index - Thérapie génique pour la DMD & physiopathologie du muscle squelettique

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Muscle cell fusion Drp1 Dilated Cardiomyopathy Liver Multi exon skipping Dystrophie musculaire de Becker Gene modifiers Cardiomyopathy Ex-vivo CD38 Becker BMD muscular dystrophy Dystrophine Epigenetics Dynamin 2 DMD Inbred C57BL BMD Centronuclear myopathy LncARN Dystrophy Homeostasis Dystrophin central domain Becker Muscular Dystrophy DHPR α1S Duchenne muscular dystrophy Metabolism Multi resolution modeling Clinical trials Duchenne muscular dystrophy DMD Autophagy Muscle development Invivo Becker muscular dystrophy BMD Mdx mouse Muscle Biology Hear Long noncoding RNA Connexins Dystrophie Musculaire de Duchenne DMD Cell Biology MES CaVβs Muscle Diseases Inhibitors Muscle Strength Hepatocellular carcinoma Muscle hypertrophy Adult muscle stem cells Long QT Antisense oligonucleotides Animals Allele‐specific silencing therapy Multiresolution modeling Skeletal muscle L-Type Becker muscular dystrophy Morphogenesis Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS Cachexia Génomique Dystrophin Animal/physiopathology Humans Genomic Knockout CTNNB1 Dystrophin-EGFP LKB1 Base Sequence DMO Cell Line CaV subunits Cells Cardiomyopathie LncRNA Energy Metabolism/drug effects Exon skipping Human Umbilical Vein Endothelial Cells Gene Expression Regulation/drug effects Mitochondrial fission Inbred mdx Cell homeostasis Immunoglobulin Fc Fragments/pharmacology Mice Cultured MiARN Calcium Channels Activin Receptors Modificateurs de gènes Heart Failure Muscle damage Molecular Sequence Data Duchenne DMD dystrophy Male Gene expression Molecular docking Dystrophie Musculaire de Becker BMD Delivery Calcium