ライフサイエンスコーパス: nucleocytoplasmic transport

1 TPase Ran and the importin proteins regulate nucleocytoplasmic transport.

2 G domain nucleoporins, which are crucial for nucleocytoplasmic transport.

3 nonsense-mediated mRNA decay pathway, and to nucleocytoplasmic transport.

4 sphorylation site which is essential for its nucleocytoplasmic transport.

5 ycine-rich nucleoporins (FG-Nups) to control nucleocytoplasmic transport.

6 e activity of Ran-GTPase, a key regulator of nucleocytoplasmic transport.

7 ndant GTPase responsible for the majority of nucleocytoplasmic transport.

8 Nuclear pore complexes (NPCs) facilitate nucleocytoplasmic transport.

9 of integral membrane proteins and/or during nucleocytoplasmic transport.

10 mplexes in the two extracts, consistent with nucleocytoplasmic transport.

11 vergence may represent a unique mechanism of nucleocytoplasmic transport.

12 o be involved in signal transduction through nucleocytoplasmic transport.

13 sport, DNA repair, chromatin remodeling, and nucleocytoplasmic transport.

14 esting an important role of the nucleolus in nucleocytoplasmic transport.

15 in is necessary and sufficient for mediating nucleocytoplasmic transport.

16 rotein assemblies that are the sole sites of nucleocytoplasmic transport.

17 acids 47-229, is also sufficient to inhibit nucleocytoplasmic transport.

18 The Ran GTPase plays a central role in nucleocytoplasmic transport.

19 on between the SUMO modification pathway and nucleocytoplasmic transport.

20 within the nucleus to inhibit bi-directional nucleocytoplasmic transport.

21 0 nucleoporins that cooperatively facilitate nucleocytoplasmic transport.

22 ellular function is the proper regulation of nucleocytoplasmic transport.

23 a small signaling GTPase that is involved in nucleocytoplasmic transport.

24 tion between the import and export phases of nucleocytoplasmic transport.

25 ction may require regulated, CRM1-dependent, nucleocytoplasmic transport.

26 n NPC-associated factor that participates in nucleocytoplasmic transport.

27 for a Brownian affinity gating mechanism for nucleocytoplasmic transport.

28 excitotoxicity, disease-associated RBPs, and nucleocytoplasmic transport.

29 ects a more global process for regulation of nucleocytoplasmic transport.

30 mplex (NPC) are fundamental to understanding nucleocytoplasmic transport.

31 oly-GR and poly-PR, has been associated with nucleocytoplasmic transport.

32 critical for understanding the mechanism of nucleocytoplasmic transport.

33 small ras-like GTPase involved in regulating nucleocytoplasmic transport.

34 ndergo degradation in the nucleus instead of nucleocytoplasmic transport.

35 d RNA sequences under conditions of impaired nucleocytoplasmic transport.

36 ulation of unspliced BDV transcripts through nucleocytoplasmic transport.

37 TPase Ran/Gsp1p, which is essential for most nucleocytoplasmic transport.

38 AN, a region that is supposed to function in nucleocytoplasmic transport.

39 125 MDa multiprotein assembly that mediates nucleocytoplasmic transport.

40 ted terminal differentiation and/or aberrant nucleocytoplasmic transport.

41 localization in notochordal cells, affecting nucleocytoplasmic transport.

42 or analyzing the effects of pore dilation on nucleocytoplasmic transport.

43 PCs) are the sole bidirectional gateways for nucleocytoplasmic transport.

44 GR and poly-PR do not directly impede active nucleocytoplasmic transport.

45 atic treatment by exploring ways to maintain nucleocytoplasmic transport.

46 PGC-1alpha in non-homologous end-joining and nucleocytoplasmic transport.

47 ation coincides with striking alterations in nucleocytoplasmic transport.

48 zation and aggregation of NUPs and defective nucleocytoplasmic transport.

49 TG (RAN) translation proteins also disrupted nucleocytoplasmic transport.

50 hting the importance of the shape effects in nucleocytoplasmic transport.

51 ) are 110-megadalton assemblies that mediate nucleocytoplasmic transport.

52 ficking and transport vesicle formation, and nucleocytoplasmic transport.

53 lex (NPC) filaments and is a docking site in nucleocytoplasmic transport.

54 nstitutes the sole gateway for bidirectional nucleocytoplasmic transport.

55 oncentration in the nucleus is important for nucleocytoplasmic transport.

