ライフサイエンスコーパス: retinoic acid receptor

1 he regulation of gene expression through the retinoic acid receptor.

2 tivation with minimal cross-signaling of the retinoic acid receptor.

3 inding to nuclear transcription factors, the retinoic acid receptors.

4 ioned close to the TSS, a process favored by retinoic acid receptors.

5 agocytic receptors including TG2 by ligating retinoic acid receptors.

6 h repeat protein 2) and STRA6 (stimulated by retinoic acid receptor 6), apparently mediated by allele

7 ector responses through their binding to the retinoic acid receptor, a ligand-activated transcription

8 oncoprotein containing the C terminus of the retinoic acid receptor-a (RARa) fused to an N-terminal p

9 cal functions, including pregnane X receptor/retinoic acid receptor activation as a potential host an

10 ntifies cancer-specific effectors within the retinoic acid receptor activation pathway among the hype

11 stic relationship between AP1 expression and retinoic acid receptor activity, increased differentiati

12 ghted in the enantioselective synthesis of a retinoic acid receptor agonist and a fatty acid amide hy

13 d be reversed by the coadministration of the retinoic acid receptor agonist, all-trans-retinoic acid,

14 in CD8(+) T cells using a dominant negative retinoic acid receptor alpha (dnRARalpha) established th

15 proteins, promyelocytic leukemia zinc finger-retinoic acid receptor alpha (PLZF-RARalpha) and RARalph

16 proteins, promyelocytic leukemia zinc finger-retinoic acid receptor alpha (PLZF-RARalpha) and RARalph

17 the expression of the promyelocytic leukemia-retinoic acid receptor alpha (PML-RAR-alpha) oncoprotein

18 tion that creates the promyelocytic leukemia-retinoic acid receptor alpha (PML-RARA) fusion oncogene.

19 es the fusion protein promyelocytic leukemia-retinoic acid receptor alpha (PML-RARA) in nearly all ca

20 ons produce a promyelocytic leukemia protein-retinoic acid receptor alpha (PML-RARalpha) fusion gene.

21 c leukemia specific promyelocytic locus gene-retinoic acid receptor alpha (PML-RARalpha) fusion prote

22 (APL) and the role of promyelocytic leukemia-retinoic acid receptor alpha (PML-RARalpha) in establish

23 The promyelocytic leukemia-retinoic acid receptor alpha (PML-RARalpha) protein of a

24 arget and degrade its ProMyelocytic Leukemia/Retinoic Acid Receptor alpha (PML/RARA) driver.

25 a (APL) cells express promyelocytic leukemia/retinoic acid receptor alpha (PML/RARalpha) fusion prote

26 is blocked by its dominant-negative form PML-retinoic acid receptor alpha (PMLRARalpha).

27 cytic leukemia (PML) protein is fused to the retinoic acid receptor alpha (RAR).

28 ed critical developmental factors, including retinoic acid receptor alpha (RARA) and homeobox D (HOXD

29 10772119 and rs883868 disrupt the binding of retinoic acid receptor alpha (RARA) and Yin and Yang 1 (

30 ranslocation, which results in fusion of the retinoic acid receptor alpha (RARA) gene to another gene

31 of the APL-associated fusion oncoprotein PML/retinoic acid receptor alpha (RARA).

32 hrough overexpression of a dominant negative retinoic acid receptor alpha (RARalpha) (dnRARalpha mice

33 dependent manners, which is mediated through retinoic acid receptor alpha (RARalpha) and retinoid X r

34 Here, we show that UTX interacts with the retinoic acid receptor alpha (RARalpha) and that this in

35 sable for spermatogenesis, and disruption of retinoic acid receptor alpha (RARalpha) function resulte

36 RARalpha, in which the PML gene fuses to the retinoic acid receptor alpha (RARalpha) gene.

37 through its fusion to the gene encoding the retinoic acid receptor alpha (RARalpha) in acute promyel

38 tinoic acid (ATRA) and other agonists of the retinoic acid receptor alpha (RARalpha) inhibit the form

39 Retinoic acid receptor alpha (RARalpha) is a transcripti

40 ML) nuclear bodies (NBs) mediated by the PML-retinoic acid receptor alpha (RARalpha) oncoprotein.

41 transcriptome analysis in APA and identified retinoic acid receptor alpha (RARalpha) signaling as a c

42 expression of a dominant-negative mutant of retinoic acid receptor alpha (RARalpha) specifically to

43 The retinoic acid receptor alpha (RARalpha) was recruited by

44 Retinoic acid receptor alpha (RARalpha) was the critical

45 rans retinoic acid, an activating ligand for retinoic acid receptor alpha (RARalpha), is used to trea

46 a (PPARgamma), vitamin D receptor (VDR), and retinoic acid receptor alpha (RARalpha).

