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Lamins A and C but Not Lamin B1 Regulate Nuclear Mechanics
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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/j.1460-2075.1987.tb02716.xopenalex-snapshot
Nuclear lamin LI of Xenopus laevis: cDNA cloning, amino acid sequence and binding specificity of a member of the lamin B subfamily.
inferredcites →https://doi.org/10.1006/excr.1993.1173openalex-snapshot
Relationship between Apoptosis and the Cell Cycle in Lymphocytes: Roles of Protein Kinase C, Tyrosine Phosphorylation, and AP1
inferredcites →https://doi.org/10.1006/excr.1995.1230openalex-snapshot
Protein-Protein Interactions between Human Nuclear Lamins Expressed in Yeast
inferredcites →https://doi.org/10.1007/s004180050138openalex-snapshot
A- and B-type lamins are differentially expressed in normal human tissues
inferredcites →https://doi.org/10.1016/0010-4809(89)90034-7openalex-snapshot
Elliptic Fourier analysis of cell and nuclear shapes
inferredcites →https://doi.org/10.1016/0092-8674(87)90634-9openalex-snapshot
Teratocarcinoma stem cells and early mouse embryos contain only a single major lamin polypeptide closely resembling lamin B
inferredcites →https://doi.org/10.1016/j.ejcb.2005.03.001openalex-snapshot
Dynamic properties of germ line-specific lamin B3: The role of the shortened rod domain
inferredcites →https://doi.org/10.1016/j.ejcb.2005.04.004openalex-snapshot
Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy
inferredcites →https://doi.org/10.1016/j.yexcr.2004.11.020openalex-snapshot
Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organization
inferredcites →https://doi.org/10.1016/s0022-510x(03)00012-1openalex-snapshot
Architectural abnormalities in muscle nuclei. Ultrastructural differences between X-linked and autosomal dominant forms of EDMD
inferredcites →https://doi.org/10.1016/s0022-510x(98)00130-0openalex-snapshot
Ultrastructural abnormality of sarcolemmal nuclei in Emery-Dreifuss muscular dystrophy (EDMD)
inferredcites →https://doi.org/10.1016/s0962-8924(02)02401-7openalex-snapshot
The nuclear lamina and inherited disease
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/ncb1104-1062openalex-snapshot
A-type lamins: Guardians of the soma?
inferredcites →https://doi.org/10.1038/nrm879openalex-snapshot
Life at the edge: the nuclear envelope and human disease
inferredcites →https://doi.org/10.1038/nrm950openalex-snapshot
Lamins: building blocks or regulators of gene expression?
inferredcites →https://doi.org/10.1073/pnas.0401424101openalex-snapshot
Lamin B1 is required for mouse development and nuclear integrity
inferredcites →https://doi.org/10.1073/pnas.0402943101openalex-snapshot
Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson–Gilford progeria syndrome
inferredcites →https://doi.org/10.1073/pnas.0408558102openalex-snapshot
Heterozygosity for Lmna deficiency eliminates the progeria-like phenotypes in Zmpste24 -deficient mice
inferredcites →https://doi.org/10.1073/pnas.85.12.4325openalex-snapshot
Heterotypic and homotypic associations between the nuclear lamins: site-specificity and control by phosphorylation.
