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The nuclear pore complex: bridging nuclear transport and gene regulation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bies.10072openalex-snapshot
Braking the silence: How heterochromatic gene repression is stopped in its tracks
inferredcites →https://doi.org/10.1002/bies.200800159openalex-snapshot
Translocation through the nuclear pore: Kaps pave the way
inferredcites →https://doi.org/10.1006/jmbi.1999.2637openalex-snapshot
Calcium-mediated structural changes of native nuclear pore complexes monitored by time-lapse atomic force microscopy
inferredcites →https://doi.org/10.1006/jsbi.1993.1045openalex-snapshot
High-Resolution Field Emission Scanning Electron Microscope Imaging of Internal Cell Structures after Epon Extraction from Sections: A New Approach to Correlative Ultrastructural and Immunocytochemical Studies
inferredcites →https://doi.org/10.1007/s00412-002-0208-2openalex-snapshot
The evolutionarily conserved single-copy gene for murine Tpr encodes one prevalent isoform in somatic cells and lacks paralogs in higher eukaryotes
inferredcites →https://doi.org/10.1007/s00412-008-0158-4openalex-snapshot
Biogenesis of mRNPs: integrating different processes in the eukaryotic nucleus
inferredcites →https://doi.org/10.1007/s00412-008-0166-4openalex-snapshot
Quality control of mRNP in the nucleus
inferredcites →https://doi.org/10.1007/s00438-007-0301-6openalex-snapshot
Different physiological relevance of yeast THO/TREX subunits in gene expression and genome integrity
inferredcites →https://doi.org/10.1016/0092-8674(85)90177-1openalex-snapshot
Localization of DNAase I-sensitive sequences to specific regions of interphase nuclei
inferredcites →https://doi.org/10.1016/0092-8674(95)90181-7openalex-snapshot
Protein import into nuclei: association and dissociation reactions involving transport substrate, transport factors, and nucleoporins
inferredcites →https://doi.org/10.1016/0092-8674(95)90331-3openalex-snapshot
The peptide repeat domain of nucleoporin Nup98 functions as a docking site in transport across the nuclear pore complex
inferredcites →https://doi.org/10.1016/1047-8477(91)90054-zopenalex-snapshot
Toward a more complete 3-D structure of the nuclear pore complex
inferredcites →https://doi.org/10.1016/j.ceb.2004.03.013openalex-snapshot
mRNA export: an assembly line from genes to nuclear pores
inferredcites →https://doi.org/10.1016/j.ceb.2008.12.004openalex-snapshot
First and last ancestors: reconstructing evolution of the endomembrane system with ESCRTs, vesicle coat proteins, and nuclear pore complexes
inferredcites →https://doi.org/10.1016/j.ceb.2009.01.007openalex-snapshot
Transcriptional memory at the nuclear periphery
inferredcites →https://doi.org/10.1016/j.ceb.2009.05.001openalex-snapshot
Nuclear pore complex biogenesis
inferredcites →https://doi.org/10.1016/j.cell.2007.01.044openalex-snapshot
Natively Unfolded Nucleoporins Gate Protein Diffusion across the Nuclear Pore Complex
inferredcites →https://doi.org/10.1016/j.cell.2007.06.024openalex-snapshot
A Saturated FG-Repeat Hydrogel Can Reproduce the Permeability Properties of Nuclear Pore Complexes
inferredcites →https://doi.org/10.1016/j.cell.2007.10.015openalex-snapshot
SnapShot: Nuclear Transport
inferredcites →https://doi.org/10.1016/j.cell.2008.08.005openalex-snapshot
THO/Sub2p Functions to Coordinate 3′-End Processing with Gene-Nuclear Pore Association
inferredcites →https://doi.org/10.1016/j.cell.2008.08.020openalex-snapshot
Highways for mRNA Transport
inferredcites →https://doi.org/10.1016/j.cell.2009.01.048openalex-snapshot
Viral RNAs: Lessons from the Enemy
inferredcites →https://doi.org/10.1016/j.cell.2009.12.054openalex-snapshot
Chromatin-Bound Nuclear Pore Components Regulate Gene Expression in Higher Eukaryotes
inferredcites →https://doi.org/10.1016/j.cell.2010.01.011openalex-snapshot
Nucleoporins Directly Stimulate Expression of Developmental and Cell-Cycle Genes Inside the Nucleoplasm
inferredcites →https://doi.org/10.1016/j.devcel.2007.03.018openalex-snapshot
SUN1 Is Required for Telomere Attachment to Nuclear Envelope and Gametogenesis in Mice
inferredcites →https://doi.org/10.1016/j.dnarep.2007.06.004openalex-snapshot
Stimulation of in vitro sumoylation by Slx5–Slx8: Evidence for a functional interaction with the SUMO pathway
inferredcites →https://doi.org/10.1016/j.febslet.2007.11.087openalex-snapshot
The nucleoporin Nup358 associates with and regulates interphase microtubules
inferredcites →https://doi.org/10.1016/j.febslet.2008.03.038openalex-snapshot
Regulation of mRNP dynamics along the export pathway
inferredcites →https://doi.org/10.1016/j.gde.2009.01.006openalex-snapshot
The nuclear envelope — a scaffold for silencing?
