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

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