inferredcites →https://doi.org/10.1074/jbc.m407705200openalex-snapshot
The Stability of the Nuclear Lamina Polymer Changes with the Composition of Lamin Subtypes According to Their Individual Binding Strengths
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.200502148openalex-snapshot
Abnormal nuclear shape and impaired mechanotransduction in emerin-deficient cells
inferredcites →https://doi.org/10.1093/hmg/ddh295openalex-snapshot
Decreased mechanical stiffness in LMNA−/− cells is caused by defective nucleo-cytoskeletal integrity: implications for the development of laminopathies
inferredcites →https://doi.org/10.1093/hmg/ddi017openalex-snapshot
Mouse model carrying H222P- Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies
inferredcites →https://doi.org/10.1093/hmg/ddi479openalex-snapshot
Loss of emerin at the nuclear envelope disrupts the Rb1/E2F and MyoD pathways during muscle regeneration
inferredcites →https://doi.org/10.1093/hmg/ddl026openalex-snapshot
The truncated prelamin A in Hutchinson–Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers
inferredcites →https://doi.org/10.1101/gad.960502openalex-snapshot
Nuclear lamins: building blocks of nuclear architecture
inferredcites →https://doi.org/10.1126/science.1122771openalex-snapshot
A Mitotic Lamin B Matrix Induced by RanGTP Required for Spindle Assembly
inferredcites →https://doi.org/10.1152/physiol.00022.2004openalex-snapshot
The Nuclear Envelope and Human Disease
inferredcites →https://doi.org/10.1172/jci19448openalex-snapshot
Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C–deficient mice
inferredcites →https://doi.org/10.1172/jci19670openalex-snapshot
Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction
inferredcites →https://doi.org/10.1172/jci27125openalex-snapshot
Prelamin A and lamin A appear to be dispensable in the nuclear lamina
inferredcites →https://doi.org/10.1242/jcs.01102openalex-snapshot
Proteins that bind A-type lamins: integrating isolated clues
inferredcites →https://doi.org/10.1242/jcs.110.19.2483openalex-snapshot
Distinct nuclear assembly pathways for lamins A and C lead to their increase during quiescence in Swiss 3T3 cells
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.114.24.4447openalex-snapshot
Nuclear envelope defects associated withLMNAmutations cause dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy
inferredcites →https://doi.org/10.1242/jcs.114.24.4459openalex-snapshot
Nuclear envelope disorganization in fibroblasts from lipodystrophic patients with heterozygous R482Q/W mutations in the lamin A/C gene
inferredcites →https://doi.org/10.1242/jcs.114.24.4557openalex-snapshot
Identification of essential genes in cultured mammalian cells using small interfering RNAs
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/1873-3468.14750openalex-snapshot
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B cell mechanobiology in health and disease: emerging techniques and insights into therapeutic responses
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Control of Mesenchymal Stem‐Cell Fate by Engineering the Nanoenvironment
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Mechanical Properties of Materials for Stem Cell Differentiation
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“Looping In” Mechanics: Mechanobiologic Regulation of the Nucleus and the Epigenome
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Neural Progenitor Cells Alter Chromatin Organization and Neurotrophin Expression in Response to 3D Matrix Degradability
inferred← citeshttps://doi.org/10.1002/advs.201901222openalex-snapshot
A Unified Linear Viscoelastic Model of the Cell Nucleus Defines the Mechanical Contributions of Lamins and Chromatin
inferred← citeshttps://doi.org/10.1002/advs.202105545openalex-snapshot
Extracellular Adhesive Cues Physically Define Nucleolar Structure and Function
inferred← citeshttps://doi.org/10.1002/advs.202201248openalex-snapshot
The Nucleus Bypasses Obstacles by Deforming Like a Drop with Surface Tension Mediated by Lamin A/C
inferred← citeshttps://doi.org/10.1002/advs.202201663openalex-snapshot
Deleterious Mechanical Deformation Selects Mechanoresilient Cancer Cells with Enhanced Proliferation and Chemoresistance
inferred← citeshttps://doi.org/10.1002/advs.202308253openalex-snapshot
Targeting Nuclear Mechanics Mitigates the Fibroblast Invasiveness in Pathological Dermal Scars Induced by Matrix Stiffening
inferred← citeshttps://doi.org/10.1002/anbr.202300042openalex-snapshot
It Takes Two to Tango: Controlling Human Mesenchymal Stromal Cell Response via Substrate Stiffness and Surface Topography
