ライフサイエンスコーパス: aryl hydrocarbon receptor

1 and that these effects are dependent on the aryl hydrocarbon receptor.

2 m cross-talk between the molecular clock and aryl hydrocarbon receptor.

3 ptophan and salicylate) as activators of the aryl hydrocarbon receptor.

4 8-tetrachlorodibenzo-p-dioxin (TCDD) via the aryl hydrocarbon receptor.

5 is pathway through a noncanonical pathway of aryl hydrocarbon receptor.

6 l microbes and innate lymphoid cells via the aryl hydrocarbon receptor.

7 AhR; Aryl hydrocarbon receptor.

8 n abundance and the enhanced activity of the aryl hydrocarbon receptor.

9 ammatory properties-partly via activation of aryl hydrocarbon receptors.

10 A ligand to the aryl hydrocarbon receptor, 2,3,7,8-tetrachlorodibenzo-p-

11 nhibition of transcriptional activity of the aryl hydrocarbon receptor, a key regulator of ILC3 maint

12 cated within a putative binding site for the aryl hydrocarbon receptor, a master regulator of IL-22 p

13 Accordingly, we show that expression of the aryl hydrocarbon receptor, a transcription factor import

14 TGF-beta1 and aryl hydrocarbon receptor activation enhanced the ERbeta

15 TGF-beta1 as well as aryl hydrocarbon receptor activation was necessary for t

16 y of Il1rl2(-/-) mice could be rescued by an aryl hydrocarbon receptor agonist, which was sufficient

17 stent with their role in detoxification, the aryl hydrocarbon receptor (Ahr) (r(2) = 0.18, p = 0.045

18 gistically elicit allergic inflammation, and aryl hydrocarbon receptor (AhR) activation and signaling

19 Aryl hydrocarbon receptor (AhR) activation by high-affin

20 Aryl hydrocarbon receptor (AhR) activation is reported t

21 Aryl hydrocarbon receptor (AhR) activation was evaluated

22 udies, we found that ZIKV infection triggers aryl hydrocarbon receptor (AHR) activation.

23 is paper deals with the characterization and aryl hydrocarbon receptor (AhR) agonist activities of a

24 il fractions were tested for the presence of aryl hydrocarbon receptor (AhR) agonist and androgen rec

25 induction of CYP450 activity in response to aryl hydrocarbon receptor (AhR) agonist omeprazole and a

26 Rodent cancer bioassays indicate that the aryl hydrocarbon receptor (AHR) agonist, 2,3,7,8-tetrach

27 an photoproduct and endogenous high-affinity aryl hydrocarbon receptor (AhR) agonist, acts as a nanom

28 Recent data define a role for the aryl hydrocarbon receptor (AHR) and diet-derived AHR lig

29 FAs upregulate IL-22 production by promoting aryl hydrocarbon receptor (AhR) and hypoxia-inducible fa

30 s and controlled IL-22 production through an aryl hydrocarbon receptor (AhR) and IL-23 receptor pathw

31 ro research suggests dioxins may bind to the aryl hydrocarbon receptor (AhR) and induce telomerase ac

32 T stimulated the expression of aryl hydrocarbon receptor (AHR) and its interaction with

33 in LKO mice correlated with the elevation of aryl hydrocarbon receptor (AHR) and mediator 1 (MED1), t

34 Activation of aryl hydrocarbon receptor (AhR) and Nrf2-mediated oxidat

35 The aryl hydrocarbon receptor (AhR) and pregnane X receptor

36 ted the ligand-operated transcription factor aryl hydrocarbon receptor (AhR) and the hepatic enzyme t

37 ia the ligand-activated transcription factor aryl hydrocarbon receptor (AHR) and the suppressor of cy

38 ses a small-molecule ligand that targets the aryl hydrocarbon receptor (AhR) and ultimately induces T

39 sion in pDCs, and the effect was reversed by aryl hydrocarbon receptor (AHR) antagonist.

