Julien Messeant

Paris, 75013, France

Last Updated: 09/26/2026

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Found 16 publications

Targeted knockdown of Smn in muscle stem cells induces non-cell autonomous loss of motor neurons.

Targeted knockdown of Smn in muscle stem cells induces non-cell autonomous loss of motor neurons.

Journal: Brain : a journal of neurology

Published: January 26, 2025

MBNL deficiency in motor neurons disrupts neuromuscular junction maintenance and gait coordination.

MBNL deficiency in motor neurons disrupts neuromuscular junction maintenance and gait coordination.

Journal: Brain : a journal of neurology

Published: April 26, 2024

GDF5 as a rejuvenating treatment for age-related neuromuscular failure.

GDF5 as a rejuvenating treatment for age-related neuromuscular failure.

Journal: Brain : a journal of neurology

Published: November 22, 2023

MuSK cysteine-rich domain antibodies are pathogenic in a mouse model of autoimmune myasthenia gravis.

MuSK cysteine-rich domain antibodies are pathogenic in a mouse model of autoimmune myasthenia gravis.

Journal: The Journal of clinical investigation

Published: June 21, 2023

New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani-Lenz syndrome.

New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani-Lenz syndrome.

Journal: Scientific reports

Published: April 03, 2023

The cell polarity protein Vangl2 in the muscle shapes the neuromuscular synapse by binding to and regulating the tyrosine kinase MuSK.

The cell polarity protein Vangl2 in the muscle shapes the neuromuscular synapse by binding to and regulating the tyrosine kinase MuSK.

Journal: Science signaling

Published: May 17, 2022

The collagen ColQ binds to LRP4 and regulates the activation of the Muscle-Specific Kinase-LRP4 receptor complex by agrin at the neuromuscular junction.

The collagen ColQ binds to LRP4 and regulates the activation of the Muscle-Specific Kinase-LRP4 receptor complex by agrin at the neuromuscular junction.

Journal: The Journal of biological chemistry

Published: April 20, 2022

Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth.

Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth.

Journal: International journal of molecular sciences

Published: October 22, 2020

New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes.

New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes.

Journal: Neurology. Genetics

Published: June 18, 2020

Desmin prevents muscle wasting, exaggerated weakness and fragility, and fatigue in dystrophic mdx mouse.

Desmin prevents muscle wasting, exaggerated weakness and fragility, and fatigue in dystrophic mdx mouse.

Journal: The Journal of physiology

Published: November 08, 2019

Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy.

Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy.

Journal: Journal of neurology

Published: May 17, 2017

Gonad-related factors promote muscle performance gain during postnatal development in male and female mice.

Gonad-related factors promote muscle performance gain during postnatal development in male and female mice.

Journal: American journal of physiology. Endocrinology and metabolism

Published: December 13, 2016

Showing 1-12 of 16

Last Updated: 09/26/2026