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Journal of Cell Science|May 4, 2012
CKIP-1 regulates mammalian and zebrafish myoblast fusionDominique Baas, Sabine Caussanel-Boude, Alexandre Guiraud, et al.
Aging Cell|January 29, 2020
Mitochondrial function in skeletal myofibers is controlled by a TRF2-SIRT3 axis over lifetimeJérôme D Robin, Maria-Sol Jacome Burbano, Han Peng, et al.
European Journal of Human Genetics : EJHG|June 19, 2023
Genetic characterization of non-5q proximal spinal muscular atrophy in a French cohort: the place of whole exome sequencingJulian Theuriet, Gorka Fernandez-Eulate, Philippe Latour, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|June 30, 2026
Muscle contribution in lipid nanoparticle mediated mRNA vaccine delivery and efficacyMathieu Repellin, Stefano Ugel, Francesco De Sanctis, et al.
ACS Medicinal Chemistry Letters|May 18, 2019
Discovery of BNC375, a Potent, Selective, and Orally Available Type I Positive Allosteric Modulator of α7 nAChRsAndrew J Harvey, Thomas D Avery, Laurent Schaeffer, et al.
Brain : a Journal of Neurology|December 1, 2022
Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathyArnaud Jacquier, Julian Theuriet, Fanny Fontaine, et al.
Elife|August 27, 2021
MACF1 controls skeletal muscle function through the microtubule-dependent localization of extra-synaptic myonuclei and mitochondria biogenesisAlireza Ghasemizadeh, Emilie Christin, Alexandre Guiraud, et al.
Neuropathology and Applied Neurobiology|December 28, 2022
MBNL-dependent impaired development within the neuromuscular system in myotonic dystrophy type 1Julie Tahraoui-Bories, Antoine Mérien, Anchel González-Barriga, et al.
Nature Communications|January 4, 2019
Genome editing in primary cells and in vivo using viral-derived Nanoblades loaded with Cas9-sgRNA ribonucleoproteinsPhilippe E Mangeot, Valérie Risson, Floriane Fusil, et al.
Journal De La Societe De Biologie|August 24, 2005
[Pathophysiological characterization of congenital myasthenic syndromes: the example of mutations in the MUSK gene]Frédéric Chevessier, Brice Faraut, Aymeric Ravel-Chapuis, et al.
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