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1 rtin beta1 and Ran-GTPase, components of the nuclear pore complex.
2 and in achieving proper configuration of the nuclear pore complex.
3 and is stabilized by an interaction with the nuclear pore complex.
4 erlie mechanistic and kinetic control in the nuclear pore complex.
5 l channel, or on the cytoplasmic face of the nuclear pore complex.
6 ng protein cargoes for transport through the nuclear pore complex.
7 eptor TAP/NXF, which guides mRNA through the nuclear pore complex.
8 d the assembly of the coatomer module of the nuclear pore complex.
9 ction of cis-acting "DNA zip codes" with the nuclear pore complex.
10 processed mRNA and transports it through the nuclear pore complex.
11 x with SUMO-modified RanGAP1 and UBC9 at the nuclear pore complex.
12 forms the basket on the nuclear side of the nuclear pore complex.
13 plex with importin-beta to interact with the nuclear pore complex.
14 eptor Crm1 to facilitate passage through the nuclear pore complex.
15 latticework coats for COPII vesicles and the nuclear pore complex.
16 , but do not alter the level of Nup98 at the nuclear pore complex.
17 clear periphery through interaction with the nuclear pore complex.
18 beta1, which drives the receptor through the nuclear pore complex.
19 Nup35 gene, which encodes a component of the nuclear pore complex.
20 sically interacts with key components of the nuclear pore complex.
21 ery and requires Nup2, suggesting a role for nuclear pore complexes.
22 cient to ensure the even distribution of the nuclear pore complexes.
23 senger RNAs (mRNAs) to the cytoplasm through nuclear pore complexes.
24 mRNAs bound to the transport factor NXF1 to nuclear pore complexes.
25 - and CENP-F-mediated anchoring of dynein to nuclear pore complexes.
26 RNAs is thought to occur exclusively through nuclear pore complexes.
27 actor NXF1 resides in the nucleoplasm and at nuclear pore complexes.
28 followed by membrane-dependent insertion of nuclear pore complexes.
29 of the AAL signal localizes in proximity to nuclear pore complexes.
30 al properties of the permeability barrier of nuclear pore complexes.
31 Grima et al. (2017) describe defects in the nuclear pore complex and impaired nucleocytoplasmic tran
32 ependent on the Nup107-160 subcomplex of the nuclear pore complex and is modulated through interactio
33 t of nucleoporins (Nups) can detach from the nuclear pore complex and move into the nuclear interior
34 or trafficking of infectious DNA through the nuclear pore complex and plasmodesmata, respectively.
35 s, might help vaults safely pass through the nuclear pore complex and potentiate their role as self-r
38 vealing the octameric arrangement of Xenopus nuclear pore complexes and by quantifying the diffusion
40 istic step in Gle1's mRNA export function at nuclear pore complexes and directly implicate altered ex
41 d in the endosomal membrane pass through the nuclear pore complexes and function as non-membrane-boun
42 compaction that facilitates movement through nuclear pore complexes and the length of transcript poly
45 stration between fluorescently labeled mRNA, nuclear pore complexes, and chromatin, we obtained globa
48 ition to suggesting functional links between nuclear pore complex architecture and cancer cell surviv
49 e nuclear periphery and interaction with the nuclear pore complex are prerequisites for gene clusteri
58 assemble on the chromatin as an intermediate nuclear pore complex before nuclear envelope formation.
59 f the three nucleoporins contains additional nuclear pore complex binding sites, distinct from those
60 nk between the Torsin/cofactor system and NE/nuclear pore complex biogenesis or homeostasis and estab
62 east, some inducible genes interact with the nuclear pore complex both when active and for several ge
66 cytosolic localization of TDP-43, including nuclear pore complex components and regulators of G2/M c
70 ous intracellular compartments including the nuclear pore complex, COPII-coated vesicles, and inside
74 rdered Phe-Gly nucleoporins (FG Nups) within nuclear pore complexes exert multivalent interactions wi
81 rins comprising the modular structure of the nuclear pore complex have been defined at atomic resolut
83 ddition to its well-defined interaction with nuclear pore complexes, here we find that Gle1 is enrich
84 omolecular complexes with an emphasis on the nuclear pore complex, holding great potential for applic
87 entional fluorophores, we have imaged single nuclear pore complexes in the nuclear membrane and aggre
89 , which is shared by several proteins of the nuclear pore complex, including those in the central cha
95 biting nuclear transport also shows that the nuclear pore complex is vulnerable to unusual cargo rece
96 is a nuclear membrane protein comprising the nuclear pore complex; its exact function in the nuclear
97 ed if ICP27 could interact directly with the nuclear pore complex itself, finding that ICP27 directly
98 lo-like kinase 1 (PLK-1) is recruited to the nuclear pore complexes, just prior to NEBD, through its
99 are stacked ER-derived membranes containing nuclear pore complex-like structures whose fate and func
102 exerts its function and whether it modulates nuclear pore complex (NPC) activity remain unknown.
