ライフサイエンスコーパス: steroid receptor

1 ked by TA through the mifepristone-sensitive steroid receptor.

2 micry to modulate sirtuin signalling through steroid receptors.

3 ansactivation to a greater extent than other steroid receptors.

4 res of this binding mode are more similar to steroid receptors.

5 spective crystal structures of the ancestral steroid receptors.

6 d -21 proteins as conserved PATs for the sex steroid receptors.

7 ting where conserved aspects exist for other steroid receptors.

8 erones that participate in the activation of steroid receptors.

9 ns that do not require activation of cognate steroid receptors.

10 ermine whether midbrain CART neurons contain steroid receptors.

11 altering the molecular pathways targeted by steroid receptors.

12 translocation and function of classical sex steroid receptors.

13 hway leading to the production of functional steroid receptors.

14 nds and redefine the quaternary structure of steroid receptors.

15 able chromatin residence times for FoxA1 and steroid receptors.

16 of transcription by ligand-activated nuclear steroid receptors.

17 ontal cortex, are densely populated with sex steroid receptors.

18 ct as agonist and/or antagonist of different steroids receptors.

19 discrete shift in ligand specificity in the steroid receptors, a family of biologically essential ho

20 Comparable regional differences in steroid receptor abundances likely regulate morph-specif

21 rs that target other sites in the pathway of steroid receptor action.

22 Steroid receptors activate gene transcription by recruit

23 trol nucleus HVC (used as a proper name) and steroid receptor activation within HVC; local coactivati

24 the mouth of the pocket play a major role in steroid receptor activation.

25 eviously unidentified level of regulation in steroid receptor activation.

26 uct of the bi-functional long non-coding RNA steroid receptor activator RNA 1 (SRA1) that is part of

27 Steroid receptor activator RNA protein (SRA1p) is the tr

28 -coding RNAs: tRNA, U2 spliceosomal RNA, and steroid receptor activator RNA.

29 s, like the group II intron, rRNA, or lncRNA steroid receptor activator.

30 a major role for FOXA1 in modulating nuclear steroid receptor activity in breast and prostate cancer,

31 Steroid receptor activity was assessed with a suite of i

32 y metabolize precursor compounds into potent steroid receptor agonists locally within bone.

33 Post-translational modification of steroid receptors allows fine-tuning different propertie

34 Steroid receptors also exist in discrete cytoplasmic org

35 The Nur77 nuclear steroid receptor and Bim, a proapoptotic BH3-only member

36 ent with selectivity for the GR versus other steroid receptors and a differentiated gene expression p

37 ysis on the intranuclear dwell times of four steroid receptors and a number of known cofactors.

38 nding domain of Ydj1 directly interacts with steroid receptors and is required for the activity of di

39 e folding of Hsp90-dependent clients such as steroid receptors and many kinases involved in cellular

40 sm through which ID activation domain of the steroid receptors and other similar transcription factor

41 e a mechanism through which ID domain of the steroid receptors and other similar transcription factor

42 eus (PMV) expresses dense collections of sex steroid receptors and receptors for metabolic cues, incl

43 uminal compartments complete with functional steroid receptors and stem/progenitor cells able to reco

44 cted on nNOS and Q78 ataxin-3 but not on the steroid receptors, and Mdm2 did not affect any of the co

45 as a chaperone for receptor protein kinases, steroid receptors, and other intracellular signaling mol

46 L2 is required for normal gene regulation by steroid receptors, and we show that estrogen receptor be

47 lthough evidence suggests that the classical steroid receptors are capable of mediating many of these

48 cribed, but the mechanisms relevant to other steroid receptors are entirely unknown.

49 Steroid receptors are found in discrete cellular locatio

50 Steroid receptors are members of a nuclear receptor tran

51 Steroid receptors are pleiotropic transcription factors

52 AR FXXLF motif region and indirectly through steroid receptor-associated p300 and p160 coactivators.

53 and AR signaling by disrupting the Pus1p-SRA-steroid receptor axis.

