ライフサイエンスコーパス: aryl hydrocarbon

1 Ligand activation of the aryl hydrocarbon (AHR) has profound effects upon the imm

2 Together with pregnane X (PXR) and aryl hydrocarbon (AHR) receptors, it is referred to as "

3 URI inhibits aryl hydrocarbon (AhR)- and estrogen receptor (ER)-media

4 verse developmental effects of environmental aryl-hydrocarbon exposure.

5 uniquely activated genes associated with the aryl hydrocarbon hydroxylase (Ah) receptor (Cyp1a1, Cyp1

6 odoxin) and ferredoxin reductase showed high aryl hydrocarbon hydroxylase activity.

7 hat HIF-2alpha and its dimerization partner, aryl hydrocarbon nuclear transferase localize to the ROR

8 o the known targets p27 and p57, we identify Aryl hydrocarbon nuclear translocator (Arnt) messenger R

9 ducible factor (HIF)-1alpha, HIF-2alpha, and aryl hydrocarbon nuclear translocator (ARNT).

10 murine models, deletion of the gene encoding aryl hydrocarbon nuclear translocator (ARNT, also known

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

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

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

14 may induce specific modes of action, such as aryl hydrocarbon receptor (AhR) agonism.

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

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

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

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

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

20 The aryl hydrocarbon receptor (AhR) also known as the dioxin

21 coordinate activation or inactivation of the aryl hydrocarbon receptor (AhR) and cyclic adenosine mon

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

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

24 lso resulted in nuclear translocation of the aryl hydrocarbon receptor (AhR) and in phosphorylation o

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

26 (-) immature NK (iNK) cells uniquely express aryl hydrocarbon receptor (AHR) and interleukin-22 (IL-2

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

42 The aryl hydrocarbon receptor (AhR) has become increasingly

43 The aryl hydrocarbon receptor (AhR) has been highlighted as

44 The aryl hydrocarbon receptor (AHR) has been known to cause

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

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

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

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

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

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

51 I3C-dependent activation of the aryl hydrocarbon receptor (AhR) initiates Rbx-1 E3 ligas

52 The aryl hydrocarbon receptor (AHR) is a basic helix-loop-he

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

54 We show here that the aryl hydrocarbon receptor (AhR) is a crucial regulator i

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

71 The aryl hydrocarbon receptor (AhR) is a ligand-dependent, b

72 The aryl hydrocarbon receptor (AhR) is a mediator of xenobio

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

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

75 Aryl hydrocarbon receptor (AhR) is a transcription facto

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

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

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

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

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

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

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

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

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

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

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

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

88 The aryl hydrocarbon receptor (AHR) is partially responsible

89 The aryl hydrocarbon receptor (AhR) is responsible for the t

90 The aryl hydrocarbon receptor (AHR) is the ligand-activated

91 Moreover, in vivo studies in aryl hydrocarbon receptor (AhR) knock-out mice demonstra

92 The aryl hydrocarbon receptor (AhR) knockout mice raised in

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

94 human fibroblasts by a candidate endogenous aryl hydrocarbon receptor (AhR) ligand 2-(1'H-indole-3'-

95 We have characterized previously a class of aryl hydrocarbon receptor (AHR) ligand termed selective

96 esidues involved in Hsp90 binding within the aryl hydrocarbon receptor (AhR) ligand-binding domain an

97 Aryl hydrocarbon receptor (AhR) ligands are important fo

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

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

100 The aryl hydrocarbon receptor (AhR) mediates induction of CY

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

102 expression of IL-22, either by mutating the aryl hydrocarbon receptor (AhR) or inhibiting AhR signal

103 The aryl hydrocarbon receptor (AhR) participates in the diff

104 The ligand-activated transcription factor aryl hydrocarbon receptor (AHR) participates in the diff

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

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

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

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

109 Here, we have shown that the aryl hydrocarbon receptor (Ahr) plays an essential role

110 The aryl hydrocarbon receptor (AHR) plays an essential role

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

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

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

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

115 The aryl hydrocarbon receptor (AHR) recognizes xenobiotics a

116 The transcription factor aryl hydrocarbon receptor (AhR) represents a promising t

117 The aryl hydrocarbon receptor (AHR) repressor (AHRR) inhibit

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

134 ll TCDD toxicities require activation of the aryl hydrocarbon receptor (AHR), a ligand-activated tran

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

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

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

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

139 e show are modified by interactions with the aryl hydrocarbon receptor (AhR), a protein functioning b

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

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

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

143 e Il17 promoter through interaction with the aryl hydrocarbon receptor (Ahr), a transcription factor

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

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

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

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

148 Aryl hydrocarbon receptor (AhR), an important regulator

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

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

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

152 achlorodibenzo-p-dioxin (TCDD), activate the aryl hydrocarbon receptor (AhR), causing it to transloca

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

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

155 ICZ), an enigmatic endogenous ligand for the aryl hydrocarbon receptor (AHR), may explain adverse phy

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

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

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

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

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

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

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

163 at the ligand-activated transcription factor aryl hydrocarbon receptor (AhR), which was induced by IL

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

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

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

167 This difference is due to a BP-selective aryl hydrocarbon receptor (AhR)-mediated recovery.

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

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

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

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

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

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

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

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

176 g tumor growth through the activation of the Aryl hydrocarbon receptor (AhR).

