ライフサイエンスコーパス: transcriptional coactivator

1 second, unrelated function in mammals, as a transcriptional coactivator.

2 In the former, free P-TEFb is a potent transcriptional coactivator.

3 of activated STAT (PIAS)-like protein and a transcriptional coactivator.

4 ntaining genes known to be regulated by this transcriptional coactivator.

5 ya during Drosophila eye development is as a transcriptional coactivator.

6 TR) through recruitment of cellular CREB and transcriptional coactivators.

7 vated protein kinase) signaling pathways and transcriptional coactivators.

8 o block DNA-binding proteins from recruiting transcriptional coactivators.

9 he PPARgamma coactivator-1 (PGC-1) family of transcriptional coactivators.

10 canonically regulated through recruitment of transcriptional coactivators.

11 nse element binding protein (CREB)-regulated transcriptional coactivator 1 (CRTC1)/mastermind-like 2

12 ion of the latent cytoplasmic CREB regulated transcriptional coactivator 2 (CRTC2).

13 Transcriptional coactivator activating signal cointegrat

14 nal coactivator with PDZ binding motif) is a transcriptional coactivator and end effector of the Hipp

15 etion mutations of CREBBP, which encodes the transcriptional coactivator and histone acetyltransferas

16 naling cascade regulates the activity of the transcriptional coactivator and oncoprotein Yorkie/Yap.

17 Eyes absent (Eya) is a highly conserved transcriptional coactivator and protein phosphatase that

18 lization of the Yes-associated protein (YAP) transcriptional coactivator and support long-term self-r

19 YAP is a transcriptional coactivator and while details of YAP reg

20 Yki and YAP are transcriptional coactivators and function as downstream

21 binding also resulted in the recruitment of transcriptional coactivators and induction of gene expre

22 ecific isoform BRDT-that largely function as transcriptional coactivators and play critical roles in

23 optosis, and DNA repair and is influenced by transcriptional coactivators and post-translational modi

24 muscle ARNT-like 1) is a regulatory hub for transcriptional coactivators and repressors that compete

25 ceptor gamma coactivator 1 (PGC-1) family of transcriptional coactivators and the estrogen-related re

26 ours, have placed EZH2 into the category of transcriptional coactivators and thus raised the possibi

27 s Tax, decreases Tax binding to the CBP/p300 transcriptional coactivator, and, by reducing Tax transc

28 are the activation of transcription factors, transcriptional coactivators, and downstream gene progra

29 The transcriptional coactivator ANGUSTIFOLIA3 (AN3) stimulat

30 ry roles of long noncoding RNAs (lncRNAs) in transcriptional coactivators are still largely unknown.

31 and offer preclinical proof of concept for a transcriptional coactivator as a therapeutic target to a

32 essive ubiquitin ligase for beta-catenin and transcriptional coactivator associated with histone acet

33 BRD4, a widely expressed transcriptional coactivator, belongs to the BET family o

34 ulatory mechanism for PIFs in which HMR is a transcriptional coactivator binding directly to PIFs and

35 igate how inhibition of the widely expressed transcriptional coactivator BRD4 leads to selective inhi

36 protein degradation using as an example the transcriptional coactivator BRD4, a protein critical for

37 iR-HSUR4-3p represses expression of the p300 transcriptional coactivator by binding the open reading

38 3, both interact with the TAZ2 domain of the transcriptional coactivator CBP at two binding sites.

39 e region of Ci can impede recruitment of the transcriptional coactivator CBP by masking its binding s

40 Here, we report that the transcriptional coactivator CBP/p300 is required to main

41 protein silencing, and the KIX domain of the transcriptional coactivator CBP/p300, critical for leuke

42 and cysteine-histidine rich region (CH1) of transcriptional coactivator CBP/p300.

