we show that the phytohormone abscisic acid (ABA) and SA antagonistically influence ce

25 The effects of the application of abscisic acid (ABA) and sucrose on the postharvest ripen

26 en the inhibitory action of the phytohormone abscisic acid (ABA) and the promoting role of light in g

27 The plant hormone abscisic acid (ABA) and the protein DELAY OF GERMINATION

28 The plant hormone abscisic acid (ABA) and the second messenger Ca(2+) are

29 driven by the rapid up-regulation of foliar abscisic acid (ABA) biosynthesis and ABA levels in angio

30 lavonoid, terpenoid, jasmonic acid (JA), and abscisic acid (ABA) biosynthesis as well as enhanced exp

31 encoding NCED3 and NCED5, two key enzymes in abscisic acid (ABA) biosynthesis.

32 SlZF2 may be involved in abscisic acid (ABA) biosynthesis/signaling, because SlZF

33 The rate-limiting abscisic acid (ABA) biosynthetic genes NINE-CIS-EPOXYCAR

34 rage for water, a process known to depend on abscisic acid (ABA) but whose molecular and cellular bas

35 ated to stress, such as heat shock proteins, abscisic acid (ABA) catabolism and its signalling pathwa

36 ) ), net assimilation (A), vein embolism and abscisic acid (ABA) concentration during dehydration wer

37 ynamics, pericarp-imposed dormancy, diaspore abscisic acid (ABA) concentration, and phenotypic plasti

38 ential, organ-level water potential and leaf abscisic acid (ABA) concentration.

39 and decreased indole-3-acetic acid (IAA) and abscisic acid (ABA) concentrations in the roots of conve

40 -3-acetic acid (IAA) increased and levels of abscisic acid (ABA) decreased from dormant to active sta

41 plants also showed strong hyposensitivity to abscisic acid (ABA) during seed germination but not in o

42 uggests that SVP2 mimics the well-documented abscisic acid (ABA) effect on the plant dehydration resp

43 In intact guard cells, abscisic acid (ABA) enhances (primes) the Ca(2+)-sensiti

44 roles in response to dehydration stress and abscisic acid (ABA) in Arabidopsis thaliana.

45 but also uncovered a novel negative role of abscisic acid (ABA) in resistance towards B. cinerea 210

46 Accumulation of the stress hormone abscisic acid (ABA) in response to drought and low water

47 % Pro, RePRP is induced by water deficit and abscisic acid (ABA) in the root elongation zone.

48 mybs1 also showed an enhanced response to abscisic acid (ABA) in the seed germination and seedling

49 The role of abscisic acid (ABA) in VPD-induced stomatal closure has

50 nates (JAs), but not salicylic acid (SA) and abscisic acid (ABA) increased in the inoculated tissues.

51 Abscisic acid (ABA) increases reactive oxygen species (R

52 Accumulation of the stress hormone abscisic acid (ABA) induces many cellular mechanisms ass

53 The phytohormone abscisic acid (ABA) influences the expression of thousan

54 Abscisic acid (ABA) inhibits, whereas gibberellin promot

55 The stress hormone abscisic acid (ABA) initiates a signaling cascade, which

56 Abscisic acid (ABA) is a drought stress signaling molecu

57 Abscisic acid (ABA) is a key phytohormone promoting abio

58 Abscisic acid (ABA) is a key phytohormone that mediates

59 Abscisic acid (ABA) is a phytohormone involved in pivota

60 Abscisic acid (ABA) is a plant growth regulator with rol

61 Abscisic acid (ABA) is a plant hormone involved in the r

62 Abscisic acid (ABA) is a plant hormone that mediates abi

63 Abscisic acid (ABA) is an important hormone for seed dev

64 The stress hormone abscisic acid (ABA) is critical for drought resistance;

65 The phytohormone abscisic acid (ABA) is critical to plant development and

66 The phytohormone abscisic acid (ABA) is important for growth, development

67 The phytohormone abscisic acid (ABA) is induced in response to abiotic st

68 Signaling by the stress phytohormone abscisic acid (ABA) is involved in acquired thermotolera

69 While the abiotic stress-related hormone abscisic acid (ABA) is known to up-regulate wax accumula

70 Abscisic acid (ABA) is the key signal in stress-induced

71 Soil flooding reduces root abscisic acid (ABA) levels in citrus, conversely to what

72 Abscisic acid (ABA) levels increase significantly in pla

73 BA INSENSITIVE GROWTH 1 (ABIG1) required for abscisic acid (ABA) mediated growth inhibition, but not

74 The sesquiterpenoid abscisic acid (ABA) mediates an assortment of responses

75 -guided design to develop opabactin (OP), an abscisic acid (ABA) mimic with up to an approximately se

76 previously undiscovered inhibitory effect of abscisic acid (ABA) on spore germination.

