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CTG⋅CAGn repeat Folding-defective proteins CLS Emerin Adeno-associated viral vector CXCR4 Coculture Endocytosis Immortalisation DM1 myoblasts Expanded repeats Human Dominant centronuclear myopathy Differentiation FoxO Duchenne muscular dystrophy Gene therapy Flavonoid Human muscle stem/progenitor cells LRP4 CDNA synthesis Myogenesis BAF MSCs Mdx Myotonic dystrophy Adhesion LTβR Gel electrophoresis Allele-specific silencing Skeletal muscle Atrial cardiac defects 3D co-culture Exon skipping Lamin A/C nuclei Mechano-transduction CXCL12 Becker muscular dystrophy Clinical trial candidate screening DMD Myotube Migration Neuromuscular junction Canine X-linked muscular dystrophy in Japan CXMD J Exon-skipping Fibrosis Chromatin HDMD/Dmd-null mice Centronuclear myopathy Alternative splicing Gene network analysis Mdx52 mice Immortalized dystrophic canine myoblast Developmental biology Dynamin 2 DsDNA break repair Laminographie KLF15 DNM2 Computer software Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS Muscle Drisapersen CMS Glucose ITSN1 CRISPR/Cas9 Cell biology Motor neuron Lamina-associated domain Acetylcholine receptor subunit epsilon Cell-penetrating peptide Insulin RNA interference Human artificial chromosomes Microarray Autophagosome BMD Mitochondrial ROS Bile acid Antisense oligonucleotide Gut microbiota Glucocorticoid-induced muscle atrophy Actin Fear response Autophagy Mechanisms of disease Eteplirsen Conjugation MT RNA/DNA Editing Antisense morpholino FSHD CFTR correctors Allele-specific silencing therapy Exondys 51 Machine learning Dystrophin ICU-acquired weakness Fibroblast Lymphotoxin-β-receptor