47 ntly demonstrated for promyelocytic leukemia-retinoic acid receptor alpha and breakpoint cluster regi

48 ed FoxP3+ T cells is mediated by the nuclear retinoic acid receptor alpha and involves T cell activat

49 Expression profiling of a retinoic acid receptor alpha coactivator protein, P/CAF,

50 Cytokines both potentiate retinoic acid receptor alpha expression and enhance its

51 esence of factors that interfere with proper retinoic acid receptor alpha function.

52 n, initially discovered as a part of the PML/retinoic acid receptor alpha fusion protein, has been fo

53 promyelocytic leukemia protein (PML) and PML-retinoic acid receptor alpha fusion protein.

54 Here, we show that retinoic acid receptor alpha not only links retinoic aci

55 e progressive multifocal leukoencephalopathy/retinoic acid receptor alpha oncoprotein, in combination

56 c acid leads to degradation of promyelocytic-retinoic acid receptor alpha protein and disappearance o

57 I/RARalpha (cellular retinol-binding protein/retinoic acid receptor alpha) expression, and led to apo

58 RARA (retinoic acid receptor alpha) haploinsufficiency is an i

59 and exposure to retinoic acid (signaling via retinoic acid receptor alpha) increased alpha4beta7 expr

60 ex containing E26 transformation-specific 1, retinoic acid receptor alpha, and HATs (p300 and p300/cA

61 me proliferator-activated receptor alpha and retinoic acid receptor alpha, enabling a mild and leaky

62 Expression of a bcr-3 isoform of retinoic acid receptor alpha-promyelocytic leukemia (RAR

63 pression of the fusion protein promyelocytic-retinoic acid receptor alpha.

64 We demonstrated that the retinoic acid receptor alpha/retinoic X receptor alpha h

65 Knockdown of Kif7, and retinoic acid receptors alpha (Rara), beta (Rarb), and g

66 a role for the TFs estrogen receptor alpha, retinoic acid receptors alpha and gamma in breast cancer

67 The retinoic acid receptors alpha, beta and gamma (RARalpha,

68 We also demonstrate that the PML retinoic acid receptor-alpha (PML-RARalpha) oncofusion p

69 ssociation of promyelocytic leukemia protein-retinoic acid receptor-alpha (PML-RARalpha) with corepre

70 igenetic landscape of promyelocytic leukemia/retinoic acid receptor-alpha (PML-RARalpha)-associated a

71 PRKAR1A (R1A)-retinoic acid receptor-alpha (R1A-RARalpha) is the sixth

72 Retinoic acid receptor-alpha (RAR alpha) is a known estr

73 th rapamycin with or without agonists of the retinoic acid receptor-alpha (RARA), and their gene expr

74 Translocations of the retinoic acid receptor-alpha (RARalpha) locus with the p

75 a was reduced by pharmacological blockade of retinoic acid receptor-alpha (RARalpha) signaling, indic

76 hesized that specific activation of a single retinoic acid receptor-alpha (RARalpha), without direct

77 s (LCL) were treated with AM580, a synthetic retinoic acid receptor-alpha agonist that upregulates CD

78 Retinoic acid receptor-alpha is the key mediator of the

79 osomal translocations that generate chimeric retinoic acid receptor-alpha proteins (x-RARalpha fusion

80 Stimulation of the Sox9 and HoxA1 genes by retinoic acid receptor-alpha was found to require both D

81 The retinoic acid receptor analog acitretin, which up-regula

82 erentiation and metabolism by activating the retinoic acid receptor and retinoid X receptor (RXR), in

83 cer therapy and that the expression level of retinoic acid receptor and RXR in tumors may be crucial

