ライフサイエンスコーパス: coactivation

1 ng of the complex and dynamic process of RTK coactivation.

2 R boxes of DRIP205 are not required for this coactivation.

3 omes and cancer phenotypes downstream of RTK coactivation.

4 bset of the ERalpha cistrome associated with coactivation.

5 ting them indirectly through augmented SRC-1 coactivation.

6 R may be the basis for the difference in CRP coactivation.

7 mer are different from those obtained during coactivation.

8 ndent activation as well as EBNALP-dependent coactivation.

9 his does not correlate as closely with Gcn5p coactivation.

10 st that Sp100 is a major mediator of EBNA-LP coactivation.

11 between AP2alpha binding and transcriptional coactivation.

12 oles in EBNA2-mediated activation and EBNALP coactivation.

13 bilized association with EBNA2 and prevented coactivation.

14 that amino acids 476 to 515 are critical for coactivation.

15 g that EBNA3C sumolation is not required for coactivation.

16 ding to androgen receptor or transcriptional coactivation.

17 ility of the EMG, as well as flexor-extensor coactivation.

18 ndent and ligand-independent interaction and coactivation.

19 especially during periods of sensory-evoked coactivation.

20 ort of the biological relevance of PI(4,5)P2 coactivation, a yeast mutant with reduced PI(4,5)P2 leve

21 ed1 stimulates its intrinsic transcriptional coactivation activity.

22 3-amino-acid sequence (789-811) required for coactivation activity.

23 Muscle activity and coactivation also decreased with motor learning.

24 365 to 545 are necessary and sufficient for coactivation and are required for SUMO-1 and SUMO-3 inte

25 erase (CARM1/PRMT4)-mediated transcriptional coactivation and arginine methylation is known to regula

26 d picture with MD regions as a whole showing coactivation and broad rule representation, but with sig

27 mic mutants are inactive for transcriptional coactivation and cancer cell growth.

28 ome-wide binding profiles for ER and GR upon coactivation and characterized the status of the chromat

29 tor translation for target selection through coactivation and competitive interaction of neural popul

30 anscriptional activity, suggesting that both coactivation and corepression are involved.

31 as competing effects on p53 activity through coactivation and decreased stability.

32 3-linked ubiquitin chains in transcriptional coactivation and demonstrate that atrogin-1 uses this me

33 A phenocopied restoration of pRB function in coactivation and differentiation assays, suggesting that

34 activation is involved after the PKC and PKA coactivation, and intrathecal administration of bradykin

35 h as cell-cycle progression, transcriptional coactivation, and mRNA processing.

36 nscriptional activation and regulated EBNALP coactivation are critical for Epstein-Barr virus-infecte

37 cleotide excision repair and transcriptional coactivation as a critical component of the NANOG, OCT4,

38 ly identified receptor tyrosine kinase (RTK) coactivation as an important mechanism by which cancer c

39 correspondence with patterns of task-evoked coactivation as well as maps of anatomical connectivity.

40 tions of AIB1 that are independent of its ER coactivation, as both approaches, ovariectomy and ER-/-

41 caudal trunk motor areas expanded; (2) trunk coactivation at cortex sites increased; (3) richness of

42 nistein, equol, and bisphenol A, whereas its coactivation at the AP-1 site is augmented by fulvestran

43 Recent advances now compute coactivation-based connectivity, connectivity-based func

44 Consistent with EBNALP coactivation being mediated by nuclear HDAC4 depletion,

45 eliable indicator of D(1)- and D(2)-receptor coactivation but not a predictor for repetitive motor be

46 the dynamic behavior of Dcp2 and attenuates coactivation by a yeast enhancer of decapping (Edc1).

47 While TCF-4N inhibited coactivation by beta-catenin of a TCF/lymphoid-enhancing

48 EF transcription factors and potentiates the coactivation by beta-catenin of other transcription fact

49 (LEF)-dependent promoter, TCF-4N potentiated coactivation by beta-catenin of several non-TCF/LEF-depe

50 Thus, we propose that TCF-4N inhibits coactivation by beta-catenin of TCF/LEF transcription fa

51 Coactivation by Dax-1 is abolished by SRA knockdown.

52 heterodimerization with RXR is required for coactivation by DRIP205.

