review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1111/FEBS.13163 |
P8608 | Fatcat ID | release_qfujh3bsevhvhki4ypkxp6ydti |
P3181 | OpenCitations bibliographic resource ID | 3097437 |
P932 | PMC publication ID | 7163960 |
P698 | PubMed publication ID | 25429850 |
P50 | author | Bastien Cautain | Q85525907 |
Richard Hill | Q39965266 | ||
Wolfgang Link | Q57975560 | ||
P2093 | author name string | Nuria de Pedro | |
P2860 | cites work | Calreticulin Is a receptor for nuclear export | Q24290720 |
Ran-binding protein 3 links Crm1 to the Ran guanine nucleotide exchange factor | Q24293261 | ||
Exportin-5 mediates the nuclear export of pre-microRNAs and short hairpin RNAs | Q24302072 | ||
The mechanism of nuclear export of Smad3 involves exportin 4 and Ran | Q24302636 | ||
Proteomic analysis of the mammalian nuclear pore complex | Q24305242 | ||
Herpes simplex virus ICP27 protein directly interacts with the nuclear pore complex through Nup62, inhibiting host nucleocytoplasmic transport pathways | Q24305296 | ||
Protein Tpr is required for establishing nuclear pore-associated zones of heterochromatin exclusion | Q24307496 | ||
Nuclear export and cytoplasmic processing of precursors to the 40S ribosomal subunits in mammalian cells. | Q24309380 | ||
Identification of a tRNA-specific nuclear export receptor | Q24314506 | ||
A novel class of RanGTP binding proteins | Q24316050 | ||
Export of importin alpha from the nucleus is mediated by a specific nuclear transport factor | Q24316152 | ||
FG-Rich Repeats of Nuclear Pore Proteins Form a Three-Dimensional Meshwork with Hydrogel-Like Properties | Q58076963 | ||
Functional dissection of the HIV-1 Rev trans-activator—Derivation of a trans-dominant repressor of Rev function | Q58611466 | ||
Kap104p-mediated nuclear import. Nuclear localization signals in mRNA-binding proteins and the role of Ran and Rna | Q73041162 | ||
Nuclear export of yeast signal recognition particle lacking srp54p by the Xpo1p/Crm1p NES-dependent pathway | Q73292066 | ||
A comparison of the activity, sequence specificity, and CRM1-dependence of different nuclear export signals | Q73598439 | ||
Ran and nuclear transport | Q77171854 | ||
Cse1p functions as the nuclear export receptor for importin alpha in yeast | Q77323192 | ||
Antagonistic effects of NES and NLS motifs determine S. cerevisiae Rna1p subcellular distribution | Q77784876 | ||
A polypeptide domain that specifies migration of nucleoplasmin into the nucleus | Q34056435 | ||
The nuclear pore complex: bridging nuclear transport and gene regulation | Q34122297 | ||
Mutational definition of the human immunodeficiency virus type 1 Rev activation domain. | Q34132236 | ||
The Ebola virus VP24 protein prevents hnRNP C1/C2 binding to karyopherin α1 and partially alters its nuclear import. | Q34222991 | ||
Nucleocytoplasmic transport enters the atomic age. | Q34245364 | ||
The human nuclear pore complex as revealed by cryo-electron tomography. | Q34282959 | ||
Inhibition of nuclear import and alteration of nuclear pore complex composition by rhinovirus | Q34344113 | ||
Nuclear export of RNA. | Q34364012 | ||
Recognition of nuclear targeting signals by Karyopherin-β proteins | Q34367559 | ||
Comparative mutagenesis of nuclear localization signals reveals the importance of neutral and acidic amino acids | Q34396948 | ||
Targeting nucleocytoplasmic transport in cancer therapy | Q34398166 | ||
SRprises along a messenger's journey | Q34400219 | ||
Pom121 links two essential subcomplexes of the nuclear pore complex core to the membrane | Q34412386 | ||
Nucleocytoplasmic traffic disorder induced by cardioviruses. | Q34434945 | ||
Effects of poliovirus infection on nucleo-cytoplasmic trafficking and nuclear pore complex composition. | Q34450018 | ||
Simple fold composition and modular architecture of the nuclear pore complex | Q34478878 | ||
Analysis of a RanGTP-regulated gradient in mitotic somatic cells | Q34506840 | ||
Classical nuclear localization signals: definition, function, and interaction with importin alpha | Q34591163 | ||
Role of the nuclear envelope in genome organization and gene expression | Q34632599 | ||
The nucleoporin Nup98 associates with the intranuclear filamentous protein network of TPR. | Q34712774 | ||
The nuclear export receptor Xpo1p forms distinct complexes with NES transport substrates and the yeast Ran binding protein 1 (Yrb1p). | Q34986205 | ||
