ライフサイエンスコーパス: transactivator

1 3 months after inactivation of tetracycline transactivator.

2 nsa serendipity alpha gene linked to the Tet-transactivator.

3 asing expression of genes controlled by this transactivator.

4 until the recent discovery of NLRC5/class I transactivator.

5 rus protein known primarily as a promiscuous transactivator.

6 silence the expression of ICP0, a key viral transactivator.

7 ins, makes the fusion protein a constitutive transactivator.

8 egatively regulated by ICP4, the major viral transactivator.

9 BHV-4), termed HORF1/2, was a very efficient transactivator.

10 Thus, IE1 is a positive, gene-specific transactivator.

11 s 1 (HSV-1) is that it acts as a promiscuous transactivator.

12 d by expressing the HCMV multifunctional IE1 transactivator.

13 d also impaired nsp1beta's function as a PRF transactivator.

14 PR/Cas9 to disrupt the gene for the class II transactivator.

15 moter for an important viral transcriptional transactivator.

16 nase activation, a classic LRP1-mediated Trk transactivator.

17 to avoid the effect of the virion-associated transactivators.

18 ral or tissue-specific 'tet-on' or 'tet-off' transactivators.

19 imulation of the spared allele by artificial transactivators.

20 tors from the primitive Cbp/p300-interacting transactivator 1 expressing (CITED1+) compartment to the

21 rotein (CBP), p300, and Cbp/p300-interacting transactivator 2 (Cited2) was increased in the amygdala

22 in the early growth response 2 (Egr2/Krox20) transactivator, a critical regulator of peripheral myeli

23 iated with up-regulation of the MHC class II transactivator, a key transcription factor with deacetyl

24 We show that the EBNA2 transactivator activates multiple MYC enhancers and reco

25 oth necessary and sufficient for PMA-induced transactivator activity in PAI-2-expressing U937 cells.

26 of IRF3 function was maintained even if IE62 transactivator activity was disrupted.

27 gnificantly decreased when the upstream EGFR transactivator ADAM17 was inhibited.

28 These transacting factors are the class II transactivator and 3 subunits of regulatory factor X (RF

29 Coexpression of this transactivator and combinations of guide RNAs in human c

30 r equation) models where the transcriptional transactivator and promoter toggle between inactive and

31 ntrol of the reverse tetracycline-controlled transactivator and the tetracycline operator minimal pro

32 genes, including those expressing additional transactivators and putative oncogenes, are induced in a

33 ICP0 also functions as a promiscuous transactivator, and it blocks repressor complexes to ena

34 esized ORF61, as well as IE62, the major VZV transactivator, appeared within 1 h, and they were targe

35 s and limits the ability of Ifh1 to act as a transactivator at RP genes.

36 of small interfering RNA targeting class II transactivator attenuates major histocompatibility compl

37 In NPC, NF-kappaB p50/p50 homodimers and the transactivator Bcl-3 were detected on the EGFR promoter.

38 the specific interplay between the cellular transactivator Brn-3a, the environmental smoking-related

39 n, suggesting that it might be not a typical transactivator but an architectural transcription factor

40 a 14-kDa viral protein that acts as a potent transactivator by binding to the transactivation-respons

41 small interfering RNA targeting of class II transactivator can reduce the capacity of human endothel

42 We previously established that the class II transactivator CIITA binds GTP and disruption of the GTP

43 The master transactivator CIITA is essential to the regulation of M

44 MHC Class II expression is controlled by the transactivator CIITA.

45 y mechanisms includes repression of class-II transactivator (CIITA) and MHC-II expression in infected

46 on strategies such as inhibition of class II transactivator (CIITA) and MHC-II expression, to survive

47 x (MHC)-II and its master regulator class II transactivator (CIITA) are downregulated in CML compared

48 as defined major histocompatibility class II transactivator (CIITA) as a key factor in mediating thes

49 Class II transactivator (CIITA) has a distinct function as the ma

50 Although complex, the co-activator class II transactivator (CIITA) is a key regulator of MHC II expr

51 The class II transactivator (CIITA) is essential for the expression o

52 Class II transactivator (CIITA) is the master regulator of MHC cl

53 Class II transactivator (CIITA) is the master regulator of the ma

54 y dependent upon the binding of the class II transactivator (CIITA) to the highly conserved promoters

55 ing on whether MHC-II genes and the class II transactivator (CIITA) were being expressed, two CTCF-de

56 ition of promoter activities of MHC class II transactivator (CIITA), IFN-gamma-activated site (GAS),

57 bition of MNV replication in vitro, class II transactivator (CIITA), interferon regulatory factor 3 (

58 An NLR protein, class II transactivator (CIITA), is a key regulator of MHC class

59 olved interactions between CTCF and class II transactivator (CIITA), the master regulator of major hi

60 show that the promoter IV (pIV) of class II transactivator (CIITA), the master regulator of MHCII ex

61 ruitment of a master regulator, the class II transactivator (CIITA), to the MHC class II promoter.

