Skeletal muscle Dystrophin Transcriptomics Laminopathies Centronuclear myopathy AAV Aged Biomarkers Mouse model Inflammation Long read sequencing Myopathies Aging Muscle Cardiomyopathy Dilated cardiomyopathy Fabry disease Thymus RNA biology Biomarker Male Cell therapy Calcium Autoimmune diseases FSHD Laminopathie Genotype phenotype correlation Thérapie génique Trinucleotide repeat expansion OPMD Treatment Glutamate Autoimmunity CMS Humans Autoantibodies Therapy Myoblasts Genetics Fibrosis Animals Congenital muscular dystrophy Myasthenia Gravis MG Motoneuron Autophagy Lamin A/C LMNA gene Exercise RNA interference PABPN1 Myogenesis Heart failure Outcome measures Alternative splicing ALS Myositis Mice Muscle regeneration LMNA Neuromuscular disease Amyotrophic lateral sclerosis Muscular dystrophy Neuromuscular junction Dynamin 2 Nuclear envelope Myopathy MBNL Laminopathy Gene therapy Satellite cells COVID-19 Lamin A/C DMD Astrocyte Dermatomyositis Rare diseases Transgenic mouse model Satellite cell Heart Myotonic dystrophy Antisense oligonucleotides Mechanotransduction Regeneration Becker muscular dystrophy Myotonic dystrophy type 1 Neuromuscular diseases Myotonic Dystrophy type 1 Congenital myopathy Actin Myasthenia gravis LMNA gene Cytoskeleton Brain Myotonic Dystrophy Rare neuromuscular diseases Errance diagnostique CTG repeat contractions Spinal muscular atrophy Cytokines CRISPRi Duchenne muscular dystrophy