ライフサイエンスコーパス: growth regulator

1 ne by plants, in which it acts as a critical growth regulator.

2 deling factor, and gibberellin (GA), a plant growth regulator.

3 et of rapamycin complex 1 (mTORC1), a master growth regulator.

4 GA3 and that the changes are unique for each growth regulator.

5 otein rendered merlin inactive as a negative growth regulator.

6 that Eif4A could be used as a dose-dependent growth regulator.

7 wth factor-beta (TGF-beta) is a bifunctional growth regulator.

8 t organic plants were less responsive to the growth regulator.

9 gulation of translation in response to a key growth regulator.

10 essors, highlighting its role as a universal growth regulator.

11 target of rapamycin (mTOR) is a central cell growth regulator.

12 nd is now designated icgR, for intracellular growth regulator.

13 onsistent with the role of Mats as a general growth regulator.

14 lls that do not produce these CRS-containing growth regulators.

15 tructural motif present in a large family of growth regulators.

16 the long sought after chalones, or negative growth regulators.

17 trolled by specific actions of extracellular growth regulators.

18 d not be rescued by treatment with exogenous growth regulators.

19 he genes encode members of the CCN family of growth regulators.

20 genes for resistance to this class of insect growth regulators.

21 to regulate the expression of some of these growth regulators.

22 despite the pleiotropic action of most known growth regulators.

23 about the mechanism of action of these plant growth regulators.

24 toplasts in the presence or absence of plant growth regulators.

25 ntially leading to the identification of new growth regulators.

26 haploid embryos in the absence of exogenous growth regulators.

27 ME INTERACTING FACTOR (PIF) family of master growth regulators.

28 l and combined effects of systemic and local growth regulators.

29 uce commercial cultivars by optimizing plant growth regulators.

30 n 6 (IL6), insulin receptor (INSR), neuronal growth regulator 1 (NEGR1), and proopiomelanocortin (POM

31 e candidate gene NEGR1 encoding the neuronal growth regulator 1, also termed neurotractin or Kilon, a

32 moter activity was further enhanced by plant growth regulators, 2,4-dichlorophenoxyacetic acid and be

33 Galectins are potent growth regulators able to bind both glycan and peptide m

34 The plant growth regulator abscisic acid (ABA) is formed by the ox

35 Further, the plant growth regulator abscisic acid (ABA) was able to mimic t

36 position of osmotic stress, and to the plant growth regulator abscisic acid (ABA).

37 permitting transcriptional activation by the growth regulator abscisic acid (ABA).

38 lt in plants that are deficient in the plant growth regulator abscisic acid (ABA).

39 ndicate that zebrafish IGFBP-2 is a negative growth regulator acting downstream in the growth hormone

40 The Hpo pathway consists of several negative growth regulators acting in a kinase cascade that ultima

41 ucan-cellulose interactions or in modulating growth regulator activity.

42 ry following CNS injury by manipulating axon growth regulators alone or in combination with activity-

43 d significantly by the addition of the plant growth regulator alpha-naphthalene acetic acid.

44 Jasmonic acid (JA), a plant growth regulator, also regulates the expression of subse

45 ifies a novel dichotomous role for TLR4 as a growth regulator and a modulator of tumor microenvironme

46 ng growth factor beta (TGF-beta) is a potent growth regulator and tumor suppressor in normal intestin

47 12-oxophytodienoic acid (OPDA) act as plant growth regulators and mediate responses to environmental

48 mouse liver cells, comparing PPs with other growth regulators and tumor promoters of known activity.

49 be induced in vitro by exposing explants to growth regulators and/or stress treatments.

50 senescence is ethylene insensitive and other growth regulators are implicated.