inferredcites →https://doi.org/10.1016/j.jsb.2003.11.010openalex-snapshot
Yeast nuclear pore complexes have a cytoplasmic ring and internal filaments
inferredcites →https://doi.org/10.1016/j.molcel.2005.12.012openalex-snapshot
Nup-PI: The Nucleopore-Promoter Interaction of Genes in Yeast
inferredcites →https://doi.org/10.1016/j.molcel.2007.01.016openalex-snapshot
Ratcheting mRNA out of the Nucleus
inferredcites →https://doi.org/10.1016/j.molcel.2009.01.033openalex-snapshot
Sus1, Cdc31, and the Sac3 CID Region Form a Conserved Interaction Platform that Promotes Nuclear Pore Association and mRNA Export
inferredcites →https://doi.org/10.1016/j.sbi.2009.02.009openalex-snapshot
Structural analysis of the nuclear pore complex by integrated approaches
inferredcites →https://doi.org/10.1016/j.str.2008.12.021openalex-snapshot
Transport-Related Structures and Processes of the Nuclear Pore Complex Studied through Molecular Dynamics
inferredcites →https://doi.org/10.1016/j.str.2009.07.014openalex-snapshot
The Nuclear Pore Complex Has Entered the Atomic Age
inferredcites →https://doi.org/10.1016/j.tcb.2003.10.007openalex-snapshot
Virtual gating and nuclear transport: the hole picture
inferredcites →https://doi.org/10.1016/j.tibs.2008.07.003openalex-snapshot
The exosome: a multipurpose RNA-decay machine
inferredcites →https://doi.org/10.1016/j.yexcr.2006.01.013openalex-snapshot
In situ SUMOylation analysis reveals a modulatory role of RanBP2 in the nuclear rim and PML bodies
inferredcites →https://doi.org/10.1016/j.yexcr.2009.10.016openalex-snapshot
Exclusion of mRNPs and ribosomal particles from a thin zone beneath the nuclear envelope revealed upon inhibition of transport
inferredcites →https://doi.org/10.1016/s0006-3495(90)82381-xopenalex-snapshot
Visualization of transport-related configurations of the nuclear pore transporter
inferredcites →https://doi.org/10.1016/s0092-8674(00)00014-3openalex-snapshot
Structural Basis for the Interaction between FxFG Nucleoporin Repeats and Importin-β in Nuclear Trafficking
inferredcites →https://doi.org/10.1016/s0092-8674(00)81900-5openalex-snapshot
A Look at Messenger RNP Moving through the Nuclear Pore
inferredcites →https://doi.org/10.1016/s0092-8674(02)00756-0openalex-snapshot
Chromatin Boundaries in Budding Yeast
inferredcites →https://doi.org/10.1016/s0092-8674(03)01026-2openalex-snapshot
Nuclear Retention of Unspliced mRNAs in Yeast Is Mediated by Perinuclear Mlp1
inferredcites →https://doi.org/10.1016/s0092-8674(03)01079-1openalex-snapshot
The Mechanisms of Vesicle Budding and Fusion
inferredcites →https://doi.org/10.1016/s0921-8777(00)00071-9openalex-snapshot
Controlling the efficiency of excision repair
inferredcites →https://doi.org/10.1016/s0962-8924(01)02144-4openalex-snapshot
Nucleocytoplasmic transport: Ran, beta and beyond
inferredcites →https://doi.org/10.1016/s1534-5807(03)00162-xopenalex-snapshot
Peering through the Pore
inferredcites →https://doi.org/10.1038/29100openalex-snapshot
Perinuclear localization of chromatin facilitates transcriptional silencing
inferredcites →https://doi.org/10.1038/emboj.2009.200openalex-snapshot
Characterisation of the passive permeability barrier of nuclear pore complexes
inferredcites →https://doi.org/10.1038/emboj.2010.54openalex-snapshot
Protein Tpr is required for establishing nuclear pore‐associated zones of heterochromatin exclusion
inferredcites →https://doi.org/10.1038/embor.2009.29openalex-snapshot
RANBP2 is an allosteric activator of the conventional kinesin‐1 motor protein, KIF5B, in a minimal cell‐free system
inferredcites →https://doi.org/10.1038/nature03588openalex-snapshot
Insights into E3 ligase activity revealed by a SUMO–RanGAP1–Ubc9–Nup358 complex
inferredcites →https://doi.org/10.1038/nature04752openalex-snapshot
SAGA interacting factors confine sub-diffusion of transcribed genes to the nuclear envelope
inferredcites →https://doi.org/10.1038/nature04845openalex-snapshot
Nuclear pore association confers optimal expression levels for an inducible yeast gene
inferredcites →https://doi.org/10.1038/nature06170openalex-snapshot
Snapshots of nuclear pore complexes in action captured by cryo-electron tomography
inferredcites →https://doi.org/10.1038/nature06404openalex-snapshot
Determining the architectures of macromolecular assemblies
inferredcites →https://doi.org/10.1038/nature06405openalex-snapshot
The molecular architecture of the nuclear pore complex
inferredcites →https://doi.org/10.1038/nature07460openalex-snapshot
Role for perinuclear chromosome tethering in maintenance of genome stability
inferredcites →https://doi.org/10.1038/nature07600openalex-snapshot
Artificial nanopores that mimic the transport selectivity of the nuclear pore complex
inferredcites →https://doi.org/10.1038/ncb1097openalex-snapshot
Minimal nuclear pore complexes define FG repeat domains essential for transport
inferredcites →https://doi.org/10.1038/ncb1604openalex-snapshot
Molecular basis for the functional interaction of dynein light chain with the nuclear-pore complex
inferredcites →https://doi.org/10.1038/ncb1733openalex-snapshot
Yeast Ataxin-7 links histone deubiquitination with gene gating and mRNA export
inferredcites →https://doi.org/10.1038/ncb1910openalex-snapshot
The DNA damage response at eroded telomeres and tethering to the nuclear pore complex
inferredcites →https://doi.org/10.1038/ncb2011openalex-snapshot
DNA zip codes control an ancient mechanism for gene targeting to the nuclear periphery
inferredcites →https://doi.org/10.1038/newbio240163a0openalex-snapshot
Nuclear Pore Complexes: “Press-Stud” Elements of Chromosomes in Pairing and Control
inferredcites →https://doi.org/10.1038/nrg2122openalex-snapshot
The nuclear envelope and transcriptional control
inferredcites →https://doi.org/10.1038/nrm2114openalex-snapshot
Molecular mechanism of the nuclear protein import cycle
inferredcites →https://doi.org/10.1038/nrm2255openalex-snapshot
