ライフサイエンスコーパス: nuclear export signal

1 the nuclear export receptor CRM1 or discrete nuclear export signal.

2 e p53 tetramer and exposure of the intrinsic nuclear export signal.

3 endence of the previously identified Gag p10 nuclear export signal.

4 thus exposing the oligomerization-regulated nuclear export signal.

5 res the adapter protein Nmd3p to provide the nuclear export signal.

6 mino-acid sequence (HDA) that functions as a nuclear export signal.

7 tion signal and TB-RBP contains a functional nuclear export signal.

8 ns and a proline-rich, pre-LIM region with a nuclear export signal.

9 is receptor toward the cytoplasm through its nuclear export signal.

10 st of the regulatory domain and disrupts the nuclear export signal.

11 Like CTE, TBE is an active nuclear export signal.

12 of mRNA and a protein reporter containing a nuclear export signal.

13 smic retention signal, which also contains a nuclear export signal.

14 recognizing proteins bearing a leucine-rich nuclear export signal.

15 h leptomycin B and was dependent on an Mypt1 nuclear export signal.

16 ion signal, a nuclear retention domain and a nuclear export signal.

17 -terminal domain and the appearance of a new nuclear export signal.

18 A third element consists of a nuclear export signal.

19 reas the C terminus of B56epsilon contains a nuclear export signal.

20 ved tryptophan residues, with a leucine-rich nuclear export signal.

21 ng that SLBP on its own does not possess any nuclear export signals.

22 ossesses functional nuclear localization and nuclear export signals.

23 is correlates with loss of centrally located nuclear export signals.

24 s well as conserved nuclear localization and nuclear export signals.

25 ibility of the NFAT nuclear localization and nuclear export signals.

26 e and functional properties of characterized nuclear export signals.

27 and will serve as an important resource for nuclear export signals.

28 s both nuclear import and supraphysiological nuclear export signals.

29 e we show that APC contains highly conserved nuclear export signals 3' adjacent to the mutation clust

30 tion of domains within Rev exon 2 includes a nuclear export signal, a large central region required f

31 ive bipartite nuclear localization signal, a nuclear export signal, a leucine-isoleucine zipper, and

32 because deletion of the NLS or addition of a nuclear export signal abolished its HR-inducing ability.

33 contains overlapping nucleolar retention and nuclear export signals, allowing its accumulation in bot

34 We here show that addition of a nuclear export signal allows zinc finger chimeric enzyme

35 sphorylation, mouse Sry contains a defective nuclear export signal analogous to a variant human SRY a

36 ns two essential protein domains, a Leu-rich nuclear export signal and a heptad repeat domain that is

37 ty is independent of MDM2 but requires a p53 nuclear export signal and acetylation of multiple lysine

38 contains a CRM1-dependent, leucine-rich-like nuclear export signal and an adjacent nuclear localizati

39 ondoA-Mlx by functioning as a CRM1-dependent nuclear export signal and as a novel binding site for 14

40 BEX3 possess a conserved leucine-rich nuclear export signal and experimental data confirmed BE

41 nker segment of the chain, which carries the nuclear export signal and includes a region of high heli

42 CM2) at the C terminus of Chk1 function as a nuclear export signal and nuclear localization signal, r

43 in-7-69Q or -92Q, which removes the putative nuclear export signal and nuclear localization signals o

44 Ajuba contained a functional nuclear export signal and shuttled into the nucleus.

45 Pab1 contains a nonessential leucine-rich nuclear export signal and shuttles between the nucleus a

46 two stretches of serine residues within the nuclear export signal and the destruction box of Snail,

47 p204 contains a nuclear export signal and was partially translocated to

48 sphorylated region, however, is not itself a nuclear export signal and we identify a region elsewhere

49 nhibits export of proteins with leucine-rich nuclear export signals and mRNAs does not inhibit Npl3p

50 Thus, the C-terminal SIM lies adjacent to a nuclear export signal, and coordinated SUMO binding by t

51 in a leucine-rich stretch, which resembles a nuclear export signal, and could be inactivated by site-

52 ts the presence of a previously unidentified nuclear export signal, and the subcellular distribution

53 be found in the cytoplasm, it has no obvious nuclear export signal, and there is no direct evidence f

54 Uap56p interacts with Rae1p directly via its nuclear export signal, and this interaction is critical

55 ee carboxy-terminal LIM domains, a potential nuclear export signal, and three proline-rich motifs, on

56 smic localization of IRF-3 is dependent on a nuclear export signal, and we demonstrate IRF-3 recognit

57 by the addition of nuclear localization and nuclear export signals, and we found that nuclear locali

58 Rather than carrying a nuclear export signal as suggested previously, we found

59 but only HDAg-L contains a CRM1-independent nuclear export signal at its C terminus.

