ライフサイエンスコーパス: nuclear localization

1 and correlates with PTEN expression and FOXO nuclear localization.

2 ospho-Ser-127 modification and promotes YAP1 nuclear localization.

3 chloroplast, without any clear evidence for nuclear localization.

4 ing the stability of hDNA2 and promoting its nuclear localization.

5 nd promotes its degradation by promoting its nuclear localization.

6 immune responses is independent of SAMHD1's nuclear localization.

7 ll area, which correlated with decreased YAP nuclear localization.

8 formation, while not affecting beta-catenin nuclear localization.

9 appropriate receptor protein expression and nuclear localization.

10 e Esrp1 peptide that is sufficient to confer nuclear localization.

11 prevented decorin-evoked TFEB induction and nuclear localization.

12 beta-catenin while CHIR99021 increased it in nuclear localization.

13 but one mutant in the cytoplasm, as well as nuclear localization.

14 we confirmed that stauprimide inhibits NME2 nuclear localization.

15 -113 is essential for catalytic activity and nuclear localization.

16 cade to control YAP-S397 phosphorylation and nuclear localization.

17 55 and Baf170 and displayed differential sub-nuclear localization.

18 ased TFEB promoter activity, expression, and nuclear localization.

19 ine residues 421 and 423 as critical for its nuclear localization.

20 ism by which cytoskeletal tension can govern nuclear localization.

21 ignals that regulate ICAP1 and, hence, KRIT1 nuclear localization.

22 motif in ZIKV and DENV NS5 proteins directs nuclear localization.

23 ature shared with HIV in which cPPTs promote nuclear localization.

24 vern Tda1 activity, while CK2 regulates Tda1 nuclear localization.

25 S89, another type I MADS box, which enhances nuclear localization.

26 of nuclease activity, as well as failure of nuclear localization.

27 ted primarily in the nucleus as loss of PTEN nuclear localization abrogated its ability to bind to an

28 lular DNA release required the enzymatic and nuclear localization activities of PAD4.

29 associated mutations result in loss of SRCAP nuclear localization, alter neural crest gene programs i

30 cologic inhibition of PKCiota decreases YAP1 nuclear localization and blocks OSC tumor growth in vitr

31 llular delivery sequence induced significant nuclear localization and cell cycle arrest in S phase, a

32 lates Hoxb13 at serine-204, resulting in its nuclear localization and cell cycle arrest.

33 s a distinct N-terminal domain that mediates nuclear localization and chromatin binding.

34 dependent regarding their protein stability, nuclear localization and chromatin recruitment and contr

35 Furthermore, phosphorylated HSF1 nuclear localization and distribution were impaired in s

36 mbled the unliganded AR (apo-AR), precluding nuclear localization and DNA binding.

37 B pathway and consequently reduces NF-kappaB nuclear localization and downregulates NF-kappaB targets

38 box deletion of MAF1 leads to increased MAF1 nuclear localization and enhanced repression of ACC1 and

39 t a SUMOylation-mediated mechanism regulates nuclear localization and function of the ICD of ErbB4 re

40 h mature HMR rescues both its plastidial and nuclear localization and functions.

41 -binding portal region, abolished both FABP1 nuclear localization and GW7647-induced PPARalpha activa

42 decreases ileal FGF15, enhances hepatic TFEB nuclear localization and improves cholesterol homeostasi

43 associated regulatory beta-subunits restrict nuclear localization and inhibit target gene induction.

44 In HPK1ARas cells, 1alpha,25(OH)2D3-induced nuclear localization and interaction of hRXRalpha are re

45 pr F34I and Q65R viral mutants, we show that nuclear localization and interaction with cullin 4A-DBB1

46 by FGF21 signal-activated PKA increases its nuclear localization and interaction with the nuclear re

47 tance to genotoxic agents by modulating YB-1 nuclear localization and interaction with the splicing f

48 l cells through the inhibition of PGC-1alpha nuclear localization and is also required for angiogenes

49 ndings indicate that androgen regulates YAP1 nuclear localization and its transcriptional activity th

50 We also demonstrate that L1 nuclear localization and mitotic chromosome association

51 SIRT1 at Ser-164 substantially inhibited its nuclear localization and modestly affected its deacetyla

52 Nuclear localization and nucleosome remodeling and histo

53 he role of individual residues of the NLS in nuclear localization and nucleotide incorporation activi

54 erminus (AAs 23-40) that mediates the CASZ1b nuclear localization and NuRD interaction.

