ライフサイエンスコーパス: localization signal

1 T (residues 16 to 24) that acts as a nuclear localization signal.

2 uclei after exposure of a C-terminal nuclear localization signal.

3 ion, although AnkG lacks a predicted nuclear localization signal.

4 n is combined with the deletion of a nuclear localization signal.

5 ng Esp1 into the nucleus with a SV40 nuclear localization signal.

6 hanges in the STAT3 dimer masked its nuclear localization signal.

7 n kinase domain with light-inducible nuclear localization signal.

8 rescent proteins sandwiched around a nuclear localization signal.

9 reas the N-terminus contains a mitochondrial localization signal.

10 uclear export signal (NES) but not a nuclear localization signal.

11 of Staufen1 into the nucleus via its nuclear localization signal.

12 omains, a proline-rich region, and a nuclear localization signal.

13 in mammalian Sun1, the SUN--nuclear envelope localization signal.

14 Its N-terminus harbors a nuclear localization signal.

15 n XPNPEP3 that was devoid of a mitochondrial localization signal.

16 scent-protein (CFP), with or without nuclear localization signal.

17 3) in sequence pattern searching for nuclear localization signal.

18 -specific activity thought to reflect a self-localization signal.

19 mportin beta family, via a conserved nuclear localization signal.

20 ll length, containing the N-terminal nuclear localization signal.

21 mediating ligand-induced exposure of nuclear localization signal.

22 e C-terminal basic stretch and basic nuclear localization signal.

23 RAF3 to the nucleus via a functional nuclear localization signal.

24 -terminal transmembrane domain and a nuclear localization signal.

25 rowing body of work on nuclear and nucleolar localization signals.

26 e 2 (AAV2) that act as nuclear and nucleolar localization signals.

27 95-100 kDa, which lacked N-terminal nuclear localization signals.

28 oised for activation by calcium and membrane-localization signals.

29 ieved by selectively mutating virion nuclear localization signals.

30 is regulated by small GTPase activators and localization signals.

31 nucleoplasmic sequences and 12% for nuclear localization signals.

32 , a nuclear import factor that binds nuclear localization signals.

33 c expression of proteins harbouring specific localization signals.

34 as little effect on KPNA7 binding to nuclear localization signals.

35 se R-motifs are found in canonical nucleolar localization signals.

36 clear import of viral genome via its nuclear localization signals.

37 ied, including a bipartite classical nuclear localization signal, a mitochondrial matrix targeting se

38 ontrol its localization, including a nuclear localization signal, a nuclear retention domain and a nu

39 uced to ablate a previously reported nuclear localization signal also resulted in a significant decre

40 ippocampal place cells, which compute a self-localization signal, also encode the relative value of p

41 to as pUL31, containing a bipartite nuclear localization signal, an intrinsically disordered region

42 r targeting sequences: two classical nuclear localization signals, an INM sorting motif, and a signal

43 2 separable functional signatures, a nuclear localization signal and a putative EDGE motif, that is c

44 to identify a structurally conserved nuclear localization signal and amino acids involved in lipid bi

45 Mutation analysis indicated that the nuclear localization signal and both the N- and C-terminal regio

46 t exons 5-15 of kazrin, encoding the nuclear localization signal and C-terminal domain, are not requi

47 of both a peptide-encoded N-terminal nuclear localization signal and C-terminal nuclear export signal

48 llular studies that HPDL has a mitochondrial localization signal and consequently localizes to mitoch

49 iced Set-beta transcript lacking the nuclear localization signal and demonstrated that the full-lengt

50 es to infection require a functional nuclear localization signal and DNA binding domain.

51 uncated Leo1(LA1186) protein lacks a nuclear localization signal and is distributed mostly in the cyt

52 The Rf4 gene product contains a nuclear localization signal and is likely to not interact direct

53 e BAG6 sequence contains a canonical nuclear localization signal and is localized predominantly in th

54 catalytic domain of PfCCT acts as a nuclear localization signal and its deletion decreases the nucle

55 TRKIN contains a nuclear localization signal and localizes to knobs earlier in pr

56 of its isoforms, DNAJB6a, contains a nuclear localization signal and regulates beta-catenin signaling

57 ior requires coordinated action of a nuclear localization signal and reversible G protein (heterotrim

58 how that ICAP1 contains a functional nuclear localization signal and that nuclear localization impair

59 oteins contain a consensus bipartite nuclear localization signal and were found in the nucleus when i

60 ng, but specific Rbfox isoforms lack nuclear localization signals and accumulate in the cytoplasm.