60 The translocation was mediated by a putative nuclear export signal at the C-terminal region of prohib

61 bipartite nuclear localization signal and a nuclear export signal at the far end of the amino termin

62 ch also contains the nucleolar retention and nuclear export signals, binds PAT1, whereas 149 residues

63 The MK2 residues 345-365, containing the nuclear export signal, block access to the p38alpha acti

64 Furthermore, deletion of the p53 nuclear export signal blocked its axonal distribution an

65 The C54 region contains no identifiable nuclear export signal but instead is required for biolog

66 Prp40 possesses two leucine-rich nuclear export signals, but little is known about the fu

67 Deleting or mutating the nuclear export signal caused SH2-B beta to lose its abil

68 on covering the Z-DNA binding domain and the nuclear export signal comprise the complete function of

69 ng site is highly conserved within the first nuclear export signal consensus sequence identified in S

70 a functional role by enhancing access to the nuclear export signal contained within its sequence.

71 olved in Crm1-mediated nuclear export of the nuclear export signal containing human immunodeficiency

72 a cellular karyopherin-beta that transports nuclear export signal-containing proteins from the nucle

73 (LMB) treatment inhibited nuclear export of nuclear export signal-containing proteins.

74 on results in a block in nuclear export of a nuclear export signal-containing reporter protein.

75 sults suggest a model wherein Rev-associated nuclear export signals cooperate to regulate the number

76 that blocked myoblast fusion, inhibited the nuclear export signal-dependent translocation of p204 to

77 domains or in the putative activation domain-nuclear export signal displayed a dominant negative phen

78 The second nuclear export signal epitope is a basic surface on the

79 ultipartite recognition of individually weak nuclear export signal epitopes may be common to CRM1 sub

80 as both a nuclear localization signal and a nuclear export signal, even though only one protein, the

81 port via the importin receptor pathway and a nuclear export signal-facilitated nuclear export through

82 ese results show that TAP can complement Rev nuclear export signal function and redirect the export o

83 o dissect M9 nuclear localization signal and nuclear export signal function.

84 the extranuclear cytoplasm by addition of a nuclear export signal (GPKAnes) promotes SGN survival as

85 Functional nuclear localization and nuclear export signals have been mapped within Axin.

86 ucleus, as well as a CRM1/exportin-dependent nuclear export signal; however, the NLS and exact pathwa

87 o a putative nuclear localization signal and nuclear export signals identified in the sea urchin KAP

88 from the nucleus during interphase using the nuclear export signal in Alp14 but is accumulated in the

89 We also identified a key nuclear export signal in beta1-chimaerin that is absent

90 The nuclear export signal in BRCA1 has been described as con

91 entification of an N-terminal Xpo1-dependent nuclear export signal in Dbp5, in addition to other sepa

92 We report evidence for a novel nuclear export signal in HAP95 and showed that the domai

93 Here we show that ATF2 possesses a nuclear export signal in its leucine zipper region and t

94 i) and (iii) depended on the presence of the nuclear export signal in p204.

95 This exposes a nuclear export signal in p53, triggering Crm1-dependent

96 We found that removal of a highly conserved nuclear export signal in the C terminus of AID causes ac

97 the N terminus of the protein and a putative nuclear export signal in the C terminus.

98 bonded structure has been argued to mask the nuclear export signal in the C-CRD that would otherwise

99 However, the sequence corresponding to the nuclear export signal in the other family members was no

100 localization signals in XLG2 and XLG3 and a nuclear export signal in XLG3, which may facilitate intr

101 this study we initially set out to identify nuclear export signals in mTOR.

