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Karyopherin-mediated import of integral inner nuclear membrane proteins
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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/(sici)1097-0061(199807)14:10<953::aid-yea293>3.0.co;2-uopenalex-snapshot
Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1002/j.1460-2075.1987.tb04720.xopenalex-snapshot
Nucleoplasmin cDNA sequence reveals polyglutamic acid tracts and a cluster of sequences homologous to putative nuclear localization signals.
inferredcites →https://doi.org/10.1002/yea.803openalex-snapshot
SRC1: an intron‐containing yeast gene involved in sister chromatid segregation
inferredcites →https://doi.org/10.1007/s00018-003-3070-3openalex-snapshot
Nucleocytoplasmic transport: taking an inventory
inferredcites →https://doi.org/10.1016/0378-1119(95)00037-7openalex-snapshot
Yeast vectors for the controlled expression of heterologous proteins in different genetic backgrounds
inferredcites →https://doi.org/10.1016/s0092-8674(03)00082-5openalex-snapshot
Regulating Access to the Genome
inferredcites →https://doi.org/10.1016/s0092-8674(03)00986-3openalex-snapshot
Cell Cycle Regulated Transport Controlled by Alterations in the Nuclear Pore Complex
inferredcites →https://doi.org/10.1016/s0955-0674(00)00101-0openalex-snapshot
The nuclear pore complex: a protein machine bridging the nucleus and cytoplasm
inferredcites →https://doi.org/10.1016/s0959-437x(03)00058-3openalex-snapshot
The laminopathies: nuclear structure meets disease
inferredcites →https://doi.org/10.1016/s1534-5807(03)00162-xopenalex-snapshot
Peering through the Pore
inferredcites →https://doi.org/10.1021/bi052156nopenalex-snapshot
Dependence of Diffusional Mobility of Integral Inner Nuclear Membrane Proteins on A-Type Lamins
inferredcites →https://doi.org/10.1038/311033a0openalex-snapshot
Sequence requirements for nuclear location of simian virus 40 large-T antigen
inferredcites →https://doi.org/10.1038/nature00935openalex-snapshot
Functional profiling of the Saccharomyces cerevisiae genome
inferredcites →https://doi.org/10.1038/nsmb1098openalex-snapshot
Importin-α-16 is a translocon-associated protein involved in sorting membrane proteins to the nuclear envelope
inferredcites →https://doi.org/10.1073/pnas.91.15.6880openalex-snapshot
Yeast Srp1p has homology to armadillo/plakoglobin/beta-catenin and participates in apparently multiple nuclear functions including the maintenance of the nucleolar structure.
inferredcites →https://doi.org/10.1074/jbc.274.41.29031openalex-snapshot
Kap104p-mediated Nuclear Import
inferredcites →https://doi.org/10.1074/jbc.274.45.32360openalex-snapshot
The Yeast Nucleoporin Nup2p Is Involved in Nuclear Export of Importin α/Srp1p
inferredcites →https://doi.org/10.1074/jbc.m106845200openalex-snapshot
Pathways Mediating the Nuclear Import of Histones H3 and H4 in Yeast
inferredcites →https://doi.org/10.1074/jbc.m112306200openalex-snapshot
Accelerating the Rate of Disassembly of Karyopherin·Cargo Complexes
inferredcites →https://doi.org/10.1074/jbc.m212725200openalex-snapshot
Bipartite Signals Mediate Subcellular Targeting of Tail-anchored Membrane Proteins in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1083/jcb.126.3.649openalex-snapshot
Isolation and characterization of Saccharomyces cerevisiae mRNA transport-defective (mtr) mutants [published erratum appears in J Cell Biol 1994 Sep;126(6):1627]
inferredcites →https://doi.org/10.1083/jcb.130.1.15openalex-snapshot
Signals and structural features involved in integral membrane protein targeting to the inner nuclear membrane.
inferredcites →https://doi.org/10.1083/jcb.131.5.1133openalex-snapshot
Two novel related yeast nucleoporins Nup170p and Nup157p: complementation with the vertebrate homologue Nup155p and functional interactions with the yeast nuclear pore-membrane protein Pom152p.
inferredcites →https://doi.org/10.1083/jcb.133.6.1153openalex-snapshot
The yeast nucleoporin Nup188p interacts genetically and physically with the core structures of the nuclear pore complex.
