ライフサイエンスコーパス: gibberellic acid

1 ion of storage proteins and the synthesis of gibberellic acid.

2 elongating in response to applied auxin plus gibberellic acid.

3 nhanced by ABA, but not by auxin, kinetin or gibberellic acid.

4 gle foliar applications of ascorbic acid and gibberellic acid.

5 of growth promoters, i.e., ascorbic acid and gibberellic acid.

6 e partially reversed with the application of gibberellic acid.

7 t of the BP gene but suppressed by exogenous gibberellic acid.

8 sis of auxin, glucosinolates, cytokinin, and gibberellic acid.

9 lied indoleacetic acid (100 micromolar) plus gibberellic acid (10 micromolar) without gravistimulatio

10 cation of a combination of ascorbic acid and gibberellic acid (120 ppm and 110 ppm) ameliorated the n

11 ), sodium chloride (NaCl; 50 and 100 mM) and gibberellic acid (2.0 and 4.0 mg/L GA(3)) to investigate

12 smotin; a cytokinin-responsive gene CKR; and gibberellic acid 20 oxidase.

13 cation of a combination of ascorbic acid and gibberellic acid (240 ppm and 220 ppm) ameliorates the n

14 rst experiment, tritiated ABA ((3)H-ABA) and gibberellic acid ((3)H-GA3) were diluted with unlabelled

15 upl3 plants are hypersensitive to gibberellic acid-3 (GA3), consistent with the role of gi

16 cate that GCT and CCT operate in parallel to gibberellic acid, a phytohormone known to regulate these

17 t not by zeatin riboside, and only weakly by gibberellic acid, abscisic acid and kinetin.

18 Gibberellic acid, abscisic acid, auxin, and ethylene had

19 The combination of gibberellic acid and benzyladenine at 200 mg/l concentra

20 , which was exposed to foliar application of gibberellic acid and benzyladenine hormones.

21 esults showed that 200 mg/l concentration of gibberellic acid and benzyladenine significantly improve

22 production of the growth-stimulating hormone gibberellic acid and downstream growth factors is first

23 ent an inverse correlation between bioactive gibberellic acid and SE in soybean, a difficult crop to

24 ansporters), ethylene, jasmonic acid, auxin, gibberellic acid, and abscisic acid responses, and respo

25 ng of plant hormones, such as abscisic acid, gibberellic acid, and auxin, are regulated by cold stres

26 hormones, most notably auxin, strigolactone, gibberellic acid, and brassinosteroids.

27 and induced by the phytohormones jasmonate, gibberellic acid, and ethylene.

28 ization, and the production of siderophores, gibberellic acid, and indole acetic acid.

29 se, mRNA levels increased in the presence of gibberellic acid, and its antagonist abscisic acid preve

30 es, and response to abscisic acid, ethylene, gibberellic acid, and jasmonic acid, suggesting these ce

31 eading to the formation of hormones, such as gibberellic acid, and other metabolites are up-regulated

32 type ubiquitin ligase: auxin, jasmonic acid, gibberellic acid, and strigolactone.

33 transcript profiling under methyl jasmonate, gibberellic acid, and yeast extract elicitations display

34 ed bushy appearance that could be rescued by gibberellic acid application.

35 Gibberellins (GAs) or gibberellic acids are ubiquitous diterpenoid phytohormon

36 sults are consistent with a role for the ABA/gibberellic acid balance in integrating dormancy-relievi

37 100 and 200 mg/l benzyladenine, and 200 mg/l gibberellic acid + benzyladenine.

38 ffects of abscisic acid and paclobutrazol, a gibberellic acid biosynthesis inhibitor, on seed germina

39 by epigenetic transcriptional activation of gibberellic acid biosynthetic enzymes via histone demeth

40 d that a putative rice CBL gene responded to gibberellic acid, but not abscisic acid, treatment.

41 s to the plant hormones jasmonate, auxin and gibberellic acid, but not brassinolide and abscisic acid

42 eurone layers maintained in vitro respond to gibberellic acid by secreting an array of proteins and p

43 that the orthogonal CIDs, abscisic acid and gibberellic acid, can be used to impart control over the

44 ughput approach revealed a role for AGL15 in gibberellic acid catabolism that is relevant to embryoge

45 acted germination and how treatments such as gibberellic acid could be used to mitigate stress.

46 ed Arabidopsis thaliana light mutants in the gibberellic acid/DELLA pathway.

47 Benzyladenine, ethylene, and gibberellic acid did not affect peroxidase gene expressi

48 The biosynthesis of gibberellic acid (GA(3)) by the fungus Fusarium fujikuro

49 symptoms that were rescued by application of gibberellic acid (GA(3)).

50 ved the applications of salicylic acid (AS); gibberellic acid (GA(3)); abscisic acid (ABA) and soluti

51 The plant hormone gibberellic acid (GA) also participates in this process,

52 The phytohormones abscisic acid (ABA) and gibberellic acid (GA) antagonistically control the shift

53 The plant hormones abscisic acid (ABA) and gibberellic acid (GA) are important regulators of the do

54 genes involved in (a)biotic stress response, gibberellic acid (GA) biosynthesis and signaling.