102 ed to YFP and either nuclear localization or nuclear export signals in N benthamiana showed that cell

103 on and mutation analyses revealed functional nuclear export signals in the amino terminus of TTP and

104 Mutation of a putative nuclear-export signal in Rad24 impairs the nuclear exclu

105 This type of leucine-rich nuclear export signal interacts with the nuclear export

106 The APOBEC1 nuclear export signal is involved in the export of ACF a

107 We conclude that the MA nuclear export signal is required to counteract the MA n

108 ed to the cytoplasm employing a heterologous nuclear export signal, it is expressed at very low level

109 re-LIM domain of Ajuba, including a putative nuclear export signal, led to an accumulation of the LIM

110 exing with MCM5 in a manner dependent upon a nuclear-export signal-like domain, blocking the recruitm

111 n of Mad4 was determined by a CRM1-dependent nuclear export signal located near the amino terminus.

112 through the recognition of the leucine-rich nuclear export signal (LR-NES).

113 Mutation of the nuclear export signal-mask in Drosophila embryos prevent

114 ation signal (cNLS)-mediated protein import, nuclear export signal-mediated protein export, and messe

115 strongly dependent on the Ran/RCC1 system as nuclear export signal-mediated protein export, U-snRNA,

116 edly diminished budding, suggesting that the nuclear export signal might reside within p10.

117 Using an M mutant with a defective nuclear export signal (MNESmut), however, we revealed th

118 export with leptomycin B or mutation of the nuclear export signal motif of Beclin 1 results in predo

119 Beclin 1 contains a leucine-rich nuclear export signal motif raising the possibility that

120 A nuclear export signal motif within the regulatory domain

121 idues 134, 135, and 136 are located within a nuclear export signal motif.

122 K-2 is regulated by nuclear localization and nuclear export signal motifs.

123 In this study we identify a canonical nuclear export signal (NES) ((537)LKKQLSTLYL(546)) locat

124 and mutagenesis analyses, we have identified nuclear export signal (NES) (19)LSLRELAI(26) of p17.

125 Scd5p-DeltaCT lacking the 9R region and its nuclear export signal (NES) accumulates in the nucleus,

126 We also identify a Crm1-dependent nuclear export signal (NES) adjacent to the Mcm3 NLS.

127 se localization is mediated by an N-terminal nuclear export signal (NES) and a C-terminal nuclear loc

128 MD3) contains a CRM-1-dependent leucine-rich nuclear export signal (NES) and a complex, dispersed nuc

129 These domains resemble, and function as, a nuclear export signal (NES) and a pattern 4 nuclear loca

130 ar transporter of ERK; experiments with hBVR nuclear export signal (NES) and nuclear localization sig

131 p27(KIP1) lacks a nuclear export signal (NES) and requires an adaptor for

132 In addition, we define the Crz1p nuclear export signal (NES) and show that it interacts w

133 ex3 association with mitochondria required a nuclear export signal (NES) and the C-terminal four amin

134 nsport signals in Exd, including a divergent nuclear export signal (NES) and two nuclear localization

135 mosome region maintenance 1 (CRM1)-dependent nuclear export signal (NES) at the AID C terminus is nec

136 Furthermore, we identified a nuclear export signal (NES) at the N terminus (AAs 176-1

137 ed motifs revealed that VHS-RNase contains a nuclear export signal (NES) but not a nuclear localizati

138 We identified a novel CRM1-dependent nuclear export signal (NES) comprising 13 amino acids (K

139 Subsequent studies identified three nuclear export signal (NES) elements.

140 ofacial development in the zebrafish, that a Nuclear Export Signal (NES) fusion protein (GFPNESWdr68)

141 ized two distinct nuclear export activities, nuclear export signal (NES) I and NES II, within the reg

142 ear exclusion of AHNAK is mediated through a nuclear export signal (NES) in a manner that depends on

143 We first reported a CRM1-dependent nuclear export signal (NES) in E1A that is conserved in

144 port of ALX, which depends on a leucine-rich nuclear export signal (NES) in its carboxyl segment and

145 udies unveiled that presence of a functional nuclear export signal (NES) in mouse PDK-1 located at am

146 ependent export of PKI requires a functional nuclear export signal (NES) in PKI and involves formatio

147 We identified a previously unknown nuclear export signal (NES) in the amino terminus of p53

148 3 nuclear export by exposing or activating a nuclear export signal (NES) in the C terminus of p53.

149 In the active oxidized form, a nuclear export signal (NES) in the carboxy-terminal cyst

150 We have identified a nuclear export signal (NES) in the highly conserved repe

151 eletion and mutagenesis studies identified a nuclear export signal (NES) in the intervening region of

152 lization signals in the basic region and one nuclear export signal (NES) in the leucine zipper domain

153 the action of a leptomycin B (LMB)-dependent nuclear export signal (NES) in the p10 domain.

