ライフサイエンスコーパス: co-activator

1 ase originally identified as a transcription co-activator.

2 ependent of the mitochondrial effects of the co-activator.

3 orylation inactivates Cdc20, a mitotic APC/C co-activator.

4 Yes-associated protein (YAP) transcriptional co-activator.

5 6) associated with the MAML1 transcriptional co-activator.

6 mulation of the beta-catenin transcriptional co-activator.

7 of POP-1 and functions as a transcriptional co-activator.

8 and association of transcription factors or co-activators.

9 arget genes; Tudor-SN is likely one of these co-activators.

10 ctivity of mERbeta isoforms with EDCs and ER co-activators.

11 cal for interactions with both receptors and co-activators.

12 receptors but also for the association with co-activators.

13 hibition is coupled to degron recognition by co-activators.

14 muscle genes through the myocardin-family of co-activators.

15 d binding sites of transcription factors and co-activators.

16 TBP also increased steroid receptor co-activator 1 (SRC-1) interaction with the PR NTD and c

17 ssociated factor (PCAF) and steroid receptor co-activator 1 (SRC-1), the full length ACTN4 protein ei

18 r peroxisome proliferator-activated receptor co-activator 1 alpha (PGC1alpha) and its splice variant

19 DNA sequence variation in PPAR gamma (PPARG) co-activator 1 alpha (PPARGC1A), a gene encoding a co-ac

20 a lipid-sensing transcription factor (PPARG co-activator 1 alpha, PPARGC1A) to age-related macular d

21 xisome proliferator-activated receptor gamma co-activator 1-alpha (PPARGC-1-alpha or PGC-1alpha), als

22 ue to increased expression of the PPAR-gamma co-activator 1-alpha.

23 8 MAPK activation and induction of PPARgamma co-activator-1 (PGC1alpha).

24 (LBD) interactions with the steroid receptor co-activator-1 (SRC-1) peptide, displacing SRC-1 binding

25 s of both receptors driving steroid receptor co-activator-1 (SRC1) interaction.

26 xisome proliferator-activated receptor gamma co-activator-1 alpha (PGC-1alpha) positively regulates t

27 the transcriptional co-activator PPAR-gamma co-activator-1 alpha (PGC1-alpha).

28 xisome proliferator-activated receptor gamma co-activator-1 alpha, positively control human OPN promo

29 element modulatory factor/androgen receptor co-activator 160), the key mediator of STAT3 ubiquitinat

30 xisome proliferator-activated receptor gamma co-activator-1a (PGC-1alpha), phosphoenolpyruvate carbox

31 xisome proliferator-activated receptor gamma co-activator 1alpha (PGC-1alpha), has emerged as a major

32 xisome proliferator-activated receptor gamma co-activator 1alpha (Pgc1alpha), leading to increased ac

33 n indirectly by modulating SP1 and PPARgamma co-activator 1alpha expression and/or activity independe

34 own of proliferator-activated receptor gamma co-activator 1alpha inhibits spinogenesis and synaptogen

35 Proliferator-activated receptor gamma co-activator 1alpha knockdown also reduces the density o

36 urons, proliferator-activated receptor gamma co-activator 1alpha overexpression increases dendritic s

37 xisome proliferator-activated receptor gamma co-activator 1alpha), a transcriptional co-activator tha

38 PPARgamma co-activator 1alpha, a co-activator of both CAR and PPAR

39 xisome proliferator-activated receptor gamma co-activator 1alpha, a master regulator of mitochondrial

40 xisome proliferator-activated receptor gamma co-activator-1alpha (PGC-1alpha) and PGC-1beta, both of

41 xisome proliferator-activated receptor gamma co-activator-1alpha (Pgc-1alpha) is critical for cardiac

42 t that proliferator-activated receptor gamma co-activator-1alpha and mitochondrial biogenesis have im

43 Proliferator-activated receptor gamma co-activator-1alpha knockdown inhibits brain-derived neu

44 ulates proliferator-activated receptor gamma co-activator-1alpha-dependent mitochondrial biogenesis b

45 xisome proliferator-activated receptor-gamma co-activator-1beta) and the nuclear receptor ERRalpha (e

46 Steroid receptor co-activator-3 (SRC-3/AIB1) is an oncogene that is ampli

47 ificantly overexpressed and nuclear receptor co-activator 4 (NCOA4) suppressed in colons of C. diffic

48 utophagy through the cargo receptor, nuclear co-activator 4.