54 We then used steroid receptor-based inducible activation system to co

55 Using a steroid receptor-based inducible activation system, we s

56 of the H295R steroidogenesis assay, and sex steroid receptor binding activity using the yeast estrog

57 cently, a novel effect of phosphorylation on steroid receptor biology was described.

58 We show that the steroid receptor BRI1 localizes to both plasma membrane

59 Basal-like "triple negative" cancers lack steroid receptors but are cytokeratin (CK) 5-positive an

60 ase the DNA-binding affinity of PR and other steroid receptors by mechanisms that are not well define

61 -containing type III J protein implicated in steroid receptor chaperoning.

62 besides Met, another member of this family, steroid receptor co-activator (SRC) is required for the

63 TBP also increased steroid receptor co-activator 1 (SRC-1) interaction with

64 uch as p300/CBP-associated factor (PCAF) and steroid receptor co-activator 1 (SRC-1), the full length

65 These data suggest the steroid receptor co-activator plays key roles in both JH

66 d binding domain (LBD) interactions with the steroid receptor co-activator-1 (SRC-1) peptide, displac

67 n 2 (AF2) surfaces of both receptors driving steroid receptor co-activator-1 (SRC1) interaction.

68 enobiotic receptor PXR with the co-activator steroid receptor co-activator-1.

69 Steroid receptor co-activator-3 (SRC-3/AIB1) is an oncog

70 ne (JH) receptor, Methoprene-tolerant (Met), steroid receptor coactivator (SRC) and GATAa but not ecd

71 tivators, VDR-interacting protein (DRIP) and steroid receptor coactivator (SRC) at different stages o

72 invasion, and metastasis, including the p160 steroid receptor coactivator (SRC) family composed of SR

73 SRC3, a highly conserved member of the steroid receptor coactivator (SRC) family, is recruited

74 the bHLH transcription factors studied, the steroid receptor coactivator (SRC) showed the most sever

75 rene-tolerant transcription factor (Met) and steroid receptor coactivator (SRC), would be expressed c

76 The steroid receptor coactivator (SRC)-1 enhances the activi

77 lencing mediator for retinoid and thyroid or steroid receptor coactivator (SRC)-1 with RARalpha versu

78 OOH-terminal interaction and are enhanced by steroid receptor coactivator (SRC)-1, whereas the bicalu

79 gamma) regulate bone metabolism, and because steroid receptor coactivator (SRC)-2 (TIF-2) enhances ER

80 Steroid receptor coactivator (SRC)-3, also called amplif

81 further dissect the roles of members of the steroid receptor coactivator (SRC)/p160 family in PR-med

82 eam target of progesterone receptor (PR) and steroid receptor coactivator (SRC-1) action in the uteru

83 Both PXR and the steroid receptor coactivator (SRC-1) were found to bind

84 receptor beta (TRbeta) gene that cannot bind steroid receptor coactivator 1 (SRC-1) and Src-1(-/-) mi

85 y less ability than dexamethasone to trigger steroid receptor coactivator 1 (SRC-1) recruitment and h

86 risk HPV type 16 (HPV16) E7 oncoprotein with steroid receptor coactivator 1 (SRC-1), an essential com

87 eciphered a previously unappreciated role of Steroid receptor coactivator 1 (SRC1) in defining the li

88 iquitination greatly enhanced recruitment of steroid receptor coactivator 1 (SRC1), a coactivator cri

89 ement binding protein binding protein (CBP), steroid receptor coactivator 1 (SRC1), and protein argin

90 TCO-mediated interaction between CAR and the steroid receptor coactivator 1 or the glucocorticoid rec

91 D bound to DAC and the fourth LXXLL motif of steroid receptor coactivator 1 reveals that the GR ligan

92 tryptophan-299 to activate hPXR; 5) recruits steroid receptor coactivator 1 to hPXR; 6) activates hPX

93 ated the recruitment of TTF-1, p65, CBP, and steroid receptor coactivator 1 to the TBE region of the

94 ta in vitro and supported the recruitment of steroid receptor coactivator 1.

