ライフサイエンスコーパス: nuclear translocation

1 activation, which may aid in regulating YAP nuclear translocation.

2 aving N-cadherin and increasing beta-catenin nuclear translocation.

3 vage of caspase-1, a step required for IL-37 nuclear translocation.

4 ing to TRIM59 binding to importin alpha5 and nuclear translocation.

5 ence, we analyzed the steps involved in DDR1 nuclear translocation.

6 ession via SAPK/JNK phosphorylation and Nrf2 nuclear translocation.

7 ress by promoting the activation of Nrf2 and nuclear translocation.

8 KPNA2), acting to reduce p65 binding and its nuclear translocation.

9 ) genes including HSP60 and GRP75, showed no nuclear translocation.

10 ivity, which stimulates SMAD3 expression and nuclear translocation.

11 s IkappaBalpha phosphorylation and NF-kappaB nuclear translocation.

12 esters NAP1L1 in the cytoplasm, blocking its nuclear translocation.

13 -activating group P65 by phosphorylation and nuclear translocation.

14 nt mTOR inhibition, thereby promoting pSTAT1 nuclear translocation.

15 log 2]) at the cell membrane, preventing its nuclear translocation.

16 ociated Nup153 is critical for its efficient nuclear translocation.

17 ad51 complex dissociation through inhibiting nuclear translocation.

18 bitor blocked STAT3 binding to myoferlin and nuclear translocation.

19 stimulated with IL-33 and resulted in NFAT1 nuclear translocation.

20 nal of ACSS2 for importin alpha5 binding and nuclear translocation.

21 plexes and was essential for TIE2/caveolin-1 nuclear translocation.

22 DG at Tyr(890) is a key stimulus for beta-DG nuclear translocation.

23 IL-6 through increased nuclear factor kappaB nuclear translocation.

24 through mTORC1-dependent repression of TFEB nuclear translocation.

25 ibility at some ER bound loci and impairs ER nuclear translocation.

26 ivated EGFR promotes FUS phosphorylation and nuclear translocation.

27 SIRT1 repression and prevents NF-kappaB p65 nuclear translocation.

28 ain, resulting in diminished DNA binding and nuclear translocation.

29 verexpressing GCB cells this caused enhanced nuclear translocation, a profoundly altered transcriptio

30 ocked NF-kappaB activation by decreasing p65 nuclear translocation, although blunting the degradation

31 activation of SAPK/JNK phosphorylation, Nrf2 nuclear translocation and antioxidant enzymes expression

32 duced increase in Keap1 and facilitated Nrf2 nuclear translocation and antioxidant gene transcription

33 Mechanistically, DMF prevents p65 nuclear translocation and attenuates its DNA binding act

34 y, PI3K/Akt-mediated SRF activation promotes nuclear translocation and binding of Egr2 to SOCS1 promo

35 ivity induces rapid CRTC1 dephosphorylation, nuclear translocation and binding to endogenous CREB.

36 oduction by B-1a cells in sepsis through its nuclear translocation and binding to putative responsive

37 rylation of PHB1 at Thr258, resulting in its nuclear translocation and binding to the Axin1 promoter.

38 hosphorylation of GAPDH is essential for its nuclear translocation and DNA repair function.

39 however, C. burnetii actively prevented CHOP nuclear translocation and downstream apoptosis in a T4SS

40 CD44 knockdown reduced NF-kappaB nuclear translocation and downstream IL-1beta and TNF-al

41 In cells, malbrancheamide attenuated GRK5 nuclear translocation and effectively blocked the hypert

42 KB/Akt-mTORC1 pathway and promotes TFEB/TFE3 nuclear translocation and enhances FAM134B transcription

43 g it contains all essential determinants for nuclear translocation and filament formation.

44 production and its ability to induce GRalpha nuclear translocation and GRE-dependent GILZ expression.

45 onsistent with these findings, impaired ITCH nuclear translocation and H1.2 polyubiquitination sensit

46 ng pathways through the drug's effect on p65 nuclear translocation and IKKbeta.