40 In silico pathway evaluation suggested the aryl hydrocarbon receptor (AhR) as one possible target o

41 monocytes underexpressed the IL-1 inhibitor aryl hydrocarbon receptor (AHR) at baseline and accumula

42 The aryl hydrocarbon receptor (AHR) belongs to the PAS (PER-

43 Xenobiotic activation of the aryl hydrocarbon receptor (AHR) by 2,3,7,8-tetrachlorodi

44 Stimulation of the aryl hydrocarbon receptor (AHR) by xenobiotics is known

45 nes and the whole liver established that the aryl hydrocarbon receptor (AhR) can disrupt G1-phase cel

46 Structural features of the aryl hydrocarbon receptor (AHR) can underlie species- an

47 aternal exposure to pollutants that bind the aryl hydrocarbon receptor (AhR) correlates with poorer a

48 es link exposure to pollutants that bind the aryl hydrocarbon receptor (AHR) during development with

49 ression in dendritic cells (DCs), as well as aryl hydrocarbon receptor (AhR) expression by CD4(+) T c

50 CN was shown to be inversely correlated with aryl hydrocarbon receptor (AHR) expression in neuroblast

51 Here we show that the transcription factor aryl hydrocarbon receptor (AHR) functions as a biosensor

52 mozygous mutation (c.1861C>T;p.Q621*) in the aryl hydrocarbon receptor (AHR) gene that perfectly co-s

53 The aryl hydrocarbon receptor (AhR) has become increasingly

54 Aryl hydrocarbon receptor (AhR) has been shown to have p

55 The evolutionarily conserved aryl hydrocarbon receptor (AhR) has been studied for its

56 The aryl hydrocarbon receptor (AhR) has roles in cell prolif

57 Although Th17 cells and the Aryl hydrocarbon receptor (AhR) have been implicated, th

58 TGF-beta signalling and consequently for the aryl hydrocarbon receptor (AhR) in conversion.

59 We identified a higher level of nuclear aryl hydrocarbon receptor (AhR) in LXA4-treated KSHV-inf

60 s study, we revealed a novel function of the aryl hydrocarbon receptor (AhR) in NASH.

61 It also explored the role of aryl hydrocarbon receptor (AhR) in NP's effect.

62 ine produced by glioblastoma cells activates aryl hydrocarbon receptor (AHR) in TAMs to modulate thei

63 stream signaling of the canonical pathway of aryl hydrocarbon receptor (AhR) in vitro, thereby induci

64 e, the ligand-activated transcription factor aryl hydrocarbon receptor (AhR) is a candidate target fo

65 The aryl hydrocarbon receptor (AhR) is a conserved, environm

66 The aryl hydrocarbon receptor (AhR) is a cytoplasmic recepto

67 The aryl hydrocarbon receptor (AhR) is a ligand-activated tr

68 The aryl hydrocarbon receptor (AhR) is a ligand-activated tr

69 The aryl hydrocarbon receptor (AhR) is a ligand-activated tr

70 Aryl hydrocarbon receptor (AHR) is a ligand-activated tr

71 The aryl hydrocarbon receptor (AhR) is a ligand-activated tr

72 The aryl hydrocarbon receptor (AhR) is a ligand-activated tr

73 The Aryl hydrocarbon receptor (AHR) is a ligand-activated tr

74 The aryl hydrocarbon receptor (AhR) is a ligand-activated tr

75 The aryl hydrocarbon receptor (Ahr) is a ligand-activated tr

76 The aryl hydrocarbon receptor (AHR) is a ligand-activated tr

77 The aryl hydrocarbon receptor (AHR) is a ligand-activated tr

78 The aryl hydrocarbon receptor (AhR) is a ligand-dependent tr

79 The aryl hydrocarbon receptor (AHR) is a ligand-dependent tr

80 The aryl hydrocarbon receptor (AhR) is a nuclear receptor th

81 The aryl hydrocarbon receptor (AhR) is a signal-regulated tr

82 cs and phenotypic profiling we show that the aryl hydrocarbon receptor (AhR) is a target of ezutromid

83 The Aryl hydrocarbon Receptor (AhR) is a transcription facto

84 The aryl hydrocarbon receptor (AhR) is a transcription facto

85 Aryl hydrocarbon receptor (AhR) is a transcription facto

86 Here, we show that the aryl hydrocarbon receptor (AhR) is activated in cells in

87 The Aryl hydrocarbon receptor (AHR) is an environment-sensin

88 The aryl hydrocarbon receptor (AhR) is an environment-sensin

89 The aryl hydrocarbon receptor (AHR) is an important regulato

90 The aryl hydrocarbon receptor (AhR) is an intracellular rece

91 The aryl hydrocarbon receptor (AHR) is critically involved i

92 Aryl hydrocarbon receptor (Ahr) is crucial for the maint

93 The aryl hydrocarbon receptor (AHR) is emerging as a pleiotr

94 The aryl hydrocarbon receptor (AHR) is expressed by immune c

95 y, we show that an environmental sensor, the aryl hydrocarbon receptor (AhR) is highly induced upon B