77 its wild-type (WT) behaviour when exposed to abscisic acid (ABA) or CaCl2 .

78 tress-induced TE-lincRNAs either after salt, abscisic acid (ABA) or cold treatments.

79 The plant hormone abscisic acid (ABA) plays a central role in the regulati

80 Abscisic acid (ABA) plays a fundamental role in plant re

81 The phytohormone abscisic acid (ABA) plays a major role in the adaptation

82 The phytohormone abscisic acid (ABA) plays a role in stresses that alter

83 The plant hormone abscisic acid (ABA) plays an important role in the plant

84 tors and PP2C co-receptors, the phytohormone abscisic acid (ABA) prevents premature germination and s

85 The phytohormone abscisic acid (ABA) promotes stomatal closure and inhibi

86 The plant hormone abscisic acid (ABA) promotes stomatal closure via multif

87 Phytohormone abscisic acid (ABA) protects seeds during water stress b

88 ing fluorine atoms in the benzyl ring of the abscisic acid (ABA) receptor agonist AM1 optimizes its b

89 tion of MSI1 or HDA19 causes upregulation of abscisic acid (ABA) receptor genes and hypersensitivity

90 Abscisic acid (ABA) receptors belong to the START domain

91 ne-associated soluble proteins, as shown for abscisic acid (ABA) receptors of the PYRABACTIN RESISTAN

92 0 protein 1), which positively regulates the abscisic acid (ABA) response in Arabidopsis.

93 The majority of the genes involved in abscisic acid (ABA) response pathway, containing the Abs

94 ABI3 also contributes to the abscisic acid (ABA) response.

95 anced without a growth penalty by modulating abscisic acid (ABA) responses either by using overexpres

96 n and other in vivo interactions with NO and abscisic acid (ABA) responses.

97 lly associated with significant increases in abscisic acid (ABA) root concentration and root hydrauli

98 n response to water deficiency by increasing abscisic acid (ABA) sensitivity.

99 lice forms that were coincident with altered abscisic acid (ABA) sensitivity.

100 Plasma membrane-associated abscisic acid (ABA) signal transduction is an integral p

101 linity, trigger a complex osmotic-stress and abscisic acid (ABA) signal transduction network.

102 Membrane-delimited abscisic acid (ABA) signal transduction plays a critical

103 h initial plant immune signaling antagonizes abscisic acid (ABA) signal transduction require further

104 nstrated CDK8 as a critical regulator in the abscisic acid (ABA) signaling and drought response pathw

105 This block is dependent upon abscisic acid (ABA) signaling and the canonical ABA sign

106 The turnover of abscisic acid (ABA) signaling core components modulates

107 with and regulates the expression of 30% of abscisic acid (ABA) signaling genes at the postsplicing

108 rsensitive DCAF1), that negatively regulates abscisic acid (ABA) signaling in Arabidopsis thaliana.

109 are central components in osmotic stress and abscisic acid (ABA) signaling pathways; however, the ups

110 Abscisic acid (ABA) signaling plays a major role in root

111 NO control of germination and crosstalk with abscisic acid (ABA) signaling through ERF-regulated expr

112 We show that ABI1, a negative regulator in abscisic acid (ABA) signaling, dephosphorylates and dest

113 or plant abiotic stress responses, including abscisic acid (ABA) signaling.

114 , JA, ethylene (ET), salicylic acid (SA) and abscisic acid (ABA) signaling.

115 known SLAC1 activation mechanisms depend on abscisic acid (ABA) signaling.

116 ly of protein phosphatases known to regulate abscisic acid (ABA) signaling.

117 ies, SeedGerm implicates a gene important in abscisic acid (ABA) signalling in seeds.