62 ith the role of CREBBP in promoting class II transactivator (CIITA)-dependent transcriptional activat

63 scription through regulation of the class II transactivator (CIITA).

64 tor for X-box 5 (RFX5) complex with class II transactivator (CIITA).

65 or histocompatibility complex (MHC) class II transactivator, CIITA, which binds to myogenin and inhib

66 This expression is initiated by the class II transactivator, CIITA.

67 or histocompatibility complex (MHC) class II transactivator, CIITA.

68 MHC class I transactivator (CITA), NLRC5 [nucleotide-binding domain

69 ced kinase1 (PINK1) and CBP/P300-interacting transactivator (CITED2).

70 Sp3 was a weaker transactivator compared to Sp1 in Drosophila D.mel-2 cel

71 rdial cells were higher in hSCF/tetracycline transactivator compared with wild-type mice 3 days post

72 biquitin prevents destabilization of the DNA-transactivator complex by the ATPases of the 26S proteas

73 ription activator (RTA), a major lytic cycle transactivator, contributes to the development of KSHV l

74 hibits promoter function of the HLA class II transactivator, decreasing expression of genes controlle

75 including Stat-3, beta-catenin, and class II transactivator-dependent antigen presentation.

76 the IE1 and IE2 proteins, known to be strong transactivators, did not.

77 studies have suggested that RBP-Jk-dependent transactivators do not function identically.

78 The viral transactivator EBNA2 is required for this switch from Wp

79 HIV-1 Tat and HTLV-1 Tax, as well as the Tas transactivator encoded by primate foamy virus, fail to i

80 esses MMP-1 expression by competing with MMP transactivator, Ets-1 for its coactivator p300.

81 Tet-regulated miR30-shRNA technology, robust transactivator expression and two fluorescent reporters

82 rescence-based quantification of reverse tet-transactivator expression.

83 can be rescued by reintroduction of class II transactivator expression.

84 The phosphatase and transactivator EYA family proteins are overexpressed in

85 e demonstrating that hnRNP K is an important transactivator for human LDLR gene transcription.

86 STAT1 is an activator of CIITA, the class II transactivator for MHC II expression; CIITA expression w

87 ic patch of ubiquitin as required to protect transactivators from destabilization by the proteasomal

88 s their own transcription by suppressing the transactivator function of the CLOCK:BMAL1 heterodimer d

89 For the Sacchromyces cerevisiae transactivator, GAL4, attachment of mono-ubiquitin preve

90 The MHC class II transactivator gene (CIITA) is an important transcriptio

91 pig transgenic for a mutant (human) class II transactivator gene, resulting in down-regulation of swi

92 was assessed by expression of p63, the IRF6-transactivator gene.

93 or, the mammalian Grainyhead-like epithelial transactivator (Get1/Grhl3), is important for epidermal

94 n overdose because of suppression of its key transactivators, hepatocyte nuclear factor (HNF)-4alpha

95 on analysis for gene transcripts of class II transactivator, HLA-DRagr;, and HLA-DRbeta1 showed maxim

96 Since herpes simplex virus type 1 transactivator ICP0 and human cytomegalovirus transactiv

97 d antisense to the viral transcript encoding transactivator ICP0.

98 -kappaB activation and is independent of the transactivator ICP27.

99 The varicella-zoster virus major transactivator, IE62, contains a potent N-terminal acidi

100 The varicella-zoster virus (VZV) major transactivator, IE62, is involved in the expression of a

101 dentified as being the major immediate-early transactivator, IE62.

102 ter was strongly stimulated by the major VZV transactivator, IE62.

103 f the SAGA transcription complex, and the RP transactivator Ifh1 as highly acetylated nonhistone spec

104 s illustrate critical roles of NLRC5/class I transactivator in MHC class I gene regulation and host d

105 Re-expressing the class II transactivator in the PELs increased expression of downs

106 oter, as well as by the actions of different transactivators, including RUNX2.

