ライフサイエンスコーパス: nuclear export signal

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

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

3 thus exposing the oligomerization-regulated nuclear export signal.

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

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

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

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

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

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

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

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

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

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

14 ors both a nuclear localization signal and a 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 the nuclear export receptor CRM1 or discrete nuclear export signal.

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

23 ossesses functional nuclear localization and nuclear export signals.

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

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

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

27 e and functional properties of characterized nuclear export signals.

28 arrying heterologous nuclear localization or nuclear export signals.

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

30 s both nuclear import and supraphysiological nuclear export signals.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

65 A mutant PKI lacking the nuclear export signal blocked gene induction but not nuc

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

86 class of transportin-specific NLSs that lack nuclear export signal function.

87 ires two proteins with putative leucine-rich nuclear export signals: Gle1p, Mex67p, and several addit

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

115 A mutation that disrupts the MA nuclear export signal (MA-M4) mislocalizes Pr55 and geno

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

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

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

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

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

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

122 A nuclear export signal motif within the regulatory domain

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

149 3 nuclear export by exposing or activating a nuclear export signal (NES) in the C terminus of p53.

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

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

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

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

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

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

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

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

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 mediated by a highly conserved leucine-rich nuclear export signal (NES) located in its tetramerizati

165 res a previously unidentified CRM1-dependent nuclear export signal (NES) located within the N-termina

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

197 -3, which had been proposed to function as a nuclear export signal (NES), instead functions globally

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

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

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

204 activity of Rev's prototypical leucine-rich 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 functional regions, including a leucine-rich nuclear export signal (NES).

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

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

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

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

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

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

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

217 nds on the adapter protein Nmd3 to provide a 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 s have identified a leptomycin B-insensitive nuclear export signal (NESAR) in the ligand-binding doma

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

250 B and thus is distinct from the leucine-rich nuclear export signal pathway mediated by CRM1.

251 Mutation of a putative nuclear export signal present in the AHR results in the

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

259 An SmgGDS nuclear export signal sequence that we identified promot

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

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

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

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

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

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

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

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

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

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

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

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

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

273 Mig1 contains a new nuclear export signal that is phosphorylated by Snf1 upo

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

275 1 has a leptomycin B-sensitive leucine-rich nuclear export signal that is required for its autophagy

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

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

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

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

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

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

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

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

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

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

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

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

288 Nuclear localization and nuclear export signals were genetically engineered into

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

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

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

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

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

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

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

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

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

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

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

300 release from GKRP, is due to a leucine-rich nuclear export signal within the protein ((300)ELVRLVLLK