inferredcites →https://doi.org/10.1083/jcb.137.4.797openalex-snapshot
A Nuclear Export Signal in Kap95p Is Required for Both Recycling the Import Factor and Interaction with the Nucleoporin GLFG Repeat Regions of Nup116p and Nup100p
inferredcites →https://doi.org/10.1083/jcb.143.7.1789openalex-snapshot
Saccharomyces cerevisiae Ndc1p Is a Shared Component of Nuclear Pore Complexes and Spindle Pole Bodies
inferredcites →https://doi.org/10.1083/jcb.143.7.1813openalex-snapshot
Specific Binding of the Karyopherin Kap121p to a Subunit of the Nuclear Pore Complex Containing Nup53p, Nup59p, and Nup170p
inferredcites →https://doi.org/10.1083/jcb.200409149openalex-snapshot
Energy- and temperature-dependent transport of integral proteins to the inner nuclear membrane via the nuclear pore
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/10.1101/gad.12.17.2673openalex-snapshot
Phosphorylation regulates association of the transcription factor Pho4 with its import receptor Pse1/Kap121
inferredcites →https://doi.org/10.1128/mcb.20.22.8468-8479.2000openalex-snapshot
Nup2p, a Yeast Nucleoporin, Functions in Bidirectional Transport of Importin α
inferredcites →https://doi.org/10.1128/mcb.22.8.2544-2555.2002openalex-snapshot
Kap121p-Mediated Nuclear Import Is Required for Mating and Cellular Differentiation in Yeast
inferredcites →https://doi.org/10.1128/mcb.23.2.534-542.2003openalex-snapshot
Binding Dynamics of Structural Nucleoporins Govern Nuclear Pore Complex Permeability and May Mediate Channel Gating
inferredcites →https://doi.org/10.1128/mmbr.65.4.570-594.2001openalex-snapshot
Transport into and out of the Nucleus
inferredcites →https://doi.org/10.1242/jcs.113.8.1471openalex-snapshot
Nup2p is located on the nuclear side of the nuclear pore complex and coordinates Srp1p/importin-α export
inferredcites →https://doi.org/10.1242/jcs.114.14.2577openalex-snapshot
Both emerin and lamin C depend on lamin A for localization at the nuclear envelope
inferredcites →https://doi.org/10.1242/jcs.115.7.1361openalex-snapshot
Intracellular trafficking of MAN1, an integral protein of the nuclear envelope inner membrane
inferredcites →https://doi.org/10.1534/genetics.105.052068openalex-snapshot
The Integral Membrane Protein Pom34p Functionally Links Nucleoporin Subcomplexes
inferredcites →https://doi.org/10.4161/cc.3.12.1316openalex-snapshot
Comparative Genomics, Evolution and Origins of the Nuclear Envelope and Nuclear Pore Complex
inferredcites →https://doi.org/10.4161/cc.3.12.1345openalex-snapshot
Ufd2, a Novel Autoantigen in Scleroderma, Regulates Sister Chromatid Separation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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The Nuclear Envelope — Structure and Protein Interactions
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Nucleoskeleton in Plants: The Functional Organization of Filaments in the Nucleus
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The Nuclear Envelope – Structure and Protein Interactions
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Nucleoskeleton in Plants: The Functional Organization of Filaments in the Nucleus
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Molecular Genetics of the Ubiquitin-Proteasome System: Lessons from Yeast
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Mechanisms of Nuclear Size Regulation in Model Systems and Cancer
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Control of Nuclear Size by NPC Proteins
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The Cell Nucleus and Its Compartments
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The Molecular Composition and Function of the Nuclear Periphery and Its Impact on the Genome
inferred← citeshttps://doi.org/10.1007/978-3-319-77309-4_5openalex-snapshot
On the Role of the Channel Nucleoporins in Nuclear Transport
inferred← citeshttps://doi.org/10.1007/978-3-319-77309-4_7openalex-snapshot
Navigating the Nuclear Envelope: One or Multiple Transport Mechanisms for Integral Membrane Proteins?
inferred← citeshttps://doi.org/10.1007/978-3-540-71058-5_2openalex-snapshot
The Plant Nuclear Envelope
inferred← citeshttps://doi.org/10.1007/s00018-012-0929-1openalex-snapshot
Many mechanisms, one entrance: membrane protein translocation into the nucleus
inferred← citeshttps://doi.org/10.1007/s00294-019-00971-1openalex-snapshot
Patrolling the nucleus: inner nuclear membrane-associated degradation
inferred← citeshttps://doi.org/10.1007/s00412-010-0289-2openalex-snapshot
Nuclear pore biogenesis into an intact nuclear envelope
inferred← citeshttps://doi.org/10.1007/s12195-016-0443-xopenalex-snapshot
On the Nuclear Pore Complex and Its Roles in Nucleo-Cytoskeletal Coupling and Mechanobiology
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?