Exporting RNA from the nucleus to the cytoplasm
inferredcites →https://doi.org/10.1038/nrm2641openalex-snapshot
Orchestrating nuclear envelope disassembly and reassembly during mitosis
inferredcites →https://doi.org/10.1038/nsmb1324openalex-snapshot
Gene regulation through nuclear organization
inferredcites →https://doi.org/10.1038/sj.emboj.7600482openalex-snapshot
Proteomic analysis identifies a new complex required for nuclear pre‐mRNA retention and splicing
inferredcites →https://doi.org/10.1038/sj.emboj.7600527openalex-snapshot
Perinuclear Mlp proteins downregulate gene expression in response to a defect in mRNA export
inferredcites →https://doi.org/10.1038/sj.emboj.7601901openalex-snapshot
SAGA and a novel Drosophila export complex anchor efficient transcription and mRNA export to NPC
inferredcites →https://doi.org/10.1042/bst0361368openalex-snapshot
KASH-domain proteins and the cytoskeletal landscapes of the nuclear envelope
inferredcites →https://doi.org/10.1073/pnas.0437902100openalex-snapshot
Disorder in the nuclear pore complex: The FG repeat regions of nucleoporins are natively unfolded
inferredcites →https://doi.org/10.1073/pnas.0500537102openalex-snapshot
A SUMO ligase is part of a nuclear multiprotein complex that affects DNA repair and chromosomal organization
inferredcites →https://doi.org/10.1073/pnas.0506345103openalex-snapshot
Simple fold composition and modular architecture of the nuclear pore complex
inferredcites →https://doi.org/10.1073/pnas.0603521103openalex-snapshot
Flexible phenylalanine-glycine nucleoporins as entropic barriers to nucleocytoplasmic transport
inferredcites →https://doi.org/10.1073/pnas.0910163107openalex-snapshot
Amyloid-like interactions within nucleoporin FG hydrogels
inferredcites →https://doi.org/10.1073/pnas.96.17.9622openalex-snapshot
The direction of transport through the nuclear pore can be inverted
inferredcites →https://doi.org/10.1074/jbc.270.23.14209openalex-snapshot
Nup358, a Cytoplasmically Exposed Nucleoporin with Peptide Repeats, Ran-GTP Binding Sites, Zinc Fingers, a Cyclophilin A Homologous Domain, and a Leucine-rich Region
inferredcites →https://doi.org/10.1074/jbc.c300522200openalex-snapshot
Differential Export Requirements for Shuttling Serine/Arginine-type mRNA-binding Proteins
inferredcites →https://doi.org/10.1074/jbc.m109.070839openalex-snapshot
Structural Basis for the Interaction between Yeast Spt-Ada-Gcn5 Acetyltransferase (SAGA) Complex Components Sgf11 and Sus1
inferredcites →https://doi.org/10.1074/jbc.m110.105890openalex-snapshot
Nucleoporin Translocated Promoter Region (Tpr) Associates with Dynein Complex, Preventing Chromosome Lagging Formation during Mitosis
inferredcites →https://doi.org/10.1074/jbc.m608741200openalex-snapshot
Actively Transcribed GAL Genes Can Be Physically Linked to the Nuclear Pore by the SAGA Chromatin Modifying Complex
inferredcites →https://doi.org/10.1074/jbc.m704054200openalex-snapshot
HSF1-TPR Interaction Facilitates Export of Stress-induced HSP70 mRNA
inferredcites →https://doi.org/10.1074/jbc.m900502200openalex-snapshot
Mutational Uncoupling of the Role of Sus1 in Nuclear Pore Complex Targeting of an mRNA Export Complex and Histone H2B Deubiquitination
inferredcites →https://doi.org/10.1074/mcp.m600309-mcp200openalex-snapshot
Rapid Evolution Exposes the Boundaries of Domain Structure and Function in Natively Unfolded FG Nucleoporins
inferredcites →https://doi.org/10.1074/mcp.m900038-mcp200openalex-snapshot
Evidence for a Shared Nuclear Pore Complex Architecture That Is Conserved from the Last Common Eukaryotic Ancestor
inferredcites →https://doi.org/10.1083/jcb.109.3.971openalex-snapshot
Protein import through the nuclear pore complex is a multistep process.
inferredcites →https://doi.org/10.1083/jcb.119.6.1429openalex-snapshot
High resolution scanning electron microscopy of the nuclear envelope: demonstration of a new, regular, fibrous lattice attached to the baskets of the nucleoplasmic face of the nuclear pores.
inferredcites →https://doi.org/10.1083/jcb.127.6.1515openalex-snapshot
Tpr, a large coiled coil protein whose amino terminus is involved in activation of oncogenic kinases, is localized to the cytoplasmic surface of the nuclear pore complex.
inferredcites →https://doi.org/10.1083/jcb.136.3.515openalex-snapshot
Identification of Protein p270/Tpr as a Constitutive Component of the Nuclear Pore Complex–attached Intranuclear Filaments
inferredcites →https://doi.org/10.1083/jcb.140.3.499openalex-snapshot
SUMO-1 Modification and Its Role in Targeting the Ran GTPase-activating Protein, RanGAP1, to the Nuclear Pore Complex
inferredcites →https://doi.org/10.1083/jcb.144.5.839openalex-snapshot
Proteins Connecting the Nuclear Pore Complex with the Nuclear Interior
inferredcites →https://doi.org/10.1083/jcb.145.4.645openalex-snapshot
A Role for RanBP1 in the Release of CRM1 from the Nuclear Pore Complex in a Terminal Step of Nuclear Export
inferredcites →https://doi.org/10.1083/jcb.152.2.411openalex-snapshot
Gradient of Increasing Affinity of Importin β for Nucleoporins along the Pathway of Nuclear Import
inferredcites →https://doi.org/10.1083/jcb.200106046openalex-snapshot
Tpr is localized within the nuclear basket of the pore complex and has a role in nuclear protein export
inferredcites →https://doi.org/10.1083/jcb.200205068openalex-snapshot
The yeast nuclear pore complex functionally interacts with components of the spindle assembly checkpoint
inferredcites →https://doi.org/10.1083/jcb.200206106openalex-snapshot
Proteomic analysis of the mammalian nuclear pore complex
inferredcites →https://doi.org/10.1083/jcb.200208169openalex-snapshot
Mps3p is a novel component of the yeast spindle pole body that interacts with the yeast centrin homologue Cdc31p
inferredcites →https://doi.org/10.1083/jcb.200308100openalex-snapshot
Spindle checkpoint proteins and chromosome–microtubule attachment in budding yeast