95 Herein, we demonstrate that Steroid Receptor Coactivator 2 (SRC-2) orchestrates a hi

96 of the oncogenic transcriptional coregulator steroid receptor coactivator 2 (SRC-2), also known as NC

97 rs that block the association of TRbeta with steroid receptor coactivator 2 (SRC2), we identified a n

98 ding between VDR and a fluorescently labeled steroid receptor coactivator 2 peptide was applied to di

99 corporated them into a sequence derived from steroid receptor coactivator 2, which interacts with est

100 ion between the vitamin D receptor (VDR) and steroid receptor coactivator 2.

101 Steroid receptor coactivator 3 (SRC-3) coactivator phosp

102 Steroid receptor coactivator 3 (SRC-3) is an oncogenic n

103 The steroid receptor coactivator 3 (SRC-3) is overexpressed

104 that ERK3 interacted with and phosphorylated steroid receptor coactivator 3 (SRC-3), an oncogenic pro

105 E3 ligases, such as C-MYC, beta-catenin, and steroid receptor coactivator 3 (SRC-3).

106 Steroid receptor coactivator 3 (SRC-3/AIB1/ACTR/NCoA-3)

107 e of an active complex of DNA-bound ERalpha, steroid receptor coactivator 3 (SRC-3/NCOA3), and a seco

108 proteins, including androgen receptor (AR), steroid receptor coactivator 3 (SRC3) and BRD4, for degr

109 Here, we report that the ER coactivator steroid receptor coactivator 3 (SRC3) is also a coactiva

110 enced by histone acetylation and require the steroid receptor coactivator 3 (SRC3), which mediates in

111 ctivation of gene expression was enhanced by steroid receptor coactivator 3 coactivator, and required

112 The steroid receptor coactivator 3 gene (SRC-3) (AIB1/ACTR/p

113 ied in breast cancer 1 (AIB1), also known as steroid receptor coactivator 3 or NCOA3, is a transcript

114 parate assays, both the recruitment of SRC3 (steroid receptor coactivator 3, a transcriptional coacti

115 Overexpression of the p160 steroid receptor coactivator ACTR is associated with bre

116 or CBP and the activation domain of the p160 steroid receptor coactivator ACTR.

117 R function by selectively competing with the steroid receptor coactivator AIB1 but not GRIP1 or SRC1

118 Overexpression and activation of the steroid receptor coactivator amplified in breast cancer

119 The steroid receptor coactivator amplified in breast cancer

120 or complex disassembly by methylation of the steroid receptor coactivator family coactivators and p30

121 In this study we explore the impact of steroid receptor coactivator inhibitor, other targeted a

122 the most active members inhibit the ERalpha/steroid receptor coactivator interaction with K i's in t

123 s induced by GR signaling, and the important steroid receptor coactivator PELP1 was also found to be

124 (Pol II), estrogen receptor alpha (ERalpha), steroid receptor coactivator proteins (SRC), and acetyla

125 stant patients showed high expression of the steroid receptor coactivator SRC-1.

126 ctivator REGgamma directs degradation of the steroid receptor coactivator SRC-3 by the 20S proteasome

127 ctivator REGgamma directs degradation of the steroid receptor coactivator SRC-3 by the 20S proteasome

128 rence (RNAi) depletions of CYC, MET, and the steroid receptor coactivator SRC/FISC.

