On the public citation graph

The SUN Protein Mps3 Is Required for Spindle Pole Body Insertion into the Nuclear Membrane and Nuclear Envelope Homeostasis

https://doi.org/10.1371/journal.pgen.1002365
0 signed · 186 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

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/10.1002/1097-0061(20000630)16:9<811::aid-yea579>3.0.co;2-8openalex-snapshot
Mutational analysis of the karmellae-inducing signal in Hmg1p, a yeast HMG-CoA reductase isozyme
inferredcites →https://doi.org/10.1002/emmm.200900051openalex-snapshot
Neurodegenerative diseases: Lessons from genome‐wide screens in small model organisms
inferredcites →https://doi.org/10.1002/yea.1130openalex-snapshot
Optimized cassettes for fluorescent protein tagging in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1006/abio.2001.5178openalex-snapshot
Quantitative Analysis and Molecular Species Fingerprinting of Triacylglyceride Molecular Species Directly from Lipid Extracts of Biological Samples by Electrospray Ionization Tandem Mass Spectrometry
inferredcites →https://doi.org/10.1007/bf02537824openalex-snapshot
Cloning of the late genes in the ergosterol biosynthetic pathway ofSaccharomyces cerevisiae—A review
inferredcites →https://doi.org/10.1007/s00018-008-8713-yopenalex-snapshot
SUN-domain and KASH-domain proteins during development, meiosis and disease
inferredcites →https://doi.org/10.1007/s00438-003-0938-8openalex-snapshot
Two-hybrid search for proteins that interact with Sad1 and Kms1, two membrane-bound components of the spindle pole body in fission yeast
inferredcites →https://doi.org/10.1016/0968-0004(90)90281-fopenalex-snapshot
The P-loop — a common motif in ATP- and GTP-binding proteins
inferredcites →https://doi.org/10.1016/j.bbaexp.2005.09.005openalex-snapshot
Stable incorporation of sequence specific repressors Ash1 and Ume6 into the Rpd3L complex
inferredcites →https://doi.org/10.1016/j.bbalip.2006.05.003openalex-snapshot
Yeast acyl-CoA synthetases at the crossroads of fatty acid metabolism and regulation
inferredcites →https://doi.org/10.1016/j.bbamcr.2008.09.001openalex-snapshot
Sun1 forms immobile macromolecular assemblies at the nuclear envelope
inferredcites →https://doi.org/10.1016/j.bbrc.2007.12.014openalex-snapshot
Characters of very ancient proteins
inferredcites →https://doi.org/10.1016/j.cell.2008.04.047openalex-snapshot
Rapid Telomere Movement in Meiotic Prophase Is Promoted By NDJ1, MPS3, and CSM4 and Is Modulated by Recombination
inferredcites →https://doi.org/10.1016/j.cell.2008.04.050openalex-snapshot
Meiotic Chromosomes Move by Linkage to Dynamic Actin Cables with Transduction of Force through the Nuclear Envelope
inferredcites →https://doi.org/10.1016/j.cell.2010.04.036openalex-snapshot
Cell Cycle-Dependent Differences in Nuclear Pore Complex Assembly in Metazoa
inferredcites →https://doi.org/10.1016/j.devcel.2009.10.018openalex-snapshot
Nuclei Take a Position: Managing Nuclear Location
inferredcites →https://doi.org/10.1016/j.devcel.2011.05.014openalex-snapshot
Perinuclear Cohibin Complexes Maintain Replicative Life Span via Roles at Distinct Silent Chromatin Domains
inferredcites →https://doi.org/10.1016/j.ejcb.2009.06.003openalex-snapshot
Dictyostelium Sun1 is a dynamic membrane protein of both nuclear membranes and required for centrosomal association with clustered centromeres
inferredcites →https://doi.org/10.1016/j.febslet.2009.10.022openalex-snapshot
Amphipathic helices and membrane curvature
inferredcites →https://doi.org/10.1016/j.phytochem.2006.06.005openalex-snapshot
Quantitative profiling of polar glycerolipid species from organs of wild-type Arabidopsis and a PHOSPHOLIPASE Dα1 knockout mutant
inferredcites →https://doi.org/10.1016/j.tins.2008.07.004openalex-snapshot
Polyglutamine neurodegeneration: protein misfolding revisited
inferredcites →https://doi.org/10.1016/s0021-9258(17)34014-0openalex-snapshot
Biochemical studies of three Saccharomyces cerevisiae acyl-CoA synthetases, Faa1p, Faa2p, and Faa3p.
