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In silico synchronization reveals regulators of nuclear ruptures in lamin A/C deficient model cells
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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/cyto.a.21153openalex-snapshot
Analysis of nucleo‐cytoplasmic shuttling of the proto‐oncogene SET/I2PP2A
inferredcites →https://doi.org/10.1007/s00018-012-1200-5openalex-snapshot
Microtubule dynamics alter the interphase nucleus
inferredcites →https://doi.org/10.1007/s00418-012-1005-5openalex-snapshot
Cytoplasmic localization of PML particles in laminopathies
inferredcites →https://doi.org/10.1007/s11010-006-9390-5openalex-snapshot
DNA damage induces N-acetyltransferase NAT10 gene expression through transcriptional activation
inferredcites →https://doi.org/10.1007/s12195-012-0257-4openalex-snapshot
Cytoplasmic Dynein: Tension Generation on Microtubules and the Nucleus
inferredcites →https://doi.org/10.1007/s12195-013-0270-2openalex-snapshot
Modulation of Nuclear Shape by Substrate Rigidity
inferredcites →https://doi.org/10.1016/j.bbagen.2010.01.002openalex-snapshot
Increased plasticity of the nuclear envelope and hypermobility of telomeres due to the loss of A–type lamins
inferredcites →https://doi.org/10.1016/j.biocel.2014.05.035openalex-snapshot
Laminopathy-inducing mutations reduce nuclear import of expressed prelamin A
inferredcites →https://doi.org/10.1016/j.bpj.2010.04.011openalex-snapshot
Actomyosin Tension Exerted on the Nucleus through Nesprin-1 Connections Influences Endothelial Cell Adhesion, Migration, and Cyclic Strain-Induced Reorientation
inferredcites →https://doi.org/10.1016/j.bpj.2012.08.041openalex-snapshot
Mechanical Activation of Cells Induces Chromatin Remodeling Preceding MKL Nuclear Transport
inferredcites →https://doi.org/10.1016/j.bpj.2015.07.006openalex-snapshot
Moving Cell Boundaries Drive Nuclear Shaping during Cell Spreading
inferredcites →https://doi.org/10.1016/j.cell.2008.11.037openalex-snapshot
Age-Dependent Deterioration of Nuclear Pore Complexes Causes a Loss of Nuclear Integrity in Postmitotic Cells
inferredcites →https://doi.org/10.1016/j.cell.2013.06.007openalex-snapshot
Catastrophic Nuclear Envelope Collapse in Cancer Cell Micronuclei
inferredcites →https://doi.org/10.1016/j.cell.2014.05.046openalex-snapshot
ATR Mediates a Checkpoint at the Nuclear Envelope in Response to Mechanical Stress
inferredcites →https://doi.org/10.1016/j.tcb.2015.08.002openalex-snapshot
Border Safety: Quality Control at the Nuclear Envelope
inferredcites →https://doi.org/10.1016/j.yexcr.2009.03.007openalex-snapshot
NAT10, a nucleolar protein, localizes to the midbody and regulates cytokinesis and acetylation of microtubules
inferredcites →https://doi.org/10.1016/j.yexcr.2009.05.003openalex-snapshot
Nuclear protein import is reduced in cells expressing nuclear envelopathy-causing lamin A mutants
inferredcites →https://doi.org/10.1038/nature14408openalex-snapshot
Spastin and ESCRT-III coordinate mitotic spindle disassembly and nuclear envelope sealing
inferredcites →https://doi.org/10.1038/nature14503openalex-snapshot
ESCRT-III controls nuclear envelope reformation
inferredcites →https://doi.org/10.1038/ng871openalex-snapshot
Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase–deficient mice
inferredcites →https://doi.org/10.1038/nprot.2013.143openalex-snapshot
Genome engineering using the CRISPR-Cas9 system
inferredcites →https://doi.org/10.1038/srep07362openalex-snapshot
Super-resolution microscopy reveals LINC complex recruitment at nuclear indentation sites
inferredcites →https://doi.org/10.1038/srep09475openalex-snapshot
Opposite rheological properties of neuronal microcompartments predict axonal vulnerability in brain injury
inferredcites →https://doi.org/10.1073/pnas.0908686106openalex-snapshot
