ライフサイエンスコーパス: indole-3-acetic acid

1 ed for polar transport of the hormone auxin (indole-3-acetic acid).

2 e gut microbiome (e.g., CMPF, phenylsulfate, indole-3-acetic acid).

3 as induced in the presence of 2,4-D and IAA (indole-3-acetic acid).

4 hydrogen peroxide, abscisic acid (ABA), and indole-3-acetic acid.

5 pression in response to exogenously supplied indole-3-acetic acid.

6 e-3-butyric acid (IBA) to the active hormone indole-3-acetic acid.

7 ecific for the carboxyl-bearing phytohormone indole-3-acetic acid.

8 duced conversion of indole-3-butyric acid to indole-3-acetic acid.

9 ty was enhanced by ethylene and inhibited by indole-3-acetic acid.

10 s was increased by treatment with 0.1 microM indole-3-acetic acid.

11 ven by the bacterially-produced phytohormone indole-3-acetic acid.

12 d response of the apx6 mutants to ABA and to indole-3-acetic acid.

13 play an important role in converting IPA to indole-3-acetic acid.

14 Indole-3-acetic acid (1 microm, 10 microm, 0.1 mm, and 1

15 m was 5-methoxy-2-methyl-1-(phenylmethyl)-1H-indole-3-acetic acid (13a).

16 ntrations of isolated uremic solutes such as indole-3-acetic acid (3.5 mug/mL), indoxyl sulfate (25 m

17 arable to that of oxindole-3-acetic acid and indole-3-acetic acid (62 picomoles per shoot).

18 seedlings to 2,3-dihydro-7-hydroxy-2-oxo-1H indole-3-acetic acid-7'-O-beta-D-glycopyranoside with th

19 d seedlings treated with different hormones (indole-3-acetic acid, abscisic acid, gibberellin, methyl

20 alicylic acid, cinnamic acid, jasmonic acid, indole-3-acetic acid, abscisic acid, unsaturated C(18) f

21 n and that these mutants show reduced auxin (indole-3-acetic acid) accumulation and auxin responses c

22 d was partially characterized as an ester of indole-3-acetic acid and a desoxyaminohexose.

23 Bacterial production of indole-3-acetic acid and attachment to algae are signifi

24 etics and thermodynamics of the oxidation of indole-3-acetic acid and derivatives and of phenols by h

25 bolic branch point between the primary auxin indole-3-acetic acid and indole glucosinolate biosynthes

26 Finally, it was found that the auxins indole-3-acetic acid and indole-3-acetamide, which were

27 that neither the naturally occurring auxins indole-3-acetic acid and indole-3-butyric acid, nor the

28 ts respond normally to the endogenous auxins indole-3-acetic acid and indole-butyric acid.

29 as purified and characterized as an ester of indole-3-acetic acid and myo-inositol.

30 fate, while for weakly bound toxins, namely, indole-3-acetic acid and p-cresyl glucuronide, an increa

31 second compound was found to be an ester of indole-3-acetic acid and the disaccharide rutinose (gluc

32 Indole-3-acetic acid and tryptophan serve as signalling

33 s (sirtinol, 2,4-dichlorophenoxyacetic acid, indole-3-acetic acid) and a host of pleiotropic phenotyp

34 ation of COR, salicylic acid, jasmonic acid, indole-3-acetic acid, and abscisic acid illustrate the p

35 l analysis of salicylic acid, jasmonic acid, indole-3-acetic acid, and abscisic acid is typically ach

36 cussed to be involved in the biosynthesis of indole-3-acetic acid, and Cytochrome P450 (CYP) 71B6 wer

37 ds including indole-3-butyric acid, 4-chloro-indole-3-acetic acid, and indole-3-propionic acid.

38 itination at baseline and that uremic serum, indole-3-acetic acid, and indoxyl sulfate significantly

39 ibution of total radioactivity, radiolabeled indole-3-acetic acid, and radiolabeled ester conjugated

40 wards small substrates including the natural indole-3-acetic acid, and the synthetic auxin 2,4-dichlo

41 t one route to produce another phytohormone, indole-3-acetic acid, and thus, AOs play important roles

42 ulation of FQR1 mRNA begins within 10 min of indole-3-acetic acid application and reaches a maximum o

43 Free indole-3-acetic acid applied to the endosperm supplies s

44 f other plant hormones, including zeatin and indole-3-acetic acid, are observed in BGL-1 lines.

