ライフサイエンスコーパス: nuclear translocation

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

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

3 ession was mediated by PEDF-induced NFkappaB nuclear translocation.

4 yme pyruvate kinase M2 (PKM2) and enable its nuclear translocation.

5 network (TGN) and recycling endosomes before nuclear translocation.

6 d ERK2 and prevents ERK2 phosphorylation and nuclear translocation.

7 importin alpha, which is crucial for IAV RNP nuclear translocation.

8 ogen receptor (AR) activity via promoting AR nuclear translocation.

9 ligands, thereby liberating the protein for nuclear translocation.

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

11 in phosphatase activity, resulting in NFATc1 nuclear translocation.

12 interacted with TFEB, and influenced TFEB's nuclear translocation.

13 orylate YAP and induce its stabilization and nuclear translocation.

14 ase phosphatase 1 increase, and a reduced GR nuclear translocation.

15 th transcription factors, facilitating their nuclear translocation.

16 nduced IFN regulatory factor 5 and NF-kB p65 nuclear translocation.

17 ctor 3 (IRF-3) at a step subsequent to their nuclear translocation.

18 ated heparan sulfate chains are required for nuclear translocation.

19 one triggers nuclear toxicity by inducing AR nuclear translocation.

20 on of IkappaBalpha, which inhibits NF-kappaB nuclear translocation.

21 driven reporter without interfering with p65 nuclear translocation.

22 transportin 2) mediates stress-induced NEMO nuclear translocation.

23 ted drug efflux; and (vii) the TAT-medicated nuclear translocation.

24 O3 degradation and preventing NF-kappaB RelA nuclear translocation.

25 on between GAPDH and Siah1, and led to GAPDH nuclear translocation.

26 nt mTOR inhibition, thereby promoting pSTAT1 nuclear translocation.

27 ivity, which stimulates SMAD3 expression and nuclear translocation.

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

29 s IkappaBalpha phosphorylation and NF-kappaB nuclear translocation.

30 ad51 complex dissociation through inhibiting nuclear translocation.

31 bitor blocked STAT3 binding to myoferlin and nuclear translocation.

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

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

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

35 n of cyclins D1-3 and cdk4, as well as their nuclear translocation, all of which are associated with

36 Overexpression of alphaB-crystallin enhanced nuclear translocation and accumulation of SMAD4 and SMAD

37 nd CR3 regions of E7 and resulted in reduced nuclear translocation and acetylation of the p65 sub-uni

38 es leading to TFEB (transcription factor EB) nuclear translocation and activation of autophagy.

39 n by high glucose was shown by its increased nuclear translocation and activation of the HIF-responsi

40 ated HIPK2/p53 activation precedes HIPK2/p53 nuclear translocation and activity.

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

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

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

44 Mechanistically, GAA promotes FoxO3 nuclear translocation and binding to the SESN2 enhancer,

45 ced stabilization of angiomotins reduces YAP nuclear translocation and decreases downstream YAP signa

46 .01), whereas baseline and TNF-alpha-induced nuclear translocation and dexamethasone-mediated suppres

47 by enhancing NF-kappaB p65 phosphorylation, nuclear translocation and DNA binding with the MCP-1 pro

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

49 tion of the MUC1-C subunit necessary for its nuclear translocation and downstream signaling.

50 vates Nf-kappaB signaling, resulting in RelA nuclear translocation and enhanced expression of pro-inf

51 ase (PI3K) p85alpha or p85beta impairs sXBP1 nuclear translocation and exacerbates DN.

52 bacter species induced nuclear factor kappaB nuclear translocation and exhibited proinflammatory prop

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

54 finally, we demonstrate that A2AR act on GR nuclear translocation and GR-dependent transcriptional r

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

56 Junctional association of YAP inhibits nuclear translocation and inactivates its transcriptiona

57 ls increased ATM phosphorylation instigating nuclear translocation and increased gamma-H2AX, triggeri

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

59 ocation and increased gamma-H2AX, triggering nuclear translocation and intensified expression of AIF.

60 The nuclear translocation and interaction of STAT3 and NFkap

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

62 ion in human disease stimulates beta-catenin nuclear translocation and is an independent predictor of

63 osphorylation and dimerization mediate c-Cbl nuclear translocation and lead to the degradation of nuc

64 Increased NF-kappaB nuclear translocation and macrophage chemoattractant pro

65 ral overexpression of NLRP12 suppressed RelB nuclear translocation and OC formation.