A perinuclear actin cap regulates nuclear shape
inferredcites →https://doi.org/10.1074/jbc.m513511200openalex-snapshot
Lamins A and C but Not Lamin B1 Regulate Nuclear Mechanics
inferredcites →https://doi.org/10.1080/19491034.2015.1050568openalex-snapshot
Sustained accumulation of prelamin A and depletion of lamin A/C both cause oxidative stress and mitochondrial dysfunction but induce different cell fates
inferredcites →https://doi.org/10.1083/jcb.147.5.913openalex-snapshot
Loss of a-Type Lamin Expression Compromises Nuclear Envelope Integrity Leading to Muscular Dystrophy
inferredcites →https://doi.org/10.1083/jcb.200306159openalex-snapshot
PLA2 activity is required for nuclear shrinkage in caspase-independent cell death
inferredcites →https://doi.org/10.1083/jcb.201210152openalex-snapshot
Physical limits of cell migration: Control by ECM space and nuclear deformation and tuning by proteolysis and traction force
inferredcites →https://doi.org/10.1083/jcb.201402003openalex-snapshot
Breaching the nuclear envelope in development and disease
inferredcites →https://doi.org/10.1088/1478-3975/10/6/065002openalex-snapshot
Probing the compressibility of tumor cell nuclei by combined atomic force–confocal microscopy
inferredcites →https://doi.org/10.1091/mbc.e04-11-1009openalex-snapshot
Lamin A/C–dependent Localization of Nesprin-2, a Giant Scaffolder at the Nuclear Envelope
inferredcites →https://doi.org/10.1093/hmg/ddm238openalex-snapshot
Nesprin-1 and -2 are involved in the pathogenesis of Emery–Dreifuss muscular dystrophy and are critical for nuclear envelope integrity
inferredcites →https://doi.org/10.1093/hmg/ddr344openalex-snapshot
Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies
inferredcites →https://doi.org/10.1111/j.1474-9726.2008.00382.xopenalex-snapshot
Increased mechanosensitivity and nuclear stiffness in Hutchinson–Gilford progeria cells: effects of farnesyltransferase inhibitors
inferredcites →https://doi.org/10.1111/j.1474-9726.2011.00750.xopenalex-snapshot
Conserved cysteine residues in the mammalian lamin A tail are essential for cellular responses to ROS generation
inferredcites →https://doi.org/10.1126/science.1063957openalex-snapshot
Dynamic Disruptions in Nuclear Envelope Architecture and Integrity Induced by HIV-1 Vpr
inferredcites →https://doi.org/10.1126/science.1127168openalex-snapshot
Lamin A-Dependent Nuclear Defects in Human Aging
inferredcites →https://doi.org/10.1126/science.1189072openalex-snapshot
Linear Arrays of Nuclear Envelope Proteins Harness Retrograde Actin Flow for Nuclear Movement
inferredcites →https://doi.org/10.1126/science.1252651openalex-snapshot
Chemical Inhibition of NAT10 Corrects Defects of Laminopathic Cells
inferredcites →https://doi.org/10.1126/science.aad7297openalex-snapshot
Nuclear envelope rupture and repair during cancer cell migration
inferredcites →https://doi.org/10.1126/science.aad7611openalex-snapshot
ESCRT III repairs nuclear envelope ruptures during cell migration to limit DNA damage and cell death
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/10.1152/physrev.00047.2005openalex-snapshot
Nuclear Lamins: Laminopathies and Their Role in Premature Ageing
inferredcites →https://doi.org/10.1172/jci19670openalex-snapshot
Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction
inferredcites →https://doi.org/10.1242/jcs.014191openalex-snapshot
Requirements for the localization of nesprin-3 at the nuclear envelope and its interaction with plectin
inferredcites →https://doi.org/10.1242/jcs.057075openalex-snapshot
Dynamics and molecular interactions of linker of nucleoskeleton and cytoskeleton (LINC) complex proteins
inferredcites →https://doi.org/10.1242/jcs.058271openalex-snapshot
Efficient cell migration requires global chromatin condensation
inferredcites →https://doi.org/10.1371/journal.pone.0111851openalex-snapshot
