ライフサイエンスコーパス: retinoid X receptor

1 ) could be bound by vitamin D receptor (VDR)/retinoid X receptor.

2 and involves direct interaction with RAR and retinoid X receptor.

3 and was dependent upon dimerization with the retinoid X receptor.

4 ein modification and heterodimerization with retinoid X receptor.

5 tor, and their obligate heterodimer partner, retinoid X receptor.

6 LXRs or their heterodimerizing partner, the retinoid X receptor.

7 overexpression of its heterodimeric partner, retinoid X receptor.

8 e PLA2g2a promoter as a heterodimer with the retinoid X receptor.

9 RA signaling were partially mediated by the retinoid X receptor.

10 elements and for heterodimerization with the retinoid X receptors.

11 embers of retinoic acid receptors (RARs) and retinoid X receptors.

12 mined the neuronally directed effects of the retinoid X receptor agonist bexarotene in an aggressive

13 and a panel of retinoid acid receptor (RAR)/retinoid X receptor agonist treatments suggested that RA

14 We investigated the effects of bexarotene (a retinoid X receptor agonist), CD1530 (a retinoic acid re

15 Alternatively, retinoid X receptor agonists partially restored myelin d

16 Human retinoid X receptor alpha (hRXRalpha) plays a critical r

17 Retinoid X receptor alpha (RXR alpha) localized througho

18 kely to be directly NRF2-dependent including retinoid X receptor alpha (RXRA).

19 port that Nuclear receptor-related 1 (Nurr1):Retinoid X receptor alpha (RXRalpha) activation has a do

20 three closely related human NRs--HNF4alpha, retinoid X receptor alpha (RXRalpha) and COUPTF2--reveal

21 way that strongly inhibits the expression of retinoid X receptor alpha (RXRalpha) and suppresses the

22 Signaling pathways regulated by retinoid x receptor alpha (RXRalpha) are involved in hep

23 tor activated receptor-gamma (PPARgamma) and retinoid X receptor alpha (RXRalpha) complex was found t

24 ferator-activated receptor gamma (PPARgamma):retinoid X receptor alpha (RXRalpha) heterodimer.

25 Although the DeltaNCARs maintain full retinoid X receptor alpha (RXRalpha) heterodimerization

26 sactivation of BSEP and SHP promoters by FXR/retinoid X receptor alpha (RXRalpha) in HepG2 cells.

27 Retinoid X receptor alpha (RXRalpha) plays a pivotal rol

28 r partner to class II nuclear receptors, the retinoid X receptor alpha (RXRalpha) plays a vital physi

29 93T, it was possible to demonstrate that the retinoid X receptor alpha (RXRalpha) plus its ligand can

30 epatocyte nuclear factor 4alpha (HNF4alpha), retinoid X receptor alpha (RXRalpha) plus peroxisome pro

31 ediated by hepatocyte nuclear factor 4alpha, retinoid X receptor alpha (RXRalpha) plus peroxisome pro

32 tocyte nuclear factor 4alpha (HNF4alpha) and retinoid X receptor alpha (RXRalpha) plus peroxisome pro

33 ptors hepatocyte nuclear factor 4 (HNF4) and retinoid X receptor alpha (RXRalpha) plus peroxisome pro

34 s predicted to interact efficiently with VDR-retinoid X receptor alpha (RXRalpha) was identified in s

35 pharmacologically perturbed the activity of retinoid X receptor alpha (RXRalpha), a key hub within t

36 The retinoid X receptor alpha (RXRalpha), a key nuclear rece

37 We have examined the role of hepatocyte retinoid X receptor alpha (RXRalpha), an essential partn

38 ctive homodimers to active heterodimers with retinoid X receptor alpha (RXRalpha), and phosphorylatio

39 depends on vitamin A signals mediated by the retinoid X receptor alpha (RXRalpha), as the systemic mu

40 Retinoid X receptor alpha (RXRalpha), functioning as eit

41 interact in an agonist-dependent manner with retinoid X receptor alpha (RXRalpha), suggesting that th

42 Pbeta), forkhead box protein A2 (FOXA2), and retinoid X receptor alpha (RXRalpha), were markedly decr

43 ln275, Arg316 and Arg371 in nuclear receptor retinoid X receptor alpha (RXRalpha), where berberine co

44 xisome proliferator-activated receptor alpha-retinoid X receptor alpha (RXRalpha), with which PGC-1be

45 retinoic acid receptor alpha (RARalpha) and retinoid X receptor alpha (RXRalpha).