45 oxIAA) and increases in the conjugated forms indole-3-acetic acid aspartic acid (IAA-Asp) and indole-

46 tors are repressed by interaction with AUXIN/INDOLE 3-ACETIC ACID (Aux/IAA) proteins.

47 ved Arabidopsis (Arabidopsis thaliana) Auxin/indole-3-acetic acid (Aux/IAA) family member.

48 The AUXIN/INDOLE-3-ACETIC ACID (Aux/IAA) genes encode short-lived

49 Auxin/indole-3-acetic acid (Aux/IAA) genes encode short-lived

50 Auxin/indole-3-acetic acid (Aux/IAA) proteins function as repr

51 xin-responsive degradation of multiple auxin/indole-3-acetic acid (Aux/IAA) proteins is essential for

52 BIF1 and BIF4 encode AUXIN/INDOLE-3-ACETIC ACID (Aux/IAA) proteins, which are key c

53 pivots on the interaction between the AUXIN/INDOLE-3-ACETIC ACID (Aux/IAA) repressor proteins and th

54 tical model revealed the centrality of auxin/indole-3-acetic acid (Aux/IAA) transcriptional corepress

55 Auxin induces the degradation of AUXIN/INDOLE-3-ACETIC ACID (AUX/IAA) transcriptional repressor

56 )/AUXIN SIGNALING F-BOX protein and an AUXIN/INDOLE-3-ACETIC ACID (Aux/IAA) transcriptional repressor

57 by facilitating proteolytic removal of auxin/indole-3-acetic acid (AUX/IAA)-inducible repressors, whi

58 n auxin response is the degradation of Auxin/Indole-3-Acetic Acid (Aux/IAA, referred to hereafter as

59 and their interaction with the plant hormone indole-3-acetic acid (auxin).

60 es encode enzymes that convert tryptophan to indole-3-acetic acid (auxin): iaaM (tryptophan mono-oxyg

61 using alpha-(2,4-dimethylphenylethyl-2-oxo)-indole-3-acetic acid (auxinole), alpha-(phenylethyl-2-ox

62 laced these CCMTs into a clade that includes indole-3-acetic acid carboxyl methyltransferases and a l

63 o lead to a sustained elevation of leaf free indole-3-acetic acid content relative to untreated contr

64 reover, cu-3 mutants retained sensitivity to indole-3-acetic acid, cytokinins, gibberellin, and absci

65 acteria raise the question as to whether the indole-3-acetic acid degradation pathway is present in h

66 , gravity affects the steady state amount of indole-3-acetic acid derived from indole-3-acetyl-myo-in

67 Asymmetric distribution of [3H]indole-3-acetic acid, derived from the applied [3H]indol

68 l defects that can be ascribed to changes in indole-3-acetic acid distribution.

69 auxin antagonist alpha-(phenyl ethyl-2-one)-indole-3-acetic acid enhanced ABA-regulated stomatal mov

70 it is the same as IAA7, a member of the IAA (indole-3-acetic acid) family of auxin-inducible genes.

71 ate flux near neuronal cells; and endogenous indole-3-acetic acid flux near the surface of Zea mays r

72 nphysiological concentrations of ethylene or indole-3-acetic acid for protracted periods (more than 2

73 eta-oxidation enzymes as in the synthesis of indole-3-acetic acid from indole-3-butyric acid.

74 a photooxidation product of the plant auxin indole-3-acetic acid, functions as an affinity label of

75 rolactone, three urolithin glucuronides, and indole-3-acetic acid glucuronide.

76 le-3-acetic acid aspartic acid (IAA-Asp) and indole-3-acetic acid glutamic acid (IAA-Glu) of 438- and

77 y for indole-3-acetic acid in Zea seedlings: Indole-3-acetic acid --> Oxindole-3-acetic acid --> 7-Hy

78 preference for the naturally occurring auxin indole 3-acetic acid (IAA) and is important for coordina

79 epicotyls were loaded symmetrically with 3H-indole 3-acetic acid (IAA) or 45Ca2+, then subjected to

80 We investigated whether the uremic solute indole-3 acetic acid (IAA) predicts clinical outcomes in

81 Indole-3 acetic acid (IAA)-induced changes in gene expre

82 years of evidence showing a pivotal role for indole-3-acetic acid (IAA or auxin) in plant development

83 m segments have implicated the plant hormone indole-3-acetic acid (IAA or auxin) in the regulation of