49 the activation of Wnt ligands, receptors and co-activators accompanies the inactivation of Wnt antago

50 Moreover, we find that the p300 co-activator acetylates H3K64, and consistent with a tra

51 or of this pathway is YAP, a transcriptional co-activator amplified in mouse and human cancers where

52 rovide evidence that G9a functions both as a co-activator and a co-repressor to enhance cellular prol

53 Z) is a WW domain-containing transcriptional co-activator and a core component of an emerging Hippo s

54 r, RORgammat encoded by Rorc, by acting as a co-activator and co-repressor of STAT3, respectively.

55 MAML1 is best known as the co-activator and effector of NOTCH-induced transcription

56 nserved component of several transcriptional co-activator and histone acetyltransferase (HAT) complex

57 ently, TRIM24 functions as a transcriptional co-activator and recruits STAT3, leading to stabilized S

58 ical interactions with the Eyes absent (Eya) co-activator and the Groucho (Gro) co-repressor, but the

59 despite unaltered protein interactions with co-activators and -repressors.

60 AD3 interacts with reprogramming factors and co-activators and co-occupies OCT4 target loci during re

61 levels and respective interactions with the co-activators and co-repressors during erythroid develop

62 y is regulated by associated transcriptional co-activators and corepressors.

63 HIF-1alpha transactivating domain to recruit co-activators and diminished target gene expression.

64 FHL1 binds to the p300/CBP co-activators and disrupts binding with HIF-1alpha.

65 than the currently known TGFbeta1 downstream co-activators and epigenetic modifications.

66 se enhancers are occupied by transcriptional co-activators and loop onto the hes1 promoter within the

67 ine-rich (SR) proteins, a family of splicing co-activators, and thereby regulate the splicing of G6PD

68 actions between TAL1 and corepressors versus co-activators are properly regulated.

69 a process called sigma appropriation, the T4 co-activator AsiA structurally remodels the sigma(70) su

70 ge promoters using an activator (MotA) and a co-activator (AsiA), which function through interactions

71 tA functions in concert with a phage-encoded co-activator, AsiA, as a molecular switch.

72 a Tet-on CHO cell reporter system, RORalpha co-activator assays and inhibition of (RORE)-LUC reporte

73 Co-activator-associated arginine methyltransferase 1 (CA

74 Here we identify co-activator-associated arginine methyltransferase 1 (CA

75 teasome subcomplex enhances the targeting of co-activator at the TFIID-dependent promoter.

76 ith other endogenous transcription factor as co-activator (ATF3-JunB) or co-repressor (ATF3-NFkappaB)

77 nt protein interfaces on the transcriptional co-activator beta-catenin provides part of the answer.

78 target genes by promoting association of the co-activator beta-catenin with TCF/LEF transcription fac

79 including some utilizing the transcriptional co-activator beta-catenin, has limited the ability of cl

80 tion between the Wnt pathway transcriptional co-activators beta-catenin/Armadillo and TCF to facilita

81 ed RORgammat-driven transcription, decreased co-activator binding and promoted interaction with co-re

82 tomistic disordered ensembles of the nuclear co-activator binding domain (NCBD) of transcription coac

83 n of the interaction kinetics of the nuclear co-activator binding domain of CREB-binding protein and

84 at the expression of PIMT, a transcriptional co-activator binding protein, was up-regulated in the so

85 y a complex network of factors that includes co-activator binding, autophosphorylation, and dephospho

86 (Nucleosome acetyltransferase of histone H4) co-activator, but not activator Rap1p (repressor-activat

87 It usually functions as a transcriptional co-activator by associating with H3K4me3 and RNA polymer

88 the binding of BMAL1 to its transcriptional co-activator CBP.