NET23/STING Promotes Chromatin Compaction from the Nuclear Envelope
inferredcites →https://doi.org/10.4161/cib.4.2.14384openalex-snapshot
A new twist on plasma membrane repair
inferredcites →https://doi.org/10.4161/nucl.18954openalex-snapshot
Transient nuclear envelope rupturing during interphase in human cancer cells
inferredcites →https://doi.org/10.4161/nucl.23388openalex-snapshot
Soft substrates normalize nuclear morphology and prevent nuclear rupture in fibroblasts from a laminopathy patient with compound heterozygous LMNA mutations
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/adfm.202410035openalex-snapshot
Engineered Nanotopographies Induce Transient Openings in the Nuclear Membrane
inferred← citeshttps://doi.org/10.1007/16833_2024_237openalex-snapshot
Intricate Synergy of Mechanical and Biochemical Cues in the Transmigration of Cancer Cells Across the Endothelium
inferred← citeshttps://doi.org/10.1007/s00018-021-04099-9openalex-snapshot
Transient nuclear lamin A/C accretion aids in recovery from vapor nanobubble-induced permeabilisation of the plasma membrane
inferred← citeshttps://doi.org/10.1007/s00018-024-05194-3openalex-snapshot
Lamin B1 curtails early human papillomavirus infection by safeguarding nuclear compartmentalization and autophagic capacity
inferred← citeshttps://doi.org/10.1007/s42764-021-00039-wopenalex-snapshot
Nuclear envelope integrity, DNA replication, damage repair and genome stability
inferred← citeshttps://doi.org/10.1016/b978-0-12-819460-7.00272-3openalex-snapshot
Nucleus | Chromatin and Nuclear Biophysics
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2017.07.013openalex-snapshot
Loss of Nuclear Envelope Integrity in Aging and Disease
inferred← citeshttps://doi.org/10.1016/j.bpj.2017.07.014openalex-snapshot
Rupture Dynamics and Chromatin Herniation in Deformed Nuclei
inferred← citeshttps://doi.org/10.1016/j.bpj.2017.08.034openalex-snapshot
Mechanics and Buckling of Biopolymeric Shells and Cell Nuclei
inferred← citeshttps://doi.org/10.1016/j.ceb.2018.02.001openalex-snapshot
Nuclear envelope rupture: little holes, big openings
inferred← citeshttps://doi.org/10.1016/j.ceb.2019.02.006openalex-snapshot
Chromatin’s physical properties shape the nucleus and its functions
inferred← citeshttps://doi.org/10.1016/j.ceb.2019.04.005openalex-snapshot
The ESCRT-machinery: closing holes and expanding roles
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.10.022openalex-snapshot
The ESCRT machinery counteracts Nesprin-2G-mediated mechanical forces during nuclear envelope repair
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2022.121735openalex-snapshot
Nuclear targeting Subcellular-delivery nanosystems for precise cancer treatment
inferred← citeshttps://doi.org/10.1016/j.jconrel.2021.06.002openalex-snapshot
Advanced mechanotherapy: Biotensegrity for governing metastatic tumor cell fate via modulating the extracellular matrix
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.nbd.2026.107630openalex-snapshot
TDP-43 and ALS - what's wrong with my membranes?
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.08.035openalex-snapshot
ESCRT-dependent control of membrane remodelling during cell division
inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.03.021openalex-snapshot
Genome instability from nuclear catastrophe and DNA damage
inferred← citeshttps://doi.org/10.1016/j.semcdb.2025.103662openalex-snapshot
Mechanics of force transmission in epithelia: From cell-to-cell propagation to nuclear response
inferred← citeshttps://doi.org/10.1016/j.taap.2025.117243openalex-snapshot
Involvement of nuclear atrophy of binucleated hepatocytes in the large micronucleus formation induced by rat hepatocarcinogen acetamide
inferred← citeshttps://doi.org/10.1016/j.tcb.2017.02.008openalex-snapshot
Bursting the Bubble – Nuclear Envelope Rupture as a Path to Genomic Instability?