inferredcites →https://doi.org/10.1016/s0092-8674(00)80295-0openalex-snapshot
The Yeast Spindle Pole Body Is Assembled around a Central Crystal of Spc42p
inferredcites →https://doi.org/10.1038/emboj.2011.242openalex-snapshot
Targeting of Nbp1 to the inner nuclear membrane is essential for spindle pole body duplication
inferredcites →https://doi.org/10.1038/emboj.2011.267openalex-snapshot
Ribosome biogenesis factors bind a nuclear envelope SUN domain protein to cluster yeast telomeres
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/nmeth.1181openalex-snapshot
A systematic library for comprehensive overexpression screens in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1038/nrm1784openalex-snapshot
How proteins produce cellular membrane curvature
inferredcites →https://doi.org/10.1038/nrm2928openalex-snapshot
The nuclear pore complex: bridging nuclear transport and gene regulation
inferredcites →https://doi.org/10.1038/nrmicro1839openalex-snapshot
Membrane lipid homeostasis in bacteria
inferredcites →https://doi.org/10.1038/nsmb1194openalex-snapshot
A general amphipathic α-helical motif for sensing membrane curvature
inferredcites →https://doi.org/10.1038/sj.emboj.7600672openalex-snapshot
The yeast lipin Smp2 couples phospholipid biosynthesis to nuclear membrane growth
inferredcites →https://doi.org/10.1042/bj20070449openalex-snapshot
DGA1 (diacylglycerol acyltransferase gene) overexpression and leucine biosynthesis significantly increase lipid accumulation in the Δsnf2 disruptant of Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1042/bj20080923openalex-snapshot
Metabolic control of transcription: paradigms and lessons from Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1073/pnas.0606165104openalex-snapshot
MPS3 mediates meiotic bouquet formation in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1073/pnas.0812037106openalex-snapshot
SUN1 and SUN2 play critical but partially redundant roles in anchoring nuclei in skeletal muscle cells in mice
inferredcites →https://doi.org/10.1074/jbc.273.29.18210openalex-snapshot
Disruption of the Saccharomyces cerevisiae FAT1 Gene Decreases Very Long-chain Fatty Acyl-CoA Synthetase Activity and Elevates Intracellular Very Long-chain Fatty Acid Concentrations
inferredcites →https://doi.org/10.1074/jbc.274.8.4671openalex-snapshot
The Saccharomyces cerevisiae FAT1 Gene Encodes an Acyl-CoA Synthetase That Is Required for Maintenance of Very Long Chain Fatty Acid Levels
inferredcites →https://doi.org/10.1074/jbc.m205375200openalex-snapshot
Profiling Membrane Lipids in Plant Stress Responses
inferredcites →https://doi.org/10.1074/jbc.m210934200openalex-snapshot
Nep98p Is a Component of the Yeast Spindle Pole Body and Essential for Nuclear Division and Fusion
inferredcites →https://doi.org/10.1074/jbc.m404324200openalex-snapshot
The Spindle Pole Body Assembly Component Mps3p/Nep98p Functions in Sister Chromatid Cohesion
inferredcites →https://doi.org/10.1074/jbc.m606654200openalex-snapshot
Control of Phospholipid Synthesis by Phosphorylation of the Yeast Lipin Pah1p/Smp2p Mg2+-dependent Phosphatidate Phosphatase
inferredcites →https://doi.org/10.1083/jcb.107.1.101openalex-snapshot
Increased amounts of HMG-CoA reductase induce "karmellae": a proliferation of stacked membrane pairs surrounding the yeast nucleus.