51 A small number of plant growth regulators are involved in the control of cell ex

52 The connections between these growth regulators are still poorly understood although s

53 y altered expression of patterning genes and growth regulators as well as a temporary loss of markers

54 These included several known growth regulators, as well as previously uncharacterized

55 imulus by generating a lateral gradient of a growth regulator at an organ's apex, later found to be a

56 The plant growth regulator auxin has now been shown to be involved

57 ks the quiescent state to high levels of the growth regulator auxin that accumulates in the QC via po

58 ombines with the action of the classic plant growth regulators auxin and cytokinin and with the actio

59 , circadian clock, and response to the plant growth regulators auxin and jasmonic acid.

60 ntegrating the responses of at least 3 major growth regulators (auxin, ethylene, jasmonic acid); (4)

61 icrotubules acting both as stress sensor and growth regulator, channels the growth and shape of the s

62 target of rapamycin (TOR) is a central cell growth regulator conserved from yeast to mammals.

63 ocrine regulation of cell growth mediated by growth regulators containing CRS.

64 allelic variation in the intron of a general growth regulator contributed to the specific reduction o

65 nduction of ethylene production by the plant growth regulator cytokinin, and promoted ACS5 degradatio

66 The growth regulator cytokinin, which also dramatically redu

67 The effect of the growth regulators differed, as alpha-naphthalene acetic

68 Here we examine the role of the growth regulator dMyc in this process during Drosophila

69 it forms a feedback regulatory loop with the growth regulator dMyc to promote cell growth, particular

70 show that local expression of the Drosophila growth regulator dMyc, a homolog of the c-myc protooncog

71 d phosphatase (cPAcP) expression, a negative growth regulator, down-regulated their p66(Shc) protein

72 of imaginal discs via Thor/4E-BP, a negative growth regulator downstream of the insulin/insulin-like

73 ial cells exhibited a broad response to this growth regulator factor depending on whether they were s

74 rCop-1 belongs to an emerging cysteine-rich growth regulator family called CCN, which includes conne

75 -like compounds reveals that members of this growth regulator family may differentially rely on ethyl

76 he angular psoralen angelicin and the insect growth regulator fenoxycarb as activators of the Ultrasp

77 iate the effects of the endothelium-produced growth regulators FGF-2 and TGF-beta1 on retinal pericyt

78 niensis are orthologs of several filamentous growth regulator (FGR) genes that also have suspected ro

79 , suggesting that the NF1 gene is a critical growth regulator for astrocytes.

80 , suggesting that the NF2 gene is a critical growth regulator for Schwann cells.

81 sequences, as well as optimization of plant growth regulators for efficient chloroplast transformati

82 hus, HCMV encodes supportive and suppressive growth regulators for optimizing its replication in huma

83 Jasmonic acid (JA) is a naturally occurring growth regulator found in higher plants.

84 n, designated migR (macrophage intracellular growth regulator; FTL_1542).

85 These include the cell growth regulator gene TGFbetaRII and the proapoptotic ge

86 The plant growth regulator gibberellin (GA) has a profound effect

87 s an enzyme required for biosynthesis of the growth regulator gibberellin (GA), is upregulated in svp

88 ts is promoted in pkl seedlings by the plant growth regulator gibberellin (GA).

89 ld usher in a new generation of agricultural growth regulators, herbicides, or defense compounds.

90 rlin or schwannomin, functions as a negative growth regulator; however, its mechanism of action is no

91 ane is important for merlin to function as a growth regulator; however, the mechanisms by which merli

92 sor protein, merlin, functions as a negative growth regulator; however, the molecular mechanisms that

93 temperature and relative humidity and insect growth regulators (IGRs).

94 trongly suggest that CHK is a novel negative growth regulator in human breast cancer.

95 may be an important transcriptional and cell growth regulator in human colon cancer.

96 ights into the function of protein 4.1B as a growth regulator in meningioma cells.

97 olatile MJ may act as a gaseous messenger or growth regulator in plants.

98 Auxin is a crucial growth regulator in plants.

99 athways of indole-3-acetic acid, the primary growth regulator in plants.

100 It may function as a negative growth regulator in the p53 signal transduction pathway.

101 r matrix production, or in response to other growth regulators in bone.

