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The lamin A/C Ig-fold undergoes cell density-dependent changes that alter epitope binding

Nucleus (Austin, Tex.), 2023-12, Vol.14 (1), p.2180206-2180206

2023

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Mechanisms of muscle degeneration, regeneration, and repair in the muscular dystrophies

Annual review of physiology, 2009-01, Vol.71 (1), p.37-57

2009

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Prelamin A, Zmpste24, misshapen cell nuclei, and progeria--new evidence suggesting that protein farnesylation could be important for disease pathogenesis

Journal of lipid research, 2005-12, Vol.46 (12), p.2531-2558

2005

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Blocking Protein Farnesyltransferase Improves Nuclear Blebbing in Mouse Fibroblasts with a Targeted Hutchinson-Gilford Progeria Syndrome Mutation

Proceedings of the National Academy of Sciences - PNAS, 2005-07, Vol.102 (29), p.10291-10296

2005

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c‐Fos separation from Lamin A/C by GDF15 promotes colon cancer invasion and metastasis in inflammatory microenvironment

Journal of cellular physiology, 2020-05, Vol.235 (5), p.4407-4421

2020

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Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644C

American journal of medical genetics. Part A, 2008-06, Vol.146A (12), p.1530-1542

2008

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Cell-cycle-dependent dynamics of nuclear pores: pore-free islands and lamins

Journal of cell science, 2006-11, Vol.119 (21), p.4442-4451

2006

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Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy

European journal of human genetics : EJHG, 2013-10, Vol.21 (10), p.1105-1111

2013

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Lamin A/C gene (LMNA) mutation associated with laminopathy: A rare cause of idiopathic acro-osteolysis

Joint, bone, spine : revue du rhumatisme, 2019-07, Vol.86 (4), p.525-527

2019

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Beta-strand-mediated dimeric formation of the Ig-like domains of human lamin A/C and B1

Biochemical and biophysical research communications, 2021-04, Vol.550, p.191-196

2021

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Modeling Skeletal Muscle Laminopathies Using Human Induced Pluripotent Stem Cells Carrying Pathogenic LMNA Mutations

Frontiers in physiology, 2018-10, Vol.9, p.1332-1332

2018

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Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria

Developmental cell, 2020-03, Vol.52 (6), p.699-713.e11

2020

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Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcription

Experimental cell research, 2003-11, Vol.291 (1), p.122-134

2003

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E3 ubiquitin ligase HECW2 targets PCNA and lamin B1

Biochimica et biophysica acta. Molecular cell research, 2018-08, Vol.1865 (8), p.1088-1104

2018

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Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers: A European Cohort Study

Journal of the American College of Cardiology, 2012-01, Vol.59 (5), p.493-500

2012

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The structure and function of lamin A/C: Special focus on cardiomyopathy and therapeutic interventions

Life sciences (1973), 2024-03, Vol.341, p.122489-122489, Article 122489

2024

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Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation

European heart journal, 2018-03, Vol.39 (10), p.853-860

2018

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Spatial distribution of lamin A/C determines nuclear stiffness and stress-mediated deformation

Journal of cell science, 2021-05, Vol.134 (10)

2021

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De Novo Variants in LMNB1 Cause Pronounced Syndromic Microcephaly and Disruption of Nuclear Envelope Integrity

American journal of human genetics, 2020-10, Vol.107 (4), p.753-762

2020

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Sensing the squeeze: nuclear mechanotransduction in health and disease

Nucleus (Austin, Tex.), 2024-12, Vol.15 (1), p.2374854

2024

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2018 ACC/AHA/HRS Guideline on the Evaluation and Management of Patients With Bradycardia and Cardiac Conduction Delay

Journal of the American College of Cardiology, 2019-08, Vol.74 (7), p.e51-e156

2019

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Lamin A/C phosphorylation at serine 22 is a conserved heat shock response to regulate nuclear adaptation during stress

Journal of cell science, 2023-02, Vol.136 (4)

2023

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Epigenetic regulation of Cebpb activation by pY19-Caveolin-2 at the nuclear periphery in association with the nuclear lamina

Biochimica et biophysica acta. Molecular cell research, 2022-12, Vol.1869 (12), p.119363-119363, Article 119363

2022

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Mice harboring a R133L heterozygous mutation in LMNA exhibited ectopic lipid accumulation, aging, and mitochondrial dysfunction in adipose tissue

The FASEB journal, 2023-02, Vol.37 (2), p.e22730-n/a

2023

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The lamin A/C Ig-fold undergoes cell density-dependent changes that alter epitope binding

Mechanisms of muscle degeneration, regeneration, and repair in the muscular dystrophies

Prelamin A, Zmpste24, misshapen cell nuclei, and progeria--new evidence suggesting that protein farnesylation could be important for disease pathogenesis

Blocking Protein Farnesyltransferase Improves Nuclear Blebbing in Mouse Fibroblasts with a Targeted Hutchinson-Gilford Progeria Syndrome Mutation

c‐Fos separation from Lamin A/C by GDF15 promotes colon cancer invasion and metastasis in inflammatory microenvironment

Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644C

Cell-cycle-dependent dynamics of nuclear pores: pore-free islands and lamins

Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy

Lamin A/C gene (LMNA) mutation associated with laminopathy: A rare cause of idiopathic acro-osteolysis

Beta-strand-mediated dimeric formation of the Ig-like domains of human lamin A/C and B1

Modeling Skeletal Muscle Laminopathies Using Human Induced Pluripotent Stem Cells Carrying Pathogenic LMNA Mutations

Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria

Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcription

E3 ubiquitin ligase HECW2 targets PCNA and lamin B1

Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers: A European Cohort Study

The structure and function of lamin A/C: Special focus on cardiomyopathy and therapeutic interventions

Lamin A/C cardiomyopathy: young onset, high penetrance, and frequent need for heart transplantation

Spatial distribution of lamin A/C determines nuclear stiffness and stress-mediated deformation

De Novo Variants in LMNB1 Cause Pronounced Syndromic Microcephaly and Disruption of Nuclear Envelope Integrity

Sensing the squeeze: nuclear mechanotransduction in health and disease

2018 ACC/AHA/HRS Guideline on the Evaluation and Management of Patients With Bradycardia and Cardiac Conduction Delay

Lamin A/C phosphorylation at serine 22 is a conserved heat shock response to regulate nuclear adaptation during stress

Epigenetic regulation of Cebpb activation by pY19-Caveolin-2 at the nuclear periphery in association with the nuclear lamina

2018 ACC/AHA/HRS Guideline on the Evaluation and Management of Patients With Bradycardia and Cardiac Conduction Delay: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society

Mice harboring a R133L heterozygous mutation in LMNA exhibited ectopic lipid accumulation, aging, and mitochondrial dysfunction in adipose tissue

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