index - Plateforme d’immortalisation MyoLine – CRM Access content directly

Last submissions

Key numbers

48 Publications with fulltext

Open Access

Chargement de la page

Keywords

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