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Kamel Mamchaoui

University of Paris
French Institute of Health and Medical Research

88

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2634

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Immortalized Canine Dystrophic Myoblast Cell Lines for Development of Peptide-Conjugated Splice-Switching Oligonucleotides.

2021 Nucleic Acid Therapeutics
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Interplay between mitochondria and reactive oxygen and nitrogen species in metabolic adaptation to hypoxia in facioscapulohumeral muscular dystrophy: potential therapeutic targets.

2021 bioRxiv
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GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome.

2020 Annals of Neurology
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Long-Term Efficacy of AAV9-U7snRNA-Mediated Exon 51 Skipping in mdx52 Mice.

2020 Molecular therapy. Methods & clinical development
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Adenylosuccinic acid therapy ameliorates murine Duchenne Muscular Dystrophy

2020 Scientific Reports
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Alternative splicing of clathrin heavy chain contributes to the switch from coated pits to plaques.

2020 Journal of Cell Biology
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Myogenin controls via AKAP6 non-centrosomal microtubule organizing center formation at the nuclear envelope

2020 bioRxiv
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Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth.

2020 International Journal of Molecular Sciences
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Simplified in vitro engineering of neuromuscular junctions between rat embryonic motoneurons and immortalized human skeletal muscle cells

2019
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A recurrent COL6A1 pseudoexon insertion causes muscular dystrophy and is effectively targeted by splice-correction therapies

2019 JCI insight
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Citations (16)