104 uncover two metformin response elements: the nuclear pore complex (NPC) and acyl-CoA dehydrogenase fa
105 ding yeast, targeting of active genes to the nuclear pore complex (NPC) and interchromosomal clusteri
108 generated nanobodies against the vertebrate nuclear pore complex (NPC) and used them in STORM imagin
109 e associated with shedding of NUP62 from the nuclear pore complex (NPC) and/or retention of NUP62 in
110 The cytoplasmic filament nucleoporins of the nuclear pore complex (NPC) are critically involved in nu
112 Elys is a conserved protein that directs nuclear pore complex (NPC) assembly in mammalian cell li
114 d important for the overall integrity of the nuclear pore complex (NPC) but not known to have cargo-s
115 show that PfSR1 is localized adjacent to the Nuclear Pore Complex (NPC) clusters in the nucleus of ea
116 directly in vitro with the FG repeats of the nuclear pore complex (NPC) components Nup62, Nup98, and
121 mechanism to explain how a component of the nuclear pore complex (NPC) could cause Htx/CHD was undef
122 1 and MAD2) were found to associate with the nuclear pore complex (NPC) during interphase and to requ
123 esized membrane proteins traffic through the nuclear pore complex (NPC) en route to the inner nuclear
125 /RanGAP1*SUMO1/Ubc9 localizes at cytoplasmic nuclear pore complex (NPC) filaments and is a docking si
126 nterest and represents a central paradigm to nuclear pore complex (NPC) function, where nuclear trans
127 nucleocytoplasmic information transfer, the nuclear pore complex (NPC) has been studied in great det
130 lluring proposal outlining functions for the nuclear pore complex (NPC) in transcription and nuclear
131 The measured active-export time through the Nuclear Pore Complex (NPC) is 18 ms, remarkably similar
136 nups) that line the transport channel of the nuclear pore complex (NPC) is investigated by means of c
137 NA (mRNA) through the aqueous channel of the nuclear pore complex (NPC) is mediated by interactions b
150 I have focused on understanding the role the nuclear pore complex (NPC) plays in maintaining this bal
152 iated Esc1, the SUMO E3 ligase Siz2, and the nuclear pore complex (NPC) protein Nup170-physically and
153 enterovirus 2A protease directly cleaves the nuclear pore complex (NPC) protein, Nup98, at amino acid
154 ring Aspergillus nidulans mitosis peripheral nuclear pore complex (NPC) proteins (Nups) disperse from
158 in receptor (p75(NTR)) is a component of the nuclear pore complex (NPC) required for glial scar forma
165 nsport, however, is tightly regulated by the nuclear pore complex (NPC) with the hydrophobic transpor
166 novirus (AdV) to the cytoplasmic face of the nuclear pore complex (NPC), a key step during delivery o
167 NPs), the translocation of mRNPs through the nuclear pore complex (NPC), and the mRNP remodeling even
168 etic modifiers that encode components of the nuclear pore complex (NPC), as well as the machinery tha
170 ls involves regulatory interactions with the nuclear pore complex (NPC), followed by translocation to
171 2, a component of the central channel of the nuclear pore complex (NPC), for forced dimerization by t
172 omponent of the cytoplasmic filaments of the nuclear pore complex (NPC), is essential for mouse embry
173 g, transport, and cytoplasmic release from a nuclear pore complex (NPC), is fast ( approximately 200
174 this study we used BioID to study the human nuclear pore complex (NPC), one of the largest macromole
176 ic reticulum to the Golgi apparatus, and the nuclear pore complex (NPC), which facilitates nucleo-cyt
189 The particles were observed to often probe nuclear pore complexes (NPC) at their nuclear face, and
193 lasmic reticulum (ER), translocation through nuclear pore complexes (NPCs) and retention on nuclear p
194 ic systems such as Saccharomyces cerevisiae, nuclear pore complexes (NPCs) and the spindle pole body
195 brane proteins, and large structures such as nuclear pore complexes (NPCs) and the spindle pole body.