inferred← citeshttps://doi.org/10.1002/cbin.10879openalex-snapshot
Intermediate filaments and cellular mechanics
inferred← citeshttps://doi.org/10.1002/cbin.11504openalex-snapshot
The multifaceted roles of nucleophagy in cancer development and therapy
inferred← citeshttps://doi.org/10.1002/cjp2.129openalex-snapshot
Intranuclear inclusions in hepatocellular carcinoma contain autophagy‐associated proteins and correlate with prolonged survival
inferred← citeshttps://doi.org/10.1002/cm.21651openalex-snapshot
Physical evidence on desmin–lamin B interaction
inferred← citeshttps://doi.org/10.1002/cm.21658openalex-snapshot
Cytoskeletal prestress: The cellular hallmark in mechanobiology and mechanomedicine
inferred← citeshttps://doi.org/10.1002/cm.21835openalex-snapshot
Microstructure‐based nuclear lamina constitutive model
inferred← citeshttps://doi.org/10.1002/dc.23941openalex-snapshot
New biological research and understanding of P apanicolaou's test
inferred← citeshttps://doi.org/10.1002/dvdy.427openalex-snapshot
A CRISPR /Cas9 zebrafish lamin A/C mutant model of muscular laminopathy
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2011.tb00343.xopenalex-snapshot
Mechanics of the Nucleus
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2016.tb00721.xopenalex-snapshot
Diseases of the Nucleoskeleton
inferred← citeshttps://doi.org/10.1002/jbio.201600198openalex-snapshot
Optomechanical measurement of the role of lamins in whole cell deformability
inferred← citeshttps://doi.org/10.1002/jcb.21485openalex-snapshot
Chromatin organization and nuclear microenvironments in cancer cells
inferred← citeshttps://doi.org/10.1002/jcp.26031openalex-snapshot
The nucleus is irreversibly shaped by motion of cell boundaries in cancer and non‐cancer cells
inferred← citeshttps://doi.org/10.1002/jcp.26336openalex-snapshot
Nucleoskeletal stiffness regulates stem cell migration and differentiation through lamin A/C
inferred← citeshttps://doi.org/10.1002/jcp.28672openalex-snapshot
Apical cell protrusions cause vertical deformation of the soft cancer nucleus
inferred← citeshttps://doi.org/10.1002/jlb.3hi1217-488ropenalex-snapshot
Frontline Science: Elevated nuclear lamin A is permissive for granulocyte transendothelial migration but not for motility through collagen I barriers
inferred← citeshttps://doi.org/10.1002/mabi.201200416openalex-snapshot
A Novel 3 D Integrated Platform for the High‐ R esolution Study of Cell Migration Plasticity
inferred← citeshttps://doi.org/10.1002/mco2.70073openalex-snapshot
At the nucleus of cancer: how the nuclear envelope controls tumor progression
inferred← citeshttps://doi.org/10.1002/path.3033openalex-snapshot
Chromosomal regions associated with prostate cancer risk localize to lamin B‐deficient microdomains and exhibit reduced gene transcription
inferred← citeshttps://doi.org/10.1002/pmic.200800019openalex-snapshot
Effects of green tea extract on lung cancer A549 cells: Proteomic identification of proteins associated with cell migration
inferred← citeshttps://doi.org/10.1002/smll.201905422openalex-snapshot
Surface Roughness Gradients Reveal Topography‐Specific Mechanosensitive Responses in Human Mesenchymal Stem Cells
inferred← citeshttps://doi.org/10.1002/smll.201907688openalex-snapshot
Nuclear Mechanics within Intact Cells Is Regulated by Cytoskeletal Network and Internal Nanostructures
inferred← citeshttps://doi.org/10.1002/smll.202506536openalex-snapshot
Evidence for Drop‐Like Nuclear Deformation in Sheared Endothelial Monolayers
inferred← citeshttps://doi.org/10.1002/stem.3098openalex-snapshot
Knockdown of formin mDia2 alters lamin B1 levels and increases osteogenesis in stem cells
inferred← citeshttps://doi.org/10.1007/8415_2010_19openalex-snapshot
Structure–Mechanical Property Changes in Nucleus arising from Breast Cancer
inferred← citeshttps://doi.org/10.1007/978-1-4614-7678-8_6openalex-snapshot
Cytoskeletal Nuclear Links in the Cardiomyocyte
inferred← citeshttps://doi.org/10.1007/978-1-4899-8032-8_1openalex-snapshot
The Nuclear Envelope and Cancer: A Diagnostic Perspective and Historical Overview
inferred← citeshttps://doi.org/10.1007/978-1-4899-8032-8_20openalex-snapshot
Nuclear Mechanics in Cancer
inferred← citeshttps://doi.org/10.1007/978-1-4939-5617-3_9openalex-snapshot
The Nuclear Lamina: From Mechanosensing in Differentiation to Cancer Cell Migration
inferred← citeshttps://doi.org/10.1007/978-1-60327-461-6_2openalex-snapshot
Mechanical Properties of Interphase Nuclei Probed by Cellular Strain Application
inferred← citeshttps://doi.org/10.1007/978-3-030-58532-7_1openalex-snapshot
The Definition of Biophysics: What Exactly is Biophysics?
