Publications by authors named "Julien Messeant"

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MuSK cysteine-rich domain antibodies are pathogenic in a mouse model of autoimmune myasthenia gravis.
Marius Halliez, Steve Cottin, Axel You, Céline Buon, Antony Grondin

J Clin Invest· August 2025

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MBNL deficiency in motor neurons disrupts neuromuscular junction maintenance and gait coordination.
Charles Frison-Roche, Célia Martin Demier, Steve Cottin, Jeanne Lainé, Ludovic Arandel

Brain· April 2025

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GDF5 as a rejuvenating treatment for age-related neuromuscular failure.
Massiré Traoré, Chiara Noviello, Amélie Vergnol, Christel Gentil, Marius Halliez

Brain· November 2024

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The collagen ColQ binds to LRP4 and regulates the activation of the Muscle-Specific Kinase-LRP4 receptor complex by agrin at the neuromuscular junction.
Thi Minh Uyen Dao, Susie Barbeau, Julien Messéant, Bruno Della-Gaspera, Tahar Bouceba

J Biol Chem· August 2023

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New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani-Lenz syndrome.
Marion Masingue, Olivia Cattaneo, Nicolas Wolff, Céline Buon, Damien Sternberg

Sci Rep· August 2023

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The cell polarity protein Vangl2 in the muscle shapes the neuromuscular synapse by binding to and regulating the tyrosine kinase MuSK.
Myriam Boëx, Steve Cottin, Marius Halliez, Stéphanie Bauché, Céline Buon

Sci Signal· May 2022

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Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth.
Daniel J Owens, Julien Messéant, Sophie Moog, Mark Viggars, Arnaud Ferry

Int J Mol Sci· December 2020

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New recessive mutations in causing severe presynaptic congenital myasthenic syndromes.
Stéphanie Bauché, Alain Sureau, Damien Sternberg, John Rendu, Céline Buon

Neurol Genet· December 2020

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Desmin prevents muscle wasting, exaggerated weakness and fragility, and fatigue in dystrophic mdx mouse.
Arnaud Ferry, Julien Messéant, Ara Parlakian, Mégane Lemaitre, Pauline Roy

J Physiol· September 2020

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Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy.
Stéphanie Bauché, Geoffroy Vellieux, Damien Sternberg, Marie-Joséphine Fontenille, Elodie De Bruyckere

J Neurol· August 2017

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Gonad-related factors promote muscle performance gain during postnatal development in male and female mice.
Vanessa Ueberschlag-Pitiot, Amalia Stantzou, Julien Messéant, Megane Lemaitre, Daniel J Owens

Am J Physiol Endocrinol Metab· July 2017

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Wnt proteins contribute to neuromuscular junction formation through distinct signaling pathways.
Julien Messéant, Jérôme Ezan, Perrine Delers, Konstantin Glebov, Carmen Marchiol

Development· May 2017

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Dystrophin restoration therapy improves both the reduced excitability and the force drop induced by lengthening contractions in dystrophic mdx skeletal muscle.
Pauline Roy, Fredérique Rau, Julien Ochala, Julien Messéant, Bodvael Fraysse

Skelet Muscle· October 2016

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MuSK frizzled-like domain is critical for mammalian neuromuscular junction formation and maintenance.
Julien Messéant, Alexandre Dobbertin, Emmanuelle Girard, Perrine Delers, Marin Manuel

J Neurosci· March 2015

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