96 The aryl hydrocarbon receptor (AhR) is involved in the regul

97 We have demonstrated that aryl hydrocarbon receptor (AhR) is overexpressed in lung

98 l exposure to contaminants that activate the aryl hydrocarbon receptor (AHR) lead to suppression of i

99 The prototypical aryl hydrocarbon receptor (AHR) ligand, 2,3,7,8-Tetrachl

100 ,2-b]carbazole (FICZ), a naturally-occurring aryl hydrocarbon receptor (AhR) ligand, allowed its biol

101 Aryl hydrocarbon receptor (AhR) ligands are important fo

102 icrobiota-derived metabolites, especially in aryl hydrocarbon receptor (AhR) ligands, bile acids and

103 lize tryptophan into metabolites that act as aryl hydrocarbon receptor (AHR) ligands.

104 els are decreased in mice fed a diet free of aryl hydrocarbon receptor (AhR) ligands.

105 udies have shown that the toxicant-activated aryl hydrocarbon receptor (AHR) may disrupt fat metaboli

106 The aryl hydrocarbon receptor (AHR) mediates the toxic effec

107 d on a few biological pathways, for example, aryl hydrocarbon receptor (AhR) or estrogen receptor (ER

108 diates its effects via the activation of the aryl hydrocarbon receptor (AhR) pathway and the subseque

109 We identified the aryl hydrocarbon receptor (AHR) pathway as a potent tumo

110 e expression data revealed activation of the aryl hydrocarbon receptor (AhR) pathway in laquinimod-tr

111 athway was significantly upregulated and the aryl hydrocarbon receptor (AhR) pathway was significantl

112 acco smoke contains numerous agonists of the aryl hydrocarbon receptor (AhR) pathway, and activation

113 sistance is linked to down regulation of the aryl hydrocarbon receptor (AHR) pathway.

114 The aryl hydrocarbon receptor (AHR) plays an important physi

115 The endogenous ligand-activated aryl hydrocarbon receptor (AHR) plays an important role

116 The aryl hydrocarbon receptor (AhR) plays an important role

117 The aryl hydrocarbon receptor (AHR) plays crucial roles in i

118 Activation of the aryl hydrocarbon receptor (AHR) promoted mo-DC different

119 The aryl hydrocarbon receptor (AHR) recognizes xenobiotics a

120 The aryl hydrocarbon receptor (AhR) represents an environmen

121 While repression of aryl hydrocarbon receptor (AHR) signaling has been shown

122 TGF-beta signaling pathway is influenced by aryl hydrocarbon receptor (AHR) signaling pathways.

123 eceptor repressor (AhRR) is known to repress aryl hydrocarbon receptor (AhR) signaling, but very litt

124 of IL-23, IL-22 production is independent of aryl hydrocarbon receptor (AhR) signaling.

125 d negatively correlates with inducibility of aryl hydrocarbon receptor (AHR) signaling.

126 These metabolites are ligands of aryl hydrocarbon receptor (AHR) signaling.

127 tions, we show that MSI2 directly attenuates aryl hydrocarbon receptor (AHR) signalling through post-

128 xia inducible factor-1alpha (HIF1-alpha) and aryl hydrocarbon receptor (AHR) supports the differentia

129 ammatory M-MO, upregulates the expression of aryl hydrocarbon receptor (AhR) target genes, and stimul

130 e a pattern of regulation in the host by the aryl hydrocarbon receptor (AhR) that is critically depen

131 we used lentivirus-mediated knockdown of the aryl hydrocarbon receptor (AHR) to demonstrate that 1023

132 th the ligand-activated transcription factor aryl hydrocarbon receptor (AHR) to drive the generation

133 orodibenzo-p-dioxin (TCDD) interact with the aryl hydrocarbon receptor (Ahr) to induce osteoclastic b

134 the therapeutic potential of activating the aryl hydrocarbon receptor (AHR) to limit ECM accumulatio