61 inery that recognizes one class of dendritic localization signals and establish its role in the polar

62 argeting motif that is distinct from nuclear localization signals and that can be computationally pre

63 protein coding genes encode multiple protein-localization signals and that, in 20-d-old adult fly hea

64 conserved Myc box regions but lacks nuclear localization signals and the bHLHZ domain essential for

65 inally truncated PTBP3 isoforms lack nuclear localization signals and/or most of the RRM1 domain and

66 sequence indicated the presence of a nuclear localization signal, and subcellular fractionation of LN

67 eacetylation sites in Msh3 overlap a nuclear localization signal, and we show that localization of Mu

68 ch TAL effectors harbor their T3 and nuclear localization signals, and activation domain.

69 t NF-kappaB dimerization properties, nuclear localization signals, and binding to cytosolic IkappaBs

70 The NKD proteins have putative nuclear localization signals, and green fluorescent protein fusi

71 ubstitution reduces KPNA7 binding to nuclear localization signals, and that this limits KPNA7 nuclear

72 occupancy, sequence conservation, and known localization signals, and their function, if any, is not

73 of selection, contain functional subcellular localization signals, and their readthrough is regulated

74 ending on TLRs' expression pattern, cellular localization, signaling, and deployment of inflammatory

75 d specific SNARE proteins thus controls KRAS localization, signaling, and tumorigenesis, and disrupti

76 For example, the NPIR and KDEL localization signals are distinctive for subfamilies, an

77 2 of ZO-2, and S261 located within a nuclear localization signal, are critical for the interaction wi

78 ivation domain at aa 31 to 185 and a nuclear localization signal at aa 23 to 29.

79 ue to the presence of a transferable nuclear localization signal at its C terminus.

80 oylation site at Lys(1172) or of the nuclear localization signal at Lys(1147) abolished L1-stimulated

81 495X FUS, which abrogates a putative nuclear localization signal at the C-terminus of FUS, in HEK-293

82 N-terminal DNA-binding domains, the nuclear localization signal becomes more highly exchanging.

83 clear-import receptor; this required nuclear localization-signal binding.

84 derived mutant LT (MCV350) lacking a nuclear localization signal binds hVam6p but fails to inhibit hV

85 se substrate is fused to a bipartite nuclear localization signal (bNLS) and nuclear export signal (NE

86 dChIRP improves the RNA genomic localization signal by >20-fold relative to previous tec

87 CK1delta catalytic activity and centrosomal localization signal (CLS) are required to rescue cilia f

88 Here we identify a modular centrosomal localization signal (CLS) localizing cyclin A to centros

89 Deletion analysis mapped the centrosomal localization signal (CLS) of CK1delta to its C-terminal

90 In Ca(2+)-OsCaM61, the basic nuclear localization signal cluster adopts an extended conformat

91 port of proteins harboring a classic nuclear localization signal (cNLS) or the spontaneous nuclear im

92 th with defects in M9- and classical nuclear localization signal (cNLS)-mediated protein import, nucl

93 We found that targeting a nuclear localization signal-containing S6 variant [NLS-S6(Rpt1)]

94 r DCL4 transcript isoform encoding a nuclear localization signal, DCL4(NLS), is present in Arabidopsi

95 , and K376A) in conjunction with the nuclear localization signal deletion did not result in cytoplasm

96 verexpression of TEF3-1, but not its nuclear localization signal-deletion mutant (TEF3-DeltaNLS), ind

97 erexpressing exogenous FUS without a nuclear localization signal (DeltaNLS-FUS), which developed prog

98 Depletion of KPNA4 attenuated nuclear localization signal-dependent transport activity and sup

99 (1D-)AR transmembrane domain 2 acts as an ER localization signal during active protein biogenesis, an

100 that the motif may act as a general nuclear localization signal for cellular RNAs.