118 The link between AtNBR1 overexpression and abscisic acid (ABA) signalling was suggested by an inter

119 usly reported to play roles in cytokinin and abscisic acid (ABA) signalling.

120 dFUS3 directly activated the promoter of the abscisic acid (ABA) synthesis key gene PdNCED3, resultin

121 lerance depends on the action of the hormone abscisic acid (ABA) that acts through a receptor-signal

122 increased in response to drought stress and abscisic acid (ABA) treatment.

123 Abscisic acid (ABA) was previously shown to mediate Arab

124 drating stresses trigger the accumulation of abscisic acid (ABA), a key plant stress-signaling hormon

125 Abscisic acid (ABA), a plant hormone synthesized from ca

126 We show that abscisic acid (ABA), an antagonist of GA, is also transp

127 ion suggested that the established ethylene, abscisic acid (ABA), and GA growth regulatory module for

128 CO4) as well as other plant hormones such as abscisic acid (ABA), auxin (IAA), and gibberellic acid (

129 lus for stomatal closure as the phytohormone abscisic acid (ABA), but underlying mechanisms remain el

130 ametric in vivo analyses of the phytohormone abscisic acid (ABA), Ca(2+), protons (H(+)), chloride (a

131 We examine the effect of osmotic stress on abscisic acid (ABA), cytokinin and ethylene responses an

132 as exchange, leaf water potential and foliar abscisic acid (ABA), during drought and through the subs

133 omata close in response to the plant hormone abscisic acid (ABA), elevated CO2 concentration, and red

134 rk of hormonal signaling cascades, including abscisic acid (ABA), ethylene, jasmonic acid (JA) and sa

135 bolism, particularly the role of the hormone abscisic acid (ABA), in functionally regulating stomatal

136 show that a catabolite of the plant hormone abscisic acid (ABA), namely phaseic acid (PA), likely em

137 ignaling, accumulation of the stress hormone abscisic acid (ABA), reprogramming of gene expression, a

138 ated levels of the dormancy-inducing hormone abscisic acid (ABA), three auxin catabolites, and cytoki

139 ngal infection and is induced by the hormone abscisic acid (ABA), which has a negative impact on resi

140 r deficit, plants produce elevated levels of abscisic acid (ABA), which improves water consumption an

141 fern sex differentiation is the phytohormone abscisic acid (ABA), which regulates the sex ratio of ma

142 ning soil-water potential, plants synthesize abscisic acid (ABA), which then triggers stomatal closur

143 al closing responses to [CO2 ] elevation and abscisic acid (ABA), while thin-shaped stomata were cont

144 ntify the Arabidopsis (Arabidopsis thaliana) abscisic acid (ABA)- and hydrogen peroxide-activated TF

145 idopsis thaliana) SnRK2 family comprises the abscisic acid (ABA)-activated protein kinases SnRK2.2, S

146 e origins and genetic diversification of the abscisic acid (ABA)-dependent seed maturation programs b

147 cription factor regulating the plant hormone abscisic acid (ABA)-independent drought response.

148 iated nitric oxide (NO) in guard cells in an abscisic acid (ABA)-independent manner.

149 ICE1) mediates the cold stress signal via an abscisic acid (ABA)-independent pathway.

150 GL4 was identified as one of the outstanding abscisic acid (ABA)-induced genes in our RNA sequencing

151 The core signaling pathway for abscisic acid (ABA)-induced stomatal closure involves pe

152 Origins of abscisic acid (ABA)-mediated metabolic control of stomat

153 otic stimuli through jasmonic acid (JA)- and abscisic acid (ABA)-mediated pathways.

154 the expression and function of AtU2AF65b in abscisic acid (ABA)-regulated flowering as well as the t

155 d in response to drought by the phytohormone abscisic acid (ABA).

156 cell wall defenses that are under control by abscisic acid (ABA).

157 ld-type under NaCl stress and in response to abscisic acid (ABA).

158 th inhibition, mediated by the plant hormone abscisic acid (ABA).

159 sponse to drought and the associated hormone abscisic acid (ABA).

160 ensitivity of stomata to the drought-hormone abscisic acid (ABA).

161 required for stomatal closure in response to abscisic acid (ABA).

162 ully elucidated but involve the phytohormone abscisic acid (ABA).

163 plant response to the drought stress hormone abscisic acid (ABA).

