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

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