84 retinoids is mediated by retinoid receptors (retinoic acid receptors and retinoid X receptors), which

85 Furthermore, a pan retinoic acid receptor antagonist (AGN193109) could less

86 nt with an inhibitor of RA biosynthesis or a retinoic acid receptor antagonist increases gata1(+) ery

87 This process was inhibited by the retinoic acid receptor antagonist LE450, showing that it

88 iescence in PSCs via a mechanism involving a retinoic acid receptor beta (RAR-beta)-dependent downreg

89 ical avulsion, we show that treatment with a retinoic acid receptor beta (RARbeta) agonist results in

90 However, the level of retinoic acid receptor beta (RARbeta) and Nur77 (NR4A1)

91 Here we show that retinoic acid receptor beta (RARbeta) controls developme

92 cell expression of the transcription factor retinoic acid receptor beta (RARbeta) is essential for v

93 Here, we identify a single target, neuronal retinoic acid receptor beta (RARbeta), which modulates t

94 volves repression of the RA-responsive gene, retinoic acid receptor beta (RARbeta), Wnt signals are w

95 ation and reexpression of the oncosuppressor retinoic acid receptor beta (RARbeta).

96 sion of retinoid homeostatic genes (encoding retinoic acid receptor beta [RARbeta], CYP26A1, and leci

97 ing E-cadherin, estrogen receptor alpha, and retinoic acid receptor beta and impaired tumor growth in

98 tochondrial dynamics in neurite outgrowth by retinoic acid receptor beta signaling.

99 tion upstream of RARB (the gene that encodes retinoic acid receptor beta) had nominal genome-wide sig

100 SIRT1 deacetylates and coactivates the retinoic acid receptor beta, a known regulator of ADAM10

101 es by deacetylating the transcription factor retinoic acid receptor beta, a potential new therapeutic

102 authors present the crystal structure of the retinoic acid receptor beta-retinoic X receptor alpha (R

103 the quaternary architecture of multi-domain retinoic acid receptor beta-retinoic X receptor alpha (R

104 Here, we explored the role of retinoic acid receptor-beta (RARbeta) signaling in remye

105 The expression of retinoic acid receptor beta2 (RAR-beta2) is frequently l

106 tly demonstrated that a transcription factor retinoic acid receptor beta2 (RARbeta2) promoted axonal

107 Here we tested the hypothesis that retinoic acid receptor beta2 (RARbeta2), critical in dev

108 es: glutathione S-transferase pi (GSTPi) and retinoic acid receptor beta2 (RARbeta2).

109 ation of an epigenetic downregulation of the retinoic acid receptor-beta2 expression in CD34 cells, a

110 e heterodimers of T3 receptor (TR) and 9-cis-retinoic acid receptor bind to the TRE both in vitro and

111 utagenesis of five cis-acting element types (retinoic acid receptor binding elements [RARE], cyclic A

112 irus infection and cooperates with activated retinoic acid receptor binding sites to further promote

113 The retinoic acid receptor binds to highly compacted chromat

114 that the physical interface between SMRT and retinoic acid receptor can be a potential therapeutic ta

115 Iterated DNA binding sites for retinoic acid receptor, CREB, and NF-kappaB family membe

116 itor cells, SMRT was critical for preventing retinoic-acid-receptor-dependent induction of differenti

117 ctivation of PPARgamma, but not PPARalpha or retinoic acid receptors, effectively induced lipid accum

118 the introduction of "photohormones" for the retinoic acid receptor, farnesoid X receptor, and estrog

119 X receptor (cholesterol efflux to lumen) and retinoic acid receptor/farnesoid X receptor (cholesterol

120 ich degrade the promyelocytic leukemia (PML)-retinoic acid receptor fusion protein.

