Jean-baptiste B. Dupont
Nantes, 44000, France
Last Updated: 09/26/2026
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Found 17 publications
Voluntary running sustains the correction of inflammation-related gene expression conferred by AAV gene therapy in mdx mice.
Journal: Molecular therapy. Advances
Published: January 17, 2025
Uncovering the Embryonic Origins of Duchenne Muscular Dystrophy.
Journal: WIREs mechanisms of disease
Published: July 05, 2024
Characterization of residual microRNAs in AAV vector batches produced in HEK293 mammalian cells and Sf9 insect cells.
Journal: Molecular therapy. Methods & clinical development
Published: February 27, 2024
Dystrophin deficiency impairs cell junction formation during embryonic myogenesis.
Journal: bioRxiv : the preprint server for biology
Published: December 18, 2023
Transcriptomic Analysis Reveals the Inability of Recombinant AAV8 to Activate Human Monocyte-Derived Dendritic Cells.
Journal: International journal of molecular sciences
Published: March 31, 2023
High-throughput, real-time monitoring of engineered skeletal muscle function using magnetic sensing.
High-throughput, real-time monitoring of engineered skeletal muscle function using magnetic sensing.
Journal: Journal of tissue engineering
Published: May 24, 2022
Erratum: Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice.
Journal: Molecular therapy. Methods & clinical development
Published: November 25, 2021
Genetic diseases in the omics era.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: July 23, 2021
Myogenesis modelled by human pluripotent stem cells: a multi-omic study of Duchenne myopathy early onset.
Journal: Journal of cachexia, sarcopenia and muscle
Published: August 27, 2020
Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice.
Journal: Molecular therapy. Methods & clinical development
Published: July 24, 2020
Last Updated: 09/26/2026