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Macromolecular transport between the nucleus and the cytoplasm: Advances in mechanism and emerging links to disease
inferred← citeshttps://doi.org/10.1016/j.bbrep.2024.101770openalex-snapshot
Multiple types of nuclear localization signals in Entamoeba histolytica
inferred← citeshttps://doi.org/10.1016/j.biopha.2019.109127openalex-snapshot
Karyopherin β1 deletion suppresses tumor growth and metastasis in colorectal cancer (CRC) by reducing MET expression
inferred← citeshttps://doi.org/10.1016/j.bpj.2016.10.004openalex-snapshot
Shape Transformation of the Nuclear Envelope during Closed Mitosis
inferred← citeshttps://doi.org/10.1016/j.ceb.2007.04.001openalex-snapshot
Lamins and lamin-associated proteins in aging and disease
inferred← citeshttps://doi.org/10.1016/j.ceb.2008.03.016openalex-snapshot
The life cycle of the metazoan nuclear envelope
inferred← citeshttps://doi.org/10.1016/j.ceb.2011.01.002openalex-snapshot
Nuclear pore complex—a coat specifically tailored for the nuclear envelope
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.2014.01.006openalex-snapshot
Traffic to the inner membrane of the nuclear envelope
inferred← citeshttps://doi.org/10.1016/j.ceb.2015.04.005openalex-snapshot
Establishment of NE asymmetry — targeting of membrane proteins to the inner nuclear membrane
inferred← citeshttps://doi.org/10.1016/j.ceb.2020.01.011openalex-snapshot
CHMPions of repair: Emerging perspectives on sensing and repairing the nuclear envelope barrier
inferred← citeshttps://doi.org/10.1016/j.ceb.2022.102115openalex-snapshot
Making and breaking the inner nuclear membrane proteome
inferred← citeshttps://doi.org/10.1016/j.cell.2007.11.038openalex-snapshot
Architecture of a Coat for the Nuclear Pore Membrane
inferred← citeshttps://doi.org/10.1016/j.cell.2008.06.022openalex-snapshot
A Network of Nuclear Envelope Membrane Proteins Linking Centromeres to Microtubules
inferred← citeshttps://doi.org/10.1016/j.cell.2010.04.036openalex-snapshot
Cell Cycle-Dependent Differences in Nuclear Pore Complex Assembly in Metazoa
inferred← citeshttps://doi.org/10.1016/j.cell.2011.09.034openalex-snapshot
Molecular Architecture of the Transport Channel of the Nuclear Pore Complex
inferred← citeshttps://doi.org/10.1016/j.cell.2014.09.012openalex-snapshot
Surveillance of Nuclear Pore Complex Assembly by ESCRT-III/Vps4
inferred← citeshttps://doi.org/10.1016/j.cell.2016.01.034openalex-snapshot
The Nuclear Pore Complex as a Flexible and Dynamic Gate
inferred← citeshttps://doi.org/10.1016/j.cellsig.2011.11.014openalex-snapshot
Nuclear localization drives α1-adrenergic receptor oligomerization and signaling in cardiac myocytes
inferred← citeshttps://doi.org/10.1016/j.cellsig.2015.12.009openalex-snapshot
Inner nuclear membrane protein Lem2 facilitates Rad3-mediated checkpoint signaling under replication stress induced by nucleotide depletion in fission yeast
inferred← citeshttps://doi.org/10.1016/j.chroma.2010.10.090openalex-snapshot
Rapid, highly efficient extraction and purification of membrane proteins using a microfluidic continuous-flow based aqueous two-phase system
inferred← citeshttps://doi.org/10.1016/j.devcel.2009.10.007openalex-snapshot
Border Control at the Nucleus: Biogenesis and Organization of the Nuclear Membrane and Pore Complexes
inferred← citeshttps://doi.org/10.1016/j.devcel.2011.05.014openalex-snapshot
Perinuclear Cohibin Complexes Maintain Replicative Life Span via Roles at Distinct Silent Chromatin Domains
inferred← citeshttps://doi.org/10.1016/j.febslet.2008.05.001openalex-snapshot
The nuclear envelope as an integrator of nuclear and cytoplasmic architecture
inferred← citeshttps://doi.org/10.1016/j.gene.2019.100006openalex-snapshot
Identification of the evolutionarily conserved nuclear envelope proteins Lem2 and MicLem2 in Tetrahymena thermophila
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2021.02.043openalex-snapshot
The nuclear transporter importin-11 regulates the Wnt/β-catenin pathway and acts as a tumor promoter in glioma
inferred← citeshttps://doi.org/10.1016/j.molcel.2006.11.001openalex-snapshot
SV40 VP2 and VP3 Insertion into ER Membranes Is Controlled by the Capsid Protein VP1: Implications for DNA Translocation out of the ER
inferred← citeshttps://doi.org/10.1016/j.molcel.2008.04.022openalex-snapshot
Structural and Functional Studies of Nup107/Nup133 Interaction and Its Implications for the Architecture of the Nuclear Pore Complex
inferred← citeshttps://doi.org/10.1016/j.molcel.2008.12.001openalex-snapshot
A Fence-like Coat for the Nuclear Pore Membrane
inferred← citeshttps://doi.org/10.1016/j.molcel.2021.11.029openalex-snapshot
Nuclear pore complexes feel the strain
inferred← citeshttps://doi.org/10.1016/j.molcel.2023.10.015openalex-snapshot
Manipulating the 3D organization of the largest synthetic yeast chromosome
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2020.111712openalex-snapshot
Chromatin rigidity provides mechanical and genome protection
inferred← citeshttps://doi.org/10.1016/j.mrrev.2015.07.004openalex-snapshot
Genetic mutations strengthen functional association of LAP1 with DYT1 dystonia and muscular dystrophy
inferred← citeshttps://doi.org/10.1016/j.proghi.2011.04.001openalex-snapshot
Taking organelles apart, putting them back together and creating new ones: Lessons from the endoplasmic reticulum
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Lamina-associated polypeptide 1: Protein interactions and tissue-selective functions
inferred← citeshttps://doi.org/10.1016/j.semcdb.2022.02.028openalex-snapshot
Nuclear envelope assembly and dynamics during development
