ライフサイエンスコーパス: coregulator

1 ce of dual coregulator functions of a master coregulator.

2 ll type-specific functions of this important coregulator.

3 ide synthesis pathways and a transcriptional coregulator.

4 he nucleus and function as a transcriptional coregulator.

5 ogenic mutations in a global transcriptional coregulator.

6 quences may also contain binding sites for a coregulator.

7 base damage, is an important transcriptional coregulator.

8 s in directing in vivo functions of a master coregulator.

9 derstood about its role as a transcriptional coregulator.

10 ical complex with the LEUNIG transcriptional coregulator.

11 phosphorylation activates it into a powerful coregulator.

12 ne-rich protein-1 (PELP1/MNAR) is a novel NR coregulator.

13 gulatory transcription factor GATA-1 and its coregulators.

14 and are involved globally as transcriptional coregulators.

15 nerships with other DNA-binding proteins and coregulators.

16 extended to understand other transcriptional coregulators.

17 ssion by recruiting diverese transcriptional coregulators.

18 ceptor (GR) is mediated by interactions with coregulators.

19 y, respond to a wide range of amino acids as coregulators.

20 actions of transcription factor proteins and coregulators.

21 f AR is mediated largely by distinct nuclear coregulators.

22 eacetylases (HDACs) are important epigenetic coregulators.

23 eptor (TR) for regulating the recruitment of coregulators.

24 ll4, and LRH-1, as statistically significant coregulators.

25 uding THAP11 and ZNF143, and transcriptional coregulators.

26 d3 transcription complexes by competing with coregulators.

27 formations that interact differentially with coregulators.

28 rough competition for their microRNA (miRNA) coregulators.

29 were initially described as transcriptional coregulators.

30 Src-1(-/-) mice to create mice deficient for coregulator action in all cell types.

31 rogram and suggest that this transcriptional coregulator acts as a bifunctional molecular switch for

32 o GCN5 or PCAF (GCN5/PCAF), other epigenetic coregulators (ADA2-A, ADA3, STAF36, and WDR5), cofactors

33 n breast cancer by inhibiting their upstream coregulator AIB1.

34 has been shown as a steroid hormone receptor coregulator and also as a crucial factor in DNA repair.

35 We have found that Pias3, a transcriptional coregulator and E3 SUMO ligase that is selectively expre

36 -1/steroid receptor coactivator-3, a nuclear coregulator and oncogene frequently amplified in human b

37 tiple mechanisms, including pioneer factors, coregulators and epigenetic modifications have been iden

38 in part by their differential utilization of coregulators and ligands.

39 tive, we retrace our steps into the field of coregulators and provide a summary of selected seminal w

40 ancer that affects ERalpha interactions with coregulators and shifts the DNA-binding signature of ERa

41 ittle is known about the identity of the key coregulators and the mechanisms by which they may potent

42 Second, coexpression of a set of 62 known NR coregulators and the six steroid receptors in 12 nonover

43 complexes containing transcription factors, coregulators, and additional non-DNA binding components.

44 disrupts the interaction between AR and its coregulators, and also increases cell survival by decrea

45 s of ERalpha expression, altered activity of coregulators, and cross-talk between the ERalpha and gro

46 hances breast cancer growth involving AR, AR coregulators, and downstream target genes.

47 e than 100 genes encoding nuclear receptors, coregulators, and their direct/indirect targets was stud

48 nscript HOTAIR is coordinated via ERs and ER coregulators, and this mechanism of HOTAIR overexpressio

49 iple coregulators at all loci, or if certain coregulators are dedicated to specific loci is unknown.

50 The interactions between VDR and coregulators are essential for VDR-mediated transcriptio

51 Transcriptional coregulators are important components of nuclear recepto

52 Chromatin coregulators are important factors in tumorigenesis and

53 RNA polymerase II transcription factors and coregulators are recruited to promoters and other regula

54 omatin-associated factor and transcriptional coregulator, as a ligand-independent macrodomain-interac

55 e Trip-Br (SERTAD) family of transcriptional coregulators, as a molecule that is required for normal

56 ll proliferation in part by altering ERalpha-coregulator association.

57 urthermore, whether GATA-1 utilizes multiple coregulators at all loci, or if certain coregulators are

58 eractions with several transcription factors/coregulators at the promoter elements of various genes.