43 upport selective bromodomain blockade of the transcriptional coactivators CBP (CREB binding protein)

44 Z1 (also known as CH1) domain of the general transcriptional coactivators CBP and p300 to control the

45 w that NLRC5 can cooperate with ATF1 and the transcriptional coactivators CBP/p300 and general contro

46 The multi-domain transcriptional coactivators CBP/p300 integrate a multit

47 ites potentiates recruitment of the Mediator transcriptional coactivator complex and transcriptional

48 of the Spt-Ada-Gcn5 acetyltransferase (SAGA) transcriptional coactivator complex in Drosophila melano

49 The transcriptional coactivator complex Mediator (MED) facil

50 EZING6 [SFR6]) subunit of the plant Mediator transcriptional coactivator complex regulates cold-respo

51 The Mediator complex is a central transcriptional coactivator complex that acts as a bridg

52 5p-containing Spt-Ada-Gcn5-acetyltransferase transcriptional coactivator complex to catalyze histone

53 Mediator is a conserved, essential transcriptional coactivator complex, but its in vivo fun

54 , MLL4 (aka KMT2D), belong to two homologous transcriptional coactivator complexes, named MLL3 and ML

55 depends on the stress-specific regulation of transcriptional coactivator complexes.

56 The Yap transcriptional coactivator controls proliferation in a

57 te pathway for triglyceride storage and as a transcriptional coactivator/corepressor for metabolic nu

58 While the transcriptional coactivator CREB binding protein (CBP) i

59 lude key host regulators such as the general transcriptional coactivator CREB binding protein (CBP),

60 vealed that the dual inhibitors depleted the transcriptional coactivator CREB-binding protein from th

61 The transcriptional coactivators CREB-binding protein (CBP)

62 when expressed ectopically, interacts with a transcriptional coactivator, CREB-binding protein (CBP),

63 (KID) and the KID-interacting domain of the transcriptional coactivator, CREB-binding protein (CBP).

64 y active form of IRF3 in the presence of its transcriptional coactivator, CREB-binding protein (CBP).

65 histone H3 Lys4 (H3K4me1) and binding of the transcriptional coactivator CREBBP (also called CBP) tha

66 nes, many of which were novel, including the transcriptional coactivators CREBBP and NCOR1, the trans

67 nse element-binding protein (CREB)-regulated transcriptional coactivator (CRTC) 3, its dissociation f

68 nse element binding protein (CREB)-regulated transcriptional coactivator (CRTC) family of transcripti

69 in modulate longevity via the CREB regulated transcriptional coactivator (CRTC)-1 in C. elegans.

70 the nuclear exclusion of the CREB-regulated transcriptional coactivator CRTC1 within pain sensory ne

71 The CREB-regulated transcriptional coactivator (CRTC1), which is required f

72 patocytes, the absence of LKB1, AMPK, or the transcriptional coactivator CRTC2 did not prevent adipon

73 ment of the CREB coactivator, cAMP-regulated transcriptional coactivators (CRTC2).

74 In mammals, CREB-regulated transcriptional coactivators (CRTCs) are a family of cof

75 eased nuclear localization of CREB-regulated transcriptional coactivators (CRTCs) in this tissue.

76 he dephosphorylation of the cAMP- responsive transcriptional coactivators (CRTCs).

77 mechanism is deregulation of CREB-regulated transcriptional coactivators (CRTCs).

78 tumor suppressor is its interaction with the transcriptional coactivators cyclic-AMP response element

79 E3, leading to direct induction of the PGC-1 transcriptional coactivators, drivers of mitochondrial b

80 a-catenins are critical regulators of Yap, a transcriptional coactivator essential for cardiomyocyte

81 he Yorkie (Yki)/Yes-associated protein (YAP) transcriptional coactivator family to control tissue gro

82 MED1 has been demonstrated to serve as a key transcriptional coactivator for AR, the mechanisms by wh

83 W1 functions as both a splicing factor and a transcriptional coactivator for induced genes.

84 nd interferes with its ability to serve as a transcriptional coactivator for T-cell factor (TCF) prot

85 indicate that ARID4A and ARID4B function as transcriptional coactivators for AR and RB and play an i

86 lts suggest that Ssdp1/2 function as crucial transcriptional coactivators for LIM complexes to specif

87 nuclear export of an essential beta-catenin transcriptional coactivator from mesoderm renders it ref

88 acetylation, PKM2 nuclear protein kinase and transcriptional coactivator functions are abolished.

