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

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Dystrophie Musculaire de Becker BMD Inhibitors Inbred mdx MES Drp1 Exon skipping LKB1 Male Gene expression Isoforms Long noncoding RNA Long QT Base Sequence Dystrophie Musculaire de Duchenne DMD L-Type Cells Génomique Molecular docking Hear Calcium CaV subunits Cell Biology Becker muscular dystrophy Dilated Cardiomyopathy Inbred C57BL Cardiomyopathy Becker Muscular Dystrophy Allele‐specific silencing therapy Dystrophin-EGFP Jonction neuromusculaire JNM Heart Failure Connexins DHPR α1S Invivo Hepatocellular carcinoma Becker BMD muscular dystrophy CaVβ1 Calcium Channels Epigenetics Multi resolution modeling Muscle Biology Duchenne muscular dystrophy Isoformes Dystrophy DMD Cell Line Dystrophin central domain Animals Homeostasis Liver Delivery Human Umbilical Vein Endothelial Cells Duchenne DMD dystrophy Dystrophine Genomic Gene Expression Regulation/drug effects Centronuclear myopathy Autophagy Knockout Becker muscular dystrophy BMD Energy Metabolism/drug effects Mdx mouse Ex-vivo Multiresolution modeling Dystrophie myotonique de type 1 DM1 Skeletal muscle Clinical trials Gene modifiers CaVβs Mitochondrial fission Metabolism CD38 Animal/physiopathology CTNNB1 Diseases Duchenne muscular dystrophy DMD BMD Multi exon skipping Cell homeostasis Activin Receptors Immunoglobulin Fc Fragments/pharmacology Antisense oligonucleotides Dynamin 2 Cachexia DMO Muscle Modificateurs de gènes Humans LncRNA LncARN Morphogenesis Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS Dystrophie musculaire de Becker Molecular Sequence Data Mice Cultured MiARN Cardiomyopathie Dystrophin Adult muscle stem cells