53 ections revealed during spontaneous activity coactivation by GCaMP3 were confirmed by intracortical m

54 Axons respond synergistically to coactivation by GDNF and EphA ligands, and these coopera

55 the livers of uninfected mice and depend on coactivation by IL-12 and IL-18 for optimum responses.

56 y toward target cells depends on synergistic coactivation by NK cell receptors such as NKG2D and 2B4.

57 substitution affected serum response factor coactivation by NKX3.1 We conclude that the polymorphic

58 intrinsic inhibitory function of RD1 and for coactivation by PIASxalpha and PIASxbeta, two members of

59 ine-specific activator sites (A1) as well as coactivation by substrate dNTP binding to a distinct set

60 n MOR-Tyr166p immunoreactivity (ir) required coactivation by the opioid agonist [D-Ala(2),methyl-Phe(

61 Accelerated hepatic DNL was due to coactivation by Vpr of liver X receptor-alpha (LXRalpha)

62 al HAT activity in vitro and transcriptional coactivation by Zta in transfected cells.

63 plays a role in acetylation of histones and coactivation, can be regulated by EBNA3C.

64 each supply a surprising degree of redundant coactivation capacity in T cells and macrophages, althou

65 e H4 transcription factor (HINFP)/p220(NPAT) coactivation complex occurs in parallel with the CDK-dep

66 lly interacts with the Notch transcriptional coactivation complex through C promoter-binding factor 1

67 We found spontaneous neuronal coactivations corresponded to intracellular UP states.

68 ata-driven approach, we analyzed large-scale coactivation data from 5,809 human imaging studies.

69 of the EBNA-LP mutants tested, including the coactivation-deficient DeltaCR3 mutant and the nonshuttl

70 5/ARA55 by both the location of its receptor coactivation domain (i.e., COOH-terminal LIM domain) and

71 tein that contains, besides other domains, 2 coactivation domains for the transcription factor Runx1/

72 inant-negative construct of TAZ in which the coactivation domains have been deleted reduces osteocalc

73 ed firing during exploration showed stronger coactivation during eSWRs and subsequent sleep-SWRs.

74 g swing, and increased antagonist leg muscle coactivation during limb loading in early stance, and (2

75 -demand (MD) regions of the human brain show coactivation during many different kinds of task perform

76 , and showed increased bursting and temporal coactivation during postexperience sleep.

77 ring rest reflected the level of their prior coactivation during the NF epoch.

78 Second, CF and PF coactivation evoked localized supralinear dendritic calc

79 omatin remodeling, histone modification, and coactivation factors.

80 This asymmetric timing window for coactivation follows the kinetics of calcium removal and

81 ining the AR-interacting FXXLF motif without coactivation function can suppress HF-enhanced AR transa

82 result, at least in part, from its defective coactivation function for HNF4alpha.

83 eceptor coactivator 1 (SRC-1) and that UBCH7 coactivation function is dependent on SRC-1.

84 ous study suggested that some of the EBNA-LP coactivation function is mediated by relocalizing histon

85 both required for the mutual interaction and coactivation function of Brd4.

86 This finding indicates that the coactivation function of c-Jun is sufficient for regulat

87 ttling is not required for efficient EBNA-LP coactivation function, and that competence for HDAC4 ass

88 Thus, inhibition of the coactivation-function of Stat3 resulted in suppression o

89 le for PELP1/pRb interactions in the maximal coactivation functions of PELP1 using cyclin D1 as one o

90 art of the yeast Mediator that shows diverse coactivation functions.

91 ower occurred even after muscle activity and coactivation had stabilized and movement changes were sm

92 The "alpha-gamma coactivation" hypothesis states that activity in a muscl

93 attenuates MUC1-induced (i) transcriptional coactivation, (ii) anchorage-independent growth, and (ii

94 ent functional imaging studies have revealed coactivation in a distributed network of cortical region

95 ay be useful in assessing the role of EBNALP coactivation in LCL growth or survival.

96 ate nuclear-cytoplasmic shuttling or EBNA-LP coactivation in the absence of a functional interaction

97 hysiological significance of transcriptional coactivation in the context of signal-dependent and cell

98 the recovered AN group, displayed increased coactivation in the left parietal cortex, encompassing t

99 Coactivation in the motor cortex and supplementary motor

100 er opioid hotspot required permissive opioid coactivation in the other (behaviorally).