66 n was IKKalpha-dependent and correlated with nuclear translocation and phosphorylation of IRF3.

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

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

69 nduced in vitro HSC activation requiring its nuclear translocation and rRNA transcriptional stimulati

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

71 Regulation of NF-kappaB nuclear translocation and stability is central to mounti

72 late endosomes by 4- to 5-fold prior to AIF nuclear translocation and subsequent glioma demise.

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

74 action involved the inhibition of NF-kappaB nuclear translocation and the decrease of Myd88 mRNA lev

75 alpha-induced NF-kappaBp65, c-Jun, and STAT3 nuclear translocation and the production of IL-6, IL-8,

76 athways, resulting in increased p50 and RelB nuclear translocation and TNFSF15 and OX40L expression.

77 Loss of MEK-ERK signaling causes FoxO3 nuclear translocation and transcriptional activation of

78 ring activity, thereby negatively regulating nuclear translocation and transcriptional activity of nu

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

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

81 Nuclear factor kappaB nuclear translocation and transcriptomic characteristics

82 eus, integrating ligand-mediated release and nuclear translocation) and duration (half-life of NICD-R

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

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

85 inhibition of NF-kappaB p65 phosphorylation, nuclear translocation, and binding of the MCP-1 promoter

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

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

88 n of NLRP12 promoted NIK stabilization, RelB nuclear translocation, and increased osteoclastogenesis

89 served that both TRES and RES suppressed the nuclear translocation, and interrupted the interaction o

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

91 osphorylation, IkappaBalpha degradation, p65 nuclear translocation, and NF-kappaB reporter activity.

92 functions, such as cooperative DNA binding, nuclear translocation, and protein-protein interactions.

93 ophila JAK kinase (hop(Tum-l)) promotes Madm nuclear translocation, and suppresses vn and integrin ex

94 ex((R))), which slows down AR activation and nuclear translocation, and the disaccharide trehalose, a

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

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

97 lthough not modulating TNF-alpha-induced p65 nuclear translocation, attenuated p65 recruitment to the

98 tivation triggers calcineurin-dependent TFEB-nuclear translocation, autophagy induction and lysosome

99 w in the present report that ApoE4 undergoes nuclear translocation, binds double-stranded DNA with hi

100 ced interferon levels was dependent on SOCS1 nuclear translocation but independent of proteasomal deg

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

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

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

104 paBalpha and p38 MAPK pathways via NF-kappaB nuclear translocation-dependent and -independent mechani

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

106 n led to increased AHR levels and subsequent nuclear translocation, followed by induced CYP1A1 gene e

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

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

109 sion prevented genotoxic stress-induced NEMO nuclear translocation, IKK/NF-kappaB activation, and inf

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

111 Decreased GR expression with impaired nuclear translocation in ASMC, associated with reduced d

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

113 of phospho-IKK-beta, -IkappaB-alpha, and p65 nuclear translocation in ECs.

114 nhanced CREB phosphorylation followed by its nuclear translocation in gastric adenocarcinoma cells.

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

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

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

118 nuclear translocation of viral DNA, and HCMV nuclear translocation in infected monocytes was observed

119 secretion, alphaSMA expression, and Smad2/3 nuclear translocation in IPF-derived HLMFs.

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

121 r (GR)-luciferase activity and facilitate GR nuclear translocation in microglial cells.

122 and endothelial cells, suggesting that HCMV nuclear translocation in monocytes is distinct from that

123 gical hypertrophy, was unable to induce GRK5 nuclear translocation in myocytes.

124 upregulates alpha-Syn protein expression and nuclear translocation in neurons of the adult rodent bra

125 ear ubiquitination and blunting of NF-kappaB nuclear translocation in response to tumour-necrosis fac

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

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

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

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

130 GH induced STAT3 phosphorylation and nuclear translocation, indicating a positive feedback lo

131 seline levels of nuclear GR were similar, GR nuclear translocation induced by dexamethasone (10(-7) M

132 rating tissues, and tumors showed that ErbB3 nuclear translocation is a common event in proliferating

133 Because glucocorticoid receptor (GR) nuclear translocation is key to the anti-inflammatory ef

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

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

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

137 horylation of AKAP12 at S732, which promotes nuclear translocation of AKAP12-ATR-pS435.