84 The plant hormone indole-3-acetic acid (IAA or auxin) mediates the elongat

85 Second, a transient gradient of free indole-3-acetic acid (IAA) across the pulvinus was appar

86 Exogenous indole-3-acetic acid (IAA) also elevated flavonoid accum

87 Indole-3-acetic acid (IAA) and 1-aminocyclopropane-1-car

88 ompared with the control group and decreased indole-3-acetic acid (IAA) and abscisic acid (ABA) conce

89 than the wild type at low concentrations of indole-3-acetic acid (IAA) and also under low nutrient c

90 tophan (Trp), including the growth regulator indole-3-acetic acid (IAA) and defense compounds against

91 binding properties of indoxyl sulfate (IS), indole-3-acetic acid (IAA) and hippuric acid (HIPA) and

92 y metabolites including the growth regulator indole-3-acetic acid (IAA) and indole glucosinolate defe

93 The auxins indole-3-acetic acid (IAA) and naphthaleneacetic acid st

94 auxin biology include synthesis of the auxin indole-3-acetic acid (IAA) and production of virulence f

95 Gretchen Hagen 3.5 (AtGH3.5) conjugates both indole-3-acetic acid (IAA) and salicylic acid (SA) to mo

96 s have suggested that AtGSTF2 interacts with indole-3-acetic acid (IAA) and the auxin transport inhib

97 the auxin precursor IBA and the active auxin indole-3-acetic acid (IAA) and those with restored respo

98 s of indole-3-acetyl-1-O-beta-D-glucose from indole-3-acetic acid (IAA) and uridine diphosphoglucose

99 h plants regulate levels of the phytohormone indole-3-acetic acid (IAA) are complex and not fully und

100 Amide-linked conjugates of indole-3-acetic acid (IAA) are putative storage or inact

101 owever, the expression of genes encoding the indole-3-acetic acid (IAA) biosynthesis enzyme TRYPTOPHA

102 Plants can regulate levels of the auxin indole-3-acetic acid (IAA) by conjugation to amino acids

103 -butyric acid (IBA) is converted into active indole-3-acetic acid (IAA) by peroxisomal beta-oxidation

104 acid (IBA) is converted to the active auxin indole-3-acetic acid (IAA) by removal of two side-chain

105 Amide-linked indole-3-acetic acid (IAA) conjugates constitute approxi

106 The formation and hydrolysis of indole-3-acetic acid (IAA) conjugates represent a potent

107 by formation and hydrolysis of amide-linked indole-3-acetic acid (IAA) conjugates.

108 Exogenous indole-3-acetic acid (IAA) enhances the constitutive exp

109 s thaliana, cotyledons and leaves synthesize indole-3-acetic acid (IAA) from tryptophan through indol

110 ence indicates that amino acid conjugates of indole-3-acetic acid (IAA) function in auxin homeostasis

111 Furthermore, homologous members of the AUX/indole-3-acetic acid (IAA) gene family mediate the actio

112 tural auxins indole-3-butyric acid (IBA) and indole-3-acetic acid (IAA) has been described in Arabido

113 Most indole-3-acetic acid (IAA) in higher plants is conjugate

114 BA), which is apparently shortened to active indole-3-acetic acid (IAA) in peroxisomes by a process s

115 The bulk of indole-3-acetic acid (IAA) in plants is found in the for

116 be the coupling between the concentration of indole-3-acetic acid (IAA) in the cambial region of a tr

117 n induces an asymmetric distribution of free indole-3-acetic acid (IAA) in the cortex-epidermis of th

118 iments show that afb4-2 is hypersensitive to indole-3-acetic acid (IAA) in the hypocotyl, indicating

119 To date, the role of the auxin indole-3-acetic acid (IAA) in this context is not well u

120 84B1, whose recombinant product glucosylated indole-3-acetic acid (IAA) in vitro.

121 PLC-ESI-MS/MS analysis showed that levels of indole-3-acetic acid (IAA) increased and levels of absci

122 ACC and indole-3-acetic acid (IAA) increased the abundance of tr

123 olated pea (Pisum sativum L.) seedlings with indole-3-acetic acid (IAA) induced within 15 min an incr

124 We show that indole-3-acetic acid (IAA) inhibition of abscisic acid (

125 Indole-3-acetic acid (IAA) is a primary phytohormone tha

126 Polar transport of the natural auxin indole-3-acetic acid (IAA) is important in a number of p

127 We further found that the free indole-3-acetic acid (IAA) level in hypocotyl regions be

128 .F.W. Meyer ecotype had significantly higher indole-3-acetic acid (IAA) levels than a UV-sensitive ec

129 nel mass and a recently reported decrease in indole-3-acetic acid (IAA) levels throughout kernel deve

130 Whereas indole-3-acetic acid (IAA) levels were elevated in young

131 tant phenotypes were rescued when endogenous indole-3-acetic acid (IAA) levels were increased by grow

132 have developed a high-throughput screen for indole-3-acetic acid (IAA) levels.