59 t binding of both, transcription factors and coregulators at the type 2 diabetes associated PPARG loc

60 Here we show that the transcriptional coregulator B cell leukemia/lymphoma 3 (Bcl3) limits gra

61 The pattern of VDR-coregulator binding affinities was very similar for the

62 of resistance, we have developed a novel ER coregulator binding modulator, ERX-11.

63 the interaction of the VDR with a library of coregulator binding motifs in the presence of two ligand

64 Small molecule inhibition of VDR-coregulator binding represents an alternative method to

65 receptor conformational changes that impact coregulator binding, transactivation and target gene exp

66 signals between dimer partners, ligands and coregulator-binding sites, thereby affecting signal tran

67 atory complexes that include both GR and the coregulator Brm, an ATPase subunit of the Swi/Snf chroma

68 Ser446 converts Bcl3 into a transcriptional coregulator by facilitating its recruitment to DNA.

69 lase 1 (LSD1) functions as a transcriptional coregulator by modulating histone methylation.

70 transcription resulting from recruitment of coregulators by the Nup98 repeat domain.

71 Overexpression of the transcriptional coregulators C-terminal binding proteins 1 and 2 (CtBP1

72 ndings establish the principle that a single coregulator can function as a signal-dependent and coord

73 rement for expression, presumably additional coregulators can mediate GATA-1 function.

74 ification of both, transcription factors and coregulators, can profoundly improve understanding of me

75 rily conserved AAA ATPase ANCCA (AAA nuclear coregulator cancer-associated protein)/ATAD2 was identif

76 We have found that the transcriptional coregulator Cited2 regulates and refines two stages of C

77 Transcriptional coregulators (coactivators and corepressors) have emerge

78 Coregulators (coactivators and corepressors) occupy the

79 Instead, a set of stage-specific coregulators collaborates with master regulators and con

80 eam effector molecules, the nuclear receptor coregulators, compared with the full agonist dexamethaso

81 architectural factor HMGA1 and the Mediator coregulator complex cooperate to enhance basal transcrip

82 The Mediator is a conserved transcriptional coregulator complex required for eukaryotic gene express

83 hormone-induced assembly of transcriptional coregulator complexes at chromatin is a process facilita

84 Most coregulator complexes contain histone-modifying enzymes

85 is achieved by signal-dependent exchange of coregulator complexes that function to read, write, and

86 anisms involving the recruitment of specific coregulator complexes to the promoters of cell cycle gen

87 ng our analyses of different transcriptional coregulator complexes.

88 llaborative regulation by HDAC1/2 containing coregulator complexes.

89 served enzymes and often coexist in the same coregulator complexes.

90 ssembly of multiprotein transcription factor-coregulator complexes.

91 d sequentially orchestrated exchange between coregulators (corepressors, coactivators).

92 ver, a detailed picture of the complexity of coregulators (CoRs) bound to a defined enhancer along wi

93 n interaction domains of the transcriptional coregulator CREB-binding protein.

94 th PPARgamma affected the recruitment of the coregulators cyclic-AMP response element-binding protein

95 ationship exists between the transcriptional coregulator Daxx, SUMO, and PML nuclear bodies.

96 establish Ldb1 as a critical transcriptional coregulator during islet alpha-, beta-, and delta-cell d

97 We conclude that the coregulator effects of melanoma antigen-A11 on the AR NH

98 tion transcription assays that depend on the coregulator effects of melanoma antigen-A11.

99 Reliance on coregulators encoded by either the host or viral genome

100 eased without detectable changes in ER or ER coregulator expression.

101 Deregulation of AR and AR coregulators, expression, or activity is involved in the

102 cally altered recruitment of transcriptional coregulator factors by SoxE proteins, displacing coactiv

103 The GATA1 coregulators FOG1 and TAL1 dissociate from mitotic chrom

104 DD4/5 is required for the recruitment of the coregulators FOG1 and the nucleosome remodeling and deac

105 selected the CThPN-specific transcriptional coregulator Fog2 for functional analysis.

106 as a positive and a negative transcriptional coregulator for discrete subsets of genes that are regul

107 Thus, G9a has a dual and selective role as a coregulator for ERalpha target genes.

108 cogene AIB1/ACTR/SRC-3 and a transcriptional coregulator for estrogen and androgen receptors and is s

109 In addition to the crucial GATA-1 coregulator Friend of GATA-1 (FOG-1), a component of the

110 n by the transcription factor GATA-1 and its coregulator Friend of GATA-1 (FOG-1).