101 K (mitogen-activated protein kinase) pathway coactivation in the prostate epithelium promotes both ep

102 Empathy often involves coactivations in further networks associated with social

103 r body localization but were dispensable for coactivation, indicating that EBNA3C sumolation is not r

104 s provides strong evidence that SRA-mediated coactivation is executed by distinct RNA motifs and not

105 D1Rs and D2Rs are not colocalized but their coactivation is necessary.

106 We hypothesized that spontaneous interareal coactivation is subserved by neuronal synchronization.

107 provided evidence that such social category coactivation manifested in neural patterns of the right

108 Meta-analytic coactivation maps of task-related increases were indepen

109 n vitro resulted in higher expression of the coactivation markers CD80, CD40, and CD70 on dendritic c

110 This continuous coactivation matrix was used to build a weighted graph t

111 This coactivation may be important for postprandial nutrient

112 nd Cl(-) both rise in oxygen-deprived cells, coactivation may more effectively trigger the activity o

113 These results imply multiple distinct RTK coactivation mechanisms and support the notion that smal

114 on of at least two different cAMP-responsive coactivation mechanisms.

115 mature DCs, the expression of CD80 and CD86 coactivation molecules, the production of IL-12p70 requi

116 The coactivation network was modular, with occipital, centra

117 Many aspects of the coactivation network were convergent with a connectivity

118 explanation for paradoxical pallidothalamic coactivations observed during behavior that raises new q

119 Coactivation of 5-HT1A and GRP receptors (GRPR) greatly

120 Coactivation of a few 10s to 100s of neurons can code se

121 This was followed by coactivation of a frontal-parietal system [superior fron

122 tivity among a large proportion of inputs or coactivation of a smaller subset of local dendrodendriti

123 o distinct biochemical activities, including coactivation of adipose triglyceride lipase and acylatio

124 can respond to glutamate spillover following coactivation of adjacent parallel fibers (PFs), indicati

125 ng mnemonic and executive tasks requires the coactivation of adult prefrontal and hippocampal network

126 dpoints are best explained as resulting from coactivation of agonist and antagonist muscles driving t

127 y step cycle and consequently there was less coactivation of agonist and antagonist muscles during th

128 a cortical origin for myoclonus and striking coactivation of agonist and antagonist muscles.

129 The biological effects of coactivation of AKT and N-Ras were then recapitulated in

130 emergence of mesenchymal components and the coactivation of AKT and STAT pathways as well as PTEN in

131 We found that coactivation of alpha(1A)- and beta(2)-AR by the nonsele

132 f events exhibiting the kinetics expected of coactivation of alpha7-nAChRs and alpha3-nAChRs.

133 thway by transactivating erbB1 receptors via coactivation of AMPA receptors (AMPARs) and metabotropic

134 teroid receptor activation within HVC; local coactivation of androgen and estrogen receptors (ARs and

135 lloproteinase (MMP)-2 and MMP-13 through its coactivation of AP-1 and PEA3.

136 of a c-Jun mutant, which is fully active in coactivation of AR but deficient in AP-1 transactivation

137 signaling through MAPK increases TIF2/GRIP1 coactivation of AR transactivation in recurrent prostate

138 Coactivation of areas implies functional connections but

139 Coactivation of astrocytic AMPARs and mGluRs caused extr

140 case in which the main contribution was from coactivation of biarticular muscles.

141 silateral ascending influences that ensure a coactivation of bilateral extraocular motoneurons with s

142 nor AKT alone promoted S-phase progression, coactivation of both kinases elicited a robust prolifera

143 iated currents in lamina II neurons requires coactivation of both PKC and PKA.

144 Coactivation of both receptors led to the canonical nega

145 Furthermore, coactivation of both receptors via repetitive afferent s

146 se correlations reflect the prior history of coactivation of brain regions, then a marked shift in co

147 yc-induced tumors, but not tumors induced by coactivation of c-Myc and Wnt-1, indicating that the ant

148 e but, more importantly, to induce effective coactivation of CD4 T cells.

149 Coactivation of cold- and heat-responsive sensory neuron

150 tic network evoked activity, with systematic coactivation of cortical areas which are components of t

151 f WWOX and ErbB-4 suppresses transcriptional coactivation of CTF by YAP in a dose-dependent manner.