107 -cell lymphotropic virus type I (HTLV-1) Tax transactivator initiates transformation in adult T-cell

108 d a podocyte-specific, doxycycline-inducible transactivator into a murine embryonic stem cell line wi

109 Mono-ubiquitylation of a transactivator is known to promote transcriptional activ

110 691-amino-acid (aa) KSHV Rta transcriptional transactivator is necessary and sufficient to reactivate

111 The Egr2/Krox20 transactivator is required for activation of many myelin

112 udes positive feedback activation of the Tat transactivator, it lacks ultrasensitivity.

113 s/human herpesvirus 8 (HHV8) ORF50 encodes a transactivator, K-Rta, which functions as the switch fro

114 different tet-transactivator/reversible tet-transactivator lines supports broad functionality of tet

115 e promotion of silencer degradation by viral transactivators may be a common mechanism for regulating

116 Transactivator-mediated cytotoxicity depends on DNA bind

117 Although FosB is likely to be involved in transactivator-mediated derepression of PAI-2 transcript

118 n the peri-infarct area of hSCF/tetracycline transactivator mice compared with wild-type mice 5 days

119 sing the responder animals with tetracycline transactivator mice under conditions in which substantia

120 Amyloid precursor protein/tetracycline transactivator mice underwent behavioral testing at 3, 6

121 -specific hSCF transgenic (hSCF/tetracycline transactivator) mice were subjected to MI.

122 acidic protein (GFAP) promoter-tetracycline transactivator mouse line with tetracycline operon-domin

123 ass I (MHC-I) transcription by disabling the transactivator NF-kappaB (p50/p65).

124 d proteolytic turnover of the promoter-bound transactivator, nor is the activator-promoter complex co

125 ur results thus identify Hgf as an important transactivator of canonical Wnt signaling that is mediat

126 e assays indicate that KLF9 itself is a weak transactivator of CYP2D6 promoter but significantly enha

127 IP4), formin-binding protein-17 (FBP-17) and transactivator of cytoskeletal assembly-1 (Toca-1), and

128 ADAM17 has been proposed to play a role as a transactivator of epidermal growth factor receptor (EGFR

129 e hypothesis that Mesp1 is a direct upstream transactivator of Etv2 during embryogenesis and that Cre

130 tein, encoded by open reading frame 57, is a transactivator of gene expression that is essential for

131 TCF7L2 acts as both a repressor and transactivator of genes, as directed by the Wnt signalin

132 These results identify KLF5 as a transactivator of HIF-1alpha and show that LPA regulates

133 ock transcription factor 1 (Hsf1) is a major transactivator of Hsp induction and has been proposed to

134 R-138, represses expression of ICP0, a viral transactivator of lytic gene expression.

135 examination and the importance of NLRC5 as a transactivator of major histocompatibility complex (MHC)

136 TA) encoded by the gene Orf50 RTA is a known transactivator of multiple viral genes, allowing it to c

137 knowledge, that a protein can function as a transactivator of ribosomal frameshifting.

138 nuclear MT1-MMP as a previously unsuspected transactivator of signaling networks central to macropha

139 s a unique and as yet, poorly characterized, transactivator of STAT1 degradation by the ubiquitin-pro

140 ous nuclear ribonucleoprotein (hnRNP) K is a transactivator of Th transcription.

141 gulates DNMT1 indirectly by targeting Sp1, a transactivator of the DNMT1 gene.

142 Klf6 acts as a gp130-sensitive transactivator of the nuclear import factor importin-alp

143 mmunodeficiency virus group specific antigen/transactivator of transcription (SIV(mac239Gag/Tat)).

144 The interaction of the HIV-1 protein transactivator of transcription (Tat) and its cognate tr

145 iption factors include NF-kappaB and the HIV transactivator of transcription (Tat) as well as the cyc

146 L deficient mice, we now reveal that the HIV transactivator of transcription (Tat) can induce BBB per

147 ion protein (TAT-SNAP-23) containing the HIV transactivator of transcription (TAT) cell-penetrating s

148 The HIV-1 protein transactivator of transcription (Tat) disrupts synaptic

149 ses in intracellular Ca(2+) level upon HIV-1 transactivator of transcription (Tat) exposure.

