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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 s (cytotoxicity; activation of the estrogen, aryl hydrocarbon, and peroxisome proliferator-activated
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                The retina-specific chaperone aryl hydrocarbon interacting protein-like 1 (AIPL1) is e
8 o the known targets p27 and p57, we identify Aryl hydrocarbon nuclear translocator (Arnt) messenger R
9 murine models, deletion of the gene encoding aryl hydrocarbon nuclear translocator (ARNT, also known
10 ms of B12/FA deficiency and cotreatment with aryl hydrocarbon portions of B12/FA rescued mice from th
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                                              Aryl hydrocarbon receptor (AhR) activation is reported t
15                                              Aryl hydrocarbon receptor (AhR) activation was evaluated
16 udies, we found that ZIKV infection triggers aryl hydrocarbon receptor (AHR) activation.
17 is paper deals with the characterization and aryl hydrocarbon receptor (AhR) agonist activities of a
18 il fractions were tested for the presence of aryl hydrocarbon receptor (AhR) agonist and androgen rec
19  induction of CYP450 activity in response to aryl hydrocarbon receptor (AhR) agonist omeprazole and a
20    Rodent cancer bioassays indicate that the aryl hydrocarbon receptor (AHR) agonist, 2,3,7,8-tetrach
21 an photoproduct and endogenous high-affinity aryl hydrocarbon receptor (AhR) agonist, acts as a nanom
22            Recent data define a role for the aryl hydrocarbon receptor (AHR) and diet-derived AHR lig
23 FAs upregulate IL-22 production by promoting aryl hydrocarbon receptor (AhR) and hypoxia-inducible fa
24 s and controlled IL-22 production through an aryl hydrocarbon receptor (AhR) and IL-23 receptor pathw
25 ro research suggests dioxins may bind to the aryl hydrocarbon receptor (AhR) and induce telomerase ac
26 in LKO mice correlated with the elevation of aryl hydrocarbon receptor (AHR) and mediator 1 (MED1), t
27                                Activation of aryl hydrocarbon receptor (AhR) and Nrf2-mediated oxidat
28                                          The aryl hydrocarbon receptor (AhR) and pregnane X receptor
29 ted the ligand-operated transcription factor aryl hydrocarbon receptor (AhR) and the hepatic enzyme t
30 ia the ligand-activated transcription factor aryl hydrocarbon receptor (AHR) and the suppressor of cy
31 ses a small-molecule ligand that targets the aryl hydrocarbon receptor (AhR) and ultimately induces T
32 sion in pDCs, and the effect was reversed by aryl hydrocarbon receptor (AHR) antagonist.
33  monocytes underexpressed the IL-1 inhibitor aryl hydrocarbon receptor (AHR) at baseline and accumula
34                                          The aryl hydrocarbon receptor (AHR) belongs to the PAS (PER-
35                 Xenobiotic activation of the aryl hydrocarbon receptor (AHR) by 2,3,7,8-tetrachlorodi
36                           Stimulation of the aryl hydrocarbon receptor (AHR) by xenobiotics is known
37 nes and the whole liver established that the aryl hydrocarbon receptor (AhR) can disrupt G1-phase cel
38                   Structural features of the aryl hydrocarbon receptor (AHR) can underlie species- an
39 aternal exposure to pollutants that bind the aryl hydrocarbon receptor (AhR) correlates with poorer a
40 es link exposure to pollutants that bind the aryl hydrocarbon receptor (AHR) during development with
41 ression in dendritic cells (DCs), as well as aryl hydrocarbon receptor (AhR) expression by CD4(+) T c
42 CN was shown to be inversely correlated with aryl hydrocarbon receptor (AHR) expression in neuroblast
43   Here we show that the transcription factor aryl hydrocarbon receptor (AHR) functions as a biosensor
44 mozygous mutation (c.1861C>T;p.Q621*) in the aryl hydrocarbon receptor (AHR) gene that perfectly co-s