47 Blockade of IFN response factor 7 nuclear translocation and inhibition of the IFN-alpha re

48 pathway mediated YAP gene expression and YAP nuclear translocation and interaction with the TEA domai

49 Increased NF-kappaB nuclear translocation and macrophage chemoattractant pro

50 AMPK inhibitors prevented Ghr-induced FOXO1 nuclear translocation and negative regulation of cell pr

51 ion in response to MSU mediated by NF-kappaB nuclear translocation and NLRP3 inflammasome activation.

52 loss of the IKK complex components prevents nuclear translocation and phosphorylation of NF-kappaB,

53 These phosphorylation events promote SRPK2 nuclear translocation and phosphorylation of SR proteins

54 r analysis reveals that IKBKE regulates GLI1 nuclear translocation and promotes the reactivation of A

55 a Gli antagonist GANT58, which inhibits Gli2 nuclear translocation and PTHrP expression in tumor cell

56 interneuron development, and promoted SATB1 nuclear translocation and repositioning within the somat

57 ficantly decreased high-mobility group box 1 nuclear translocation and secretion in neurons, an effec

58 tiffness-induced CCN1 activates beta-catenin nuclear translocation and signaling and that this contri

59 he TGF-beta pathway in osteoblasts, enhanced nuclear translocation and target gene expression, and in

60 and LRP6 co-receptors, enabling beta-catenin nuclear translocation and TCF/LEF-dependent gene transac

61 RT1) repression and stimulates NF-kappaB p65 nuclear translocation and transactivation of NF-kappaB t

62 R-mediated FUS phosphorylation regulates FUS nuclear translocation and transcription of a major profi

63 ereby PGE(2) promotes Yap dephosphorylation, nuclear translocation and transcriptional activity by si

64 Moreover, oncogenic Kras promoted nuclear translocation and transcriptional activity of SO

65 olic beta-catenin stabilization promotes its nuclear translocation and transcriptional activity.

66 ng a molecular basis for hormone-independent nuclear translocation and transcriptional enhancement.

67 duced IkappaB phosphorylation, NF-kappaB p65 nuclear translocation, and activity of the NF-kappaB-spe

68 ses implicate dysregulation of ciliogenesis, nuclear translocation, and an epigenetic mechanism that

69 he TGF-beta signaling pathway, but not their nuclear translocation, and depended on oxygen availabili

70 sphorylation promotes mTORC1 signaling, IRF3 nuclear translocation, and IFN-beta production.

71 father's lymphocytes showed reduced pSTAT4, nuclear translocation, and impaired IFN-gamma production

72 R83C showed reduced nuclear translocation, and neither mutant was able to re

73 rylation of AMPKalpha Thr172, reduced SREBP2 nuclear translocation, and Srebf2 mRNA expression.

74 This leads to NRF1 dimerization, nuclear translocation, and the up-regulation of nuclear-

75 Deregulation of CRTC1 dephosphorylation, nuclear translocation, and transcriptional function are

76 and FOXO3a phosphorylation, increased FOXO3a nuclear translocation, and upregulated high temperature

77 t the onset of differentiation and undergoes nuclear translocation as differentiation progresses.

78 a/macrophages irrespective of similar pSTAT1 nuclear translocation as in infected controls.

79 The evaluation of competition relied on a nuclear translocation assay applied in a three-color ima

80 omogeneous time-resolved fluorescence assay, nuclear translocation assay, and immunofluorescence.

81 ormal IkappaBalpha degradation and NF-kappaB nuclear translocation but significantly reduced NF-kappa

82 T. gondii and IL-10 inhibited virus-induced nuclear translocation, but not phosphorylation, of IFN r

83 e applied to the nucleus directly drives YAP nuclear translocation by decreasing the mechanical restr

84 We tracked TNF-stimulated NF-kappaB RelA nuclear translocation by live-cell imaging and then quan

85 the NRON complex affects PER and CRY protein nuclear translocation, dampens amplitude, and alters per

86 amin A expression, as well as YAP and MRTF-A nuclear translocation did not show consistent trends bet

87 iptional performance of GR, but no impact on nuclear translocation, dimerization, or DNA binding capa

88 -267 by Ack1/TNK2 tyrosine kinase results in nuclear translocation, DNA binding, and androgen-depende

89 different types of stresses induce distinct nuclear translocation dynamics of the general stress-res