inferredcites →https://doi.org/10.1083/jcb.114.4.745openalex-snapshot
MPS1 and MPS2: novel yeast genes defining distinct steps of spindle pole body duplication.
inferredcites →https://doi.org/10.1083/jcb.122.4.743openalex-snapshot
NDC1: a nuclear periphery component required for yeast spindle pole body duplication
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.132.5.887openalex-snapshot
Spc42p: a phosphorylated component of the S. cerevisiae spindle pole body (SPD) with an essential function during SPB duplication.
inferredcites →https://doi.org/10.1083/jcb.134.4.949openalex-snapshot
Aberrant mitosis in fission yeast mutants defective in fatty acid synthetase and acetyl CoA carboxylase.
inferredcites →https://doi.org/10.1083/jcb.134.5.1141openalex-snapshot
Targeting and function in mRNA export of nuclear pore complex protein Nup153.
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.148.5.883openalex-snapshot
In Vitro Formation of the Endoplasmic Reticulum Occurs Independently of Microtubules by a Controlled Fusion Reaction
inferredcites →https://doi.org/10.1083/jcb.153.4.709openalex-snapshot
A Link between the Synthesis of Nucleoporins and the Biogenesis of the Nuclear Envelope
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.200509124openalex-snapshot
Coupling of the nucleus and cytoplasm: Role of the LINC complex
inferredcites →https://doi.org/10.1083/jcb.200601062openalex-snapshot
The Sad1-UNC-84 homology domain in Mps3 interacts with Mps2 to connect the spindle pole body with the nuclear envelope
inferredcites →https://doi.org/10.1083/jcb.200702120openalex-snapshot
The yeast integral membrane protein Apq12 potentially links membrane dynamics to assembly of nuclear pore complexes
inferredcites →https://doi.org/10.1083/jcb.200704108openalex-snapshot
Functional association of Sun1 with nuclear pore complexes
inferredcites →https://doi.org/10.1083/jcb.200706040openalex-snapshot
Telomere anchoring at the nuclear periphery requires the budding yeast Sad1-UNC-84 domain protein Mps3
inferredcites →https://doi.org/10.1083/jcb.200806174openalex-snapshot
ER membrane–bending proteins are necessary for de novo nuclear pore formation
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.200810030openalex-snapshot
Role of the Ndc1 interaction network in yeast nuclear pore complex assembly and maintenance
inferredcites →https://doi.org/10.1083/jcb.200902101openalex-snapshot
A ZYG-12–dynein interaction at the nuclear envelope defines cytoskeletal architecture in the C. elegans gonad
inferredcites →https://doi.org/10.1083/jcb.200906068openalex-snapshot
Bringing KASH under the SUN: the many faces of nucleo-cytoskeletal connections
inferredcites →https://doi.org/10.1083/jcb.200910043openalex-snapshot
Pom33, a novel transmembrane nucleoporin required for proper nuclear pore complex distribution
inferredcites →https://doi.org/10.1083/jcb.201011017openalex-snapshot
Targeting of the SUN protein Mps3 to the inner nuclear membrane by the histone variant H2A.Z
inferredcites →https://doi.org/10.1083/jcb.201012154openalex-snapshot
POM121 and Sun1 play a role in early steps of interphase NPC assembly
inferredcites →https://doi.org/10.1091/mbc.6.11.1535openalex-snapshot
Identification of the sequences in HMG-CoA reductase required for karmellae assembly.
inferredcites →https://doi.org/10.1091/mbc.7.5.769openalex-snapshot
Different subcellular localization of Saccharomyces cerevisiae HMG-CoA reductase isozymes at elevated levels corresponds to distinct endoplasmic reticulum membrane proliferations.