89 e provide genetic evidence that this generic transcriptional coactivator functions as a positive modi

90 transcriptional coactivator (CRTC) family of transcriptional coactivators has been proposed to promot

91 The cellular transcriptional coactivator HCF-1 is required for initia

92 nistic insight into how SPIN1 functions as a transcriptional coactivator, here we purified its intera

93 cell adhesion and as the T-cell factor (TCF) transcriptional coactivator in canonical Wnt (wingless-r

94 on of PGC-1beta and studied the role of this transcriptional coactivator in dietary-induced steatosis

95 directly targets CREB-binding protein, a key transcriptional coactivator in IFN signaling, thereby in

96 at binds to acetylated histones and is a key transcriptional coactivator in mammals.

97 We propose Integrator as a crucial transcriptional coactivator in MAPK signaling, which cou

98 While it functions in the nucleus as a transcriptional coactivator in phytochrome signaling to

99 ingle gene for beta-catenin, which is also a transcriptional coactivator in Wnt signaling.

100 onic stem cells that Sp5/8 are gene-specific transcriptional coactivators in the Wnt/beta-catenin pat

101 orted as a negative regulator of SIRT1 and a transcriptional coactivator, in the regulation of Wnt/be

102 DE-ON-PETIOLE1 (BOP1) and BOP2, which encode transcriptional coactivators, in the SAM during vegetati

103 PGC-1alpha is a transcriptional coactivator induced by exercise that giv

104 llular domain, which associates with several transcriptional coactivators involved in nuclear signali

105 ying mechanism by which TDRD3 functions as a transcriptional coactivator is unknown.

106 The family of three MAML transcriptional coactivators is crucial for Notch signal

107 plants to humans and best characterized as a transcriptional coactivator, is also the prototype for a

108 As a transcriptional coactivator, LSD1 is necessary for desil

109 ibit NOTCH signaling by associating with the transcriptional coactivator MAML1.

110 show that members of the Myocardin family of transcriptional coactivators, MASTR and MRTF-A, are up-r

111 binding region of one of these proteins, the transcriptional coactivator Mbf1, to a region distinct f

112 uired the megakaryoblastic leukemia 1 (MKL1) transcriptional coactivator-mediated mechanosensing path

113 ted transcription factors (MRTFs), which are transcriptional coactivators mediating cell-specific fun

114 n polymerization-dependent activation of the transcriptional coactivator megakaryoblastic leukemia 1

115 ed through GPCRs and RhoA, one utilizing the transcriptional coactivator myocardin-related transcript

116 rmation via control of the G-actin-regulated transcriptional coactivator myocardin-related transcript

117 ogen receptor required the expression of the transcriptional coactivator NCoR.

118 Because BCL9 is a critical transcriptional coactivator of beta-catenin that is aber

119 f active beta-catenin protein, the essential transcriptional coactivator of canonical Wnt signaling,

120 HCF1 is known as a transcriptional coactivator of herpes simplex virus (HSV

121 PHD3 is a transcriptional coactivator of HIF-1alpha in nucleus pul

122 njury involves the role of beta-catenin as a transcriptional coactivator of HIF-1alpha signaling, whi

123 dependent kinase 9 (CDK9), which serves as a transcriptional coactivator of HIV-1 gene expression.