Nucleocytoplasmic transport: navigating the channel | Q35092062 | ||
Biology and biophysics of the nuclear pore complex and its components | Q35195849 | ||
Prediction of leucine-rich nuclear export signal containing proteins with NESsential | Q35198286 | ||
NESmapper: accurate prediction of leucine-rich nuclear export signals using activity-based profiles | Q35261339 | ||
Nucleocytoplasmic transport: taking an inventory | Q35541034 | ||
Virtual gating and nuclear transport: the hole picture | Q35587487 | ||
Regulation of JAK-STAT signalling in the immune system | Q35605437 | ||
Nuclear export of mRNA: from the site of transcription to the cytoplasm | Q35761786 | ||
Importin α: a multipurpose nuclear-transport receptor | Q35879618 | ||
Importin beta: conducting a much larger cellular symphony | Q35938681 | ||
Nuclear envelope budding enables large ribonucleoprotein particle export during synaptic Wnt signaling | Q36020221 | ||
Translocation through the nuclear pore complex: selectivity and speed by reduction-of-dimensionality | Q36090722 | ||
Modularity within the architecture of the nuclear pore complex. | Q36101124 | ||
Snurportin1, an m3G-cap-specific nuclear import receptor with a novel domain structure | Q24316296 | ||
Co-activation of RanGTPase and inhibition of GTP dissociation by Ran-GTP binding protein RanBP1 | Q24316332 | ||
Exp5 exports eEF1A via tRNA from nuclei and synergizes with other transport pathways to confine translation to the cytoplasm | Q24317462 | ||
The human homologue of yeast CRM1 is in a dynamic subcomplex with CAN/Nup214 and a novel nuclear pore component Nup88 | Q24322912 | ||
A cap-binding protein complex mediating U snRNA export | Q24336104 | ||
RanBP3 influences interactions between CRM1 and its nuclear protein export substrates | Q24522587 | ||
The role of exportin-t in selective nuclear export of mature tRNAs | Q24533485 | ||
Importin 13: a novel mediator of nuclear import and export | Q24535585 | ||
A masked NES in INI1/hSNF5 mediates hCRM1-dependent nuclear export: implications for tumorigenesis | Q24536149 | ||
Exportin-5-mediated nuclear export of eukaryotic elongation factor 1A and tRNA | Q24537714 | ||
ICP27 interacts with the RNA export factor Aly/REF to direct herpes simplex virus type 1 intronless mRNAs to the TAP export pathway | Q24538841 | ||
Exportin 5 is a RanGTP-dependent dsRNA-binding protein that mediates nuclear export of pre-miRNAs | Q24540256 | ||
Identification of different roles for RanGDP and RanGTP in nuclear protein import | Q24561933 | ||
Exportin 7 defines a novel general nuclear export pathway | Q24563375 | ||
A proteasome inhibitor prevents activation of NF-kappa B and stabilizes a newly phosphorylated form of I kappa B-alpha that is still bound to NF-kappa B | Q24568234 | ||
Rules for nuclear localization sequence recognition by karyopherin beta 2 | Q24600321 | ||
Structural basis for leucine-rich nuclear export signal recognition by CRM1 | Q24604395 | ||
The yeast RNA1 gene product necessary for RNA processing is located in the cytosol and apparently excluded from the nucleus | Q24678911 | ||
The yeast nuclear pore complex: composition, architecture, and transport mechanism | Q24680784 | ||
A role for RanBP1 in the release of CRM1 from the nuclear pore complex in a terminal step of nuclear export | Q24682010 | ||
CRM1-mediated recycling of snurportin 1 to the cytoplasm | Q24682405 | ||
Ran-binding protein 3 is a cofactor for Crm1-mediated nuclear protein export | Q24685628 | ||
Nuclear export of proteins and drug resistance in cancer | Q27012444 | ||
mRNA export and the TREX complex | Q27026569 | ||
Structural basis for the interaction between FxFG nucleoporin repeats and importin-beta in nuclear trafficking | Q27625995 | ||
Structure of Nup58/45 suggests flexible nuclear pore diameter by intermolecular sliding | Q27644208 | ||
A fence-like coat for the nuclear pore membrane | Q27653292 | ||
Crystal structure of the nuclear export receptor CRM1 in complex with Snurportin1 and RanGTP | Q27655147 | ||
Nuclear import mechanism of the EJC component Mago-Y14 revealed by structural studies of importin 13 | Q27659349 | ||
Structural and functional analysis of the interaction between the nucleoporin Nup98 and the mRNA export factor Rae1 | Q27661891 | ||
NES consensus redefined by structures of PKI-type and Rev-type nuclear export signals bound to CRM1 | Q27665346 | ||