inferredcites →https://doi.org/10.1091/mbc.8.11.2119openalex-snapshot
Nuclear Pore Complex Number and Distribution throughout the Saccharomyces cerevisiae Cell Cycle by Three-Dimensional Reconstruction from Electron Micrographs of Nuclear Envelopes
inferredcites →https://doi.org/10.1091/mbc.9.10.2803openalex-snapshot
A Late Mitotic Regulatory Network Controlling Cyclin Destruction inSaccharomyces cerevisiae
inferredcites →https://doi.org/10.1091/mbc.e04-08-0703openalex-snapshot
Analysis of a Spindle Pole Body Mutant Reveals a Defect in Biorientation and Illuminates Spindle Forces
inferredcites →https://doi.org/10.1091/mbc.e05-07-0668openalex-snapshot
TheSaccharomyces cerevisiaeSpindle Pole Body (SPB) Component Nbp1p Is Required for SPB Membrane Insertion and Interacts with the Integral Membrane Proteins Ndc1p and Mps2p
inferredcites →https://doi.org/10.1091/mbc.e05-09-0839openalex-snapshot
Yeast Nuclear Envelope Subdomains with Distinct Abilities to Resist Membrane Expansion
inferredcites →https://doi.org/10.1091/mbc.e09-07-0555openalex-snapshot
Structural Mutants of the Spindle Pole Body Cause Distinct Alteration of Cytoplasmic Microtubules and Nuclear Dynamics in Multinucleated Hyphae
inferredcites →https://doi.org/10.1093/emboj/17.22.6449openalex-snapshot
A novel complex of membrane proteins required for formation of a spherical nucleus
inferredcites →https://doi.org/10.1093/emboj/19.3.421openalex-snapshot
The Bbp1p–Mps2p complex connects the SPB to the nuclear envelope and is essential for SPB duplication
inferredcites →https://doi.org/10.1093/genetics/137.1.55openalex-snapshot
Isolation and characterization of a mutant of Saccharomyces cerevisiae with pleiotropic deficiencies in transcriptional activation and repression.
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.524209openalex-snapshot
The SESA network links duplication of the yeast centrosome with the protein translation machinery
inferredcites →https://doi.org/10.1104/pp.115.3.875openalex-snapshot
Membrane Fluidity and Temperature Perception
inferredcites →https://doi.org/10.1126/science.1180823openalex-snapshot
The Genetic Landscape of a Cell
inferredcites →https://doi.org/10.1126/science.273.5277.953openalex-snapshot
Activation of the Budding Yeast Spindle Assembly Checkpoint Without Mitotic Spindle Disruption
inferredcites →https://doi.org/10.1126/science.6547247openalex-snapshot
Allylamine Derivatives: New Class of Synthetic Antifungal Agents Inhibiting Fungal Squalene Epoxidase
inferredcites →https://doi.org/10.1128/ec.3.2.447-458.2004openalex-snapshot
A Novel Allele of Saccharomyces cerevisiae NDC1 Reveals a Potential Role for the Spindle Pole Body Component Ndc1p in Nuclear Pore Assembly
inferredcites →https://doi.org/10.1128/jb.124.1.511-523.1975openalex-snapshot
Behavior of spindles and spindle plaques in the cell cycle and conjugation of Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1128/mcb.16.12.7161openalex-snapshot
A Yeast Acetyl Coenzyme A Carboxylase Mutant Links Very-Long-Chain Fatty Acid Synthesis to the Structure and Function of the Nuclear Membrane-Pore Complex
inferredcites →https://doi.org/10.1128/mcb.24.23.10479-10491.2004openalex-snapshot
Yeast Shuttling SR Proteins Npl3p, Gbp2p, and Hrb1p Are Part of the Translating mRNPs, and Npl3p Can Function as a Translational Repressor
inferredcites →https://doi.org/10.1128/mcb.26.10.3738-3751.2006openalex-snapshot
SUN1 Interacts with Nuclear Lamin A and Cytoplasmic Nesprins To Provide a Physical Connection between the Nuclear Lamina and the Cytoskeleton
inferredcites →https://doi.org/10.1146/annurev-cellbio-100109-104037openalex-snapshot
Interactions Between Nuclei and the Cytoskeleton Are Mediated by SUN-KASH Nuclear-Envelope Bridges
inferredcites →https://doi.org/10.1146/annurev.biophys.093008.131357openalex-snapshot