46 ncer cell apoptosis mediated via the nuclear retinoid X receptor alpha (RXRalpha).

47 oblastoma tumor suppressor protein (pRb) and retinoid X receptor alpha (RXRalpha).

48 onstitutive androstane receptor (CAR, NR1I3)/retinoid X receptor alpha (RXRalpha, NR2B1) heterodimer

49 mation weight matrix for vitamin D3 receptor/retinoid X receptor alpha (VDR/RXRalpha) binding sites w

50 Retinoid X receptor alpha [RXRalpha; nuclear receptor (N

51 Ethanol feeding decreased PPARalpha/retinoid X receptor alpha binding in electrophoretic mob

52 hereby implicating activation of a PPARgamma-retinoid X receptor alpha complex.

53 ited the DNA binding activity of a PPARgamma/retinoid X receptor alpha heterodimeric complex.

54 X receptor (FXR) via a direct binding of FXR/retinoid X receptor alpha heterodimers to a highly conse

55 Cotreatment with a retinoid X receptor alpha ligand, 9-cis-retinoic acid, d

56 d to this site as a monomer, because neither retinoid X receptor alpha nor retinoid X receptor beta a

57 Ralpha, induced the recruitment of PPARalpha:retinoid x receptor alpha, but not PPARgamma coactivator

58 stored the DNA binding activity of PPARalpha/retinoid X receptor alpha, induced mRNA levels of PPARal

59 itation studies confirmed the recruitment of retinoid X receptor alpha, PPARalpha, and PGC1alpha on t

60 Surprisingly, occupancies of FXR, retinoid X receptor alpha, RNA polymerase II, and epigen

61 eptor, constitutive androstane receptor, and retinoid X receptor alpha.

62 d miR193 expression via transcription factor retinoid X receptor alpha.

63 istent with this suggestion, it appears that retinoid X receptor alpha/farnesoid X receptor alpha and

64 dogenous PPARgamma together with its partner retinoid-X receptor alpha (RXRalpha).

65 eptor gamma (PPAR-gamma) and its co-receptor retinoid-X-receptor alpha (RXR-alpha).

66 -2 motif of CAR3 and is markedly enhanced by retinoid X receptor-alpha (RXR) cotransfection.

67 r expression of vitamin D receptor (VDR) and retinoid X receptor-alpha (RXR) has not been investigate

68 In cohort 1, retinoid X receptor-alpha (RXRA) chr9:136355885+ and end

69 Association of the retinoid X receptor-alpha (RXRA) coreceptor to PML/RARA

70 Retinoid X receptor-alpha (RXRalpha) binds to DNA either

71 ing protein-alpha (Cebpalpha), Cebpbeta, and retinoid x receptor-alpha (Rxralpha) compared with untre

72 how here that keratinocytic nuclear receptor retinoid X receptor-alpha (RXRalpha) regulates mouse ker

73 In addition, coexpression of retinoid X receptor-alpha (RXRalpha) resulted in nuclear

74 brate drugs were abrogated in the absence of retinoid X receptor-alpha (RXRalpha), a molecule known t

75 n availability as hepatic nuclear PPARgamma, retinoid X receptor-alpha (RXRalpha), and PPARgamma/RXRa

76 roach designed to identify novel ligands for retinoid X receptor-alpha (RXRalpha).

77 ing binding to other molecules including the retinoid X receptor-alpha (RXRalpha).

78 Nuclear receptors including retinoid X receptor-alpha and peroxisome proliferator-ac

79 d 14, and normal melanocyte distribution and retinoid X receptor-alpha expression.

80 The vitamin D receptor/retinoid X receptor-alpha heterodimer (VDRRXRalpha) regu

81 specific target genes.The vitamin D receptor/retinoid X receptor-alpha heterodimer (VDRRXRalpha) regu

82 ferator responsiveness via the PPARgamma and retinoid X receptor-alpha heterodimer.

83 Heterodimerization of PPARalpha to the retinoid X receptor-alpha resulted in even larger increa

84 ranscriptional regulation via binding of VDR.retinoid X receptor-alpha to discrete DNA motifs.

