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