89 by Plk1, which triggers association with the co-activator CBP.

90 mRNAs, whereas concentrations of the T-cell co-activators CD80 and CD86 increased in parallel with r

91 by catalysing the incorporation of the APC/C co-activator, CDC20, into a complex called the mitotic c

92 Furthermore, the metaphase APC co-activator, Cdc20, is specifically recruited to the ba

93 ion rate of 15 known substrates of the APC/C co-activator Cdh1 under normal conditions and conditions

94 gene, and fzr-1, an orthologue to the APC/C co-activator Cdh1, completely eliminates the essential r

95 mainly in neuronal contexts, when using the co-activator Cdh1/Fzr.

96 sition upon stimulation of the enzyme by its co-activator CGI-58.

97 tors (GTFs), RNA polymerase II (RNA pol II), co-activators, co-repressors, and more.

98 NA binding domain and a conserved N-terminal co-activator/co-repressor (COAR) domain consisting of A1

99 ntially induced in GSCs by a HIF1alpha/STAT3 co-activator complex and stabilizes Notch1 protein at th

100 chitecture of an estrogen receptor (ERalpha) co-activator complex bound to DNA.

101 The conserved Mediator co-activator complex has an essential role in the regula

102 TA1/polymerase II/activator protein-1 (AP-1) co-activator complex interacts with the FosB-gene chroma

103 The co-activator complex is deeply conserved and includes th

104 a component of the MEDIATOR transcriptional co-activator complex led us to address its involvement i

105 The conserved co-activator complex Mediator enables regulated transcri

106 The transcription co-activator complex SAGA is recruited to gene promoters

107 iated factor complex (PAFc) is an epigenetic co-activator complex that makes direct contact with MLL

108 port that depletion of the components of the co-activator complex, Mediator, specifically and potentl

109 es of the Tup1-Cyc8 co-repressor and Swi-Snf co-activator complexes.

110 ses are conserved components of COMPASS-like co-activator complexes.

111 quired for the T3-induced recruitment of the co-activator CREB-binding protein (CBP) and release of n

112 Cdc45 association with the MCM ring and GINS co-activator, critical for CMG assembly.

113 lcineurin and CREB-regulated transcriptional co-activator (Crtc).

114 ct of silencing CREB-regulated transcription co-activators (CRTC).

115 ding protein (Creb1) and its transcriptional co-activators (Crtc1-3) as targets of miR-17, miR-144, a

116 ssion via the de-phosphorylation of the CREB co-activator CRTC2 (ref. 1).

117 fferentiation via the activation of the CREB co-activator CRTC2.

118 romotes dephosphorylation of transcriptional co-activators CRTC2/3 resulting in enhanced gluconeogeni

119 sphorylation of CREB-regulated transcription co-activators (CRTCs) whose aberrant activation is linke

120 d protein (YAP) are critical transcriptional co-activators downstream of the Hippo pathway involved i

121 tial activator SIRT1, or its binding partner/co-activator EP300 inhibited RGZ induction of PPARgamma-

122 tivation of the enhancers and recruitment of co-activators, exemplified by p300, causing both enhance

123 ion of the transcription factor Six1 and its co-activator Eya1, develops into placodes and ultimately

124 er the methyltransferase and transcriptional co-activator EZH2 controls the differentiation clock of

125 icate that tissue-restricted transcriptional co-activators facilitate cell-specific Wnt/Wingless sign

126 e GRF-INTERACTING FACTOR (GIF) transcription co-activator family of Arabidopsis thaliana (Arabidopsis

127 Drosophila CREB-binding protein (dCBP) is a co-activator for Caudal-regulated activation of ftz.

128 In the nucleus, beta-catenin acted as a co-activator for IRF3-mediated transcription.

129 findings suggest a novel role for BTG2 as a co-activator for NFE2L2 in up-regulating cellular antiox

130 s, stabilizing beta-catenin, a transcription co-activator for OPN expression.