85 pha, but were decreased in mice deficient in retinoid X receptor-alpha, the major heterodimerization

86 receptor 4 and the ligand-binding domains of retinoid X receptor and retinoic acid receptor by observ

87 ith a selective PPARgamma antagonist or with retinoid X receptor and retinoic acid receptor ligands p

88 clear receptors that heterodimerize with the retinoid X receptor and then modulate at the transcripti

89 ediated by preferential interactions between retinoid X receptors and CYP4F promoter elements in epid

90 inoic acid receptors (retinoic acid receptor/retinoid X receptor) and glucocorticoid receptors are re

91 Sult2A1 chromatin to recruit VDR, RXR-alpha (retinoid X receptor) and PXR in mice injected with D(3)

92 lets, also in vitro translated PPARgamma and retinoid X receptor, and chromatin immunoprecipitation a

93 The glucocorticoid receptor, retinoid X receptor, and p53 underwent similar processin

94 by nuclear receptors retinoic acid receptor, retinoid X receptor, and thyroid hormone receptor and in

95 ic identity were linked to RUNX2, C/EBPbeta, retinoid X receptor, and vitamin D receptor binding site

96 th retinoic acid receptor, does not activate retinoid-X receptor, and is not a substrate for CYP26s,

97 unctional expression cloning approach, a gag-retinoid X receptor beta (gag-RXRbeta) fusion protein wa

98 ecause neither retinoid X receptor alpha nor retinoid X receptor beta antibody supershifted the prote

99 nscription factors PPARalpha, PPARdelta, and retinoid X receptor beta; and (c) liver development asso

100 , all found in the MHC class III region; and retinoid X receptor, beta (RXRB),which resides in the MH

101 lly bind tretinoin and alitretinoin, whereas retinoid-X receptors bind only alitretinoin.

102 21 gene transcription was mediated by an FXR/retinoid X receptor binding site in the 5'-flanking regi

103 ites identified two vitamin D receptor (VDR)/retinoid X receptor binding sites in the 1-kb promoter r

104 s 1,25(OH)(2)D(3) induces rapid VDR and RXR (retinoid X receptor) binding to the Cyp24a1 gene in both

105 adipocyte differentiation favored PPARgamma, retinoid X receptor, C/EBPalpha, and C/EBPbeta binding s

106 peroxisome proliferator-activated receptor, retinoid X receptor, CCAAT/enhancer binding protein, and

107 element was associated with the VD receptor/retinoid X receptor complex in vitro.

108 Coexpression of TRbetaA1 with retinoid X receptor did not enhance regulation.

109 er and show that binding of the liganded VDR.retinoid X receptor directly impacts both the distal and

110 f Fgf15 by vitamin A is mediated through the retinoid X receptor/farnesoid X receptor heterodimer and

111 imal promoter recruit retinoic acid receptor/retinoid X receptor from a distal RARE to form an enhanc

112 Disruption of retinoid X receptor function in young macrophages, using

113 Signaling via the retinoid X receptor gamma (RXR-gamma) has been shown to

114 ormone receptor siRNA library, we identified retinoid X receptor gamma (RXRgamma) instead as being in

115 receptors, retinoic acid receptor alpha and retinoid X receptor gamma, were up-regulated in response

116 D receptor (VDR), which heterodimerizes with retinoid X receptor, gamma (RXRG).

117 a direct transcriptional target for the LXR/retinoid X receptor heterodimer and that the ability of

118 forms a complex with the vitamin D receptor.retinoid X receptor heterodimer in electrophoresis mobil

119 (NRs), especially the liver X receptor (LXR)/retinoid X receptor heterodimer, as an important event i

120 ery in the peroxisome proliferator-activated/retinoid X receptor heterodimer.

121 IP205 in the context of a DNA-bound FXR/RXR (retinoid X receptor) heterodimer.

122 TRAP220 interacted predominantly with the TR.retinoid X receptor heterodimeric pair in a ligand-depen

123 id not exhibit any defects in DNA binding or retinoid X receptor heterodimerization and was transcrip

124 Rather, LXR/retinoid X receptor heterodimers bound directly to a con

125 oic acid can activate retinoic acid receptor/retinoid X receptor heterodimers but not retinoid X rece

126 aling did not involve reduced binding of LXR/retinoid X receptor heterodimers to target gene promoter

127 hormone receptor (TR) homodimers, but not TR-retinoid X receptor heterodimers, to thyroid hormone res

128 s of the LXRbeta homodimer and LXRalpha:RXR (retinoid X receptor) heterodimers explains differences i

129 s are further magnified in the presence of a retinoid X receptor heteromeric partner.

