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Marc Bitoun

Showing results (41-50 of 54) with videos related to

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Nature Genetics|October 18, 2005
Mutations in dynamin 2 cause dominant centronuclear myopathyMarc Bitoun, Svetlana Maugenre, Pierre-Yves Jeannet, et al.
The Journal of Cell Biology|May 7, 2014
Actin scaffolding by clathrin heavy chain is required for skeletal muscle sarcomere organizationStéphane Vassilopoulos, Christel Gentil, Jeanne Lainé, et al.
Elife|April 21, 2023
Caveolae and Bin1 form ring-shaped platforms for T-tubule initiationEline Lemerle, Jeanne Lainé, Marion Benoist, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsyVerity McClelland, Thomas Cullup, Istvan Bodi, et al.
Scientific Reports|July 6, 2017
Dynamin-2 mutations linked to Centronuclear Myopathy impair actin-dependent trafficking in muscle cellsArlek M González-Jamett, Ximena Baez-Matus, María José Olivares, et al.
The American Journal of Pathology|June 11, 2025
Early endosome disturbance and endolysosomal pathway dysfunction in Duchenne muscular dystrophyJulie Chassagne, Nathalie Da Silva, Ines Akrouf, et al.
Neuropathology and Applied Neurobiology|June 15, 2023
A centronuclear myopathy-causing mutation in dynamin-2 disrupts neuronal morphology and excitatory synaptic transmission in a murine model of the diseaseJorge Arriagada-Diaz, Carolina Flores-Muñoz, Bárbara Gómez-Soto, et al.
Science Progress|April 2, 2025
The synaptic availability of GluA1 is reduced in hippocampal neurons of a murine model of dynamin-2 linked autosomal dominant centronuclear myopathyCarolina Flores-Muñoz, Marjorie Labraña-Allende, Michelle Mattar-Araos, et al.
Journal of Neuropathology and Experimental Neurology|August 23, 2013
Skeletal muscle biopsy analysis in reducing body myopathy and other FHL1-related disordersEdoardo Malfatti, Montse Olivé, Ana Lía Taratuto, et al.
EMBO Reports|March 11, 2025
SH3KBP1 promotes skeletal myofiber formation and functionality through ER/SR architecture integrityAlexandre Guiraud, Nathalie Couturier, Emilie Christin, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Nature Genetics|October 18, 2005
Mutations in dynamin 2 cause dominant centronuclear myopathyMarc Bitoun, Svetlana Maugenre, Pierre-Yves Jeannet, et al.
The Journal of Cell Biology|May 7, 2014
Actin scaffolding by clathrin heavy chain is required for skeletal muscle sarcomere organizationStéphane Vassilopoulos, Christel Gentil, Jeanne Lainé, et al.
Elife|April 21, 2023
Caveolae and Bin1 form ring-shaped platforms for T-tubule initiationEline Lemerle, Jeanne Lainé, Marion Benoist, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsyVerity McClelland, Thomas Cullup, Istvan Bodi, et al.
Scientific Reports|July 6, 2017
Dynamin-2 mutations linked to Centronuclear Myopathy impair actin-dependent trafficking in muscle cellsArlek M González-Jamett, Ximena Baez-Matus, María José Olivares, et al.
The American Journal of Pathology|June 11, 2025
Early endosome disturbance and endolysosomal pathway dysfunction in Duchenne muscular dystrophyJulie Chassagne, Nathalie Da Silva, Ines Akrouf, et al.
Neuropathology and Applied Neurobiology|June 15, 2023
A centronuclear myopathy-causing mutation in dynamin-2 disrupts neuronal morphology and excitatory synaptic transmission in a murine model of the diseaseJorge Arriagada-Diaz, Carolina Flores-Muñoz, Bárbara Gómez-Soto, et al.
Science Progress|April 2, 2025
The synaptic availability of GluA1 is reduced in hippocampal neurons of a murine model of dynamin-2 linked autosomal dominant centronuclear myopathyCarolina Flores-Muñoz, Marjorie Labraña-Allende, Michelle Mattar-Araos, et al.
Journal of Neuropathology and Experimental Neurology|August 23, 2013
Skeletal muscle biopsy analysis in reducing body myopathy and other FHL1-related disordersEdoardo Malfatti, Montse Olivé, Ana Lía Taratuto, et al.
EMBO Reports|March 11, 2025
SH3KBP1 promotes skeletal myofiber formation and functionality through ER/SR architecture integrityAlexandre Guiraud, Nathalie Couturier, Emilie Christin, et al.
Pageof 6