135 t loss, liberated PCBs act as ligands of the aryl hydrocarbon receptor (AhR) to negatively influence

136 y, StemRegenin 1 (SR1), an antagonist of the aryl hydrocarbon receptor (AhR) transcription factor kno

137 rrepresentation of cognate sequences for the aryl hydrocarbon receptor (AhR) transcription factor, wh

138 promote NK cell IL-10, and activation of the aryl hydrocarbon receptor (AHR) was also required for ma

139 These metabolites are ligands of the aryl hydrocarbon receptor (AhR)(6), and AhR-mediated sig

140 ealthspan in worms and flies depend upon the aryl hydrocarbon receptor (AHR), a conserved detector of

141 cities require binding and activation of the aryl hydrocarbon receptor (AhR), a ligand activated tran

142 TCDD is a potent activator of the aryl hydrocarbon receptor (AHR), a ligand activated tran

143 The aryl hydrocarbon receptor (AhR), a ligand-activated memb

144 the modulation of the immune response by the aryl hydrocarbon receptor (AhR), a ligand-activated tran

145 The aryl hydrocarbon receptor (AhR), a ligand-activated tran

146 The aryl hydrocarbon receptor (AhR), a ligand-activated tran

147 or Gb3 synthesis, and it also identified the aryl hydrocarbon receptor (AHR), a ligand-activated tran

148 Interestingly, the aryl hydrocarbon receptor (AhR), a ligand-dependent tran

149 lecular weight PAHs are known ligands of the aryl hydrocarbon receptor (AhR), a nuclear receptor that

150 ly polar structure, kynurenine activates the aryl hydrocarbon receptor (AHR), a PER, ARNT, SIM (PAS)

151 The aryl hydrocarbon receptor (AhR), a regulator of xenobiot

152 Here we show that the aryl hydrocarbon receptor (AhR), a transcription factor

153 -derived metabolites that signal through the aryl hydrocarbon receptor (AHR), a transcription factor

154 The aryl hydrocarbon receptor (AhR), a transcription factor

155 We propose that the aryl hydrocarbon receptor (AhR), a unique chemical senso

156 y, bioassays indicative of activation of the aryl hydrocarbon receptor (AhR), activation of the pregn

157 The aryl hydrocarbon receptor (AHR), also known as the dioxi

158 DO2 in TNBC cells was sufficient to activate aryl hydrocarbon receptor (AhR), an endogenous kynurenin

159 Aryl hydrocarbon receptor (AhR), an important regulator

160 amely, the pregnane X receptor (PXR) and the aryl hydrocarbon receptor (AhR), and itsinteractions wit

161 tors constitutive androstane receptor (CAR), aryl hydrocarbon receptor (AhR), and Nrf2.

162 nes represent known ligands of the mammalian aryl hydrocarbon receptor (AHR), and UPEC infection of A

163 Dioxin exposure, acting through the aryl hydrocarbon receptor (AHR), blocked eyelid closure

164 The aryl hydrocarbon receptor (AhR), for many years almost e

165 cript levels of five gene targets, including aryl hydrocarbon receptor (Ahr), interleukin-1 beta (Il1

166 to compare relative risks of activating the aryl hydrocarbon receptor (AhR), nuclear factor erythroi

167 ntrols, we found that coal tar activated the aryl hydrocarbon receptor (AHR), resulting in induction

168 and the anti-lipogenic transcription factor aryl hydrocarbon receptor (Ahr), the latter of which we

169 Because IS is an agonist of the aryl hydrocarbon receptor (AHR), we first examined the r

170 is the ligand-activated transcription factor aryl hydrocarbon receptor (AhR), which binds TB virulenc

171 -induced Jag1 expression was mediated by the aryl hydrocarbon receptor (AhR), which bound to and acti

172 The aryl hydrocarbon receptor (AHR), which has been central

173 primarily depend on its ability to activate aryl hydrocarbon receptor (AhR), which is a ligand-depen

174 their toxic action through activation of the aryl hydrocarbon receptor (AhR), which is believed to re

175 te, are agonists of the transcription factor aryl hydrocarbon receptor (AhR), which is widely express

176 heir barrier functions through activation of aryl hydrocarbon receptor (AhR)- nuclear factor erythroi

177 sed in vitro and in vivo studies to quantify aryl hydrocarbon receptor (AhR)-dependent effects of PCB

178 uction of anti-inflammatory cytokines via an aryl hydrocarbon receptor (AhR)-dependent mechanism.

