Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype
Comparison of lamin A, lamin C, and LA ⌬ 50 structures. ( A ) The 12... | Download Scientific Diagram
The UMD-LMNA database: the gene
Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria - ScienceDirect
What Should the Cardiologist know about Lamin Disease? | AER Journal
Lamin A Truncation in Hutchinson-Gilford Progeria | Science
JCI - Good news in the nuclear envelope: loss of lamin A might be a gain
David R. Liu on Twitter: "The mutation (discovered by @NIHDirector's lab in 2003) results in progerin, a toxic protein that damages nuclei. So providing more healthy LMNA is not a solution, and
Frontiers | Diversity of Nuclear Lamin A/C Action as a Key to Tissue-Specific Regulation of Cellular Identity in Health and Disease
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization | PNAS
Cells | Free Full-Text | Consequences of Lmna Exon 4 Mutations in Myoblast Function
The structural and gene expression hypotheses in laminopathic diseases—not so different after all | Molecular Biology of the Cell
Frontiers | The Broad Spectrum of LMNA Cardiac Diseases: From Molecular Mechanisms to Clinical Phenotype
Lamin - Wikipedia
Lamin and the heart | Heart
Normal processing of lamin A from mRNA to mature lamin A. (A) Normal... | Download Scientific Diagram
When Lamins Go Bad: Nuclear Structure and Disease: Cell
Pathogenic LMNA variants disrupt cardiac lamina-chromatin interactions and de-repress alternative fate genes - ScienceDirect
Lamin A/C protein (top), gene structure (middle), and localization of... | Download Scientific Diagram
Pre-Lamin A/C - Wikipedia
Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging | European Journal of Human Genetics