131 ivation domain from the p160 transcriptional co-activator for thyroid hormone and retinoid receptors.

132 eracts with, and serves as a transcriptional co-activator for, Lef1 and beta-catenin.

133 Perilipin 5 promotes PGC-1alpha co-activator function by disinhibiting SIRT1 deacetylase

134 at the inhibition of the YAP transcriptional co-activator function by PTPN14 is mediated through thei

135 ses reveal that CARM1 exerts transcriptional co-activator function on autophagy-related and lysosomal

136 Merm1 binds the GR co-activator GRIP1 but not GR.

137 uitment of the elongation factor P-TEFb, the co-activator GRIP1, the chromatin remodeling factor BRG1

138 ococcus pneumoniae, the core enzyme GtfA and co-activator GtfB form an OGT complex to glycosylate the

139 iogenesis in yeast (i.e. the transcriptional co-activator Hap4p) is positively regulated by the cellu

140 Knockdown of GATA6 or transcriptional co-activator/histone acetyltransferase p300 decreased AQ

141 se metabolism, acting as its transcriptional co-activator in endothelial cells.

142 YAP1 is a transcriptional co-activator in the Hippo signaling pathway, and YAP1-in

143 The role of co-activators in establishing this long-range interactio

144 nsferases (HATs) that act as transcriptional co-activators in multiple signalling pathways.

145 tential involvement of these transcriptional co-activators in skeletal myopathies.

146 The potential role of c-Jun and specific co-activators in the action of TGF-beta was investigated

147 rylation-dependent interaction of Elk-1 with co-activators, including histone acetyltransferases and

148 mechanisms driving differential beta-catenin/co-activator interactions and their role in adult somati

149 C) signaling regulates specific beta-catenin/co-activator interactions to promote adult progenitor ce

150 We show that the SRY-box 10 (SOX10) co-activator interacts and forms transcriptional complex

151 Creb3l3 mRNA, which encode a transcriptional co-activator involved in energy metabolism and a liver-s

152 owth factor (LEDGF/p75) is a transcriptional co-activator involved in targeting human immunodeficienc

153 function as non-DNA-binding transcriptional co-activators involved in regulating metabolic and devel

154 We demonstrate that ABHD5, a lipolytic co-activator, is ectopically expressed in CRC-associated

155 to regulate the epigenetic activity of an ER co-activator KDM3A, ACK1 modulates HOXA1 expression in t

156 We report that ACK1 phosphorylates the ER co-activator, KDM3A, a H3K9 demethylase, at an evolution

157 amily member) interacts with transcriptional co-activators like CREB-binding protein (CBP) and its pa

158 ranscription factor and one of its principal co-activators, MAL.

159 We further show that co-activator MED1 recruitment to the UBE2C enhancers is

160 e actin cytoskeleton and the transcriptional co-activator MKL1 (MAL).

161 action between serum response factor and its co-activator myocardin was reduced by overexpression of

162 r serum-response factor (SRF) along with its co-activator, myocardin-related transcription factor-A (

163 ecreased expression of progesterone receptor co-activators (NCOA1, -2 and -3, and CREBBP) towards ter

164 of miR-146b, downregulation of the PPARgamma co-activator NCOA4, and PPARgamma, leading to upregulati

165 o bind DNA and that a putative transcription co-activator NDP52 relieves the auto-inhibition of MVI t

166 eptor-gamma coactivator 1alpha, PGC1 related co-activator, nuclear respiratory factor 1, transcriptio

167 We have linked the co-activator of a lipid-sensing transcription factor (PP

168 work identifies the MLL complex as a crucial co-activator of AR and a potential therapeutic target in

169 r of MLL fusion-positive leukemia, acts as a co-activator of AR signaling.

170 ional target of androgen receptor (AR), is a co-activator of AR.

171 at the overexpression of the transcriptional co-activator of beta-catenin, transcription factor 7-lik

172 PPARgamma co-activator 1alpha, a co-activator of both CAR and PPARbeta/delta, was up-regu

173 is a negative regulator of p53 levels and a co-activator of estrogen receptor.