inferredcites →https://doi.org/10.1083/jcb.200405168openalex-snapshot
Mlp-dependent anchorage and stabilization of a desumoylating enzyme is required to prevent clonal lethality
inferredcites →https://doi.org/10.1083/jcb.200504140openalex-snapshot
The nuclear pore complex–associated protein, Mlp2p, binds to the yeast spindle pole body and promotes its efficient assembly
inferredcites →https://doi.org/10.1083/jcb.200505159openalex-snapshot
Telomere tethering at the nuclear periphery is essential for efficient DNA double strand break repair in subtelomeric region
inferredcites →https://doi.org/10.1083/jcb.200509061openalex-snapshot
The mobile nucleoporin Nup2p and chromatin-bound Prp20p function in endogenous NPC-mediated transcriptional control
inferredcites →https://doi.org/10.1083/jcb.200608141openalex-snapshot
Simple kinetic relationships and nonspecific competition govern nuclear import rates in vivo
inferredcites →https://doi.org/10.1083/jcb.200702154openalex-snapshot
A nuclear envelope protein linking nuclear pore basket assembly, SUMO protease regulation, and mRNA surveillance
inferredcites →https://doi.org/10.1083/jcb.200704108openalex-snapshot
Functional association of Sun1 with nuclear pore complexes
inferredcites →https://doi.org/10.1083/jcb.200803098openalex-snapshot
The inner nuclear membrane protein Src1 associates with subtelomeric genes and alters their regulated gene expression
inferredcites →https://doi.org/10.1083/jcb.200804098openalex-snapshot
The nuclear export factor Xpo1p targets Mad1p to kinetochores in yeast
inferredcites →https://doi.org/10.1083/jcb.200810029openalex-snapshot
The nucleoporins Nup170p and Nup157p are essential for nuclear pore complex assembly
inferredcites →https://doi.org/10.1083/jcb.200810059openalex-snapshot
Sem1 is a functional component of the nuclear pore complex–associated messenger RNA export machinery
inferredcites →https://doi.org/10.1083/jcb.200811012openalex-snapshot
Spatiotemporal control of mitosis by the conserved spindle matrix protein Megator
inferredcites →https://doi.org/10.1091/mbc.12.8.2433openalex-snapshot
Amino Acid Substitutions of Coiled-Coil Protein Tpr Abrogate Anchorage to the Nuclear Pore Complex but Not Parallel, In-Register Homodimerization
inferredcites →https://doi.org/10.1091/mbc.e04-03-0165openalex-snapshot
Nucleoporins as Components of the Nuclear Pore Complex Core Structure and Tpr as the Architectural Element of the Nuclear Basket
inferredcites →https://doi.org/10.1091/mbc.e04-07-0579openalex-snapshot
Megator, an Essential Coiled-Coil Protein that Localizes to the Putative Spindle Matrix during Mitosis inDrosophila
inferredcites →https://doi.org/10.1091/mbc.e05-01-0011openalex-snapshot
Interactions between Mad1p and the Nuclear Transport Machinery in the YeastSaccharomyces cerevisiae
inferredcites →https://doi.org/10.1091/mbc.e05-08-0715openalex-snapshot
Nup153 Affects Entry of Messenger and Ribosomal Ribonucleoproteins into the Nuclear Basket during Export
inferredcites →https://doi.org/10.1091/mbc.e07-02-0123openalex-snapshot
Nucleoporins Prevent DNA Damage Accumulation by Modulating Ulp1-dependent Sumoylation Processes
inferredcites →https://doi.org/10.1091/mbc.e07-11-1162openalex-snapshot
In Vivo Dynamics of Drosophila Nuclear Envelope Components
inferredcites →https://doi.org/10.1091/mbc.e08-08-0878openalex-snapshot
Mlp1 Acts as a Mitotic Scaffold to Spatially Regulate Spindle Assembly Checkpoint Proteins inAspergillus nidulans
inferredcites →https://doi.org/10.1093/carcin/bgp081openalex-snapshot
Enhanced genomic instabilities caused by deregulated microtubule dynamics and chromosome segregation: a perspective from genetic studies in mice
inferredcites →https://doi.org/10.1093/emboj/18.15.4332openalex-snapshot
Dbp5, a DEAD‐box protein required for mRNA export, is recruited to the cytoplasmic fibrils of nuclear pore complex via a conserved interaction with CAN/Nup159p
inferredcites →https://doi.org/10.1093/emboj/21.11.2664openalex-snapshot
The permeability barrier of nuclear pore complexes appears to operate via hydrophobic exclusion
inferredcites →https://doi.org/10.1093/emboj/21.3.387openalex-snapshot
Modular self‐assembly of a Y‐shaped multiprotein complex from seven nucleoporins
inferredcites →https://doi.org/10.1093/emboj/cdf335openalex-snapshot
The yeast THO complex and mRNA export factors link RNA metabolism with transcription and genome instability
inferredcites →https://doi.org/10.1093/genetics/162.2.603openalex-snapshot
Transcription and Double-Strand Breaks Induce Similar Mitotic Recombination Events in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1093/nar/gkm373openalex-snapshot
A new connection of mRNP biogenesis and export with transcription-coupled repair
inferredcites →https://doi.org/10.1101/gad.1307205openalex-snapshot
Developmentally induced changes in transcriptional program alter spatial organization across chromosomes
inferredcites →https://doi.org/10.1101/gad.1419506openalex-snapshot
The locus control region is required for association of the murine β-globin locus with engaged transcription factories during erythroid maturation
inferredcites →https://doi.org/10.1101/gad.1506607openalex-snapshot
SWI/SNF is required for transcriptional memory at the yeast GAL gene cluster
inferredcites →https://doi.org/10.1101/gad.1677208openalex-snapshot
Tpr directly binds to Mad1 and Mad2 and is important for the Mad1–Mad2-mediated mitotic spindle checkpoint
inferredcites →https://doi.org/10.1101/gad.1782209openalex-snapshot
Mechanisms that regulate localization of a DNA double-strand break to the nuclear periphery
inferredcites →https://doi.org/10.1101/gad.1787509openalex-snapshot
Yeast telomerase and the SUN domain protein Mps3 anchor telomeres and repress subtelomeric recombination
inferredcites →https://doi.org/10.1101/gad.1805309openalex-snapshot
Life on the edge: telomeres and persistent DNA breaks converge at the nuclear periphery: Figure 1.