179 r findings uncover an activin-A-induced IRF4-aryl hydrocarbon receptor (AhR)-dependent transcriptiona

180 All extracts induced aryl hydrocarbon receptor (Ahr)-regulated mRNAs, malform

181 Aryl hydrocarbon receptor (AhR)-related CYP1A4 mRNA leve

182 roduction in murine T cells through inducing aryl hydrocarbon receptor (AhR)-retinoic acid receptor-r

183 this induction was abrogated by CH223191, an aryl hydrocarbon receptor (AhR)-specific antagonist.

184 narof are mediated through activation of the aryl hydrocarbon receptor (AhR).

185 its hepatotoxicity through activation of the aryl hydrocarbon receptor (AhR).

186 mediated primarily through activation of the aryl hydrocarbon receptor (AHR).

187 insults and express the transcription factor aryl hydrocarbon receptor (AhR).

188 ynurenine pathway, producing ligands for the aryl hydrocarbon receptor (AHR).

189 r adverse outcomes through activation of the aryl hydrocarbon receptor (AhR).

190 e il22 promoter and its interaction with the aryl hydrocarbon receptor (AhR).

191 12 and FA function as natural antagonists of aryl hydrocarbon receptor (AhR).

192 ar translocation of the transcription factor aryl hydrocarbon receptor (AHR).

193 ion and activity of the transcription factor aryl hydrocarbon receptor (AhR).

194 s in vitro and in vivo, which is mediated by aryl hydrocarbon receptor (AhR).

195 onmental contaminant, is a potent ligand for aryl hydrocarbon receptor (AhR).

196 kin homeostasis is largely controlled by the aryl hydrocarbon receptor (AhR).

197 ls, IAA activated an inflammatory nongenomic aryl hydrocarbon receptor (AhR)/p38MAPK/NF-kappaB pathwa

198 ently been shown to be endogenous ligands of aryl hydrocarbon receptor (AhR; a unique cellular chemic

199 forms together with the transcription factor aryl-hydrocarbon receptor (AhR), compared to unprimed co

200 pothesis that coplanar PCBs act at adipocyte aryl hydrocarbon receptors (AhRs) to promote adipose inf

201 netic and functional similarities in species aryl hydrocarbon receptors (AHRs), which mediate DLC sen

202 Mechanistically, the aryl hydrocarbon receptor, along with STAT3 and c-Maf, a

203 ould parallel that in other clients like the aryl hydrocarbon receptor and HIF1alpha, which also inte

204 hobicity in two bioassays, indicative of the aryl hydrocarbon receptor and oxidative stress response

205 es known to be specifically regulated by the aryl hydrocarbon receptor and oxidative stress.

206 ghly expressed CD90 ( approximately 63%) and aryl hydrocarbon receptor and produced IL-17 ( approxima

207 ed in this process through activation of the aryl hydrocarbon receptor and subsequent mitochondrial r

208 te the ligand-activated transcription factor aryl hydrocarbon receptor and, consequently, antiinflamm

209 leotide-polymorphisms and upon activation of aryl-hydrocarbon-receptor and oxygen-mediated pathways.

210 particulate matter caused activation of the aryl hydrocarbon receptor, and phosphorylation of histon

211 SIRT1 also promotes activation of the aryl hydrocarbon receptor, and the aryl hydrocarbon rece

212 on the ligand-activated transcription factor aryl hydrocarbon receptor, and the third on how docosano

213 associated with increased transcription from aryl hydrocarbon receptor- and oxidative stress-regulate

214 drocarbon receptor signaling pathway, as the aryl hydrocarbon receptor antagonist GNF-351 modified ap

215 ility and safety of StemRegenin-1 (SR-1), an aryl hydrocarbon receptor antagonist that expands CD34+

216 ve and tolerant populations, we identify the aryl hydrocarbon receptor-based signaling pathway as a s

217 Four CpGs border sequences carrying aryl hydrocarbon receptor binding sites and enhancer-spe

218 Aryl hydrocarbon receptor blockade prevented differentia

219 Both depend on RORgammat and aryl hydrocarbon receptor, but NKp46(+)ILC3s also requir

220 nduces the expression of CYP2E1, CYP1A2, and aryl hydrocarbon receptor, but not of CYP3A4, hepatocyte

221 ound mutations further demonstrated that the aryl hydrocarbon receptor, but not RORgammat, was requir

222 ted with increased levels of MUC2, LYZ1, and aryl hydrocarbon receptor, but reduced levels of SLC2A5.