196 eraction of non-chromosomal DNA circles with nuclear pore complexes (NPCs) and thereby promotes their
197 hp1:Sem1:Sus1:Cdc31 (TREX2) complex binds to nuclear pore complexes (NPCs) and, in addition to integr
208 long-term protein persistence, we found that nuclear pore complexes (NPCs) are maintained over a cell
213 e nucleus, possibly due to delocalization of nuclear pore complexes (NPCs) at the nuclear envelope.
219 of mitosis and modulates distribution of the nuclear pore complexes (NPCs) during mitotic NE expansio
220 Nucleocytoplasmic transport is mediated by nuclear pore complexes (NPCs) embedded in the nuclear en
226 es can lead to an uneven distribution of the nuclear pore complexes (NPCs) in the interphase nuclear
229 s sentrin-specific proteases, or SENPs) with nuclear pore complexes (NPCs) is conserved in eukaryotic
230 artmentalization by the nuclear envelope and nuclear pore complexes (NPCs) is essential for cell func
231 epletions suggest that translocation through nuclear pore complexes (NPCs) is rate-limiting and restr
232 Passive macromolecular diffusion through nuclear pore complexes (NPCs) is thought to decrease dra
233 cleus and cytoplasm, is tightly regulated by nuclear pore complexes (NPCs) made up of nucleoporins (N
240 ntial macromolecular protein assemblies: the nuclear pore complexes (NPCs) that enable nucleocytoplas
241 of select nucleoporin proteins (Nups) within nuclear pore complexes (NPCs) to disrupt karyopherin-dep
243 heir preintegration complexes (PICs) through nuclear pore complexes (NPCs) within nuclear envelopes.
244 to p53-SUMO-1 and their accumulation in the nuclear pore complexes (NPCs), as well as their persiste
246 e requires a dedicated transport system: (1) nuclear pore complexes (NPCs), embedded in the nuclear e
247 Nucleocytoplasmic transport is mediated by nuclear pore complexes (NPCs), enormous assemblies compo
248 horylation-driven partial disassembly of the nuclear pore complexes (NPCs), increasing their permeabi
249 ucleocytoplasmic transport are maintained by nuclear pore complexes (NPCs), large structures composed
250 known as the constituent building blocks of nuclear pore complexes (NPCs), membrane-embedded channel
251 ucleocytoplasmic transport is facilitated by nuclear pore complexes (NPCs), which are massive protein
260 les and contribute to the quality control of nuclear pore complexes (NPCs); whether these processes a
261 air; neuron pruning; extraction of defective nuclear pore complexes; nuclear envelope reformation; pl
262 sample preservation with a structure of the nuclear pore complex obtained from a single tomogram.
263 P214) are differentially distributed between nuclear pore complexes on the flattened surfaces and per
265 uding capsid transport, decapsidation at the nuclear pore complex, particle assembly, and secondary e
268 ter Blobel, on the structure and function of nuclear pore complexes; Peter Walter, on the unfolded pr
273 that the Arabidopsis (Arabidopsis thaliana) nuclear pore complex protein Nup88/MOS7 is essential for
276 the Sad1p, UNC-84 domain protein Klaroid and nuclear pore complex proteins were mislocalized to the c
278 ults suggest that LNO1 is a component of the nuclear pore complex required for mature mRNA export fro
279 Analysis of a large dynamic structure-the nuclear pore complex-revealed variations detectable at t
283 provided a high-resolution understanding of nuclear pore complex structure and transport, revealing
284 ELLPs were associated with chromatin and the nuclear pore complex, the central transport channels tha
285 ssical nuclear import pathway, involving the nuclear pore complex, the small GTPase Ran, and cellular
287 human cells, this dynein pool is anchored to nuclear pore complexes through RanBP2-Bicaudal D2 (BICD2
289 rate complicated molecular gates such as the nuclear pore complex to control the transport of biologi
291 functions with cis-encoded DNA elements and nuclear pore complexes to regulate interchromosomal gene
292 ion of identical daughter nuclei by coupling nuclear pore complexes to the segregating chromosomes.
294 G-Nups for its entire trajectory through the nuclear pore complex until RanGTP severs the cargo-Nup b
295 onal hsp-16.2/41 promoter interacts with the nuclear pore complex upon activation by heat shock in th
296 entary studies that Plk1 is recruited to the nuclear pore complex upon mitotic entry, where it acts w
297 the cellular substrates, particularly in the nuclear pore complex, used by these proteases were indee
299 oscopy (AFM) to the nuclear envelope and the nuclear pore complexes, we demonstrate that disposition
300 ants, and 3) transcripts being enriched near nuclear pore complexes when components of the mRNA expor
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