152 SRCAP is implicated in the transcriptional coactivation of cyclic AMP- and steroid-dependent promot

153 PPARgamma coactivator-1 alpha (PGC-1 alpha) coactivation of CYP7A1 reporter activity, whereas a domi

154 icated that this is mediated by AC5, because coactivation of D(2) and mGluRs could induce LTD in wild

155 the catalytic domain of Dcp2, and show that coactivation of decapping by Dcp2 is linked to formation

156 vating receptors, such as 2B4 or CD16, or by coactivation of different receptor combinations.

157 e cohort of clinical samples showed frequent coactivation of EGFR and SFKs in glioblastoma patients.

158 ALK secondary mutation but instead harbored coactivation of EGFR signaling.

159 However, PIASx-mediated coactivation of Elk-1 occurs in an E3 activity-independe

160 K for survival, it also contained concurrent coactivation of epidermal growth factor receptor (EGFR)

161 Moreover, coactivation of ER and IKKbeta promoted cell migration a

162 Taken together, our findings suggest that coactivation of ER and the canonical NFkappaB pathway pr

163 tiple domains of this protein play a role in coactivation of ERalpha and in interactions with ERalpha

164 These results demonstrate that coactivation of ERalpha by DRIP150 in ZR-75 cells is NR

165 Coactivation of ERalpha by DRIP150 in ZR-75 cells was ac

166 Coactivation of ERalpha by DRIP205 does not require NR b

167 ; however, unlike p160 coactivators, DRIP205 coactivation of ERalpha does not require NR boxes.

168 ining these sequences were not necessary for coactivation of ERalpha.

169 nteraction with ErbB-4 has no effect on this coactivation of ErbB-4.

170 HDAC3 coactivation of ERRalpha is mediated by deacetylation of

171 , all phosphorylation sites are required for coactivation of estrogen and androgen receptors, but not

172 helia and is required to modulate AIB1/SRC-3 coactivation of estrogen receptor alpha (ERalpha), proge

173 Coactivation of FGFR1 and FGFR3 promoted symmetrical div

174 nclude that neuronal ensembles, built by the coactivation of flexible groups of neurons, are emergent

175 interaction participating in transcriptional coactivation of genes encoding G(1) phase regulatory pro

176 The coactivation of GIRK and SK channels represents a novel

177 Coactivation of human NK cells via CD16 and IL-12 induce

178 ation of extrinsic tongue muscles but by the coactivation of intrinsic and extrinsic protrudor and re

179 and in xenografted mice was dependent on the coactivation of JAK2/STAT3 and MEK/ERK1/2 in neuroblasto

180 nduction, and investigated the net effect of coactivation of M(1) and alpha1 receptors on the magnitu

181 Coactivation of mAChRs and mGluRs also induced a long-la

182 These findings provide a mechanism for LGP2 coactivation of MDA5 and a biological context for MDA5-R

183 interaction with LGP2 specifically prevents coactivation of MDA5 signaling and that LGP2's negative

184 Coactivation of mGluR1/5 and DR1/5 also enhanced cAMP-re

185 Coactivation of mGluR1/5 and DR1/5 with (S)-3,5-dihydrox

186 iably represented by momentary, simultaneous coactivation of microbands of adjacent Purkinje cells.

187 Coactivation of MOR and SSTR2 in PDAC cells led to incre

188 types, such as cardiomyocytes, this leads to coactivation of multiple downstream pathways.

189 inherent resistance mechanism in GBM is the coactivation of multiple receptor tyrosine kinases, whic

190 t that, in the absence of direct experience, coactivation of multiple relevant memories can provide a

191 ivation often overlaps and crosstalk between coactivation of multiple signaling cascades can result i

192 We found that coactivation of N-methyl-D-aspartate receptors (NMDAR) a

193 Coactivation of N-methyl-D-aspartate receptors (NMDARs)

194 We found that coactivation of N-methyl-D-aspartate receptors (NMDARs)

195 Coactivation of neonatal moDCs through Dectin-1 allows T

196 tial diffusion will determine the convergent coactivation of neuroblasts and stem cells, and provide

197 Here, we tested whether coactivation of neurons across macaque ACC and PFC would

198 n effect commonly interpreted to reflect the coactivation of neurons due to anatomically shared input

199 eceptors, but not all sites are required for coactivation of NF-kappaB.

200 novel function of GITR/GITRL in pDC-mediated coactivation of NK cells.

