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

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

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

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

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

5 The top hit was SNW1, a splicing factor and transcriptional coactivator.

6 tivator 1-alpha (PGC1A) is a fasting-induced transcriptional coactivator.

7 nd was identified as a putative oncogene and transcriptional coactivator.

8 canonically regulated through recruitment of transcriptional coactivators.

9 works between transcriptional activators and transcriptional coactivators.

10 0 are closely related acetyltransferases and 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 nal coactivator with PDZ binding motif) is a transcriptional coactivator and end effector of the Hipp

14 The EZH2 TAD directly interacts with the transcriptional coactivator and histone acetyltransferas

15 form 2 (PKM2) is a key glycolytic enzyme and transcriptional coactivator and is critical for tumor me

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

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

18 YAP1 is a transcriptional coactivator and the principal effector o

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

20 Yki and YAP are transcriptional coactivators and function as downstream

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

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

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

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

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

26 The transcriptional coactivator ANGUSTIFOLIA3 (AN3) stimulat

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

28 ts two downstream effectors, the YAP and TAZ transcriptional coactivators, are drivers of tumor growt

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

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

31 In Wnt/beta-catenin signaling, the transcriptional coactivator beta-catenin is regulated by

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

33 tural transitions that may enable subsequent transcriptional coactivator binding.

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

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

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

37 -binding factor alpha1, mediator subunit 12, transcriptional coactivator CBP and TATA-box binding pro

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

39 tate the recruitment of Transportion and the transcriptional coactivator CBP.

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

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

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

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

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

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

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

47 5p-containing Spt-Ada-Gcn5-acetyltransferase transcriptional coactivator complex to catalyze histone

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

49 of the Spt-Ada-Gcn5 Acetyltransferase (SAGA) transcriptional coactivator complex.

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

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

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

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

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

55 The transcriptional coactivators CREB-binding protein (CBP)

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

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

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

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

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

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

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

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

64 The cAMP-regulated transcriptional coactivators (CRTCs) are a newly discove

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

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

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

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

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

70 say and suggest that LUG could function as a transcriptional coactivator during leaf blade developmen

71 A genome-wide shRNA screen identified the transcriptional coactivators EHMT2, EHMT1, and CBX3 as i

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

87 P7 was involved in the activation of YAP1 (a transcriptional coactivator in the Hippo pathway), which

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

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

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

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

92 PDZ-binding motif (TAZ), the key downstream transcriptional coactivators inhibited by LATS1/2.

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

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

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

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

97 oactivator with PDZ-binding motif (Taz), two transcriptional coactivators known to be activated by WN

98 As a transcriptional coactivator, LSD1 is necessary for desil

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

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

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

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

103 Mechanosensitive transcriptional coactivators MRTF-A and YAP/TAZ regulate

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

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

106 OXR2 affects the nuclear localization of the transcriptional coactivator NPR1, a master regulator of

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

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

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

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

111 centromeric protein, SGO2, serves as a novel transcriptional coactivator of HSF1, contributing to PIC

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

113 NCOA4 is a transcriptional coactivator of nuclear hormone receptors

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

115 We report that DLC1 is a regulator of YAP, a transcriptional coactivator of proliferation-promoting a

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

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

118 sferase mixed-lineage leukemia-4 (MLL4) is a transcriptional coactivator of the BA-sensing nuclear re

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

120 Yes-associated protein (YAP), the main transcriptional coactivator of the Hippo pathway, integr

121 Here, we show that the transcriptional coactivator of the Hippo pathway, Yorkie

122 d JEG-3 clones, we herein show that YAP, the transcriptional coactivator of the Hippo signaling pathw

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

124 ZMIZ1 is a transcriptional coactivator of the protein inhibitor of

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

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

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

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

129 The transcriptional coactivator p300 mediates histone acetyl

130 advances, the mechanism by which the HAT and transcriptional coactivator p300 mediates tumorigenesis

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

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

133 horylation and inactivation of the HIF1alpha transcriptional coactivator p300.

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

135 disrupting their interaction with the common transcriptional coactivator p300.

136 The transcriptional coactivator p300/CBP possesses both hist

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

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

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

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

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

142 The transcriptional coactivator peroxisome proliferator-acti

143 The transcriptional coactivator peroxisome proliferator-acti

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

145 The transcriptional coactivator peroxisome proliferator-acti

146 84 increased expression of the mitochondrial transcriptional coactivator peroxisome proliferator-acti

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

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

149 Transcriptional coactivators, peroxisome proliferator-ac

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

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

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

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

154 neurite outgrowth in ZIP12 deficient cells. Transcriptional coactivator PGC-1alpha, mitochondrial su

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

156 SIRT1 increases the levels of the transcriptional coactivator PGC1a and the secreted molec

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

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

159 onal corepressor and the ANGUSTIFOLIA3 (AN3) transcriptional coactivator play important roles in leaf