111 ukemogenesis, which often functions with the coregulator Friend of GATA-1 (FOG-1).

112 1 regulates target genes with or without the coregulator Friend of GATA-1 (FOG-1).

113 ctivation only at target genes requiring the coregulator Friend of GATA-1 (FOG-1).

114 We conclude that the coregulator function of MAGE-11 extends to isoform-speci

115 spective to the molecular governance of dual coregulator functions of a master coregulator.

116 Deregulated expression of coregulators has been implicated in diverse disease stat

117 e first authentic coregulator, more than 400 coregulators have been identified and characterized, and

118 evidence suggests that nuclear receptor (NR) coregulators have potential to act as master genes and t

119 ssociate physically with the transcriptional coregulator HCF-1 (host cell factor 1) and recruit HCF-1

120 teins and proteolysis of the transcriptional coregulator HCF-1.

121 of ES cells, binds with its transcriptional coregulator, Hcf-1, to a highly conserved enhancer eleme

122 issense mutation in a global transcriptional coregulator, HCFC1, was identified in the index case.

123 domain, but Lin11, Isl-1, Mec-3 (LIM) domain coregulator Hic-5 (TGFB1I1) binds to the relatively unch

124 we examined recruitment of nuclear receptor coregulators, histone modifications and RNA polymerase I

125 ion of MYC with the abundant transcriptional coregulator host cell factor-1 (HCF-1).

126 The coregulator hydrogen peroxide-inducible clone 5 (Hic-5)

127 Among the many coregulators identified were all of the subunits of the

128 Several key transcription factors and coregulators important to peripheral nerve myelination h

129 uclear receptor interacting factor 3 (NRIF3) coregulator in a wide variety of breast cancer cells sel

130 oma protein), functions as a transcriptional coregulator in many fundamental cellular processes.

131 abundance, primate-specific steroid receptor coregulator in normal tissues of the human reproductive

132 NPR1 is a key transcriptional coregulator in plant defense responses.

133 lysis suggested that addition of the nuclear coregulators in a multivariable analysis with ER and E2

134 ssion and activity of androgen receptor (AR) coregulators in prostate cancer is an important mechanis

135 ggests potentially significant new roles for coregulators in renal cancer biology.

136 role of specific nuclear receptors and their coregulators in the dynamic control of mitochondrial bio

137 ic combinations of transcription factors and coregulators in the fine tuning of organismal metabolism

138 s-associated protein 1 (MTA1), a dual master coregulator, in epithelial cells, and that MTA1 status i

139 ion of Zfp521, a zinc finger transcriptional coregulator, in prehypertrophic chondrocytes.

140 R-mediated gene regulation is enhanced by AR coregulators, inactivation of those coregulators is emer

141 These coregulators include the cell-type-specific multi-zinc f

142 en stimulation, ERalpha recruits a number of coregulators, including both coactivators and corepresso

143 TR-FRET-based competitive ligand binding and coregulator interaction assays to screen 2693 compounds

144 which contains a conserved nuclear receptor-coregulator interaction motif IXXLL.

145 tein via interruption of the AR-AR selective coregulator interaction.

146 ifies the measurement of ligand-modulated TR-coregulator interactions and should improve the overall

147 D2 also disrupts androgen receptor-coregulator interactions in ex vivo cultures of primary

148 Thus, coregulator interactions of Pu.1 were examined by immuno

149 de evidence that targeting androgen receptor-coregulator interactions using peptidomimetics may be a

150 monstrate the unexpectedly dynamic nature of coregulator interactions within enhancer complexes, whic

151 on and activation as well as the dynamics of coregulator interactions within the enhancer complex.

152 RIP140 is a transcriptional coregulator involved in energy homeostasis, ovulation, a

153 far, the only example of a nuclear receptor coregulator involved in suppression of kidney cancer and

154 ed by AR coregulators, inactivation of those coregulators is emerging as a promising therapy for pros

155 nce of interactions between GATA-1 and other coregulators is poorly understood.

156 s, the glucocorticoid receptor (GR), and its coregulators is poorly understood.

