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 ansactivation to a greater extent than other steroid receptors.

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

4 spective crystal structures of the ancestral steroid receptors.

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

6 ting where conserved aspects exist for other steroid receptors.

7 erones that participate in the activation of steroid receptors.

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

9 ermine whether midbrain CART neurons contain steroid receptors.

10 nds and redefine the quaternary structure of 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 able chromatin residence times for FoxA1 and steroid receptors.

15 of transcription by ligand-activated nuclear steroid receptors.

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

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

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

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

20 Yet, the distinct roles of these proteins in steroid receptor action are poorly understood.

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

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

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

24 eviously unidentified level of regulation in steroid receptor activation.

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

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

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

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

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

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

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

32 Steroid receptors also exist in discrete cytoplasmic org

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

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

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

36 a now demonstrate the oncogenic potential of steroid receptors and implicate altered AR function and

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

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

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

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

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

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

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

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

45 ion, we hypothesized that nNOS cells contain steroid receptors, and the testosterone-induced restorat

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 calreticulin, and caspase 3 and decreases in steroid receptor co-activator 1, Grp78/BiP, and annexin

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

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

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

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

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

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

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

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

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 ne receptors involves the recruitment of the steroid receptor coactivator (SRC)/p160 coactivator LXXL

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

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

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

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

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

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

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

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

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

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

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

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 rect interaction of the liganded TRbeta with steroid receptor coactivator 3 (SRC-3), which recruits p

106 Steroid receptor coactivator 3 (SRC-3/AIB1) interacts wi

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

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

109 as a model, we have investigated the role of steroid receptor coactivator 3 (SRC3) in gene activation

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

111 We have previously shown that steroid receptor coactivator 3 (SRC3) is expressed and u

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

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

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

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

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

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

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

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

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

121 The steroid receptor coactivator amplified in breast cancer

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

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

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

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

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

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

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

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

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

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

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

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

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

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 corticosterone and the fourth LXXLL motif of steroid receptor coactivator-1 (SRC1-4).

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

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

144 rinsic activity of p160 coactivators such as steroid receptor coactivator-1 and promoted the interact

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

146 and promoted the interaction between PR and steroid receptor coactivator-1 in a mammalian two-hybrid

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

181 Steroid receptor coactivators (SRCs) regulate nuclear re

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

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

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

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

186 Currently, steroid receptor coactivators have been proposed to medi

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

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

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

190 160 coactivators to hormone response element-steroid receptor complexes has been difficult to investi

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

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

193 also known as immunophilins) in hormone-free steroid receptor complexes.

194 70 and Hsp90 interactions during assembly of steroid receptor complexes.

195 Steroid receptors comprise a homologous family of ligand

196 Steroid receptors comprise an evolutionarily conserved f

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

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

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

200 (20-45 min), p300 is recruited to ERalpha by steroid receptor coregulators (SRCs) for enhancer matura

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

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

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

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

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

206 Despite that steroid receptors engage nucleosome-remodeling complexes

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

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

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

210 these effects are initiated through altered steroid receptor expression; however, the immediate down

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

212 ERK5 induces the Nur77 orphan steroid receptor family members.

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

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

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

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

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

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

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

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

221 Steroid receptors have classically been described as lig

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

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

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

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

226 or coactivator 3 (SRC-3/AIB1) interacts with steroid receptors in a ligand-dependent manner to activa

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

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

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

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

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

232 s PIP(2) and that aldosterone stimulation of steroid receptors induces PIP(3) formation.

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

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

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

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

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

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

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

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

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

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

255 e normal mammary gland does not occur in the steroid-receptor positive cells but rather in adjacent c

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 Because of their interactions with other steroid receptors, steroid-metabolizing enzymes, or othe

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

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 al L/HX7LL motif, selectively present in sex steroid receptors, that causes recruitment of TAB2 as a

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

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

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

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

293 methylation of histones and coactivation of steroid receptor transcription.

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

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

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

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

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

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

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