Lipids and Cholesterol as Regulators of Traffic in the Endomembrane System
inferredcites →https://doi.org/10.1146/annurev.cellbio.20.022003.114106openalex-snapshot
THE BUDDING YEAST SPINDLE POLE BODY: Structure, Duplication, and Function
inferredcites →https://doi.org/10.1186/1471-2121-8-47openalex-snapshot
Immobility, inheritance and plasticity of shape of the yeast nucleus
inferredcites →https://doi.org/10.1242/dev.126.14.3171openalex-snapshot
UNC-84 localizes to the nuclear envelope and is required for nuclear migration and anchoring during C. elegans development
inferredcites →https://doi.org/10.1242/jcs.01528openalex-snapshot
Intranuclear membrane structure formations by CaaX-containing nuclear proteins
inferredcites →https://doi.org/10.1242/jcs.055046openalex-snapshot
Integral membrane proteins Brr6 and Apq12 link assembly of the nuclear pore complex to lipid homeostasis in the endoplasmic reticulum
inferredcites →https://doi.org/10.1371/journal.pone.0015426openalex-snapshot
Identification of Saccharomyces cerevisiae Spindle Pole Body Remodeling Factors
inferredcites →https://doi.org/10.1534/genetics.110.119149openalex-snapshot
Changes in the Nuclear Envelope Environment Affect Spindle Pole Body Duplication in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.4161/cc.6.1.3647openalex-snapshot
The Nuclear Envelope and Spindle Pole Body-Associated Mps3 Protein Bind Telomere Regulators and Function in Telomere Clustering

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4162077openalex-extracted
A Membrane Sensing Mechanism Couples Local Lipid Metabolism to Protein Degradation at the Inner Nuclear Membrane
inferred← citeshttps://doi.org/10.1002/9781118492833.ch17openalex-snapshot
Size Scaling of Subcellular Organelles and Structures inXenopus laevisandXenopus tropicalis
inferred← citeshttps://doi.org/10.1002/jcb.24178openalex-snapshot
Shaping the nucleus: Factors and forces
inferred← citeshttps://doi.org/10.1002/jcp.25355openalex-snapshot
The Malleable Nature of the Budding Yeast Nuclear Envelope: Flares, Fusion, and Fenestrations
inferred← citeshttps://doi.org/10.1007/978-1-4899-8032-8_25openalex-snapshot
Mechanisms of Nuclear Size Regulation in Model Systems and Cancer
inferred← citeshttps://doi.org/10.1007/978-3-642-41566-1_2openalex-snapshot
Subnuclear Architecture of Telomeres and Subtelomeres in Yeast
inferred← citeshttps://doi.org/10.1007/s00294-017-0699-2openalex-snapshot
Position matters: multiple functions of LINC-dependent chromosome positioning during meiosis
inferred← citeshttps://doi.org/10.1007/s00294-021-01176-1openalex-snapshot
The challenge of staying in shape: nuclear size matters
inferred← citeshttps://doi.org/10.1007/s00412-013-0417-xopenalex-snapshot
The diverse functional LINCs of the nuclear envelope to the cytoskeleton and chromatin
inferred← citeshttps://doi.org/10.1016/b978-0-12-397920-9.00004-4openalex-snapshot
LINC Complex Proteins in Development and Disease
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2015.03.001openalex-snapshot
Nuclear Envelope and Chromatin, Lock and Key of Genome Integrity
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2015.11.001openalex-snapshot
New Insights into Mechanisms and Functions of Nuclear Size Regulation
inferred← citeshttps://doi.org/10.1016/j.biochi.2024.08.002openalex-snapshot
Behind the stoNE wall: A fervent activity for nuclear lipids
inferred← citeshttps://doi.org/10.1016/j.ceb.2012.09.001openalex-snapshot
Remodeling the nuclear membrane during closed mitosis
inferred← citeshttps://doi.org/10.1016/j.ceb.2013.08.002openalex-snapshot
Breaking down the wall: the nuclear envelope during mitosis
inferred← citeshttps://doi.org/10.1016/j.ceb.2014.01.003openalex-snapshot
Sizing and shaping the nucleus: mechanisms and significance