inferred← citeshttps://doi.org/10.1007/978-3-030-93306-7_9openalex-snapshot
Mechanics of Microsporidian Polar Tube Firing
inferred← citeshttps://doi.org/10.1007/978-3-032-00537-3_1openalex-snapshot
Role of Nuclear Lamins in the Regulation of the Genome: Focus on CardioLaminopathy
inferred← citeshttps://doi.org/10.1007/978-3-032-00537-3_3openalex-snapshot
Tubular Lamin- and Emerin-Lined Nuclear Envelope Invaginations Isolate Chromatin Domains for Gene Expression Regulation
inferred← citeshttps://doi.org/10.1007/978-3-032-00537-3_4openalex-snapshot
Genetics and cancer-related Laminopathies: Involvement of Lamins and Lamin-Chromatin Interactions
inferred← citeshttps://doi.org/10.1007/978-3-032-19509-8_9openalex-snapshot
Setting Up to Divide: Nuclear Mechanotransduction in the Regulation of Mitosis
inferred← citeshttps://doi.org/10.1007/978-3-032-22285-5_5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-319-15263-9_9openalex-snapshot
The Nuclear Envelope in Cardiac Health and Disease
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Navigating the Nuclear Envelope: One or Multiple Transport Mechanisms for Integral Membrane Proteins?
inferred← citeshttps://doi.org/10.1007/978-3-319-95294-9_3openalex-snapshot
Mechanics of the Cell Nucleus
inferred← citeshttps://doi.org/10.1007/978-3-319-96445-4_5openalex-snapshot
Endothelial Nuclear Lamina in Mechanotransduction Under Shear Stress
inferred← citeshttps://doi.org/10.1007/978-94-007-7726-2_7openalex-snapshot
A Role for the Nuclear Lamina Shape in Cell Senescence and Aging
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inferred← citeshttps://doi.org/10.1007/s00018-019-03037-0openalex-snapshot
Nuclear pore protein TPR associates with lamin B1 and affects nuclear lamina organization and nuclear pore distribution
inferred← citeshttps://doi.org/10.1007/s00018-021-04084-2openalex-snapshot
The wide and growing range of lamin B-related diseases: from laminopathies to cancer
inferred← citeshttps://doi.org/10.1007/s00018-023-04968-5openalex-snapshot
Mechanical stress confers nuclear and functional changes in derived leukemia cells from persistent confined migration
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/s00412-014-0484-7openalex-snapshot
Do lamin A and lamin C have unique roles?