56 Nups in the nuclear pore, and mechanisms of nucleocytoplasmic transport.

57 ptors (Karyopherins (Kaps)) that orchestrate nucleocytoplasmic transport.

58 mbers (karyopherins) mediate the majority of nucleocytoplasmic transport.

59 t, consistent with its essential function in nucleocytoplasmic transport.

60 ility of Cic by controlling the rates of its nucleocytoplasmic transport.

61 was originally identified as a regulator of nucleocytoplasmic transport [1] and subsequently found t

62 is sufficient to decrease DPR levels, rescue nucleocytoplasmic transport abnormalities, and improve s

63 The nucleocytoplasmic transport activity was not dependent o

64 esponse to changes in membrane synthesis and nucleocytoplasmic transport, altering nuclear size.

65 studies offered clues that mHTT may disrupt nucleocytoplasmic transport and a mutation of an NUP can

66 nisms that remain poorly defined, defects in nucleocytoplasmic transport and accumulations of specifi

67 occupancy of multiple RPEL motifs regulates nucleocytoplasmic transport and activity of MAL.

68 entify polyglutamine-dependent inhibition of nucleocytoplasmic transport and alteration of nuclear in

69 In addition, LKB1 nucleocytoplasmic transport and AMPK activation in respo

70 utant that is used extensively in studies of nucleocytoplasmic transport and cell-cycle progression.

71 nuclear pore complex (NPC) has dual roles in nucleocytoplasmic transport and chromatin organization.

72 uclear pore complex (NPC) is responsible for nucleocytoplasmic transport and constitutes a hub for co

73 lts confirm that CAN plays a crucial role in nucleocytoplasmic transport and imply an essential role

74 MO E3 ligase activity that functions in both nucleocytoplasmic transport and mitosis.

75 oughout the cell cycle, including interphase nucleocytoplasmic transport and mitotic spindle assembly

76 Arginine methylation can affect both nucleocytoplasmic transport and protein-protein interact

77 To further explore the role of Kap123p in nucleocytoplasmic transport and ribosome biogenesis, we

78 ntial for many cellular processes, including nucleocytoplasmic transport and spindle assembly.

79 ranslational regulation of p53 comprises its nucleocytoplasmic transport and subsequent proteasomal d

80 lays a cell type-specific role in regulating nucleocytoplasmic transport and that this function is es

81 like U1 and U5 RNAs in their bi-directional nucleocytoplasmic transport and their 5'-cap hypermethyl

82 infection, E1B-55K is required for efficient nucleocytoplasmic transport and translation of late vira

83 te phase, E1B-55K modulates the preferential nucleocytoplasmic transport and translation of the late

84 are down-regulated during stress, including nucleocytoplasmic transport and translation, as well as

85 Ran, which provides spatial information for nucleocytoplasmic transport and various mitotic processe

86 p62 at the nuclear envelope (probably during nucleocytoplasmic transport) and also in nucleoli, clear

87 romised nuclear envelope integrity, impaired nucleocytoplasmic transport, and accumulation of DNA dou

88 tion of host gene expression, disablement of nucleocytoplasmic transport, and disruption of the host

89 ical for cellular processes such as mitosis, nucleocytoplasmic transport, and nuclear envelope format

90 ct role of the disorder within FG repeats in nucleocytoplasmic transport, and resolves the apparent c

91 he nuclear pore complexes (NPCs) that enable nucleocytoplasmic transport, and the spindle pole bodies

92 latory elements (INS) that impair stability, nucleocytoplasmic transport, and translation by unknown

93 c nuclear permeability barrier and selective nucleocytoplasmic transport are maintained by nuclear po

94 virus (RSV) Gag protein undergoes transient nucleocytoplasmic transport as an intrinsic step in viru

95 ycine (FG) repeats play an important role in nucleocytoplasmic transport as they bind to transport re

96 Here we demonstrate that nucleocytoplasmic transport at the membrane domain surro

97 position of NE-localized proteins along the nucleocytoplasmic transport axis.

98 The RanGTPase acts as a master regulator of nucleocytoplasmic transport by controlling assembly and

99 n et al. provide evidence for the control of nucleocytoplasmic transport by protein kinase signaling

100 Hence, the direction and velocity of nucleocytoplasmic transport can be determined simultaneo

101 We have examined whether signal-mediated nucleocytoplasmic transport can be regulated by phosphor

102 Thus, to overcome the limited capacity for nucleocytoplasmic transport, cells requiring increased n

103 and Nup107, thereby provoking inhibition of nucleocytoplasmic transport, clearance of nuclear TDP-43

104 We suggest that defects in the nucleocytoplasmic transport components may be a general

105 dependent on a tRNA structure necessary for nucleocytoplasmic transport, consistent with primer sele

106 Defective nucleocytoplasmic transport contributes to C9-ALS/FTD, b

107 tain this conformation throughout the entire nucleocytoplasmic transport cycle.