130 tor/retinoid X receptor heterodimers but not retinoid X receptor homodimers in reporter cell assays.

131 signaling through heterodimerization with a retinoid X receptor homologue Ultraspiracle (USP), the o

132 eceptor, EcR, which heterodimerizes with the retinoid X receptor homologue Ultraspiracle.

133 association of the ligand-binding domain of retinoid X receptor in the presence and absence of 9-cis

134 )2D3-independent interaction between VDR and retinoid X receptors in primary keratinocytes, indicatin

135 that mediates promoter induction by LXR/RXR (retinoid X receptor) in transfection assays.

136 tilizing an undefined retinoic acid receptor/retinoid X receptor-independent mechanism.

137 al proliferator-activated receptor-gamma and retinoid X receptor inhibit expression of CYP3a13 at the

138 bition of IL-1beta-dependent genes by active retinoid X receptors involves antagonism of NF-kappaB si

139 We observe the formation of homodimers of retinoid X receptor ligand binding domain upon addition

140 of alpha-synuclein toxicity and suggest that retinoid X receptor ligands with appropriate pharmacolog

141 peroxisome proliferator-activated receptor, retinoid X receptor, liver X receptor, and activating pr

142 Similarly, ablation of retinoid X receptors loosens PML/RARA DNA binding, induc

143 udes the binding of the liver X receptor and retinoid X receptor (LXR/RXR) heterodimer to the DR-4 el

144 miferana ultraspiracle (CfUSP), Mus musculus retinoid X receptor (MmRXR) to either GAL4 DNA binding d

145 of matrix metalloproteases, liver X receptor/retinoid X receptor, nuclear factor erythroid 2-related

146 etic ligand for the nuclear hormone receptor retinoid X receptor, on the expression of matrix metallo

147 inoic acid, a retinoic acid receptor-, and a retinoid X receptor pan-agonist were unable to induce NA

148 how that expression of genes involved in the retinoid X receptor pathway are decreased with ageing in

149 These results reveal the retinoid X receptor pathway as a positive regulator of m

150 Retinoid X receptor:peroxisome proliferative-activated r

151 Anti-miR-21 enhanced PPARalpha/retinoid X receptor (PPARalpha/RXR) activity and downstr

152 rogram in mammary epithelial cells through a retinoid X receptor/PPARgamma-mediated mechanism.

153 13 promoter shows putative binding sites for retinoid X receptor, pregnane X receptor, and estrogen r

154 ), through binding to retinoic acid receptor-retinoid X receptor (RAR-RXR) heterodimers bound at RA r

155 er partner (SHP), and retinoic acid receptor/retinoid X receptor (RAR/RXR).

156 perfamily including retinoic acid receptors, retinoid X receptors (RAR and RXR, respectively), and pe

157 tg2 promoter and show that the element binds retinoid X receptor/RAR heterodimers in vitro, is occupi

158 on in response to 9-cis-RA as evident by the retinoid X receptor response element-luciferase assays.

159 In this review we focus on the role of retinoid X receptor, retinoic acid receptor, peroxisome

160 and migration, lower retinol, and abolished retinoid X receptor/retinoid A receptor transcriptional

161 ds bound to the ligand binding domain of the retinoid X receptor reveal key structural aspects that e

162 tinoid related orphan receptor Ror beta, and retinoid X receptor Rxr gamma.

163 ither BADGE nor BPA activated or antagonized retinoid "X" receptor (RXR) or PPARgamma in transient tr

164 were synthesized and assessed for selective retinoid X receptor (RXR) agonism.

165 thalenyl]-1-propenyl ) benzoic acid) and RAR/retinoid X receptor (RXR) agonist (9-cis-RA) promote exp

166 ious data demonstrate that bexarotene (Bex), retinoid X receptor (RXR) agonist, reduces soluble and i

167 Examination of three retinoid X receptor (RXR) agonists [Targretin (TRG), UAB

168 However, the expression of retinoid X receptor (RXR) alpha, peroxisomal proliferato

169 s unable to bind its nuclear binding partner retinoid X receptor (RXR) alpha.