55 , and NUP43 transcripts is uncorrelated with nuclear localization and paraspeckle association.

56 (FABP1), GW7647 treatment increases FABP1's nuclear localization and potentiates GW7647-mediated PPA

57 eus and cytosol, whereas RFA4 shows specific nuclear localization and promotes nuclear degradation of

58 Here we show unique nuclear localization and regulation of gene transcriptio

59 Hippo pathway regulation due to constitutive nuclear localization and resistance to degradation of th

60 Most noncoding transcripts exhibit nuclear localization and several have been shown to play

61 did not affect heat-induced oligomerization, nuclear localization and specific DNA binding but inhibi

62 ound that NS5 SIM sites are required for NS5 nuclear localization and that SUMO sites regulate NS5 NB

63 s provide a mechanism for regulation of Bag6 nuclear localization and the functional integrity of the

64 induces resistance to BETi, by promoting TAZ nuclear localization and transcriptional activity.

65 d that ALS-associated Sod1 mutations reduced nuclear localization and, consequently, impaired the ant

66 crophthalmia-associated transcription factor nuclear localization, and Chromatin immuno-Precipitation

67 /Thr-to-alanine variants displayed increased nuclear localization, and NACA dephosphorylation was ass

68 rogates cytoplasmic assemblies, promotes ARF nuclear localization, and results in an altered transcri

69 he transcription factor Yap8, promoting Yap8 nuclear localization, and stimulating the transcription

70 lation cycle by promoting TDG function, TET1 nuclear localization, and TET/TDG association.

71 critical for STAT3 phosphorylation at Y705, nuclear localization, and transcription activation.

72 late embryonic periods, and this activity is nuclear localization- and TEAD transcription factor-depe

73 ngle-membrane vacuoles or cytosol, with some nuclear localization apparent.

74 ACLY phosphorylation and nuclear localization are necessary for its role in promo

75 enced by decreased percent androgen receptor nuclear localization (%ARNL) and increased microtubule b

76 romotes EGF-induced EGFR internalization and nuclear localization, associated with induction of EGFR-

77 lls post 24-h serum starvation showed PACS-1 nuclear localization at G(1)-S phase of the cell cycle.

78 mbranous localization, whereas mutant showed nuclear localization; both nuclear and non-nuclear local

79 sponsive transcription factor Crz1 undergoes nuclear localization bursts during the pheromone respons

80 lements that contributed multiplicatively to nuclear localization, but the conserved DNA binding resi

81 transcriptional activation and constitutive nuclear localization, bypassing the need for dimerizatio

82 We found that Raf1-tr has increased nuclear localization compared with full-length Raf1, and

83 ions that otherwise modulate PBX1 stability, nuclear localization, DNA binding, and transcriptional a

84 Moreover, ACOT1 exhibited partial nuclear localization during fasting and cAMP/cAMP-depend

85 t activation resulted in efficient Set2-LANS nuclear localization followed by H3K36me3 deposition in

86 Furthermore, we show that VOZ TFs require nuclear localization for their contribution to BABA-IR b

87 o our knowledge, this is the first time that nuclear localization has been mapped for any geminiviral

88 though several RNA sequences responsible for nuclear localization have been identified-such as repeat

89 ctional nuclear localization signal and that nuclear localization impairs the ability of ICAP1 to sup

90 It distinguishes sub-nuclear localization in 13 distinct substructures and di

91 LPS also increased SETD1 nuclear localization in a p65-dependent fashion and the

92 LOPMENT) protein family, and we observed its nuclear localization in barley protoplasts.

93 n and early tumour initiation and displays a nuclear localization in both mouse and human adenomas.

94 Finally, spliced TERT mRNA had primarily nuclear localization in cancer cells and induced pluripo

95 te Cascade expression, complex formation and nuclear localization in human cells, and demonstrate pro

96 tly, EDP-305 decreased TGF-beta1-induced YAP nuclear localization in human kidney 2 cells by increasi

97 uxin-responsive gene expression and exhibits nuclear localization in regions of high auxin responsive

98 tudies have highlighted the importance of AR nuclear localization in SBMA pathogenesis; therefore, in

99 This was accompanied by diminished ATF6 nuclear localization in stressed senescent cells.

100 primary myoblasts, both MTF1 expression and nuclear localization increased.