129 SRC-3/AIB1 is a steroid receptor coactivator with potent growth-promotin

130 xes, DRIP (VDR-interacting protein) and SRC (steroid receptor coactivator), during keratinocyte diffe

131 Also, coactivator binding studies with a steroid receptor coactivator-1 (receptor interaction dom

132 Steroid receptor coactivator-1 (SRC-1 or NCOA1) is overe

133 In breast cancer, steroid receptor coactivator-1 (SRC-1) expression positi

134 Here, we show that Steroid Receptor Coactivator-1 (SRC-1) interacts with a

135 Steroid receptor coactivator-1 (SRC-1) is a coactivator

136 o part of the active receptor complex is the steroid receptor coactivator-1 (SRC-1) which interacts w

137 Steroid receptor coactivator-1 (SRC-1), a coregulatory p

138 During the decade since the discovery of steroid receptor coactivator-1 (SRC-1), the first authen

139 lpha), which requires co-activators, such as steroid receptor coactivator-1 (SRC-1), to facilitate th

140 rs recruit coactivator proteins, such as the steroid receptor coactivator-1 (SRC1).

141 r activator RNA 1 (SRA1) that is part of the steroid receptor coactivator-1 acetyltransferase complex

142 e interactions of hCAR with the coactivators steroid receptor coactivator-1 and glucocorticoid recept

143 eases the functional interaction between the steroid receptor coactivator-1 and hPXR but not mouse PX

144 e nuclear receptor interacting domain of the steroid receptor coactivator-1 as a model for exploring

145 BEL attenuated the agonist-induced steroid receptor coactivator-1 interaction with hPXR, an

146 ene and also remarkably reduces basal MR and steroid receptor coactivator-1 recruitment, unraveling a

147 t insulin facilitated the recruitment of the steroid receptor coactivator-1 to the SREBP-1c promoter.

148 interaction with fatty acid metabolites and steroid receptor coactivator-1 while increasing PPARalph

149 d to spironolactone, finerenone inhibits MR, steroid receptor coactivator-1, and RNA polymerase II bi

150 glucose increased PPARalpha interaction with steroid receptor coactivator-1, DNA binding, and transac

151 to bind the IL-4 promoter in the presence of steroid receptor coactivator-1, indicating that PPARalph

152 gate binding and dissociation of full-length steroid receptor coactivator-1a (SRC1a) from full-length

153 reviously demonstrated the potential role of steroid receptor coactivator-2 (SRC-2) as a co-regulator

154 sly shown that the transcriptional regulator steroid receptor coactivator-2 (SRC-2) controls activati

155 y androgen receptor (AR) and its coregulator steroid receptor coactivator-2 (SRC-2) enhances mitochon

156 Loss of steroid receptor coactivator-2 (SRC-2) results in a reve

157 es and in HepG2 cells reduced recruitment of steroid receptor coactivator-2 by RORalpha at an endogen

158 gh-throughput screening to identify SMIs for steroid receptor coactivator-3 (SRC-3 or AIB1), a large

159 Here we demonstrate that reprogramming steroid receptor coactivator-3 (SRC-3) function by chang

160 Molecular Cell, Yu et al. reported that the steroid receptor coactivator-3 (SRC-3) has a novel cytop

161 ctivator amplified in breast cancer 1 (AIB1)/steroid receptor coactivator-3 (SRC-3) have been shown t

162 ent study aimed to elucidate the role of the steroid receptor coactivator-3 (SRC-3) in thyroid carcin

163 oncogene amplified in breast cancer 1 (AIB1)/steroid receptor coactivator-3 (SRC-3) induces mammary t

164 Here, we show that the oncogenic steroid receptor coactivator-3 (SRC-3) is a critical reg

165 Steroid receptor coactivator-3 (SRC-3) is a histone acet

166 Steroid receptor coactivator-3 (SRC-3) is a transcriptio

167 Phosphorylation and activity of the Steroid Receptor Coactivator-3 (SRC-3) is reduced upon H

168 Estrogen receptor (ER) recruits steroid receptor coactivator-3 (SRC-3) primary coactivat

169 y also caused a failure in downregulation of steroid receptor coactivator-3 (SRC-3), a potent ERalpha