170 hether apocarotenoids activate or antagonize retinoid X receptor (RXR) alpha.

171 served enrichment for liver X receptor (LXR)/retinoid X receptor (RXR) and farnesoid X receptor/RXR n

172 AEG-1 interacts with retinoid X receptor (RXR) and inhibits RXR function.

173 r that can form a heterodimeric complex with retinoid X receptor (RXR) and initiate transcription of

174 hormone receptor, which heterodimerizes with retinoid X receptor (RXR) and regulates transcription of

175 g protein (C/EBP), HNF3, and heterodimers of retinoid X receptor (RXR) and retinoic acid receptor (RA

176 The synthesis and bioactivity of the retinoid X receptor (RXR) antagonist 4-[(3'-n-butyl-5',6

177 ale gastropods, because of the activation of retinoid X receptor (RXR) at very low environmental conc

178 10R slightly but significantly decreased FXR/retinoid X receptor (RXR) binding affinity but enhanced

179 cognizable half site that is required for TR/retinoid X receptor (RXR) binding.

180 As a promiscuous dimerization partner the retinoid X receptor (RXR) can contribute to signaling by

181 The nuclear receptor retinoid X receptor (RXR) can regulate transcription thr

182 oth VDREs bound the vitamin D receptor (VDR)-retinoid X receptor (RXR) complex and drove reporter gen

183 rough interactions of NF-kappaB with the PXR.retinoid X receptor (RXR) complex.

184 eracts with retinoic acid receptor (RAR) and retinoid X receptor (RXR) constitutively, but hormone bi

185 hat competed with a normally functioning VDR-retinoid X receptor (RXR) dimer for binding to the vitam

186 Ligands that activate the nuclear receptor retinoid X receptor (RXR) display potent anticarcinogeni

187 or, a transcriptional corepressor) from a TR*retinoid X receptor (RXR) heterodimer bound to a DR+4 th

188 multiprotein complex that assembles on a TR.retinoid X receptor (RXR) heterodimer in HeLa nuclear ex

189 ferator activated receptor-alpha (PPARalpha)/retinoid X receptor (RXR) heterodimer promotes transcrip

190 5(OH)(2)D(3)) via a vitamin D receptor (VDR)/retinoid X receptor (RXR) heterodimer that binds to two

191 These response elements directly bind FXR/retinoid X receptor (RXR) heterodimers and confer the ac

192 cription by binding to RA receptor (RAR) and retinoid X receptor (RXR) heterodimers.

193 Retinoid X receptor (RXR) is a combinatorial partner for

194 The nuclear receptor retinoid X receptor (RXR) is a ligand-activated transcri

195 Retinoid X receptor (RXR) is the binding partner for PPA

196 As retinoid X receptor (RXR) is the mammalian homolog of US

197 anisms underlying the anti-cancer effects of retinoid X receptor (RXR) ligand (rexinoid) therapy are

198 The three-dimensional structure of the retinoid X receptor (RXR) ligand binding domain has been

199 ed receptor gamma (PPARgamma) interacts with retinoid X receptor (RXR) on PPAR response elements (PPR

200 tion was achieved through the binding of PXR-retinoid X receptor (RXR) or CAR-RXR heterodimers to dir

201 The retinoid X receptor (RXR) partners with numerous nuclear

202 Retinoid X receptor (RXR) plays a central role in the re

203 orphan receptors and, in particular, of the retinoid X receptor (RXR) positioned nuclear receptors a

204 Retinoid X receptor (RXR) regulates key cellular respons

205 Retinoid X receptor (RXR) regulates several key function

206 In vitro studies demonstrated that the retinoid X receptor (RXR) retinoid, bexarotene, at biolo

207 itamin D receptor (VDR) FokI AA genotype and retinoid X receptor (RXR) rs7861779 TT genotype were ass

208 3254), are described and evaluated for their retinoid X receptor (RXR) selective agonism.

209 sed here expressed all RA receptor (RAR) and retinoid X receptor (RXR) subtypes (as detected by North

210 mechanisms that may cause aberrations in the retinoid X receptor (RXR) subunits, RXR-alpha and RXR-be

211 binding of retinoic acid receptor (RAR) and retinoid X receptor (RXR) to a dominant site in enhancer

212 he conventional retinoic acid receptor (RAR)/retinoid X receptor (RXR) to activate CREB.