101 th the GO-203 inhibitor, which blocks MUC1-C nuclear localization, induced DNA double-strand breaks a

102 Similar to AtMYC2, MpMYCs showed nuclear localization, interaction with JASMONATE-ZIM-DOM

103 a phosphorylation significantly disrupts its nuclear localization, interaction with VDR, intra-nuclea

104 onine and adenine auxotrophy of Ppmet6 Thus, nuclear localization is essential for the stability and

105 on at the molecular level to regulate YAP1's nuclear localization is still puzzling.

106 y SMAX1 domains that are responsible for its nuclear localization, KAR-induced degradation, associati

107 Collectively, the data suggest that nuclear localization may be important for AtDRO1 functio

108 nts defective in dNTPase activity (HD/RN) or nuclear localization (mNLS).

109 between the cytoplasm and nucleus due to its nuclear localization (NLS) and export sequences (NES).

110 In this study, we manipulated three putative nuclear localization (NLS1 to -3) and two potential nucl

111 n the FABP1 helical cap affected neither its nuclear localization nor PPARalpha activation.

112 ORC1 and WNT signaling pathways, and exhibit nuclear localization of activated PKA.

113 is a broadly expressed nuclear protein, and nuclear localization of AFFL-2 is necessary for its role

114 , and promoted protein expression as well as nuclear localization of AHRR.

115 Nuclear localization of androgen receptor (AR) directs t

116 involve the VHL-impacted ubiquitination and nuclear localization of AR.

117 Interestingly, nuclear localization of aSyn, and the effect on gene exp

118 rturbs pro-cancerous Wnt signaling including nuclear localization of beta-catenin and E-cadherin.

119 Concurrently, Dkk1 prevents nuclear localization of beta-catenin by restricting its

120 ase kinase 3beta (GSK3beta) deactivation and nuclear localization of beta-catenin critical to osteoge

121 tivation triggers Akt signaling and enhances nuclear localization of beta-catenin in osteoblasts.

122 The nuclear localization of beta-catenin is the defining ste

123 in transfected cells, which resulted in the nuclear localization of beta-catenin.

124 port by leptomycin B resulted in predominant nuclear localization of C3G.

125 tivated before significant downregulation of nuclear localization of Cic and demonstrated that their

126 The N termini also promote nuclear localization of CLKs, but their transport mechan

127 ion to this scaffolding role, TRIB1 promotes nuclear localization of COP1 by disrupting an intramolec

128 testinal ins-7 transcription, and diminished nuclear localization of DAF-16/FOXO.

129 In addition, KPNA2 mediated nuclear localization of E2F1 and E2F7, where they in tur

130 However, the mechanisms controlling the nuclear localization of FLIL33 or its stability in cells

131 diated by functional activation and enhanced nuclear localization of forkhead box protein O1 transcri

132 ignificantly higher percentage of cells with nuclear localization of gammaH2AX & p16 than non-OSA ind

133 long with increased prevalence of cells with nuclear localization of gammaH2AX & p16.

134 We also found that the nuclear localization of Gene 33 is regulated by its 14-3

135 1 interaction plays an important role in the nuclear localization of HBx.

136 F6-mediated polyubiquitination abolishes the nuclear localization of hDNA2, consequently impairing DN

137 Additionally, in progressing HSK lesions, nuclear localization of HIF-2alpha protein was detected

138 se data suggest that the kinase activity and nuclear localization of HIPK2 are essential for the prod

139 ines concomitantly with increases in piRNAs, nuclear localization of HIWI2 and an increase in H3K9me3

140 response to osmotic stress, and promoted the nuclear localization of Hog1 upon exposure of cells to a

141 Sp1 require the N-terminal pyrin domain and nuclear localization of IFI16, but not the HIN domains i

142 ctate the global genome organization and the nuclear localization of individual chromosomes are not f

143 -like antagonist, INS-37, which promotes the nuclear localization of intestinal HLH-30/TFEB, a key pr

144 rylation of ITCH at Ser257 by AKT led to the nuclear localization of ITCH and ubiquitination of H1.2.

145 Increased expression and nuclear localization of LEF1 are also observed in cystic

146 Heat inactivation of HIV-1 blocks nuclear localization of LysRS, but treatment with a reve

147 se M18BP1/CENP-C interaction cause defective nuclear localization of M18BP1 in interphase, resulting

148 siRNA knockdown of TRPV4 enhanced nuclear localization of mechanosensitive transcription f

149 developing C. elegans embryos and depends on nuclear localization of MET-2.

150 d function primarily inside the nucleus, but nuclear localization of mRNAs has been considered rare i

151 We conclude that nuclear localization of MS is a unique feature of respir

152 iquitination increases protein stability and nuclear localization of mutant PTEN.