108 zymes in ubiquitination, carrier proteins in nucleocytoplasmic transport, cyclin-dependent kinase in

109 n (RanGAP) at the nuclear pore, resulting in nucleocytoplasmic transport deficit and accumulation of

110 ce in the eye have specific requirements for nucleocytoplasmic transport, despite involving processes

111 ion, whereas inhibitors of transcription and nucleocytoplasmic transport did not.

112 -FTD spectrum disorder, including autophagy, nucleocytoplasmic transport, DNA damage repair, pre-mRNA

113 We propose that L inhibits nucleocytoplasmic transport during infection by disrupti

114 To study nucleocytoplasmic transport during multicellular develop

115 ever little is known about the regulation of nucleocytoplasmic transport during the formation of myof

116 ta and ste5ts), indicating that reduction in nucleocytoplasmic transport enhances mating proficiency.

117 nt signalling pathways rely on bidirectional nucleocytoplasmic transport events through the nuclear p

118 ll GTPase Ran is essential for virtually all nucleocytoplasmic transport events.

119 uction of securin by APC is regulated by the nucleocytoplasmic transport factors Rae1 and Nup98.

120 ave been proposed to mediate the movement of nucleocytoplasmic transport factors.

121 of numerous biological processes, including nucleocytoplasmic transport, genomic stability, and gene

122 rtial sequestration of factors essential for nucleocytoplasmic transport (Gle1 and RanGAP1), and intr

123 The separate components of nucleocytoplasmic transport have been well characterized

124 n, suggesting a potential link between DPRs, nucleocytoplasmic transport impairments and TDP-43 patho

125 may lead to unique insights into the role of nucleocytoplasmic transport in adrenal function and neur

126 and serves as the sole conduit to facilitate nucleocytoplasmic transport in eukaryotes.

127 s) are key cellular transporter that control nucleocytoplasmic transport in eukaryotic cells, but its

128 cts in the nuclear pore complex and impaired nucleocytoplasmic transport in Huntington's disease (HD)

129 Therefore, we evaluated the NPC and nucleocytoplasmic transport in multiple models of HD, in

130 s provide evidence for an important role for nucleocytoplasmic transport in the pathogenic mechanism

131 Virtually nothing is known about nucleocytoplasmic transport in these parasites (phylum A

132 th mutations in many other genes involved in nucleocytoplasmic transport, including SRP1 (alpha-impor

133 (Phe) mutants that retained the capacity for nucleocytoplasmic transport, indicative of overall intac

134 tment of heterozygous ahctf1 larvae with the nucleocytoplasmic transport inhibitor, Selinexor, comple

135 sses of mRNA metabolism, including splicing, nucleocytoplasmic transport,initiation of translation, a

136 Nucleocytoplasmic transport involves assembly and moveme

137 Interference with nucleocytoplasmic transport is a strategy employed by ce

138 Dysfunction in nucleocytoplasmic transport is also an emerging theme in

139 permeability, selectivity, and the speed of nucleocytoplasmic transport is an assembly of natively u

140 p53 nucleocytoplasmic transport is carried out by a bipartit

141 Receptor-mediated nucleocytoplasmic transport is dependent on the GTPase R

142 We conclude that the directionality of nucleocytoplasmic transport is determined mainly by the

143 stablished general background information on nucleocytoplasmic transport is discussed.

144 In animal models of HD, nucleocytoplasmic transport is disrupted and its restora

145 Deficient nucleocytoplasmic transport is emerging as a pathogenic

146 Altered nucleocytoplasmic transport is emerging as a prominent p

147 Nucleocytoplasmic transport is facilitated by nuclear po

148 Disruption of nucleocytoplasmic transport is increasingly implicated i

149 Nucleocytoplasmic transport is mediated by nuclear pore

150 Nucleocytoplasmic transport is mediated by nuclear pore

151 Nucleocytoplasmic transport is mediated by the interacti

152 Nucleocytoplasmic transport is mediated by the interplay

153 s, and is changed only if gene expression or nucleocytoplasmic transport is modulated.

