ライフサイエンスコーパス: abscisic acid

1 pression decreased after exposure to NaCl or abscisic acid.

2 and cellular stress responses downstream of abscisic acid.

3 is rapidly downregulated by the phytohormone abscisic acid.

4 correlated with increased responsiveness to abscisic acid.

5 high salinity, drought, and the phytohormone abscisic acid.

6 ed by the signaling cascades of ethylene and abscisic acid.

7 nd in the presence of ethylene substrate and abscisic acid.

8 salicylic acid, ethylene, jasmonic acid, and abscisic acid.

9 nscription factors and factors controlled by abscisic acid.

10 etrazolium salts and a higher sensitivity to abscisic acid.

11 is differentially regulated by stresses and abscisic acid.

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

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

14 pathway and signalling by the plant hormone abscisic acid.

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

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

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

18 phytes do not conform to the standard active abscisic acid (ABA) -mediated stomatal control model, we

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

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

21 The plant hormone abscisic acid (ABA) acts both as a developmental signal

22 mino acid levels, and elevated metabolism of abscisic acid (ABA) and auxin in drying apx6 mutant seed

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

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

25 function mutants have reduced sensitivity to abscisic acid (ABA) and germinate earlier than the wild

26 Abscisic acid (ABA) and gibberellin (GA) signalling resp

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

28 To study the role of abscisic acid (ABA) and gibberellins (GA) in pre-maturit

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

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

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

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

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

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

35 ulates the abundance of proteins involved in abscisic acid (ABA) biosynthesis and the ABA response, w

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

37 ng a gene encoding a key regulated enzyme in abscisic acid (ABA) biosynthesis, 9-cis-EPOXYCAROTENOID

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

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

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

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

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

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

44 -3-acetic acid (IAA) increased and levels of abscisic acid (ABA) decreased from dormant to active sta

45 t over-express AtMBP-1 are hypersensitive to abscisic acid (ABA) during seed germination and show def

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

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

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

49 The hormone abscisic acid (ABA) has a central role in regulation of

50 Abscisic acid (ABA) has been shown to promote arbuscule

51 tases (PP2Cs), established repressors of the abscisic acid (ABA) hormonal pathway, interact with the

52 Although the importance of abscisic acid (ABA) in plant development and response to

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

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

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

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

57 losure occurs as water tension and levels of abscisic acid (ABA) increase in the leaf, but the intera

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

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

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

61 The abscisic acid (ABA) inducible RD29B gene of Arabidopsis

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

63 Abscisic acid (ABA) inhibits, whereas gibberellin promot

64 Abscisic acid (ABA) is a central player in plant respons

65 Abscisic acid (ABA) is a global regulator in stress resp

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

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

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

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

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

71 Abscisic acid (ABA) is a plant hormone that regulates pl

72 Abscisic acid (ABA) is a well-studied regulator of stoma

73 Abscisic acid (ABA) is an essential molecule in plant ab

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

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

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

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

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

79 Because abscisic acid (ABA) is recognized as the critical hormon

80 Abscisic acid (ABA) is shown to mediate the alternative

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

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

83 lso observed between isoprene production and abscisic acid (ABA) levels in the fruit cortex, which we

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

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

86 criptome coexpression analysis revealed that abscisic acid (ABA) metabolism/signaling genes were disp

87 Abscisic acid (ABA) modulates root growth in plants grow

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

89 ening and of the effect of the plant hormone abscisic acid (ABA) on this process.

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

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

92 ell proteins altered by redox in response to abscisic acid (ABA) or methyl jasmonate (MeJA) were iden

93 It is well known that abscisic acid (ABA) plays a central role in the regulati

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

95 The phytohormone abscisic acid (ABA) plays a key role in the plant respon

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

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

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

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

100 Thus, we show that DDA1 binds to the abscisic acid (ABA) receptor PYL8, as well as PYL4 and P

101 The discovery of the START family of abscisic acid (ABA) receptors places these proteins at t

102 Abscisic acid (ABA) regulates numerous physiological and

103 Quiescence is correlated with sustained abscisic acid (ABA) response in LRs and is dependent upo

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

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

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

107 Plant hormone abscisic acid (ABA) serves as an integrator of environme

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

109 eaf, PstDC3000 has been shown to up-regulate abscisic acid (ABA) signaling and thereby suppress salic

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

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

112 dividual metabolites have been implicated in abscisic acid (ABA) signaling in guard cells, but a meta

113 To study how PP2A is involved in abscisic acid (ABA) signaling in plants, we studied the

114 kinase 2s (SnRK2s) are central components of abscisic acid (ABA) signaling pathways.