inferred← citeshttps://doi.org/10.1007/s00418-011-0792-4openalex-snapshot
Reorganization of the nuclear lamina and cytoskeleton in adipogenesis
inferred← citeshttps://doi.org/10.1007/s00418-017-1618-9openalex-snapshot
Nuclear organization during in vitro differentiation of porcine mesenchymal stem cells (MSCs) into adipocytes
inferred← citeshttps://doi.org/10.1007/s00418-026-02526-1openalex-snapshot
Lamin subtype expression in Merkel-cell carcinoma: its relation to polyomavirus infection and tumor metastasis
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inferred← citeshttps://doi.org/10.1007/s10237-014-0558-8openalex-snapshot
Bio-chemo-mechanical models for nuclear deformation in adherent eukaryotic cells
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inferred← citeshttps://doi.org/10.1007/s10237-024-01836-4openalex-snapshot
Simulation and experimental study on the influence of lamina on nanoneedle penetration into the cell nucleus
inferred← citeshttps://doi.org/10.1007/s10409-018-00836-9openalex-snapshot
Nuclear mechanics during and after constricted migration
inferred← citeshttps://doi.org/10.1007/s10439-008-9618-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10577-008-1232-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11357-018-0020-4openalex-snapshot
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Hutchinson–Gilford Progeria Syndrome: A Premature Aging Disease
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inferred← citeshttps://doi.org/10.1007/s12195-014-0342-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12195-016-0439-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12195-017-0513-8openalex-snapshot
Expression of Nuclear Lamin Proteins in Endothelial Cells is Sensitive to Cell Passage and Fluid Shear Stress
inferred← citeshttps://doi.org/10.1007/s12195-018-0518-yopenalex-snapshot
Nuclear Lamin Protein C Is Linked to Lineage-Specific, Whole-Cell Mechanical Properties
inferred← citeshttps://doi.org/10.1007/s12195-022-00734-yopenalex-snapshot
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Mapping cytoskeletal stress concentrations and nuclear stresses during confined cell migration
inferred← citeshttps://doi.org/10.1007/s40610-016-0032-8openalex-snapshot
Cell Mechanosensitivity Is Enabled by the LINC Nuclear Complex
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The Cellular Mastermind(?)—Mechanotransduction and the Nucleus
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Nuclear Forces and Cell Mechanosensing
inferred← citeshttps://doi.org/10.1016/b978-0-12-397920-9.00006-8openalex-snapshot
Functional Architecture of the Cell's Nucleus in Development, Aging, and Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-418680-4.00021-xopenalex-snapshot
Selenium and Senescence
inferred← citeshttps://doi.org/10.1016/b978-0-12-803480-4.00014-4openalex-snapshot
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Biophysical regulation of epidermal fate and function
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.abb.2015.11.005openalex-snapshot
The role of endothelial mechanosensitive genes in atherosclerosis and omics approaches
inferred← citeshttps://doi.org/10.1016/j.abb.2020.108718openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.abb.2021.108829openalex-snapshot
Cell stretchers and the LINC complex in mechanotransduction
inferred← citeshttps://doi.org/10.1016/j.addr.2023.114722openalex-snapshot
Mechanotherapy in oncology: Targeting nuclear mechanics and mechanotransduction
inferred← citeshttps://doi.org/10.1016/j.arr.2021.101264openalex-snapshot
Deterioration of nuclear morphology and architecture: A hallmark of senescence and aging
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2012.11.019openalex-snapshot
A role for β-dystroglycan in the organization and structure of the nucleus in myoblasts
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.08.200openalex-snapshot
Linkage between lipid droplet formation and nuclear deformation in HeLa human cervical cancer cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.05.102openalex-snapshot
Mutated lamin A modulates stiffness in muscle cells
inferred← citeshttps://doi.org/10.1016/j.biocel.2022.106300openalex-snapshot
The multifaceted role of micronuclei in tumour progression: A whole organism perspective.