154 Nucleocytoplasmic transport is sustained by karyopherins

155 Nucleocytoplasmic transport is tightly regulated by the

156 the functional role of this modification in nucleocytoplasmic transport is unclear.

157 igate the impact of each DPR on the nucleus, nucleocytoplasmic transport machinery and TDP-43 localis

158 asm, it may mediate a connection between the nucleocytoplasmic transport machinery and the endosomal

159 To further our understanding of how the nucleocytoplasmic transport machinery interfaces with it

160 As RCC1 is an important component of the nucleocytoplasmic transport machinery, we find that dRCC

161 concomitantly can interact with the soluble nucleocytoplasmic transport machinery.

162 exportins represent an essential part of the nucleocytoplasmic transport machinery.

163 rovides several binding sites for the mobile nucleocytoplasmic transport machinery.

164 rovides a multitude of binding sites for the nucleocytoplasmic transport machinery.

165 common mechanism for SUMOylation to regulate nucleocytoplasmic transport may lie in the interplay bet

166 e propose that RB inactivation, via aberrant nucleocytoplasmic transport, may disrupt normal cell dif

167 the NPC, taking a central role in the vital nucleocytoplasmic transport mechanism.

168 g key insights into evolution, assembly, and nucleocytoplasmic transport mechanisms.

169 gradient of RanGTP on chromatin that directs nucleocytoplasmic transport, mitotic spindle assembly an

170 ll GTPase Ran is best known for its roles in nucleocytoplasmic transport, mitotic spindle assembly, a

171 ifunctional small GTPase that is involved in nucleocytoplasmic transport, mitotic spindle assembly, a

172 y of GTPases, is best known for its roles in nucleocytoplasmic transport, mitotic spindle fiber assem

173 n guanosine triphosphatase (GTPase) controls nucleocytoplasmic transport, mitotic spindle formation,

174 d23 is localized in the cytosol in rna1-1, a nucleocytoplasmic transport mutant, and it forms reduced

175 disrupted neurodevelopment, and compromised nucleocytoplasmic transport (NCT) functions.

176 Disrupted nucleocytoplasmic transport (NCT) has been implicated in

177 Defective nucleocytoplasmic transport (NCT) has emerged as a contr

178 Although defects in nucleocytoplasmic transport (NCT) is reported ALS and ot

179 Although defects in nucleocytoplasmic transport (NCT) may be central to the

180 This necessitates nucleocytoplasmic transport (NCT) to bypass nuclear pore

181 The NUP107 complex is important for nucleocytoplasmic transport, nuclear envelope assembly,

182 nslation; however, the mechanism(s) by which nucleocytoplasmic transport occurs and how Dbp5 specific

183 Nucleocytoplasmic transport occurs exclusively through n

184 Nucleocytoplasmic transport occurs through gigantic prot

185 Nucleocytoplasmic transport occurs through nuclear pore

186 To understand how the vital process of nucleocytoplasmic transport occurs, the contribution of

187 ite mutant TA accumulation in NE structures, nucleocytoplasmic transport of a reporter protein was un

188 Nuclear eIF4E functions in nucleocytoplasmic transport of a subset of transcripts i

189 the canonical Wnt pathway by regulating the nucleocytoplasmic transport of beta-catenin rather than

190 ant function of small GTPases in the cell is nucleocytoplasmic transport of both proteins and RNA.

191 Retroviral replication requires the nucleocytoplasmic transport of both spliced and unsplice

192 Dynamic nucleocytoplasmic transport of E-M factors regulates cel

193 Therefore, we characterized the nucleocytoplasmic transport of each of the heterogeneous

194 te the structural features that underlie the nucleocytoplasmic transport of FABP4.

195 gs define a possible mechanism for regulated nucleocytoplasmic transport of Gln3p by phosphorylation

196 roductive infection, including the selective nucleocytoplasmic transport of late viral mRNA.

197 1 phosphorylation at S307, which directs the nucleocytoplasmic transport of LKB1 and consequent AMPK

198 We investigated the mechanism of nucleocytoplasmic transport of LKB1 in response to its c

199 role that can be considered dependent on the nucleocytoplasmic transport of macromolecules (i.e. is t

200 The nuclear pore complex mediates nucleocytoplasmic transport of macromolecules in eukaryo

201 In eukaryotes, the nucleocytoplasmic transport of macromolecules is mainly

202 Nucleocytoplasmic transport of macromolecules is regulat

203 The NPC regulates nucleocytoplasmic transport of macromolecules, utilizing

204 of the nuclear-pore complex, which regulates nucleocytoplasmic transport of macromolecules.