101 A2 function for endosomal escape and nuclear localization signals for nuclear targeting and (ii) trig

102 d, nonactivating fatty acids inhibit nuclear localization signal formation by destabilizing this acti

103 d this localization is dictated by a nuclear localization signal found in the Adi3 T-loop extension,

104 s was restricted to the PM by fusing to a PM localization signal from the Rit GTPase, the resulting p

105 One isoform loses the putative nuclear localization signal, generating c-Drosha.

106 ET genes was investigated by pAtTET::NUCLEAR LOCALIZATION SIGNAL-GREEN FLUORESCENT PROTEIN/beta-GLUCU

107 erized region of Dnmt3a1 including a nuclear localization signal, has very low activity in TKO mESCs,

108 amino acids of MxB to function as a nuclear localization signal; however, the ability of the N-termi

109 he interaction was mediated by two nucleolar localization signals identified by bioinformatics and mu

110 idues 11-27 and an isoleucine-lysine nuclear localization signal (IK-NLS) motif at residues 35-40.

111 ference, together with the lack of a nuclear localization signal in any of the AnkA orthologues, sugg

112 Mutation of the nuclear localization signal in CELF1 abolished the ability to do

113 Mutations in the nuclear localization signal in EEEV capsid protein have an addit

114 s have been shown to deteriorate the nuclear localization signal in FUS and thereby facilitate cytopl

115 aerin localizes to the nucleus via a nuclear localization signal in its N terminus.

116 ion of PHLPP1 depends on a bipartite nuclear localization signal in its unique N-terminal extension.

117 We identified a nuclear localization signal in NAMPT and amino acid substitution

118 A nuclear localization signal in ORF2 was necessary for inhibiting

119 hinge domain, we identified a novel nuclear localization signal in the A/B domain of thyroid hormone

120 uch nonlinear processing generates an object-localization signal in the apical dendritic tuft of laye

121 ism whereby L takes advantage of the nuclear localization signal in the COOH region of 2A to enhance

122 rotein, which is positioned within a nuclear localization signal in the cyclophilin A-binding loop, i

123 king elements, including a canonical nuclear localization signal in the extreme C terminus and a nucl

124 essing human TDP-43 with a defective nuclear localization signal in the forebrain (hTDP-43-DeltaNLS),

125 Along with the known nuclear localization signal in the hinge domain, we identified a

126 lization is mediated by a complex cis-acting localization signal in the nos 3' untranslated region th

127 logical pathway and examined for subcellular localization signals in an effort to identify possible s

128 We found putative nuclear localization signals in NEMO whose mutations disrupted s

129 uttling protein, and it contains two nuclear localization signals in the basic region and one nuclear

130 We identified two critical nuclear localization signals in the central, poorly characterize

131 st import factors that interact with nuclear localization signals in the Gag MA and NC domains.

132 features include enhancement of the nuclear localization signals in the nucleocapsid protein and dis

133 ion studies identified and confirmed nuclear localization signals in XLG2 and XLG3 and a nuclear expo

134 Cdk5 has no intrinsic nuclear localization signal; in the absence of p27, two weak nuc

135 expressing full-length HDM-2 with a membrane-localization signal into untransformed MCF-10-2A cells n

136 ically disordered domains containing nuclear localization signals into the central channel for direct

137 A nuclear localization signal is embedded between PRR and WH2 and

138 reen fluorescent protein (GFP) and a nuclear localization signal is fused to the amino terminus of GF

139 -terminal region of NPM1 where its nucleolar localization signal is located.

140 It contains a nuclear localization signal KRKR motif in the N-terminus.

141 P-43 protein, as a disruption of its nuclear localization signal leads to mislocalization and aggrega

142 screen for novel factors associated with RNA localization signals mediating minus end-directed mRNA t

143 LANA1(S) proteins lack an N-terminal nuclear localization signal motif, and some isoforms differ from

144 r through an atypical basic patch PY nuclear localization signal motif.

145 sequences do not correspond to known nuclear localization signal motifs, they represent a new motif f

146 te thus acts as a widespread microtubule tip localization signal (MtLS).

147 ed with recombinant NEMO but not the nuclear localization signal mutant version and induced nuclear i

148 Utilizing a p53 nuclear localization signal mutant, whose nuclear import is comp

149 AP (AAP2) nuclear (NLS) and nucleolar (NoLS) localization signals near the carboxy-terminal region of

150 In these proteins, a nuclear localization signal (NLS) and an intrinsically disordere

151 st substrates that carry a classical nuclear localization signal (NLS) and bind to importin alpha1, S

152 nal region of FMDV 3D that acts as a nuclear localization signal (NLS) and in template binding is als

153 on protein between RecA containing a nuclear localization signal (NLS) and the DNA-binding domain of

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

155 quence analyses revealed a potential nuclear localization signal (NLS) at the C terminus of IPSE/alph

156 P24 recognizes a unique nonclassical nuclear localization signal (NLS) binding site on KPNA5 that is

157 is only the second to have a defined nuclear localization signal (NLS) consensus.