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2011.11.047openalex-snapshot
The role of microtopography in cellular mechanotransduction
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2013.09.095openalex-snapshot
Multifunctional polymer scaffolds with adjustable pore size and chemoattractant gradients for studying cell matrix invasion
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2019.119300openalex-snapshot
Matrix promote mesenchymal stromal cell migration with improved deformation via nuclear stiffness decrease
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2019.119443openalex-snapshot
From perinuclear to intranuclear localization: A cell-penetrating peptide modification strategy to modulate cancer cell migration under mild laser irradiation and improve photothermal therapeutic performance
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2019.119739openalex-snapshot
Substrate curvature as a cue to guide spatiotemporal cell and tissue organization
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2019.119743openalex-snapshot
Cell engineering: Biophysical regulation of the nucleus
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2020.119854openalex-snapshot
Dimensionality changes actin network through lamin A/C and zyxin
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2020.120420openalex-snapshot
Adaptive architecture and mechanoresponse of epithelial cells on a torus
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2020.120572openalex-snapshot
Steering cell behavior through mechanobiology in 3D: A regenerative medicine perspective
inferred← citeshttps://doi.org/10.1016/j.bios.2016.03.015openalex-snapshot
The IsoStretcher: An isotropic cell stretch device to study mechanical biosensor pathways in living cells
inferred← citeshttps://doi.org/10.1016/j.bone.2021.116023openalex-snapshot
At the nuclear envelope of bone mechanobiology
inferred← citeshttps://doi.org/10.1016/j.bpj.2009.02.048openalex-snapshot
Influence of Lamin A on the Mechanical Properties of Amphibian Oocyte Nuclei Measured by Atomic Force Microscopy
inferred← citeshttps://doi.org/10.1016/j.bpj.2013.06.023openalex-snapshot
Macro- to Microscale Strain Transfer in Fibrous Tissues is Heterogeneous and Tissue-Specific
inferred← citeshttps://doi.org/10.1016/j.bpj.2015.05.029openalex-snapshot
Microconstriction Arrays for High-Throughput Quantitative Measurements of Cell Mechanical Properties
inferred← citeshttps://doi.org/10.1016/j.bpj.2015.07.025openalex-snapshot
Migration in Confined 3D Environments Is Determined by a Combination of Adhesiveness, Nuclear Volume, Contractility, and Cell Stiffness
inferred← citeshttps://doi.org/10.1016/j.bpj.2016.08.011openalex-snapshot
A Chemomechanical Model for Nuclear Morphology and Stresses during Cell Transendothelial Migration
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.bpj.2018.08.029openalex-snapshot
Actin Dynamics Couples Extracellular Signals to the Mobility and Molecular Stability of Telomeres
inferred← citeshttps://doi.org/10.1016/j.bpj.2019.02.013openalex-snapshot
A Nondimensional Model Reveals Alterations in Nuclear Mechanics upon Hepatitis C Virus Replication
inferred← citeshttps://doi.org/10.1016/j.bpj.2019.02.029openalex-snapshot
Breast Cancer Cells Adapt Contractile Forces to Overcome Steric Hindrance
inferred← citeshttps://doi.org/10.1016/j.bpj.2020.04.001openalex-snapshot
Chromatin and Cytoskeletal Tethering Determine Nuclear Morphology in Progerin-Expressing Cells
inferred← citeshttps://doi.org/10.1016/j.bpj.2020.11.1200openalex-snapshot
Spatial Distribution of Lamin a Determines Nuclear Stiffness and Stress-Mediated Deformation
inferred← citeshttps://doi.org/10.1016/j.bpj.2021.05.017openalex-snapshot
Depletion of HP1α alters the mechanical properties of MCF7 nuclei
inferred← citeshttps://doi.org/10.1016/j.bpj.2024.03.034openalex-snapshot
Single-cell mechanical assay unveils viscoelastic similarities in normal and neoplastic brain cells