150 culture model, we show that the HIV protein transactivator of transcription (Tat) initially potentia

151 HIV-1 transactivator of transcription (TAT) is an arginine-ric

152 neutralizing mAb against extracellular HIV-1 transactivator of transcription (Tat) is important for t

153 HIV transactivator of transcription (Tat) is released from i

154 yte function, we evaluated the impact of HIV transactivator of transcription (Tat) on Wnt/beta-cateni

155 A transactivator of transcription (TAT) peptide strategy w

156 A peptide of CRMP-2 fused to the HIV transactivator of transcription (TAT) protein (TAT-CBD3)

157 ism(s) by which viral proteins such as HIV-1 Transactivator of Transcription (Tat) protein can activa

158 Because HIV-1 Transactivator of Transcription (Tat) protein continues

159 We find that the HIV transactivator of transcription (Tat) protein manipulate

160 Human immunodeficiency virus type 1 (HIV-1) transactivator of transcription (Tat) protein possesses

161 hondria would repair the defect, we used the transactivator of transcription (TAT) protein transducti

162 the signaling and neuroprotective effect of transactivator of transcription (TAT) protein transducti

163 ter (DAT) is the target of cocaine and HIV-1 transactivator of transcription (Tat) protein.

164 sion in transgenic mice expressing the HIV-1 transactivator of transcription (Tat) protein.

165 neurotoxic factors such as the viral protein transactivator of transcription (Tat) that potentiate NM

166 ein-driven, doxycycline-inducible HIV type-1 transactivator of transcription (Tat) transgenic mouse m

167 Here, we investigated the effects of HIV-1 transactivator of transcription (Tat), a protein release

168 Surprisingly, transactivator of transcription (Tat), an early virus-en

169 The HIV-1 transactivator of transcription (Tat), combined with fib

170 HIV Tat protein, which is the transactivator of transcription (Tat), plays a key role

171 To examine events triggering combined transactivator of transcription (Tat)- and morphine-indu

172 Moreover, purified recombinant transactivator of transcription (TAT)-conjugated R18 pro

173 Here, we expressed transactivator of transcription (TAT)-fused proteins, So

174 leased neurotoxins such as the HIV-1 protein transactivator of transcription (Tat).

175 y conjugated to the cell-penetrating peptide transactivator of transcription (TAT).

176 t infect neurons, but viral proteins such as transactivator of transcription and glycoprotein 120, or

177 In vitro, the HIV-1 regulatory protein transactivator of transcription induces SOCS3 in human a

178 studies, co-exposure with morphine enhanced transactivator of transcription neurotoxicity towards cu

179 Synergistic effects of morphine on transactivator of transcription neurotoxicity were great

180 Similar morphine-transactivator of transcription synergy was also observe

181 s of its cyclin T1 subunit with the HIV Tat (transactivator of transcription) protein and TAR (transa

182 Kinetic analysis of the HIV-1 Tat (transactivator of transcription)-positive transcription

183 ting neurotoxic interactions of morphine and transactivator of transcription, and support the emergin

184 present in the HIV-1-infected brain, such as transactivator of transcription, inhibits antiviral IFN-

185 n studies with the clade C sequence of HIV-1 transactivator of transcription, which did not cause neu

186 Morphine enhanced transactivator of transcription-induced inflammatory eff

187 Morphine co-exposure significantly enhanced transactivator of transcription-induced neuron death whe

188 VPA also inhibited HIV-1 transactivator of transcription-induced release of sCD40

189 us (HCMV) IE2 86-kDa protein is an essential transactivator of viral and cellular gene expression.

190 Tat is a potent transactivator of viral gene expression required for HIV

191 ation assays indicated that AP-1 is a potent transactivator of XT-I promoter and that IL-1beta-induce

192 on receptor (AHR) and mediator 1 (MED1), two transactivators of Cyp1a2.

193 nscription factor Nkx2-5 is one of the major transactivators of the ANF gene in the developing heart.

194 MEL-18 suppressed SUMOylation of the ESR1 transactivators p53 and SP1, thereby driving ESR1 transc

195 ransactivator ICP0 and human cytomegalovirus transactivator pp71 also stimulate the degradation of ce

196 Some transactivator-promoter complexes are highly dynamic due

197 factor Tat is known for its transcriptional transactivator properties, we present evidence for an un

198 The viral transactivator protein (Tat) plays an essential role in

199 rom the human immunodeficiency virus 1 (HIV) transactivator protein (TAT) to mesoporous silica nanopa

200 r CCL2 that of neuroprotection against HIV-1 transactivator protein (Tat) toxicity in rat primary mid

201 tion of CD8(+) T cells, and the frequency of transactivator protein (Tax)-specific CD8(+) CTLs, thoug

202 ansporter (DAT) promoter-driven tetracycline transactivator protein (tTA), we expressed mito-PstI exc

203 e we provide evidence that hepatitis B virus transactivator protein HBx stimulates the expression of

204 Transactivator protein HBx, a major regulator of cellula

205 homomultimerization of the virus's essential transactivator protein IE2 at nuclear PML bodies.

