ライフサイエンスコーパス: gibberellic acid

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

2 e partially reversed with the application of gibberellic acid.

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

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

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

6 elongating in response to applied auxin plus gibberellic acid.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

50 Gibberellic acid (GA) promotes hydrolase production, whe

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

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

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

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

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

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

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

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

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

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

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

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

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

64 Gibberellic acid (GA)-mediated cell expansion initiates

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

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

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

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

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

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

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

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

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

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

75 0-fold or more within 24 h of treatment with gibberellic acid (GA3).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

107 Gibberellic acid signaling, which antagonizes the ABA pa

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

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

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

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

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

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

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

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

116 Gibberellic acid treatment stimulates the rate of tensio

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

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

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