153 Decreased nuclear localization of nBMP2 in the nBmp2NLS(tm) mouse

154 tor of beta-catenin activation, by mediating nuclear localization of NFkappaBp65 and beta-catenin.

155 restingly, cell proliferation, migration and nuclear localization of nuclear factor of activated T-ce

156 In this study, we demonstrate nuclear localization of p-STAT(Y705), with significant o

157 Nuclear localization of P. pastoris MS (PpMS) was abroga

158 quely long half-life and unprecedented basal nuclear localization of p53 in NEFs, naked mole-rat p53

159 atment significantly elevated expression and nuclear localization of PAK4 in correlation with inducti

160 mmunohistochemical analyses showed increased nuclear localization of phosphorylated JUN and SMAD prot

161 Nuclear localization of phosphorylated-IRF7 was most pro

162 Moreover, the nuclear localization of PINN-1 is altered in dapk-1 muta

163 We have shown previously that nuclear localization of PKCdelta is necessary and suffic

164 Repressing the expression or nuclear localization of Polkappa might prevent drug resi

165 at R742A as well as D113R mutations abrogate nuclear localization of PpMS and its ability to reverse

166 croscopy, we confirmed the mitochondrial and nuclear localization of RIbeta in cultured neurons.

167 By contrast, enhanced nuclear localization of RPW8.2 by adding an NLS to it re

168 PV4 activation and volume expansion controls nuclear localization of RUNX2, but not YAP, to promote o

169 However, whether the dNTPase activity and nuclear localization of SAMHD1 are required for its supp

170 we report that the dNTPase activity, but not nuclear localization of SAMHD1, is important for its sup

171 beta) pathway, exposure to ligand stimulates nuclear localization of Smad proteins, which then regula

172 hermore, loss of PRL-3 efficiently abolished nuclear localization of STAT3 and reduced its occupancy

173 We also show frequent loss of TFF1 with nuclear localization of STAT3 in human gastric cancers.

174 PstGSRE1 disrupted nuclear localization of TaLOL2 and suppressed ROS-mediat

175 Nuclear localization of TFPI-2 contributed to inhibition

176 signaling involving VE-cadherin, triggering nuclear localization of the Hippo pathway transcriptiona

177 we show that ICAP1 phosphorylation controls nuclear localization of the ICAP1-KRIT1 complex.

178 Moreover, the nuclear localization of the mutant protein in transfecte

179 tem cell (ESC) differentiation by inhibiting nuclear localization of the MYC transcription factor NME

180 eactive oxygen species production, increased nuclear localization of the NRF2 transcription factor, i

181 MUC1-C regulated nuclear localization of the polycomb group proteins BMI1

182 Nuclear localization of the pro-osteoblastic factor RUNX

183 d group of LMNB1 result in a decrease in the nuclear localization of the protein and an increase in m

184 ve membrane-binding domain also affected the nuclear localization of the protein.

185 in the N-terminal part of Rep is pivotal for nuclear localization of the Rep protein from Tomato yell

186 to TLC1 is a pre-requisite for formation and nuclear localization of the telomerase holoenzyme.

187 t chain kinase in the cytoplasm and enhanced nuclear localization of the transcription factor NFAT.

188 n peptide flg22 Moreover, AtOXR2 affects the nuclear localization of the transcriptional coactivator

189 The expression and nuclear localization of the transcriptional coactivators

190 ility are paralleled by modifications in the nuclear localization of the transcriptional regulator YA

191 ermeability, significant cellular uptake and nuclear localization of these Cu complexes was observed.

192 hion, and is required to maintain levels and nuclear localization of TLC1.

193 Finally, an impaired nuclear localization of TRADD triggers cell death throug

194 cient B cell progenitors exhibited increased nuclear localization of transcription factor binding to

195 tically, we found that DMF treatment reduced nuclear localization of transcriptional coactivator with

196 ent with NAM is sufficient to facilitate the nuclear localization of TyrRS that activates PARP1.

197 e forming a heterodimer with AR-FL to induce nuclear localization of unliganded AR-FL, AR-V7 does not

198 of virus entry in a manner dependent on the nuclear localization of Vpr and its interaction with the

199 Bcl-6, c-Myc), reduced proliferation (Ki67), nuclear localization of XPO1 cargos (p53, PTEN), and inc

200 In particular, ARF knockdown reduced non-nuclear localization of YAP which led to an increase in

201 in nucleus that may further lead to the non-nuclear localization of YAP.