133 leaves is paralleled by an increase in free indole-3-acetic acid (IAA) levels.

134 Indole-3-acetic acid (IAA) methyltransferase (IAMT) is a

135 Either 5-[3H]indole-3-acetic acid (IAA) or 5-[3H]indole-3-acetyl-myo-

136 Cuttings treated with indole-3-acetic acid (IAA) or subjected to salt stress s

137 est that the enzymatic reactions involved in indole-3-acetic acid (IAA) production via IPyA are diffe

138 Indole-3-acetic acid (IAA) promotes ethylene biosynthesi

139 es facilitates ubiquitination of auxin (aux)/indole-3-acetic acid (IAA) repressor proteins in the pre

140 although AgNO(3) dramatically decreased root indole-3-acetic acid (IAA) responsiveness in inhibition

141 ized carrier proteins to transport the auxin indole-3-acetic acid (IAA) to target tissues.

142 first enzyme-catalyzed reaction leading from indole-3-acetic acid (IAA) to the myo-inositol esters of

143 companied by a rapid increase in radioactive indole-3-acetic acid (IAA) transport and its accumulatio

144 mutation significantly enhance radiolabeled indole-3-acetic acid (IAA) transport in both the acropet

145 Root basipetal and acropetal indole-3-acetic acid (IAA) transport increase with ACC t

146 were to determine whether both polarities of indole-3-acetic acid (IAA) transport occur in roots of A

147 Indole-3-acetic acid (IAA) was identified in F. distichu

148 the promotion of lateral root initiation by indole-3-acetic acid (IAA) was reduced as the IAA concen

149 Indole-3-acetic acid (IAA), a major plant auxin, is prod

150 of bacterial cultures and the production of indole-3-acetic acid (IAA), a ubiquitous plant hormone t

151 onversion of indole-3-pyruvic acid (IPyA) to indole-3-acetic acid (IAA), acting downstream of CKRC1/T

152 The auxin, indole-3-acetic acid (IAA), and auxin efflux inhibitors,

153 rabidopsis genes were specifically active on indole-3-acetic acid (IAA), and one was active on both I

154 ant-associated microbes synthesize the auxin indole-3-acetic acid (IAA), and several IAA biosynthetic

155 In addition to MeJA and indole-3-acetic acid (IAA), axr1-24 had decreased sensit

156 synthesis and degradation of the main auxin, indole-3-acetic acid (IAA), by sugars requires changes i

157 IBA is converted to the more abundant auxin, indole-3-acetic acid (IAA), in a mechanism that parallel

158 l mechanisms to regulate levels of the auxin indole-3-acetic acid (IAA), including the formation and

159 The native auxin, indole-3-acetic acid (IAA), is a major regulator of plan

160 A plant growth-promoting substance, such as indole-3-acetic acid (IAA), known to be produced by G. d

161 nscripts that were consistently regulated by indole-3-acetic acid (IAA), partitioning into 60 cluster

162 stasis of the major form of auxin in plants, indole-3-acetic acid (IAA), remains unclear.

163 Indole-3-acetic acid (IAA), the main naturally occurring

164 an antagonistic manner to that of the auxin indole-3-acetic acid (IAA), the mechanism by which remai

165 Levels of indole-3-acetic acid (IAA), the primary auxin, are tight

166 When combined with plant auxin, indole-3-acetic acid (IAA), the SPE fraction shows a syn

167 changes in auxin metabolism, mediated by the indole-3-acetic acid (IAA)-amido synthetase Gretchen Hag

168 Conjugation to amino acids by indole-3-acetic acid (IAA)-amido synthetases is an impor

169 ulation of a conjugated form of the hormone, indole-3-acetic acid (IAA)-Asp, to promote disease devel

170 We show that the expression of an indole-3-acetic acid (IAA)-modified protein from bean se

171 a that are resistant to growth inhibition by indole-3-acetic acid (IAA)-phenylalanine have been isola

172 al root primordia; decreased auxin maxima in indole-3-acetic acid (IAA)-treated root apical meristems

173 The most abundant natural auxin is indole-3-acetic acid (IAA).

174 ly via its conversion to the principal auxin indole-3-acetic acid (IAA).

