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Humans Male Myotonic dystrophy type 1 Acute coronary syndrome Exercice Muscular dystrophy Autophagy CONGENITAL MYATHENIC SYNDROME RNA splicing Exercise Genotype phenotype correlation PacBio Skeletal muscle Astrocytes Dystrophie Myotonique Duchenne muscular dystrophy Transcriptomics ACETYLCHOLINESTERASE Myelin Oligodendrocyte Myotonic dystrophy mouse models Myotonic Dystrophy Acetylcholinesterase knockout mouse Myotonic dystrophy Cell penetrating peptide GABA Aging Expression Dilated cardiomyopathy KNOCKOUT MICE DMPK Glutamate Gene therapy MBNL Brain dysfunction Myotonic Dystrophy type 1 DMSXL mice Desmin Cell model Long read sequencing Astrocyte Neuron ARN In vivo Quantitative microdialysis Glucocorticoids Heart failure Acetylcholinesterase deficiency Mice Lc3 Glial cells Hypoxia Gene editing Fibrosis BIOLOGIE MOLECULAIRE Trinucleotide Repeat Expansion Maximal force CRISPRi GSK3␤ Centronuclear myopathy CMS Thérapie génique Antisense oligonucleotides Dynamin 2 Dystrophin Transgenic mouse model Mouse models RNA interference Central nervous system CTG repeat instability Antisense oligonucleotide Glucocorticoid-receptor Myostatin Trinucleotide repeat expansion Intermediate filament CTG repeats Brain PCR Cardiac muscle AAV Mouse model Dystrophie myotonique Motoneuron Cytoskeleton Transgenic mouse Alternative splicing CTG repeat contractions Cell culture model Myotonic Dystrophy Type 1 Muscle Knockout DM1 Animals CRISPR/Cas9 Oligodendrocytes Heart Therapy Gene Therapy Diaphragm RNA biology