inferred← citeshttps://doi.org/10.1016/j.str.2008.03.007openalex-snapshot
Importin-β: Structural and Dynamic Determinants of a Molecular Spring
inferred← citeshttps://doi.org/10.1016/j.str.2015.04.017openalex-snapshot
Distinctive Properties of the Nuclear Localization Signals of Inner Nuclear Membrane Proteins Heh1 and Heh2
inferred← citeshttps://doi.org/10.1016/j.str.2019.11.003openalex-snapshot
Flexible and Extended Linker Domains Support Efficient Targeting of Heh2 to the Inner Nuclear Membrane
inferred← citeshttps://doi.org/10.1016/j.tcb.2007.02.004openalex-snapshot
Barrier-to-autointegration factor – a BAFfling little protein
inferred← citeshttps://doi.org/10.1016/j.tcb.2012.11.004openalex-snapshot
Nuclear size regulation: from single cells to development and disease
inferred← citeshttps://doi.org/10.1016/j.tcb.2013.10.006openalex-snapshot
Destination: inner nuclear membrane
inferred← citeshttps://doi.org/10.1016/j.tcb.2015.08.002openalex-snapshot
Border Safety: Quality Control at the Nuclear Envelope
inferred← citeshttps://doi.org/10.1016/j.tins.2009.04.001openalex-snapshot
Nucleocytoplasmic protein shuttling: the direct route in synapse-to-nucleus signaling
inferred← citeshttps://doi.org/10.1016/j.virol.2008.06.031openalex-snapshot
Membrane binding properties of EBV gp110 C-terminal domain; evidences for structural transition in the membrane environment
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.12.030openalex-snapshot
Centrosome attachment to the C. elegans male pronucleus is dependent on the surface area of the nuclear envelope
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.12.038openalex-snapshot
Involvement of an inner nuclear membrane protein, Nemp1, in Xenopus neural development through an interaction with the chromatin protein BAF
inferred← citeshttps://doi.org/10.1016/j.yexcr.2007.03.012openalex-snapshot
Proteins that associate with lamins: Many faces, many functions
inferred← citeshttps://doi.org/10.1016/j.yexcr.2007.03.028openalex-snapshot
“Laminopathies”: A wide spectrum of human diseases
inferred← citeshttps://doi.org/10.1021/acs.jproteome.2c00281openalex-snapshot
Shared and Distinctive Neighborhoods of Emerin and Lamin B Receptor Revealed by Proximity Labeling and Quantitative Proteomics
inferred← citeshttps://doi.org/10.1038/emboj.2010.119openalex-snapshot
A classical NLS and the SUN domain contribute to the targeting of SUN2 to the inner nuclear membrane
inferred← citeshttps://doi.org/10.1038/emboj.2011.242openalex-snapshot
Targeting of Nbp1 to the inner nuclear membrane is essential for spindle pole body duplication
inferred← citeshttps://doi.org/10.1038/nature05170openalex-snapshot
Spatially regulated ubiquitin ligation by an ER/nuclear membrane ligase
inferred← citeshttps://doi.org/10.1038/nature06170openalex-snapshot
Snapshots of nuclear pore complexes in action captured by cryo-electron tomography
inferred← citeshttps://doi.org/10.1038/nature06277openalex-snapshot
Transformation and diversification in early mammal evolution
inferred← citeshttps://doi.org/10.1038/nature06405openalex-snapshot
The molecular architecture of the nuclear pore complex
inferred← citeshttps://doi.org/10.1038/nature07460openalex-snapshot
Role for perinuclear chromosome tethering in maintenance of genome stability
inferred← citeshttps://doi.org/10.1038/ncb2076openalex-snapshot
Nuclear transport receptor goes moonlighting
inferred← citeshttps://doi.org/10.1038/ncomms8159openalex-snapshot
The tethering of chromatin to the nuclear envelope supports nuclear mechanics
inferred← citeshttps://doi.org/10.1038/nm.3669openalex-snapshot
Subcellular localization of coagulation factor II receptor-like 1 in neurons governs angiogenesis
inferred← citeshttps://doi.org/10.1038/nrm2165openalex-snapshot
Highway to the inner nuclear membrane: rules for the road
inferred← citeshttps://doi.org/10.1038/onc.2010.157openalex-snapshot
Nuclear trafficking of the epidermal growth factor receptor family membrane proteins
inferred← citeshttps://doi.org/10.1038/s41467-020-16033-xopenalex-snapshot
Nucleoplasmic signals promote directed transmembrane protein import simultaneously via multiple channels of nuclear pores
inferred← citeshttps://doi.org/10.1038/s41467-020-19885-5openalex-snapshot
Yeast Nup84-Nup133 complex structure details flexibility and reveals conservation of the membrane anchoring ALPS motif
inferred← citeshttps://doi.org/10.1038/s41467-023-39150-9openalex-snapshot
Co-translational binding of importins to nascent proteins
inferred← citeshttps://doi.org/10.1038/s41467-024-54811-zopenalex-snapshot
Seipin governs phosphatidic acid homeostasis at the inner nuclear membrane
inferred← citeshttps://doi.org/10.1038/s41467-025-67659-8openalex-snapshot
Mechanism of alternative splicing of yeast HEH1 through competing 5’ splice sites
inferred← citeshttps://doi.org/10.1038/s41580-025-00881-wopenalex-snapshot
Structure, function and assembly of nuclear pore complexes
inferred← citeshttps://doi.org/10.1038/s41598-020-75852-6openalex-snapshot
ESCRT-III controls nuclear envelope deformation induced by progerin
inferred← citeshttps://doi.org/10.1039/b703878jopenalex-snapshot
Communication between the cytoskeleton and the nuclear envelope to position the nucleus
inferred← citeshttps://doi.org/10.1042/bc20070033openalex-snapshot
Retention and mobility of the mammalian lamin B receptor in the plant nuclear envelope
inferred← citeshttps://doi.org/10.1042/bst0361373openalex-snapshot
Inner nuclear membrane protein transport is mediated by multiple mechanisms
inferred← citeshttps://doi.org/10.1042/bst0380278openalex-snapshot
Nesprin isoforms: are they inside or outside the nucleus?