175 r 2,4-dichlorophenoxyacetic acid (2,4-D) and indole-3-acetic acid (IAA).

176 estigated the sensitivity of rhd1-4 roots to indole-3-acetic acid (IAA).

177 remain sensitive to the more abundant auxin indole-3-acetic acid (IAA).

178 didate precursor of the plant growth hormone indole-3-acetic acid (IAA).

179 or produces high concentrations of the auxin indole-3-acetic acid (IAA).

180 nt hormone, usually occurring in the form of indole-3-acetic acid (IAA).

181 logical responses like the endogenous auxin, indole-3-acetic acid (IAA).

182 s peroxisomal beta-oxidation to release free indole-3-acetic acid (IAA).

183 nclude camalexin, indole glucosinolates, and indole-3-acetic acid (IAA); however, the steps in their

184 ynthesis pathway and increases in the auxin [indole-3-acetic acid (IAA)] biosynthesis pathway.

185 static regulation of the phytohormone auxin [indole-3-acetic acid (IAA)] is essential to plant growth

186 Spatial regulation of the plant hormone indole-3-acetic acid (IAA, or auxin) is essential for pl

187 The Trp conjugate with indole-3-acetic acid (IAA-Trp) produced a similar respon

188 he biosynthesis of the main auxin in plants (indole-3-acetic acid [IAA]) has been elucidated recently

189 The plant hormone auxin (indole-3-acetic acid [IAA]) is found both free and conju

190 The phytohormone auxin (indole-3-acetic acid [IAA]) plays a fundamental role in

191 rile (IAN; a possible precursor of the auxin indole-3-acetic acid [IAA]) was carried out under mild c

192 (1-NAA); however, traditional auxins (e.g., indole-3-acetic acid [IAA], 2,4-D, 1-NAA) have no effect

193 IAR3 hydrolyzes an inactive form of auxin (indole-3-acetic acid [IAA]-alanine) and releases bioacti

194 er to survey the entire literature on auxin (indole-3-acetic acid, IAA) action in all plants, with sp

195 The phytohormone auxin (indole-3-acetic acid, IAA) is a small organic molecule t

196 ycerol and each of two inhibitors of hKAT I: indole-3-acetic acid (IAC) and Tris.

197 The polar movement of [(3)H]indole-3-acetic acid in both hypocotyl sections and prim

198 s roots and increases the retention of [(3)H]indole-3-acetic acid in root tips of maize.

199 pplied to the endosperm supplies some of the indole-3-acetic acid in the mesocotyl but essentially no

200 induction of primary auxin response genes by indole-3-acetic acid in the presence of growth-inhibitor

201 bution and chemical form of the radiolabeled indole-3-acetic acid in the shoot depending upon whether

202 ic acid-glucoside is a natural metabolite of indole-3-acetic acid in Z. mays seedlings.

203 route as the principal catabolic pathway for indole-3-acetic acid in Zea seedlings: Indole-3-acetic a

204 etic acid, and radiolabeled ester conjugated indole-3-acetic acid, in the shoots was then determined.

205 ns of auxin response factors (ARF) and auxin/indole 3-acetic acid inducible proteins regulate transcr

206 ly of transcription factors as well as AUXIN/INDOLE-3-ACETIC ACID INDUCIBLE (AUX/IAA) proteins that r

207 analyses revealed that expression of several indole-3-acetic acid-inducible genes, including Aux/IAA,

208 P, and the auxin-inducible genes MONOPTEROS, INDOLE-3-ACETIC ACID INDUCIBLE1 (IAA1), and IAA19.

209 /SL signaling, D14-LIKE2, KAR-UP F-BOX1, and INDOLE-3-ACETIC ACID INDUCIBLE1, is rescued in smax1 max

210 t increases in the expression of some genes (INDOLE-3-ACETIC ACID-INDUCIBLE1 and PHYTOCHROME B ACTIVA

211 ated tissues and others through signaling of INDOLE-3-ACETIC ACID INDUCIBLE28 (IAA28), CRANE (IAA18),

212 The auxin indole-3-acetic acid is a key plant hormone essential fo

213 Indole-3-acetic acid is oxidized to oxindole-3-acetic ac

214 According to the classic model, the auxin indole-3-acetic acid is produced in the shoot tip and tr

215 We propose that the level of indole-3-acetic acid is regulated by the flux of indole-

216 We also show that the widespread auxin, indole-3-acetic acid, is synthesized by a parallel pathw

217 In particular, indole-3-acetic acid levels declined after ABA treatment

218 ed within 12 h of increasing the R:FR, while indole-3-acetic acid levels did not change.