45                                          The aryl hydrocarbon receptor (AhR) has become increasingly
46                                              Aryl hydrocarbon receptor (AhR) has been shown to have p
47                 The evolutionarily conserved aryl hydrocarbon receptor (AhR) has been studied for its
48                                          The aryl hydrocarbon receptor (AhR) has roles in cell prolif
49                  Although Th17 cells and the Aryl hydrocarbon receptor (AhR) have been implicated, th
50 TGF-beta signalling and consequently for the aryl hydrocarbon receptor (AhR) in conversion.
51      We identified a higher level of nuclear aryl hydrocarbon receptor (AhR) in LXA4-treated KSHV-inf
52 s study, we revealed a novel function of the aryl hydrocarbon receptor (AhR) in NASH.
53                 It also explored the role of aryl hydrocarbon receptor (AhR) in NP's effect.
54 ine produced by glioblastoma cells activates aryl hydrocarbon receptor (AHR) in TAMs to modulate thei
55 stream signaling of the canonical pathway of aryl hydrocarbon receptor (AhR) in vitro, thereby induci
56 e, the ligand-activated transcription factor aryl hydrocarbon receptor (AhR) is a candidate target fo
57                                          The aryl hydrocarbon receptor (AhR) is a conserved, environm
58                                          The aryl hydrocarbon receptor (AhR) is a cytoplasmic recepto
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                                              Aryl hydrocarbon receptor (AHR) is a ligand-activated tr
63                                          The 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-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                                          The aryl hydrocarbon receptor (AhR) is a ligand-dependent tr
71                                          The aryl hydrocarbon receptor (AHR) is a ligand-dependent tr
72                                          The aryl hydrocarbon receptor (AhR) is a nuclear receptor th
73 cs and phenotypic profiling we show that the aryl hydrocarbon receptor (AhR) is a target of ezutromid
74                                          The Aryl hydrocarbon Receptor (AhR) is a transcription facto
75                                          The aryl hydrocarbon receptor (AhR) is a transcription facto
76                                              Aryl hydrocarbon receptor (AhR) is a transcription facto
77                       Here, we show that the aryl hydrocarbon receptor (AhR) is activated in cells in
78                                          The Aryl hydrocarbon receptor (AHR) is an environment-sensin
79                                          The aryl hydrocarbon receptor (AHR) is an important regulato
80                                          The aryl hydrocarbon receptor (AhR) is an intracellular rece
81                                          The aryl hydrocarbon receptor (AHR) is critically involved i
82                                          The aryl hydrocarbon receptor (AHR) is emerging as a pleiotr
83                                          The aryl hydrocarbon receptor (AHR) is expressed by immune c
84 y, we show that an environmental sensor, the aryl hydrocarbon receptor (AhR) is highly induced upon B
85                                          The aryl hydrocarbon receptor (AhR) is involved in the regul
86                    We have demonstrated that aryl hydrocarbon receptor (AhR) is overexpressed in lung
87 l exposure to contaminants that activate the aryl hydrocarbon receptor (AHR) lead to suppression of i
88                             The prototypical aryl hydrocarbon receptor (AHR) ligand, 2,3,7,8-Tetrachl
89 ,2-b]carbazole (FICZ), a naturally-occurring aryl hydrocarbon receptor (AhR) ligand, allowed its biol
90                                              Aryl hydrocarbon receptor (AhR) ligands are important fo
91 icrobiota-derived metabolites, especially in aryl hydrocarbon receptor (AhR) ligands, bile acids and
92 lize tryptophan into metabolites that act as aryl hydrocarbon receptor (AHR) ligands.
93 els are decreased in mice fed a diet free of aryl hydrocarbon receptor (AhR) ligands.
94                                          The aryl hydrocarbon receptor (AHR) mediates the toxic effec
95 d on a few biological pathways, for example, aryl hydrocarbon receptor (AhR) or estrogen receptor (ER
96 diates its effects via the activation of the aryl hydrocarbon receptor (AhR) pathway and the subseque
97                            We identified the aryl hydrocarbon receptor (AHR) pathway as a potent tumo
98 e expression data revealed activation of the aryl hydrocarbon receptor (AhR) pathway in laquinimod-tr
99 athway was significantly upregulated and the aryl hydrocarbon receptor (AhR) pathway was significantl
100 acco smoke contains numerous agonists of the aryl hydrocarbon receptor (AhR) pathway, and activation
101 sistance is linked to down regulation of the aryl hydrocarbon receptor (AHR) pathway.