102 po effector YAP was amongst the top positive growth regulators in both screens.

103 the cadherin family have been implicated as growth regulators in multiple tumor types.

104 Irregularities in the role of opioids as growth regulators in relationship to the more than 500,0

105 two protein 4.1 family members are critical growth regulators in the pathogenesis of meningiomas.

106 BMP-2 and BMP-4 may serve as negative growth regulators in the retina and RPE that are downreg

107 The jasmonate family of growth regulators includes the isoleucine (Ile) conjugat

108 nvironmental cues such as light and internal growth regulators including plant steroid hormones, bras

109 mber of an emerging gene family that encodes growth regulators, including the connective tissue growt

110 e amino acid tryptophan (Trp), including the growth regulator indole-3-acetic acid (IAA) and defense

111 mportant secondary metabolites including the growth regulator indole-3-acetic acid (IAA) and indole g

112 The plant growth regulators indole-butyric acid, 6-benzylaminopuri

113 UVEC contain elevated levels of the negative growth regulator interleukin (IL)-1alpha.

114 s were identified, comprising cell cycle and growth regulators, invasion regulators, signalling and d

115 We have identified p33ING1b, a negative growth regulator involved in the p53 pathway, as a SAP30

116 Auxins are growth regulators involved in virtually all aspects of p

117 The control of cell division by growth regulators is critical to proper shoot and root d

118 trol and "soft" pesticides, including insect growth regulators, is currently under development both i

119 uxins, which are an important class of plant growth regulators, is not known.

120 e was identical to a relatively new class of growth regulators known as granulins, which have tertiar

121 Central to this process are several growth regulators known as plant hormones or phytohormon

122 Recent evidence, however, has suggested that growth regulators may mediate KNOX activity in a variety

123 p27(KIP1) and other growth regulators may selectively suppress the prolifera

124 he Hippo pathway kinase LATS/Warts (Wts) and growth regulator Melted generates mutually exclusive pho

125 ore pathway kinase, which interacts with the growth regulator melted in a double-negative feedback lo

126 inase of the Hippo pathway and the PH-domain growth regulator Melted regulates the choice between 'pa

127 ulate the Hippo pathway kinase Warts and the growth regulator Melted; two opposing factors of a bi-st

128 g pathway, an evolutionarily conserved organ growth regulator, modulate ACD in Drosophila.

129 in, CCI-779, and RAD001) of the pivotal cell growth regulator mTOR.

130 ted with reduced activity of the master cell growth regulator mTORC1.

131 that in the absence of the endogenous muscle growth regulator myostatin, regeneration of muscle is en

132 trongly suggest that CHK is a novel negative growth regulator of HRG-mediated ErbB-2/neu and Src fami

133 k homologous kinase (CHK) acts as a negative growth regulator of human breast cancer through inhibiti

134 atase, is proposed to function as a negative growth regulator of prostate cancer (PCa) cells in part

135 GDF-8 (myostatin) is a negative growth regulator of skeletal muscle, and myostatin-defic

136 ), its predicted ligand, are strong positive growth regulators of the Drosophila melanogaster larval

137 Western blotting of key growth regulators or growth and migratory responses were

138 dopsis thaliana) seedlings without exogenous growth regulators or stress treatments.

139 cription of genes which function as negative growth regulators or tumor suppressors.

140 It depends on the growth regulator p53 and a protein p53 induces, the cycl

141 hat reduced activity of the gibberellin (GA) growth regulator pathway promotes meristematic activity,

142 Ethylene is an important plant growth regulator perceived by membrane-bound ethylene re

143 The residue dynamics of plant growth regulators (PGR) forchlorfenuron (CPPU), 6-benzyl

144 s in the normal prostate indicate that these growth regulators play key roles in prostatic developmen

145 try to downstream calcium-sensitive synaptic growth regulators provides an efficient activity-depende

146 hantia polymorpha LRL gene acts as a general growth regulator required for rhizoid development, a fun

147 Exploration of down-stream growth regulators revealed that loss of beta and gamma,

148 well as the apical localization of root hair growth regulator ROP2 is oscillated in rhd3 Interestingl

149 d by mutations in the gene NF2, encoding the growth regulator schwannomin (also known as merlin).

