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