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

139 hondrial depolarization with the release and nuclear translocation of apoptotis-inducing factor (AIF)

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

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

142 Furthermore, LPA treatment initiates nuclear translocation of beta-catenin and transcriptiona

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

144 inactivation, cytoplasmic accumulation, and nuclear translocation of beta-catenin to induce EMT in h

145 ) which coincided with dephosphorylation and nuclear translocation of beta-catenin, a major canonical

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

147 port that Lzap, a tumor suppressor, controls nuclear translocation of beta-catenin.

148 enescence mediated by p16(INK4a) by inducing nuclear translocation of Bmi1 because of sustained activ

149 quitination by Nedd4 E3 ligases, followed by nuclear translocation of BRAT1.

150 rons show increased expression of Ndfip1 and nuclear translocation of BRAT1.

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

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

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

154 Deletion of Lkb1 results in a cytoplasm to nuclear translocation of CRTC3 in brown adipocytes, wher

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

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

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

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

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

160 ession of the nuclear receptor PPARalpha and nuclear translocation of forkhead box O 1, which cause c

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

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

163 tivation, triggering the phosphorylation and nuclear translocation of FoxO3a, and leading to an incre

164 Nuclear translocation of Gal-1, in turn, was regulated b

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

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

167 Nuclear translocation of HDA6 was also elevated in the h

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

169 ause decreased phosphorylation and increased nuclear translocation of HDAC4/5 and CRTC2.

170 ion and disrupts Hippo signaling, leading to nuclear translocation of Hippo signaling effector Yes-as

171 ses S326 phosphorylation, trimerization, and nuclear translocation of HSF1, and the transcription of

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

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

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

175 tion of TLR9-mediated NF-kappaB and MAPK and nuclear translocation of IRF7 were greatly enhanced by M

176 f NFATC3 greatly reduced the CpG DNA-induced nuclear translocation of IRF7, which resulted in impaire

177 nd cytosolic fractions further confirmed the nuclear translocation of LASP-1 upon chemokine and growt

178 in the tumor microenvironment could trigger nuclear translocation of LASP-1.Treatment of human breas

179 ctivated ERK increased the protein level and nuclear translocation of mechanosensitive Yes-associated

180 ate that agonists are able to induce partial nuclear translocation of MR but fail to produce transact

181 Xrs2/Nbs1 is essential for nuclear translocation of Mre11, but its role as a compon

182 llular contacts, which induces Rho-dependent nuclear translocation of MRTF.

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

184 f SCCRO in vivo by inhibiting SCCRO-promoted nuclear translocation of neddylation components and resu

185 e beta (IKKbeta) and p38 phosphorylation and nuclear translocation of NF-kappaB and AP-1.

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

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

188 a-5p increased IkappaBalpha level, prevented nuclear translocation of NF-kappaB p65 and ultimately su

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

190 Finally, elevation of nuclear translocation of NF-kappaB p65/p50 and caspase-3

191 clooxygenase-2 (COX-2) was decreased and the nuclear translocation of NF-kappaB was attenuated after

192 Nuclear translocation of NF-kappaB was detected by immun

193 ore, phycocyanin promotes the activation and nuclear translocation of NF-kappaB, which plays an impor

194 ase Calpha (PKCalpha) activity to facilitate nuclear translocation of NF-kappaB/Jun N-terminal protei

195 the expression of cytokines by facilitating nuclear translocation of NFAT and dephosphorylation of d

196 stitutive activation of calcineurin, whereas nuclear translocation of NFAT is associated with increas

197 of ICa, T mediated by PKCalpha, which caused nuclear translocation of NFAT.

198 d a PKCalpha-mediated increase in ICa, T and nuclear translocation of NFAT.

199 AA represses GLI1 expression by stimulating nuclear translocation of NFATc1, which then binds the GL

200 isition of chemoresistance by perturbing the nuclear translocation of NFkappaB in preexisting CSCs.

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

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

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

204 lycemia-associated oxidative stress inhibits nuclear translocation of Nrf2 and impairs activation of

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

206 The sustained nuclear translocation of Nrf2 in chronically infected cu

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

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

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

210 In glomerular endothelial cells, the nuclear translocation of nuclear factor-kappaB, which wa

211 ISO-induced cardiac hypertrophy by inducing nuclear translocation of Nur77 in cardiomyocytes.

212 rescent protein) reporter cells and enhanced nuclear translocation of Nurr1 primary microglia.

213 TGF-beta1 evoked nuclear translocation of p-Smad2 and p-Smad3 in TGF-beta

214 IF-JAK1-STAT3 signaling that delays eventual nuclear translocation of p16(INK4a).

215 lies in prevention of senescence mediated by nuclear translocation of p16(INK4a).