206 not initiated because the tegument-delivered transactivator protein pp71 fails to enter the nucleus a

207 ORF50, the gene that encodes the major lytic transactivator protein RTA, while mLANA did not, suggest

208 with a mutation in the major immediate-early transactivator protein RTA.

209 The interaction between the HIV-1 transactivator protein Tat and TAR (transactivation resp

210 The HIV-1 transactivator protein Tat is implicated in the neuronal

211 The interaction of the HIV-1 transactivator protein Tat with its transactivation resp

212 The HTLV-1 transactivator protein Tax controls many critical cellul

213 is produced by cells that express the HTLV-1 transactivator protein Tax, and that the increased CCL22

214 hrough induction of the oncogenic HTLV-1 Tax transactivator protein.

215 irectly binding promoters and enhancer-bound transactivator proteins.

216 romote transcriptional activation of certain transactivator proteins.

217 ulates expression of the immediate-early EBV transactivator R.

218 ein genes requires TFIID and the DNA-binding transactivator Rap1.

219 an upstream silencer (PAUSE-1), and a distal transactivator region between -5100 and -3300, which app

220 The distal transactivator region is inducible by the phorbol ester

221 nes (RPGs) by making direct contact with the transactivator repressor activator protein 1 (Rap1).

222 x virus type 1 is an E3 ubiquitin ligase and transactivator required for the efficient switch between

223 KSHV K-RTA has been shown to be the major transactivator required for the initiation of lytic reac

224 inding specifically to its cognate site, the transactivator response element (TAR), Tat mediates a st

225 interaction of TOE1 with the viral specific transactivator response element as part of the inhibitor

226 ette that comprises an HSP70B promoter and a transactivator-responsive promoter and (ii) transactivat

227 transactivator-responsive promoter and (ii) transactivator-responsive promoters that drive the ICP4

228 (76%) harbored mutations in the tetracycline transactivator, resulting in expression of the MYC trans

229 reover, breeding these mice to different tet-transactivator/reversible tet-transactivator lines suppo

230 transcripts and proteins of the master lytic transactivator RTA (ORF50), early lytic genes ORF57 and

231 The Epstein-Barr virus (EBV) lytic transactivator Rta activates promoters through direct bi

232 ing sequences of ORF50-encoding reactivation transactivator Rta and A6-encoding bZIP protein genes.

233 e sites now respond exclusively to the viral transactivator RTA and no longer to the host mediator IC

234 on interacted with the EBV immediate early R transactivator (Rta) and was found to inhibit Rta transa

235 early gene product of gammaHV68, replication transactivator (RTA), functions as a ubiquitin E3 ligase

236 or open reading frame 50 (ORF50)/replication transactivator (RTA)-induced activation.

237 D2))-directed reverse tetracycline-dependent transactivator (rtTA) and the tetracycline-responsive el

238 line (Dox)-regulated reverse transcriptional transactivator (rtTA) have many applications in biomedic

239 cell (PEC)-specific PEC-reverse-tetracycline transactivator (rtTA) transgenic mouse also efficiently

240 erse tetracycline-controlled transcriptional transactivator (rtTA), one with self-reporting GFP activ

241 ond cassette contains a reverse tetracycline transactivator, rtTA(M2), which directs the expression o

242 in (mVEcad) promoter for the expression of a transactivator, rtTA2S-M2; and the other driven by an in

243 ion is not well defined in terms of the host transactivator(s) required for iNOS gene expression.

244 e, which expresses a tetracycline-responsive transactivator selectively in the stratified squamous ep

245 e the expression of the reverse tetracycline transactivator (SP-C-rtTA) enabled functional analysis o

246 king gI promoter elements that bind cellular transactivators, specificity factor 1 (Sp1) and upstream

247 ter fidelity is most reliant on histone gene transactivators (Spt10, Spt21) and H3-H4 chaperones (Asf

248 into a heterologous tetracycline-repressible transactivator such that the transactivator transcript i

249 cell types using the tetracycline-dependent transactivator system.

250 ain disrupts the interaction between the HIV transactivator Tat and P-TEFb and suppresses the ability

251 ess HIV transcription both through the viral transactivator Tat and via Tat-independent mechanisms.