inferred← citeshttps://doi.org/10.1016/j.ceb.2016.03.016openalex-snapshot
Mixing and matching nuclear envelope remodeling and spindle assembly strategies in the evolution of mitosis
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.10.021openalex-snapshot
Mitotic Nuclear Envelope Breakdown and Spindle Nucleation Are Controlled by Interphase Contacts between Centromeres and the Nuclear Envelope
inferred← citeshttps://doi.org/10.1016/j.dnarep.2025.103903openalex-snapshot
Overcoming natural replication barriers formed by DNA structures and the role of repositioning to the nuclear periphery
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.11.008openalex-snapshot
LINC complexes and nuclear positioning
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.2015.08.002openalex-snapshot
Border Safety: Quality Control at the Nuclear Envelope
inferred← citeshttps://doi.org/10.1016/j.tcb.2016.11.005openalex-snapshot
Chromosomes Orchestrate Their Own Liberation: Nuclear Envelope Disassembly
inferred← citeshttps://doi.org/10.1016/j.tibs.2013.04.001openalex-snapshot
Poring over pores: nuclear pore complex insertion into the nuclear envelope
inferred← citeshttps://doi.org/10.1038/s41467-024-48382-2openalex-snapshot
Fate of telomere entanglements is dictated by the timing of anaphase midregion nuclear envelope breakdown
inferred← citeshttps://doi.org/10.1074/jbc.m115.688374openalex-snapshot
Endoplasmic Reticulum-resident Heat Shock Protein 90 (HSP90) Isoform Glucose-regulated Protein 94 (GRP94) Regulates Cell Polarity and Cancer Cell Migration by Affecting Intracellular Transport
inferred← citeshttps://doi.org/10.1080/00275514.2019.1659091openalex-snapshot
Spindle pole body duplication defective yeast cells are more prone to membrane damage
inferred← citeshttps://doi.org/10.1080/19420889.2021.1939942openalex-snapshot
Regulation of diverse nuclear shapes: pathways working independently, together
inferred← citeshttps://doi.org/10.1080/19491034.2019.1644593openalex-snapshot
Regulation of inner nuclear membrane associated protein degradation
inferred← citeshttps://doi.org/10.1083/jcb.201408118openalex-snapshot
Ndj1, a telomere-associated protein, regulates centrosome separation in budding yeast meiosis
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.201709009openalex-snapshot
The budding yeast RSC complex maintains ploidy by promoting spindle pole body insertion
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.201809045openalex-snapshot
Yeast centrosome components form a noncanonical LINC complex at the nuclear envelope insertion site
inferred← citeshttps://doi.org/10.1083/jcb.202004196openalex-snapshot
The N-terminus of Sfi1 and yeast centrin Cdc31 provide the assembly site for a new spindle pole body
inferred← citeshttps://doi.org/10.1083/jcb.202210059openalex-snapshot
Distinct domains in Ndc1 mediate its interaction with the Nup84 complex and the nuclear membrane
inferred← citeshttps://doi.org/10.1083/jcb.202304026openalex-snapshot
A membrane-sensing mechanism links lipid metabolism to protein degradation at the nuclear envelope
inferred← citeshttps://doi.org/10.1091/mbc.e11-07-0600openalex-snapshot
Acetylation of the SUN protein Mps3 by Eco1 regulates its function in nuclear organization
inferred← citeshttps://doi.org/10.1091/mbc.e12-08-0602openalex-snapshot
An auxiliary, membrane-based mechanism for nuclear migration in budding yeast
inferred← citeshttps://doi.org/10.1091/mbc.e13-11-0699openalex-snapshot
Regulation of spindle pole body assembly and cytokinesis by the centrin-binding protein Sfi1 in fission yeast
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.e18-09-0585openalex-snapshot
Expression of TorsinA in a heterologous yeast system reveals interactions with lumenal domains of LINC and nuclear pore complex components
