The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy | Nature Communications
Lamin A/C Antibody | Cell Signaling Technology
Generation of Lamin A/C gene (Lmna) exon 4 mutations using CRISPR/Cas... | Download Scientific Diagram
Tyrosine phosphorylation of lamin A by Src promotes disassembly of nuclear lamina in interphase | Life Science Alliance
Dual Specificity Phosphatase 4 Mediates Cardiomyopathy Caused by Lamin A/C (LMNA) Gene Mutation* - Journal of Biological Chemistry
What Should the Cardiologist know about Lamin Disease? | AER Journal
Laminopathies | IntechOpen
Phosphorylated Lamin A/C in the nuclear interior binds active enhancers associated with abnormal transcription in progeria | bioRxiv
Amelioration of desmin network defects by αB-crystallin overexpression confers cardioprotection in a mouse model of dilated cardiomyopathy caused by LMNA gene mutation - ScienceDirect
Pre-Lamin A/C - Wikipedia
A novel lamin A/C mutation in a Dutch family with premature atherosclerosis - Atherosclerosis
Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes | Journal of Medical Genetics
Cells | Free Full-Text | Consequences of Lmna Exon 4 Mutations in Myoblast Function | HTML
Structural basis for lamin assembly at the molecular level | Nature Communications
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
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
Lamin A/C protein (top), gene structure (middle), and localization of... | Download Scientific Diagram
LBR and Lamin A/C Sequentially Tether Peripheral Heterochromatin and Inversely Regulate Differentiation - ScienceDirect
A novel lamin A/C gene mutation causing spinal muscular atrophy phenotype with cardiac involvement: report of one case | BMC Neurology | Full Text
What Should the Cardiologist know about Lamin Disease? | AER Journal
Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease | NEJM
LMNA-R249W produces Lamin A/C aggregates upon terminal skeletal... | Download Scientific Diagram
Cureus | Lamin A/C Cardiomyopathy with E203K Pathogenic Mutation