90 lly interacts with PD-L1 and facilitates its nuclear translocation, enhancing the transcription of th

91 uation of TGF-beta signaling, Smads and XBP1 nuclear translocation, expression of GRP78 and XBP1 (ER

92 NRF2-dependent OSGIN1 expression induced P53 nuclear translocation following MMF administration, lead

93 oplasmic beta-catenin result in insufficient nuclear translocation for full Wnt target gene transcrip

94 totoxic T lymphocyte effector functions.NFAT nuclear translocation has been shown to be required for

95 NF-kappaB nuclear translocation, IL-1 beta and TNF-alpha gene expr

96 elated factor 2 (Nrf2) gene expression, Nrf2 nuclear translocation in bronchial epithelial cells, and

97 ction of p65 phosphorylation and accelerated nuclear translocation in cells exposed to Pg LPS.

98 A CDK inhibitor blocks p53-RS's nuclear translocation in HCC, whereas CDK4 interacts wit

99 TFEB phosphorylation, feedback inhibits TFEB nuclear translocation in hepatocytes.

100 raction with coactivators and enhancing hCAR nuclear translocation in HPHs.

101 PEG3 for TFEB transcriptional induction and nuclear translocation in human umbilical vein endothelia

102 f both stimuli via the dynamics of NF-kappaB nuclear translocation in individual cells, suggesting th

103 n receptor alpha (ERalpha) and activates its nuclear translocation in mESCs.

104 is able to efficiently block STAT1 and STAT2 nuclear translocation in order to impair transcriptional

105 zation, hormone-dependent monomerization and nuclear translocation in PC-3 and COS-1 cells, by utiliz

106 monstrated that COX-2 was induced and showed nuclear translocation in two neuronal cell lines - mouse

107 ion, NF-kappaB binding to DNA, and NF-kappaB nuclear translocation in WT mice was exacerbated in MIOX

108 Keap1 inhibition increased Nrf2 nuclear translocation, increased antioxidant gene expres

109 phorylates TFEB at Ser467 and represses TFEB nuclear translocation independently of mechanistic targe

110 Nuclear translocation is important in MLP-mediated signa

111 th live cell reporters, we discover that ERK nuclear translocation is regulated in a graded manner in

112 on 6 to 9 (ARM6-9) of KAP3, required for its nuclear translocation, is also necessary and sufficient

113 it mediates PKCdelta-dependent NF-kappaB-p65 nuclear translocation, leading to inflammasome priming,

114 plays additional roles in human disease, its nuclear translocation mechanism remains unresolved.

115 f impaired SNAI1 proteasomal degradation and nuclear translocation, might be a sign of a diseased pro

116 F508del CFTR correctors induced Nrf2 nuclear translocation, Nrf2-dependent luciferase activit

117 ion, which enhances IkappaB degradation, p65 nuclear translocation, nuclear exit of MKL, and sequestr

118 ng a hypoxia-tracer, we show that HIF-1alpha nuclear translocation occurred both in hypoxic and non-h

119 ctivation, enhanced spine Ca(2+) transients, nuclear translocation of a CaM shuttle, and nuclear CaMK

120 chaperones have been shown to play a role in nuclear translocation of a variety of proteins including

121 Notably, FCHSD2 depletion results in the nuclear translocation of active extracellular signal-reg

122 n of glioblastoma stem-like cells drives the nuclear translocation of an intracellular fragment of OD

123 evented 5alpha- dihydrotestosterone-mediated nuclear translocation of AR and induced proteasomal degr

124 rt which otherwise dominates over import and nuclear translocation of AR as a transcription factor.