157 e of combinational PTM codes on histones and coregulators is profoundly shaped by regulatory interpla

158 tivity by the androgen receptor (AR) and its coregulators is required for male reproductive developme

159 One such group of ubiquitously expressed coregulators is the metastasis-associated protein (MTA)

160 us, while Med1 is a context-dependent GATA-1 coregulator, it also exerts specialized functions in ery

161 -2 or SRC-3, we hypothesized that permissive coregulator levels comprise a necessary adipogenic equil

162 The widely expressed transcriptional coregulator, ligand-dependent corepressor (LCoR), initia

163 We propose a coregulator matrix model in which distinct combinations

164 nt nuclear receptors at different domains by coregulator may lead to differential receptor transactiv

165 Reliance on cellular coregulators may allow KSHV to adjust its lytic program

166 ncreasingly accepted that steroidal receptor coregulators may also function in the cytoplasmic compar

167 CoR and HDACs, indicating that this class of coregulators may play a previously unrecognized role dur

168 P-ribosyl)ation of transcription factors and coregulators, mediated by the poly(ADP-ribose) polymeras

169 (CITED2), a mechanosensitive transcriptional coregulator, mediates this chondroprotective effect of m

170 GATA-1 corepressor expands the repertoire of coregulators mediating establishment/maintenance of the

171 ich is the primate-specific steroid receptor coregulator melanoma antigen-A11 (MAGE-A11).

172 The MTA1 coregulator (metastatic tumor antigen 1), a component of

173 r coactivator-1 (SRC-1), the first authentic coregulator, more than 400 coregulators have been identi

174 the recently established role for the master coregulator MTA1 and MTA1-containing nuclear remodeling

175 ically interacts with bodies enriched in the coregulator NCoA-2, DNA-dependent foci and chromatin tar

176 identified component of the transcriptional coregulator network, was found to interact with the Nucl

177 e independent of Smad4, the almost universal coregulator of canonical TGFbeta signaling.

178 Lipin 1 is a coregulator of DNA-bound transcription factors and a pho

179 identified Tip60 as the first dual-function coregulator of ERbeta1.

180 uman hepatoma cells and identified AMPK as a coregulator of FXR.

181 zation and acts as a nuclear transcriptional coregulator of gene expression.

182 These observations establish PML as a coregulator of IFN-gamma-induced MHC class II expression

183 These results demonstrate that FUS is a coregulator of MITF activity and provide new insights in

184 ng noncoding RNA, LincRNA-Tnfaip3, acts as a coregulator of NF-kappaB to modulate inflammatory gene t

185 PGC1alpha is a key transcriptional coregulator of oxidative metabolism and thermogenesis.

186 protein Bcl3 is primarily a transcriptional coregulator of p52 and p50 homodimers.

187 , this work identifies CHD4 as an epigenetic coregulator of PAX3-FOXO1 activity, providing rational e

188 pendent chromatin remodeler, acts as crucial coregulator of PAX3-FOXO1 activity.

189 We found that COUP-TFII functions as a coregulator of Prox1 to control several lineage-specific

190 38 MAP kinase (p38K)/Mef2/MnSOD pathway is a coregulator of stress and life span.

191 Thus, p300 is the dominant coregulator of the CBP/p300 pair for androgen-regulated

192 that TET2 protein is a cofactor of EBNA2 and coregulator of the EBV type III latency program and DNA

193 icate that HO-1 plays an important role as a coregulator of the erythroid differentiation process.

194 tor-gamma coactivator-1alpha (PGC-1alpha), a coregulator of the GCs receptor (GR), and that the overe

195 GRIP1, a GR ligand-dependent coregulator of the p160 family can potentiate or inhibit

196 teracting protein (GRIP)1, a transcriptional coregulator of the p160 family, which is recruited to th

197 The histone acetyltransferase TIP60 is a coregulator of transcription factors and is implicated i

198 Lhx6 and -8 act as transcription factors and coregulators of cell lineage specification.

199 hether other cell surface molecules serve as coregulators of EMS1.

200 and -beta serve as inducible transcriptional coregulators of genes involved in mitochondrial biogenes

201 ormone receptors; NCoR2) are well-recognized coregulators of nuclear receptor (NR) action.

202 osphatases, Cdc25C and PP2Acalpha, which are coregulators of the G(2)-M checkpoint, are inhibited by

203 ry biomarker C-reactive protein as prominent coregulators of the observed annual pulse increases.

204 es and the tight packing of multiple TFs and coregulators on stretches of regulatory DNA.

205 Estrogen receptor (ER) coregulator overexpression promotes carcinogenesis and/o

206 damage response protein and transcriptional coregulator PARP-1.

207 ers, demonstrated that the estrogen receptor coregulator PELP1 is a proto-oncogene.