154 calization signal (NLS) and a CRM1-dependent nuclear export signal (NES) in the SUMO protease SENP2.

155 Both contain a nuclear export signal (NES) in their C-terminal domain a

156 ased on its ability to interact with the Rev nuclear export signal (NES) in yeast two-hybrid assays.

157 The consensus pattern of Nuclear Export Signal (NES) is a short sequence motif th

158 The AID nuclear export signal (NES) is found at the carboxyl ter

159 Similarly to the NLS, the nuclear export signal (NES) is not apparent in the prima

160 The leucine-rich nuclear export signal (NES) is the only known class of t

161 nit dissociation required for exposing p53's nuclear export signal (NES) is unnecessary for p53 nucle

162 The leucine-rich nuclear export signal (NES) is used to shuttle large cel

163 nstrated that PCNA relocalization involved a nuclear export signal (NES) located from Ile-11 to Ile-2

164 analysis identified a putative leucine-rich nuclear export signal (NES) motif that overlaps with the

165 Nuclear export signal (NES) motifs function as essential

166 , we identified three novel CRM1-independent nuclear export signal (NES) motifs in the ligand-binding

167 a fide nuclear localization signal (NLS) and nuclear export signal (NES) motifs, and constitutively s

168 A leucine-rich nuclear export signal (NES) near the C terminus of RanBP

169 in for nuclear export and a receptor for the nuclear export signal (NES) of Daxx.

170 terminal region of prohibitin; fusion of the nuclear export signal (NES) of prohibitin to green fluor

171 ues 177 to 198 of BR1 contain a leucine-rich nuclear export signal (NES) of the type found in the Rev

172 amino acid substitutions in the leucine-rich nuclear export signal (NES) sequence (residues 90-100) a

173 lear localizing signal (NLS) sequences and a nuclear export signal (NES) sequence whose functions wer

174 n their N termini an MAPK-docking site and a nuclear export signal (NES) sequence, which are known to

175 w encode proteins with putative leucine-rich nuclear export signal (NES) sequences that fit the conse

176 ce that displays similarities to a canonical nuclear export signal (NES) that also binds CRM1/exporti

177 inal domain of Ssb1p contains a leucine-rich nuclear export signal (NES) that is necessary and suffic

178 Here, we describe for Tbx5 a nuclear export signal (NES) that is recognized by the CR

179 Here, we show that CALM contains a nuclear export signal (NES) that mediates cytoplasmic lo

180 Lysine 151 is adjacent to a nuclear export signal (NES) that resembles a consensus N

181 xclusively by nuclear exclusion, driven by a nuclear export signal (NES) that restricts GEN1 actions

182 in indicate that Tax contains a leucine-rich nuclear export signal (NES) that, when fused to green fl

183 is end, we fused a prototypical leucine-rich nuclear export signal (NES) to GFP as a cargo model and

184 A nuclear export signal (NES) was also recognized in p73s

185 A nuclear export signal (NES) was characterized in the C t

186 A functional nuclear export signal (NES) was identified in the C term

187 A nuclear export signal (NES) was identified within the am

188 In addition, a putative nuclear export signal (NES) was identified, and mutation

189 Additionally, a novel nuclear export signal (NES) was identified, which includ

190 A nuclear export signal (NES) was previously identified wi

191 nally, we identify a cryptic CRM-1-dependent nuclear export signal (NES) within ZIC3, and identify a

192 or Msn5 to Nmd3, lacking its Crm1-dependent nuclear export signal (NES), all functioned in export.

193 Nuclear receptors lack a leucine-rich nuclear export signal (NES), and export is insensitive t

194 rtite nuclear localization signal (bNLS) and nuclear export signal (NES), as well as to a fluorescent

195 all thirteen residues is required to mask a nuclear export signal (NES), cause full exposure of a nu

196 -3, which had been proposed to function as a nuclear export signal (NES), instead functions globally

197 I1 is a nuclear protein and harbors a masked nuclear export signal (NES), the transdominant negative

198 The nuclear export signal (NES)-binding groove of CRM1 is ab

199 Glu571 of CRM1 is located in its nuclear export signal (NES)-binding groove, suggesting t

200 We compiled >200 nuclear export signal (NES)-containing CRM1 cargoes in a

201 nts of the pathway that exports leucine-rich nuclear export signal (NES)-containing proteins from the

202 ild-type (wt) SOD1 exposes a normally buried nuclear export signal (NES)-like sequence.

