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Marc Bitoun

University of Paris

16

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242

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A centronuclear myopathy-causing mutation in dynamin-2 perturbs the actin-dependent structure of dendritic spines leading to excitatory synaptic defects in a murine model of the disease

2021 bioRxiv
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Satellite cells deficiency and defective regeneration in dynamin 2-related centronuclear myopathy.

2021 The FASEB Journal
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Correlative SICM-FCM reveals changes in morphology and kinetics of endocytic pits induced by disease-associated mutations in dynamin

2019 The FASEB Journal
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Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model

2019 Scientific Reports
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Clathrin plaques and associated actin anchor intermediate filaments in skeletal muscle

2019 Molecular Biology of the Cell
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TRAITEMENT PAR SILENÇAGE SPÉCIFIQUE D'UN ALLÈLE, DESTINÉ À DES MALADIES ASSOCIÉES À LA DYNAMINE 2

2018
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Clathrin plaques form mechanotransducing platforms

2018 bioRxiv
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Mechanosensitive clathrin platforms anchor desmin intermediate filaments in skeletal muscle

2018 bioRxiv
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Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy

2017 Molecular therapy. Nucleic acids
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Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations

2014 Brain
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