inferred← citeshttps://doi.org/10.1091/mbc.e20-02-0146openalex-snapshot
Yeast pericentrin/Spc110 contains multiple domains required for tethering the γ-tubulin complex to the centrosome
inferred← citeshttps://doi.org/10.1091/mbc.e21-05-0239openalex-snapshot
Redistribution of centrosomal proteins by centromeres and Polo kinase controls partial nuclear envelope breakdown in fission yeast
inferred← citeshttps://doi.org/10.1093/femsyr/fov089openalex-snapshot
Reduction ofS. cerevisiaePom34 protein level by SESA network is related to membrane lipid composition
inferred← citeshttps://doi.org/10.1101/2020.12.01.406553openalex-snapshot
Redistribution of centrosomal proteins by centromeres and Polo kinase controls partial nuclear envelope breakdown in fission yeast
inferred← citeshttps://doi.org/10.1101/2025.06.08.658251openalex-snapshot
The fastest movements and the most extreme deformations of the cell nucleus are driven by microtubules in the model fungus Podospora anserina
inferred← citeshttps://doi.org/10.1101/343939openalex-snapshot
Identification and characterization of genes encoding the nuclear envelope LINC complex in the monocot species Zea mays
inferred← citeshttps://doi.org/10.1101/cshperspect.a040477openalex-snapshot
The Diverse Cellular Functions of Inner Nuclear Membrane Proteins
inferred← citeshttps://doi.org/10.1111/boc.70024openalex-snapshot
The Nuclear Envelope Proteins Esc1 and Mps3 Differentially Impact Sterol Gradients in Budding Yeast
inferred← citeshttps://doi.org/10.1128/ec.00101-15openalex-snapshot
Yeast Integral Membrane Proteins Apq12, Brl1, and Brr6 Form a Complex Important for Regulation of Membrane Homeostasis and Nuclear Pore Complex Biogenesis
inferred← citeshttps://doi.org/10.1128/jvi.00330-17openalex-snapshot
Integrity of the Linker of Nucleoskeleton and Cytoskeleton Is Required for Efficient Herpesvirus Nuclear Egress
inferred← citeshttps://doi.org/10.1128/mbio.00216-25openalex-snapshot
SUN-domain proteins of the malaria parasite Plasmodium falciparum are essential for proper nuclear division and DNA repair
inferred← citeshttps://doi.org/10.1128/mbio.01455-26openalex-snapshot
Fast and tortuous: extreme deformations and fast movements of the cell nucleus are driven by microtubules in the model fungus Podospora anserina
inferred← citeshttps://doi.org/10.1128/mbio.02236-22openalex-snapshot
Niemann-Pick Type C Proteins Are Required for Sterol Transport and Appressorium-Mediated Plant Penetration of Colletotrichum orbiculare
inferred← citeshttps://doi.org/10.1146/annurev-genet-120116-024733openalex-snapshot
Big Lessons from Little Yeast: Budding and Fission Yeast Centrosome Structure, Duplication, and Function
inferred← citeshttps://doi.org/10.11575/prism/26597openalex-snapshot
Interaction of the NuA4 Complex and Chromatin Modifications with the DNA Damage Tolerance Pathway
inferred← citeshttps://doi.org/10.1186/s12864-015-1755-2openalex-snapshot
Evolutionary engineering of a wine yeast strain revealed a key role of inositol and mannoprotein metabolism during low-temperature fermentation
inferred← citeshttps://doi.org/10.1242/bio.20122188openalex-snapshot
Rules of engagement: centrosome–nuclear connections in a closed mitotic system
inferred← citeshttps://doi.org/10.1242/jcs.154997openalex-snapshot
The KASH protein Kms2 coordinates mitotic remodeling of the spindle pole body
inferred← citeshttps://doi.org/10.1242/jcs.164160openalex-snapshot
Sphingolipids regulate telomere clustering by affecting transcriptional levels of genes involved in telomere homeostasis
inferred← citeshttps://doi.org/10.1242/jcs.186700openalex-snapshot
LINCing the eukaryotic tree of life – towards a broad evolutionary comparison of nucleocytoplasmic bridging complexes
inferred← citeshttps://doi.org/10.1242/jcs.221390openalex-snapshot