102                                          The aryl hydrocarbon receptor (AHR) plays an important physi
103              The endogenous ligand-activated aryl hydrocarbon receptor (AHR) plays an important role
104                                          The aryl hydrocarbon receptor (AhR) plays an important role
105                                          The aryl hydrocarbon receptor (AHR) plays crucial roles in i
106                            Activation of the aryl hydrocarbon receptor (AHR) promoted mo-DC different
107                                          The aryl hydrocarbon receptor (AHR) recognizes xenobiotics a
108                                          The aryl hydrocarbon receptor (AhR) represents an environmen
109                          While repression of aryl hydrocarbon receptor (AHR) signaling has been shown
110  TGF-beta signaling pathway is influenced by aryl hydrocarbon receptor (AHR) signaling pathways.
111 eceptor repressor (AhRR) is known to repress aryl hydrocarbon receptor (AhR) signaling, but very litt
112 of IL-23, IL-22 production is independent of aryl hydrocarbon receptor (AhR) signaling.
113 d negatively correlates with inducibility of aryl hydrocarbon receptor (AHR) signaling.
114             These metabolites are ligands of aryl hydrocarbon receptor (AHR) signaling.
115 tions, we show that MSI2 directly attenuates aryl hydrocarbon receptor (AHR) signalling through post-
116 xia inducible factor-1alpha (HIF1-alpha) and aryl hydrocarbon receptor (AHR) supports the differentia
117 ammatory M-MO, upregulates the expression of aryl hydrocarbon receptor (AhR) target genes, and stimul
118 e a pattern of regulation in the host by the aryl hydrocarbon receptor (AhR) that is critically depen
119 we used lentivirus-mediated knockdown of the aryl hydrocarbon receptor (AHR) to demonstrate that 1023
120 th the ligand-activated transcription factor aryl hydrocarbon receptor (AHR) to drive the generation
121 orodibenzo-p-dioxin (TCDD) interact with the aryl hydrocarbon receptor (Ahr) to induce osteoclastic b
122  the therapeutic potential of activating the aryl hydrocarbon receptor (AHR) to limit ECM accumulatio
123 t loss, liberated PCBs act as ligands of the aryl hydrocarbon receptor (AhR) to negatively influence
124 y, StemRegenin 1 (SR1), an antagonist of the aryl hydrocarbon receptor (AhR) transcription factor kno
125 rrepresentation of cognate sequences for the aryl hydrocarbon receptor (AhR) transcription factor, wh
126 promote NK cell IL-10, and activation of the aryl hydrocarbon receptor (AHR) was also required for ma
127         These metabolites are ligands of the aryl hydrocarbon receptor (AhR)(6), and AhR-mediated sig
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 modulation of the immune response by the aryl hydrocarbon receptor (AhR), a ligand-activated tran
132                                          The aryl hydrocarbon receptor (AhR), a ligand-activated tran
133                                          The aryl hydrocarbon receptor (AhR), a ligand-activated tran
134 or Gb3 synthesis, and it also identified the aryl hydrocarbon receptor (AHR), a ligand-activated tran
135                           Interestingly, the aryl hydrocarbon receptor (AhR), a ligand-dependent tran
136 lecular weight PAHs are known ligands of the aryl hydrocarbon receptor (AhR), a nuclear receptor that
137 ly polar structure, kynurenine activates the aryl hydrocarbon receptor (AHR), a PER, ARNT, SIM (PAS)
138                                          The aryl hydrocarbon receptor (AhR), a regulator of xenobiot
139                        Here we show that the aryl hydrocarbon receptor (AhR), a transcription factor
140 -derived metabolites that signal through the aryl hydrocarbon receptor (AHR), a transcription factor
141                                          The aryl hydrocarbon receptor (AhR), a transcription factor
142                          We propose that the aryl hydrocarbon receptor (AhR), a unique chemical senso
143 y, bioassays indicative of activation of the aryl hydrocarbon receptor (AhR), activation of the pregn
144                                          The aryl hydrocarbon receptor (AHR), also known as the dioxi
145 DO2 in TNBC cells was sufficient to activate aryl hydrocarbon receptor (AhR), an endogenous kynurenin
146                                              Aryl hydrocarbon receptor (AhR), an important regulator
147 amely, the pregnane X receptor (PXR) and the aryl hydrocarbon receptor (AhR), and itsinteractions wit
148 tors constitutive androstane receptor (CAR), aryl hydrocarbon receptor (AhR), and Nrf2.