158 studies that UNE-S harbours a robust nuclear localization signal (NLS) directing SerRS to the nucleus

159 ein domains, including the canonical nuclear localization signal (NLS) in the AR hinge region.

160 be the identification of a potential nuclear localization signal (NLS) in the C-terminal region of I2

161 translocate proteins that contain a nuclear localization signal (NLS) into the nucleus.

162 thin the MeCP2 protein sequence, the nuclear localization signal (NLS) is reported to reside between

163 A nuclear localization signal (NLS) knock-out mutant N did not act

164 dy documents multifunctionality of a nuclear localization signal (NLS) located at the N-terminal regi

165 importin alpha/beta from a bipartite nuclear localization signal (NLS) located in the tail domain [14

166 analysis suggests that a monopartite nuclear localization signal (NLS) may reside in the N-terminal l

167 Consistent with the presence of a nuclear localization signal (NLS) motif within the GmHSP40.1 cod

168 on domain although it does possess a nuclear localization signal (NLS) motif, whilst Cry3 lacks both

169 acterized the importin-alpha binding nuclear localization signal (NLS) of rat ChREBP, identifying it

170 We found that, in addition to the nuclear localization signal (NLS) of XPA, importin-alpha4 or/and

171 26 and Ser828, located in a putative nuclear localization signal (NLS) on the Drosophila melanogaster

172 x virus 1 (HSV-1) mutant lacking the nuclear localization signal (NLS) on the ICP0 gene (0DeltaNLS) i

173 The nuclear localization signal (NLS) polypeptide of RelA, the canon

174 Moreover, acetylation of Skp2 in the nuclear localization signal (NLS) promotes its cytoplasmic reten

175 ING4 is known to bind p53 via its nuclear localization signal (NLS) region and to enhance transcri

176 Remarkably, this nuclear localization signal (NLS) sequence motif is also importa

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

178 (L858R, EGFRvIII), or mutated in the nuclear localization signal (NLS) sequence.

179 ed the structure and conservation of nuclear localization signal (NLS) sequences previously identifie

180 he ring component anillin contains a nuclear localization signal (NLS) that binds to importin and is

181 protein VP1-2 contains an N-terminal nuclear localization signal (NLS) that is critical for capsid ro

182 Here we identify a TIM nuclear localization signal (NLS) that is required for appropria

183 ting on RNA (ADAR1) carries a unique nuclear localization signal (NLS) that overlaps one of its doubl

184 SAP11 contains a bipartite nuclear localization signal (NLS) that targets this effector to

185 otein (GFP) reporter fusion assays a nuclear localization signal (NLS) that was mapped to a 23-amino-

186 of influenza virus A/WSN/33 when its nuclear localization signal (NLS) was disrupted by R101S and R10

187 nt mouse, nBmp2NLS(tm), in which the nuclear localization signal (NLS) was inactivated to prevent nuc

188 ear localization, and a nonclassical nuclear localization signal (NLS) was mapped to a short, highly

189 Ser238 neighbors a nuclear localization signal (NLS) whose function is blocked by p

190 port that Nurr1 contains a bipartite nuclear localization signal (NLS) within its DNA binding domain

191 Both HDAgs contain a nuclear localization signal (NLS), but only HDAg-L contains a CR

192 f topo IIalpha, while preserving the nuclear localization signal (NLS), enhances the decatenation che

193 translocated into the nucleus via a nuclear localization signal (NLS), specific among keratins, wher

194 is coimported into the nucleus with nuclear localization signal (NLS)-bearing paralogues in the NMCP

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

196 s required in the nucleus to release nuclear localization signal (NLS)-containing cargo from import r

197 Notably, the PB2 nuclear localization signal (NLS)-containing domain translocates

198 embrane and modulates its binding to nuclear localization signal (NLS)-containing proteins that regul

199 esmata, targeted to the nucleus in a nuclear localization signal (NLS)-dependent manner, where it loc

200 phate (RanGTP) gradient that imports nuclear localization signal (NLS)-specific cargoes (NLS-cargoes)

201 lasts harboring mutations in the FUS nuclear localization signal (NLS).

202 triphosphohydrolase (dNTPase) with a nuclear localization signal (NLS).

203 dual amino acids of the FMDV 3D(pol) nuclear localization signal (NLS).