125 In particular, RAPGEF5 regulates the nuclear translocation of beta-catenin independently of b

126 g of CD8(+) T cells induces a TNIK-dependent nuclear translocation of beta-catenin with consecutive W

127 endocytosis did not affect accumulation and nuclear translocation of beta-catenin, as measured by si

128 ling in the neoplastic epithelium to promote nuclear translocation of beta-catenin, cellular prolifer

129 In HEK293 cells HP produced nuclear translocation of beta-catenin, together with a r

130 ular activation of c-Jun was demonstrated by nuclear translocation of c-Jun, enhanced phosphorylation

131 The knockdown of KPNB1 reduced nuclear translocation of c-Myc, the expression of downst

132 nscription factor RelA was enhanced, whereas nuclear translocation of c-Rel was decreased in A20-defi

133 sclosed that Importin 4 (IPO4) augmented the nuclear translocation of CEBPD through nuclear localizat

134 ll line HuT78 activates the Notch pathway by nuclear translocation of cleaved Notch1 intracellular do

135 between CLOCK and BMAL1 and interferes with nuclear translocation of CLOCK both in vivo and in vitro

136 ed decorin and increased phosphorylation and nuclear translocation of CREB.

137 rzA, displayed normal alkaline tolerance and nuclear translocation of CrzA was unaffected by ambient

138 Various stress conditions induce the nuclear translocation of cytosolic glyceraldehyde-3-phos

139 e found that BMP-2 stimulated expression and nuclear translocation of Dlx3 and Osx in odontoblasts bo

140 e ERK1/2-importin7 interaction, inhibits the nuclear translocation of ERK1/2, and arrests active ERK1

141 Our study indicates that targeting the nuclear translocation of ERK1/2, in combination with MEK

142 e of the hallmarks of the ERK cascade is the nuclear translocation of ERK1/2, which is important main

143 changes in the kinase domain that result in nuclear translocation of ERK5 and stimulation of gene tr

144 This is achieved by preventing nuclear translocation of FoxO1 (Forkhead box protein O1)

145 the LKB1-AMPK axis, thereby facilitating the nuclear translocation of FoxO1 and activation of key glu

146 eleases Gli2 from SuFu binding, resulting in nuclear translocation of Gli2 and transcription of parat

147 Loss of WASp impedes nuclear translocation of GOLPH3 and its colocalization w

148 ity without disrupting dexamethasone-induced nuclear translocation of GR.

149 ing protein calmodulin (CaM), which leads to nuclear translocation of GRK5 and promotion of cardiac h

150 Moreover, LRRK2 stimulated nuclear translocation of HDAC3 via the phoshorylation of

151 o laminin and integrin alpha6beta1-dependent nuclear translocation of HIF1alpha.

152 ich Vpx orchestrates the challenging task of nuclear translocation of HIV-2/SIV genome in nondividing

153 to rhinovirus and viral mimics and decreased nuclear translocation of interferon regulatory factors.

154 ConA induced nuclear translocation of interferon-regulatory factor-1

155 hermore, NS1 blocked the phosphorylation and nuclear translocation of IRF3 upon stimulation by variou

156 STING-mediated IFN production is mediated by nuclear translocation of IRF3 whereas TLR9-mediated acti

157 TAK1 and IKKbeta activation, leading to the nuclear translocation of IRF5 and induction of inflammat

158 se findings suggest that syndecan-4 mediates nuclear translocation of MLP in the heart.

159 form a stable complex that is essential for nuclear translocation of NAMPT.

160 tion signal (NLS) was inactivated to prevent nuclear translocation of nBMP2 while still allowing the

161 3) SIRT1 activation prevented nuclear translocation of NF-kappaB (p65), which, in turn

162 idinecarbonitrile) and IKK 16 prevented both nuclear translocation of NF-kappaB and activation of a N

163 to an inflammatory phenotype associated with nuclear translocation of NF-kappaB and production of IL-

164 Treatment with an A(2A)AR agonist decreased nuclear translocation of NF-kappaB and subsequent produc

165 h STING signalosomes and interferes with the nuclear translocation of NF-kappaB and the induction of

166 hronic antipsychotic drug exposure increases nuclear translocation of NF-kappaB in both mouse and hum

167 cFOS, STAT3, p38-MAPK, AKT and IKKs, and the nuclear translocation of NF-kappaB p-65 subunit whereas

168 Further, suppression of mTOR facilitated nuclear translocation of NF-kappaB p65.

169 Nuclear translocation of NF-kappaB was detected by immun

170 iR-301a-mediated inhibition of NKRF enhances nuclear translocation of NF-kappaB, which, in turn, resu

171 ociated with enhanced activation of RhoA and nuclear translocation of NF-kappaB.