121 Expression levels of retinoic acid receptor gamma (NR1B3/RARG, encodes RARgam

122 We provide evidence that the retinoic acid receptor gamma (RAR-G) plays a major role

123 We previously found that retinoic acid receptor gamma (RARgamma) agonist blocks h

124 Retinoic acid synthesis enzyme, RALDH2, and retinoic acid receptor gamma (RARgamma) are expressed in

125 Here we report that the cytoplasmic retinoic acid receptor gamma (RARgamma) controls recepto

126 Interestingly, overexpression of retinoic acid receptor gamma (RARgamma) strongly inhibit

127 Retinoic acid receptor gamma 2 (RARgamma2) is the major

128 , the authors show that the nuclear receptor retinoic acid receptor gamma is released from the nucleu

129 e (a retinoid X receptor agonist), CD1530 (a retinoic acid receptor gamma selective agonist), and the

130 arathyroid hormone-related protein receptor, retinoic acid receptor gamma, matrix metalloproteinase 1

131 The depletion of transcripts of retinoic-acid receptor gamma from oocytes increases oct4

132 The proteins include the retinoic-acid-receptor gamma, a known repressor of oct4

133 tially prevented in mice receiving a nuclear retinoic acid receptor-gamma (RAR-gamma) agonist.

134 rs of vitamin D receptor (VDR)/RXR-alpha and retinoic acid receptor-gamma (RAR-gamma)/RXR-beta are bo

135 Using reporter assays, ChIP assays, and retinoic acid receptor-gamma (RARgamma) knockout ESC lin

136 Here, we showed that retinoic acid receptor-gamma (RARgamma) was cytoplasmic

137 d the signaling of retinoic acid through the retinoic acid receptor gene rarab.

138 , addition of all-trans-retinal did activate retinoic acid receptors in cultured cells.

139 PR also increased ACER2 expression through a retinoic acid receptor-independent and caspase-dependent

140 Retinoic acid via retinoic acid receptors induced expression of the intest

141 l cholesterol homeostasis via two receptors: retinoic acid receptor/liver X receptor (cholesterol eff

142 Nuclear retinoic acid receptors mediate most but not all of the

143 DEAB treatment also caused a decrease in retinoic acid receptor-mediated signaling within human H

144 caused by an erroneous signaling mediated by retinoic acid receptors on the MMP-1 promoter and leads

145 imal expression changes were associated with retinoic acid receptor or vitamin D receptor heterodimer

146 we focus on the role of retinoid X receptor, retinoic acid receptor, peroxisome proliferator-associat

147 elastase (NE) cleaves promyelocytic leukemia-retinoic acid receptor (PML-RAR)alpha (PR), the fusion p

148 We identified several retinoic acid receptor (RAR) agonists that reduced secre

149 The retinoic acid receptor (RAR) alpha, beta(2), and gamma i

150 nvestigated how the human (h) ADA3 regulates retinoic acid receptor (RAR) alpha-mediated transactivat

151 s direct further monocytic maturation, while retinoic acid receptor (RAR) and C/EBPepsilon direct gra

152 cription by activating the nuclear receptors retinoic acid receptor (RAR) and peroxisome proliferator

153 The retinoic acid receptor (RAR) and retinoid X receptor (RX

154 RA augmentation involved the binding of retinoic acid receptor (RAR) and retinoid X receptor (RX

155 the dimerization and DNA binding behavior of retinoic acid receptor (RAR) and retinoid X receptor (RX

156 ctivate TRAIL-R1 expression was inhibited by retinoic acid receptor (RAR) antagonists or siRNAs, but

157 We show here the role of retinoic acid receptor (RAR) beta and alpha signalling i

158 CYP26A1 and retinoic acid receptor (RAR) beta were found to be great

159 Retinoic acid receptor (RAR) binds Ngn2 and is thereby r

160 ivity for RXR and minimal crossover onto the retinoic acid receptor (RAR) compared to all-trans-retin

161 RA is the ligand of the retinoic acid receptor (RAR) family of transcription fac

162 The retinoic acid receptor (RAR) gamma agonist CD1530 was as

163 We have previously shown that retinoic acid receptor (RAR) gamma-deficient mice have h

164 Nuclear receptors including retinoic acid receptor (RAR) have been proposed to play

165 s6 promoter is specifically activated by the retinoic acid receptor (RAR) in response to its natural

166 Here, we identify a new role for the retinoic acid receptor (RAR) in the anterior of the embr

167 ed dissect the intrinsic role of each of the retinoic acid receptor (RAR) isoforms in the clonal expa

168 eover, transgenic donor T cells expressing a retinoic acid receptor (RAR) response element luciferase

169 Here, we show that CBFA2T3 represses retinoic acid receptor (RAR) target gene expression and

170 sion of lamin-A is known to be controlled by retinoic acid receptor (RAR) transcription factors, but

