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

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