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Marc Bitoun

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
2016 · Daniel J Klionsky, Kotb Abdelmohsen, et al. · Autophagy · 5,851
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Guidelines for the use and interpretation of assays for monitoring autophagy
2016 · Klionsky, Daniel J, Abdelmohsen, Kotb, et al. · 4,799
Mutations in dynamin 2 cause dominant centronuclear myopathy
2005 · Marc Bitoun, Svetlana Maugenre, et al. · Nature Genetics · 499
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Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset
2007 · Marc Bitoun, Jorge A. Bevilacqua, et al. · Annals of Neurology · 164
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Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy
2012 · Johann Böhm, Valérie Biancalana, et al. · Human Mutation · 147
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Dynamin 2 and human diseases
2010 · Anne-Cécile Durieux, Bernard Prudhon, et al. · Journal of Molecular Medicine · 146
A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice
2010 · Anne-Cécile Durieux, Alban Vignaud, et al. · Human Molecular Genetics · 144
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization
2010 · J. A. Bevilacqua, N. Monnier, et al. · Neuropathology and Applied Neurobiology · 127
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Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene
2007 · Heinz Jungbluth, Haiyan Zhou, et al. · Neuromuscular Disorders · 127
“Necklace” fibers, a new histological marker of late-onset MTM1-related centronuclear myopathy
2008 · Jorge A. Bevilacqua, Marc Bitoun, et al. · Acta Neuropathologica · 124
Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations
2014 · Johann Böhm, Valérie Biancalana, et al. · Brain · 117
Centronuclear Myopathies
2011 · Norma B. Romero, Marc Bitoun · Seminars in Pediatric Neurology · 117
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Expanding the clinical, pathological and MRI phenotype of DNM2-related centronuclear myopathy
2010 · Rachel D. Susman, Susana Quijano-Roy, et al. · Neuromuscular Disorders · 117
Phenotype of a Patient With Recessive Centronuclear Myopathy and a Novel Bin1 Mutation
2010 · K. G. Claeys, T. Maisonobe, et al. · Neurology · 92
Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis
2009 · Marc Bitoun, Anne-Cécile Durieux, et al. · Human Mutation · 90
An alternative mechanism of clathrin-coated pit closure revealed by ion conductance microscopy
2012 · Andrew I. Shevchuk, Pavel Novak, et al. · The Journal of Cell Biology · 87
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Reducing dynamin 2 (DNM2) rescues DNM2 -related dominant centronuclear myopathy
2018 · Suzie Buono, Jacob A. Ross, et al. · Proceedings of the National Academy of Sciences · 76
Actin scaffolding by clathrin heavy chain is required for skeletal muscle sarcomere organization
2014 · Stéphane Vassilopoulos, Christel Gentil, et al. · The Journal of Cell Biology · 76
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A Centronuclear Myopathy – Dynamin 2 Mutation Impairs Autophagy in Mice
2012 · Anne‐Cécile Durieux, Stéphane Vassilopoulos, et al. · Traffic · 76
Erratum
2016 · Klionsky D. J., Abdelmohsen K., et al. · Autophagy · 68
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Allele‐specific silencing therapy for Dynamin 2‐related dominant centronuclear myopathy
2017 · Delphine Trochet, Bernard Prudhon, et al. · EMBO Molecular Medicine · 64
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A DNM2 Centronuclear Myopathy Mutation Reveals a Link between Recycling Endosome Scission and Autophagy
2020 · Claudia Puri, Marco M. Manni, et al. · Developmental Cell · 58
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Clathrin plaques and associated actin anchor intermediate filaments in skeletal muscle
2019 · Agathe Franck, Jeanne Lainé, et al. · Molecular Biology of the Cell · 57
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A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: Clinical and pathological findings
2008 · Marc Bitoun, Tanya Stojkovic, et al. · Neuromuscular Disorders · 57
Gene expression of the transporters and biosynthetic enzymes of the osmolytes in astrocyte primary cultures exposed to hyperosmotic conditions
2000 · Marc Bitoun, Marcel Tappaz · Glia · 56
Works count: 123
Citation count: 14,310
H-index: 36
I10-index: 52
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