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

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