55 le regulators, cell wall metabolism enzymes, gibberellic acid (GA) biosynthesis enzymes, and auxin re

56 rapidly when aleurone cells are treated with gibberellic acid (GA) but not abscisic acid (ABA).

57 companied by higher expression levels of the gibberellic acid (GA) catabolic enzyme StGA2ox1.

58 The plant hormone gibberellic acid (GA) controls many physiological proces

59 Ethylene accelerates petal senescence, while gibberellic acid (GA) delays this process.

60 by abscisic acid (ABA) and downregulated by gibberellic acid (GA) during seed germination.

61 orrelated genes predicted that the auxin and gibberellic acid (GA) hormone pathways both contribute t

62 In the aleurone cells of the cereal grain, gibberellic acid (GA) induces the secretion of hydrolase

63 Gibberellic acid (GA) is both necessary and sufficient t

64 The phytohormone gibberellic acid (GA) is critical for environmentally se

65 It is well established that the phytohormone gibberellic acid (GA) is involved in supplemental FR-ind

66 Interestingly, exogenous application of gibberellic acid (GA) not only enhanced SAR in wild-type

67 We tested the effect of gibberellic acid (GA) on sex determination through exoge

68 tive cross talk with salicylic acid (SA) and gibberellic acid (GA) pathways.

69 Gibberellic acid (GA) promotes germination, stem/hypocot

70 Gibberellic acid (GA) promotes hydrolase production, whe

71 i') of tall fescue (Festuca arundinacea) and gibberellic acid (GA) regulation of LER were associated

72 orters, we mapped auxin, cytokinin (CK), and gibberellic acid (GA) response patterns in maize (Zea ma

73 that DELLA proteins, which are repressors of gibberellic acid (GA) signaling and function at the nexu

74 rowth and development, negatively regulating gibberellic acid (GA) signaling and positively regulatin

75 F9, 2 DELLA family proteins that repress the gibberellic acid (GA) signaling pathway.

76 rtilization and is associated with auxin and gibberellic acid (GA) signaling.

77 posed to restrict shoot growth by modulating gibberellic acid (GA) signaling.

78 The plant hormone gibberellic acid (GA) stimulates the secretion of hydrol

79 nding, maturation of contractile fibers, and gibberellic acid (GA) stimulation of tension wood format

80 s with the proteosome inhibitor MG132 or the gibberellic acid (GA) synthesis inhibitor paclobutrazol

81 ins involved in auxin, brassinosteroid (BR), gibberellic acid (GA), abscisic acid (ABA) and ethylene

82 programmed cell death (PCD) when exposed to gibberellic acid (GA), but incubation in abscisic acid (

83 hormones such as abscisic acid (ABA), auxin, gibberellic acid (GA), cytokinin (CK), brassinosteroids

84 ution of the other plant hormones, including gibberellic acid (GA), is largely unknown.

85 re, we show that also another plant hormone, gibberellic acid (GA), shows asymmetric action during gr

86 etween ABA, which represses germination, and gibberellic acid (GA), which promotes germination, under

87 transcriptional repressor regulating light-, gibberellic acid (GA)-, and abscisic acid (ABA)-responsi

88 appear to regulate fruit patterning through gibberellic acid (GA)-DELLA signalling, revealing a cent

89 Gibberellic acid (GA)-mediated cell expansion initiates

90 wall-loosening EXPANSIN (EXPA) genes promote gibberellic acid (GA)-mediated germination, identifying

91 urone layers or protoplasts are incubated in gibberellic acid (GA).

92 of the phytohormones jasmonic acid (JA) and gibberellic acid (GA).

93 by high nitrate plus sugars and in shoots by gibberellic acid (GA).

94 uch as abscisic acid (ABA), auxin (IAA), and gibberellic acid (GA).

95 e in M202 also upregulated by treatment with gibberellic acid (GA).

96 g Cr/kg soil), as well as the application of gibberellic acid (GA3 = 5 mg/L solution) with and withou

97 Both gibberellic acid (GA3) and abscisic acid (ABA) regulate

98 rfenuron (CPPU), 6-benzylaminopurine (6-BA), gibberellic acid (GA3) and ethephon in grape are present

99 ffect the degradation rate of IAA1::LUC, and gibberellic acid (GA3) and salicylic acid (SA) did not s

100 igate the individual and combined effects of gibberellic acid (GA3) application and biofertilizer (Ag

101 hese issues, the use of activated carbon and gibberellic acid (GA3) are considered valuable amendment

102 Application of gibberellic acid (GA3) rescued impaired germination of k

103 unilaterally with indoleacetic acid (IAA) or gibberellic acid (GA3) with or without gravistimulation

104 d by gravistimulus, indoleacetic acid (IAA), gibberellic acid (GA3), and fusicoccin (FC).

105 0-fold or more within 24 h of treatment with gibberellic acid (GA3).

