ライフサイエンスコーパス: growth regulator

1 pha-cypermethrin and pyriproxyfen (an insect growth regulator).

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

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

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

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

6 otein rendered merlin inactive as a negative growth regulator.

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

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

9 RXC9 as the candidate stress resilience root growth regulator.

10 19 insecticides, 17 fungicides, and a plant growth regulator.

11 Auxin is a crucial plant growth regulator.

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

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

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

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

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

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

18 ated peptidases destabilize various positive growth regulators.

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

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

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

22 trolled by specific actions of extracellular growth regulators.

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

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

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

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

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

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

29 iation study among DEGs to identify key leaf growth regulators.

30 ntially leading to the identification of new growth regulators.

31 timations, and management decisions of plant growth regulators.

32 g, grapevine producers apply different plant growth regulators.

33 er 2 weeks, revealing known and unknown root growth regulators.

34 in and its capacity to produce alkaloids and growth regulators.

35 despite the pleiotropic action of most known growth regulators.

36 voidance and interacts with several negative growth regulators.

37 haploid embryos in the absence of exogenous growth regulators.

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

39 ivate defence responses are photomorphogenic growth regulators.

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

41 uce commercial cultivars by optimizing plant growth regulators.

42 Neuronal growth regulator 1 (NEGR1) and neurotrimin (NTM) are abu

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

44 nt T2D (P < 1.25 x 10-3), including neuronal growth regulator 1 (NeGR1; hazard ratio per SD 0.85; P =

45 Supplementation of neuronal growth regulator 1 reverses this neurodegenerative effec

46 g cell populations, including NEGR (neuronal growth regulator 1) and NRNX (neurexin) pathways.

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

48 ice, that show reduced secretion of neuronal growth regulator 1.

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

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

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

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

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

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

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

56 Thus, GT1 and VRS1 maintain their potency as growth regulators across vast timescales and in distinct

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

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

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

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

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

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

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

64 conserved and unique nature of this critical growth regulator and its role in multiple aspects of pla

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

66 Auxin and brassinosteroids (BR) are crucial growth regulators and display overlapping functions duri

67 12-oxophytodienoic acid (OPDA) act as plant growth regulators and mediate responses to environmental

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

69 ticides, fungicides, herbicides, acaricides, growth regulators and veterinary drugs in honey samples.

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

71 evated temperature in conjunction with plant growth regulator application.

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

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

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

75 One way to achieve this is by using plant growth regulators as a tool for plant growth management.

76 re obtained by utilizing components of these growth regulators as markers for genetic lineage tracing

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

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

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

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

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

82 eds back on a polar transport network of the growth regulator auxin.

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

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

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

86 seven biorational insecticides [five insect growth regulators (Buprofezin, Fenoxycarb, Pyriproxyfen,

87 We formulate how growth regulators can be used to control the formation o

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

89 alian target of rapamycin) is a central cell growth regulator connecting cellular metabolism and grow

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

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

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

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

94 The growth regulator cytokinin, which also dramatically redu

95 nation and proteasomal degradation of master growth regulators-DELLA proteins-mediated by the SCF(SLY

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

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

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

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

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

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

102 females, protein and gene expression of cell growth regulators, e.g. p15 and p21, which inhibit cell

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

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

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

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

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

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

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

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

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

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

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

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

115 phyllotaxy, implicating PP2C phosphatases as growth regulators functioning under favorable conditions

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

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

118 Involvement of the growth regulator gibberellin (GA) in the control of flow

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

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

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

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

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

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

125 d candidate chemical insecticides and insect growth regulator (IGR) can be used for indoor residual s

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

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

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

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

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

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

132 Auxin is a crucial growth regulator in plants.

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

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

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

136 ssinosteroids (BRs) are widely used as plant growth regulators in modern agriculture.

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

138 en Revolution genes, encode conserved master growth regulators in plants.

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

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

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

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

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

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

145 reatment with elevated temperature and plant growth regulators increased UPR activation, as assessed

146 ora of abiotic and biotic stresses and plant growth regulators indicating a complex regulatory networ

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

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

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

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

151 However, many common growth regulators intervene in both situations.

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

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

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

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

156 pamycin (TOR) kinase, a widely conserved pro-growth regulator, is hyperactive, and that, unlike cell

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

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

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

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

161 Insect growth regulators, like S-methoprene, are heavily relied

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

163 is increasing evidence that commercial plant growth regulators may protect against abiotic stressors

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

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

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

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

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

169 thways ), as well as pyriproxyfen (an insect growth regulator mimicking an insect juvenile hormone wh

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

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

172 Inhibition of the master growth regulator mTORC1 (mechanistic target of rapamycin

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

174 Cholesterol activates the master growth regulator, mTORC1 kinase, by promoting its recrui

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

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

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

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

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

180 Changing the concentration of plant growth regulator of the initiation medium did not signif

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

182 k was to evaluate the influence of different growth regulators on the mineral and total phenolic cont

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

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

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

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

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

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

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

190 wth promoting rhizobacteria (PGPR) and plant growth regulators (PGRs) can be applied to improve the g

191 tors via rhythmic transcription of the nodal growth regulators, PHYTOCHROME-INTERACTING FACTORs (PIFs

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

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

194 chlorfenapyr and clothianidin) and an insect growth regulator ( Pyriproxyfen) resulted in complete ov

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

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

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

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

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

200 Several growth regulators such as auxins, cytokinins and caroten

201 o found a differential accumulation of other growth regulators such as brassinosteroids, cytokinin, m

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

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

204 activity controls the abundance of hypocotyl growth regulators, such as DWF1, through ubiquitin-media

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

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

207 nal nutrient stores with reactivation of the growth regulator target of rapamycin complex 1 (TORC1).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

227 DELLA proteins are conserved master growth regulators that play a central role in controllin

228 olesterol-dependent activation of the master growth regulator, the protein kinase mechanistic target

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

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

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

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

233 The intrinsic axonal growth regulators, their interaction and roles that enab

234 By functionally connecting two essential growth regulators, these results underpin a novel and cr

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

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

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

238 We propose that plant growth regulator treatment induces bZIP60 mRNA splicing

239 pressed in poplar to test its potential as a growth regulator under non-stress conditions.

240 itans as carriers of pyriproxyfen, an insect growth regulator, under semi-field conditions in three d

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

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

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

244 Unexpectedly, SOX9, a hair follicle growth regulator, was aberrantly expressed throughout th

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

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

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

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

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

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

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