115 Abscisic acid (ABA) signaling plays a critical role in r

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

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

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

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

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

121 encode rate-limiting enzymes in proline and abscisic acid (ABA) synthesis, respectively.

122 ole process is regulated by the phytohormone abscisic acid (ABA) through ABSCISIC ACID INSENSITIVE 3

123 species relies on high levels of the hormone abscisic acid (ABA) to close stomata during water stress

124 xpression increased with high temperature or abscisic acid (ABA) treatment.

125 -type Arabidopsis was responsive to heat and abscisic acid (ABA) treatment.

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

127 Abscisic acid (ABA) was found (up to 53.7 mg/kg) with th

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

129 Levels of the classical stress phytohormone abscisic acid (ABA) were also mainly enhanced by drought

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

131 arbon and water relations, are controlled by abscisic acid (ABA), both metabolically and hydraulicall

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

133 nts were hypersensitive to the plant hormone abscisic acid (ABA), displaying enhanced ABA-mediated in

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

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

136 ositively regulated by MeJA but repressed by abscisic acid (ABA), ethylene, and H2O2, while LjLTP6 wa

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

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

139 Potential roles of abscisic acid (ABA), of transcription factors (TFs) from

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

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

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

143 s insensitive to auxin and was stimulated by abscisic acid (ABA), which restored the inhibitory effec

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

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

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

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 OST1 activation is controlled through abscisic acid (ABA)-induced inhibition of type 2 protein

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

152 Interestingly, various osmotic stress/abscisic acid (ABA)-inducible genes were up-regulated in

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

154 ID INSENSITIVE5 (ABI5) is a key regulator of abscisic acid (ABA)-mediated seed germination and postge

155 e protein kinase, is a positive regulator in abscisic acid (ABA)-mediated stomatal response, but OST1

156 analysis of AtTim17-1 further identified an abscisic acid (ABA)-responsive element, which binds ABA-

157 gate the effects of environmental stress the abscisic acid (ABA)-responsive transcription factor ABI5

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

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

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

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

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

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

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

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

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

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

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

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

170 r motifs, most notably those associated with abscisic acid (ABA).

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

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

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

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

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

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

177 moderate local but not systemic induction of abscisic acid after infection of leaves with Psj.

178 Data on phenolics and abscisic acids allowed the discrimination and classifica

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

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

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

182 urther demonstrate that the orthogonal CIDs, abscisic acid and gibberellic acid, can be used to impar

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

184 owed impaired glucose metabolism and altered abscisic acid and gibberellin levels.

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

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

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

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

192 aling cascade of interactions among glucose, abscisic acid, and gibberellins.

193 ulators of root development including auxin, abscisic acid, and nitrate.

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

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

196 nses to drought, to the water stress hormone abscisic acid, and to pathogen attack, and it is essenti

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

198 fication of 36 compounds: 24 flavonoids, two abscisic acids, and 10 phenolic acids and their derivati

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 ins mediating chloroplast-localized steps of abscisic acid biosynthesis are expressed to a lower exte

203 accumulated oil bodies and responded to the abscisic acid biosynthesis inhibitor fluridone, which br

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

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

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

207 hydrated roots, associated with an increased abscisic acid concentration in leaves under topsoil dryi

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

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

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

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

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

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

214 ealed eighty-five compounds, including three abscisic acid derivatives, five limonoid glycosides, twe

215 and treatment with phytohormones, including abscisic acid, ethephon, methyljasmonate, 2,4-dichloroph

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

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

218 on of aliphatic glucosinolates is related to abscisic acid formation.

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

220 th early gibberellin-dependent flowering and abscisic acid hypersensitivity at seed germination.