inferredcites →https://doi.org/10.1101/gad.1823209openalex-snapshot
Gene loops function to maintain transcriptional memory through interaction with the nuclear pore complex
inferredcites →https://doi.org/10.1105/tpc.106.049239openalex-snapshot
NUCLEAR PORE ANCHOR, theArabidopsisHomolog of Tpr/Mlp1/Mlp2/Megator, Is Involved in mRNA Export and SUMO Homeostasis and Affects Diverse Aspects of Plant Development
inferredcites →https://doi.org/10.1111/j.1462-5822.2005.00679.xopenalex-snapshot
Viral interactions with the cytoskeleton: a hitchhiker's guide to the cell
inferredcites →https://doi.org/10.1111/j.1600-0854.2005.00270.xopenalex-snapshot
Mechanisms of Receptor‐Mediated Nuclear Import and Nuclear Export
inferredcites →https://doi.org/10.1111/j.1600-0854.2007.00564.xopenalex-snapshot
A Microtubule‐Facilitated Nuclear Import Pathway for Cancer Regulatory Proteins
inferredcites →https://doi.org/10.1111/j.1600-0854.2009.00944.xopenalex-snapshot
Messenger RNA Export from the Nucleus: A Series of Molecular Wardrobe Changes
inferredcites →https://doi.org/10.1126/science.1068768openalex-snapshot
Subnuclear Compartmentalization of Immunoglobulin Loci During Lymphocyte Development
inferredcites →https://doi.org/10.1126/science.1124196openalex-snapshot
Nuclear Pores Form de Novo from Both Sides of the Nuclear Envelope
inferredcites →https://doi.org/10.1126/science.1132516openalex-snapshot
FG-Rich Repeats of Nuclear Pore Proteins Form a Three-Dimensional Meshwork with Hydrogel-Like Properties
inferredcites →https://doi.org/10.1126/science.1145980openalex-snapshot
Nanomechanical Basis of Selective Gating by the Nuclear Pore Complex
inferredcites →https://doi.org/10.1126/science.1162790openalex-snapshot
Functional Targeting of DNA Damage to a Nuclear Pore-Associated SUMO-Dependent Ubiquitin Ligase
inferredcites →https://doi.org/10.1126/science.1181369openalex-snapshot
Comprehensive Mapping of Long-Range Interactions Reveals Folding Principles of the Human Genome
inferredcites →https://doi.org/10.1128/ec.00225-09openalex-snapshot
Flexible Gates: Dynamic Topologies and Functions for FG Nucleoporins in Nucleocytoplasmic Transport
inferredcites →https://doi.org/10.1128/mcb.00870-06openalex-snapshot
Cotranscriptional Recruitment to the mRNA Export Receptor Mex67p Contributes to Nuclear Pore Anchoring of Activated Genes
inferredcites →https://doi.org/10.1128/mcb.01675-09openalex-snapshot
Dominant Role for Signal Transduction in the Transcriptional Memory of Yeast GAL Genes
inferredcites →https://doi.org/10.1128/mmbr.65.4.570-594.2001openalex-snapshot
Transport into and out of the Nucleus
inferredcites →https://doi.org/10.1139/o08-101openalex-snapshot
The molecular basis of chromatin dynamics during nucleotide excision repairThis paper is one of a selection of papers published in this Special Issue, entitled 29th Annual International Asilomar Chromatin and Chromosomes Conference, and has undergone the Journal’s usual peer review process.
inferredcites →https://doi.org/10.1186/1471-2121-6-32openalex-snapshot
Crosstalk between the actin cytoskeleton and Ran-mediated nuclear transport
inferredcites →https://doi.org/10.1242/jcs.040154openalex-snapshot
The nuclear pore component Nup358 promotes transportin-dependent nuclear import
inferredcites →https://doi.org/10.1242/jcs.110.8.927openalex-snapshot
A Drosophila Tpr protein homolog is localized both in the extrachromosomal channel network and to nuclear pore complexes
inferredcites →https://doi.org/10.1242/jcs.111.2.223openalex-snapshot
Active nuclear pore complexes in Chironomus: visualization of transporter configurations related to mRNP export
inferredcites →https://doi.org/10.1261/rna.764108openalex-snapshot
Sus1, Sac3, and Thp1 mediate post-transcriptional tethering of active genes to the nuclear rim as well as to non-nascent mRNP
inferredcites →https://doi.org/10.1371/journal.pbio.0020342openalex-snapshot
Gene Recruitment of the Activated INO1 Locus to the Nuclear Membrane
inferredcites →https://doi.org/10.1371/journal.pbio.0020380openalex-snapshot
Components of Coated Vesicles and Nuclear Pore Complexes Share a Common Molecular Architecture
inferredcites →https://doi.org/10.1371/journal.pbio.0050081openalex-snapshot
H2A.Z-Mediated Localization of Genes at the Nuclear Periphery Confers Epigenetic Memory of Previous Transcriptional State
inferredcites →https://doi.org/10.1371/journal.pbio.1000008openalex-snapshot
An Endoribonuclease Functionally Linked to Perinuclear mRNP Quality Control Associates with the Nuclear Pore Complexes
inferredcites →https://doi.org/10.1371/journal.pcbi.0030125openalex-snapshot
Efficiency, Selectivity, and Robustness of Nucleocytoplasmic Transport
inferredcites →https://doi.org/10.1371/journal.pcbi.1000145openalex-snapshot
Intramolecular Cohesion of Coils Mediated by Phenylalanine–Glycine Motifs in the Natively Unfolded Domain of a Nucleoporin
inferredcites →https://doi.org/10.1371/journal.pgen.1000364openalex-snapshot
Genome-Wide Analysis of Factors Affecting Transcription Elongation and DNA Repair: A New Role for PAF and Ccr4-Not in Transcription-Coupled Repair
inferredcites →https://doi.org/10.1371/journal.pgen.1000846openalex-snapshot
Nuclear Pore Proteins Nup153 and Megator Define Transcriptionally Active Regions in the Drosophila Genome
inferredcites →https://doi.org/10.4161/cc.3.12.1345openalex-snapshot
Ufd2, a Novel Autoantigen in Scleroderma, Regulates Sister Chromatid Separation
inferredcites →https://doi.org/10.4161/cc.9.1.10317openalex-snapshot
Opening the DNA repair toolbox: Localization of DNA double strand breaks to the nuclear periphery
inferredcites →https://doi.org/10.4161/rna.6.3.8330openalex-snapshot
Mechanisms of nuclear mRNA quality control
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Recessive NUP54 Variants Underlie Early‐Onset Dystonia with Striatal Lesions
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Passive permeability and effective pore size of HeLa cell nuclear membranes
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Functional Droplet Interface Bilayers
inferred← citeshttps://doi.org/10.1007/978-3-662-46430-4_22openalex-snapshot
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Large-Scale Nuclear Architecture and Transcriptional Control
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Coordinating Replication with Transcription
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Transport and Communication Across the Nuclear Envelope
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Molecular Mechanisms Defining the Structural Basis for Self-Association of the FUS Low-Complexity Domain
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Phosphoproteomics of colon cancer metastasis: comparative mass spectrometric analysis of the isogenic primary and metastatic cell lines SW480 and SW620
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Nucleoporin Nup98 participates in flowering regulation in a CONSTANS-independent mode
inferred← citeshttps://doi.org/10.1007/s00412-010-0289-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00412-010-0298-1openalex-snapshot
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Autophagy as a consequence of seasonal functions of testis and epididymis in adult male European bison (Bison bonasus, Linnaeus 1758)
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Oncoprotein SET dynamically regulates cellular stress response through nucleocytoplasmic transport in breast cancer
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The mRNA export pathway in plants
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Physical model of the nuclear membrane permeability mechanism
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Proteomics: A tool to decipher cold tolerance
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Phenotypic evolution of cancer cells: structural requirements for survival
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Transcription and Epigenetic Regulation
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Regulation of Nucleocytoplasmic Transport in Skeletal Muscle
inferred← citeshttps://doi.org/10.1016/b978-0-12-394310-1.00003-5openalex-snapshot
Effect of Viral Infection on the Nuclear Envelope and Nuclear Pore Complex
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Cilia and Flagella
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Analysis of DEAD-Box Proteins in mRNA Export
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Epigenetic gene regulation and stem cell function
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The Nuclear Lamina and Genome Organization
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Transcription and Epigenetic Regulation
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Nucleoporins in Retroviral Replication
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Known types of membrane-less organelles and biomolecular condensates
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MicroRNA turnover and nuclear function
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Nuclear transport protein suppresses Tau neurodegeneration
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Nuclear Envelope and Chromatin, Lock and Key of Genome Integrity
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The Multifaceted Contributions of Chromatin to HIV-1 Integration, Transcription, and Latency
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Loss of Nuclear Envelope Integrity in Aging and Disease
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Biallelic Mutations in Nuclear Pore Complex Subunit NUP107 Cause Early-Childhood-Onset Steroid-Resistant Nephrotic Syndrome
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Distinct Gene Expression Profiles Define Anaplastic Grade in Retinoblastoma
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Nucleocytoplasmic transport under stress conditions and its role in HSP70 chaperone systems
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2011.12.001openalex-snapshot
mRNA export and the TREX complex
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2011.12.006openalex-snapshot
Ubiquitin and assembly of export competent mRNP
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2011.12.010openalex-snapshot
Nuclear organization and chromatin dynamics in yeast: Biophysical models or biologically driven interactions?