inferred← citeshttps://doi.org/10.1016/j.bpj.2024.11.3322openalex-snapshot
Metabolically intact nuclei are fluidized by the activity of the chromatin remodeling motor BRG1
inferred← citeshttps://doi.org/10.1016/j.bpj.2026.02.030openalex-snapshot
Hypoxia-driven changes in nuclear morphology as a determinant of cell migration
inferred← citeshttps://doi.org/10.1016/j.cbpc.2018.03.006openalex-snapshot
Abnormal nuclear morphology is independent of longevity in a zmpste24 -deficient fish model of Hutchinson-Gilford progeria syndrome (HGPS)
inferred← citeshttps://doi.org/10.1016/j.ceb.2010.10.015openalex-snapshot
Nuclear mechanics during cell migration
inferred← citeshttps://doi.org/10.1016/j.ceb.2011.10.001openalex-snapshot
Nuclear mechanics in differentiation and development
inferred← citeshttps://doi.org/10.1016/j.ceb.2016.01.011openalex-snapshot
Squish and squeeze — the nucleus as a physical barrier during migration in confined environments
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.2020.03.001openalex-snapshot
The role of the cell nucleus in mechanotransduction
inferred← citeshttps://doi.org/10.1016/j.ceb.2023.102222openalex-snapshot
Mechanisms controlling the mechanical properties of the nuclei
inferred← citeshttps://doi.org/10.1016/j.ceb.2023.102267openalex-snapshot
Lamins as structural nuclear elements through evolution
inferred← citeshttps://doi.org/10.1016/j.ceb.2023.102280openalex-snapshot
Intermediate filaments in the heart: The dynamic duo of desmin and lamins orchestrates mechanical force transmission
inferred← citeshttps://doi.org/10.1016/j.ceb.2026.102668openalex-snapshot
Nuclear adaptation in cell migration
inferred← citeshttps://doi.org/10.1016/j.cell.2013.06.052openalex-snapshot
Orchestrated Intron Retention Regulates Normal Granulocyte Differentiation
inferred← citeshttps://doi.org/10.1016/j.cellsig.2026.112449openalex-snapshot
Oncometabolite D-2-hydroxyglutarate regulates actin dynamics and nuclear homeostasis in IDH1-mutant glioma
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.08.018openalex-snapshot
Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112893openalex-snapshot
An oncogenic isoform of septin 9 promotes the formation of juxtanuclear invadopodia by reducing nuclear deformability
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114373openalex-snapshot
The condensation of HP1α/Swi6 imparts nuclear stiffness
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114692openalex-snapshot
Confinement controls the directional cell responses to fluid forces
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114852openalex-snapshot
Heterogeneous force response of chromatin in isolated nuclei
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.118126openalex-snapshot
EpCAM-dependent membrane mechanics regulate nuclear deformation and promote gastric cancer metastasis
inferred← citeshttps://doi.org/10.1016/j.cub.2013.11.009openalex-snapshot
Nuclear Mechanics and Mechanotransduction in Health and Disease
inferred← citeshttps://doi.org/10.1016/j.cub.2020.11.037openalex-snapshot
Nuclear Deformation Causes DNA Damage by Increasing Replication Stress
inferred← citeshttps://doi.org/10.1016/j.cub.2024.10.015openalex-snapshot
Nuclear deformability facilitates apical nuclear migration in the developing zebrafish retina
inferred← citeshttps://doi.org/10.1016/j.devcel.2008.07.013openalex-snapshot
The Impact of Gene Location in the Nucleus on Transcriptional Regulation
inferred← citeshttps://doi.org/10.1016/j.devcel.2009.10.018openalex-snapshot
Nuclei Take a Position: Managing Nuclear Location
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.04.020openalex-snapshot
Mechanosensing by the Lamina Protects against Nuclear Rupture, DNA Damage, and Cell-Cycle Arrest
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.10.023openalex-snapshot
ERK1/2 Phosphorylation of FHOD Connects Signaling and Nuclear Positioning Alternations in Cardiac Laminopathy
