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Deletion of the Lmna gene in fibroblasts causes senescence-associated dilated cardiomyopathy by activating the double-stranded DNA damage response and induction of senescence-associated secretory phenotype
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The alternative splicing of LMNA produces the progerin variant that is... | Download Scientific Diagram
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LMNA mutations detected in patients. (A) Representation of mutations... | Download Scientific Diagram
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Pathogenic LMNA variants disrupt cardiac lamina-chromatin interactions and de-repress alternative fate genes - ScienceDirect
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Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy: Molecular Therapy - Nucleic Acids
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Integrated analysis reveals the alterations that LMNA interacts with euchromatin in LMNA mutation-associated dilated cardiomyopathy | Clinical Epigenetics | Full Text
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Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging | European Journal of Human Genetics
Whole-Exome Sequencing to Identify a Novel LMNA Gene Mutation Associated with Inherited Cardiac Conduction Disease | PLOS ONE
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