124 coactivator 1alpha (PGC-1alpha), a critical transcriptional coactivator of metabolic genes, acts as

125 NCOA4 is a transcriptional coactivator of nuclear hormone receptors

126 coactivator-1alpha (PGC-1alpha) is a potent transcriptional coactivator of oxidative metabolism and

127 receptor RNA activator (SRA), functions as a transcriptional coactivator of PPARgamma and promotes ad

128 Bzeta, an atypical IkappaB family member and transcriptional coactivator of selected NF-kappaB target

129 ardin-related transcription factor (MRTF), a transcriptional coactivator of serum response factor (SR

130 Myocardin functions as a transcriptional coactivator of SRF and is sufficient and

131 s) induces the activity of Yorkie (Yki), the transcriptional coactivator of the Hippo pathway, by ind

132 Our data indicate that TRBP is a novel transcriptional coactivator of the Notch signaling pathw

133 ZMIZ1 is a transcriptional coactivator of the protein inhibitor of

134 ers, which enter the nucleus and function as transcriptional coactivators of plant defense genes.

135 ol of bile acid homeostasis) and as critical transcriptional coactivators of the circadian TFs, RORs.

136 Mediator is a highly conserved transcriptional coactivator organized into four modules,

137 us studies establishing the XPC complex as a transcriptional coactivator, our findings underscore two

138 regulation because they have to compete with transcriptional coactivator p300 for binding to p53.

139 t(8;21) translocation, is acetylated by the transcriptional coactivator p300 in leukemia cells isola

140 red binding of the histone acetyltransferase/transcriptional coactivator p300 to this same region, ca

141 R-132 and miR-26a, as negative regulators of transcriptional coactivator p300, a component of the IFN

142 emonstrate here that ATF5 interacts with the transcriptional coactivator p300, which acetylates ATF5

143 odomain/PHD finger (bromo/PHD) region of the transcriptional coactivator p300.

144 disrupting their interaction with the common transcriptional coactivator p300.

145 horylation and inactivation of the HIF1alpha transcriptional coactivator p300.

146 The transcriptional coactivator p300/CBP possesses both hist

147 ens epithelium-derived growth factor (LEDGF)/transcriptional coactivator p75 are an emerging class of

148 Accumulating evidence implicates the transcriptional coactivator peroxisome proliferator acti

149 84 increased expression of the mitochondrial transcriptional coactivator peroxisome proliferator-acti

150 ccumulating evidence strongly implicates the transcriptional coactivator peroxisome proliferator-acti

151 The transcriptional coactivator peroxisome proliferator-acti

152 The transcriptional coactivator peroxisome proliferator-acti

153 A direct SIRT1 substrate is the transcriptional coactivator peroxisome proliferator-acti

154 in a strong interaction between YY1 and the transcriptional coactivator peroxisome proliferator-acti

155 breast cancer by ectopically expressing the transcriptional coactivator peroxisome proliferator-acti

156 The effects of YAP are mediated by the transcriptional coactivator peroxisome proliferator-acti

157 (ADRB2), cAMP production, and import of the transcriptional coactivator peroxisome proliferator-acti

158 xpression of downstream targets, Myc and the transcriptional coactivator peroxisome proliferator-acti

159 We show here that the transcriptional coactivators peroxisome proliferator-act

160 The role of MFN2's transcriptional coactivator, peroxisome proliferator-act

161 Transcriptional coactivators, peroxisome proliferator-ac

162 ial biogenesis and glycolysis, controlled by transcriptional coactivator PGC-1alpha and HIF, respecti

163 heat production in brown adipocytes are the transcriptional coactivator PGC-1alpha and its splicing

164 Correspondingly, levels of the transcriptional coactivator PGC-1alpha fell by 35%, sugg

165 The transcriptional coactivator PGC-1alpha is a master regul

166 Underexpression of the transcriptional coactivator PGC-1alpha is causally linke

167 etyltransferase promoting acetylation of the transcriptional coactivator PGC-1alpha to control hepati

168 e acetylation (suggesting inhibition) of the transcriptional coactivator PGC-1alpha, downregulating e

169 and mitochondrial alterations and repressed transcriptional coactivator PGC-1alpha.

170 PARIS represses the expression of the transcriptional coactivator, PGC-1alpha and the PGC-1alp

171 increased expression of the AMPK-target and transcriptional coactivator PGC1alpha in Fnip1 null skel

172 ive phosphorylation (OxPhos) mediated by the transcriptional coactivator PGC1alpha.