205 Ran GTPase is required for nucleocytoplasmic transport of many types of cargo.

206 Moreover, the role of nucleocytoplasmic transport of mature mRNA during liver

207 enetic information is regulated by selective nucleocytoplasmic transport of messenger RNA:protein com

208 ype suggests that this protein regulates the nucleocytoplasmic transport of molecules involved in sev

209 est that polyadenylation is required for the nucleocytoplasmic transport of mRNA and that Rev interac

210 Saccharomyces cerevisiae and facilitates the nucleocytoplasmic transport of mRNA-binding proteins thr

211 TAP and NxT1, both of which are involved in nucleocytoplasmic transport of mRNA.

212 recombination and the proper processing and nucleocytoplasmic transport of mRNA.

213 rus has been used as a model system to study nucleocytoplasmic transport of mRNA.

214 hat Arabidopsis AtNUP160 is critical for the nucleocytoplasmic transport of mRNAs and that it plays i

215 roteins may occur at NPCs and facilitate the nucleocytoplasmic transport of mRNAs.

216 We therefore investigated the nucleocytoplasmic transport of NP from influenza virus A

217 indings suggest a role of phosphorylation in nucleocytoplasmic transport of NP.

218 In addition these mutations affect nucleocytoplasmic transport of Npl3p.

219 rt receptors (karyopherins) that mediate the nucleocytoplasmic transport of protein and RNA cargoes.

220 Active nucleocytoplasmic transport of protein and RNA in eukary

221 investigated possible roles of xNup98 in the nucleocytoplasmic transport of proteins and RNAs by anal

222 Regulated nucleocytoplasmic transport of proteins is central to ce

223 naling in mammalian cells, and regulation of nucleocytoplasmic transport of RBP-J may contribute to f

224 distribution, vaults may be involved in the nucleocytoplasmic transport of ribosomes and/or mRNA.

225 The general molecular mechanisms involved in nucleocytoplasmic transport of RNA are only beginning to

226 inson-Gilford progeria syndrome inhibits the nucleocytoplasmic transport of several factors with key

227 eIF-4E is involved in nucleocytoplasmic transport of specific mRNAs including

228 bodies may participate in the regulation of nucleocytoplasmic transport of specific mRNAs.

229 ated with PML nuclear bodies, eIF4E mediates nucleocytoplasmic transport of specific transcripts, and

230 key translation factor and as a promoter of nucleocytoplasmic transport of specific transcripts.

231 Possible functions for this complex in nucleocytoplasmic transport of spliced mRNA, as well as

232 JAK/STAT signaling through their control of nucleocytoplasmic transport of STAT92E.

233 tly how these interactions contribute to the nucleocytoplasmic transport of substrates remains unclea

234 etition between autocatalytic processing and nucleocytoplasmic transport of the initial TRz transcrip

235 This impairs the nucleocytoplasmic transport of the tumor necrosis factor

236 cy virus type 1 (HIV-1) is essential for the nucleocytoplasmic transport of unspliced and partially s

237 protein export pathway in order to allow the nucleocytoplasmic transport of unspliced viral RNA.

238 Nucleocytoplasmic transport of viral ribonucleoproteins

239 lone does not produce discernable defects in nucleocytoplasmic transport or cell viability.

240 This is not due to a general decline in nucleocytoplasmic transport or to occlusion or loss of n

241 with recent reports showing that DPRs affect nucleocytoplasmic transport, our results point to an imp

242 tions with components of the endocytosis and nucleocytoplasmic transport pathways, regulated by p300-

243 t factors underlie the efficiency of certain nucleocytoplasmic transport pathways.

244 we recently established its crucial role in nucleocytoplasmic transport processes and cell cycle pro

245 with the Ran-GTPase support also its role in nucleocytoplasmic transport processes.

246 Here we analyzed the nucleocytoplasmic transport properties of both Gag prote

247 e divided into two groups according to their nucleocytoplasmic transport properties.