149 nes represent known ligands of the mammalian aryl hydrocarbon receptor (AHR), and UPEC infection of A
150          Dioxin exposure, acting through the aryl hydrocarbon receptor (AHR), blocked eyelid closure
151                                          The aryl hydrocarbon receptor (AhR), for many years almost e
152 cript levels of five gene targets, including aryl hydrocarbon receptor (Ahr), interleukin-1 beta (Il1
153  to compare relative risks of activating the aryl hydrocarbon receptor (AhR), nuclear factor erythroi
154 ntrols, we found that coal tar activated the aryl hydrocarbon receptor (AHR), resulting in induction
155  and the anti-lipogenic transcription factor aryl hydrocarbon receptor (Ahr), the latter of which we
156              Because IS is an agonist of the aryl hydrocarbon receptor (AHR), we first examined the r
157 is the ligand-activated transcription factor aryl hydrocarbon receptor (AhR), which binds TB virulenc
158 -induced Jag1 expression was mediated by the aryl hydrocarbon receptor (AhR), which bound to and acti
159                                          The aryl hydrocarbon receptor (AHR), which has been central
160  primarily depend on its ability to activate aryl hydrocarbon receptor (AhR), which is a ligand-depen
161 their toxic action through activation of the aryl hydrocarbon receptor (AhR), which is believed to re
162 te, are agonists of the transcription factor aryl hydrocarbon receptor (AhR), which is widely express
163 heir barrier functions through activation of aryl hydrocarbon receptor (AhR)- nuclear factor erythroi
164 uction of anti-inflammatory cytokines via an aryl hydrocarbon receptor (AhR)-dependent mechanism.
165 r findings uncover an activin-A-induced IRF4-aryl hydrocarbon receptor (AhR)-dependent transcriptiona
166                         All extracts induced aryl hydrocarbon receptor (Ahr)-regulated mRNAs, malform
167                                              Aryl hydrocarbon receptor (AhR)-related CYP1A4 mRNA leve
168 roduction in murine T cells through inducing aryl hydrocarbon receptor (AhR)-retinoic acid receptor-r
169 this induction was abrogated by CH223191, an aryl hydrocarbon receptor (AhR)-specific antagonist.
170 narof are mediated through activation of the aryl hydrocarbon receptor (AhR).
171 its hepatotoxicity through activation of the aryl hydrocarbon receptor (AhR).
172 mediated primarily through activation of the aryl hydrocarbon receptor (AHR).
173 insults and express the transcription factor aryl hydrocarbon receptor (AhR).
174 ynurenine pathway, producing ligands for the aryl hydrocarbon receptor (AHR).
175 r adverse outcomes through activation of the aryl hydrocarbon receptor (AhR).
176 e il22 promoter and its interaction with the aryl hydrocarbon receptor (AhR).
177 12 and FA function as natural antagonists of aryl hydrocarbon receptor (AhR).
178 ar translocation of the transcription factor aryl hydrocarbon receptor (AHR).
179 ion and activity of the transcription factor aryl hydrocarbon receptor (AhR).
180 s in vitro and in vivo, which is mediated by aryl hydrocarbon receptor (AhR).
181 onmental contaminant, is a potent ligand for aryl hydrocarbon receptor (AhR).