Evidence for a role of CRM1 in signal-mediated nuclear protein export | Q29620231 | ||
Sequence requirements for nuclear location of simian virus 40 large-T antigen | Q29620588 | ||
Karyopherins: from nuclear-transport mediators to nuclear-function regulators | Q30434629 | ||
STRADalpha regulates LKB1 localization by blocking access to importin-alpha, and by association with Crm1 and exportin-7. | Q30441588 | ||
Interaction of HTLV-1 Tax protein with calreticulin: implications for Tax nuclear export and secretion | Q30442529 | ||
Imaging of single-molecule translocation through nuclear pore complexes | Q30832298 | ||
A protein inventory of human ribosome biogenesis reveals an essential function of exportin 5 in 60S subunit export | Q30991604 | ||
Flexible phenylalanine-glycine nucleoporins as entropic barriers to nucleocytoplasmic transport | Q33246576 | ||
H2A.Z-mediated localization of genes at the nuclear periphery confers epigenetic memory of previous transcriptional state | Q33279444 | ||
An electron microscope study of the nuclear membrane | Q33311818 | ||
Nuclear export signal consensus sequences defined using a localization-based yeast selection system | Q33371970 | ||
Depletion of nucleophosmin via transglutaminase 2 cross-linking increases drug resistance in cancer cells | Q33375544 | ||
Ebolavirus VP24 binding to karyopherins is required for inhibition of interferon signaling | Q33558506 | ||
Comparative genomic evidence for a complete nuclear pore complex in the last eukaryotic common ancestor. | Q33719317 | ||
Mechanistic consequences of hnRNP C binding to both RNA termini of poliovirus negative-strand RNA intermediates | Q33826732 | ||
A leucine-rich nuclear export signal in the p53 tetramerization domain: regulation of subcellular localization and p53 activity by NES masking | Q33890625 | ||
Gatekeepers of the nucleus | Q33927537 | ||
RanGTP-regulated interactions of CRM1 with nucleoporins and a shuttling DEAD-box helicase | Q33959492 | ||
Nuclear import by karyopherin-βs: Recognition and inhibition | Q34024485 | ||
CRM1 is an export receptor for leucine-rich nuclear export signals | Q27860453 | ||
The GTPase superfamily: conserved structure and molecular mechanism | Q27860524 | ||
Nuclear export of microRNA precursors | Q27860686 | ||
Yeast Ran-binding protein 1 (Yrb1) shuttles between the nucleus and cytoplasm and is exported from the nucleus via a CRM1 (XPO1)-dependent pathway | Q27936568 | ||
Yeast Los1p has properties of an exportin-like nucleocytoplasmic transport factor for tRNA | Q27937371 | ||
Nuclear export of 60s ribosomal subunits depends on Xpo1p and requires a nuclear export sequence-containing factor, Nmd3p, that associates with the large subunit protein Rpl10p | Q27937695 | ||
Regulated nucleo/cytoplasmic exchange of HOG1 MAPK requires the importin beta homologs NMD5 and XPO1. | Q27937992 | ||
Homeodomain of yeast repressor alpha 2 contains a nuclear localization signal | Q27938014 | ||
Roles of phosphorylation sites in regulating activity of the transcription factor Pho4. | Q27938391 | ||
Nmd3p is a Crm1p-dependent adapter protein for nuclear export of the large ribosomal subunit | Q27939125 | ||
Kap104p imports the PY-NLS-containing transcription factor Tfg2p into the nucleus | Q27939454 | ||
Exportin 1 (Crm1p) is an essential nuclear export factor | Q27939696 | ||
Telomere tethering at the nuclear periphery is essential for efficient DNA double strand break repair in subtelomeric region | Q27940251 | ||
Integrated structural analysis of the human nuclear pore complex scaffold | Q28115760 | ||
Biogenesis and nuclear export of ribosomal subunits in higher eukaryotes depend on the CRM1 export pathway | Q28116115 | ||
The HIV-1 Rev activation domain is a nuclear export signal that accesses an export pathway used by specific cellular RNAs | Q28131708 | ||
Protein import into nuclei: association and dissociation reactions involving transport substrate, transport factors, and nucleoporins | Q28131733 | ||
Vesicular stomatitis virus matrix protein inhibits host cell gene expression by targeting the nucleoporin Nup98 | Q28139522 | ||
Molecular dissection of the importin beta1-recognized nuclear targeting signal of parathyroid hormone-related protein | Q28201295 | ||
Exporting RNA from the nucleus to the cytoplasm | Q28245155 | ||
Identification of a nuclear export receptor for tRNA | Q28265348 | ||
