Deficiency of emerin contributes differently to the pathogenesis of skeletal and cardiac muscles in LmnaH222P/H222P mutant mice - Wada, Eiji; Kato, Megumi; Yamashita, Kaori; Kokuba, Hiroko; Liang, Wen-Chen; Bonne, Gisèle; Hayashi, Yukiko K. (PloS one, 2019)
Keywords: Abnormalities; Age; Aging - pathology; Animal models; Animal tissues; Animals; Biology and Life Sciences; Breeding; Cardiac muscle; Cardiomyopathy; Cardiotoxins; Cell cycle; Cell Nucleus - pathology; Cell Nucleus - ultrastructure; Cells (biology); Cellular Biology; Dystrophy; Emery-Dreifuss muscular dystrophy; Fibrosis; Gene expression; Genes; Genetics; Kinases; Lamin Type A - genetics; Life Sciences; Medicine and Health Sciences; Membrane Proteins - deficiency; Membrane Proteins - metabolism; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Muscle, Skeletal - pathology; Muscle, Skeletal - physiopathology; Muscle, Skeletal - ultrastructure; Muscles; Muscular dystrophy; Musculoskeletal system; Mutation; Myocardium - pathology; Myocardium - ultrastructure; Myopathy; Nuclear membranes; Nuclear Proteins - deficiency; Nuclear Proteins - metabolism; Pathogenesis; Pathology; Pediatrics; Phenotype; Phenotypes; Proteins; Regeneration; Research and Analysis Methods; Satellite cells; Signal transduction; Skeletal muscle; Japan; Taiwan