201 This potentiation requires coactivation of NMDA and mGlu5 receptors and a postsynap

202 This form of plasticity requires coactivation of NMDA receptors (NMDARs).

203 Our results provide evidence that D-serine coactivation of NMDA receptors and endothelial nitric ox

204 ynergistic phosphorylation of ERK induced by coactivation of NMDA receptors and mGluR5 was blocked by

205 Coactivation of Notch allows accumulation of far greater

206 Coactivation of p38 in DRG neurons and spinal microglia

207 this coregulator, thereby facilitating SMRT coactivation of p53-dependent gene expression.

208 Furthermore, WWOX is able to inhibit coactivation of p73 by YAP.

209 pmental program results from the reiterative coactivation of pathways that are largely inactive in ve

210 Compared to PF stimulation alone, coactivation of PF and CF synapses greatly enhanced endo

211 the TCR) proliferation, IL-2 secretion, and coactivation of phosphatidylinositol 3-kinase.

212 es prostate cancer metastasis in response to coactivation of PI3-kinase and Ras signaling pathways in

213 his transcriptional activity is required for coactivation of PPARdelta by ERK5 in C2C12 cells.

214 athways: (1) it increases FXR mRNA levels by coactivation of PPARgamma and HNF4alpha to enhance FXR g

215 Inductive signaling leads to the coactivation of regulatory pathways for specifying gener

216 on) is processive during the transcriptional coactivation of select transcription factors and can ser

217 phosphorylate NKX3.1 had no effect on NKX3.1 coactivation of serum response factor.

218 Coactivation of spinal alpha(2)-adrenergic receptors (AR

219 ring the early phase of PGC development, and coactivation of STAT and Ras is required for PGC prolife

220 h a dual intracellular cascade that requires coactivation of Stat6 and Stat1 to impact transcriptiona

221 anisms including methylation of histones and coactivation of steroid receptor transcription.

222 This work indicates that although coactivation of steroid-dependent transcription by SRA i

223 ence that motor plans in PMd emerge from the coactivation of such attractor modules, heterogeneous in

224 on of prosurvival signaling triggered by the coactivation of synaptic and extrasynaptic receptors.

225 racts with beta-catenin and can suppress its coactivation of T cell factor 4 (Tcf4) in prostate cance

226 uman CCA cell lines, driven, in part, by YAP coactivation of TBX5.

227 Our findings show how coactivation of the AKT and CAT pathways in hepatocytes

228 Coactivation of the apoC-III/A-IV promoter region by PGC

229 ow that the nuclear localization of FHL2 and coactivation of the AR is driven by calpain cleavage of

230 that the responses were greatly increased by coactivation of the cells with either recombinant interl

231 mation required fast GABAergic transmission, coactivation of the dopamine D1 and NMDA receptor, and d

232 n alone causes long-term potentiation (LTP), coactivation of the heterosynaptic CF input, which evoke

233 Prominent coactivation of the hippocampus, detected in all groups,

234 ralized pain syndromes may be stress-induced coactivation of the hypothalamo-pituitary-adrenal and sy

235 The E2AD was essential for EBNALP coactivation of the latent membrane protein 1 promoter i

236 expression is likely due to the simultaneous coactivation of the liver X receptor, LXRalpha, a nuclea

237 After investigating the effect of coactivation of the NMDAR and the Gs-coupled beta-adrene

238 cognitive demand, patients showed increasing coactivation of the primary motor cortex and supplementa

239 single receptor activation, suggesting that coactivation of the receptors can lead to novel antagoni

240 ve mice to increase dopamine release through coactivation of the receptors CRFR1 and CRFR2.

241 l1 (Arntl) and Rev-erbalpha (Nr1d1), through coactivation of the ROR family of orphan nuclear recepto

242 subgroup of medulloblastoma characterized by coactivation of the Sonic hedgehog (SHH) and CXCR4 pathw

243 ve autonomic blockers, could be explained by coactivation of the sympathetic and cardiovagal outflows

244 stic SF-1 and sex-determining region Y (SRY) coactivation of the testis development gene SOX9.

245 Coactivation of the TLR3 and TLR7 pathways synchronizes

246 Coactivation of the TTF-1 and NKX2-8 pathways identified

247 Furthermore, lung cancer cell lines showing coactivation of the TTF-1 and NKX2-8 pathways were shown

248 ng of prostanoid biosynthesis toward PGE2 by coactivation of the two enzymes.

249 Interestingly, coactivation of these receptors with the beta-adrenergic

250 d within a session, arguing against a simple coactivation of these regions.