219 of this enzyme in the homeostatic control of indole-3-acetic acid levels in Zea mays is discussed.

220 Jasmonic acid and indole-3-acetic acid levels were also found to increase

221 hypocotyls contained considerably lower free indole-3-acetic acid levels when compared with wild-type

222 nhibitor response1/auxin-related f-box-auxin/indole-3-acetic acid-mediated auxin-signaling machinery

223 ft1-2, and 35S:PFT1 seedlings in response to indole-3-acetic acid, naphthaleneacetic acid, and the po

224 uding a number of transcripts encoding Auxin/Indole-3-Acetic Acids, negative regulators of auxin sign

225 pe dilution, accounting for 19% of the ester indole-3-acetic acid of the shoot.

226 id in the shoot depending upon whether 5-[3H]indole-3-acetic acid or 5-[3H]indole-3-acetyl-myo-inosit

227 d an auxin-inhibitor (a-(phenyl ethyl-2-one)-indole-3-acetic acid (PEO-IAA)), together with the MIR17

228 c acid (auxinole), alpha-(phenylethyl-2-oxo)-indole-3-acetic acid (PEO-IAA), and 5-fluoroindole-3-ace

229 Indole-3-acetic acid (plant auxin) has low toxicity but

230 atranscriptome analyses that show widespread indole-3-acetic acid production by Sulfitobacter-related

231 Auxin/indole-3-acetic acid protein (Aux/IAA) luciferase (LUC)

232 ene family products, together with the AUXIN/INDOLE-3-ACETIC ACID proteins, regulate auxin-mediated t

233 intermediate indole-3-pyruvic acid (IPA) and indole-3-acetic acid rescues the tir2 short hypocotyl ph

234 This compound was also formed from labeled indole-3-acetic acid supplied to intact seedlings and ro

235 m cell division via secretion of the hormone indole-3-acetic acid, synthesized by the bacterium using

236 se mutant, but it also is less responsive to indole-3-acetic acid, synthetic auxins, auxin transport

237 1 seedlings accumulate nearly threefold more indole-3-acetic acid than the wild type.

238 oxygenases participates in converting IPA to indole-3-acetic acid, the main auxin in plants.

239 Indole-3-acetic acid, the major form of auxin in higher

240 unds related to the biosynthetic pathways of indole-3-acetic acid, the primary growth regulator in pl

241 trations but maintain wild-type responses to indole-3-acetic acid, the principle active auxin.

242 tration of the in vitro enzymic oxidation of indole-3-acetic acid to oxindole-3-acetic acid in higher

243 tic acid in the mesocotyl but essentially no indole-3-acetic acid to the coleoptile or primary leaves

244 perm provides both free and ester conjugated indole-3-acetic acid to the mesocotyl and coleoptile.

245 nositol and 1 picomole per plant per hour of indole-3-acetic acid to the shoot and thus is comparable

246 with auxin-regulated proteolysis of an auxin/indole-3-acetic acid transcription factor, and two impar

247 Basipetal indole-3-acetic acid transport and gravitropism are redu

248 The are mutant has increased indole-3-acetic acid transport and greater sensitivity t

249 We demonstrate that 2,4-D, but not indole-3-acetic acid transport is affected by mutations

250 avitropic response, a reduction in basipetal indole-3-acetic acid transport, and a delay in the asymm

251 Y6) mutant makes no flavonoids, has elevated indole-3-acetic acid transport, and exhibits a delayed g

252 ings exhibit increased and reduced basipetal indole-3-acetic acid transport, respectively.

253 function inhibits gravitropism and basipetal indole-3-acetic acid transport.

254 Cel1 and Cel5 mRNA decreased 99% when indole-3-acetic acid was added during ethylene treatment

255 contrast, Cel6 mRNA increased slightly when indole-3-acetic acid was added.

256 m was applied unilaterally to the cap and 3H-indole-3-acetic acid was applied to the basal cut surfac

257 Esters of indole-3-acetic acid were extracted and purified from th

258 l as enzymes that act upon jasmonic acid and indole-3-acetic acid were identified.

259 nd 3-mercaptopropionate, and the plant auxin indole 3-acetic acid, were released by S. elongatus at m

260 eld [3H]indole-3-acetyl-myo-inositol and [3H]indole-3-acetic acid which were then transported to the