106 Gibberellic acids (GAs) are key plant hormones, regulati

107 e, various applications of ascorbic acid and gibberellic acid have been applied as foliar sprays to m

108 eembryonated transgenic grain incubated with gibberellic acid; (iii) a 35% increase in the ratio of r

109 eq data to examine the role of cytokinin and gibberellic acid in P(i) deficiency-induced cluster root

110 We demonstrate interaction between auxin and gibberellic acid in the promotion of SE and document an

111 Perturbation of protein secretion in gibberellic acid-induced aleurone layers by two independ

112 ncept, we demonstrate that the plant hormone gibberellic acid induces a spatial gradient in mechanica

113 The results indicate that gibberellic acid induces accumulation of growth regulato

114 Tomato transcripts of Gibberellic Acid Insensitive (SlGAI) and Cathepsin D Pro

115 ngle DELLA family transcription factor gene (GIBBERELLIC ACID INSENSITIVE (SpGAI)) and observed inflo

116 ) Gibberellic Acid Insensitive, Repressor of Gibberellic Acid Insensitive, and Scarecrow (GRAS)-type

117 ic mutant screen a petunia (Petunia hybrida) Gibberellic Acid Insensitive, Repressor of Gibberellic A

118 Signal Transduction1 subfamily of GRAS (for Gibberellic Acid-Insensitive (GAI), Repressor of GAI, an

119 plants, named after the first three members: GIBBERELLIC ACID-INSENSITIVE, REPRESSOR of GAI, and SCAR

120 d et al. (2016) find that the hormone signal gibberellic acid is key in integrating these responses,

121 luding that for different hormones as auxin, gibberellic acid, jasmonic acid and abscisic acid, light

122 caused extreme bending away from that side; gibberellic acid, kinetin, and abscisic acid were withou

123 e perception of day length periodicity or in gibberellic acid metabolism.

124 its function is related to the regulation of gibberellic acid metabolism.

125 its function is related to the regulation of gibberellic acid metabolism.

126 ite-nonselective process was shown with both gibberellic acid methyl ester and brefeldin A using only

127 Abscisic acid, auxin, gibberellic acid, methyl jasmonic acid, and salicylic ac

128 h loss of repression as an initial effect of gibberellic acid on transcription of those genes, althou

129 Signaling via gibberellic acid, on the other hand, turned out to be es

130 tic acid, jasmonic acid, salicylic acid, and gibberellic acid or by wounding, temperature, and light,

131 ent, but could not be completely overcome by gibberellic acid or physical removal of the seed materna

132 t hap3b plants showed earlier flowering upon gibberellic acid or vernalization treatment, which means

133 lls treated with the hormones abscisic acid, gibberellic acid, or both.

134 than wild-type, likely by downregulating the gibberellic acid pathway genes PhGAI, creating a more co

135 whereas GID1b probably functions to regulate gibberellic acid perception in reproductive organs.

136 ene for dw as a non-functional allele of the gibberellic acid receptor GID1c.

137 LP2-AtMIA40 complex in negatively regulating gibberellic acid-related processes during seed germinati

138 work also includes a number of ethylene- and gibberellic acid-related transcription factors with esta

139 thaliana, we examine molecular variation at GIBBERELLIC ACID REQUIRING 1 (GA1) and test for associat

140 accessions, dampens ethylene production and gibberellic acid responsiveness during submergence, econ

141 h inhibition may occur via interference with gibberellic acid signaling or responsiveness.

142 Gibberellic acid signaling, which antagonizes the ABA pa

143 RESSOR-OF-GA (RGA) and RGA-LIKE3 involved in gibberellic acid signaling; and MOTHER-OF-FT-AND-TFL1 (M

144 feeding with a sucrose, t-cinnamic acid, and gibberellic acid solution; presumably restoring cellular

145 hat was classified as a member of the Snakin/Gibberellic Acid Stimulated in Arabidopsis protein famil

146 Gibberellic Acid Stimulated Transcript (GAST)-like genes

147 psis 10) and the monocot rice (Oryza sativa; Gibberellic Acid Stimulated Transcript-Related 9) sugges

148 gonizing the ability of ABA to down-regulate gibberellic acid-stimulated alpha-amylase production.

149 the dicot Arabidopsis (Arabidopsis thaliana; Gibberellic Acid-Stimulated Arabidopsis 10) and the mono

150 Reversal of the phenotype with exogenous gibberellic acid suggests that NSPHAN, acting via KNOX r

151 s lower in aleurone protoplasts incubated in gibberellic acid than in those incubated in abscisic aci

152 Application of gibberellic acid to glabrous ga1-3 plants consistently i

153 Application of gibberellic acid to WT plants growing in SD conditions a

154 Gibberellic acid treatment stimulates the rate of tensio

155 tion than lecrka4.1-1, while the response to gibberellic acid was not affected in lecrka4.1-1 and lec

156 nt hormones (e.g. ethylene, brassinosteroid, gibberellic acid) were significantly changed in the 35S:

157 sic acid (ABA), which promotes dormancy, and gibberellic acid, which promotes germination.