164 g-term treatments of polyethylene glycol and abscisic acid (ABA).

165 aves, hydraulic waves, electric signals, and abscisic acid (ABA).

166 regulating the levels of the stress hormone abscisic acid (ABA).

167 tomatal closure, specifically in response to abscisic acid (ABA).

168 ion that is coincident with the depletion of abscisic acid (ABA).

169 ic stresses, and enhanced the sensitivity to abscisic acid (ABA).

170 o biochemical regulation by the phytohormone abscisic acid (ABA).

171 achidonic acid (AA), jasmonic acid (JA), and abscisic acid (ABA).

172 Pro), and accumulation of the stress hormone abscisic acid (ABA).

173 l movements in response to CO(2) , light and abscisic acid (ABA).

174 during early seedling growth in response to abscisic acid (ABA).

175 abiotic stresses, plants produce the hormone abscisic acid (ABA).

176 ID DIOXIGENASE 3 (NCED3) expression, lead to abscisic acid accumulation, and trigger hormone response

177 related genes coincide with pathogen-induced abscisic acid accumulation.

178 Abscisic acid also promoted poplar defense against rust

179 step in the biosynthesis of the phytohormone abscisic acid and a component of a major abiotic stress-

180 Conversely, basal levels of abscisic acid and aphid feeding-induced cytokinins were

181 Moreover, the role of abscisic acid and diterpenes (gibberellins) in germinati

182 osition and degradation by the phytohormones abscisic acid and ethylene.

183 nt stresses, mediated by the stress hormones abscisic acid and ethylene.

184 ession analyses of genes associated with the abscisic acid and gibberellin biosynthetic pathways and

185 H1 variants that are induced by drought and abscisic acid and have been implicated in mediating adap

186 rved that PME34 transcription was induced by abscisic acid and highly expressed in guard cells.

187 selected plant hormones (auxins, cytokinins, abscisic acid and jasmonates), and in the nutrient compo

188 gulating phytohormones such as gibberellins, abscisic acid and jasmonic acid, but surprisingly, not a

189 -type responses to the inhibitory effects of abscisic acid and paclobutrazol (an inhibitor of gibbere

190 ion, sodium chloride, low temperature, heat, abscisic acid and salicylic acid treatments.

191 an early flowering phenotype, resistance to abscisic acid and tolerance to osmotic stress.

192 nthesis to counter the inhibitory effects of abscisic acid and, therefore, promote germination at hig

193 alicylates, auxins, trans-jasmonic acid, and abscisic acid) and the transcript levels of their biosyn

194 Genes related to responses to salt, osmotic, abscisic acid, and drought treatments were specifically

195 ic acid (JA), jasmonoyl-Ile, salicylic acid, abscisic acid, and indole-3-acetic acid were compromised

196 d gibberellic acid, but not brassinolide and abscisic acid, and that SGT1b and its homologue SGT1a ar

197 ys evoked by the drought and stress hormone, abscisic acid, and the circadian clock.

198 F1B was transient, induced by drought, cold, abscisic acid, and wounding treatments.

199 luminating one aspect of the brassinosteroid/abscisic acid antagonism.

200 The relative content of ethylene, abscisic acid, anthocyanins, total carotenoids and total

201 Abscisic acid, auxin, gibberellic acid, methyl jasmonic

202 constitutively elevated transcript levels of abscisic acid biosynthetic genes and bark/vegetative sto

203 xogenous application of the defence hormones abscisic acid, brassinolides (applied as epibrassinolide

204 rs include auxins, gibberellins, cytokinins, abscisic acid, brassinosteroids, polyamines, strigolacto

205 ifying K(+) -channel) were hypersensitive to abscisic acid, but insensitive to drought, suggesting a

206 its, including water use efficiency, growth, abscisic acid concentration (ABA), and proline concentra

207 ort system, or if metabolism, primarily high abscisic acid concentration, might delay recovery.

208 is correlated with a decrease in guard cell abscisic acid content and an increase in jasmonic acid c

209 n the late stages with an increase in foliar abscisic acid content.

210 red in leaves, both indole-3-acetic acid and abscisic acid contents were decreased in the mutant, whe

211 Endogenous abscisic acid contents were reduced in both mutants, and

212 etic approaches, we further demonstrate that abscisic acid controls the activity of BAM1 and AMY3 in

213 fferent temperatures, and in the presence of abscisic acid, copper, kinetin, nitrate, and sucrose.