208 r, nuclear receptor coactivator-2 (Tif2), in coregulator peptide recruitment assays.

209 ciation of both PPARbeta/delta and PPARgamma coregulator peptides in response to ligand activation, c

210 complex that was devoid of ERRgamma and the coregulator peroxisome proliferator-activated receptor g

211 udies suggest that PRDM16 and its associated coregulators PPARgamma coactivator-1alpha (PGC-1alpha) a

212 rough the progesterone receptor (PR) and its coregulators prepares the human endometrium for receptiv

213 Here we report our study of endogenous human coregulator protein complex networks obtained from integ

214 Rgamma modulator characteristics by inducing coregulator protein interactions, PPARgamma-dependent ex

215 e "open" chromatin compartment together with coregulator proteins essential for regulation of gene ex

216 Coregulator proteins play key roles in transcriptional c

217 involving LXXLL motifs in androgen receptor-coregulator proteins such as PELP1 using a novel, small

218 tory elements of target genes and recruiting coregulator proteins to remodel chromatin and regulate t

219 ar receptors that function coordinately with coregulator proteins.

220 ing, via interaction with critical oncogenic coregulator proteins.

221 of DNA-bound functional dimers positions the coregulators proteins.

222 pose energy homeostasis via these metabolism coregulators, provides a potential therapeutic strategy

223 ; the response regulator RcsB; the accessory coregulator RcsA; and an outer membrane bound lipoprotei

224 y impact SF-1 function, the conformation and coregulator recruitment of fully sumoylated SF-1 LBD pro

225 -binding surface, consistent with an altered coregulator recruitment profile.

226 d that INT131 mediates a distinct pattern of coregulator recruitment to PPAR gamma.

227 -L1 is mediated by differential RA-dependent coregulator recruitment to the receptor/Glucocorticoid R

228 Additional studies of coregulator recruitment using ChIP-chip analysis reveale

229 -fold vs. E2) is enhanced at several levels (coregulator recruitment, chromatin binding); nevertheles

230 we show that MAGE-11 is an isoform-specific coregulator responsible for the greater transcriptional

231 Quantitative proteomics also found the coregulator RING1 and YY1 binding protein (RYBP) whose m

232 ere, we demonstrate that the transcriptional coregulator RIP140 regulates intestinal homeostasis and

233 PXR and RXRalpha bind to the transcriptional coregulator SRC-1 with higher affinity when they are par

234 rogen receptors ERalpha and ERbeta, with key coregulators (SRC3 and RIP140) and chromatin binding sit

235 is recruited to ERalpha by steroid receptor coregulators (SRCs) for enhancer maturation and maintena

236 pregulation of the oncogenic transcriptional coregulator steroid receptor coactivator 2 (SRC-2), also

237 cal interactions of TBP with transcriptional coregulator subunits and with the general transcription

238 iological processes through interaction with coregulators such as AR trapped clone-27 (ART-27).

239 ational modifications (PTMs) on histones and coregulators such as corepressors, coactivators, DNA-bin

240 trogen receptors (ERs) along with various ER coregulators such as histone methylases MLL1 (mixed line

241 Estrogen receptors (ERs) and ER coregulators such as mixed lineage leukemia (MLL) histon

242 Although binding sites for DNA and coregulators such as SRC1 are distinct and at distal reg

243 adipose tissue, nuclear receptors and their coregulators, such as peroxisome proliferator-activated

244 re complex than is generally recognized, and coregulators, such as Tax, likely play a critical role i

245 DC-specific transcript (DC-SCRIPT) as an NR coregulator, suppressing type I steroid NRs estrogen rec

246 The coregulator switch is mediated by B-Myb and c-Myb, which

247 essful transition between these two phases ("coregulator switching") is required for proper enhancer

248 Thus, Hic-5 is a versatile coregulator that acts by multiple gene-specific mechanis

249 g protein 140 (RIP140) is a nuclear receptor coregulator that affects a wide spectrum of biological p

250 s of melanoma antigen gene protein-11, an AR coregulator that binds the AR FXXLF motif and targets AF

251 vator-1alpha (PGC-1alpha), a transcriptional coregulator that binds to numerous transcription factors

252 c demethylase 1 (KDM1A) is a transcriptional coregulator that can function in both the activation and

253 yltransferase 1 (CARM1) is a dual functional coregulator that facilitates transcription initiation by

254 erosum SELF-PRUNING 6A), a FLOWERING LOCUS T coregulator that functions as a signal for tuberization.