174 ssociated protein (YAP) is a transcriptional co-activator of hippo signaling pathway, which plays an

175 NPAT is a key co-activator of histone gene transcription, whereas FLAS

176 the nuclear translocation of beta-catenin, a co-activator of IFNbeta enhanceosome.

177 pha (PGC-1alpha), a critical transcriptional co-activator of metabolic gene expression, functions to

178 udies clearly indicate that PHD3 serves as a co-activator of NF-kappaB signaling activity in NP cells

179 ne methyltransferase 6 (PRMT6) is a specific co-activator of normal and mutant AR and that the intera

180 mouse model, in which an essential cytosolic co-activator of Nox2 is lost, to characterize bone metab

181 CRABP2 is a transcriptional co-activator of retinoic acid signaling.

182 d the binding between TAp63gamma and p300, a co-activator of TAp63gamma, and consequently counteracte

183 Vav3 is a novel co-activator of the AR.

184 Here we show that Ndfip1, a co-activator of the E3 ubiquitin ligase Itch, restricts

185 ted protein (YAP) is a major transcriptional co-activator of the Hippo pathway.

186 YAP is a transcriptional co-activator of the Hippo signaling pathway that is esse

187 ivator 1 alpha (PPARGC1A), a gene encoding a co-activator of the LCPUFA-sensing PPARG-retinoid X rece

188 he RNA helicase p68 (DDX5) is an established co-activator of the p53 tumour suppressor that itself ha

189 m phosphorylating YAP, a key transcriptional co-activator of the TE-specifying gene Cdx2.

190 TAZ was a critical co-activator of the TH17-defining transcription factor R

191 sent study we identified Tudor-SN as a novel co-activator of the transcription factor peroxisome prol

192 ation and degradation of beta-catenin, a key co-activator of Wnt-induced transcription.

193 r work has focused on targeting AR directly, co-activators of AR signaling, which may represent new t

194 CRTC isoforms are co-activators of CREB-regulated transcription by a CREB

195 wed that Kto and Skd are not transcriptional co-activators of Rel2 or other key factors of the IMD pa

196 Interestingly, the classical co-activators of SMAD3 complexes, p300 and CBP, were not

197 Ligands and co-activators of the omega-3 LCPUFA sensing PPAR-RXR axi

198 Eya proteins are essential co-activators of the Six family of transcription factors

199 that certain isoforms of AUF1 can serve as "co-activators" of TTP family protein binding to RNA.

200 anscription factor that acts in concert with co-activators or co-repressors to control the activity o

201 PPARgamma requires various co-activators or co-repressors, which may dynamically as

202 ongation, potentially through recruitment of co-activators or release of co-repressors with unique ro

203 e present at the Stra6 RARE; 2) RA increases co-activator p300 (KAT3B) binding and histone H3 Lys-27

204 Interestingly, only depletion of co-activator P300 resulted in the decrease of Foxo1 mRNA

205 sulted in recruitment of the transcriptional co-activator p300 to a Bcl11b-repressed promoter with su

206 significantly reduced owing to depletion of co-activator p300 upon treatment with triptolide.

207 dependent recruitment of the transcriptional co-activator p300.

208 upting the cooperation of C/EBPbeta with the co-activator p300.

209 a-catenin with either of the homologous Kat3 co-activators, p300 or CREB-binding protein, differentia

210 transcription and protein levels of the Cdk5 co-activator p35 through ERK1/2, resulting in an increas

211 Nuclear receptor co-activator peroxisome proliferator-activated receptor

212 esis was most likely mediated by the nuclear co-activators peroxisome proliferator-activated receptor

213 The co-activator, peroxisome proliferator-activated receptor

214 an OPN showed that ERRalpha and its obligate co-activator, peroxisome proliferator-activated receptor

215 sity, enhanced expression of transcriptional co-activator PGC-1alpha and increased mitochondrial fatt

216 evels of a gluconeogenic enzyme G6Pase and a co-activator PGC-1alpha were all markedly decreased.