182 kin homeostasis is largely controlled by the 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                                TGF-beta1 and aryl hydrocarbon receptor activation enhanced the ERbeta
186                         TGF-beta1 as well as aryl hydrocarbon receptor activation was necessary for t
187 y of Il1rl2(-/-) mice could be rescued by an aryl hydrocarbon receptor agonist, which was sufficient
188 ould parallel that in other clients like the aryl hydrocarbon receptor and HIF1alpha, which also inte
189 hobicity in two bioassays, indicative of the aryl hydrocarbon receptor and oxidative stress response
190 es known to be specifically regulated by the aryl hydrocarbon receptor and oxidative stress.
191 ghly expressed CD90 ( approximately 63%) and aryl hydrocarbon receptor and produced IL-17 ( approxima
192 ed in this process through activation of the aryl hydrocarbon receptor and subsequent mitochondrial r
193 te the ligand-activated transcription factor aryl hydrocarbon receptor and, consequently, antiinflamm
194 drocarbon receptor signaling pathway, as the aryl hydrocarbon receptor antagonist GNF-351 modified ap
195 ility and safety of StemRegenin-1 (SR-1), an aryl hydrocarbon receptor antagonist that expands CD34+
196          Four CpGs border sequences carrying aryl hydrocarbon receptor binding sites and enhancer-spe
197                                              Aryl hydrocarbon receptor blockade prevented differentia
198   Effects of developmental activation of the aryl hydrocarbon receptor by 2,3,7,8-tetrachlorodibenzo-
199       Activation of the transcription factor aryl hydrocarbon receptor by 2,3,7,8-tetrachlorodibenzo-
200 he group 3 innate lymphoid cell (ILC3) in an aryl hydrocarbon receptor dependent manner.
201  that IL-23-mediated restoration of IL-22 is aryl hydrocarbon receptor dependent, whereas IL-17 requi
202 hen PP cells were treated with CH-223191, an aryl hydrocarbon receptor inhibitor.
203          The molecular mechanisms leading to aryl hydrocarbon receptor interacting protein (AIP) muta
204                Here, we have identified AIP (aryl hydrocarbon receptor interacting protein) as a new
205 lic mutations in the photoreceptor-expressed aryl hydrocarbon receptor interacting protein-like 1 (AI
206            Mutant P351Delta12 human isoform, aryl hydrocarbon receptor interacting protein-like 1 (hA
207 of P351Delta12 hAIPL1 and the mouse isoform, aryl hydrocarbon receptor interacting protein-like 1 (mA
208                                   Defects in aryl hydrocarbon receptor interacting protein-like1 (AIP
209 on of the aryl hydrocarbon receptor, and the aryl hydrocarbon receptor ligand restores FLG expression
210 inarof, a bacteria-derived polyphenol, is an aryl hydrocarbon receptor ligand that attenuated inflamm
211 ct 6-formylindolo[3,2-b]carbazole (FICZ), an aryl hydrocarbon receptor ligand, has been found to be a
212       AHR and its heterodimerization partner aryl hydrocarbon receptor nuclear translocator (ARNT) be
213 eted the HIF-alpha dimerization partner, the aryl hydrocarbon receptor nuclear translocator (ARNT) in
214        We demonstrate that the expression of aryl hydrocarbon receptor nuclear translocator (ARNT) is
215                        Our data suggest that aryl hydrocarbon receptor nuclear translocator (ARNT) pl
216  hypoxia-inducible factor complex (HIF-alpha.aryl hydrocarbon receptor nuclear translocator (ARNT)) r
217                            The expression of aryl hydrocarbon receptor nuclear translocator (ARNT), a
218  and NPAS3 must each heterodimerize with the aryl hydrocarbon receptor nuclear translocator (ARNT), t
219 and a constitutively expressed beta subunit, aryl hydrocarbon receptor nuclear translocator (ARNT).