204 o the nucleus, it does not possess a nuclear localization signal (NLS).

205 otif which functions as an efficient nuclear localization signal (NLS).

206 volutionarily conserved multipartite nuclear localization signal (NLS).

207 boxy-terminal 143 residues contain a nuclear localization signal (NLS).

208 ver, M protein mutants with weakened nuclear localization signals (NLS) and deficient nuclear interac

209 clear translocation of CEBPD through nuclear localization signals (NLS) to activate PRKDC-mediated DN

210 0-nm diameter) and without (< 10 nm) nuclear localization signals (NLS), macroscopic transport rates

211 , proline/serine (PS) domain and two nuclear localization signals (NLS).

212 CAPN5 possesses two nuclear localization signals (NLS): an N-terminal monopartite NL

213 rminal residues (1-45) including the nuclear localization signal (NLS1) are dispensable.

214 idues within the peptides containing nuclear localization signals (NLSs) 1 and 2 were non-acetylated,

215 ant pathogen Phytophthora sojae uses nuclear localization signals (NLSs) for translocation of protein

216 al nucleocytoplasmic import pathway, nuclear localization signals (NLSs) in cargo proteins are recogn

217 rins that engage the two independent nuclear localization signals (NLSs) in Gag.

218 Importin alpha1 can bind classical nuclear localization signals (NLSs) in two NLS-binding sites, kn

219 l with mutations that inactivate the nuclear localization signals (NLSs) of Apc (Apc(mNLS)).

220 ecific interaction of importins with nuclear localization signals (NLSs) of cargo proteins not only m

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

222 their bacterial homologues, possess nuclear localization signals (NLSs) to enter the cell nucleus du

223 proteins have been shown to contain nuclear localization signals (NLSs), although its biological rol

224 ia the EHM-targeting signals and the nuclear localization signals (NLSs), as well as the nuclear expo

225 ospholipase A(2) (PLA(2)) domain and nuclear localization signals (NLSs).

226 s of influenza A viruses contain two nuclear localization signals (NLSs): a well-studied monopartite

227 lpha and NRF-2beta contain intrinsic nuclear localization signals (NLSs): the Ets domain within NRF-2

228 tches of basic amino acids-nuclear/nucleolar localization signals (NLSs/NoLSs).

229 modular signals for nuclear import (nuclear localization signals, NLSs) and export (nuclear export s

230 Here, we show that NSs contains a nucleolar localization signal (NoLS) and induces disorganization o

231 to target the nucleolus through a nucleolar localization signal (NoLS) localized between residues 33

232 leolus, and deletion of a putative nucleolus localization signal (NoLS) within its N-terminal moiety

233 nce that is predicted to contain a nucleolar localization signal (NoLS), only p8 is found in the nucl

234 lus, suggesting that it contains a nucleolar localization signal (NoLS).

235 orylation at S659, which exposed the nuclear localization signal of ACSS2 for importin alpha5 binding

236 sphorylation sites reside around the nuclear localization signal of Alp7, and the phosphodeficient al

237 ith point mutations in the canonical nuclear localization signal of CMAS, which relocated the enzyme

238 that was dependent on the functional nuclear localization signal of ErbB4.

239 redicted deleterious variants in the nuclear localization signal of Heterogeneous Nuclear Ribonucleop

240 to bind to HIV-1 capsid and (ii) the nuclear localization signal of MxB, which is important for the a

241 glycerol medium, and removal of the nuclear localization signal of Rat1, the nuclear homolog of Xrn1

242 bic domain and a proximal C-terminal nuclear localization signal of VP4 were required for (i) cytolys

243 This is because the predicted nuclear localization signals of HMR are nonfunctional, and there

244 nd this reduction requires the mitochondrial localization signals of Opa3.

245 We identified two nuclear localization signals of Stp1 and found that the N-termin

246 ion sites: one (short form) with the nuclear localization signal only, exclusively localized in the n

247 BP12) fused to a cellular 'address' (nuclear localization signal or nuclear export sequence).

248 srupting Arl13b's palmitoylation site, cilia localization signal, or GTPase handling altered the Shh

249 trated via the assembly of stable QD-nuclear localization signal peptide bioconjugates that promoted

250 in its free form or in complex with nuclear localization signal peptides as the starting conformatio

251 Mutation of the nuclear localization signal prevented detectable levels of AtLAZ

252 not a truncated version lacking the nuclear localization signal protects from pathogenic TDP-43-medi

