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Direct Synthesis of Lamin A, Bypassing Prelamin A Processing, Causes Misshapen Nuclei in Fibroblasts but No Detectable Pathology in Mice* - Journal of Biological Chemistry
Direct Synthesis of Lamin A, Bypassing Prelamin A Processing, Causes Misshapen Nuclei in Fibroblasts but No Detectable Pathology in Mice* - Journal of Biological Chemistry

Phosphorylated Lamin A/C in the nuclear interior binds active enhancers associated with abnormal transcription in progeria | bioRxiv
Phosphorylated Lamin A/C in the nuclear interior binds active enhancers associated with abnormal transcription in progeria | bioRxiv

Frontiers | Effect of Occurrence of Lamin A/C (LMNA) Genetic Variants in a Cohort of 101 Consecutive Apparent “Lone AF” Patients: Results and Insights
Frontiers | Effect of Occurrence of Lamin A/C (LMNA) Genetic Variants in a Cohort of 101 Consecutive Apparent “Lone AF” Patients: Results and Insights

Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies | Circulation: Genomic and Precision Medicine
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies | Circulation: Genomic and Precision Medicine

Modeling of lamin A/C mutation premature cardiac aging using patient-specific induced pluripotent stem cells | Aging
Modeling of lamin A/C mutation premature cardiac aging using patient-specific induced pluripotent stem cells | Aging

Lamin A/C (4C11) Mouse mAb | Cell Signaling Technology
Lamin A/C (4C11) Mouse mAb | Cell Signaling Technology

Lamin A/C-Related Cardiac Disease | Circulation: Cardiovascular Genetics
Lamin A/C-Related Cardiac Disease | Circulation: Cardiovascular Genetics

Cardiovascular Medicine - Lamin A/C cardiomyopathy: case report and review of the literature
Cardiovascular Medicine - Lamin A/C cardiomyopathy: case report and review of the literature

Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease | NEJM
Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease | NEJM

Familial lamin A/C mutation cardiomyopathy with arrhythmia substrate detected by cardiac magnetic resonance imaging and electroanatomical mapping - International Journal of Cardiology
Familial lamin A/C mutation cardiomyopathy with arrhythmia substrate detected by cardiac magnetic resonance imaging and electroanatomical mapping - International Journal of Cardiology

Lamin A/C-Related Cardiac Disease | Circulation: Cardiovascular Genetics
Lamin A/C-Related Cardiac Disease | Circulation: Cardiovascular Genetics

Frontiers | The Broad Spectrum of LMNA Cardiac Diseases: From Molecular Mechanisms to Clinical Phenotype
Frontiers | The Broad Spectrum of LMNA Cardiac Diseases: From Molecular Mechanisms to Clinical Phenotype

Phosphorylated Lamin A/C in the nuclear interior binds active enhancers associated with abnormal transcription in progeria | bioRxiv
Phosphorylated Lamin A/C in the nuclear interior binds active enhancers associated with abnormal transcription in progeria | bioRxiv

Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease - Journal of Molecular and Cellular Cardiology
Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease - Journal of Molecular and Cellular Cardiology

Phosphorylation of Lamin A/C at serine 22 modulates Nav1.5 function - Olaopa - 2021 - Physiological Reports - Wiley Online Library
Phosphorylation of Lamin A/C at serine 22 modulates Nav1.5 function - Olaopa - 2021 - Physiological Reports - Wiley Online Library

Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications - International Journal of Cardiology
Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications - International Journal of Cardiology

Clinical and Functional Characterization of a Novel Mutation in Lamin A/C Gene in a Multigenerational Family with Arrhythmogenic Cardiac Laminopathy | PLOS ONE
Clinical and Functional Characterization of a Novel Mutation in Lamin A/C Gene in a Multigenerational Family with Arrhythmogenic Cardiac Laminopathy | PLOS ONE

PE Anti-Lamin A + Lamin C antibody [EPR4100] (ab210433) | Abcam
PE Anti-Lamin A + Lamin C antibody [EPR4100] (ab210433) | Abcam

Structure of the asymmetric unit of the human lamin A/C fragment. a... | Download Scientific Diagram
Structure of the asymmetric unit of the human lamin A/C fragment. a... | Download Scientific Diagram

MedShare | Facebook
MedShare | Facebook

Pulmonary vein isolation treats symptomatic AF in a patient with Lamin A/C mutation: case report and review of the literature | SpringerLink
Pulmonary vein isolation treats symptomatic AF in a patient with Lamin A/C mutation: case report and review of the literature | SpringerLink

A novel mutation in LAMIN A/C is associated with isolated early-onset atrial fibrillation and progressive atrioventricular block followed by cardiomyopathy and sudden cardiac death - Heart Rhythm
A novel mutation in LAMIN A/C is associated with isolated early-onset atrial fibrillation and progressive atrioventricular block followed by cardiomyopathy and sudden cardiac death - Heart Rhythm

Lamin A/C Antibody | Cell Signaling Technology
Lamin A/C Antibody | Cell Signaling Technology

Anti-Lamin A + C Antibody (A12573) | Antibodies.com
Anti-Lamin A + C Antibody (A12573) | Antibodies.com

A typical laminopathy ECG, showing first-degree atrioventricular block... | Download Scientific Diagram
A typical laminopathy ECG, showing first-degree atrioventricular block... | Download Scientific Diagram

Localization of the R189W mutation in lamin A/C gene and lamin A/C... | Download Scientific Diagram
Localization of the R189W mutation in lamin A/C gene and lamin A/C... | Download Scientific Diagram