inferred← citeshttps://doi.org/10.1021/acsnano.8b01860openalex-snapshot
Targeted Perturbation of Nuclear Envelope Integrity with Vapor Nanobubble-Mediated Photoporation
inferred← citeshttps://doi.org/10.1038/s41389-019-0136-0openalex-snapshot
ESCRT-III is necessary for the integrity of the nuclear envelope in micronuclei but is aberrant at ruptured micronuclear envelopes generating damage
inferred← citeshttps://doi.org/10.1038/s41416-020-01176-xopenalex-snapshot
Squeezing through the microcirculation: survival adaptations of circulating tumour cells to seed metastasis
inferred← citeshttps://doi.org/10.1038/s41420-020-00327-6openalex-snapshot
Apoptotic stress induces Bax-dependent, caspase-independent redistribution of LINC complex nesprins
inferred← citeshttps://doi.org/10.1038/s41420-020-0256-5openalex-snapshot
The nuclear envelope: target and mediator of the apoptotic process
inferred← citeshttps://doi.org/10.1038/s41467-025-65994-4openalex-snapshot
LRRC59 cooperates with nuclear transporters to restrain the nuclear envelope repair machinery and safeguard genome integrity
inferred← citeshttps://doi.org/10.1038/s41556-018-0038-yopenalex-snapshot
Emerging views of the nucleus as a cellular mechanosensor
inferred← citeshttps://doi.org/10.1038/s41563-019-0563-5openalex-snapshot
Mutant lamins cause nuclear envelope rupture and DNA damage in skeletal muscle cells
inferred← citeshttps://doi.org/10.1038/s41598-024-56613-1openalex-snapshot
A high-content screen reveals new regulators of nuclear membrane stability
inferred← citeshttps://doi.org/10.1042/bst20170442openalex-snapshot
Fantastic nuclear envelope herniations and where to find them
inferred← citeshttps://doi.org/10.1042/bst20250351openalex-snapshot
Nuclear envelope rupture and resealing: mechanisms, consequences, and disease implications
inferred← citeshttps://doi.org/10.1063/5.0082656openalex-snapshot
Nuclear lamins: Structure and function in mechanobiology
inferred← citeshttps://doi.org/10.1080/15384101.2020.1836441openalex-snapshot
The adenoviral protein E4orf4: a probing tool to decipher mechanical stress-induced nuclear envelope remodeling in tumor cells
inferred← citeshttps://doi.org/10.1080/15384101.2021.1892320openalex-snapshot
Barrier-to-autointegration factor: a first responder for repair of nuclear ruptures
inferred← citeshttps://doi.org/10.1080/19336918.2016.1247144openalex-snapshot
Deregulation of focal adhesion formation and cytoskeletal tension due to loss of A-type lamins
inferred← citeshttps://doi.org/10.1080/19491034.2017.1292191openalex-snapshot
Consequences of a tight squeeze: Nuclear envelope rupture and repair
inferred← citeshttps://doi.org/10.1080/19491034.2020.1806661openalex-snapshot
Interplay of the nuclear envelope with chromatin in physiology and pathology
inferred← citeshttps://doi.org/10.1080/19491034.2024.2352203openalex-snapshot
Crosstalk between mitotic reassembly and repair of the nuclear envelope
inferred← citeshttps://doi.org/10.1083/jcb.201609102openalex-snapshot
Nuclear envelope rupture: Actin fibers are putting the squeeze on the nucleus
inferred← citeshttps://doi.org/10.1083/jcb.201805122openalex-snapshot
Adenoviral protein E4orf4 interacts with the polarity protein Par3 to induce nuclear rupture and tumor cell death
inferred← citeshttps://doi.org/10.1083/jcb.202101165openalex-snapshot
Micronuclei in Kif18a mutant mice form stable micronuclear envelopes and do not promote tumorigenesis
inferred← citeshttps://doi.org/10.1083/jcb.202201024openalex-snapshot
Nucleoplasmic lamin C rapidly accumulates at sites of nuclear envelope rupture with BAF and cGAS
inferred← citeshttps://doi.org/10.1083/jcb.202208123openalex-snapshot
Small lipid droplets are rigid enough to indent a nucleus, dilute the lamina, and cause rupture
inferred← citeshttps://doi.org/10.1091/mbc.e17-06-0374openalex-snapshot
Dynein pulling forces counteract lamin-mediated nuclear stability during nuclear envelope repair
inferred← citeshttps://doi.org/10.1091/mbc.e17-06-0410openalex-snapshot
Chromatin histone modifications and rigidity affect nuclear morphology independent of lamins
inferred← citeshttps://doi.org/10.1091/mbc.e19-05-0286openalex-snapshot
Physicochemical mechanotransduction alters nuclear shape and mechanics via heterochromatin formation
inferred← citeshttps://doi.org/10.1091/mbc.e19-05-0286-topenalex-snapshot
Physicochemical mechanotransduction alters nuclear shape and mechanics via heterochromatin formation
inferred← citeshttps://doi.org/10.1091/mbc.e23-07-0292openalex-snapshot