253 identified a novel proline-tyrosine nuclear localization signal (PY-NLS) in DJ-1, and we found that

254 portin recognizes a proline-tyrosine nuclear localization signal (PY-NLS) in the N-terminal tail of N

255 Mutations in the proline/tyrosine-nuclear localization signal (PY-NLS) of the Fused in Sarcoma pro

256 a1- and 2-dependent proline-tyrosine nuclear localization signal (PY-NLS), which has a unique interve

257 Here, we show that the PY-type nuclear localization signal (PY-NLS)/karyopherinbeta2 (Kapbeta2)

258 o species are due to gain/loss of cis-acting localization signals rather than to differences in the R

259 rins for Rrp6 nuclear import and the nuclear localization signals recognized by them.

260 go proteins, including the classical nuclear localization signals, recognized by the adaptor importin

261 e adaptor importin-alpha, and the PY nuclear localization signals, recognized by transportin-1.

262 -characterized basic amino acid-rich nuclear localization signal region at positions 101 to 105, M1 c

263 onstrate that the positively charged nuclear localization signal region in the tail in apo-OsCaM61 is

264 etylated lysine is in the N-terminal nuclear localization signal region.

265 ction as a nuclear export signal and nuclear localization signal, respectively.

266 r truncated Ptpmt1 lacking the mitochondrial localization signal restored the differentiation capabil

267 of mouse and human, and contained nucleolar localization signal, RNA-binding domain and several phos

268 nuc-ErbB3 possesses a functional nuclear localization signal sequence and binds to chromatin.

269 ls showed that all of them contain a nuclear localization signal sequence flanking to the K1 segment

270 The C terminus encompassing the nuclear localization signal sequesters the enzyme in the nucleus

271 g proteins (EBs) through the microtubule tip localization signal SKIP, which lies N terminal to MCAK'

272 d to nuclei, through the fusion with nuclear localization signal, still exerts strong antiproliferati

273 last targeting signal and a putative nuclear localization signal, suggesting that they are dual targe

274 playing an established mitochondria-specific localization signal targets mitochondria, and that an in

275 DP-43 variant with a mutation in the nuclear localization signal (TDP-43-NLS).

276 Orc6 and Orc1 each contain a single nuclear localization signal that is essential for nuclear locali

277 However, because hDNA2 lacks the nuclear localization signal that is found in its yeast homolog,

278 hat residues (20)KY(21) constitute a nuclear localization signal that is not required for the ability

279 -1314 possesses a conserved putative nuclear localization signal that may facilitate the nuclear targ

280 elements consists of a high-affinity nuclear localization signal that mediates indirect tethering to

281 with importin alpha via a classical nuclear localization signal that recruits importin alpha to the

282 Although different ER localization signals that exhibit varying affinities for

283 by mutating Ser rich clusters of the nuclear localization signal to Ala abolished nuclear import and

284 termines whether AGR2 requires a specific ER localization signal to be functionally active.

285 Fyn biosensor with a light-inducible nuclear localization signal to demonstrate that the Fyn kinase a

286 have expressed KpnI fused to a mitochondrial localization signal to induce a specific mitochondrial d

287 rallels effects of the attachment of nuclear localization signal to Sis1, indicating that Cur1 acts o

288 Using a Giardia nuclear localization signal to target dCas9 to both nuclei, we d

289 fuse the ADAR2 domain, tagged with a nuclear localization signal, to an RNA binding peptide from bact

290 In addition to its nuclear localization signal, translocation of M1 to the nucleus

291 The localization signal was compared with ER-specific dyes.

292 n, which could be reversed after the nuclear localization signal was deleted.

293 inal 25 amino acids to function as a nuclear localization signal was not required for restriction.

294 1 (FHY1) and fhy1-like, an intrinsic nuclear localization signal was proposed to be involved in the n

295 PAD4 or PADV), the only PADI with a nuclear localization signal, was previously shown to act in myel

296 tNLS algorithm uncovered a potential nuclear localization signal, whereas the algorithm DBS-Pred retu

297 The Orc6 nuclear localization signal, which is essential for Orc6 functio

298 dreCmas1 was mediated by a bipartite nuclear localization signal, which seemed irrelevant for other e

299 ICAP1 contains a nuclear localization signal within an unstructured, N-terminal r

300 nd-sensing beta2 loop and a tertiary nuclear localization signal within the alpha-helical cap of the