171 Activation of retinoic acid receptor (RAR) with all-trans-retinoic aci

172 luding Sonic hedgehog (Shh), Wingless (Wnt), retinoic acid receptor (RAR), and bone morphogenetic pro

173 ite adipocytes by selectively activating the retinoic acid receptor (RAR), recruiting the coactivator

174 -cells by overexpressing a dominant-negative retinoic acid receptor (RAR)-alpha mutant (RARdn) using

175 Retinoic acid receptor (RAR)-beta signaling is involved

176 ially due to the epigenetic silencing of the retinoic acid receptor (RAR)-beta The histone deacetylas

177 mice, potently induced BMP2 in WT MSCs in a retinoic acid receptor (RAR)-dependent manner, suggestin

178 interaction, AEG-1 profoundly inhibited RXR/retinoic acid receptor (RAR)-mediated transcriptional ac

179 While human ILCPs express low levels of retinoic acid receptor (RAR)-related orphan receptor C (

180 ediated suppression of the expression of the retinoic acid receptor (RAR)-related orphan receptor gam

181 Tconv and Treg express similar levels of the retinoic acid receptor (RAR).

182 transport RA from the cytosol to the nuclear retinoic acid receptor (RAR).

183 roteins such as promyelocytic leukemia (PML)-retinoic acid receptor (RAR)alpha and promyelocytic leuk

184 Notably, the expression of retinoic acid receptor (RAR-beta) and retinoid X recepto

185 Podocytes expressed most isoforms of retinoic acid receptors (RAR) and retinoid X receptors (

186 4-HBR is shown to exhibit binding to the retinoic acid receptors (RAR) at concentrations necessar

187 sms by which progesterone receptors (PR) and retinoic acid receptors (RAR) regulate CK5 expression an

188 ty of distinct transcription factors such as retinoic acid receptors (RAR), peroxisome-proliferator-a

189 ABP2), fatty acid-binding protein 5 (FABP5), retinoic acid receptors (RAR-alpha, -beta, -gamma), and

190 otein between a tumor suppressor PML and the retinoic acid receptor RARalpha.

191 15;17) chromosomal translocation which fuses retinoic acid receptor (RARalpha) to PML is almost alway

192 riptional signaling, including reductions in retinoic acid receptor (RARalpha, RARbeta2 and RARgamma)

193 is also a high-affinity antagonist of all 3 retinoic acid receptors (RARalpha, RARbeta, and RARgamma

194 NA sequence derived from the promoter of the retinoic acid receptor (RARE) gene.

195 The retinoic acid receptors (RARs or rars) and the thyroid h

196 Retinoic acid receptors (RARs) alpha, beta and gamma are

197 lability of nuclear hormone receptors called retinoic acid receptors (RARs) and retinoid receptors (R

198 somer, 9-cis-retinoic acid (9cRA), activates retinoic acid receptors (RARs) and retinoid X receptors

199 se retinoids are mediated through members of retinoic acid receptors (RARs) and retinoid X receptors.

200 acting motifs and selectively interacts with retinoic acid receptors (RARs) and rexinoid receptor (RX

201 Retinoic acid receptors (RARs) are members of the nuclea

202 ession due to AP-1 inhibition resulting from retinoic acid receptors (RARs) competing for limiting am

203 Retinoic acid receptors (RARs) heterodimerize with retin

204 r to explore the paracrine role of adipocyte retinoic acid receptors (RARs) in mammary morphogenesis.

205 ge organ of vitamin A, but activation of the retinoic acid receptors (RARs) in mouse liver and in hum

206 Retinoic acid receptors (RARs) mediate RA effects by dir

207 called nuclear receptors, which includes the retinoic acid receptors (RARs) responsible for mediating

208 In this study, we target specific retinoic acid receptors (RARs) to either PD duplicate (R

209 al cofactor that directly interacts with the retinoic acid receptors (RARs) to modulate retinoic acid

210 noic acid leads to activation and binding of retinoic acid receptors (RARs) to the Hox1-Hox5 chromati

211 igand-activated transcription factors termed retinoic acid receptors (RARs), but this hormone can als

212 1 (TNIP1) is a corepressor of agonist-bound retinoic acid receptors (RARs).

