index - Plateforme d’immortalisation MyoLine – CRM

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51 Publications avec texte intégral

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CFTR correctors ICU-acquired weakness Cell Therapy CDNA synthesis Expanded repeats Immortalisation Lamin A/C nuclei Exon skipping Autophagy Myotube Myogenesis CXCR4 Cell-penetrating peptide Human artificial chromosomes Coculture CMS Conjugation Antisense morpholino CRISPR/Cas9 Muscle CTG⋅CAGn repeat DiPRO1 Exon Skipping DM1 myoblasts DMD Centronuclear myopathy Bile acid Exondys 51 Autophagosome Gene network analysis Fear response Glucose Myotonic dystrophy Clinical trial candidate screening Emerin Folding-defective proteins Dystrophin Motor neuron Lymphotoxin-β-receptor Laminographie Cell biology Adhesion Adeno-associated viral vector Skeletal muscle Human Gene therapy Fibroblast Machine learning Becker muscular dystrophy Exon-skipping HDMD/Dmd-null mice Developmental biology RNA interference Gut microbiota Lamina-associated domain Alternative splicing Differentiation Fibrosis Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS Canine X-linked muscular dystrophy in Japan CXMD J Dynamin 2 LRP4 Immortalized dystrophic canine myoblast Antisense oligonucleotide Migration Human muscle stem/progenitor cells Actin 3D co-culture Glucocorticoid-induced muscle atrophy Gene Therapy Eteplirsen KLF15 Duchenne muscular dystrophy DsDNA break repair DNM2 BMD Chromatin Atrial cardiac defects Drisapersen Flavonoid MSCs Computer software Mdx Gel electrophoresis ITSN1 Allele-specific silencing BAF FSHD FoxO Duchenne Muscular Dystrophy Acetylcholine receptor subunit epsilon Endocytosis MT RNA/DNA Editing Dominant centronuclear myopathy CXCL12 CLS Allele-specific silencing therapy LTβR Insulin Neuromuscular junction