217 nsferase-1, and the integral transcriptional co-activator Pgc-1alpha were significantly downregulated

218 xisome proliferator-activated receptor gamma co-activator (PGC)-1alpha promoter.

219 isome proliferators-activated receptor-gamma co-activator (PGC)-1alpha, a critical master of ROS meta

220 Cyclin E and its co-activator, phospho-cyclin-dependent kinase 2 (p-CDK2)

221 n muscle are mediated by the transcriptional co-activator PPAR-gamma co-activator-1 alpha (PGC1-alpha

222 the mitochondrial biogenesis transcriptional co-activator PPARgamma coactivator 1alpha (PGC-1alpha).

223 on of the adipogenic regulator PPARG and its co-activator PPARGC1B, and reduced expression of LPL.

224 ranscriptional mechanism.The transcriptional co-activator Prdm16 regulates browning of white adipose

225 bly checkpoint proteins Mad2, Mad3 and APC/C co-activator protein Cdc20), we reveal the molecular bas

226 F2C-bound sites by the SAP domain-containing co-activator protein myocardin, and we show that paired

227 cer may occur through increased levels of AR co-activator proteins.

228 ates Lys63-linked ubiquitination of the AP-1 co-activator RACO-1, leading to RACO-1 protein stabiliza

229 Mediator is a transcriptional co-activator recruited to enhancers by DNA-binding activ

230 Inhibition of co-activator recruitment to RXR and activation of NF-kap

231 sactivation due at least in part to impaired co-activator recruitment.

232 omoter occupancy and p300, a transcriptional co-activator, recruitment resulting in a defect in targe

233 was recently described as a transcriptional co-activator regulated by miR-135b in vestibular hair ce

234 langiectasia locus (NPAT), a transcriptional co-activator required for expression of histone genes in

235 tion of the NTD to facilitate the binding of co-activators required for maximal transcriptional activ

236 Thus, BRG1 is a SOX10 co-activator, required to establish the melanocyte linea

237 roporin Fps1, in part, by displacing channel co-activators (Rgc1/2).

238 ere we use mathematical modelling to infer a co-activator role for LIGHT-REGULATED WD1 (LWD1) in CCA1

239 one fold-containing subunits of TFIID and of co-activator SAGA are important for the assembly of thes

240 s1p is a common component of transcriptional co-activator, SAGA (Spt-Ada-Gcn5-Acetyltransferase), and

241 ow that cells stably depleted of LKB1 or its co-activator STRADalpha have increased phosphorylation o

242 ns are assembled, and how they interact with co-activators, substrates and regulatory proteins is lim

243 ranscriptional activators via recruitment of co-activators such as EP300, whereas KLF3 and related me

244 ) interacts efficiently with transcriptional co-activators such as p300/CBP-associated factor (PCAF)

245 sets of target genes through recruitment of co-activators such as the RNA polymerase II-interacting

246 ear receptor alpha (ERalpha), which requires co-activators, such as steroid receptor coactivator-1 (S

247 ast cancer by activating the transcriptional co-activator TAZ.

248 lation of beta-catenin and its transcription co-activator Tcf4 led to activation of Wnt/beta-catenin

249 The Eya1 gene encodes a transcriptional co-activator that acts with Six1 to control the developm

250 A point mutation in the Gal1 co-activator that disrupts the interaction with the Gal8

251 ssociated protein (YAP) is a transcriptional co-activator that has been associated with bladder cance

252 recruitment of Gcn5 (also known as Kat2a), a co-activator that has been implicated in transcription i

253 SAGA complex is a conserved, multifunctional co-activator that has broad roles in eukaryotic transcri

254 amma co-activator 1alpha), a transcriptional co-activator that has powerful effects on mitochondria;

255 n-like protein 2 (MKL2) is a transcriptional co-activator that in response to RhoA and cytoskeletal a

256 d also its homologue TAZ) is a transcription co-activator that mediates the biological functions of t

257 otein (Yap) has emerged as a transcriptional co-activator that modulates tissue homeostasis in respon

258 n-expressor of PR1 (NPR1) is a transcription co-activator that plays a central role in regulating the