251 ed) intensity to rule out the possibility of coactivation of this structure caused by the current spr

252 In contrast, the coactivation of TLR4 and IFN-gamma receptors results in

253 atients with Omenn syndrome, indicating that coactivation of TRAIL-R and TCR represents a mechanism t

254 p75-mediated Rac activation is modulated by coactivation of Trk, identifying Rac GTPase as one of th

255 is suggests that the cohort of patients with coactivation of TTF-1 and NKX2-8 pathways appears to be

256 ortantly, the poor prognosis associated with coactivation of TTF-1 and NKX2-8 was validated in 2 othe

257 specific effector function was stimulated by coactivation of Valpha14 iNKT cells using alpha-galactos

258 and that network events are composed of the coactivation of variable subsets of these clusters, whic

259 ions, we studied the effects of DA-glutamate coactivation on pyramidal cell excitability in brain sli

260 omotion (reciprocal innervation) and stance (coactivation pattern).

261 Manipulating coactivation patterns can alter perception in ways that

262 Whether these coactivation patterns have any physiological reality wit

263 Neuron pairs exhibited coactivation patterns organized within beta-frequency ti

264 , we found that this brain area shows strong coactivation patterns with nearly all of the value-assoc

265 The coactivation period of leg flexors and extensors, which

266 The coactivation potential of PGC-1alpha requires an intact

267 oylation mutant showed a drastically reduced coactivation potential.

268 on in Dcp2, suggest a structural pathway for coactivation, predict that Dcp1 directly contacts the ca

269 rovide structural insight into the versatile coactivation profile of PGC-1alpha and can readily be ex

270 ons were clustered based on their functional coactivation profiles across all the experiments stored

271 At the cellular level, Notch/Kras coactivation promotes rapid reprogramming of acinar cell

272 , mutagenesis of this docking site unearthed coactivation properties for FCRL5 that were orchestrated

273 of activation frequency, climbing fiber (CF) coactivation provides an instructive signal that further

274 y and decreased surface expression of CD2, a coactivation receptor.

275 Ligands of coactivation receptors 2B4 and NKG2D segregated into cen

276 en the nucleus and cytoplasm is required for coactivation remains to be clarified.

277 ne-specific coactivator of EBNA2 and whether coactivation requires interaction between these proteins

278 Coactivation requires that the cooperating target sites

279 EBNALP coactivation requires the EBNA2 acidic activation domain

280 2X channels interact functionally, such that coactivation results in cross-inhibition of one or both

281 spatial scales on the basis of meta-analytic coactivation, revealing three broad functional zones alo

282 s RNA-binding domains in contexts related to coactivation, RNA-processing and possibly prokaryotic tr

283 Here, we demonstrate a specific ion coactivation (SICA) effect at the interfaces of transien

284 ic pH at a physiological temperature provide coactivation signals, allowing virus association with me

285 tives take the form of time-invariant muscle coactivations ("spatial" synergies) or time-varying musc

286 xhibit a secondary effect that modulates the coactivation strength.

287 ear targeting of a Vav3 PH mutant rescued AR coactivation, suggesting that nuclear localization is an

288 ites SNr GABA neurons via D(1)-D(5) receptor coactivation that enhances constitutively active TRPC3 c

289 Simultaneous coactivation through Dectin-1 and TLRs induced robust se

290 These data suggested that Rac1 and Cdc42 coactivation was essential to smoke-promoted cell migrat

291 changes indicative of endogenous AP3 factor coactivation were also observed.

292 Two modes of coactivation were observed, one that was dependent on th

293 t stimulation-induced patterns of interareal coactivation were reactivated in the absence of stimulat

294 89%) were preceded by ICNA and sympathovagal coactivation, whereas 11% were preceded by ICNA and stel

295 ession repressed EBNA2 activation and EBNALP coactivation, whereas other HDACs had little effect.

296 al zones that exhibited discrete patterns of coactivation with cortical brain regions across distinct

297 EBNALP coactivation with EBNA2 was found to dominate over NCoR

298 ecause EBNALPd10 dominantly inhibited EBNALP coactivation with EBNA2, EBNALPd10 expression in LCLs ma

299 shown synergistic increases in signaling on coactivation with fibroblast growth factor 2 (FGF2) and

300 h motor learning and (2) muscle activity and coactivation would parallel changes in metabolic power.