inferred← citeshttps://doi.org/10.1042/bst0380307openalex-snapshot
The plant nuclear envelope in focus
inferred← citeshttps://doi.org/10.1073/pnas.0703186104openalex-snapshot
Early sorting of inner nuclear membrane proteins is conserved
inferred← citeshttps://doi.org/10.1073/pnas.0907453106openalex-snapshot
Structural and functional analysis of Nup120 suggests ring formation of the Nup84 complex
inferred← citeshttps://doi.org/10.1073/pnas.0909373106openalex-snapshot
Structure of a trimeric nucleoporin complex reveals alternate oligomerization states
inferred← citeshttps://doi.org/10.1073/pnas.1302655110openalex-snapshot
Ring cycle for dilating and constricting the nuclear pore
inferred← citeshttps://doi.org/10.1073/pnas.1613916114openalex-snapshot
LEM2 recruits CHMP7 for ESCRT-mediated nuclear envelope closure in fission yeast and human cells
inferred← citeshttps://doi.org/10.1073/pnas.1903764116openalex-snapshot
Mapping the native organization of the yeast nuclear pore complex using nuclear radial intensity measurements
inferred← citeshttps://doi.org/10.1074/jbc.m110.158659openalex-snapshot
The Translocon Sec61β Localized in the Inner Nuclear Membrane Transports Membrane-embedded EGF Receptor to the Nucleus
inferred← citeshttps://doi.org/10.1074/jbc.m110.187062openalex-snapshot
The Yeast Homolog of Heme Oxygenase-1 Affords Cellular Antioxidant Protection via the Transcriptional Regulation of Known Antioxidant Genes
inferred← citeshttps://doi.org/10.1074/jbc.m609201200openalex-snapshot
Inner Nuclear Membrane Proteins Asi1, Asi2, and Asi3 Function in Concert to Maintain the Latent Properties of Transcription Factors Stp1 and Stp2
inferred← citeshttps://doi.org/10.1074/jbc.m611094200openalex-snapshot
Cell Nuclei Spin in the Absence of Lamin B1
inferred← citeshttps://doi.org/10.1074/jbc.m802903200openalex-snapshot
An Unconventional Diacylglycerol Kinase That Regulates Phospholipid Synthesis and Nuclear Membrane Growth
inferred← citeshttps://doi.org/10.1074/jbc.m809117200openalex-snapshot
The Kap60-Kap95 Karyopherin Complex Directly Regulates Phosphatidylcholine Synthesis
inferred← citeshttps://doi.org/10.1074/mcp.m000035-mcp201openalex-snapshot
A Bimodal Distribution of Two Distinct Categories of Intrinsically Disordered Structures with Separate Functions in FG Nucleoporins
inferred← citeshttps://doi.org/10.1074/mcp.m112.026856openalex-snapshot
Identification of Importin α 7 Specific Transport Cargoes Using a Proteomic Screening Approach
inferred← citeshttps://doi.org/10.1074/mcp.m700407-mcp200openalex-snapshot
Discovering Novel Interactions at the Nuclear Pore Complex Using Bead Halo
inferred← citeshttps://doi.org/10.1080/19491034.2015.1035844openalex-snapshot
ESCRTs breach the nuclear border
inferred← citeshttps://doi.org/10.1080/21541248.2017.1282402openalex-snapshot
New insights into mechanisms of nuclear translocation of G-protein coupled receptors
inferred← citeshttps://doi.org/10.1083/jcb.200701139openalex-snapshot
A role for Rab5 in structuring the endoplasmic reticulum
inferred← citeshttps://doi.org/10.1083/jcb.200703002openalex-snapshot
An in vitro nuclear disassembly system reveals a role for the RanGTPase system and microtubule-dependent steps in nuclear envelope breakdown
inferred← citeshttps://doi.org/10.1083/jcb.200704108openalex-snapshot
Functional association of Sun1 with nuclear pore complexes
inferred← citeshttps://doi.org/10.1083/jcb.200710022openalex-snapshot
Membrane-anchored growth factor, HB-EGF, on the cell surface targeted to the inner nuclear membrane
inferred← citeshttps://doi.org/10.1083/jcb.200803098openalex-snapshot
The inner nuclear membrane protein Src1 associates with subtelomeric genes and alters their regulated gene expression
inferred← citeshttps://doi.org/10.1083/jcb.200912045openalex-snapshot
