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Genes | Free Full-Text | LMNA Mutations G232E and R482L Cause Dysregulation of Skeletal Muscle Differentiation, Bioenergetics, and Metabolic Gene Expression Profile
Genes | Free Full-Text | LMNA Mutations G232E and R482L Cause Dysregulation of Skeletal Muscle Differentiation, Bioenergetics, and Metabolic Gene Expression Profile

Prelamin-A/C - Wikipedia
Prelamin-A/C - Wikipedia

Frontiers | Effect of Occurrence of Lamin A/C (LMNA) Genetic Variants in a Cohort of 101 Consecutive Apparent “Lone AF” Patients: Results and Insights
Frontiers | Effect of Occurrence of Lamin A/C (LMNA) Genetic Variants in a Cohort of 101 Consecutive Apparent “Lone AF” Patients: Results and Insights

Schematic representation of MADA pathogenic mutations in LMNA gene... | Download Scientific Diagram
Schematic representation of MADA pathogenic mutations in LMNA gene... | Download Scientific Diagram

Prelamin-A/C - Wikipedia
Prelamin-A/C - Wikipedia

LMNA Gene - GeneCards | LMNA Protein | LMNA Antibody
LMNA Gene - GeneCards | LMNA Protein | LMNA Antibody

Lamin A Truncation in Hutchinson-Gilford Progeria | Science
Lamin A Truncation in Hutchinson-Gilford Progeria | Science

LMNA - an overview | ScienceDirect Topics
LMNA - an overview | ScienceDirect Topics

Epigenetic clock for skin and blood cells applied to Hutchinson Gilford Progeria Syndrome and ex vivo studies - Figure f3 | Aging
Epigenetic clock for skin and blood cells applied to Hutchinson Gilford Progeria Syndrome and ex vivo studies - Figure f3 | Aging

Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy: Molecular Therapy - Nucleic Acids
Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy: Molecular Therapy - Nucleic Acids

Prelamin-A/C - Wikipedia
Prelamin-A/C - Wikipedia

Modulation of cytoskeleton in cardiomyopathy caused by mutations in LMNA gene | American Journal of Physiology-Cell Physiology
Modulation of cytoskeleton in cardiomyopathy caused by mutations in LMNA gene | American Journal of Physiology-Cell Physiology

The role of genetic mutations in genes LMNA, PPARG, PLIN1, AKT2, CIDEC in Köbberling–Dunnigan Syndrome
The role of genetic mutations in genes LMNA, PPARG, PLIN1, AKT2, CIDEC in Köbberling–Dunnigan Syndrome

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

Hutchinson-Gilford progeria patient-derived cardiomyocyte model of carrying LMNA gene variant c.1824 C > T | SpringerLink
Hutchinson-Gilford progeria patient-derived cardiomyocyte model of carrying LMNA gene variant c.1824 C > T | SpringerLink

The LMNA gene and its putative association with human ageing
The LMNA gene and its putative association with human ageing

LMNA » Laboratory Testing and Research
LMNA » Laboratory Testing and Research

What Should the Cardiologist know about Lamin Disease? | AER Journal
What Should the Cardiologist know about Lamin Disease? | AER Journal

Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging | European Journal of Human Genetics
Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging | European Journal of Human Genetics

Variation in the Lamin A/C Gene | Arteriosclerosis, Thrombosis, and Vascular Biology
Variation in the Lamin A/C Gene | Arteriosclerosis, Thrombosis, and Vascular Biology

What Should the Cardiologist know about Lamin Disease? | AER Journal
What Should the Cardiologist know about Lamin Disease? | AER Journal

Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes | Journal of Medical Genetics
Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes | Journal of Medical Genetics

PDF] LMNA cardiomyopathy: cell biology and genetics meet clinical medicine | Semantic Scholar
PDF] LMNA cardiomyopathy: cell biology and genetics meet clinical medicine | Semantic Scholar

Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype
Frontiers | The Emerging Role of Lamin C as an Important LMNA Isoform in Mechanophenotype

Schematic structure of LMNA. In the upper panel, filled boxes indicate... | Download Scientific Diagram
Schematic structure of LMNA. In the upper panel, filled boxes indicate... | Download Scientific Diagram

CRISPR base editor treats premature-aging syndrome | Signal Transduction and Targeted Therapy
CRISPR base editor treats premature-aging syndrome | Signal Transduction and Targeted Therapy

Frontiers | Exploring the Crosstalk Between LMNA and Splicing Machinery Gene Mutations in Dilated Cardiomyopathy
Frontiers | Exploring the Crosstalk Between LMNA and Splicing Machinery Gene Mutations in Dilated Cardiomyopathy