213 family of nuclear transcription factors, the retinoic acid receptors (RARs).

214 l profile limited primarily to activation of retinoic acid receptors (RARs).

215 r family of transcription factors, including retinoic acid receptors (RARs).

216 activities that are mediated by the nuclear retinoic acid receptors (RARs).

217 to express sufficient amounts of endogenous retinoic acid receptors (RARs).

218 es gene transcription via binding to nuclear retinoic acid receptors (RARs).

219 min A to retinoic acid (RA), which activates retinoic acid receptors (RARs).

220 found that HCV-specific IL-17-producing and retinoic acid receptor related orphan receptorgammat-exp

221 Retinoic acid receptor-related orphan nuclear receptor a

222 Adalimumab therapy led to a reduction in retinoic acid receptor-related orphan nuclear receptor C

223 TGF-beta had no effect on the expression of retinoic acid receptor-related orphan nuclear receptor g

224 gh small-molecule thymus-specific isoform of retinoic acid receptor-related orphan nuclear receptor g

225 nd blocking antibodies in mice, we show that retinoic acid receptor-related orphan nuclear receptor g

226 cells are distinguished by expression of the retinoic acid receptor-related orphan nuclear receptor R

227 rentiation of Th17 cells is dependent on the retinoic acid receptor-related orphan nuclear receptor R

228 fy STAT3-induced transcription of IL-17A and retinoic acid receptor-related orphan nuclear receptor,

229 ugh inducing aryl hydrocarbon receptor (AhR)-retinoic acid receptor-related orphan nuclear receptor-g

230 gival expressions of interleukin (IL)-17 and retinoic acid receptor-related orphan receptor (ROR) gam

231 synergizes with IL-1beta and IL-23 to drive retinoic acid receptor-related orphan receptor (ROR)-gam

232 and activators of transcription (STAT)3 and retinoic acid receptor-related orphan receptor (ROR)-gam

233 Herein, we show that FOXP3 interacts with retinoic acid receptor-related orphan receptor (ROR)alph

234 rcadian expression of BMAL1 is influenced by retinoic acid receptor-related orphan receptor alpha (RO

235 of Molecular Cell, Lee et al. show that the retinoic acid receptor-related orphan receptor alpha (RO

236 n this study, we demonstrate that the 730 kb retinoic acid receptor-related orphan receptor alpha (RO

237 Here we showed that retinoic acid receptor-related orphan receptor alpha (RO

238 on in CRP in EAs (P </= 6.8 x 10(-4)) and in retinoic acid receptor-related orphan receptor alpha (RO

239 d receptor-related orphan receptor C [RORC], retinoic acid receptor-related orphan receptor alpha [RO

240 Retinoic acid receptor-related orphan receptor C (RORc,

241 TH17 lineage (retinoic acid receptor-related orphan receptor C [RORC],

242 an Th17 cells by enhancing the expression of retinoic acid receptor-related orphan receptor C through

243 sive analysis reveals an unexpected role for retinoic acid receptor-related orphan receptor gamma (RO

244 Retinoic acid receptor-related orphan receptor gamma (RO

245 Here we show that retinoic acid receptor-related orphan receptor gamma (RO

246 tor gamma(-/-) T cells by MSCs revealed that retinoic acid receptor-related orphan receptor gamma is

247 T cells and GATA-binding protein 3 (but not retinoic acid receptor-related orphan receptor gamma or

248 pin RNA (shRNA) to CD30(+) T cells to target retinoic acid receptor-related orphan receptor gamma t (

249 regulation by impairing microbiota-dependent retinoic acid receptor-related orphan receptor gamma t (

250 sion of Foxp3(+) T(reg) cell generation from retinoic acid receptor-related orphan receptor gamma(-/-

251 Th17 cells with characteristic expression of retinoic acid receptor-related orphan receptor gamma-t (

252 Moreover, STAT3 regulated the expression of retinoic acid receptor-related orphan receptor gamma-T (

253 Retinoic acid receptor-related orphan receptor gamma-t (

254 ins under the control of keratin 5, CD4, and retinoic acid receptor-related orphan receptor gamma.