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.01.030openalex-snapshot
Lamin B2 Levels Regulate Polyploidization of Cardiomyocyte Nuclei and Myocardial Regeneration
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.10.011openalex-snapshot
Mechanical Adaptability of Tumor Cells in Metastasis
inferred← citeshttps://doi.org/10.1016/j.drudis.2022.103438openalex-snapshot
Gold nanoparticles as antiangiogenic and antimetastatic agents
inferred← citeshttps://doi.org/10.1016/j.drup.2022.100881openalex-snapshot
Paclitaxel resistance related to nuclear envelope structural sturdiness
inferred← citeshttps://doi.org/10.1016/j.ejcb.2016.06.007openalex-snapshot
Causes and consequences of nuclear envelope alterations in tumour progression
inferred← citeshttps://doi.org/10.1016/j.exer.2020.108373openalex-snapshot
Iris stromal cell nuclei deform to more elongated shapes during pharmacologically-induced miosis and mydriasis
inferred← citeshttps://doi.org/10.1016/j.exphem.2025.104863openalex-snapshot
Ontogenetic drivers of neutrophil heterogeneity
inferred← citeshttps://doi.org/10.1016/j.gde.2022.101959openalex-snapshot
Molecular genetic mechanisms of dilated cardiomyopathy
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e36583openalex-snapshot
The destruction of cytoplasmic skeleton leads to the change of nuclear structure and the looseness of lamin A submicroscopic network
inferred← citeshttps://doi.org/10.1016/j.ijcard.2022.06.038openalex-snapshot
The LMNA p.R541C mutation causes dilated cardiomyopathy in human and mice
inferred← citeshttps://doi.org/10.1016/j.jbiomech.2008.01.009openalex-snapshot
Muscle dystrophy single point mutation in the 2B segment of lamin A does not affect the mechanical properties at the dimer level
inferred← citeshttps://doi.org/10.1016/j.jbiomech.2009.09.002openalex-snapshot
In the middle of it all: Mutual mechanical regulation between the nucleus and the cytoskeleton
inferred← citeshttps://doi.org/10.1016/j.jbiomech.2015.05.004openalex-snapshot
Mechanical trapping of the nucleus on micropillared surfaces inhibits the proliferation of vascular smooth muscle cells but not cervical cancer HeLa cells
inferred← citeshttps://doi.org/10.1016/j.jbiomech.2016.10.034openalex-snapshot
Nuclear mechanical resilience but not stiffness is modulated by αII-spectrin
inferred← citeshttps://doi.org/10.1016/j.jbiomech.2020.110012openalex-snapshot
Isolated Nuclei Stiffen in Response to Low Intensity Vibration
inferred← citeshttps://doi.org/10.1016/j.jbiomech.2025.112579openalex-snapshot
Endothelial cytoskeleton in mechanotransduction and vascular diseases
inferred← citeshttps://doi.org/10.1016/j.jgg.2017.09.003openalex-snapshot
Tissue-specific genome editing of laminA/C in the posterior silk glands of Bombyx mori
inferred← citeshttps://doi.org/10.1016/j.jmps.2025.106322openalex-snapshot
A mechanochemical model for dynamic deformation and adaptive stiffening of cell nuclei
inferred← citeshttps://doi.org/10.1016/j.jprot.2009.12.004openalex-snapshot
Protein profile in HBx transfected cells: A comparative iTRAQ-coupled 2D LC-MS/MS analysis
inferred← citeshttps://doi.org/10.1016/j.jsb.2011.05.015openalex-snapshot
Structure and stability of the lamin A tail domain and HGPS mutant
inferred← citeshttps://doi.org/10.1016/j.jtho.2025.07.027openalex-snapshot
Metastatic Organotropism in Small Cell Lung Cancer
inferred← citeshttps://doi.org/10.1016/j.lfs.2018.09.026openalex-snapshot
Understanding lamin proteins and their roles in aging and cardiovascular diseases
inferred← citeshttps://doi.org/10.1016/j.matbio.2019.01.001openalex-snapshot
Nuclear softening is essential for protease-independent migration
inferred← citeshttps://doi.org/10.1016/j.mbm.2025.100164openalex-snapshot
Mechanical cues enhance chondrocyte function: Insights from mechanoreception, regulation, and biological responses
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