214 positions in the zeaxanthin epoxidase gene (ABSCISIC ACID DEFICIENT 1/ZEAXANTHIN EPOXIDASE, or ABA1/

215 as reflected by the gradual up-regulation of abscisic acid-dependent and C-REPEAT-BINDING FACTOR path

216 nRK2s) are key signaling elements regulating abscisic acid-dependent plant development and responses

217 Abscisic acid enhances the COP1-mediated degradation of

218 t, together with jasmonates, salicylate, and abscisic acid, ethylene is important in steering stress

219 l enrichment for proteins involved in auxin, abscisic acid, ethylene, and brassinosteroid signaling,

220 companied with changes in hormones including abscisic acid, gibberellin, jasmonic acid, indole-3-acet

221 c stresses, particularly dehydration through abscisic acid; however, their role through accumulation

222 ive expression of hypoxia response genes and abscisic acid hypersensitivity.

223 d in response to the essential plant hormone abscisic acid in a mechanism that is primarily independe

224 an altered expression of genes responsive to abscisic acid in roots.

225 ity to repress responses to the phytohormone abscisic acid in the root.

226 signaling, and highlight the special role of abscisic acid in this process.

227 BII was repressed by auxins and activated by abscisic acid, in parallel to the ripening process.

228 s of salicylic acid (SA), jasmonic acid, and abscisic acid increased in rust-infected leaves and acti

229 lanta, both forms are negative regulators of abscisic acid-induced SnRK2 activity and regulate plant

230 uring fusicoccin-induced stomatal opening or abscisic acid-induced stomatal closure, indicating that

231 erences in light-induced stomatal opening or abscisic acid-induced stomatal closure; however, they di

232 pmental Cell, Gui et al. (2016) show that an abscisic acid-inducible remorin protein in rice directly

233 genes through transcription factors such as ABSCISIC ACID INSENSITIVE (ABI3).

234 o its homoeolog GmABI3a, which maintains the ABSCISIC ACID INSENSITIVE 3 (ABI3)-like function in modu

235 e active stage, whereas those related to the abscisic acid insensitive 3(ABI3), the cytoskeleton and

236 turation genes LEAFY COTYLEDON 1/2 (LEC1/2), ABSCISIC ACID INSENSITIVE 3, FUSCA 3 and WRINKLED 1 is u

237 r (Populus x canescens) lines: wild type and abscisic acid-insensitive (abi1) with functionally impai

238 Abscisic acid-insensitive 5 (ABI5) is an essential and c

239 splicing and reduced transcript abundance of ABSCISIC ACID-INSENSITIVE 5 (ABI5), which encodes an act

240 An abscisic-acid-insensitive mutant, abi1, showed altered s

241 ing, and mRNA splicing, including targets of ABSCISIC ACID INSENSITIVE3 (ABI3) and PHYTOCHROME INTERA

242 Arabidopsis thaliana ABSCISIC ACID INSENSITIVE3 (ABI3) is a transcription fac

243 mutants using the developmentally regulated ABSCISIC ACID INSENSITIVE3 (ABI3) promoter.

244 a B3 domain, namely LEAFY COTYLEDON2 (LEC2), ABSCISIC ACID INSENSITIVE3 (ABI3), and FUSCA3 (ABI3/FUS3

245 nt soybean embryo regulatory factors such as ABSCISIC ACID INSENSITIVE3 and FUSCA3 and provide a work

246 SCARECROW and the sugar signaling component ABSCISIC ACID INSENSITIVE4, despite the requirement for

247 we identified the bZIP transcription factor ABSCISIC ACID INSENSITIVE5 (ABI5).

248 ignaling through ERF-regulated expression of ABSCISIC ACID INSENSITIVE5 (ABI5).