213 (FXR), which binds as a heterodimer with the retinoid X receptor (RXR) to the FXR response element (F

214 g a co-activator of the LCPUFA-sensing PPARG-retinoid X receptor (RXR) transcription complex, may inf

215 A-I and is induced by liver X receptor (LXR)/retinoid X receptor (RXR) transcription factors.

216 a functional heterodimer between EcR and the retinoid X receptor (RXR) upon application of the chemic

217 (NRs) function as obligate heterodimers with retinoid X receptor (RXR), allowing integration of ligan

218 receptors (PPARs) form heterodimers with the retinoid X receptor (RXR), and PPAR-gamma has been inten

219 ion: thyroid hormone receptor beta (TRbeta), retinoid X receptor (RXR), and PPARalpha.

220 iption factors retinoic acid receptor (RAR), retinoid X receptor (RXR), and Sp-1 exhibited >2-fold in

221 a (PPARgamma) and its heterodimeric partner, retinoid X receptor (RXR), are effective agents for the

222 Nuclear receptors, such as the retinoid X receptor (RXR), are proteins that regulate a

223 by activating the retinoic acid receptor and retinoid X receptor (RXR), indirectly influencing RXR he

224 ndrostane receptor, pregnane X receptor, and retinoid X receptor (RXR), modulate acetaminophen (APAP)

225 r hormone receptors that heterodimerize with retinoid X receptor (RXR), such as thyroid receptors, pe

226 Exposure to agonists of retinoid X receptor (RXR), the obligate heterodimer part

227 imers and heterodimers with PPARgamma or the retinoid X receptor (RXR), thereby competing with PPARga

228 Activation of the retinoid X receptor (RXR), which is involved in cell pro

229 selective ablation of the nuclear receptors retinoid X receptor (RXR)-alpha and RXR-beta in mouse ep

230 f hepatocyte nuclear factor (HNF)-1alpha and retinoid X receptor (RXR)-alpha to investigate whether a

231 am promoter-transcription factor (COUP-TF1), retinoid X receptor (RXR)-gamma, thyroid hormone recepto

232 s controlled by the transcription regulation retinoid X receptor (RXR)-liver X receptor (LXR) system.

233 We have identified a novel retinoid X receptor (RXR)-mediated APC-independent pathw

234 tes fundamental biological processes through retinoid X receptor (RXR)-mediated gene expression, mole

235 However, when used in combination with a retinoid X receptor (RXR)-selective ligand, tazarotene c

236 We and others have shown that retinoid X receptor (RXR)-selective retinoids or "rexino

237 gh-affinity retinoid acid receptor (RAR)- or retinoid X receptor (RXR)-selective retinoids.

238 bexarotene, and their analysis in acting as retinoid X receptor (RXR)-specific agonists.

239 s an obligate heterodimer (CAR-RXR) with the retinoid X receptor (RXR).

240 dies to the vitamin D receptor (VDR) and the retinoid X receptor (RXR).

241 while 9-cis-retinoic acid also binds to the retinoid X receptor (RXR).

242 hormone metabolism as a heterodimer with the retinoid X receptor (RXR).

243 subfamily function as heterodimers with the retinoid X receptor (RXR).

244 ion by binding DNA as a heterodimer with the Retinoid X receptor (RXR).

245 ligand of Nurr1's heterodimerization partner retinoid X receptor (RXR).

246 Retinoid X receptor (RXR)/retinoic acid receptor (RAR) h

247 Retinoid X receptor (RXR)alpha is an essential partner o

248 PCR analyses showed increased PPAR mRNA and retinoid X receptor (RXR)alpha mRNA expression after exp

249 Because the effect of retinoid X receptor (RXR)alpha on arterial mononuclear l

250 The constitutive androstane (CAR) and retinoid X receptors (RXR) are ligand-mediated transcrip

251 The thyroid (TR) and retinoid X receptors (RXR) belong to the nuclear recepto

252 Bexarotene, a selective agonist for Retinoid X receptors (RXR) improves cognitive deficits a

253 soforms of retinoic acid receptors (RAR) and retinoid X receptors (RXR) with the exception of RXRgamm

254 RAR pan-agonists and Am580, but not retinoid X receptors (RXR)-agonists, stimulate the expre

255 D receptor (VDR), which heterodimerizes with retinoid X receptors (RXR).

256 id receptors (RAR-alpha, -beta, -gamma), and retinoid X receptors (RXR-alpha, -beta, -gamma) was perf

257 ion of retinoic acid receptor (RAR-beta) and retinoid X receptors (RXR-beta, -gamma) was significantl

258 Most studies on the nuclear retinoid-X receptor (RXR) have focused on its role as a

259 tor-activated receptor gamma (PPARgamma) and retinoid-X receptor (RXR) ligands on AIB3(+/-)/PyMT cell

260 ysone Receptor (EcR) and Ultraspiracle (USP)/Retinoid-X Receptor (RXR).