The nucleoporin Nup188 controls passage of membrane proteins across the nuclear pore complex
inferred← citeshttps://doi.org/10.1083/jcb.201007098openalex-snapshot
Pom121 links two essential subcomplexes of the nuclear pore complex core to the membrane
inferred← citeshttps://doi.org/10.1083/jcb.201009068openalex-snapshot
System analysis shows distinct mechanisms and common principles of nuclear envelope protein dynamics
inferred← citeshttps://doi.org/10.1083/jcb.201011017openalex-snapshot
Targeting of the SUN protein Mps3 to the inner nuclear membrane by the histone variant H2A.Z
inferred← citeshttps://doi.org/10.1083/jcb.201103171openalex-snapshot
Functional evolution of nuclear structure
inferred← citeshttps://doi.org/10.1083/jcb.201409127openalex-snapshot
Diffusion and retention are major determinants of protein targeting to the inner nuclear membrane
inferred← citeshttps://doi.org/10.1083/jcb.201409133openalex-snapshot
Live imaging and modeling of inner nuclear membrane targeting reveals its molecular requirements in mammalian cells
inferred← citeshttps://doi.org/10.1083/jcb.201607043openalex-snapshot
Analysis of membrane proteins localizing to the inner nuclear envelope in living cells
inferred← citeshttps://doi.org/10.1083/jcb.201808024openalex-snapshot
The anaphase-promoting complex regulates the degradation of the inner nuclear membrane protein Mps3
inferred← citeshttps://doi.org/10.1083/jcb.201910119openalex-snapshot
Cdc42 GTPase regulates ESCRTs in nuclear envelope sealing and ER remodeling
inferred← citeshttps://doi.org/10.1083/jcb.202103030openalex-snapshot
Atg39 selectively captures inner nuclear membrane into lumenal vesicles for delivery to the autophagosome
inferred← citeshttps://doi.org/10.1083/jcb.202409120openalex-snapshot
Visualizing nuclear pore complex plasticity with pan-expansion microscopy
inferred← citeshttps://doi.org/10.1091/mbc.e06-04-0292openalex-snapshot
The Unfolded Protein Response Transducer Ire1p Contains a Nuclear Localization Sequence Recognized by Multiple β Importins
inferred← citeshttps://doi.org/10.1091/mbc.e08-07-0704openalex-snapshot
Analysis of Prelamin A Biogenesis Reveals the Nucleus to be a CaaX Processing Compartment
inferred← citeshttps://doi.org/10.1091/mbc.e08-10-0987openalex-snapshot
Prm3p Is a Pheromone-induced Peripheral Nuclear Envelope Protein Required for Yeast Nuclear Fusion
inferred← citeshttps://doi.org/10.1091/mbc.e10-06-0554openalex-snapshot
Lumenal interactions in nuclear pore complex assembly and stability
inferred← citeshttps://doi.org/10.1091/mbc.e10-08-0733openalex-snapshot
Multiple mechanisms actively target the SUN protein UNC-84 to the inner nuclear membrane
inferred← citeshttps://doi.org/10.1091/mbc.e14-07-1175openalex-snapshot
Size-dependent leak of soluble and membrane proteins through the yeast nuclear pore complex
inferred← citeshttps://doi.org/10.1091/mbc.e15-03-0184openalex-snapshot
Conservation of inner nuclear membrane targeting sequences in mammalian Pom121 and yeast Heh2 membrane proteins
inferred← citeshttps://doi.org/10.1091/mbc.e16-07-0544openalex-snapshot
A mitotic nuclear envelope tether for Gle1 also affects nuclear and nucleolar architecture
inferred← citeshttps://doi.org/10.1091/mbc.e18-04-0223openalex-snapshot
Nup2 performs diverse interphase functions inAspergillus nidulans
inferred← citeshttps://doi.org/10.1091/mbc.e20-09-0584openalex-snapshot
Heh2/Man1 may be an evolutionarily conserved sensor of NPC assembly state
inferred← citeshttps://doi.org/10.1091/mbc.e22-05-0189openalex-snapshot
A role for Nup153 in nuclear assembly reveals differential requirements for targeting of nuclear envelope constituents
inferred← citeshttps://doi.org/10.1093/bib/bbn043openalex-snapshot
Facts from text: can text mining help to scale-up high-quality manual curation of gene products with ontologies?
