p.S143P mutant lamin A/C is more nucleoplasmic than WT lamin A/C and... | Download Scientific Diagram
Altered Chromosomal Positioning, Compaction, and Gene Expression with a Lamin A/C Gene Mutation | PLOS ONE
Laminopathies | IntechOpen
Structural basis for lamin assembly at the molecular level | Nature Communications
Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes | Journal of Medical Genetics
Dual Specificity Phosphatase 4 Mediates Cardiomyopathy Caused by Lamin A/C (LMNA) Gene Mutation* - Journal of Biological Chemistry
A novel lamin A/C gene mutation causing spinal muscular atrophy phenotype with cardiac involvement: report of one case | BMC Neurology | Full Text
The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy | Nature Communications
Cureus | Lamin A/C Cardiomyopathy with E203K Pathogenic Mutation
Tyrosine phosphorylation of lamin A by Src promotes disassembly of nuclear lamina in interphase | Life Science Alliance
What Should the Cardiologist know about Lamin Disease? | AER Journal
Cardiovascular Medicine - Lamin A/C cardiomyopathy: case report and review of the literature
Frontiers | Role of Lamin A/C Gene Mutations in the Signaling Defects Leading to Cardiomyopathies
LBR and Lamin A/C Sequentially Tether Peripheral Heterochromatin and Inversely Regulate Differentiation - ScienceDirect
A case of lamin A/C mutation cardiomyopathy with overlap features of ARVC: A critical role of genetic testing - International Journal of Cardiology
Localization of the R189W mutation in lamin A/C gene and lamin A/C... | Download Scientific Diagram
Familial lamin A/C mutation cardiomyopathy with arrhythmia substrate detected by cardiac magnetic resonance imaging and electroanatomical mapping - International Journal of Cardiology
Variation in the Lamin A/C Gene | Arteriosclerosis, Thrombosis, and Vascular Biology
LMNA-R249W produces Lamin A/C aggregates upon terminal skeletal... | Download Scientific Diagram
Amelioration of desmin network defects by αB-crystallin overexpression confers cardioprotection in a mouse model of dilated cardiomyopathy caused by LMNA gene mutation - ScienceDirect
What Should the Cardiologist know about Lamin Disease? | AER Journal
Pre-Lamin A/C - Wikipedia
Generation of Lamin A/C gene (Lmna) exon 4 mutations using CRISPR/Cas... | Download Scientific Diagram
Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype
