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1 zation and aggregation of NUPs and defective nucleocytoplasmic transport.
2     Nuclear pore complexes (NPCs) facilitate nucleocytoplasmic transport.
3  of integral membrane proteins and/or during nucleocytoplasmic transport.
4 mplexes in the two extracts, consistent with nucleocytoplasmic transport.
5 vergence may represent a unique mechanism of nucleocytoplasmic transport.
6 o be involved in signal transduction through nucleocytoplasmic transport.
7 esting an important role of the nucleolus in nucleocytoplasmic transport.
8 in is necessary and sufficient for mediating nucleocytoplasmic transport.
9 rotein assemblies that are the sole sites of nucleocytoplasmic transport.
10  acids 47-229, is also sufficient to inhibit nucleocytoplasmic transport.
11       The Ran GTPase plays a central role in nucleocytoplasmic transport.
12 hting the importance of the shape effects in nucleocytoplasmic transport.
13 on between the SUMO modification pathway and nucleocytoplasmic transport.
14 within the nucleus to inhibit bi-directional nucleocytoplasmic transport.
15 0 nucleoporins that cooperatively facilitate nucleocytoplasmic transport.
16 ellular function is the proper regulation of nucleocytoplasmic transport.
17 a small signaling GTPase that is involved in nucleocytoplasmic transport.
18 tion between the import and export phases of nucleocytoplasmic transport.
19 ction may require regulated, CRM1-dependent, nucleocytoplasmic transport.
20 n NPC-associated factor that participates in nucleocytoplasmic transport.
21 for a Brownian affinity gating mechanism for nucleocytoplasmic transport.
22 ects a more global process for regulation of nucleocytoplasmic transport.
23 mplex (NPC) are fundamental to understanding nucleocytoplasmic transport.
24  critical for understanding the mechanism of nucleocytoplasmic transport.
25 small ras-like GTPase involved in regulating nucleocytoplasmic transport.
26 ndergo degradation in the nucleus instead of nucleocytoplasmic transport.
27 d RNA sequences under conditions of impaired nucleocytoplasmic transport.
28 ulation of unspliced BDV transcripts through nucleocytoplasmic transport.
29 TPase Ran/Gsp1p, which is essential for most nucleocytoplasmic transport.
30 AN, a region that is supposed to function in nucleocytoplasmic transport.
31  125 MDa multiprotein assembly that mediates nucleocytoplasmic transport.
32 ted terminal differentiation and/or aberrant nucleocytoplasmic transport.
33 ) are 110-megadalton assemblies that mediate nucleocytoplasmic transport.
34 lex (NPC) filaments and is a docking site in nucleocytoplasmic transport.
35 nstitutes the sole gateway for bidirectional nucleocytoplasmic transport.
36 oncentration in the nucleus is important for nucleocytoplasmic transport.
37  Nups in the nuclear pore, and mechanisms of nucleocytoplasmic transport.
38 ptors (Karyopherins (Kaps)) that orchestrate nucleocytoplasmic transport.
39 mbers (karyopherins) mediate the majority of nucleocytoplasmic transport.
40 t, consistent with its essential function in nucleocytoplasmic transport.
41 ility of Cic by controlling the rates of its nucleocytoplasmic transport.
42 TPase Ran and the importin proteins regulate nucleocytoplasmic transport.
43 G domain nucleoporins, which are crucial for nucleocytoplasmic transport.
44 nonsense-mediated mRNA decay pathway, and to nucleocytoplasmic transport.
45 sphorylation site which is essential for its nucleocytoplasmic transport.
46 TG (RAN) translation proteins also disrupted nucleocytoplasmic transport.
47 e activity of Ran-GTPase, a key regulator of nucleocytoplasmic transport.
48 ndant GTPase responsible for the majority of nucleocytoplasmic transport.
49  was originally identified as a regulator of nucleocytoplasmic transport [1] and subsequently found t
50                                          The nucleocytoplasmic transport activity was not dependent o
51  studies offered clues that mHTT may disrupt nucleocytoplasmic transport and a mutation of an NUP can
52  occupancy of multiple RPEL motifs regulates nucleocytoplasmic transport and activity of MAL.
53 entify polyglutamine-dependent inhibition of nucleocytoplasmic transport and alteration of nuclear in
54                            In addition, LKB1 nucleocytoplasmic transport and AMPK activation in respo
55 utant that is used extensively in studies of nucleocytoplasmic transport and cell-cycle progression.
56 nuclear pore complex (NPC) has dual roles in nucleocytoplasmic transport and chromatin organization.
57 uclear pore complex (NPC) is responsible for nucleocytoplasmic transport and constitutes a hub for co
58 lts confirm that CAN plays a crucial role in nucleocytoplasmic transport and imply an essential role
59 MO E3 ligase activity that functions in both nucleocytoplasmic transport and mitosis.
60 oughout the cell cycle, including interphase nucleocytoplasmic transport and mitotic spindle assembly
61         Arginine methylation can affect both nucleocytoplasmic transport and protein-protein interact
62    To further explore the role of Kap123p in nucleocytoplasmic transport and ribosome biogenesis, we
63 ntial for many cellular processes, including nucleocytoplasmic transport and spindle assembly.
64 ranslational regulation of p53 comprises its nucleocytoplasmic transport and subsequent proteasomal d
65 lays a cell type-specific role in regulating nucleocytoplasmic transport and that this function is es
66  like U1 and U5 RNAs in their bi-directional nucleocytoplasmic transport and their 5'-cap hypermethyl
67 infection, E1B-55K is required for efficient nucleocytoplasmic transport and translation of late vira
68 te phase, E1B-55K modulates the preferential nucleocytoplasmic transport and translation of the late
69  Ran, which provides spatial information for nucleocytoplasmic transport and various mitotic processe
70 p62 at the nuclear envelope (probably during nucleocytoplasmic transport) and also in nucleoli, clear
71 romised nuclear envelope integrity, impaired nucleocytoplasmic transport, and accumulation of DNA dou
72 tion of host gene expression, disablement of nucleocytoplasmic transport, and disruption of the host
73 ical for cellular processes such as mitosis, nucleocytoplasmic transport, and nuclear envelope format
74 ct role of the disorder within FG repeats in nucleocytoplasmic transport, and resolves the apparent c
75 he nuclear pore complexes (NPCs) that enable nucleocytoplasmic transport, and the spindle pole bodies
76 latory elements (INS) that impair stability, nucleocytoplasmic transport, and translation by unknown
77 c nuclear permeability barrier and selective nucleocytoplasmic transport are maintained by nuclear po
78 ycine (FG) repeats play an important role in nucleocytoplasmic transport as they bind to transport re
79                     Here we demonstrate that nucleocytoplasmic transport at the membrane domain surro
80  The RanGTPase acts as a master regulator of nucleocytoplasmic transport by controlling assembly and
81 n et al. provide evidence for the control of nucleocytoplasmic transport by protein kinase signaling
82     We have examined whether signal-mediated nucleocytoplasmic transport can be regulated by phosphor
83   Thus, to overcome the limited capacity for nucleocytoplasmic transport, cells requiring increased n
84  dependent on a tRNA structure necessary for nucleocytoplasmic transport, consistent with primer sele
85 tain this conformation throughout the entire nucleocytoplasmic transport cycle.
86 zymes in ubiquitination, carrier proteins in nucleocytoplasmic transport, cyclin-dependent kinase in
87 ce in the eye have specific requirements for nucleocytoplasmic transport, despite involving processes
88 ion, whereas inhibitors of transcription and nucleocytoplasmic transport did not.
89 -FTD spectrum disorder, including autophagy, nucleocytoplasmic transport, DNA damage repair, pre-mRNA
90                   We propose that L inhibits nucleocytoplasmic transport during infection by disrupti
91                                     To study nucleocytoplasmic transport during multicellular develop
92 ever little is known about the regulation of nucleocytoplasmic transport during the formation of myof
93 ta and ste5ts), indicating that reduction in nucleocytoplasmic transport enhances mating proficiency.
94 ll GTPase Ran is essential for virtually all nucleocytoplasmic transport events.
95 uction of securin by APC is regulated by the nucleocytoplasmic transport factors Rae1 and Nup98.
96 ave been proposed to mediate the movement of nucleocytoplasmic transport factors.
97  of numerous biological processes, including nucleocytoplasmic transport, genomic stability, and gene
98 rtial sequestration of factors essential for nucleocytoplasmic transport (Gle1 and RanGAP1), and intr
99                   The separate components of nucleocytoplasmic transport have been well characterized
100 may lead to unique insights into the role of nucleocytoplasmic transport in adrenal function and neur
101 and serves as the sole conduit to facilitate nucleocytoplasmic transport in eukaryotes.
102 s) are key cellular transporter that control nucleocytoplasmic transport in eukaryotic cells, but its
103 cts in the nuclear pore complex and impaired nucleocytoplasmic transport in Huntington's disease (HD)
104          Therefore, we evaluated the NPC and nucleocytoplasmic transport in multiple models of HD, in
105 s provide evidence for an important role for nucleocytoplasmic transport in the pathogenic mechanism
106             Virtually nothing is known about nucleocytoplasmic transport in these parasites (phylum A
107 th mutations in many other genes involved in nucleocytoplasmic transport, including SRP1 (alpha-impor
108 (Phe) mutants that retained the capacity for nucleocytoplasmic transport, indicative of overall intac
109 sses of mRNA metabolism, including splicing, nucleocytoplasmic transport,initiation of translation, a
110                                              Nucleocytoplasmic transport involves assembly and moveme
111                            Interference with nucleocytoplasmic transport is a strategy employed by ce
112                               Dysfunction in nucleocytoplasmic transport is also an emerging theme in
113  permeability, selectivity, and the speed of nucleocytoplasmic transport is an assembly of natively u
114                                          p53 nucleocytoplasmic transport is carried out by a bipartit
115                            Receptor-mediated nucleocytoplasmic transport is dependent on the GTPase R
116       We conclude that the directionality of nucleocytoplasmic transport is determined mainly by the
117 stablished general background information on nucleocytoplasmic transport is discussed.
118                                              Nucleocytoplasmic transport is facilitated by nuclear po
119                                              Nucleocytoplasmic transport is mediated by nuclear pore
120                                              Nucleocytoplasmic transport is mediated by nuclear pore
121                                              Nucleocytoplasmic transport is mediated by the interacti
122                                              Nucleocytoplasmic transport is mediated by the interplay
123                                              Nucleocytoplasmic transport is sustained by karyopherins
124 asm, it may mediate a connection between the nucleocytoplasmic transport machinery and the endosomal
125      To further our understanding of how the nucleocytoplasmic transport machinery interfaces with it
126     As RCC1 is an important component of the nucleocytoplasmic transport machinery, we find that dRCC
127  concomitantly can interact with the soluble nucleocytoplasmic transport machinery.
128 exportins represent an essential part of the nucleocytoplasmic transport machinery.
129 rovides several binding sites for the mobile nucleocytoplasmic transport machinery.
130 rovides a multitude of binding sites for the nucleocytoplasmic transport machinery.
131 common mechanism for SUMOylation to regulate nucleocytoplasmic transport may lie in the interplay bet
132 e propose that RB inactivation, via aberrant nucleocytoplasmic transport, may disrupt normal cell dif
133  the NPC, taking a central role in the vital nucleocytoplasmic transport mechanism.
134 gradient of RanGTP on chromatin that directs nucleocytoplasmic transport, mitotic spindle assembly an
135 ifunctional small GTPase that is involved in nucleocytoplasmic transport, mitotic spindle assembly, a
136 ll GTPase Ran is best known for its roles in nucleocytoplasmic transport, mitotic spindle assembly, a
137 y of GTPases, is best known for its roles in nucleocytoplasmic transport, mitotic spindle fiber assem
138 n guanosine triphosphatase (GTPase) controls nucleocytoplasmic transport, mitotic spindle formation,
139          The NUP107 complex is important for nucleocytoplasmic transport, nuclear envelope assembly,
140                                              Nucleocytoplasmic transport occurs exclusively through n
141                                              Nucleocytoplasmic transport occurs through gigantic prot
142                                              Nucleocytoplasmic transport occurs through nuclear pore
143       To understand how the vital process of nucleocytoplasmic transport occurs, the contribution of
144 ite mutant TA accumulation in NE structures, nucleocytoplasmic transport of a reporter protein was un
145                   Nuclear eIF4E functions in nucleocytoplasmic transport of a subset of transcripts i
146  the canonical Wnt pathway by regulating the nucleocytoplasmic transport of beta-catenin rather than
147 ant function of small GTPases in the cell is nucleocytoplasmic transport of both proteins and RNA.
148          Retroviral replication requires the nucleocytoplasmic transport of both spliced and unsplice
149              Therefore, we characterized the nucleocytoplasmic transport of each of the heterogeneous
150 te the structural features that underlie the nucleocytoplasmic transport of FABP4.
151 gs define a possible mechanism for regulated nucleocytoplasmic transport of Gln3p by phosphorylation
152 roductive infection, including the selective nucleocytoplasmic transport of late viral mRNA.
153 1 phosphorylation at S307, which directs the nucleocytoplasmic transport of LKB1 and consequent AMPK
154             We investigated the mechanism of nucleocytoplasmic transport of LKB1 in response to its c
155 role that can be considered dependent on the nucleocytoplasmic transport of macromolecules (i.e. is t
156            The nuclear pore complex mediates nucleocytoplasmic transport of macromolecules in eukaryo
157                           In eukaryotes, the nucleocytoplasmic transport of macromolecules is mainly
158                                              Nucleocytoplasmic transport of macromolecules is regulat
159                            The NPC regulates nucleocytoplasmic transport of macromolecules, utilizing
160                   Ran GTPase is required for nucleocytoplasmic transport of many types of cargo.
161                        Moreover, the role of nucleocytoplasmic transport of mature mRNA during liver
162 enetic information is regulated by selective nucleocytoplasmic transport of messenger RNA:protein com
163 ype suggests that this protein regulates the nucleocytoplasmic transport of molecules involved in sev
164 est that polyadenylation is required for the nucleocytoplasmic transport of mRNA and that Rev interac
165 Saccharomyces cerevisiae and facilitates the nucleocytoplasmic transport of mRNA-binding proteins thr
166  TAP and NxT1, both of which are involved in nucleocytoplasmic transport of mRNA.
167  recombination and the proper processing and nucleocytoplasmic transport of mRNA.
168 rus has been used as a model system to study nucleocytoplasmic transport of mRNA.
169 hat Arabidopsis AtNUP160 is critical for the nucleocytoplasmic transport of mRNAs and that it plays i
170 roteins may occur at NPCs and facilitate the nucleocytoplasmic transport of mRNAs.
171                We therefore investigated the nucleocytoplasmic transport of NP from influenza virus A
172 indings suggest a role of phosphorylation in nucleocytoplasmic transport of NP.
173           In addition these mutations affect nucleocytoplasmic transport of Npl3p.
174 rt receptors (karyopherins) that mediate the nucleocytoplasmic transport of protein and RNA cargoes.
175                                       Active nucleocytoplasmic transport of protein and RNA in eukary
176 investigated possible roles of xNup98 in the nucleocytoplasmic transport of proteins and RNAs by anal
177                                    Regulated nucleocytoplasmic transport of proteins is central to ce
178  distribution, vaults may be involved in the nucleocytoplasmic transport of ribosomes and/or mRNA.
179 The general molecular mechanisms involved in nucleocytoplasmic transport of RNA are only beginning to
180 inson-Gilford progeria syndrome inhibits the nucleocytoplasmic transport of several factors with key
181                        eIF-4E is involved in nucleocytoplasmic transport of specific mRNAs including
182  bodies may participate in the regulation of nucleocytoplasmic transport of specific mRNAs.
183 ated with PML nuclear bodies, eIF4E mediates nucleocytoplasmic transport of specific transcripts, and
184  key translation factor and as a promoter of nucleocytoplasmic transport of specific transcripts.
185       Possible functions for this complex in nucleocytoplasmic transport of spliced mRNA, as well as
186  JAK/STAT signaling through their control of nucleocytoplasmic transport of STAT92E.
187 tly how these interactions contribute to the nucleocytoplasmic transport of substrates remains unclea
188 etition between autocatalytic processing and nucleocytoplasmic transport of the initial TRz transcrip
189                             This impairs the nucleocytoplasmic transport of the tumor necrosis factor
190 cy virus type 1 (HIV-1) is essential for the nucleocytoplasmic transport of unspliced and partially s
191 protein export pathway in order to allow the nucleocytoplasmic transport of unspliced viral RNA.
192                                              Nucleocytoplasmic transport of viral ribonucleoproteins
193      This is not due to a general decline in nucleocytoplasmic transport or to occlusion or loss of n
194 with recent reports showing that DPRs affect nucleocytoplasmic transport, our results point to an imp
195 t factors underlie the efficiency of certain nucleocytoplasmic transport pathways.
196  we recently established its crucial role in nucleocytoplasmic transport processes and cell cycle pro
197 with the Ran-GTPase support also its role in nucleocytoplasmic transport processes.