202 ation of Cx43 hemichannels was necessary for nuclear localization of Yap/Taz and induction of prolife

203 kPa) led to a decrease in the cell area and nuclear localization of YAP/TAZ, and subsequent stiffeni

204 . 3.5 to 28 kPa) increased the cell area and nuclear localization of YAP/TAZ.

205 sarcoma cell lines, immunoblotting confirmed nuclear localization of YAP1 and TAZ, corresponding to t

206 Nuclear localization of YAP1-MAMLD1 protein is mediated

207 hexosamine biosynthetic pathway (HBP) allows nuclear localization of YAP1.

208 interactions caused either AHR constitutive nuclear localization or failure to translocate to nucleu

209 With the addition of a DNA-nuclear localization peptide component in the same NF, n

210 These interactions regulate nuclear localization, phase separation, and stress granu

211 W7647 requires FABP1-dependent transport and nuclear localization processes.

212 RTKs can translocate to the nucleus via a nuclear localization sequence (NLS) present on the recep

213 viral nucleoprotein (NP) via its N-terminal nuclear localization sequence (NLS).

214 e LSD1 complex through its domain containing nuclear localization sequence and phosphorylation sites.

215 ely accrues from a phosphorylation-sensitive nuclear localization sequence located in the PLD.

216 fused to a yellow fluorescent protein and a nuclear localization sequence to simplify quantitative n

217 trol, PELP1-wt, or mutant PELP1 in which the nuclear localization sequence was altered, resulting in

218 h IPSE or IPSE-NLS (a mutant of IPSE lacking nuclear localization sequence).

219 e central region of ING5, which contains the nuclear localization sequence, is flexible and disordere

220 Located in the nuclear localization sequence, K510 acetylation disrupte

221 isoform of TDP2, DeltaN-TDP2, which omits a nuclear localization sequence.

222 neered variants of Cas12a with two different nuclear localization sequences (NLS) on the C terminus p

223 ally, we identify two previously undescribed nuclear localization sequences in the DBD.

224 asmic-nuclear transitions, several classical nuclear localization sequences in the N terminus of the

225 y of importin-alpha (Imp-alpha) to recognize nuclear localization sequences, without effecting the Im

226 Anillin contains a conserved nuclear localization signal (NLS) at its C-terminus that

227 A nuclear localization signal (NLS) knock-out mutant N did

228 uctural analysis suggests that a monopartite nuclear localization signal (NLS) may reside in the N-te

229 s simplex virus 1 (HSV-1) mutant lacking the nuclear localization signal (NLS) on the ICP0 gene (0Del

230 The 3D(pol) N terminus encodes a nuclear localization signal (NLS) sequence,MRKTKLAPT, im

231 d that the ring component anillin contains a nuclear localization signal (NLS) that binds to importin

232 ted mutant mouse, nBmp2NLS(tm), in which the nuclear localization signal (NLS) was inactivated to pre

233 at CRWN4 is coimported into the nucleus with nuclear localization signal (NLS)-bearing paralogues in

234 Here, we developed nuclear localization signal (NLS)-conjugated polymersome

235 plasma membrane and modulates its binding to nuclear localization signal (NLS)-containing proteins th

236 triphosphate (RanGTP) gradient that imports nuclear localization signal (NLS)-specific cargoes (NLS-

237 leoside triphosphohydrolase (dNTPase) with a nuclear localization signal (NLS).

238 f individual amino acids of the FMDV 3D(pol) nuclear localization signal (NLS).

239 rtin beta1- and 2-dependent proline-tyrosine nuclear localization signal (PY-NLS), which has a unique

240 owed us to identify a structurally conserved nuclear localization signal and amino acids involved in

241 ivities of both a peptide-encoded N-terminal nuclear localization signal and C-terminal nuclear expor

242 The Rf4 gene product contains a nuclear localization signal and is likely to not interac

243 thin the catalytic domain of PfCCT acts as a nuclear localization signal and its deletion decreases t

244 TRKIN contains a nuclear localization signal and localizes to knobs earli

245 try to show that ICAP1 contains a functional nuclear localization signal and that nuclear localizatio

246 Mutations in the nuclear localization signal in EEEV capsid protein have

247 a7p-chimaerin localizes to the nucleus via a nuclear localization signal in its N terminus.