170 Steroid receptor coactivator-3 (SRC-3)/AIB1 is a member

171 Steroid receptor coactivator-3 (SRC-3/AIB1) is an oncoge

172 sphorylated alternate-spliced isoform of the steroid receptor coactivator-3 (SRC-3Delta4) bridges EGF

173 d crystallographic studies, we identify that steroid receptor coactivator-3 (SRC3) (also named as amp

174 exes did not readily recruit the coactivator steroid receptor coactivator-3 (SRC3) or ER to the PS2 p

175 ociated with the displacement of ERalpha and steroid receptor coactivator-3 from the target EBRs lead

176 shown that TR recruits the coactivator SRC3 (steroid receptor coactivator-3) and that coactivator rec

177 ceptor-associated coactivator 3 (RAC3)/AIB-1/steroid receptor coactivator-3, a nuclear coregulator an

178 Our previous research revealed that steroid receptor coactivators (Src)-1 and -2 serve a cri

179 The three members of the p160 family of steroid receptor coactivators (SRC-1, SRC-2, and SRC-3)

180 growth pathways on which cancer cells rely, steroid receptor coactivators (SRC-1, SRC-2, and SRC-3)

181 interplay and demonstrated that it requires steroid receptor coactivators (SRC-2, SRC-3) and the med

182 B-613, a potent small molecule stimulator of steroid receptor coactivators (SRCs) attenuates patholog

183 Thus far, a mechanistic role for steroid receptor coactivators (SRCs) in the progression

184 The p160 steroid receptor coactivators (SRCs) SRC-1, SRC-2 [nucle

185 AR and its steroid receptor coactivators (SRCs; SRC-1, -2 and -3) w

186 CI, Gao and colleagues present evidence that steroid receptor coactivators 1 and 2 (SRC-1 and SRC-2)

187 Here, we evaluated the contribution of steroid receptor coactivators 1 and 2 (SRC-1 and SRC-2),

188 in the recruitment of RNA polymerase II and steroid receptor coactivators SRC-2 and SRC-3, and chang

189 s reactivation of mutant p53, stimulation of steroid receptor coactivators, and induction of protein

190 plicing in a manner differing from the other steroid receptor coactivators.

191 man (Tai) protein is homologous to the human steroid-receptor coactivators SRC1-3 and activates trans

192 lting in a more selective destabilization of steroid receptors compared with kinase clients.

193 160 coactivators to hormone response element-steroid receptor complexes has been difficult to investi

194 e tetratricopeptide repeat proteins found in steroid receptor complexes, and Fkbp51 is an androgen re

195 Originally discovered as a component of steroid receptor complexes, it is now known to regulate

196 Steroid receptors comprise a homologous family of ligand

197 Steroid receptors comprise an evolutionarily conserved f

198 plasm and nucleus that stabilizes unliganded steroid receptors, controls the catalytic activity of ce

199 GE-A11) is a low-abundance, primate-specific steroid receptor coregulator in normal tissues of the hu

200 oteins, one of which is the primate-specific steroid receptor coregulator melanoma antigen-A11 (MAGE-

201 (20-45 min), p300 is recruited to ERalpha by steroid receptor coregulators (SRCs) for enhancer matura

202 to injury and in methyl-binding proteins and steroid receptor coregulatory proteins are also reported

203 ivate the oestrogen receptor/ER and the worm steroid receptor DAF-12.

204 processes as well as in the therapeutics of steroid receptor-dependent diseases.

205 We will review how steroid receptor-dependent genomic signaling is affected

206 ntradicts the traditional understanding that steroid receptors dimerize in the absence of DNA, it is

207 in two distinct proliferative phases via the steroid receptors EcR and Usp and their downstream targe

208 SL was correlated with the LXR target genes, steroid receptor element-binding protein 1c and ATP bind

209 Despite that steroid receptors engage nucleosome-remodeling complexes

210 s simplex viral vector to express a chimeric steroid receptor ("ERGR") which binds glucocorticoids ye