220   With hypoxia, the stabilized HIF-alpha and aryl hydrocarbon receptor nuclear translocator (ARNT, al
221 d the transport of two transcription factors-aryl hydrocarbon receptor nuclear translocator and sine
222 he circadian clock transcriptional activator aryl hydrocarbon receptor nuclear translocator-like (Bma
223 f circadian clock transcriptional activators aryl hydrocarbon receptor nuclear translocator-like (Bma
224                 The circadian rhythm-related aryl hydrocarbon receptor nuclear translocator-like 2 (A
225                         The brain and muscle aryl hydrocarbon receptor nuclear translocator-like prot
226 rcadian reporter construct [brain and muscle aryl hydrocarbon receptor nuclear translocator-like:luci
227 ptional factor BMAL1 (brain and muscle ARNT [aryl hydrocarbon receptor nuclear translocator]-like pro
228 etabolic enzyme activity, likely through the aryl hydrocarbon receptor pathway, and generation of rea
229                  This effect depended on the aryl hydrocarbon receptor pathway.
230 n Hepa-1 cells but not for expression of the aryl hydrocarbon receptor protein.
231                 Transgenic overexpression of aryl hydrocarbon receptor repressor (AhRR) and AhR-media
232                                          The aryl hydrocarbon receptor repressor (AhRR) is known to r
233 okers, including an intragenic region of the aryl hydrocarbon receptor repressor gene (AHRR; cg055759
234                         We further found the aryl hydrocarbon receptor signaling pathway plays an imp
235 e to PPIs was partially mediated through the aryl hydrocarbon receptor signaling pathway, as the aryl
236 of immunology, presenting information on the aryl hydrocarbon receptor signaling pathway, the immunom
237  antigen-specific TH22 cells is dependent on aryl hydrocarbon receptor signaling.
238  sporadic differentiation through xenobiotic aryl hydrocarbon receptor signaling.
239 ferentiation, indole acts via the xenobiotic aryl hydrocarbon receptor to increase expression of the
240   IDO1 interacted non-enzymatically with the aryl hydrocarbon receptor to inhibit activation of NOTCH
241                The transcription factor AHR (aryl hydrocarbon receptor) drives the expression of gene
242     We postulate a hypothesis where the AhR (aryl hydrocarbon receptor) mediates aberrant cell growth
243 nhibition of transcriptional activity of the aryl hydrocarbon receptor, a key regulator of ILC3 maint
244 cated within a putative binding site for the aryl hydrocarbon receptor, a master regulator of IL-22 p
245  Accordingly, we show that expression of the aryl hydrocarbon receptor, a transcription factor import
246                         Mechanistically, the aryl hydrocarbon receptor, along with STAT3 and c-Maf, a
247  particulate matter caused activation of the aryl hydrocarbon receptor, and phosphorylation of histon
248        SIRT1 also promotes activation of the aryl hydrocarbon receptor, and the aryl hydrocarbon rece
249 on the ligand-activated transcription factor aryl hydrocarbon receptor, and the third on how docosano
250                 Both depend on RORgammat and aryl hydrocarbon receptor, but NKp46(+)ILC3s also requir
251 nduces the expression of CYP2E1, CYP1A2, and aryl hydrocarbon receptor, but not of CYP3A4, hepatocyte
252 ound mutations further demonstrated that the aryl hydrocarbon receptor, but not RORgammat, was requir
253 ted with increased levels of MUC2, LYZ1, and aryl hydrocarbon receptor, but reduced levels of SLC2A5.
254 ndogenous ligand of the transcription factor aryl hydrocarbon receptor, could change the expression o
255 , which, along with the environmental sensor aryl hydrocarbon receptor, forms a multipartite transcri
256 ly increase cellular viability, activate the aryl hydrocarbon receptor, increase double-strand DNA br
257 ith other PDE4 inhibitors, an agonist of the aryl hydrocarbon receptor, Janus kinase inhibitors, and
258 h were associated with gene dysregulation in aryl hydrocarbon receptor, stress-response, and thyroid
259 transcription 3 and the cell cycle regulator aryl hydrocarbon receptor, the data suggest a disturbed
260 totype, is independent of suppression of the aryl hydrocarbon receptor, which targets cells with more
261 l for Th9, via suppressing the expression of aryl hydrocarbon receptor, without an increase in IL-10.
