Schematic of the LMNA gene and lamin A protein indicating... | Download Scientific Diagram
References in Lamins and Lamin-Associated Proteins in Gastrointestinal Health and Disease - Gastroenterology
Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy | Genetics in Medicine
Cancers | Free Full-Text | Lamin A/C: Function in Normal and Tumor Cells | HTML
When Lamins Go Bad: Nuclear Structure and Disease: Cell
Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype | Cell and Developmental Biology
An EDMD Mutation in C. elegans Lamin Blocks Muscle-Specific Gene Relocation and Compromises Muscle Integrity - ScienceDirect
Lamin A Truncation in Hutchinson-Gilford Progeria
JCI - Good news in the nuclear envelope: loss of lamin A might be a gain
Lamin and the heart | Heart
Lamin gene evolution in insects. (A) Phylogenetic tree of insects. The... | Download Scientific Diagram
Figure 1 | Pharmacotherapy to gene editing: potential therapeutic approaches for Hutchinson–Gilford progeria syndrome | SpringerLink
What Should the Cardiologist know about Lamin Disease? | AER Journal
Schematic of the LMNA gene and lamin A protein indicating mutations.
Structural basis for lamin assembly at the molecular level | Nature Communications
CRISPR base editor treats premature-aging syndrome | Signal Transduction and Targeted Therapy
Role of A‐ and B‐type lamins in nuclear structure–function relationships - Patil - 2021 - Biology of the Cell - Wiley Online Library
Lamin mutation location predicts cardiac phenotype severity: combined analysis of the published literature | Open Heart
LMNA Gene - GeneCards | LMNA Protein | LMNA Antibody
Comparison of lamin A, lamin C, and LA ⌬ 50 structures. ( A ) The 12... | Download Scientific Diagram
Dual Specificity Phosphatase 4 Mediates Cardiomyopathy Caused by Lamin A/C (LMNA) Gene Mutation* - Journal of Biological Chemistry
Pre-Lamin A/C - Wikipedia
Phosphorylated Lamin A/C in the Nuclear Interior Binds Active Enhancers Associated with Abnormal Transcription in Progeria - ScienceDirect