172 that the NRON scaffolding complex regulates nuclear translocation of NFAT and its signaling.

173 Mechanistically, phenformin induces the nuclear translocation of NFATc1 in keratinocytes in an A

174 ation duration, the LV showed an increase in nuclear translocation of NFkappaB (p65), whereas the RV

175 exposure of PHH to HBV particles resulted in nuclear translocation of NFkappaB, followed by the expre

176 KKbeta phosphorylation but did not block the nuclear translocation of NFkappaB, which was surprising,

177 d IRF5 translocation to the nucleus, but not nuclear translocation of NFkappaB.

178 oter reporter activity and etoposide induced nuclear translocation of NFkappaB.

179 lays an important role in the activation and nuclear translocation of Notch intracellular domain (NIC

180 t maternal piRNAs, which prevents precocious nuclear translocation of NRDE-3 in the early embryo.

181 and NF-kappaB or inhibition of AKT prevented nuclear translocation of Nrf1.

182 mic reticulum (ER) stress elicited prominent nuclear translocation of Nrf2 in 100% of HCV infected he

183 The sustained nuclear translocation of Nrf2 in chronically infected cu

184 (ERK1/2), NF-kappaB, and Nrf2 activation and nuclear translocation of Nrf2, and it reduced the expres

185 malized the ER-stress response and prevented nuclear translocation of Nrf2, whereas HCV clearance by

186 increased reactive oxygen species and caused nuclear translocation of Nrf2, which in turn upregulated

187 We quantified an increased nuclear translocation of nuclear factor erythroid 2-rela

188 Moreover, increased BMP signaling promoted nuclear translocation of nuclear factor-activated T-cell

189 ted mmp-3 promoter activity with concomitant nuclear translocation of nuclear factor-kappaB (NF-kappa

190 an increase in both the cellular content and nuclear translocation of p-S552 beta-catenin after 15 mi

191 ntegrin subunits and TGF-beta receptors, and nuclear translocation of p-SMAD2 in hASCs.

192 enetic deficiency inhibits mitochondrial and nuclear translocation of p53 in cultured cells and in AP

193 alization in a p65-dependent fashion and the nuclear translocation of p65 as mediated through SETD1,

194 Immunostaining revealed the blocking of nuclear translocation of p65 in gingival fibroblasts.

195 IkappaBalpha phosphorylation, and suppressed nuclear translocation of p65 in RAW264.7 cells induced b

196 The nuclear translocation of P65 was partially prevented by

197 osphorylated IKKalpha/beta and IkappaBalpha, nuclear translocation of p65, and iNOS expression.

198 lpha (IkappaBalpha) and p65 phosphorylation, nuclear translocation of p65, and regulation of target g

199 paBalpha and degradation of IkappaBalpha and nuclear translocation of p65, and suppressed basal level

200 ed activation of NF-kappaB via inhibition of nuclear translocation of p65-NFkappaB, the transcription

201 of IkappaBalpha and the phosphorylation and nuclear translocation of p65.

202 ERK, CREB, and Ser-727 of STAT3 and induced nuclear translocation of pCaMKII.

203 l molecules targeting the NFAT pathway alter nuclear translocation of PER and CRY proteins and impact

204 an cells, and we showed how the mobility and nuclear translocation of PER2 are regulated by casein ki

205 gnaling cascade, which, in turn, induces the nuclear translocation of phospho-Nrf2 protein to regulat

206 We analyzed cellular content and nuclear translocation of phosphorylated (p)-serine 552 (

207 We have previously shown that nuclear translocation of PKCdelta is necessary and suffi

208 Nuclear translocation of Prom1 and these molecules is pa

209 cells treated with IFN-alpha, it blocks the nuclear translocation of pSTAT1 by interacting with the

210 Radiation stimulated nuclear translocation of Rad51 in an HDAC4-dependent man

211 Akt activity mediates growth factor-induced nuclear translocation of Raptor, a regulatory scaffoldin

212 ) levels can be independently regulated, and nuclear translocation of receptor tyrosine kinases (RTKs

213 igase which dephosphorylates IkB and impedes nuclear translocation of RelA (p65), thus repressing onc

214 appaB activation, as shown by the absence of nuclear translocation of RelA with a decreased expressio

215 coholic liver disease, we detected increased nuclear translocation of RELB and increased levels of LT

216 duced BCR and NF-kappaB signaling, inhibited nuclear translocation of RelB and p50, and decreased Bcl

217 er diseases have increased levels of LTB and nuclear translocation of RELB.

