Lamin and the heart | Heart
Frontiers | The Broad Spectrum of LMNA Cardiac Diseases: From Molecular Mechanisms to Clinical Phenotype | Physiology
Lamin A/C protein (top), gene structure (middle), and localization of... | Download Scientific Diagram
Comparison of lamin A, lamin C, and LA ⌬ 50 structures. ( A ) The 12... | Download Scientific Diagram
Structural basis for lamin assembly at the molecular level | Nature Communications
JCI - Good news in the nuclear envelope: loss of lamin A might be a gain
Lamins: building blocks or regulators of gene expression? | Nature Reviews Molecular Cell Biology
Lamin A Truncation in Hutchinson-Gilford Progeria
LMNA - 维基百科，自由的百科全书
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
Generation of Lamin A/C gene (Lmna) exon 4 mutations using CRISPR/Cas... | Download Scientific Diagram
Do lamin A and lamin C have unique roles? | SpringerLink
An EDMD Mutation in C. elegans Lamin Blocks Muscle-Specific Gene Relocation and Compromises Muscle Integrity - ScienceDirect
Lamin mutation location predicts cardiac phenotype severity: combined analysis of the published literature | Open Heart
Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype | Cell and Developmental Biology
The structural and gene expression hypotheses in laminopathic diseases—not so different after all | Molecular Biology of the Cell
The lamin protein family | Genome Biology | Full Text
Pre-Lamin A/C - Wikipedia
Biogenesis of lamin A and progerin in the cell. The left picture... | Download Scientific Diagram
Localization of the R189W mutation in lamin A/C gene and lamin A/C... | Download Scientific Diagram
LBR and Lamin A/C Sequentially Tether Peripheral Heterochromatin and Inversely Regulate Differentiation: Cell
Variation in the Lamin A/C Gene | Arteriosclerosis, Thrombosis, and Vascular Biology
PLOS ONE: Clinical and Functional Characterization of a Novel Mutation in Lamin A/C Gene in a Multigenerational Family with Arrhythmogenic Cardiac Laminopathy