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

161 Moreover, deletion of the transcriptional coactivator PPARgamma coactivator 1alpha

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

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

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

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

166 nt studies have implicated the Hippo pathway transcriptional coactivator protein YAP1 as an additiona

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

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

169 cytes via interactions with PGC1alpha, a key transcriptional coactivator regulating gluconeogenesis,

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

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

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

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

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

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

176 cleaved CTT of PC1 (PC1-CTT) stimulates the transcriptional coactivator TAZ (Wwtr1), an essential co

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

178 1 and PC2 (encoded by Pkd1 and Pkd2) and the transcriptional coactivator TAZ form a mechanosensing co

179 inase signaling and nuclear translocation of transcriptional coactivator TAZ, inhibition of which mit

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

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

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

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

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

185 gamma coactivator 1-alpha (PGC-1alpha) is a transcriptional coactivator that controls expression of

186 ity leads to inactivation of Yorkie (Yki), a transcriptional coactivator that drives expression of gr

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

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

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

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

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

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

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

194 PGC1alpha is a transcriptional coactivator that promotes mitochondrial

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

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

197 ed target of Yes-associated protein (YAP), a transcriptional coactivator that regulates cell growth a

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

199 (MYOCD) is the founding member of a class of transcriptional coactivators that bind the serum-respons

200 YAP and TAZ are transcriptional coactivators that function as effectors

201 However, transcriptional coactivators that mediate their developm

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

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

204 as alternative, nonglycolysis functions as a transcriptional coactivator to enhance the transcription

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

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

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

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

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

210 any available beta-catenin, the Wnt pathway transcriptional coactivator, to the adherens junctions i

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

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

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

214 ells induced yes-associated protein 1 (YAP1)/transcriptional coactivator with PDZ binding motif (TAZ)

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

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

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

218 transcription factors Yes-associated protein/Transcriptional coactivator with PDZ domain (YAP/TAZ) an

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

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

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

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

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

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

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

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

227 effectors, Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ)

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

229 targets of Yes-associated protein (Yap) and transcriptional coactivator with PDZ-binding motif (Taz)

230 Yes-associated protein (YAP) and its homolog transcriptional coactivator with PDZ-binding motif (TAZ)

231 omologs (Smads)/Yes-associated protein (YAP)/Transcriptional coactivator with PDZ-binding motif (TAZ)

232 reased cellular senescence and inhibition of transcriptional coactivator with PDZ-binding motif (TAZ)

233 tivation of Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ)

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

235 ding (C-X-C motif) chemokine 10 (Cxcl10) and transcriptional coactivator with PDZ-binding motif (Taz)

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

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

238 l cofactors Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ,

239 ven EGFR, p53, Rac1b, yes-associated protein/transcriptional coactivator with PDZ-binding motif activ

240 ranscription factors, yes-associated protein/transcriptional coactivator with PDZ-binding motif via r

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

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

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

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

245 In a hyperactivated transcriptional coactivator with PDZ-binding motif-drive

246 nscription factor and Yes-associated protein/transcriptional coactivator with PDZ-binding motif.

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

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

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

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

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

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

253 The transcriptional coactivator YAP has been identified as a

254 Although the Hippo transcriptional coactivator YAP is considered oncogenic

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

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

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

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

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

260 The transcriptional coactivators YAP and TAZ mediate this fe

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

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

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

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

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

266 nd LATS1/2, as well as downstream effectors, transcriptional coactivators YAP and TAZ.

267 The Hippo pathway transcriptional coactivators YAP/TAZ were implicated as

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

269 The transcriptional coactivator YAP1 (yes-associated protein

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

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

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

273 In particular, the transcriptional coactivator YAP1 rescued cell viability

274 uire amplification and overexpression of the transcriptional coactivator Yap1.

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

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

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

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

279 n bind both F-actin and the neurosuppressive transcriptional coactivator Yes-associated protein (YAP)

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

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

282 ells similarly showed cytosolic retention of transcriptional coactivator Yes-associated protein (YAP)

283 Transcriptional coactivator yes-associated protein (YAP)

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

285 1 and 2 (LATS1/2) control activation of the transcriptional coactivators Yes-associated protein (YAP

286 We examined the role of the Hippo pathway transcriptional coactivators Yes-associated protein (YAP

287 Further, CS-GRP78 activated the transcriptional coactivators Yes-associated protein (YAP

288 e expression and nuclear localization of the transcriptional coactivators Yes-associated protein (YAP

289 (LATS)1 and 2, which serve to inactivate the transcriptional coactivators Yes-associated protein (YAP

290 helial cells, there is an early induction of transcriptional coactivator, Yes-associated protein (YAP

291 restricts tissue growth by inactivating the transcriptional coactivator Yki.

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

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

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

295 in Drosophila to promote the activity of the transcriptional coactivator Yorkie (Yki), the sole fly h

296 rosophila by restricting the activity of the transcriptional coactivator Yorkie (Yki), which normally

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

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

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

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