Jocelyn F. Laporte

Inserm U1258, CNRS UMR7104, 1 Rue Laurent Fries
Illkirch-graffenstaden, 67404, France

Last Updated: 09/26/2026

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Found 406 publications

Circulating MYOM3 fragments reflect disease severity and therapeutic efficacy in tubular aggregate myopathy and Stormorken syndrome.

Circulating MYOM3 fragments reflect disease severity and therapeutic efficacy in tubular aggregate myopathy and Stormorken syndrome.

Journal: Human molecular genetics

Published: January 28, 2026

Clinical, Histological, and Genetic Characterization of a Large Cohort of 49 Patients With Nebulin-Related Congenital Myopathy.

Clinical, Histological, and Genetic Characterization of a Large Cohort of 49 Patients With Nebulin-Related Congenital Myopathy.

Journal: Human mutation

Published: January 25, 2026

BIN1 overexpression rescues cardiac but not skeletal muscle defects in a mouse model of caveolinopathy.

BIN1 overexpression rescues cardiac but not skeletal muscle defects in a mouse model of caveolinopathy.

Journal: Human molecular genetics

Published: January 14, 2026

DNM2 lipid binding drives centronuclear myopathy and represents a potential therapeutic target.

DNM2 lipid binding drives centronuclear myopathy and represents a potential therapeutic target.

Journal: JCI insight

Published: January 08, 2026

Muscle-Specific DNM2 Overexpression Improves Charcot-Marie-Tooth Disease In Vivo and Reveals a Narrow Therapeutic Window in Skeletal Muscle.

Muscle-Specific DNM2 Overexpression Improves Charcot-Marie-Tooth Disease In Vivo and Reveals a Narrow Therapeutic Window in Skeletal Muscle.

Journal: International journal of molecular sciences

Published: December 04, 2025

The MYOCAPTURE project: Capturing the elusive mutations behind congenital myopathies

The MYOCAPTURE project: Capturing the elusive mutations behind congenital myopathies

Journal: Medecine sciences : M/S

Published: November 28, 2025

Integrative Multi-Omics and Network Analyses Reveal Pathogenic and Protective Pathways in Centronuclear Myopathies.

Integrative Multi-Omics and Network Analyses Reveal Pathogenic and Protective Pathways in Centronuclear Myopathies.

Journal: International journal of molecular sciences

Published: September 11, 2025

Myomerger-derived peptide enhances skeletal muscle tropism and reduces liver transduction of lipid nanoparticles for gene delivery.

Myomerger-derived peptide enhances skeletal muscle tropism and reduces liver transduction of lipid nanoparticles for gene delivery.

Journal: Molecular therapy. Nucleic acids

Published: July 15, 2025

Evidence for the Dimuon Decay of the Higgs Boson in pp Collisions with the ATLAS Detector.

Evidence for the Dimuon Decay of the Higgs Boson in pp Collisions with the ATLAS Detector.

Journal: Physical review letters

Published: July 08, 2025

STIM1 Reduction Prevents Tubular Aggregate Formation and Compromises Muscle Performance in Ageing Mice.

STIM1 Reduction Prevents Tubular Aggregate Formation and Compromises Muscle Performance in Ageing Mice.

Journal: Journal of cachexia, sarcopenia and muscle

Published: June 23, 2025

Myosin inhibition partially rescues the myofiber proteome in X-linked myotubular myopathy.

Myosin inhibition partially rescues the myofiber proteome in X-linked myotubular myopathy.

Journal: JCI insight

Published: May 07, 2025

Tamoxifen treatment fails to improve muscle dysfunction in a model of recessive RYR1-linked centronuclear myopathy.

Tamoxifen treatment fails to improve muscle dysfunction in a model of recessive RYR1-linked centronuclear myopathy.

Journal: Disease models & mechanisms

Published: May 02, 2025

Showing 1-12 of 406

Last Updated: 09/26/2026