Pre-Lamin A/C - Wikipedia
Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease | NEJM
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes | Journal of Medical Genetics
When Lamins Go Bad: Nuclear Structure and Disease: Cell
What Should the Cardiologist know about Lamin Disease? | AER Journal
Frontiers | The Broad Spectrum of LMNA Cardiac Diseases: From Molecular Mechanisms to Clinical Phenotype
The Cardiomyopathy Lamin A/C D192G Mutation Disrupts Whole-Cell Biomechanics in Cardiomyocytes as Measured by Atomic Force Microscopy Loading-Unloading Curve Analysis | Scientific Reports
Altered Chromosomal Positioning, Compaction, and Gene Expression with a Lamin A/C Gene Mutation | PLOS ONE
Mechanisms of allelic and clinical heterogeneity of lamin A/C phenotypes
Cardiovascular Medicine - Lamin A/C cardiomyopathy: case report and review of the literature
A case of lamin A/C mutation cardiomyopathy with overlap features of ARVC: A critical role of genetic testing - International Journal of Cardiology
The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy | Nature Communications
Frontiers | Role of Lamin A/C Gene Mutations in the Signaling Defects Leading to Cardiomyopathies
Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype
LMNA-R249W produces Lamin A/C aggregates upon terminal skeletal... | Download Scientific Diagram
Lamin A/C protein (top), gene structure (middle), and localization of... | Download Scientific Diagram
p.S143P mutant lamin A/C is more nucleoplasmic than WT lamin A/C and... | Download Scientific Diagram
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 lamin A/C mutation in a Dutch family with premature atherosclerosis - Atherosclerosis
Amelioration of desmin network defects by αB-crystallin overexpression confers cardioprotection in a mouse model of dilated cardiomyopathy caused by LMNA gene mutation - ScienceDirect
Variation in the Lamin A/C Gene | Arteriosclerosis, Thrombosis, and Vascular Biology
Pre-Lamin A/C - Wikipedia
Tyrosine phosphorylation of lamin A by Src promotes disassembly of nuclear lamina in interphase | Life Science Alliance