173 functional, chromatin-associated protein and transcriptional coactivator positive coactivator 4 (PC4/

174 ne kinase STK32B and one (rs17590046) in the transcriptional coactivator PPARGC1A were associated wit

175 that Nf2 functions by inhibiting the Yap/Taz transcriptional coactivators, probably through a mechani

176 d by a 190-kb 5' genomic region of Cited1, a transcriptional coactivator protein for CBP/p300.

177 ing of its alpha-subunit (HIF-1alpha) to the transcriptional coactivator protein p300.

178 t-Hippo signaling acts via a non-DNA-binding transcriptional coactivator protein, Yorkie.

179 nd nutritional supplies, the PGC-1 family of transcriptional coactivators regulates mitochondrial bio

180 muscular atrophy, impairs its function as a transcriptional coactivator regulating an extensive netw

181 hieve complete deletion of beta-catenin, the transcriptional coactivator required for canonical Wnt s

182 Bzeta, an atypical IkappaB family member and transcriptional coactivator required for the selective e

183 The transcriptional coactivator SRC-3 plays a key role in en

184 her with phosphorylation and activity of the transcriptional coactivator SRC-3.

185 The transcriptional coactivator Sub1 has been implicated in

186 present study, we show that miR-101 targets transcriptional coactivator SUB1 homolog (Saccharomyces

187 ell varies drastically depending on lineage, transcriptional coactivators such as BETs would be expec

188 lted in histone modifications, activation of transcriptional coactivators, such as p300/CBP, and accu

189 endent ACDs rely on nuclear asymmetry of the transcriptional coactivator SYS-1/beta-catenin between d

190 quiescence was mediated by the Hippo pathway transcriptional coactivator TAZ and, ultimately, led to

191 1 and PC2 (encoded by Pkd1 and Pkd2) and the transcriptional coactivator TAZ form a mechanosensing co

192 ilization of the tyrosine kinase ABL and the transcriptional coactivator TAZ.

193 Hippo pathway transcriptional coactivators TAZ and YAP and the TGF-bet

194 ed the efficiency of Rap1 binding to a known transcriptional coactivator TFIID-binding target, Taf5.

195 Myocardin is a muscle-restricted transcriptional coactivator that activates a serum respo

196 PPARGC1A is a transcriptional coactivator that binds to and coactivate

197 rase (SAGA) chromatin-modifying complex is a transcriptional coactivator that contains four different

198 lts highlight a role for SNAPC1 as a general transcriptional coactivator that functions through elong

199 or, alpha subunit-like effector A (Cidea), a transcriptional coactivator that has been implicated in

200 Myocardin is a muscle lineage-restricted transcriptional coactivator that has been shown to trans

201 r gamma coactivator 1alpha (PGC-1alpha) is a transcriptional coactivator that in hippocampus is highl

202 has been well characterized as an important transcriptional coactivator that interacts both with seq

203 jor target of this kinase cascade is YAP1, a transcriptional coactivator that is inactivated by Hippo

204 ECs was enhanced by BCL9, a Wnt-beta-catenin transcriptional coactivator that is selectively expresse

205 p300 is a transcriptional coactivator that participates in many im

206 PGC-1alpha is a transcriptional coactivator that plays a central role in

207 man homolog of trithorax in Drosophila, is a transcriptional coactivator that plays an essential role

208 ssociated protein (YAP) is a Hippo signaling transcriptional coactivator that plays pivotal roles in

209 PGC-1alpha is a transcriptional coactivator that powerfully regulates ma

210 teroid receptor coactivator 3 or NCOA3, is a transcriptional coactivator that promotes cancer cell pr

211 cle-specific overexpression of PGC-1alpha, a transcriptional coactivator that promotes mitochondrial

212 PGC1alpha is a transcriptional coactivator that promotes mitochondrial

213 known as PGC-1alpha; encoded by Ppargc1a), a transcriptional coactivator that regulates broad program