218 c study showed the inhibition of EGFR caused nuclear translocation of S6K1 for binding with MDM2 in r

219 We show that RanBP6 silencing impairs nuclear translocation of signal transducer and activator

220 sCYLD mediates ubiquitination and nuclear translocation of SMAD7 and thereby decreases tra

221 ed by decreased STAT1/STAT2 phosphorylation, nuclear translocation of STAT1, and expression of IFN-al

222 aining revealed that the virus prevented the nuclear translocation of STAT2 molecules, confirming the

223 rance induction of monocytes associated with nuclear translocation of STAT3 and BCL-3 as relevant mec

224 Myosin phosphorylation leads to nuclear translocation of Taz, which together with Tead1a

225 the T4SS, as a Dot/Icm mutant showed reduced nuclear translocation of TFEB and TFE3.

226 rectly interacted with TFEB and promoted the nuclear translocation of TFEB.

227 ates Aqp2 transcription through induction of nuclear translocation of the acetyltransferase EP300, wh

228 d adrenal explant culture supernatant induce nuclear translocation of the androgen receptor in female

229 ditis elegans, mitochondrial damage leads to nuclear translocation of the ATFS-1 transcription factor

230 chanistically, this phenotype is ascribed to nuclear translocation of the basic helix-loop-helix tran

231 Aversive learning requires nuclear translocation of the cGMP-dependent protein kina

232 ification in RPE cells, which coincides with nuclear translocation of the lysosomal stress-sensing tr

233 TNF-induced nuclear translocation of the NF-kappaB subunit p65 and N

234 of NF-kappaB inhibitor alpha in IECs led to nuclear translocation of the NF-kappaB subunit p65 and r

235 d extracellular signal-regulated kinase 1/2; nuclear translocation of the NF-kappaB subunit p65; and

236 e optimal IkappaB kinase phosphorylation and nuclear translocation of the nuclear factor kappa light

237 te precursor cells associated with increased nuclear translocation of the nuclear factor of activated

238 multipotent mesenchymal cells stimulated the nuclear translocation of the PC1 C-terminal tail/TAZ (PC

239 F-beta signaling via high-content imaging of nuclear translocation of the profibrotic transcription f

240 Regeneration coincides with nuclear translocation of the putative mechanotransducer

241 ing epithelial oxidative stress and inducing nuclear translocation of the signaling protein beta-cate

242 ut inhibiting IFN-induced phosphorylation or nuclear translocation of the STAT1 and STAT2 transcripti

243 no other tryptophan metabolite promotes the nuclear translocation of the transcription factor aryl h

244 Increased production and nuclear translocation of the transcription factor ATF4 a

245 ts antiretroviral responses by promoting the nuclear translocation of the transcription factor EB (TF

246 upregulate autophagic genes by inducing the nuclear translocation of the transcription factor EB (TF

247 complementation, triggers TCRs and activates nuclear translocation of the transcription factor nuclea

248 ssion through a conserved pathway leading to nuclear translocation of the transcriptional effector Yk

249 ated impaired S1P cleavage, which prohibited nuclear translocation of the transcriptionally active fo

250 sulting in distinct cellular trafficking and nuclear translocation of the virus compared to that in o

251 TGFbeta1 stimulation promotes nuclear translocation of the WWP2 isoforms containing th

252 eneity, which was positively associated with nuclear translocation of the YAP/TAZ transcriptional co-

253 The nuclear translocation of these transcription factors was

254 Rap and rapalogs induced autophagic flux via nuclear translocation of transcription factor EB (TFEB).

255 This triggered the nuclear translocation of transcription factor EB, a know

256 pro-inflammatory mediators and viral-induced nuclear translocation of transcription factors from Nucl

257 ch resulted in increased phosphorylation and nuclear translocation of transcription factors NFkappaB,

258 d stimulated them with TNFalpha and analyzed nuclear translocation of transcription regulators -NFkap

259 ncreased focal adhesion kinase signaling and nuclear translocation of transcriptional coactivator TAZ

260 Additional factors, including nuclear translocation of UBQLN2, may facilitate its acti

261 (UPR) by interacting with and regulating the nuclear translocation of XBP-1s, a transcription factor

262 al rise in p38 phosphorylation activated the nuclear translocation of XBP1, which together with the t

263 ced cytosolic mislocalization, prevented the nuclear translocation of XRCC4-DNA ligase 4.

