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

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