211 It has also been shown that steroid receptors exist outside the nucleus in many orga

212 However, the organization, gonadal steroid receptor expression, and activity of nPGi affere

213 y structure analysis of other members of the steroid receptor family (estrogen, androgen, and progest

214 ERK5 induces the Nur77 orphan steroid receptor family members.

215 cocorticoid receptor (GR) is a member of the steroid receptor family of ligand-activated transcriptio

216 ctionally known phosphorylation sites in the steroid receptor family of transcription factors are loc

217 iously found that the ancestor of the entire steroid receptor family was highly specific for estrogen

218 Androgen receptor (AR), a member of the steroid receptor family, is a transcription factor that

219 ain (DBD) not shared by other members of the steroid receptor family.

220 r, there is compelling evidence for membrane steroid receptors for estrogen in hypothalamic and other

221 itin ligase function that targets, e.g., the steroid receptors for proteasomal degradation.

222 The N-terminal domain (NTD) of steroid receptors harbors a transcriptional activation f

223 Steroid receptors have classically been described as lig

224 lmitoylation and membrane trafficking of the steroid receptor in all organs.

225 ene to study the biological function of this steroid receptor in the epithelial compartment at define

226 s masked the biological significance of this steroid receptor in the mammary epithelium.

227 set of 62 known NR coregulators and the six steroid receptors in 12 nonoverlapping mouse brain regio

228 on to the well-characterized role of the sex steroid receptors in fertility and reproduction, organs

229 (A(max)) in gene induction and repression by steroid receptors in general and glucocorticoid receptor

230 and neuroendocrine secretions, expression of steroid receptors in GnIH-ir nuclei, and GnIH inhibition

231 TRPM3 channels form ionotropic steroid receptors in the plasma membrane of pancreatic b

232 The transcriptional activity of steroid receptors, including AR, is dependent on interac

233 d PRMT6 interaction occurs through the PRMT6 steroid receptor interaction motif, LXXLL, and the AR ac

234 nsgenic mouse model in which growth factor - steroid receptor interactions were explored.

235 rring more efficient functioning of this sex steroid receptor is associated with "masculinization" of

236 Ligand-mediated gene induction by steroid receptors is a multistep process characterized b

237 to have actions via binding to their cognate steroid receptors, it is becoming clearer that steroids

238 Structure activity studies and steroid receptor knockdown suggest that flurandrenolide

239 However, steroid receptor ligand-binding domains (LBDs) are inher

240 targets to selectively inhibit membrane sex steroid receptor localization and function.

241 In the past 40 years, steroid receptors localized to the nucleus have been rec

242 ving cells to develop a single-cell model of steroid-receptor mediated gene activation.

243 However, little is known about the steroid receptor-mediated molecular mechanisms of action

244 ctively, these data provide insight into sex steroid receptor-mediated regulation of androgen-inactiv

245 a dual-functional coregulator that regulates steroid receptor-mediated transcription and alternative

246 reported to be a coactivator that regulates steroid receptor-mediated transcription and alternative

247 Recent studies indicate that steroid receptor-mediated transcriptional initiation is

248 ins, including MAO, tyrosine kinases, BACE1, steroid receptors, mGlu5 receptors, FFA1/GPR40, and HIV-

249 ta suggest that CpdA is a unique dual-target steroid receptor modulator that has a high potential for

250 c factors that contribute to the function of steroid receptor modulators, providing valuable insight

251 r research on pregnancy hormones and risk of steroid receptor-negative cancers is needed to further c

252 that tumor growth in nude rats bearing human steroid receptor-negative MCF-7 breast tumors can be sig

253 viduals with a common genetic variant in the steroid receptor (NR3C1) gene.

254 The orphan steroid receptor, Nur77, is thought to be a central part

255 However, the identity of the steroid receptor PAT(s) is unknown.

256 e of three evolutionarily diverged ancestral steroid receptor proteins using the Zipping and Assembly

257 e divergence in the evolutionary path of the steroid receptor proteins.