150 ethylamino)succinamic acid, 160 Da), a plant growth regulator, selectively inhibits the KDM2/7 JmjC s

151 Several growth regulators such as auxins, cytokinins and caroten

152 ne constituents and as precursors to steroid growth regulators such as brassinosteroids.

153 ing may be to oppose the effects of negative growth regulators such as p53.

154 ay also stimulate the expression of positive growth regulators, such as insulin-like growth factor II

155 tion of several important protooncogenes and growth-regulators, such as Myc and FGF-2, can start at C

156 Auxin is a key plant growth regulator that also impacts plant-pathogen intera

157 omplex 1 (mTORC1) protein kinase is a master growth regulator that becomes activated at the lysosome

158 Ethylene is a gaseous plant growth regulator that controls a multitude of developmen

159 Abscisic acid (ABA) is a plant growth regulator that has a potential to increase antiox

160 factor (TGF) beta is a pre-eminent negative growth regulator that has antiproliferative effects on a

161 get of rapamycin (TOR) kinase is a conserved growth regulator that integrates nutrient signals and mo

162 t origin, ethylene evolved into an important growth regulator that is essential for myriad plant deve

163 omplex 1 (mTORC1) protein kinase is a master growth regulator that is stimulated by amino acids.

164 indicate that UCN represents a unique plant growth regulator that maintains planar growth of integum

165 ed by a substantial rise in abscisic acid, a growth regulator that may be an important component of t

166 These studies suggest that TIG3 may be a growth regulator that mediates some of the growth suppre

167 he biosynthesis of ethylene, a gaseous plant growth regulator that plays numerous roles in the growth

168 omplex 1 (mTORC1) protein kinase is a master growth regulator that responds to multiple environmental

169 mTOR complex I (mTORC1) is a central growth regulator that senses amino acids through a pathw

170 The mTORC1 kinase is a master growth regulator that senses many environmental cues, in

171 The mTORC1 kinase is a master growth regulator that senses numerous environmental cues

172 proposed that fw2.2 encodes a negative fruit-growth regulator that underlies natural fruit-size varia

173 Phytohormones are plant growth regulators that are involved in almost every aspe

174 CYR61 is a member of an emerging family of growth regulators that includes the human connective tis

175 Three negative growth regulators, the HMG-CoA reductase inhibitor lovas

176 Compared with other growth regulators, the profile of PP-induced gene expres

177 are regulated by at least two types of cell growth regulators: the retinoblastoma protein family and

178 These genes function as positive growth regulators; the coincidence of high transcript le

179 Type 2C protein phosphatases act as negative growth regulators to restrain growth during drought.

180 Although TORC1 is the more central growth regulator, TORC2 has also been shown to affect ce

181 secreted higher levels of the negative hair growth regulators transforming growth factor beta 1 and

182 ein and exhibits dual ligand (CRS-containing growth regulators (v-sis gene product and insulin-like g

183 The response of the CAt2 gene to plant growth regulators was examined.

184 synergism between the two different types of growth regulators was seen only when both classes of mol

185 By documenting some oncogenic growth regulators, we pave the way for future investigat

186 growth factor-A (VEGF-A) and VEGF-C (cancer growth regulators) were measured after 82 days.

187 ian target of rapamycin (mTOR) is a key cell growth regulator, which forms two distinct functional co

188 atterns-growth" model, a persistently acting growth regulator whose distribution is pre-patterned by

189 Abscisic acid (ABA) is a plant growth regulator with roles in senescence, fruit ripenin

190 propose that SfaD and FadA are both positive growth regulators with partially overlapping functions a

191 ones belong to two distinct classes of plant growth regulators, yet both can promote cell elongation