252 that the human immunodeficiency virus (HIV) transactivator Tat inhibits the SIRT1 deacetylase, resul

253 ansduction of human immunodeficiency virus 1-transactivator (Tat) protein and linked to the mitochond

254 iciency virus type 1 (HIV-1) transcriptional transactivator (Tat) recruits the positive transcription

255 ne permeabilization peptide (transcriptional transactivator, TAT).

256 urotoxic viral proteins, including the viral transactivator, tat.

257 HTLV-1 transactivator Tax also binds HLX2, and this interaction

258 leukemia virus (HTLV) type 1 transcriptional transactivator Tax is an oncogene sufficient to produce

259 The viral transactivator Tax is regarded as the oncoprotein respon

260 sers, and the viral genome encodes the viral transactivator Tax, which is highly homologous to the tr

261 ve up-regulation of interferon-gamma and its transactivator Tbx21/Tbet, and amelioration of autoimmun

262 tory protein-reverse tetracycline-controlled transactivator/tetracycline operator-VEGF-C double-trans

263 Using a rtTA transactivator/tetracycline promoter approach allowing i

264 development and adult life, we used an rtTA transactivator/tetracycline promoter approach that allow

265 ever, the precise mechanisms and outcomes of transactivator-TFIID interaction remain unclear.

266 The properties of XND1, a transactivator that depends on multiple linear RBR-inter

267 ICP0, a promiscuous transactivator that enhances the expression of genes int

268 The gene switch comprises (i) a transactivator that is activated by a narrow class of an

269 NA-binding proteins, we created a Cas9-based transactivator that is targeted to DNA sequences by guid

270 s from biallelic gene disruption in class II transactivator that leaves other essential properties of

271 HIV-1 Tat is a viral transactivator that strongly stimulates the processivity

272 cetylases (HDACs) because pp71, the tegument transactivator that travels to the nucleus and inactivat

273 n of the Mpz gene is controlled by two major transactivators that coordinate Schwann cell development

274 mportant roles for the BZLF1 immediate early transactivator, the BHRF1 vBcl-2 homologue, and a novel

275 One such NLR protein is the MHC class II transactivator, the master regulator of MHC class II gen

276 ein Tax, which is believed to act as a viral transactivator through its interactions with a variety o

277 t NLRC5 acts in a manner similar to class II transactivator to drive MHC expression and revealed NLRC

278 ine-repressible transactivator such that the transactivator transcript is disrupted in male splice va

279 ondary somatic mutations in the tetracycline transactivator transgene, MMTV-rtTA, rendering gene expr

280 a-myosin heavy chain reverse transcriptional transactivator transgenic mice, and the double-transgeni

281 increase dendritic development, we tested a transactivator trap assay and found that the C456S varia

282 lies in the assumption that the tetracycline transactivator (TTA) acts as an inert control element an

283 ryos to drive expression of the tetracycline transactivator (tTA), the transcription factor commonly

284 he absence of tetracycline, the tetracycline transactivator (tTAV) accumulates, resulting in female d

285 ic mice carrying the tetracycline-responsive transactivator under the control of the liver activator

286 a (AML), we used a Vav promoter-tetracycline transactivator (Vav-tTA)-driven repressible TRE-NRAS(G12

287 f SVV open reading frame 61 (ORF61), a viral transactivator, was detected most frequently in latently

288 used insulinomas transfected with the CIITA transactivator, which resulted in their expression of cl

289 the tetracycline/doxycycline-controlled Tet-transactivator, while tolerated well during development

290 Here, we test whether CBP/p300-interacting transactivator with ED-rich tail 2 (CITED2), a mechanose

291 CITED2 (CBP/p300-interacting transactivator with ED-rich tail 2) is essential for neu

292 ITED2 (CREB-binding protein/p300 interacting transactivator with ED-rich tail).

293 Cited2 (CBP/p300-interacting transactivator with glutamic acid (E)/aspartic acid (D)-

294 CREB-binding protein (CBP)/p300 interacting transactivator with glutamic acid (Glu) and aspartic aci

295 lementbinding protein [CBP]/p300-interacting transactivators with glutamic acid [E] and aspartic acid

296 usly expressed in GBM cells are strong viral transactivators with oncogenic properties.

297 ctivating expression of Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domai

298 with ArsA were selected by either repressed transactivator yeast two-hybrid or reverse yeast two-hyb

299 olish the SUMOylation of the EBV lytic cycle transactivator ZTA was dependent on both BGLF4 SUMO bind

300 o lytic replication is governed by two viral transactivators, Zta and Rta.