198                         Here we analyzed the nucleocytoplasmic transport properties of both Gag prote
199 e divided into two groups according to their nucleocytoplasmic transport properties.
200                                     Rev is a nucleocytoplasmic transport protein that directly binds
201  show that importin beta, a well established nucleocytoplasmic transport protein, interacts with comp
202 irst time revealed a novel role that MOG1, a nucleocytoplasmic transport protein, plays in cardiac ph
203 1 have been shown to regulate transcription, nucleocytoplasmic transport, protein stability, and prot
204 estration and impairment of nuclear HR23 and nucleocytoplasmic transport proteins is an outcome of, a
205 g karyopherins and effectors of Ran-mediated nucleocytoplasmic transport, providing insight into pote
206 s will continue to be applied to outstanding nucleocytoplasmic transport questions, and that the appr
207  defective mutants, a nonsense allele of the nucleocytoplasmic transport receptor, Kap104, was identi
208 rm1 is a member of the karyopherin family of nucleocytoplasmic transport receptors and mediates the e
209 abidopsis ortholog of the importin beta-like nucleocytoplasmic transport receptors exportin 5 in mamm
210 e RanGTPase cycle provides directionality to nucleocytoplasmic transport, regulating interactions bet
211                         Continuous cycles of nucleocytoplasmic transport require disassembly of trans
212 answer by other means, yet the complexity of nucleocytoplasmic transport requires that interpretation
213  included 1) mRNAs within the nucleolus when nucleocytoplasmic transport, rRNA biogenesis, or RNA pro
214 3, where a cluster of consensus sites near a nucleocytoplasmic transport signal is confined to a spec
215 ant ZIC3 proteins identified the presence of nucleocytoplasmic transport signals.
216 ntrols multiple cellular processes including nucleocytoplasmic transport, spindle assembly, and nucle
217 es in multiple cellular processes, including nucleocytoplasmic transport, spindle formation, and post
218          The small GTPase Ran is involved in nucleocytoplasmic transport, spindle formation, nuclear
219 P) is important to Ran signaling involved in nucleocytoplasmic transport, spindle organization, and p
220                        The Ran GTPase drives nucleocytoplasmic transport, stabilizes mitotic spindles
221                   The fundamental process of nucleocytoplasmic transport takes place through the nucl
222  is blocked by an inhibitor of Ran-dependent nucleocytoplasmic transport, the Matrix protein of vesic
223 the role of nuclear pore complexes (NPCs) in nucleocytoplasmic transport, the mechanism of NPC assemb
224                          As the sole site of nucleocytoplasmic transport, the nuclear pore complex (N
225                                              Nucleocytoplasmic transport, the trafficking of macromol
226               The nuclear pore complex gates nucleocytoplasmic transport through a massive, eight-fol
227                        Cardioviruses disrupt nucleocytoplasmic transport through the activity of thei
228      The nuclear pore complex (NPC) mediates nucleocytoplasmic transport through the nuclear envelope
229 f G4C2 repeat expansion is the compromise of nucleocytoplasmic transport through the nuclear pore, re
230        There is significant evidence linking nucleocytoplasmic transport to cell cycle control.
231 ights into how these nucleoporins coordinate nucleocytoplasmic transport to mount a robust immune res
232       These results demonstrate that maximum nucleocytoplasmic transport velocities can be modulated
233 unidentified cellular molecules that undergo nucleocytoplasmic transport via a pathway that is not as
234   Nuclear transport receptors (NTRs) mediate nucleocytoplasmic transport via their affinity for unstr
235                              Although global nucleocytoplasmic transport was not significantly altere
236          Consistent with a potential role in nucleocytoplasmic transport, we found that HST interacts
237 easomal degradation and proteins involved in nucleocytoplasmic transport were sequestered by poly(GA)
238 s detected by FRET methods; the kinetics for nucleocytoplasmic transport were unaffected by mutations
239 echanics is essential for characterizing the nucleocytoplasmic transport, which has a central importa
240  pore complex encloses a central channel for nucleocytoplasmic transport, which is thought to consist
241                This mechanism may coordinate nucleocytoplasmic transport with other mitogenic effects
242  model of an intact NPC structure to examine nucleocytoplasmic transport with refined spatial and tem
243  The nuclear pore complex (NPC) mediates all nucleocytoplasmic transport, yet its structure and bioge

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