258 c knockout of a long non-coding RNA (lncRNA) steroid receptor RNA activator (SRA) (SRAKO) are resista

259 smic RISC proteins PACT, TRBP, and Dicer are steroid receptor RNA activator (SRA) binding NR coregula

260 Steroid receptor RNA Activator (SRA) is a long, noncodin

261 d secondary structure of a human lncRNA, the steroid receptor RNA activator (SRA), 0.87 kB in size.

262 Both SF-1 and Dax-1 bind to steroid receptor RNA activator (SRA), a coactivator that

263 p68 (DDX5) and its associated noncoding RNA, steroid receptor RNA activator (SRA), form a complex wit

264 have recently shown that the non-coding RNA, steroid receptor RNA activator (SRA), functions as a tra

265 In a widely accepted model, the steroid receptor RNA activator protein (SRA protein; SRA

266 acterized by exquisite potency and favorable steroid receptor selectivity and pharmacokinetic profile

267 he role of pioneer can be reversed, with the steroid receptors serving to enhance binding of FoxA1.

268 chaperone activity of SNCG on stimulation of steroid receptor signaling in mammary gland and, thus in

269 ires pseudouridylation by Pus1p to stimulate steroid receptor signaling.

270 ein-based multiprotein chaperone complex for steroid receptor signaling.

271 C-3 transcriptional coregulatory activity in steroid receptor signalings.

272 as emerged as a critical mediator of nuclear steroid receptor signalling, manifest at least in part t

273 ide receptor imaging for 3 receptor systems--steroid receptors, somatostatin receptors, and growth fa

274 In the future, we hope to fully characterize steroid receptor-specific functions in the brain.

275 ription factor FoxA1 is a global mediator of steroid receptor (SR) action in hormone-dependent cancer

276 FKBP52, FKBP51, Cyp40, and PP5 are found in steroid receptor (SR) complexes, but their receptor-spec

277 Multiple steroid receptors (SR) have been proposed to localize to

278 Steroid receptors (SRs) are the largest family of metazo

279 olecular requirements for the recognition of steroid receptors (SRs) by the lincRNA growth arrest-spe

280 Classical sex steroid receptors (SRs) localize at the plasma membranes

281 ydrolysis and the activation of a kinase and steroid receptor substrate in yeast cells.

282 In contrast to other steroid receptors, such as ERalpha, the activation funct

283 g extracellular signal-regulated kinases and steroid receptors, suggesting that MVP is likely to be i

284 VitD interaction with other steroid receptor superfamily receptors in peripheral blo

285 thyroid hormone receptors are members of the steroid receptor superfamily that interact with their DN

286 well studied in specific regions, brain-wide steroid receptor targets and mediators remain largely un

287 orrelations of mRNA expression levels of six steroid receptors that we provide constitute a rich reso

288 both the apo- and hormone-bound forms of the steroid receptor to modulate its affinity for ligand, wh

289 oadened the search for and identification of steroid receptors to include nonnuclear sites in synapse

290 ing immunophilins FKBP51 and FKBP52 modulate steroid receptor trafficking and hormone-dependent biolo

291 ts activity of the androgen receptor (AR), a steroid receptor transcription factor required for PCa g

292 methylation of histones and coactivation of steroid receptor transcription.

293 fic expression of MAGE-11 results in greater steroid receptor transcriptional activity through direct

294 ecedented Fkbp52 function, direct control of steroid receptor transcriptional activity.

295 Lysine acetyltransferases interact with steroid receptors upon binding of an agonist and are rec

296 KDACs have been shown to interact with steroid receptors upon binding to an antagonist.

297 on by androgens makes it distinct from other steroid receptors, which are typically ubiquitinated and

298 (H100)Trp, converts 1E9 into a high-affinity steroid receptor with a ligand recognition profile simil

299 be identified through spatial correlation of steroid receptors with genome-wide mRNA expression acros

300 ctural basis of agonism versus antagonism in steroid receptors with potential implications for drug d