203 nds on the adapter protein Nmd3 to provide a nuclear export signal (NES).

204 l nuclear localization signal and C-terminal nuclear export signal (NES).

205 4 and 192 that functions as a CRM1-dependent nuclear export signal (NES).

206 nd contains a single functional leucine-rich nuclear export signal (NES).

207 bserved, and this suggests the presence of a nuclear export signal (NES).

208 r import signals and an exportin-1-dependent nuclear export signal (NES).

209 activity of Rev's prototypical leucine-rich nuclear export signal (NES).

210 functional regions, including a leucine-rich nuclear export signal (NES).

211 Thus, it presumably contains a nuclear export signal (NES).

212 if, whereas the C-terminal region contains a nuclear export signal (NES).

213 to the NLS, Smad1 also contains a functional nuclear export signal (NES).

214 of STAT1 were found to encode a leucine-rich nuclear export signal (NES).

215 xported from nuclei due to the activity of a nuclear export signal (NES).

216 nce homologous to the recently characterized nuclear export signal (NES).

217 toplasm during infection using an N-terminal nuclear export signal (NES).

218 its DNA binding domain and two leucine-rich nuclear export signals (NES) in its ligand binding domai

219 LS) located at its C-terminal domain and two nuclear export signals (NES) located in its N- and C-ter

220 uR-pp32 and APRIL-which contain leucine-rich nuclear export signals (NES) recognized by the export re

221 y cytokines, we examined their sequences for nuclear export signals (NES).

222 ation signal (NLS) in the basic region and a nuclear exporting signal (NES) in the leucine zipper dom

223 Moreover, induced expression of the nuclear exporting signal (NES)-fused form of Rb caused d

224 localization (NLS1 to -3) and two potential nuclear export signals (NES1 and -2) within MSH3.

225 s have identified a leptomycin B-insensitive nuclear export signal (NESAR) in the ligand-binding doma

226 Classical nuclear export signals (NESs) are short cognate peptides

227 However, neither the nuclear export signals (NESs) for the ribosomal subunits

228 r export receptor CRM1 binds highly variable nuclear export signals (NESs) in hundreds of different c

229 r export of proteins containing leucine-rich nuclear export signals (NESs) is mediated by the NES rec

230 is mediated by two intrinsic, leucine-rich, nuclear export signals (NESs) located near the amino ter

231 rt of diverse cargos containing leucine-rich nuclear export signals (NESs) through complex formation

232 localization signals (NLSs), as well as the nuclear export signals (NESs), in RPW8.2 is critical for

233 eds of proteins through recognition of their nuclear export signals (NESs), which are highly variable

234 everal consensus CRM1 (exportin 1)-dependent nuclear export signals (NESs).

235 no acid region with homology to leucine-rich nuclear export signals (NESs).

236 factor for proteins containing leucine-rich nuclear export signals (NESs).

237 ithin sequences homologous to Crm1-dependent nuclear export signals (NESs).

238 lear localization signals, NLSs) and export (nuclear export signals, NESs).

239 ophagy (Atg3) or recombinant NIC tagged to a nuclear export signal (NIC-NES), restored autophagy and

240 Although MA lacks the canonical leucine-rich nuclear export signal, nuclear export is mediated throug

241 Disruption of the classic nuclear export signal of 14-3-3sigma inactivated its abi

242 The nuclear export signal of AR (NES(AR)) has an important r

243 this approach, we were able to identify the nuclear export signal of BLV Rex.

244 Deletion of the nuclear export signal of CHK1 led to its hyperphosphoryl

245 In fact, mutational studies targeting the nuclear export signal of ChREBP also identified a distin

246 tions of the nuclear localization signal and nuclear export signal of MyoD restrict ubiquitination an

247 ocked gene induction, demonstrating that the nuclear export signal of PKI can override a strong nucle

248 ormation and reveal how the binding site for nuclear export signals of cargoes is modulated by differ

249 des conforming to the canonical leucine-rich nuclear export signal, of which 3 were found by reporter

250 catalytic mechanism involving the masking of nuclear export signals on NF-AT targeted by Crm1.