177 contaminants, known as potent ligands of the aryl hydrocarbon receptor (AhR).

178 -inducer (LTi)-like subsets that express the aryl hydrocarbon receptor (AHR).

179 phase I clinical trials, is a ligand of the aryl hydrocarbon receptor (AhR).

180 udies show that SR1 acts by antagonizing the aryl hydrocarbon receptor (AHR).

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

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

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

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

185 esticus) and common tern (Sterna hirundo) to aryl hydrocarbon receptor 1 (AHR1)-dependent changes in

186 HR tomcod exhibited variants in the aryl hydrocarbon receptor 2 (AHR2) that were nearly abse

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

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

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

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

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

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

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

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

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

196 nhibits mouse 3'IghRR activation and induces aryl hydrocarbon receptor binding to dioxin response ele

197 Aryl hydrocarbon receptor blockade prevented differentia

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

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

200 of the ligand-activated transcription factor aryl hydrocarbon receptor by 2-(1'H-indole-3'-carbonyl)-

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

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

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

204 nital amaurosis (LCA) caused by mutations in Aryl hydrocarbon receptor interacting protein like-1 (Ai

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

206 Defects in the photoreceptor-specific gene aryl hydrocarbon receptor interacting protein-like 1 (Ai

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

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

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

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

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

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

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

214 Activated aryl hydrocarbon receptor may interact with latent Epste

215 were reduced by 1,25-D(3), whereas IL-21 and aryl hydrocarbon receptor mRNA remained unchanged.

216 hypoxia-inducible factor 1alpha (HIF1alpha)/aryl hydrocarbon receptor nuclear translocator (ARNT) an

217 rategy that led to the identification of the aryl hydrocarbon receptor nuclear translocator (ARNT) as

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

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

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

221 The aryl hydrocarbon receptor nuclear translocator (ARNT) is

222 The aryl hydrocarbon receptor nuclear translocator (ARNT) is

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

224 The aryl hydrocarbon receptor nuclear translocator (ARNT) se

225 alpha subunit and a constitutively expressed aryl hydrocarbon receptor nuclear translocator (ARNT) su

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

227 unoglobulin heavy chain enhancer 3', and the aryl hydrocarbon receptor nuclear translocator (ARNT), d

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

229 ible factor (HIF) basic helix-loop-helix Per-aryl hydrocarbon receptor nuclear translocator (ARNT)-Si

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

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

232 ) and a constitutively present beta subunit, aryl hydrocarbon receptor nuclear translocator (HIFbeta/

233 cates to the nucleus where it dimerizes with aryl hydrocarbon receptor nuclear translocator and modul

234 ng the core clock component brain and muscle aryl hydrocarbon receptor nuclear translocator like 1 (B

235 ne hepatoma Hepa1c1c7 cells and its AhR- and aryl hydrocarbon receptor nuclear translocator-deficient

236 breaks in AhR-deficient cells compared with aryl hydrocarbon receptor nuclear translocator-deficient

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

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

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

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

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

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

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

244 This effect depended on the aryl hydrocarbon receptor pathway.

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

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

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

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

249 Aryl hydrocarbon receptor signaling is severely impaired

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

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

252 AHRR and CYP1A1 play a key role in the aryl hydrocarbon receptor signaling pathway, which media

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

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

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

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

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

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

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

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

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

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

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

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

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

266 ABCG2 coincided with increased occupancy of aryl hydrocarbon receptor, Sp1, and Nrf2 within the ABCG

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

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

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

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

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

272 by TCDD, and antagonist studies supported an aryl hydrocarbon receptor-dependent activation, which wa

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

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

275 Here we show that homozygous deletion of the aryl hydrocarbon receptor-interacting protein (AIP), a s

276 ar chaperones, including Hsp90, p23, and the aryl hydrocarbon receptor-interacting protein (AIP), als

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

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

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

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

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

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

283 8-tetrachlorodibenzo-p-dioxin (TCDD) via the aryl hydrocarbon receptor.

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

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

286 ry effects of kynurenine are mediated by the aryl hydrocarbon receptor.

287 adhesion kinase (FAK)/RhoA alteration by the aryl-hydrocarbon receptor (AhR) agonist 3-methylcholanth

288 ed single nucleotide polymorphisms (SNPs) in aryl-hydrocarbon receptor (AHR) and cytochrome P450 1A1

289 d in cultured cells following treatment with Aryl-hydrocarbon receptor (Ahr) ligands including the ub

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

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

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

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

294 que for TAA at 1 week (Folh1, Cubn), whereas aryl-hydrocarbon receptor signaling might be important f

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

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

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

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

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

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