249 EEP ON GOING (KEG), a known repressor of the ABSCISIC ACID INSENSITIVE5 transcription factor in absci

250 Abscisic acid is a key phytohormone produced in response

251 Abscisic acid is a phytohormone found in fruits and vege

252 Abscisic acid is a phytohormone regulating plant growth,

253 abscisic acid levels peaked, suggesting that abscisic acid is involved in root aging-related processe

254 d MAPK), phytohormones (auxin, gibberellins, abscisic acid, JA and SA), and secondary metabolites (es

255 a key regulatory hub, integrating ethylene, abscisic acid, jasmonate, and redox signaling in the pla

256 led that infection increased accumulation of abscisic acid, jasmonates, and salicylic acid in wild ty

257 g stress response, most notably genes in the abscisic acid, jasmonic acid and salicylic acid pathways

258 ogenous SA levels and dramatically decreased abscisic acid levels in both shoot and root.

259 At this time point, root abscisic acid levels peaked, suggesting that abscisic ac

260 induction of TaNCED-5BS results in elevated abscisic acid levels, reduced host transpiration and wat

261 s auxin, gibberellic acid, jasmonic acid and abscisic acid, light, and circadian regulated elements.

262 stomatal aperture following incubation with abscisic acid, malate, or citrate.

263 d makes plants hypersensitive to a subset of abscisic acid-mediated responses.

264 tase, is additionally regulated by ethylene, abscisic acid, nitric oxid, and other phytohormones.

265 ndicate that an apocarotenoid, distinct from abscisic acid or strigolactone, is specifically required

266 nt of wheat, separately, with jasmonic acid, abscisic acid or with the avirulent race, CYR23, of the

267 ve the signaling molecules jasmonic acid and abscisic acid, or autophagy, but associates with salicyl

268 demand and soil drought, possibly involving abscisic acid production in leaves.

269 and the involvement of both ZmFDL1/MYB94 and abscisic acid regulatory pathways.

270 low mitotic activity and high expression of abscisic acid response genes.

271 acid (ABA) response pathway, containing the Abscisic Acid Responsive Element (ABRE) element within t

272 This study further reveals that the altered abscisic acid responsiveness of hy5 mutants is modulated

273 rk analysis predicted altered integration of abscisic acid sensing/signaling with ethylene and jasmon

274 activity, and several phenotypes, including abscisic acid sensitivity during germination, vegetative

275 th increased gibberellin content and reduced abscisic acid sensitivity during germination.

276 0, that cause defoliation either by altering abscisic acid sensitivity, hormone disruption, or sensit

277 hatases belonging to clade A are involved in abscisic acid signaling and control seed dormancy.

278 s responses in plants, for example by gating abscisic acid signaling and suppressing thermoresponsive

279 roots appeared to be oppositely affected by abscisic acid signaling compared with the salt stress re

280 partners, and also modulate gibberellin and abscisic acid signaling to regulate diverse developmenta

281 erall mild drought stress response comprised abscisic acid signaling, proline metabolism, and cell wa

282 lder rosette leaves through the phytohormone abscisic acid signaling, whereas this antagonistic effec

283 IC ACID INSENSITIVE5 transcription factor in abscisic acid signaling.

284 spectively) closely associated with DOG1 and abscisic acid signalling and suggest a model for the con

285 y, mediated by alteration of gibberellin and abscisic acid signalling.

286 One was a response to abscisic acid that resulted in dehydration, increases in

287 s accompanied by an enhanced accumulation of abscisic acid, the constitutive expression of genes enco

288 including the phytohormones gibberellin and abscisic acid, through conserved cis-motifs present in t

289 sensitivity to salinity, osmotic stress, and abscisic acid treatment at the seedling stage, and a red

290 and ARLs in different tissues, stresses and abscisic acid treatment highlighted temporal and spatial

291 In contrast, abscisic acid treatment or osmotic stress of P. patens d

292 Abscisic acid treatment promoted JAZ12 degradation, and

293 aize seedlings exposed to drought as well as abscisic acid treatment, which implies coordinated chang

294 ssed during pathogen infection, drought, and abscisic acid treatment.

295 ied its hyposensitive responses to auxin and abscisic acid treatments and enhanced far-red light/phyA

296 -B, dehydration, NaCl, methyl jasmonate, and abscisic acid treatments indicating its possible role in

297 tative proteomic analysis was used to detect abscisic acid-triggered persulfidation that reveals a ma

298 ought conditions or exogenous application of abscisic acid) was accompanied by crystal decomposition

299 ted an effect that is separable from that of abscisic acid, which is associated with water stress.

300 hormones jasmonate-isoleucine conjugate and abscisic acid, which represents a likely mechanism for i