inferred← citeshttps://doi.org/10.1093/bioinformatics/btm064openalex-snapshot
Clustering by common friends finds locally significant proteins mediating modules
inferred← citeshttps://doi.org/10.1093/femsre/fuad021openalex-snapshot
Nuclear genome organization in fungi: from gene folding to Rabl chromosomes
inferred← citeshttps://doi.org/10.1093/jb/mvad017openalex-snapshot
Inner nuclear membrane proteins Lem2 and Bqt4 interact with different lipid synthesis enzymes in fission yeast
inferred← citeshttps://doi.org/10.1093/jb/mvm219openalex-snapshot
Till Disassembly Do Us Part: A Happy Marriage of Nuclear Envelope and Chromatin
inferred← citeshttps://doi.org/10.1093/plphys/kiag415openalex-snapshot
NUP107-160 nuclear pore sub-complex members determine symbiotic ion channel localization in legumes
inferred← citeshttps://doi.org/10.1097/fjc.0000000000000165openalex-snapshot
Nuclear Compartmentalization of α1-Adrenergic Receptor Signaling in Adult Cardiac Myocytes
inferred← citeshttps://doi.org/10.1098/rstb.2011.0090openalex-snapshot
Ecology and evolution of mammalian biodiversity
inferred← citeshttps://doi.org/10.1099/vir.0.009035-0openalex-snapshot
Autographa californica multiple nucleopolyhedrovirus ORF 23 null mutant produces occlusion-derived virions with fewer nucleocapsids
inferred← citeshttps://doi.org/10.1101/049148openalex-snapshot
Chm7 and Heh1 form a nuclear envelope subdomain for nuclear pore complex quality control
inferred← citeshttps://doi.org/10.1101/049312openalex-snapshot
LEM2 recruits CHMP7 for ESCRT-mediated nuclear envelope closure in fission yeast and human cells
inferred← citeshttps://doi.org/10.1101/2020.07.11.196790openalex-snapshot
STING Promotes Breast Cancer Cell Survival by an Inflammatory-Independent Nuclear Pathway Enhancing the DNA Damage Response
inferred← citeshttps://doi.org/10.1101/2022.05.11.491529openalex-snapshot
Shared and distinctive neighborhoods of emerin and LBR revealed by proximity labeling and quantitative proteomics
inferred← citeshttps://doi.org/10.1101/451583openalex-snapshot
LEM domain proteins control the efficiency of adaptation through copy number variation
inferred← citeshttps://doi.org/10.1101/cshperspect.a000612openalex-snapshot
The Budding Yeast Nucleus
inferred← citeshttps://doi.org/10.1101/cshperspect.a041264openalex-snapshot
Structure and Function of the Nuclear Pore Complex
inferred← citeshttps://doi.org/10.1101/sqb.2010.75.004openalex-snapshot
Three-Dimensional Organization of Chromatids by Nuclear Envelope-Associated Structures
inferred← citeshttps://doi.org/10.1101/sqb.2010.75.033openalex-snapshot
The Mechanism of Nucleocytoplasmic Transport through the Nuclear Pore Complex
inferred← citeshttps://doi.org/10.1104/pp.113.220863openalex-snapshot
Nuclear Calcium Signaling in Plants
inferred← citeshttps://doi.org/10.1111/boc.201400013openalex-snapshot
Human RAD23 homolog A is required for the nuclear translocation of apoptosis‐inducing factor during induction of cell death
inferred← citeshttps://doi.org/10.1111/febs.15307openalex-snapshot
New kid on the block: lipid droplets in the nucleus
inferred← citeshttps://doi.org/10.1111/gtc.12385openalex-snapshot
Inner nuclear membrane protein Lem2 augments heterochromatin formation in response to nutritional conditions
inferred← citeshttps://doi.org/10.1111/gtc.12557openalex-snapshot
Lem2 is retained at the nuclear envelope through its interaction with Bqt4 in fission yeast
inferred← citeshttps://doi.org/10.1111/j.1365-2443.2011.01544.xopenalex-snapshot
Inner nuclear membrane protein Ima1 is dispensable for intranuclear positioning of centromeres
inferred← citeshttps://doi.org/10.1111/j.1471-4159.2006.04382.xopenalex-snapshot
Nuclear localization of functional metabotropic glutamate receptor mGlu1 in HEK293 cells and cortical neurons: role in nuclear calcium mobilization and development
inferred← citeshttps://doi.org/10.1111/j.1600-0854.2009.00956.xopenalex-snapshot
Mechanism and a Peptide Motif for Targeting Peripheral Proteins to the Yeast Inner Nuclear Membrane
inferred← citeshttps://doi.org/10.1111/j.1600-0854.2010.01060.xopenalex-snapshot
Nuclear Targeting of an Endosomal E3 Ubiquitin Ligase
inferred← citeshttps://doi.org/10.1111/j.1600-0854.2010.01119.xopenalex-snapshot
Truncated Isoforms of Kap60 Facilitate Trafficking of Heh2 to the Nuclear Envelope
inferred← citeshttps://doi.org/10.1111/j.1600-0854.2012.01341.xopenalex-snapshot