Actin contraction controls nuclear blebbing and rupture independent of actin confinement
inferred← citeshttps://doi.org/10.1091/mbc.e25-02-0057openalex-snapshot
Lamin B1 and LAP2β resist cytoskeletal force to maintain lamin A/C meshwork organization and preserve nuclear integrity
inferred← citeshttps://doi.org/10.1093/bfgp/elab012openalex-snapshot
The functional impact of nuclear reorganization in cellular senescence
inferred← citeshttps://doi.org/10.1093/nar/gkac726openalex-snapshot
The BAF A12T mutation disrupts lamin A/C interaction, impairing robust repair of nuclear envelope ruptures in Nestor–Guillermo progeria syndrome cells
inferred← citeshttps://doi.org/10.1093/pnasnexus/pgae527openalex-snapshot
Roles of the lamin A-specific tail region in the localization to sites of nuclear envelope rupture
inferred← citeshttps://doi.org/10.1093/toxsci/kfad131openalex-snapshot
Formation of hepatocyte cytoplasmic inclusions and their contribution to methylcarbamate-induced hepatocarcinogenesis in F344 rats
inferred← citeshttps://doi.org/10.1098/rsbl.2020.0302openalex-snapshot
The nuclear envelope: LINCing tissue mechanics to genome regulation in cardiac and skeletal muscle
inferred← citeshttps://doi.org/10.1101/2022.09.01.506190openalex-snapshot
Small, fat-filled lipid droplets remain spherical as they indent a nucleus, dilute the lamina, and cause rupture
inferred← citeshttps://doi.org/10.1101/476630openalex-snapshot
ESCRT-III accumulates in micronuclei with ruptured nuclear envelopes
inferred← citeshttps://doi.org/10.1111/acel.13143openalex-snapshot
Nuclear envelope dysfunction and its contribution to the aging process
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-020520-120627openalex-snapshot
Nuclear Membrane Rupture and Its Consequences
inferred← citeshttps://doi.org/10.1152/physiol.00029.2017openalex-snapshot
Bypassing Border Control: Nuclear Envelope Rupture in Disease
inferred← citeshttps://doi.org/10.1242/jcs.261547openalex-snapshot
Transcription inhibition suppresses nuclear blebbing and rupture independently of nuclear rigidity
inferred← citeshttps://doi.org/10.1371/journal.pone.0170688openalex-snapshot
Accurate Detection of Dysmorphic Nuclei Using Dynamic Programming and Supervised Classification
inferred← citeshttps://doi.org/10.1371/journal.pone.0195664openalex-snapshot
Automated analysis of cell migration and nuclear envelope rupture in confined environments
inferred← citeshttps://doi.org/10.17912/micropub.biology.001103openalex-snapshot
Nuclear shape is affected differentially by loss of lamin A, lamin C, or both lamin A and C
inferred← citeshttps://doi.org/10.3389/fcell.2022.1018102openalex-snapshot
The role of prelamin A post-translational maturation in stress response and 53BP1 recruitment
inferred← citeshttps://doi.org/10.3389/fcell.2022.989217openalex-snapshot
The LEM-ESCRT toolkit: Repair and maintenance of the nucleus
inferred← citeshttps://doi.org/10.3390/cells11030347openalex-snapshot
Current Methods and Pipelines for Image-Based Quantitation of Nuclear Shape and Nuclear Envelope Abnormalities
inferred← citeshttps://doi.org/10.3390/cells8030231openalex-snapshot
Deciphering Nuclear Mechanobiology in Laminopathy
inferred← citeshttps://doi.org/10.3390/cells9030712openalex-snapshot
Mitochondria in the Nuclei of Rat Myocardial Cells
inferred← citeshttps://doi.org/10.3390/microorganisms7050149openalex-snapshot
The Chlamydia trachomatis Extrusion Exit Mechanism Is Regulated by Host Abscission Proteins
inferred← citeshttps://doi.org/10.3410/f.735359149.793562715openalex-snapshot
Faculty Opinions recommendation of Chromatin's physical properties shape the nucleus and its functions.
inferred← citeshttps://doi.org/10.64898/2026.06.29.735225openalex-snapshot
CRISPR-Engineered hiPSC-derived Cardiomyocytes Reveal Divergent Responses to Loss and Defective Processing of A-type Lamins
inferred← citeshttps://doi.org/10.70675/fcbf63f9z5dc9z40e6z888cz9c26ac6e9766openalex-snapshot
DNA damage-induced nuclear envelope rupture : A new cancer vulnerability
inferred← citeshttps://doi.org/10.7554/elife.45284openalex-snapshot
An ESCRT-LEM protein surveillance system is poised to directly monitor the nuclear envelope and nuclear transport system
inferred← citeshttps://doi.org/10.7554/elife.59999openalex-snapshot
CDK1 controls CHMP7-dependent nuclear envelope reformation
inferred← citeshttps://doi.org/10.7554/elife.63972openalex-snapshot
HP1α is a chromatin crosslinker that controls nuclear and mitotic chromosome mechanics
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