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2012.01.015openalex-snapshot
Regulated nucleocytoplasmic transport during gametogenesis
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2012.02.011openalex-snapshot
To the pore and through the pore: A story of mRNA export kinetics
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2011.03.008openalex-snapshot
Expression of nucleocytoplasmic transport machinery: Clues to regulation of spermatogenic development
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2013.09.003openalex-snapshot
Werner complex deficiency in cells disrupts the Nuclear Pore Complex and the distribution of lamin B1
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.12.128openalex-snapshot
Characterization of the ptr5 gene involved in nuclear mRNA export in fission yeast
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.04.042openalex-snapshot
Leptomycin B alters the subcellular distribution of CRM1 (Exportin 1)
inferred← citeshttps://doi.org/10.1016/j.bbrep.2015.03.003openalex-snapshot
Intrinsically disordered proteins in the nucleus of human cells
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Multiple types of nuclear localization signals in Entamoeba histolytica
inferred← citeshttps://doi.org/10.1016/j.bpj.2011.01.061openalex-snapshot
Biophysical Coarse-Grained Modeling Provides Insights into Transport through the Nuclear Pore Complex
inferred← citeshttps://doi.org/10.1016/j.bpj.2018.05.034openalex-snapshot
Enhanced Nucleocytoplasmic Transport due to Competition for Elastic Binding Sites
inferred← citeshttps://doi.org/10.1016/j.bpj.2019.11.026openalex-snapshot
Bound-State Diffusion due to Binding to Flexible Polymers in a Selective Biofilter
inferred← citeshttps://doi.org/10.1016/j.bpj.2024.08.024openalex-snapshot
C9orf72 polyPR interaction with the nuclear pore complex
inferred← citeshttps://doi.org/10.1016/j.cbpa.2013.04.027openalex-snapshot
Visualizing molecular diffusion through passive permeability barriers in cells: conventional and novel approaches
inferred← citeshttps://doi.org/10.1016/j.ceb.2011.12.013openalex-snapshot
A jumbo problem: mapping the structure and functions of the nuclear pore complex
inferred← citeshttps://doi.org/10.1016/j.ceb.2012.01.009openalex-snapshot
Trafficking to uncharted territory of the nuclear envelope
inferred← citeshttps://doi.org/10.1016/j.ceb.2014.02.001openalex-snapshot
The multifunctional nuclear pore complex: a platform for controlling gene expression
inferred← citeshttps://doi.org/10.1016/j.ceb.2019.01.002openalex-snapshot
Poring over chromosomes: mitotic nuclear pore complex segregation
inferred← citeshttps://doi.org/10.1016/j.cell.2012.02.058openalex-snapshot
Hikeshi, a Nuclear Import Carrier for Hsp70s, Protects Cells from Heat Shock-Induced Nuclear Damage
inferred← citeshttps://doi.org/10.1016/j.cell.2014.01.010openalex-snapshot
Nuclear Pores Protect Genome Integrity by Assembling a Premitotic and Mad1-Dependent Anaphase Inhibitor
inferred← citeshttps://doi.org/10.1016/j.cell.2015.10.069openalex-snapshot
Gene Essentiality Is a Quantitative Property Linked to Cellular Evolvability
inferred← citeshttps://doi.org/10.1016/j.cell.2016.07.042openalex-snapshot
Nuclear Pore Permeabilization Is a Convergent Signaling Event in Effector-Triggered Immunity
inferred← citeshttps://doi.org/10.1016/j.cell.2017.08.048openalex-snapshot
Structure of FUS Protein Fibrils and Its Relevance to Self-Assembly and Phase Separation of Low-Complexity Domains
inferred← citeshttps://doi.org/10.1016/j.cell.2017.09.033openalex-snapshot
Natively Unfolded FG Repeats Stabilize the Structure of the Nuclear Pore Complex
inferred← citeshttps://doi.org/10.1016/j.cell.2021.12.015openalex-snapshot
Comprehensive structure and functional adaptations of the yeast nuclear pore complex
inferred← citeshttps://doi.org/10.1016/j.cell.2024.07.020openalex-snapshot
The molecular architecture of the nuclear basket
inferred← citeshttps://doi.org/10.1016/j.cell.2025.07.025openalex-snapshot
The small GTPase Ran defines nuclear pore complex asymmetry
inferred← citeshttps://doi.org/10.1016/j.celrep.2012.07.007openalex-snapshot
The Oncogene eIF4E Reprograms the Nuclear Pore Complex to Promote mRNA Export and Oncogenic Transformation
inferred← citeshttps://doi.org/10.1016/j.celrep.2013.10.013openalex-snapshot
High-Frequency Promoter Firing Links THO Complex Function to Heavy Chromatin Formation
inferred← citeshttps://doi.org/10.1016/j.celrep.2014.08.021openalex-snapshot
Telomerase RNA TLC1 Shuttling to the Cytoplasm Requires mRNA Export Factors and Is Important for Telomere Maintenance
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2025.144145openalex-snapshot
Exposure to environmentally relevant levels of DEHP during development modifies the distribution and expression patterns of androgen receptors in the anterior pituitary in a sex-specific manner
inferred← citeshttps://doi.org/10.1016/j.chom.2016.10.004openalex-snapshot
A Herpesvirus Protein Selectively Inhibits Cellular mRNA Nuclear Export
inferred← citeshttps://doi.org/10.1016/j.cirep.2024.200148openalex-snapshot
Nucleoporin 43 inhibits NF-κB pathway by targeting TRAF6 in miiuy croaker, Miichthys miiuy
inferred← citeshttps://doi.org/10.1016/j.cis.2016.05.012openalex-snapshot
Protein intrinsic disorder-based liquid–liquid phase transitions in biological systems: Complex coacervates and membrane-less organelles
inferred← citeshttps://doi.org/10.1016/j.crmeth.2022.100357openalex-snapshot
Protein fluorescent labeling in live yeast cells using scFv-based probes
inferred← citeshttps://doi.org/10.1016/j.cub.2012.08.043openalex-snapshot
Nuclear Transport: Shifting Gears in Fungal Nuclear and Cytoplasmic Organization
inferred← citeshttps://doi.org/10.1016/j.cub.2012.10.026openalex-snapshot
Evolution of Gene Regulation: Hybrid Networks Breed Diversity
inferred← citeshttps://doi.org/10.1016/j.cub.2012.10.037openalex-snapshot
Nuclear Transport: Beginning to Gel?