251 Mutation of a nuclear export signal or treatment with leptomycin B cau

252 endent phosphorylation of Stu2 adjacent to a nuclear export signal prevents nuclear accumulation of S

253 iction to cytoplasm, through the fusion with nuclear export signal, prevents these effects (in each c

254 tment with leptomycin B, an inhibitor of the nuclear export signal receptor, dramatically enhanced bo

255 One subdomain is an Exportin-dependent nuclear export signal requiring three conserved hydropho

256 the cytoplasm with nuclear localization and nuclear export signals, respectively, showed concordance

257 alization of Klp67A to the cytoplasm using a nuclear export signal resulted in the disassembly of the

258 e-and find that the RcRE resembles the HIV-1 nuclear export signal, RRE.

259 er, this carboxyl-portion of p100 contains a nuclear export signal(s), which is required for effectiv

260 An SmgGDS nuclear export signal sequence that we identified promot

261 he septum to the nucleus, suggesting it is a nuclear export signal sequence.

262 mouse lines in which nuclear localization or nuclear export signal sequences have been placed N-termi

263 Systematic mutation of putative nuclear export signal sequences in APC-25 decreases APC-

264 m and nucleus due to the presence of NLS and nuclear export signal sequences in the CIITA protein.

265 ns canonical nuclear localization signal and nuclear export signal sequences necessary for its locali

266 ral possible nuclear localization signal and nuclear export signal sequences.

267 in 1) protein is a receptor for leucine-rich nuclear export signal sequences.

268 Mutation of the nuclear export signal site in the Rev portion had no eff

269 Furthermore, we found that deletion of the nuclear export signal strongly suppressed toxicity, sugg

270 d that promoting AR export with an exogenous nuclear export signal substantially reduces its aggregat

271 ve nuclear localization (TDP-43-DeltaNLS) or nuclear export signals (TDP-43-DeltaNES).

272 NXF3 contains a novel Crm1-dependent nuclear export signal that compensates in cis for the lo

273 Unexpectedly, TPP1 contains a functional nuclear export signal that directly controls the amount

274 red cells indicates that Prospero contains a nuclear export signal that is masked by the Prospero dom

275 pter protein Nmd3p to provide a leucine-rich nuclear export signal that is recognized by the export r

276 1 has a leptomycin B-sensitive leucine-rich nuclear export signal that is required for its autophagy

277 on (61-74 amino acids) was identified as the nuclear export signal that participated in CRM1-dependen

278 Mutations within an HIV Rev-like nuclear export signal that resembles a nuclear receptor

279 CPEB2, -3, and -4 have conserved nuclear export signals that are not present in CPEB.

280 tion signal; in the absence of p27, two weak nuclear export signals that bind CRM1 cause it to shuttl

281 x has defined nuclear localization (NLS) and nuclear export signals that enable shuttling between the

282 , Rad24 appears to function as an attachable nuclear-export signal that enhances the nuclear export o

283 ransfected cells and uses a highly conserved nuclear export signal to exit nuclei.

284 rokaryon analysis, we have localized the Vpr nuclear export signal to the second leucine-rich helix,

285 p204 from which the nuclear export signal was deleted was not translocated,

286 A construct in which a nuclear export signal was fused to the N terminus of p11

287 Additionally, a nuclear export signal was identified in the N terminus o

288 A truncated form of RanBP1 (lacking its nuclear export signal) was able to complement the yrb1(t

289 Nuclear localization and nuclear export signals were genetically engineered into

290 two leucine-rich sequences similar to known nuclear export signals were not required for Mig1 export

291 ral portion of the HDAC3 protein possesses a nuclear export signal, whereas the C-terminal part of HD

292 hat CD151 is a critical novel host factor of nuclear export signaling whereby the IAV nuclear export

293 Although CHP1 contains nuclear export signals, whether its nuclear and cytoplas

294 ults in extra C-terminal residues encoding a nuclear export signal, which causes NPM1c+ to be localiz

295 It unmasks the nuclear export signal, which is part of the second C-ter

296 localization signal (NLS) and a leucine-rich nuclear export signal, which regulate Nrf2 shuttling in

297 within the C terminus of REKLES contain its nuclear export signal, whose regulation is primarily res

298 be inhibited with leptomycin B, indicating a nuclear export signal within STAT2 is recognized by the

299 Additionally, the presence of a nuclear export signal within Tax and its active secretio

300 contingent upon the function of an intrinsic nuclear export signal within the carboxyl terminus of ST