261 ranscription factor II (ARP-1/COUP-TFII) and retinoid X receptor (RXRalpha) as the protein factors th

262 Retinoid X receptor (RXRalpha) is activated by 9-cis-ret

263 totic effect was associated with loss of the retinoid X receptor (RXRalpha) protein in the adenocarci

264 ns of retinoic acid receptor (RARLBD) and of retinoid X receptor (RXRLBD).

265 Bexarotene-activated retinoid X receptors (RXRs) ameliorate memory deficits i

266 ic acid receptors (RARs) heterodimerize with retinoid X receptors (RXRs) and bind to RA response elem

267 Retinoid X receptors (RXRs) are important transcriptiona

268 Here, we demonstrate that retinoid X receptors (RXRs) are key elements of the tran

269 iferator-activated receptors (PPARs) and the retinoid X receptors (RXRs) are ligand-activated transcr

270 The retinoid X receptors (RXRs) are members of the family of

271 Retinoid X receptors (RXRs) are nuclear receptors that c

272 Retinoid X receptors (RXRs) are obligate partners for se

273 Retinoic acid receptors (RARs) and retinoid X receptors (RXRs) are transcription factors th

274 Retinoid X receptors (RXRs) comprise a family of nuclear

275 sms underlying neuritogenesis, we found that retinoid X receptors (RXRs) control neuritogenesis.

276 Retinoids that activate the nuclear retinoid X receptors (RXRs) display potential for chemop

277 Retinoid X receptors (RXRs) function as ligand-activated

278 activates retinoic acid receptors (RARs) and retinoid X receptors (RXRs) in vitro.

279 t activation of liver X receptors (LXRs) and retinoid X receptors (RXRs) inhibits apoptotic responses

280 rodimeric binding partners of PPARgamma, the retinoid X receptors (RXRs), showed additive enhancement

281 Agonists of retinoid X receptors (RXRs), which include the natural 9

282 (RA) are mediated by RA receptors (RARs) and retinoid X receptors (RXRs).

283 reas rexinoids are selective ligands for the retinoid X receptors (RXRs).

284 -RA for RA receptors (RARs) and 9-cis-RA for retinoid X receptors (RXRs).

285 s of retinoic acid (RA) signaling, including retinoid X receptors (RXRs).

286 a and liver X receptors in coordination with retinoid X receptors (RXRs).

287 Purpose: Bexarotene is a retinoid X receptor-selective retinoid that has preclini

288 vious studies of the retinoid, bexarotene, a retinoid X receptor-specific ligand, have indicated that

289 e expression of known retinoic acid receptor/retinoid X receptor target genes, whereas GW0742 did not

290 lly targeted by bexarotene, a ligand for the retinoid X receptor that forms heterodimers with Nurr1.

291 factors are the retinoic acid receptor, the retinoid X receptor, the hepatocyte nuclear factor 4alph

292 monstrated specific binding of PPARgamma and retinoid X receptor to the human and mouse pdx-1 x PPREs

293 omoted binding of the vitamin D receptor and retinoid X receptor to the promoters of osteoblastic tar

294 tation assay demonstrated binding of RAR and retinoid X receptor to the RA response element.

295 )2D3 increased recruitment of Vdr and rodent retinoid X receptor to the Shp promoter.

296 Binding of the vitamin D/retinoid-X receptor (VDR/RXRalpha) heterodimer to the AC

297 ts with a DNA response element known to bind retinoid X receptor-VDR heterodimers.

298 inoid receptors (retinoic acid receptors and retinoid X receptors), which are nuclear transcription f

299 DHA stimulates the retinoid X receptor, which reportedly regulates the expr

300 specific nuclear retinoic-acid receptors and retinoid-X receptors, which are encoded by separate gene