223 Effects of developmental activation of the aryl hydrocarbon receptor by 2,3,7,8-tetrachlorodibenzo-

224 Activation of the transcription factor aryl hydrocarbon receptor by 2,3,7,8-tetrachlorodibenzo-

225 ndogenous ligand of the transcription factor aryl hydrocarbon receptor, could change the expression o

226 he group 3 innate lymphoid cell (ILC3) in an aryl hydrocarbon receptor dependent manner.

227 that IL-23-mediated restoration of IL-22 is aryl hydrocarbon receptor dependent, whereas IL-17 requi

228 s close homolog Cyp1a1 was upregulated in an aryl hydrocarbon receptor-dependent manner, hence indica

229 ugh reactive oxygen species production in an aryl hydrocarbon receptor-dependent mechanism.

230 The transcription factor AHR (aryl hydrocarbon receptor) drives the expression of gene

231 , which, along with the environmental sensor aryl hydrocarbon receptor, forms a multipartite transcri

232 ted to xenobiotic metabolism (pregnane X and aryl hydrocarbon receptors), hormone-mediated modes of a

233 derivatives of tryptophan that activated the aryl-hydrocarbon receptor in CD4(+) T cells, allowing Th

234 ly increase cellular viability, activate the aryl hydrocarbon receptor, increase double-strand DNA br

235 The pattern of PER-, BMAL-, and aryl hydrocarbon receptor-induced P450 gene expression a

236 hen PP cells were treated with CH-223191, an aryl hydrocarbon receptor inhibitor.

237 The molecular mechanisms leading to aryl hydrocarbon receptor interacting protein (AIP) muta

238 Here, we have identified AIP (aryl hydrocarbon receptor interacting protein) as a new

239 lic mutations in the photoreceptor-expressed aryl hydrocarbon receptor interacting protein-like 1 (AI

240 Mutant P351Delta12 human isoform, aryl hydrocarbon receptor interacting protein-like 1 (hA

241 of P351Delta12 hAIPL1 and the mouse isoform, aryl hydrocarbon receptor interacting protein-like 1 (mA

242 Defects in aryl hydrocarbon receptor interacting protein-like1 (AIP

243 Aryl hydrocarbon receptor-interacting protein (AIP) muta

244 , a genome-wide CRISPR screen identified the aryl hydrocarbon receptor-interacting protein (AIP), a c

245 Aryl hydrocarbon receptor-interacting protein-like 1 (AI

246 Aryl hydrocarbon receptor-interacting protein-like 1 (AI

247 Aryl hydrocarbon receptor-interacting protein-like 1 (AI

248 of PDE6 relies on the chaperone activity of aryl hydrocarbon receptor-interacting protein-like 1 (AI

249 ations in either the enzyme itself or AIPL1 (aryl hydrocarbon receptor-interacting protein-like 1), l

250 erogenic molecule (ligand for the endogenous aryl-hydrocarbon receptor; ITE) were injected i.p. four

251 ith other PDE4 inhibitors, an agonist of the aryl hydrocarbon receptor, Janus kinase inhibitors, and

252 on of the aryl hydrocarbon receptor, and the aryl hydrocarbon receptor ligand restores FLG expression

253 inarof, a bacteria-derived polyphenol, is an aryl hydrocarbon receptor ligand that attenuated inflamm

254 ct 6-formylindolo[3,2-b]carbazole (FICZ), an aryl hydrocarbon receptor ligand, has been found to be a

255 Activated aryl hydrocarbon receptor may interact with latent Epste

256 llowed the ranking of wetland sites based on aryl hydrocarbon receptor-mediated end points; EROD acti

257 lonies based on the efficacy of eliciting an aryl hydrocarbon receptor-mediated response.