216 t inhibition transitioned to senescence with nuclear translocation of p16(INK4a).

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

218 in cells with intracellular Cn, LPS-induced nuclear translocation of p65 is both amplified and susta

219 ajor Cn capsular polysaccharide, LPS-induced nuclear translocation of p65 is inhibited, whereas in ce

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

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

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

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

224 on, along with increased phosphorylation and nuclear translocation of p65.

225 hosphorylation (palpha-Syn) of alpha-Syn and nuclear translocation of palpha-Syn.

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

227 hance its stability and importin 13-mediated nuclear translocation of PDCD5.

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

229 iferation and a significant reduction in the nuclear translocation of pERK.

230 by interaction with importin7 and subsequent nuclear translocation of pERK.

231 operated Ca(2+) entry (SOCE), SOCE-dependent nuclear translocation of pGFP-NFAT1, and NFAT-dependent

232 t that Sema 3A regulates phosphorylation and nuclear translocation of phosphatase and tensin homolog

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

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

235 r YAP1 association with SMADs and subsequent nuclear translocation of receptor-activated SMAD2.

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

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

238 ere, we show that adipogenic stimuli trigger nuclear translocation of S6K1, leading to H2BS36 phospho

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

240 ng protein synthesis before hormone-inducing nuclear translocation of Six1 or Eya1.

241 bind receptors to induce phosphorylation and nuclear translocation of SMAD transcription factors (R-S

242 ia enhanced expression, phosphorylation, and nuclear translocation of SMAD2/3.

243 irectional phosphorylation mechanism and the nuclear translocation of SRSF1 demonstrating that the in

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

245 Prestwick library) that block ligand-induced nuclear translocation of Stat3 and identified piperlongu

246 In addition, nuclear translocation of TFEB requires phagosome complet

247 show that Fcgamma receptor activation causes nuclear translocation of TFEB, a transcription factor th

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

249 ecies production in ASM cells, and inhibited nuclear translocation of the anti-oxidative response reg

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

251 from the extracellular compartment; and (iv) nuclear translocation of the Ca(2+)-regulated nuclear fa

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

253 inflammatory genes, which is associated with nuclear translocation of the early gene Egr-1 In conclus

254 er HIV infection, correlating with increased nuclear translocation of the gene repressor C-terminal-b

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

256 cystathionine suppressed phosphorylation and nuclear translocation of the NF-kappaB p65 protein, as w

257 ow increased degradation of IkappaBalpha and nuclear translocation of the NF-kappaB p65 subunit toget

258 Furthermore, the nuclear translocation of the NF-kappaB subunit c-Rel was

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

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

261 ced IL-8 release parallel with inhibition of nuclear translocation of the NF-kappaB subunit, p65 (eac

262 -induced TRPC6 channel activation stimulated nuclear translocation of the nuclear factor of activated

263 Nuclear translocation of the nuclear factor of activated

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

265 Regulated nuclear translocation of the PER/CRY repressor complex i

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

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

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

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

270 Keap1 knockdown led to increased nuclear translocation of transcription factors NF-kappaB

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

272 Disruption of the TGN significantly reduced nuclear translocation of viral DNA, and HCMV nuclear tra

273 We also documented transient nuclear translocation of wild-type SHOC2 upon EGF stimul

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

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

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

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

278 d the ensuing c-Src signaling drive a unique nuclear translocation pattern that promotes productive i

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

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

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

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

283 K2 inhibitor to block phosphorylation of the nuclear translocation signal in pERK resulted in greatly

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

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

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

287 Moreover, NFATC3 nuclear translocation, synaptopodin degradation, integri

288 applying force on the nucleus to facilitate nuclear translocation through tight spaces.

289 ndergoing AMPK-dependent phosphorylation and nuclear translocation to activate Sirt1 deacetylase acti

290 re activated through deacetylation-dependent nuclear translocation to forestall the progression of th

291 Instead, the average period of NF-kappaB nuclear translocation varies considerably among single c

292 agment induces SMAD1/5/8 phosphorylation and nuclear translocation via ERK1/2 and P38 signaling.

293 +) influx through CaV1 channels triggers CaM nuclear translocation via local Ca(2+) signaling.

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 h muscle actin (alpha-SMA), and NFkappaB p65 nuclear translocation were quantified with Western blott

298 cdks in human beta-cells but are capable of nuclear translocation when overexpressed.

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

300 iabetes had a higher degree of FHL2 podocyte nuclear translocation, which was positively associated w