214 PGC-1alpha is an inducible transcriptional coactivator that regulates cellular ener

215 r gamma coactivator 1alpha (PGC-1alpha) is a transcriptional coactivator that regulates diverse aspec

216 tor gamma coactivator 1beta (PGC-1beta) is a transcriptional coactivator that regulates metabolism an

217 PGC-1alpha is a transcriptional coactivator that regulates mitochondrial

218 YAP and TAZ are transcriptional coactivators that function as effectors

219 However, transcriptional coactivators that mediate their developm

220 (MAML2) (C1/M2) oncoprotein comprised of two transcriptional coactivators, the CRTC1 and the NOTCH/RB

221 irment of which converts nuclear-WASp from a transcriptional coactivator to a corepressor of nuclear

222 ultikinase (IPMK) acts noncatalytically as a transcriptional coactivator to mediate induction of nume

223 levels of FA oxidation enzymes, up-regulated transcriptional coactivators to drive oxidative metaboli

224 neral insights into how cancer cells exploit transcriptional coactivators to maintain oncogenic gene

225 n which AEG-1 interferes with recruitment of transcriptional coactivators to RXR, preventing transcri

226 ent kinase 9 (CDK9)/cyclin T1 and other host transcriptional coactivators to the HIV-1 promoter.

227 hx3-LIM domains are essential for recruiting transcriptional coactivators to the Isl1-Lhx3 complex.

228 text of fear extinction, PCAF functions as a transcriptional coactivator, which may facilitate the fo

229 slational modification in the recruitment of transcriptional coactivators, which may allow transcript

230 activates yes-associated protein 1 (YAP) and transcriptional coactivator with a PDZ-binding domain (T

231 Spindlin1 (SPIN1) is a transcriptional coactivator with critical functions in e

232 This study identifies a transcriptional coactivator with diversified functions i

233 MF treatment reduced nuclear localization of transcriptional coactivator with PDZ binding motif (TAZ)

234 ipogenic proteins such as GATA-3, KLF-2, and transcriptional coactivator with PDZ binding motif (TAZ)

235 ectors Yap (Yes-associated protein) and Taz (transcriptional coactivator with PDZ binding motif) in t

236 TAZ (transcriptional coactivator with PDZ binding motif) is a

237 tion of the Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding domain (TAZ

238 We show that FGF18 induces transcriptional coactivator with PDZ-binding motif (TAZ)

239 tivation of the Yes-associated protein (YAP)/transcriptional coactivator with PDZ-binding motif (TAZ)

240 ator Yorkie [Yki-Yes-activated protein (YAP)/transcriptional coactivator with PDZ-binding motif (TAZ)

241 m effectors Yes-associated protein (YAP) and Transcriptional coactivator with PDZ-binding motif (TAZ)

242 factors Yes-associated protein 1 (YAP1) and transcriptional coactivator with PDZ-binding motif (TAZ)

243 is pathway, Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ)

244 Transcriptional coactivator with PDZ-binding motif (TAZ)

245 ancer Genome Atlas (TCGA), we identified the transcriptional coactivator with PDZ-binding motif (TAZ)

246 Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ)

247 nt roles of Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ)

248 YAP (Yes-associated protein) and TAZ (transcriptional coactivator with PDZ-binding motif) are

249 ctors, Yap (yes-associated protein) and Taz (transcriptional coactivator with PDZ-binding motif), as

250 homologues, Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif, enco

251 netics of both early (Yes-associated protein/Transcriptional coactivator with PDZ-binding motif, YAP/

252 d protein (YAP), an evolutionarily conserved transcriptional coactivator with potent oncogenic potent

253 Overexpression of PGC-1alpha, a transcriptional coactivator with roles in both mitochond

254 Nuclear CTNNB1 acts as a transcriptional coactivator with TCF/LEF transcription f

255 p300 (EP300) and CBP (CREBBP) are transcriptional coactivators with histone acetyltransfer

256 s absent (EYA) family proteins are conserved transcriptional coactivators with intrinsic protein phos

257 protein (CBP) and p300 are highly homologous transcriptional coactivators with unique, non-redundant

258 y, the tumor suppressor Nf2 (Merlin) and the transcriptional coactivator Yap (Yap1), regulate guidepo

259 The transcriptional coactivator YAP has been identified as a

260 The Hippo pathway regulates the transcriptional coactivator YAP to control cell prolifer

261 Here, we focused on the transcriptional coactivator YAP, a critical component of

262 re associated with increased activity of the transcriptional coactivator YAP, which is due at least i

263 ession by phosphorylating and inhibiting the transcriptional coactivator YAP.