inferred← citeshttps://doi.org/10.1016/j.cub.2014.08.012openalex-snapshot
An Assay for Clogging the Ciliary Pore Complex Distinguishes Mechanisms of Cytosolic and Membrane Protein Entry
inferred← citeshttps://doi.org/10.1016/j.devcel.2011.11.021openalex-snapshot
A Change in Nuclear Pore Complex Composition Regulates Cell Differentiation
inferred← citeshttps://doi.org/10.1016/j.devcel.2015.02.017openalex-snapshot
Nuclear Pore Basket Proteins Are Tethered to the Nuclear Envelope and Can Regulate Membrane Curvature
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.08.006openalex-snapshot
A Nucleoporin Docks Protein Phosphatase 1 to Direct Meiotic Chromosome Segregation and Nuclear Assembly
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.01.002openalex-snapshot
Nucleoporin Seh1 controls murine neocortical development via transcriptional repression of p21 in neural stem cells
inferred← citeshttps://doi.org/10.1016/j.ejcb.2011.04.004openalex-snapshot
Lighting up the nuclear pore complex
inferred← citeshttps://doi.org/10.1016/j.febslet.2015.09.008openalex-snapshot
Crystal structure of human nuclear pore complex component NUP43
inferred← citeshttps://doi.org/10.1016/j.gde.2025.102375openalex-snapshot
The Yin and Yang of replicative aging and rejuvenation
inferred← citeshttps://doi.org/10.1016/j.gim.2025.101555openalex-snapshot
Pathogenic XPO1 variants cause a dominant neurodevelopmental disorder
inferred← citeshttps://doi.org/10.1016/j.jbc.2026.113343openalex-snapshot
O-GlcNAcylation is a mitochondrial-nuclear signal that regulates passive transport through the nuclear pore complex
inferred← citeshttps://doi.org/10.1016/j.jmb.2016.03.015openalex-snapshot
The Structure Inventory of the Nuclear Pore Complex
inferred← citeshttps://doi.org/10.1016/j.jmbbm.2025.107247openalex-snapshot
Mechanical force sensitive pioneer transcription factors and super-enhancers
inferred← citeshttps://doi.org/10.1016/j.jsb.2010.09.015openalex-snapshot
Conformational dynamics of supramolecular protein assemblies
inferred← citeshttps://doi.org/10.1016/j.jsb.2011.11.006openalex-snapshot
Nuclear transport of baculovirus: Revealing the nuclear pore complex passage
inferred← citeshttps://doi.org/10.1016/j.mce.2023.112009openalex-snapshot
Androgen receptor nucleocytoplasmic trafficking – A one-way journey
inferred← citeshttps://doi.org/10.1016/j.molbiopara.2016.07.008openalex-snapshot
The nuclear envelope and gene organization in parasitic protozoa: Specializations associated with disease
inferred← citeshttps://doi.org/10.1016/j.molcel.2012.09.020openalex-snapshot
Nuclear Pore Component Nup98 Is a Potential Tumor Suppressor and Regulates Posttranscriptional Expression of Select p53 Target Genes
inferred← citeshttps://doi.org/10.1016/j.molcel.2013.08.001openalex-snapshot
Integral Nuclear Pore Proteins Bind to Pol III-Transcribed Genes and Are Required for Pol III Transcript Processing in C. elegans
inferred← citeshttps://doi.org/10.1016/j.molcel.2025.08.035openalex-snapshot
The nuclear pore complex connects energy sensing to transcriptional plasticity in longevity
inferred← citeshttps://doi.org/10.1016/j.nano.2017.02.006openalex-snapshot
Regulation of human GDNF gene expression in nigral dopaminergic neurons using a new doxycycline-regulated NTS-polyplex nanoparticle system
inferred← citeshttps://doi.org/10.1016/j.neuron.2017.03.032openalex-snapshot
Huntington’s Disease: Nuclear Gatekeepers Under Attack
inferred← citeshttps://doi.org/10.1016/j.patter.2025.101262openalex-snapshot
Discovering the nuclear localization signal universe through a deep learning model with interpretable attention units
inferred← citeshttps://doi.org/10.1016/j.pbi.2020.10.006openalex-snapshot
Structural and functional insight into the nuclear pore complex and nuclear transport receptors in plant stress signaling
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112545openalex-snapshot
FERONIA interacts with NPL4 to regulate immunity gene mRNA nucleocytoplasmic transport in response to plant immunity
inferred← citeshttps://doi.org/10.1016/j.prp.2020.152836openalex-snapshot
NUP37 silencing induces inhibition of cell proliferation, G1 phase cell cycle arrest and apoptosis in non-small cell lung cancer cells
inferred← citeshttps://doi.org/10.1016/j.resmic.2011.01.014openalex-snapshot
Nuclear architecture, genome and chromatin organisation in Trypanosoma brucei
inferred← citeshttps://doi.org/10.1016/j.sbi.2014.06.001openalex-snapshot
Different subunits belonging to the same protein complex often exhibit discordant expression levels and evolutionary properties
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.05.004openalex-snapshot
The functional versatility of the nuclear pore complex proteins
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.05.021openalex-snapshot
Structural dynamics of the nuclear pore complex
inferred← citeshttps://doi.org/10.1016/j.str.2010.09.005openalex-snapshot
The NPC-Transporter, A Ghost in the Machine
inferred← citeshttps://doi.org/10.1016/j.str.2012.03.008openalex-snapshot
Solution Structure of the ESCRT-I and -II Supercomplex: Implications for Membrane Budding and Scission
inferred← citeshttps://doi.org/10.1016/j.str.2012.03.025openalex-snapshot
The Human Nuclear Pore Complex as Revealed by Cryo-Electron Tomography
inferred← citeshttps://doi.org/10.1016/j.talanta.2024.127367openalex-snapshot
Outer-surface covering of nanochannels with hydrogel for anti-protein-interference on the ion current
inferred← citeshttps://doi.org/10.1016/j.talanta.2026.129380openalex-snapshot