264 Intriguingly, nuclear translocation of YAP and TAZ induced by Lats1/2-

265 d destabilized LATS and resulted in enhanced nuclear translocation of YAP and TAZ, accompanied with a

266 osine phosphorylation and strong, continuous nuclear translocation of YAP in ECs that is dependent on

267 ical constraints results in accumulation and nuclear translocation of Yap, which triggers proliferati

268 Post-transcriptional modifications and nuclear translocation of YAP1 are crucial for its nuclea

269 to elucidate the mechanism of regulation of nuclear translocation of Yes-associated protein (YAP) un

270 ore, elevated cAMP inhibited mitogen-induced nuclear-translocation of MKL1 and MKL2 in VSMCs but not

271 Targeting FUS nuclear translocation offers a new antifibrotic therapy.

272 Fluticasone-induced GRalpha nuclear translocation, phosphorylation at serine 211 and

273 Upon light-induced nuclear translocation, phytochrome (phy) sensory photore

274 appaB transactivation, and delayed NF-kappaB nuclear translocation, presumably via delayed kinetics o

275 lamina that interferes with nucleokinesis, a nuclear translocation process required for neuronal migr

276 down ATF4 decreased NRF2 expression and its nuclear translocation, reduced HO-1 expression and incre

277 a cell-penetrating peptide that inhibits FUS nuclear translocation reduces FUS nuclear content and co

278 ally modulating PD-L1 acetylation blocks its nuclear translocation, reprograms the expression of immu

279 We show that DDR1 nuclear translocation requires collagen-mediated recepto

280 l site affecting protein phosphorylation and nuclear translocation, resulting in CVID with adrenocort

281 aling and STAT1 activation, it precluded the nuclear translocation specifically of STAT1 in response

282 escent phenotype, correlating with NF-kappaB nuclear translocation, suggesting a mechanism of toleran

283 ependent transactivation ability and altered nuclear translocation, suggesting abnormal interactions

284 LPA signaling induced NFAT1 nuclear translocation, suggesting that autocrine LPA syn

285 ownregulation of NFKBIB by siRNA led to RELA nuclear translocation that could bind to the KIT promote

286 ) by inhibiting NF-kappaB activation and its nuclear translocation (the root cause for inflammation i

287 thesis, or hypoxia) also triggers SnRK1alpha nuclear translocation, thereby controlling induced but n

288 FFSS signaling drives class IIa HDAC nuclear translocation through a signaling pathway involv

289 athways of the target cell and mediate their nuclear translocation through components of the nuclear

290 hat photoluminescent Pdots provide selective nuclear translocation to hepatocellular carcinoma cells

291 esenchymal transition (EMT) and beta-catenin nuclear translocation to promote cell migration and inva

292 fferential roles for RSLD phosphorylation in nuclear translocation versus regulation of APA.

293 tivated T cells 1 (NFATc1) and regulates its nuclear translocation via interaction with Ppia, and thi

294 Aldosterone-stimulated MR nuclear translocation was blocked by the 11beta-HSD2 inh

295 HDAC3 phosphorylation and its nuclear translocation were increased in response to 6-hy

296 The activation of Nrf2 and its nuclear translocation were prevented by ER-stress and PE

297 iated YAP1 dephosphorylation and promote its nuclear translocation which induces a pro-survival gene

298 lly, CD82 modulates TLR9-dependent NF-kappaB nuclear translocation, which is critical for inflammator

299 disrupts TFEB phosphorylation, allowing its nuclear translocation, which is synergized by increased

300 ed-forward activates TFEB via promoting TFEB nuclear translocation, while bile acid-induced fibroblas