248 o system, transport disruption is not due to nucleocytoplasmic transport protein sequestration, nor b

249 Rev is a nucleocytoplasmic transport protein that directly binds

250 show that importin beta, a well established nucleocytoplasmic transport protein, interacts with comp

251 irst time revealed a novel role that MOG1, a nucleocytoplasmic transport protein, plays in cardiac ph

252 1 have been shown to regulate transcription, nucleocytoplasmic transport, protein stability, and prot

253 estration and impairment of nuclear HR23 and nucleocytoplasmic transport proteins is an outcome of, a

254 g karyopherins and effectors of Ran-mediated nucleocytoplasmic transport, providing insight into pote

255 s will continue to be applied to outstanding nucleocytoplasmic transport questions, and that the appr

256 defective mutants, a nonsense allele of the nucleocytoplasmic transport receptor, Kap104, was identi

257 rm1 is a member of the karyopherin family of nucleocytoplasmic transport receptors and mediates the e

258 abidopsis ortholog of the importin beta-like nucleocytoplasmic transport receptors exportin 5 in mamm

259 e RanGTPase cycle provides directionality to nucleocytoplasmic transport, regulating interactions bet

260 Continuous cycles of nucleocytoplasmic transport require disassembly of trans

261 answer by other means, yet the complexity of nucleocytoplasmic transport requires that interpretation

262 Rather, disruptions in Dbp5 nucleocytoplasmic transport result in tRNA export defect

263 included 1) mRNAs within the nucleolus when nucleocytoplasmic transport, rRNA biogenesis, or RNA pro

264 n autoregulatory loop and tightly controlled nucleocytoplasmic transport - safeguard its normal funct

265 fferentially control passive and facilitated nucleocytoplasmic transport, setting the rules for the m

266 3, where a cluster of consensus sites near a nucleocytoplasmic transport signal is confined to a spec

267 ant ZIC3 proteins identified the presence of nucleocytoplasmic transport signals.

268 ntrols multiple cellular processes including nucleocytoplasmic transport, spindle assembly, and nucle

269 es in multiple cellular processes, including nucleocytoplasmic transport, spindle formation, and post

270 The small GTPase Ran is involved in nucleocytoplasmic transport, spindle formation, nuclear

271 P) is important to Ran signaling involved in nucleocytoplasmic transport, spindle organization, and p

272 The Ran GTPase drives nucleocytoplasmic transport, stabilizes mitotic spindles

273 The fundamental process of nucleocytoplasmic transport takes place through the nucl

274 is blocked by an inhibitor of Ran-dependent nucleocytoplasmic transport, the Matrix protein of vesic

275 the role of nuclear pore complexes (NPCs) in nucleocytoplasmic transport, the mechanism of NPC assemb

276 As the sole site of nucleocytoplasmic transport, the nuclear pore complex (N

277 As the only gateway governing nucleocytoplasmic transport, the nuclear pore complex (N

278 dipeptide repeats produced by C9-HRE disrupt nucleocytoplasmic transport, the proteins that become re

279 Nucleocytoplasmic transport, the trafficking of macromol

280 The nuclear pore complex gates nucleocytoplasmic transport through a massive, eight-fol

281 Cardioviruses disrupt nucleocytoplasmic transport through the activity of thei

282 The nuclear pore complex (NPC) mediates nucleocytoplasmic transport through the nuclear envelope

283 f G4C2 repeat expansion is the compromise of nucleocytoplasmic transport through the nuclear pore, re

284 There is significant evidence linking nucleocytoplasmic transport to cell cycle control.

285 ights into how these nucleoporins coordinate nucleocytoplasmic transport to mount a robust immune res

286 These results demonstrate that maximum nucleocytoplasmic transport velocities can be modulated

287 unidentified cellular molecules that undergo nucleocytoplasmic transport via a pathway that is not as

288 Nuclear transport receptors (NTRs) mediate nucleocytoplasmic transport via their affinity for unstr

289 Although global nucleocytoplasmic transport was not significantly altere

290 Consistent with a potential role in nucleocytoplasmic transport, we found that HST interacts

291 causal role of poly-GR or poly-PR on active nucleocytoplasmic transport, we measured nuclear import

292 easomal degradation and proteins involved in nucleocytoplasmic transport were sequestered by poly(GA)

293 s detected by FRET methods; the kinetics for nucleocytoplasmic transport were unaffected by mutations

294 echanics is essential for characterizing the nucleocytoplasmic transport, which has a central importa

295 r studies indicate that RCC1 variants affect nucleocytoplasmic transport, which is crucial for health

296 pore complex encloses a central channel for nucleocytoplasmic transport, which is thought to consist

297 racts with RAN and normally functions in the nucleocytoplasmic transport while exerts its pathogenic

298 This mechanism may coordinate nucleocytoplasmic transport with other mitogenic effects

299 model of an intact NPC structure to examine nucleocytoplasmic transport with refined spatial and tem

300 The nuclear pore complex (NPC) mediates all nucleocytoplasmic transport, yet its structure and bioge