The HIV-1 rev trans-activator acts through a structured target sequence to activate nuclear export of unspliced viral mRNA | Q28279502 | ||
Molecular basis for specificity of nuclear import and prediction of nuclear localization | Q28296734 | ||
Nucleo-cytoplasmic distribution of human hnRNP proteins: a search for the targeting domains in hnRNP A1 | Q28302458 | ||
PHAX, a mediator of U snRNA nuclear export whose activity is regulated by phosphorylation | Q28511197 | ||
Nuclear localization of NF-ATc by a calcineurin-dependent, cyclosporin-sensitive intramolecular interaction | Q28616185 | ||
HIV-1 structural gene expression requires binding of the Rev trans-activator to its RNA target sequence | Q28646785 | ||
Identification of a signal for rapid export of proteins from the nucleus | Q29547742 | ||
A short amino acid sequence able to specify nuclear location | Q29547781 | ||
CRM1 is responsible for intracellular transport mediated by the nuclear export signal | Q29547861 | ||
Structural biology of nucleocytoplasmic transport | Q29615350 | ||
Transport into and out of the nucleus | Q29615611 | ||
Analysis and prediction of leucine-rich nuclear export signals | Q29619228 | ||
The SR protein family of splicing factors: master regulators of gene expression | Q29619935 | ||
The GTP-binding protein Ran/TC4 is required for protein import into the nucleus | Q29620192 | ||
Inhibition of nuclear protein import by nonhydrolyzable analogues of GTP and identification of the small GTPase Ran/TC4 as an essential transport factor | Q29620193 | ||
Structural basis for assembly and disassembly of the CRM1 nuclear export complex | Q36220837 | ||
NESdb: a database of NES-containing CRM1 cargoes | Q36234505 | ||
A nuclear export signal is essential for the cytosolic localization of the Ran binding protein, RanBP1. | Q36237387 | ||
The cytoplasmic filaments of the nuclear pore complex are dispensable for selective nuclear protein import | Q36323649 | ||
Karyopherin flexibility in nucleocytoplasmic transport | Q36432992 | ||
ValidNESs: a database of validated leucine-rich nuclear export signals | Q36491242 | ||
Protein sequence requirements for function of the human T-cell leukemia virus type 1 Rex nuclear export signal delineated by a novel in vivo randomization-selection assay | Q36561338 | ||
The role of nuclear envelope calcium in modifying nuclear pore complex structure | Q36562700 | ||
Nup358/RanBP2 attaches to the nuclear pore complex via association with Nup88 and Nup214/CAN and plays a supporting role in CRM1-mediated nuclear protein export | Q36572321 | ||
Severe acute respiratory syndrome coronavirus protein 6 accelerates murine hepatitis virus infections by more than one mechanism. | Q36747726 | ||
Nuclear pore complexes: guardians of the nuclear genome | Q36829705 | ||
Dynamic trafficking of STAT5 depends on an unconventional nuclear localization signal | Q37061528 | ||
Nucleocytoplasmic transport of proteins | Q37087415 | ||
Leader-induced phosphorylation of nucleoporins correlates with nuclear trafficking inhibition by cardioviruses | Q37099800 | ||
Mengovirus-induced rearrangement of the nuclear pore complex: hijacking cellular phosphorylation machinery | Q37127856 | ||
Rhinovirus 3C protease can localize in the nucleus and alter active and passive nucleocytoplasmic transport | Q37247979 | ||
CRM1-mediated nuclear export of proteins and drug resistance in cancer | Q37320237 | ||
First and last ancestors: reconstructing evolution of the endomembrane system with ESCRTs, vesicle coat proteins, and nuclear pore complexes | Q37388173 | ||
Bidirectional increase in permeability of nuclear envelope upon poliovirus infection and accompanying alterations of nuclear pores. | Q37492721 | ||
mRNA nuclear export at a glance | Q37506920 | ||
Importins and beyond: non-conventional nuclear transport mechanisms | Q37528567 | ||
Linking gene regulation to mRNA production and export. | Q37827981 | ||
The structure of the nuclear pore complex | Q37865519 | ||
Calcium regulation of nucleocytoplasmic transport | Q37870091 | ||
mRNA export and cancer | Q37907202 | ||
Protein localization in disease and therapy. | Q37947248 | ||
New clues to understand the role of THO and other functionally related factors in mRNP biogenesis | Q37972238 | ||
Functional architecture of the nuclear pore complex | Q38009349 | ||
Nuclear trafficking of proteins from RNA viruses: potential target for antivirals? | Q38023068 | ||