Amperometric ion-selective nanoelectrodes for bioanalytical sensing and imaging
inferred← citeshttps://doi.org/10.1016/j.tcb.2011.06.002openalex-snapshot
Biological hydrogels as selective diffusion barriers
inferred← citeshttps://doi.org/10.1016/j.tcb.2013.03.004openalex-snapshot
Aiding and abetting cancer: mRNA export and the nuclear pore
inferred← citeshttps://doi.org/10.1016/j.tcb.2015.10.004openalex-snapshot
Super-Resolution Microscopy: From Single Molecules to Supramolecular Assemblies
inferred← citeshttps://doi.org/10.1016/j.tcb.2022.02.006openalex-snapshot
Integrating mechanical signals into cellular identity
inferred← citeshttps://doi.org/10.1016/j.urolonc.2022.05.019openalex-snapshot
Up-regulation of POM121 is linked to prostate cancer aggressiveness and serves as a prognostic biomarker
inferred← citeshttps://doi.org/10.1016/j.virusres.2013.09.003openalex-snapshot
New insights in the role of nucleoporins: A bridge leading to concerted steps from HIV-1 nuclear entry until integration
inferred← citeshttps://doi.org/10.1016/j.xcrp.2024.102111openalex-snapshot
Nanoimaging of SARS-CoV-2 viral invasion toward the nucleus and genome
inferred← citeshttps://doi.org/10.1017/cbo9781139012751.010openalex-snapshot
Dynamic network models of protein complexes
inferred← citeshttps://doi.org/10.1021/ac403607sopenalex-snapshot
Ion Permeability of the Nuclear Pore Complex and Ion-Induced Macromolecular Permeation as Studied by Scanning Electrochemical and Fluorescence Microscopy
inferred← citeshttps://doi.org/10.1021/acs.analchem.2c03076openalex-snapshot
Quantitative Structural Proteomics Unveils the Conformational Changes of Proteins under the Endoplasmic Reticulum Stress
inferred← citeshttps://doi.org/10.1021/acs.analchem.2c04216openalex-snapshot
Inner Wall and Outer Surface Distinguished Solid-State Nanopores for Sensing
inferred← citeshttps://doi.org/10.1021/acs.analchem.9b00796openalex-snapshot
Probing High Permeability of Nuclear Pore Complexes by Scanning Electrochemical Microscopy: Ca2+ Effects on Transport Barriers
inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.5b00694openalex-snapshot
Acridine Orange Conjugated Polymersomes for Simultaneous Nuclear Delivery of Gemcitabine and Doxorubicin to Pancreatic Cancer Cells
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00667openalex-snapshot
Single-Molecule Localization Microscopy in Eukaryotes
inferred← citeshttps://doi.org/10.1021/acs.macromol.4c01092openalex-snapshot
Electrophoretic Translocation of Star-Shaped Polymers through Single Solid-State Nanopores
inferred← citeshttps://doi.org/10.1021/acs.nanolett.3c00743openalex-snapshot
Molecular Recognition in Confined Space Elucidated with DNA Nanopores and Single-Molecule Force Microscopy
inferred← citeshttps://doi.org/10.1021/acs.nanolett.3c00852openalex-snapshot
Investigating Uncertainties in Single-Molecule Localization Microscopy Using Experimentally Informed Monte Carlo Simulation
inferred← citeshttps://doi.org/10.1021/acsami.8b18288openalex-snapshot
Antisense Oligonucleotide-Conjugated Nanostructure-Targeting lncRNA MALAT1 Inhibits Cancer Metastasis
inferred← citeshttps://doi.org/10.1021/acschembio.4c00833openalex-snapshot
Chemically Induced Nuclear Pore Complex Protein Degradation via TRIM21
inferred← citeshttps://doi.org/10.1021/acschembio.9b00606openalex-snapshot
Leveraging New Definitions of the LxVP SLiM To Discover Novel Calcineurin Regulators and Substrates
inferred← citeshttps://doi.org/10.1021/acsmacrolett.1c00740openalex-snapshot
Design and Synthesis of Shikimoylated-Polypeptides for Nuclear Specific Internalization
inferred← citeshttps://doi.org/10.1021/acsnano.5c05817openalex-snapshot
Bimodal Mechanical Response of Membrane Necks: Implications for the Nuclear Envelope
inferred← citeshttps://doi.org/10.1021/am503045bopenalex-snapshot
Cell-Imprinted Substrates Act as an Artificial Niche for Skin Regeneration
inferred← citeshttps://doi.org/10.1021/ja311080jopenalex-snapshot
Nanoscale Mechanism of Molecular Transport through the Nuclear Pore Complex As Studied by Scanning Electrochemical Microscopy
inferred← citeshttps://doi.org/10.1021/jacs.1c05550openalex-snapshot
DNA-Origami NanoTrap for Studying the Selective Barriers Formed by Phenylalanine-Glycine-Rich Nucleoporins
inferred← citeshttps://doi.org/10.1021/jacsau.5c00774openalex-snapshot
Molecular Interactions within Nanoconfinement of Model DNA Nanostructures Controlled by Compensatory Kinetics as Revealed by Single-Molecule Fluorescence Analysis
inferred← citeshttps://doi.org/10.1038/emboj.2011.109openalex-snapshot
A novel assay identifies transcript elongation roles for the Nup84 complex and RNA processing factors
inferred← citeshttps://doi.org/10.1038/leu.2017.62openalex-snapshot
MLL is essential for NUP98-HOXA9-induced leukemia
inferred← citeshttps://doi.org/10.1038/nbt.2281openalex-snapshot
Tandem fluorescent protein timers for in vivo analysis of protein dynamics
inferred← citeshttps://doi.org/10.1038/ncb2450openalex-snapshot
A size-exclusion permeability barrier and nucleoporins characterize a ciliary pore complex that regulates transport into cilia
inferred← citeshttps://doi.org/10.1038/ncomms6978openalex-snapshot
RNA export factor Ddx19 is required for nuclear import of the SRF coactivator MKL1
inferred← citeshttps://doi.org/10.1038/ncomms9882openalex-snapshot
Combining Spinach-tagged RNA and gene localization to image gene expression in live yeast
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