Physiopathologie des maladies neuromusculaires
Chef d'équipe : Jocelyn LAPORTE
Département : Médecine translationnelle et neurogénétique
Jocelyn LAPORTE
Chercheur
Directeur de recherche Inserm
jocelyn@igbmc.fr
Équipe(s)
Sous-groupe(s)
Publications
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2018
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Discordant manifestations in Italian brothers with GNE myopathy
- Maria-Teresa Dotti
- Alessandro Malandrini
- Xavière Lornage
- Andrea Mignarri
- Teresa Anna Cantisani
- Johann Böhm
- Jocelyn Laporte
- Edoardo Malfatti
J Neurol Sci ; Volume: 386 ; Page: 1-3
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Reducing dynamin 2 (DNM2) rescues DNM2-related dominant centronuclear myopathy
- Suzie Buono
- Jacob Ross
- Hichem Tasfaout
- Yotam Levy
- Christine Kretz
- Leighla Tayefeh
- John Matson
- Shuling Guo
- Pascal Kessler
- Brett Monia
- Marc Bitoun
- Julien Ochala
- Jocelyn Laporte
- Belinda Cowling
Proceedings of the National Academy of Sciences of the United States of America ; Volume: 115 ; Page: 11066-11071
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2017
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Allele-specific silencing therapy for Dynamin 2-related dominant centronuclear myopathy
- Delphine Trochet
- Bernard Prudhon
- Maud Beuvin
- Cécile Peccate
- Stéphanie Lorain
- Laura Julien
- Sofia Benkhelifa-Ziyyat
- Aymen Rabai
- Kamel Mamchaoui
- Arnaud Ferry
- Jocelyn Laporte
- Pascale Guicheney
- Stéphane Vassilopoulos
- Marc Bitoun
Circulation. Arrhythmia and electrophysiology ; Volume: 10 ; Page: 428-431
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Amphiphysin (BIN1) negatively regulates dynamin 2 for normal muscle maturation
- Belinda Cowling
- Ivana Prokic
- Hichem Tasfaout
- Aymen Rabai
- Frédéric Humbert
- Bruno Rinaldi
- Anne‐sophie Nicot
- Christine Kretz
- Sylvie Friant
- Aurelien Roux
- Jocelyn Laporte
Journal of Clinical Investigation ; Volume: 127 ; Page: 4477-4487
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IFN-β-induced reactive oxygen species and mitochondrial damage contribute to muscle impairment and inflammation maintenance in dermatomyositis
- Alain Meyer
- Gilles Laverny
- Yves Allenbach
- Elise Grelet
- Vanessa Ueberschlag
- Andoni Echaniz-Laguna
- Béatrice Lannes
- Ghada Alsaleh
- Anne Laure Charles
- François Singh
- Joffrey Zoll
- Evelyne Lonsdorfer
- François Maurier
- Olivier Boyer
- Jacques-Eric Gottenberg
- Anne Sophie Nicot
- Jocelyn Laporte
- Olivier Benveniste
- Daniel Metzger
- Jean Sibilia
- ...
Acta Neuropathologica ; Volume: 134 ; Page: 655-666
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Myotubularins and associated neuromuscular diseases
- Helene Tronchere
- Alessandra Bolino
- Jocelyn Laporte
- Bernard Payrastre
Journal of clinical lipidology ; Volume: 7 ; Page: 151-162
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WANTED – Dead or alive: Myotubularins, a large disease-associated protein family
- Matthieu Raess
- Sylvie Friant
- Belinda S. Cowling
- Jocelyn Laporte
Advances in Biological Regulation ; Volume: 63 ; Page: 49-58
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Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy
- Vanessa Schartner
- Norma Romero
- Sandra Donkervoort
- Susan Treves
- Pinki Munot
- Tyler Pierson
- Ivana Dabaj
- Edoardo Malfatti
- Irina Zaharieva
- Francesco Zorzato
- Osario Abath Neto
- Guy Brochier
- Xavière Lornage
- Bruno Eymard
- Ana Taratuto
- Johann Böhm
- Hernan Gonorazky
- Leigh Ramos-Platt
- Lucy Feng
- Rahul Phadke
- ...
Acta Neuropathologica ; Volume: 133 ; Page: 517-533
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Nonlethal CHRNA1-Related Congenital Myasthenic Syndrome with a Homozygous Null Mutation
- Osorio Abath Neto
- Carlos Heise
- Cristiane de Araújo Martins Moreno
- Eduardo de Paula Estephan
- Lilia Mesrob
- Doris Lechner
- Anne Boland
- Jean-François Deleuze
- Acary Souza Bulle Oliveira
- Umbertina Reed
- Valerie Biancalana
- Jocelyn Laporte
- Edmar Zanoteli
Canadian Journal of Neurological Sciences ; Volume: 44 ; Page: 125-127
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ORAI1 mutations with distinct channel gating defects in tubular aggregate myopathy
- Johann Bohm
- Monica Bulla
- Jill Urquhart
- Edoardo Malfatti
- Simon Williams
- James O'Sullivan
- Anastazja Szlauer
- Catherine Koch
- Giovanni Baranello
- Martin Mora
- Michela Ripolone
- Raffaella Violano
- Maurizio Moggio
- Helen Kingston
- Timothy Dawson
- Christian Degoede
- John Nixon
- Anne Boland
- Jean-François Deleuze
- Norma Romero
- ...
Human Mutation ; Volume: 38 ; Page: 426-438
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