Nuclear Import of Exogenous FGF 1 Requires the ER ‐Protein LRRC 59 and the Importins Kpn α1 and Kpn β1
inferred← citeshttps://doi.org/10.1111/j.1600-0854.2012.01378.xopenalex-snapshot
Rab6‐Mediated Retrograde Transport Regulates Inner Nuclear Membrane Targeting of Caveolin‐2 in Response to Insulin
inferred← citeshttps://doi.org/10.1111/tra.12048openalex-snapshot
Quantitative Analysis of Membrane Protein Transport Across the Nuclear Pore Complex
inferred← citeshttps://doi.org/10.1124/pr.112.007203openalex-snapshot
Cardiac Alpha1-Adrenergic Receptors: Novel Aspects of Expression, Signaling Mechanisms, Physiologic Function, and Clinical Importance
inferred← citeshttps://doi.org/10.1126/science.1205741openalex-snapshot
Long Unfolded Linkers Facilitate Membrane Protein Import Through the Nuclear Pore Complex
inferred← citeshttps://doi.org/10.1126/science.abm9798openalex-snapshot
Architecture of the linker-scaffold in the nuclear pore
inferred← citeshttps://doi.org/10.1128/ec.00225-09openalex-snapshot
Flexible Gates: Dynamic Topologies and Functions for FG Nucleoporins in Nucleocytoplasmic Transport
inferred← citeshttps://doi.org/10.1128/jvi.00021-13openalex-snapshot
Mapping of Sequences in Pseudorabies Virus pUL34 That Are Required for Formation and Function of the Nuclear Egress Complex
inferred← citeshttps://doi.org/10.1128/jvi.00386-08openalex-snapshot
Glycoproteins Required for Entry Are Not Necessary for Egress of Pseudorabies Virus
inferred← citeshttps://doi.org/10.1128/jvi.00874-08openalex-snapshot
Effects of Lamin A/C, Lamin B1, and Viral U S 3 Kinase Activity on Viral Infectivity, Virion Egress, and the Targeting of Herpes Simplex Virus U L 34-Encoded Protein to the Inner Nuclear Membrane
inferred← citeshttps://doi.org/10.1128/jvi.01046-18openalex-snapshot
Influenza A Virus Utilizes Low-Affinity, High-Avidity Interactions with the Nuclear Import Machinery To Ensure Infection and Immune Evasion
inferred← citeshttps://doi.org/10.1128/jvi.01756-06openalex-snapshot
Glycoprotein M of Herpes Simplex Virus 1 Is Incorporated into Virions during Budding at the Inner Nuclear Membrane
inferred← citeshttps://doi.org/10.1128/jvi.05484-11openalex-snapshot
Structural Determinants for Nuclear Envelope Localization and Function of Pseudorabies Virus pUL34
inferred← citeshttps://doi.org/10.1128/jvi.07047-11openalex-snapshot
The Simian Virus 40 Late Viral Protein VP4 Disrupts the Nuclear Envelope for Viral Release
inferred← citeshttps://doi.org/10.1128/mcb.00482-08openalex-snapshot
A Novel Nuclear Signaling Pathway for Thromboxane A2Receptors in Oligodendrocytes: Evidence for Signaling Compartmentalization during Differentiation
inferred← citeshttps://doi.org/10.1128/mmbr.00005-16openalex-snapshot
The Epigenetic Pathways to Ribosomal DNA Silencing
inferred← citeshttps://doi.org/10.1134/s0006297907130032openalex-snapshot
Nucleocytoplasmic transport of proteins
inferred← citeshttps://doi.org/10.1134/s1990747816030156openalex-snapshot
Origin and early evolution of the nuclear envelope
inferred← citeshttps://doi.org/10.1146/annurev-biochem-031622-025802openalex-snapshot
Nucleocytoplasmic Transport
inferred← citeshttps://doi.org/10.1146/annurev-biochem-060109-151030openalex-snapshot
The Structure of the Nuclear Pore Complex
inferred← citeshttps://doi.org/10.1146/annurev-biophys-050511-102328openalex-snapshot
Functional Architecture of the Nuclear Pore Complex
inferred← citeshttps://doi.org/10.1158/0008-5472.can-07-5291openalex-snapshot
Transmembrane Protein 18 Enhances the Tropism of Neural Stem Cells for Glioma Cells
inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-08-2813openalex-snapshot
Nuclear Translocation of the Epidermal Growth Factor Receptor Family Membrane Tyrosine Kinase Receptors
inferred← citeshttps://doi.org/10.1186/1471-2121-8-47openalex-snapshot
Immobility, inheritance and plasticity of shape of the yeast nucleus
inferred← citeshttps://doi.org/10.1186/1745-6150-5-7openalex-snapshot
Origin of the cell nucleus, mitosis and sex: roles of intracellular coevolution
inferred← citeshttps://doi.org/10.1186/gb-2008-9-s2-s14openalex-snapshot
Gene mention normalization and interaction extraction with context models and sentence motifs
inferred← citeshttps://doi.org/10.1194/jlr.m800632-jlr200openalex-snapshot
Nuclear export of the rate-limiting enzyme in phosphatidylcholine synthesis is mediated by its membrane binding domain
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