255 ene protein-A11 (MAGE-11) is an AR selective coregulator that increases AR transcriptional activity.

256 Herein, we show that CoAA is a dual-function coregulator that inhibits G(1)-S transition in human kid

257 ing to melanoma antigen-A11 (MAGE-11), an AR coregulator that is also primate-specific.

258 cells and acts as an ERalpha transcriptional coregulator that is recruited by 17beta-estradiol to the

259 eucine rich protein 1) is a nuclear receptor coregulator that is upregulated during breast cancer pro

260 eucine-rich protein 1) is a nuclear receptor coregulator that plays an important role in ER signaling

261 RERE is a widely-expressed nuclear receptor coregulator that positively regulates retinoic acid sign

262 y protein 4 (LMO4) is a transcription factor coregulator that promotes the assembly of multiprotein c

263 ivator activator (CoAA) is a dual-functional coregulator that regulates steroid receptor-mediated tra

264 a antigen gene protein 11 (MAGE-11) is an AR coregulator that specifically binds the AR NH(2)-termina

265 F3 is an estrogen-inducible nuclear receptor coregulator that stimulates estrogen receptor-alpha (ERa

266 CgrC proteins of Pseudomonas aeruginosa are coregulators that are required for the phase-variable ex

267 ases and a host of transcription factors and coregulators that control their activity during transcri

268 foundation of our knowledge for the now 350+ coregulators that have been identified to date.

269 Ldb1 and Ldb2 are coregulators that mediate Lin11-Isl1-Mec3 (LIM)-homeodom

270 roid receptor RNA activator (SRA) binding NR coregulators that target steroid-responsive promoters an

271 on can alter the selective binding of TFs to coregulators, that prior binding events can lead to sele

272 While FOG-1 is an established GATA-1 coregulator, the importance of interactions between GATA

273 el of metastasis-associated protein 1 (MTA1) coregulator, the physiological role of the MTA1 coactiva

274 proteomic technique, we identified a new AR coregulator, the transcription factor Grainyhead-like 2

275 e activity of transcriptional regulators and coregulators, there are few examples of core components

276 o the DAD limits HDAC3 interaction with this coregulator, thereby facilitating SMRT coactivation of p

277 fferent tissues expressing different sets of coregulators, thus facilitating the goal of developing t

278 Through coregulator titrations, we could determine the affinity

279 tor of hematopoiesis GATA-1 recruits diverse coregulators to chromatin, which mediate transcriptional

280 cell type- and cell state-specific array of coregulators to control gene transcription.

281 ational changes that recruit transcriptional coregulators to promoter elements.

282 CSL interacts with coregulators to repress and activate transcription from

283 optosis regulator 1 (CCAR1), a transcription coregulator, to the PPARgamma gene GBRs.

284 his screen was directed against a variety of coregulators, transcription modifiers, signaling molecul

285 liver fluke Opisthorchis viverrini and this coregulator using both an Mta1(-/-) mouse model of infec

286 Thus, GR restricts actions of its own coregulator via CDK9-mediated phosphorylation to a subse

287 on of MTA1 (metastasis-associated protein 1) coregulator via NF-kappaB signaling in hepatic cells.

288 GR recruits many coregulators via the well-characterized AF2 interaction

289 Recruitment of these coregulators was likely responsible for the increase in

290 y in eukaryotic transcription is provided by coregulators, which are recruited by DNA-binding factors

291 summary, this study has identified a new AR coregulator with a multifaceted role in prostate cancer,

292 een the roles for BRCA1 as a transcriptional coregulator with control of its expression via an autore

293 d blocks the interaction between a subset of coregulators with both native and mutant forms of ER.

294 Among the various transcriptional coregulators with which HNF4alpha interacts, peroxisome

295 riptional activity of AR is modulated by the coregulators with which it interacts, and consequently d

296 ecific master regulators and transcriptional coregulators within developmental stage-specific enhance

297 The sigma-like factor YvrI and coregulator YvrHa activate transcription from a small se

298 esults indicate that YvrI and its associated coregulators YvrHa and YvrL are required for the regulat

299 cell factor 1 (Ebf1) and the transcriptional coregulator Zfp521 as components of the machinery that r

300 inc finger unit found in the transcriptional coregulator ZNF217 recognizes DNA but with an affinity a