255 Retinoic acid receptor-related orphan receptor gammat (R

256 s response is driven by the master regulator retinoic acid receptor-related orphan receptor gammat (R

257 decrease in STAT3 phosphorylation as well as retinoic acid receptor-related orphan receptor gammaT (R

258 In addition, the level of retinoic acid receptor-related orphan receptor gammat mR

259 on and intracellular expression of IL-17 and retinoic acid receptor-related orphan receptor gammat) w

260 beta into GF mice induces the development of retinoic acid receptor-related orphan receptor gammat-ex

261 -17 production and coexpression of GATA3 and retinoic acid receptor-related orphan receptor gammat.

262 the biology surrounding the nuclear receptor retinoic acid receptor-related orphan receptor-gamma (RO

263 ivo, despite relatively normal expression of retinoic acid receptor-related orphan receptor-gammaT (R

264 The retinoic acid receptor-related orphan receptor-gammat (R

265 levels of IL-17A, IL-17F, IL-22, CCL-20, and retinoic acid receptor-related orphan receptor-gammat mR

266 Retinoic acid receptor-related orphan receptor-gammat-po

267 Retinoic acid receptor-related orphan receptors (RORs) r

268 ence for one family of orphan receptors, the retinoic acid receptor-related orphan receptors (RORs),

269 The retinoic acid receptor-related orphan receptors alpha an

270 The retinoic acid receptor-related orphan receptors RORalpha

271 Retinoic acid receptor-related receptor alpha (RORalpha)

272 me proliferator-activated receptor alpha and retinoic acid receptor-related receptor alpha, RAR may a

273 Retinoic-acid-receptor-related orphan receptor alpha (RO

274 In particular, the nuclear hormone receptor retinoic-acid-receptor-related orphan receptor gamma (RO

275 We show that loss of retinoic-acid-receptor-related orphan receptor-gammat-po

276 The nuclear receptors retinoic-acid-receptor-related orphan receptors alpha an

277 ributable to high dependence of promoters of retinoic-acid-receptor-related orphan receptors on the C

278 could be rescued by exogenous expression of retinoic-acid-receptor-related orphan receptors or a con

279 Ligand-activated retinoic acid receptors repressed Nur77 induction and fu

280 , the retinoic acid-induced tumor suppressor retinoic acid receptor responder 1 (RARRES1) has no know

281 Retinoic acid receptor responder 2 (RARRES2) is transcri

282 pothalamic ependymal cells, such as Rarres2 (retinoic acid receptor responder [tazarotene induced] 2)

283 ated by RA signaling that is mediated by the retinoic acid receptor responder protein 1 (RARRES1).

284 trans retinoic acid (RA), through binding to retinoic acid receptor-retinoid X receptor (RAR-RXR) het

285 ha and p300 at the proximal promoter recruit retinoic acid receptor/retinoid X receptor from a distal

286 id not; RA increased the expression of known retinoic acid receptor/retinoid X receptor target genes,

287 on as homo- or heterodimers such as TR:9-cis retinoic acid receptor (RXR).

288 e elements led to a high affinity binding of retinoic acid receptor/RXR heterodimer to the retinoic a

289 d are key molecules that target retinoid and retinoic acid receptors (RXRs and RARs), leading to phys

290 ar, we demonstrate that MLL2 participates in retinoic acid receptor signaling by promoting retinoic a

291 bopoietin (Tpo) gene as a target of the SMRT-retinoic acid receptor signaling pathway in bone marrow

292 The retinoid increase drives intrinsic retinoic acid receptor signaling, and activation occurs

293 set of vertebrate transcription factors, the retinoic acid receptor superfamily.

294 monji-domain containing gene JMJD3, a direct retinoic-acid-receptor target that functions as a histon

295 This process required RARalpha, a nuclear retinoic acid receptor that doubles as a cytoplasmic ret

296 All-trans RA binds to its nuclear retinoic acid receptors that are expressed in lymphoid c

297 These transcription factors are the retinoic acid receptor, the retinoid X receptor, the hep

298 virus expressing a dominant negative form of retinoic acid receptor type alpha blocks the reappearanc

299 erestingly, although the unliganded TR/9-cis-retinoic acid receptor was able to recruit corepressors

300 with Nr2f2, p300 (also known as Ep300) and a retinoic acid receptor, which is recruited to the retino