248 ed function of PHLPP1 depends on a bipartite nuclear localization signal in its unique N-terminal ext

249 We identified a nuclear localization signal in NAMPT and amino acid subs

250 capsid protein, which is positioned within a nuclear localization signal in the cyclophilin A-binding

251 trafficking elements, including a canonical nuclear localization signal in the extreme C terminus an

252 A nuclear localization signal is embedded between PRR and

253 e these sequences do not correspond to known nuclear localization signal motifs, they represent a new

254 However, because hDNA2 lacks the nuclear localization signal that is found in its yeast h

255 eered a Fyn biosensor with a light-inducible nuclear localization signal to demonstrate that the Fyn

256 rions parallels effects of the attachment of nuclear localization signal to Sis1, indicating that Cur

257 Using a Giardia nuclear localization signal to target dCas9 to both nucl

258 xpression, which could be reversed after the nuclear localization signal was deleted.

259 ICAP1 contains a nuclear localization signal within an unstructured, N-te

260 Deacetylation sites in Msh3 overlap a nuclear localization signal, and we show that localizati

261 region 2 of ZO-2, and S261 located within a nuclear localization signal, are critical for the intera

262 ncharacterized region of Dnmt3a1 including a nuclear localization signal, has very low activity in TK

263 We fuse the ADAR2 domain, tagged with a nuclear localization signal, to an RNA binding peptide f

264 Depletion of KPNA4 attenuated nuclear localization signal-dependent transport activity

265 n-fluorescent-protein (CFP), with or without nuclear localization signal.

266 n, and (3) in sequence pattern searching for nuclear localization signal.

267 of the importin beta family, via a conserved nuclear localization signal.

268 were full length, containing the N-terminal nuclear localization signal.

269 way for mediating ligand-induced exposure of nuclear localization signal.

270 both the C-terminal basic stretch and basic nuclear localization signal.

271 red a Fyn kinase domain with light-inducible nuclear localization signal.

272 ha, a nuclear-import receptor; this required nuclear localization-signal binding.

273 However, M protein mutants with weakened nuclear localization signals (NLS) and deficient nuclear

274 d the nuclear translocation of CEBPD through nuclear localization signals (NLS) to activate PRKDC-med

275 ycete plant pathogen Phytophthora sojae uses nuclear localization signals (NLSs) for translocation of

276 karyopherins that engage the two independent nuclear localization signals (NLSs) in Gag.

277 The specific interaction of importins with nuclear localization signals (NLSs) of cargo proteins no

278 ngaged via the EHM-targeting signals and the nuclear localization signals (NLSs), as well as the nucl

279 tinct host import factors that interact with nuclear localization signals in the Gag MA and NC domain

280 These features include enhancement of the nuclear localization signals in the nucleocapsid protein

281 intrinsically disordered domains containing nuclear localization signals into the central channel fo

282 karyopherins for Rrp6 nuclear import and the nuclear localization signals recognized by them.

283 , in which TAL effectors harbor their T3 and nuclear localization signals, and activation domain.

284 E344Q substitution reduces KPNA7 binding to nuclear localization signals, and that this limits KPNA7

285 trast, has little effect on KPNA7 binding to nuclear localization signals.

286 Nuclear-import receptors (NIRs) bind nuclear-localization signals (NLSs) of protein cargo in

287 an acetylation-dependent regulation of PD-L1 nuclear localization that governs immune-response gene e

288 domain also plays a critical role in hLysRS nuclear localization, thus facilitating noncanonical fun

289 ing hypothesis that influenza virus exploits nuclear localization to delay activation of the innate i

290 Mutations lacking nuclear localization uncover a novel mechanism whereby l

291 tus loss-of-function alleles decrease Dorsal nuclear localization ventrally, where Toll signals are h

292 s conditions and expression of CTT1 Msn2-GFP nuclear localization was increased in the siw14Delta.

293 d dipeptides were present in the nucleus and nuclear localization was necessary and sufficient for th

294 d nuclear localization; both nuclear and non-nuclear localization were observed in HCT116-P.

295 itionally, the K252 SUMOylation site and NS5 nuclear localization were required for ZIKV NS5 to regul

296 om coalescing into PBs without affecting its nuclear localization, whereas overexpression of PCH1 dra

297 The inhibitory effect of AnkG requires its nuclear localization, which depends on p32-dependent int

298 ect the slope of the correlation between YAP nuclear localization with area, but did decrease overall

299 r import function, with NLS1 responsible for nuclear localization within full-length MSH3.

300 tly as competitive antagonists, blocking AhR nuclear localization, XRE binding, and target gene induc