262 associated with increased transcription from aryl hydrocarbon receptor- and oxidative stress-regulate
263 ve and tolerant populations, we identify the aryl hydrocarbon receptor-based signaling pathway as a s
264 s close homolog Cyp1a1 was upregulated in an aryl hydrocarbon receptor-dependent manner, hence indica
265 ugh reactive oxygen species production in an aryl hydrocarbon receptor-dependent mechanism.
266              The pattern of PER-, BMAL-, and aryl hydrocarbon receptor-induced P450 gene expression a
267                                              Aryl hydrocarbon receptor-interacting protein (AIP) muta
268 , a genome-wide CRISPR screen identified the aryl hydrocarbon receptor-interacting protein (AIP), a c
269                                              Aryl hydrocarbon receptor-interacting protein-like 1 (AI
270                                              Aryl hydrocarbon receptor-interacting protein-like 1 (AI
271                                              Aryl hydrocarbon receptor-interacting protein-like 1 (AI
272  of PDE6 relies on the chaperone activity of aryl hydrocarbon receptor-interacting protein-like 1 (AI
273 ations in either the enzyme itself or AIPL1 (aryl hydrocarbon receptor-interacting protein-like 1), l
274 llowed the ranking of wetland sites based on aryl hydrocarbon receptor-mediated end points; EROD acti
275 lonies based on the efficacy of eliciting an aryl hydrocarbon receptor-mediated response.
276 ve model was applied to predict variation of aryl hydrocarbon receptor-mediated toxic potencies among
277  and that these effects are dependent on the aryl hydrocarbon receptor.
278 m cross-talk between the molecular clock and aryl hydrocarbon receptor.
279 ptophan and salicylate) as activators of the aryl hydrocarbon receptor.
280 8-tetrachlorodibenzo-p-dioxin (TCDD) via the aryl hydrocarbon receptor.
281 is pathway through a noncanonical pathway of aryl hydrocarbon receptor.
282                                         AhR; Aryl hydrocarbon receptor.
283 l microbes and innate lymphoid cells via the aryl hydrocarbon receptor.
284 n abundance and the enhanced activity of the aryl hydrocarbon receptor.
285 forms together with the transcription factor aryl-hydrocarbon receptor (AhR), compared to unprimed co
286 derivatives of tryptophan that activated the aryl-hydrocarbon receptor in CD4(+) T cells, allowing Th
287 pted to manipulate the expressions of FLRL2, aryl-hydrocarbon receptor nuclear translocator-like (Arn
288                    Four CpG sites within the aryl-hydrocarbon receptor repressor (AHRR) associate wit
289 ng heaviness and also DNA methylation at the aryl-hydrocarbon receptor repressor (AHRR) locus, but we
290 questionnaires as well as DNA methylation in aryl-hydrocarbon receptor repressor (AHRR), a sentinel e
291 (LIMR), enhanced the interaction of LIMR and aryl-hydrocarbon receptor repressor (AHRR), and promoted
292 erogenic molecule (ligand for the endogenous aryl-hydrocarbon receptor; ITE) were injected i.p. four
293  prominent example is hypomethylation of the aryl hydrocarbon-receptor repressor (AHRR) locus, which
294 ese regulatory factors, we identify AHR, the aryl hydrocarbon-receptor which controls a healthy immun
295 leotide-polymorphisms and upon activation of aryl-hydrocarbon-receptor and oxygen-mediated pathways.
296 pothesis that coplanar PCBs act at adipocyte aryl hydrocarbon receptors (AhRs) to promote adipose inf
297 netic and functional similarities in species aryl hydrocarbon receptors (AHRs), which mediate DLC sen
298 ted to xenobiotic metabolism (pregnane X and aryl hydrocarbon receptors), hormone-mediated modes of a
299 ammatory properties-partly via activation of aryl hydrocarbon receptors.
300 entially expressed BALF proteins also map to aryl hydrocarbon signaling, communication between innate

 
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