258 ve model was applied to predict variation of aryl hydrocarbon receptor-mediated toxic potencies among

259 We postulate a hypothesis where the AhR (aryl hydrocarbon receptor) mediates aberrant cell growth

260 AHR and its heterodimerization partner aryl hydrocarbon receptor nuclear translocator (ARNT) be

261 eted the HIF-alpha dimerization partner, the aryl hydrocarbon receptor nuclear translocator (ARNT) in

262 We demonstrate that the expression of aryl hydrocarbon receptor nuclear translocator (ARNT) is

263 Our data suggest that aryl hydrocarbon receptor nuclear translocator (ARNT) pl

264 hypoxia-inducible factor complex (HIF-alpha.aryl hydrocarbon receptor nuclear translocator (ARNT)) r

265 The expression of aryl hydrocarbon receptor nuclear translocator (ARNT), a

266 and NPAS3 must each heterodimerize with the aryl hydrocarbon receptor nuclear translocator (ARNT), t

267 and a constitutively expressed beta subunit, aryl hydrocarbon receptor nuclear translocator (ARNT).

268 With hypoxia, the stabilized HIF-alpha and aryl hydrocarbon receptor nuclear translocator (ARNT, al

269 d the transport of two transcription factors-aryl hydrocarbon receptor nuclear translocator and sine

270 he circadian clock transcriptional activator aryl hydrocarbon receptor nuclear translocator-like (Bma

271 f circadian clock transcriptional activators aryl hydrocarbon receptor nuclear translocator-like (Bma

272 The circadian rhythm-related aryl hydrocarbon receptor nuclear translocator-like 2 (A

273 The brain and muscle aryl hydrocarbon receptor nuclear translocator-like prot

274 rcadian reporter construct [brain and muscle aryl hydrocarbon receptor nuclear translocator-like:luci

275 ptional factor BMAL1 (brain and muscle ARNT [aryl hydrocarbon receptor nuclear translocator]-like pro

276 pted to manipulate the expressions of FLRL2, aryl-hydrocarbon receptor nuclear translocator-like (Arn

277 etabolic enzyme activity, likely through the aryl hydrocarbon receptor pathway, and generation of rea

278 hanced by IL-21 expression through the c-Maf/aryl hydrocarbon receptor pathway, independent of APCs.

279 This effect depended on the aryl hydrocarbon receptor pathway.

280 n Hepa-1 cells but not for expression of the aryl hydrocarbon receptor protein.

281 Transgenic overexpression of aryl hydrocarbon receptor repressor (AhRR) and AhR-media

282 The aryl hydrocarbon receptor repressor (AhRR) is known to r

283 okers, including an intragenic region of the aryl hydrocarbon receptor repressor gene (AHRR; cg055759

284 prominent example is hypomethylation of the aryl hydrocarbon-receptor repressor (AHRR) locus, which

285 Four CpG sites within the aryl-hydrocarbon receptor repressor (AHRR) associate wit

286 ng heaviness and also DNA methylation at the aryl-hydrocarbon receptor repressor (AHRR) locus, but we

287 questionnaires as well as DNA methylation in aryl-hydrocarbon receptor repressor (AHRR), a sentinel e

288 (LIMR), enhanced the interaction of LIMR and aryl-hydrocarbon receptor repressor (AHRR), and promoted

289 We further found the aryl hydrocarbon receptor signaling pathway plays an imp

290 e to PPIs was partially mediated through the aryl hydrocarbon receptor signaling pathway, as the aryl

291 of immunology, presenting information on the aryl hydrocarbon receptor signaling pathway, the immunom

292 antigen-specific TH22 cells is dependent on aryl hydrocarbon receptor signaling.

293 sporadic differentiation through xenobiotic aryl hydrocarbon receptor signaling.

294 h were associated with gene dysregulation in aryl hydrocarbon receptor, stress-response, and thyroid

295 transcription 3 and the cell cycle regulator aryl hydrocarbon receptor, the data suggest a disturbed

296 ferentiation, indole acts via the xenobiotic aryl hydrocarbon receptor to increase expression of the

297 IDO1 interacted non-enzymatically with the aryl hydrocarbon receptor to inhibit activation of NOTCH

298 ese regulatory factors, we identify AHR, the aryl hydrocarbon-receptor which controls a healthy immun

299 totype, is independent of suppression of the aryl hydrocarbon receptor, which targets cells with more

300 l for Th9, via suppressing the expression of aryl hydrocarbon receptor, without an increase in IL-10.