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

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

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

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

225 y when overexpressed, potentially as part of abscisic acid-induced repression of pathogen response ge

226 induced root growth arrest and inhibition of abscisic acid-induced stomatal closing.

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

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

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

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

231 the phytohormone abscisic acid (ABA) through ABSCISIC ACID INSENSITIVE 3 (ABI3); a B3 domain transcri

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

233 Moreover, novel morphological and abscisic acid-insensitive seed germination mutants were

234 idopsis clade-A PROTEIN PHOSPHATASE2C mutant abscisic acid-insensitive1 (abi1-1) does not close the s

235 Relative suppression of abscisic acid insensitive3 (ABI3) and ABI5 expression, t

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

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

238 Although FUSCA3 and abscisic acid insensitive3 are required for L1L and bZIP

239 ABI3 (for ABSCISIC ACID INSENSITIVE3), a transcription factor of t

240 y an interaction between the closely related ABSCISIC ACID-INSENSITIVE3 (ABI3), FUSCA3 (FUS3), and LE

241 genes of interest involved in embryogenesis (abscisic acid-insensitive3 and FUSCA3) were found to be

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

243 TO ABSCISIC ACID18 and transcription factor ABSCISIC ACID-INSENSITIVE4 (ABI4), in ZFP3 overexpressio

244 he basic Leucine zipper transcription factor ABSCISIC ACID INSENSITIVE5 (ABI5) is a key regulator of

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

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

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

248 Abscisic acid is a key phytohormone produced in response

249 Abscisic acid is a phytohormone regulating plant growth,

250 Abscisic acid is an essential hormone for seed dormancy.

251 Further screens showed that the phytohormone abscisic acid is required for the DE response, positivel

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

253 s not cluster with clade A phosphatases, and abscisic acid levels and sensitivity are unaltered in th

254 arbon fixation as well as for maintenance of abscisic acid levels for responding to environmental cha

255 sistance, increased transpiration, decreased abscisic acid levels, and increased salicylic acid level

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

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

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

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

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

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

262 ingly, rh3-4 seedlings have lower amounts of abscisic acid prior to recovery of their chloroplasts, a

263 ology to mammalian lipid transport and plant abscisic acid receptor proteins and are predicted to hav

264 s, including methyl jasmonate, ethylene, and abscisic acid, regulated RIP2 protein expression.

265 ied RECEPTOR-LIKE PROTEIN KINASE1 (RPK1), an abscisic acid-related receptor, as the most likely gene

266 This work characterizes ABSCISIC ACID RESPONSE ELEMENT-BINDING FACTOR2 (VvABF2),

267 ent on BRC1, among them a set of upregulated abscisic acid response genes and two networks of cell cy

268 IVE 4 and SUPPRESSOR OF FRIGIDA4 to regulate abscisic acid responses and flowering time, respectively

269 that a single amino acid substitution in an abscisic acid-responsive kinase, AtMPK12, causes reducti

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

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

272 rtially correlated with natural variation in abscisic acid sensitivity and different Na(+)/K(+) ratio

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

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

275 INSENSITIVE3), a transcription factor of the abscisic acid signal transduction pathway, plays a major

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

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

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

279 The COAR domain mediates abscisic acid signaling via a physical interaction with

280 Hydropatterning is independent of endogenous abscisic acid signaling, distinguishing it from a classi

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

282 lation of potassium channel activity through abscisic acid signaling, transporter activity by a WNK k

283 IC ACID INSENSITIVE5 transcription factor in abscisic acid signaling.

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

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

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

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

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

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

290 Abscisic acid treatment promoted JAZ12 degradation, and

291 th upstream ABRE elements were responsive to abscisic acid treatment.

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

293 cations of the jasmonic acid methyl ester or abscisic acid triggered systemic immunity to Xtc.

294 Simultaneously, abscisic acid was determined, particularly in dehydrated

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

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

297 e that TIP-AQPs affect the induction of leaf abscisic acid, which leads to increased levels of transp

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

299 Transgenic lines underproducing abscisic acid, with lower hydraulic conductivity and hig

300 to report the levels of the stress hormone, abscisic acid, within cells in living plants in real-tim