Moving to the core: spatiotemporal analysis of Forkhead box O (FOXO) and nuclear factor-κB (NF-κB) nuclear translocation | Q38066579 | ||
Nuclear trafficking in health and disease | Q38188343 | ||
I kappa B interacts with the nuclear localization sequences of the subunits of NF-kappa B: a mechanism for cytoplasmic retention | Q38325326 | ||
Nup214 is required for CRM1-dependent nuclear protein export in vivo | Q38411212 | ||
Differential processing of nuclear pore complex proteins by rhinovirus 2A proteases from different species and serotypes | Q38631844 | ||
High-content screening of natural products reveals novel nuclear export inhibitors | Q39094551 | ||
Cse1p is involved in export of yeast importin alpha from the nucleus | Q39576650 | ||
The arginine-rich domains present in human immunodeficiency virus type 1 Tat and Rev function as direct importin beta-dependent nuclear localization signals | Q39610897 | ||
The permeability barrier of nuclear pore complexes appears to operate via hydrophobic exclusion | Q39647313 | ||
A PY-NLS nuclear targeting signal is required for nuclear localization and function of the Saccharomyces cerevisiae mRNA-binding protein Hrp1. | Q39647788 | ||
Thyroid hormone receptor alpha1 follows a cooperative CRM1/calreticulin-mediated nuclear export pathway. | Q39959148 | ||
Severe acute respiratory syndrome coronavirus open reading frame (ORF) 3b, ORF 6, and nucleocapsid proteins function as interferon antagonists | Q40208162 | ||
Crm1 is a mitotic effector of Ran-GTP in somatic cells | Q40418909 | ||
Expanding the definition of the classical bipartite nuclear localization signal | Q41113075 | ||
Heat-stable inhibitors of cAMP-dependent protein kinase carry a nuclear export signal. | Q41408510 | ||
Snapshots of nuclear pore complexes in action captured by cryo-electron tomography | Q41624126 | ||
Processing of the precursor of NF-kappa B by the HIV-1 protease during acute infection | Q41687257 | ||
Exportin 4 mediates a novel nuclear import pathway for Sox family transcription factors | Q41879312 | ||
Severe acute respiratory syndrome coronavirus ORF6 antagonizes STAT1 function by sequestering nuclear import factors on the rough endoplasmic reticulum/Golgi membrane | Q42624738 | ||
Design of peptide inhibitors for the importin alpha/beta nuclear import pathway by activity-based profiling | Q42808317 | ||
RNA nuclear export is blocked by poliovirus 2A protease and is concomitant with nucleoporin cleavage. | Q43269551 | ||
Nucleocytoplasmic shuttling of the thyroid hormone receptor alpha | Q43552383 | ||
Stimulation of nuclear export and inhibition of nuclear import by a Ran mutant deficient in binding to Ran-binding protein 1. | Q43559962 | ||
Nuclear export of 5S rRNA-containing ribonucleoprotein complexes requires CRM1 and the RanGTPase cycle | Q44220022 | ||
Inhibition of nuclear import mediated by the Rev-arginine rich motif by RNA molecules. | Q44339479 | ||
A SOX9 defect of calmodulin-dependent nuclear import in campomelic dysplasia/autosomal sex reversal | Q44480806 | ||
Cytoplasmic localization of mitogen-activated protein kinase kinase directed by its NH2-terminal, leucine-rich short amino acid sequence, which acts as a nuclear export signal | Q45300833 | ||
The protein kinase CK2 site (Ser111/112) enhances recognition of the simian virus 40 large T-antigen nuclear localization sequence by importin | Q45762248 | ||
Binding dynamics of isolated nucleoporin repeat regions to importin-beta | Q46843299 | ||
Nanomechanical basis of selective gating by the nuclear pore complex | Q46966189 | ||
Prediction of nuclear export signals using weighted regular expressions (Wregex). | Q47681206 | ||
Nanomechanical interactions of phenylalanine-glycine nucleoporins studied by single molecule force-volume spectroscopy | Q50165583 | ||
CRM1-mediated nuclear export: to the pore and beyond. | Q50336102 | ||
SnapShot: nuclear transport. | Q51974366 | ||
A Saturated FG-Repeat Hydrogel Can Reproduce the Permeability Properties of Nuclear Pore Complexes | Q58076940 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | nucleus | Q40260 |
P304 | page(s) | 445-462 | |
P577 | publication date | 2015-02-01 | |
P1433 | published in | FEBS Journal | Q1388041 |
P1476 | title | Components and regulation of nuclear transport processes | |
P478 | volume | 282 |
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