264 ffening resulted in mechanoactivation of the transcriptional coactivators YAP and TAZ (WWTR1).

265 the protein kinases Lats1 and Lats2, and the transcriptional coactivators Yap and Taz [4-6].

266 The key effectors of this pathway, transcriptional coactivators Yap and Taz, are expressed

267 d Lats2, which phosphorylate and inhibit the transcriptional coactivators Yap and Taz, in nephron pro

268 unctions to phosphorylate and inactivate the transcriptional coactivators YAP and TAZ, which control

269 d triggering the nuclear localization of the transcriptional coactivators YAP and TAZ, which serve to

270 phosphorylation and nuclear exclusion of the transcriptional coactivators YAP and TAZ.

271 rotein-coupled receptors act upstream of the transcriptional coactivators YAP/TAZ.

272 raining the growth-promoting function of the transcriptional coactivator, YAP.

273 rther demonstrated the nuclear expression of transcriptional coactivator YAP1 in the limbal and corne

274 Phosphorylation of the transcriptional coactivator YAP1 is a key event in defin

275 Here we show that the transcriptional coactivator YAP1 is a major determinant

276 In particular, the transcriptional coactivator YAP1 rescued cell viability

277 uire amplification and overexpression of the transcriptional coactivator Yap1.

278 We show that the Hippo pathway transcriptional coactivators Yap1 and Wwtr1 are specific

279 ppo pathway signaling, via modulation of the transcriptional coactivator Yes-associated protein (YAP)

280 nd nuclear exclusion of the growth-promoting transcriptional coactivator Yes-associated protein (YAP)

281 retention and functional inactivation of the transcriptional coactivator YES-associated protein (YAP)

282 The transcriptional coactivator Yes-associated protein (YAP)

283 esponse factor (SRF) and the other using the transcriptional coactivator Yes-associated protein (YAP)

284 The recent discovery that the transcriptional coactivator Yes-associated protein (Yap)

285 S1) kinase that inhibits the activity of the transcriptional coactivator yes-associated protein (YAP)

286 d abundance, and nuclear localization of the transcriptional coactivator Yes-associated protein 1 (Ya

287 nuclear localization of the mechanoreactive transcriptional coactivator Yes-associated protein.

288 1 and 2 (LATS1/2) control activation of the transcriptional coactivators Yes-associated protein (YAP

289 restricts tissue growth by inactivating the transcriptional coactivator Yki.

290 mediary kinase Wts/Lats to phosphorylate the transcriptional coactivator Yki/YAP/TAZ.

291 ivator Taiman (Tai) interacts with the Hippo transcriptional coactivator Yorkie (Yki) and promotes ex

292 e proteins by RNA interference regulated the transcriptional coactivator Yorkie (Yki) either positive

293 The transcriptional coactivator Yorkie (Yki) mediates transc

294 ates tissue growth in Drosophila through the transcriptional coactivator Yorkie (Yki).

295 ette that phosphorylates and inactivates the transcriptional coactivator Yorkie (Yki).

296 Phosphorylation of the transcriptional coactivator Yorkie (Yki)/YAP by Warts do

297 The transcriptional coactivator Yorkie (Yki, a YES-Associate

298 he heart of the Hpo pathway is the progrowth transcriptional coactivator Yorkie [Yki-Yes-activated pr

299 conserved residues in the WW domains of the transcriptional coactivator Yorkie, and Myopic colocaliz

300 that negatively regulate the activity of the transcriptional coactivator Yorkie.