Identification and characterization of genes encoding the nuclear envelope LINC complex in the monocot species Zea mays
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006830openalex-snapshot
Cleavage of the SUN-domain protein Mps3 at its N-terminus regulates centrosome disjunction in budding yeast meiosis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008911openalex-snapshot
The role of gene dosage in budding yeast centrosome scaling and spontaneous diploidization
inferred← citeshttps://doi.org/10.1515/hsz-2014-0267openalex-snapshot
Making the LINC: SUN and KASH protein interactions
inferred← citeshttps://doi.org/10.1534/g3.112.004614openalex-snapshot
Genetic Analysis of Mps3 SUN Domain Mutants inSaccharomyces cerevisiaeReveals an Interaction with the SUN-Like Protein Slp1
inferred← citeshttps://doi.org/10.1534/g3.120.401864openalex-snapshot
The Genetic and Physical Interactomes of the Saccharomyces cerevisiae Hrq1 Helicase
inferred← citeshttps://doi.org/10.1534/genetics.112.141465openalex-snapshot
Integrity and Function of theSaccharomyces cerevisiaeSpindle Pole Body Depends on Connections Between the Membrane Proteins Ndc1, Rtn1, and Yop1
inferred← citeshttps://doi.org/10.1534/genetics.115.178012openalex-snapshot
Sec66-Dependent Regulation of Yeast Spindle-Pole Body Duplication Through Pom152
inferred← citeshttps://doi.org/10.2139/ssrn.5384588openalex-snapshot
The Fastest Movements and the Most Extreme Deformations of the Cell Nucleus are Driven by Microtrubules in the Model Fungus Podospora Anserina
inferred← citeshttps://doi.org/10.3389/fcell.2020.594092openalex-snapshot
SWR1-Independent Association of H2A.Z to the LINC Complex Promotes Meiotic Chromosome Motion
inferred← citeshttps://doi.org/10.3389/fgene.2017.00060openalex-snapshot
The Emerging Role of the Cytoskeleton in Chromosome Dynamics
inferred← citeshttps://doi.org/10.3389/fgene.2020.00136openalex-snapshot
SUNny Ways: The Role of the SUN-Domain Protein Mps3 Bridging Yeast Nuclear Organization and Lipid Homeostasis
inferred← citeshttps://doi.org/10.3389/fpls.2016.00118openalex-snapshot
GIP Contributions to the Regulation of Centromere at the Interface Between the Nuclear Envelope and the Nucleoplasm
inferred← citeshttps://doi.org/10.3390/biom11010054openalex-snapshot
Nuclear Ubiquitin-Proteasome Pathways in Proteostasis Maintenance
inferred← citeshttps://doi.org/10.3390/cells12050706openalex-snapshot
Tuning between Nuclear Organization and Functionality in Health and Disease
inferred← citeshttps://doi.org/10.3390/ijms24129829openalex-snapshot
A Yeast Mitotic Tale for the Nucleus and the Vacuoles to Embrace
inferred← citeshttps://doi.org/10.3410/f.735320249.793579977openalex-snapshot
Faculty Opinions recommendation of Yeast centrosome components form a noncanonical LINC complex at the nuclear envelope insertion site.
inferred← citeshttps://doi.org/10.4161/nucl.20148openalex-snapshot
Nuclear envelope insertion of spindle pole bodies and nuclear pore complexes
inferred← citeshttps://doi.org/10.4161/nucl.23387openalex-snapshot
LINCing complex functions at the nuclear envelope
inferred← citeshttps://doi.org/10.4161/nucl.24088openalex-snapshot
How plants LINC the SUN to KASH
inferred← citeshttps://doi.org/10.4161/nucl.29793openalex-snapshot
Requirement of the spindle pole body for targeting and/or tethering proteins to the inner nuclear membrane
inferred← citeshttps://doi.org/10.7554/elife.55694openalex-snapshot
The wtf4 meiotic driver utilizes controlled protein aggregation to generate selective cell death
inferred← citeshttps://doi.org/10.7916/d8k64wmqopenalex-snapshot
Distinct Nuclear-Cytoskeletal LINCages Position the Nucleus for Homeostasis, Polarization and Migration
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.