259 In conclusion, RAC3 is a novel ERalpha co-activator that promotes cell migration and has progno

260 describe its oncogenic role as a HIF-1alpha co-activator that regulates the HIF-1 transcriptional ne

261 inding protein (CBP) are key transcriptional co-activators that are essential for a multitude of cell

262 Cdc20 and Cdh1 are WD40-containing APC co-activators that bind destruction boxes (DB) and KEN b

263 00/CBP, which are ubiquitous transcriptional co-activators that interact with a variety of sequence-s

264 In the presence of its co-activator, the siderophore bacillibactin (BB), the Bt

265 By inhibiting YAP and TAZ transcription co-activators, the Hippo pathway regulates cell prolifer

266 n with p300 and recruitment of this critical co-activator to promoters.

267 eta-catenin from acting as a transcriptional co-activator to TCF, yet without affecting its stability

268 co-repressors and facilitates recruitment of co-activators to activate transcription.

269 ription in part by controlling the access of co-activators to their transcription factor partners.

270 ors LRH-1's interaction with transcriptional co-activators to up-regulate gene expression.

271 ntified the RNA helicase DHX15 as a novel AR co-activator using a yeast mutagenesis screen and reveal

272 ing protein co-activators, we depleted these co-activators using adenoviral shRNAs.

273 hrough cAMP-response element-binding protein co-activators, we depleted these co-activators using ade

274 ls for MYC and EBNA2 (an EBV transcriptional co-activator) were significantly enriched in the promote

275 e expression indirectly inhibits the YAP/TAZ co-activators, which maintain the clonogenic potential o

276 CBP/p300 are transcription co-activators whose binding is a signature of enhancers,

277 of this pathway are YAP/TAZ, transcriptional co-activators whose dysfunction contributes to epithelia

278 Transcriptional co-activator with a PDZ binding domain (TAZ) is a WW dom

279 Transcriptional co-activator with PDZ-binding motif (TAZ) and Yes-associ

280 associated protein (YAP) and transcriptional co-activator with PDZ-binding motif (TAZ) are its target

281 associated protein (YAP) and transcriptional co-activator with PDZ-binding motif (TAZ), are required

282 Hippo pathway effectors TAZ (transcriptional co-activator with PDZ-binding motif) and YAP (Yes-associ

283 As Camtas can function as co-activators with NK2 proteins in other tissues, we exp

284 -terminal domain (A/B), as a transcriptional co-activator, without ELK1 hyper-phosphorylation.

285 reduces the activity of the transcriptional co-activator YAP and the expression of the NOTCH ligand

286 Binding of the transcriptional co-activator YAP with the transcription factor TEAD stim

287 of the Hippo kinase pathway transcriptional co-activator YAP.

288 The transcriptional co-activators YAP and TAZ are key regulators of organ si

289 We discovered that Tead1 and co-activators Yap and Taz are required for Pmp22 express

290 e and inhibit the downstream transcriptional co-activators YAP and TAZ, which are implicated in vario

291 of MST1/2 and LATS1/2 and the transcription co-activators YAP/TAZ.

292 y, the Hippo pathway and its transcriptional co-activator Yes-associated protein (YAP) have been show

293 sulting in activation of the transcriptional co-activator yes-associated protein (YAP).

294 g overexpressed AIP4 and the transcriptional co-activator Yes-associated protein (YAP).

295 The transcriptional co-activator Yes-associated protein 1 (YAP1), a key nucl

296 MST2 negatively regulate the transcriptional co-activators yes-associated protein 1 and WW domain con

297 osphorylation of the oncogenic transcription co-activator Yki/YAP.

298 the interaction between the transcriptional co-activator Yorkie (Yki) and the transcription factor S

299 nuclear localization of the transcriptional co-activator Yorkie and initiation of growth and prolife

300 or the Hippo pathway and its transcriptional co-activator Yorkie in controlling Drosophila glial prol

301 t suppressed by removing the transcriptional co-activator Yorkie, suggesting that these roles of Fat