Clinical and Functional Characterization of a Novel Mutation in Lamin A/C Gene in a Multigenerational Family with Arrhythmogenic Cardiac Laminopathy | PLOS ONE
Direct Synthesis of Lamin A, Bypassing Prelamin A Processing, Causes Misshapen Nuclei in Fibroblasts but No Detectable Pathology in Mice* - Journal of Biological Chemistry
Role of nuclear Lamin A/C in cardiomyocyte functions - Carmosino - 2014 - Biology of the Cell - Wiley Online Library
Modeling of lamin A/C mutation premature cardiac aging using patient-specific induced pluripotent stem cells | Aging
Cardiovascular Medicine - Lamin A/C cardiomyopathy: case report and review of the literature
Lamin A/C Antibody | Cell Signaling Technology
Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease | NEJM
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Clinical and Functional Characterization of a Novel Mutation in Lamin A/C Gene in a Multigenerational Family with Arrhythmogenic Cardiac Laminopathy | PLOS ONE
Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria - ScienceDirect
Familial lamin A/C mutation cardiomyopathy with arrhythmia substrate detected by cardiac magnetic resonance imaging and electroanatomical mapping - International Journal of Cardiology
Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype
Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications - International Journal of Cardiology
IJMS | Free Full-Text | Lamin A/C and the Immune System: One Intermediate Filament, Many Faces | HTML
Autosomal dominant dilated cardiomyopathy with atrioventricular block: a lamin A/C defect-related disease - ScienceDirect
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
Refractory ventricular arrhythmia in a patient with Lamin A/C (LMNA) cardiomyopathy successfully treated with thoracic bilateral stellate ganglionectomy - HeartRhythm Case Reports
Phosphorylation of Lamin A/C at serine 22 modulates Nav1.5 function - Olaopa - 2021 - Physiological Reports - Wiley Online Library
Structure of the asymmetric unit of the human lamin A/C fragment. a... | Download Scientific Diagram
PE Anti-Lamin A + Lamin C antibody [EPR4100] (ab210433) | Abcam
Pulmonary vein isolation treats symptomatic AF in a patient with Lamin A/C mutation: case report and review of the literature | SpringerLink
Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease - Journal of Molecular and Cellular Cardiology