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Wires Mechanisms of Disease|October 24, 2024
Uncovering the Embryonic Origins of Duchenne Muscular DystrophyPhilip Barrett, Ke'ale W Louie, Jean-Baptiste Dupont, et al.
Molecular Therapy. Advances|May 15, 2026
Voluntary running sustains the correction of inflammation-related gene expression conferred by AAV gene therapy in mdx miceClaire Yuan, Shelby E Hamm, David L Mack, et al.
Molecular Therapy. Methods & Clinical Development|September 2, 2024
Characterization of residual microRNAs in AAV vector batches produced in HEK293 mammalian cells and Sf9 insect cellsMagalie Penaud-Budloo, Emilie Lecomte, Quentin Lecomte, et al.
International Journal of Molecular Sciences|July 14, 2023
Transcriptomic Analysis Reveals the Inability of Recombinant AAV8 to Activate Human Monocyte-Derived Dendritic CellsSamer Masri, Laure Carré, Nicolas Jaulin, et al.
Human Molecular Genetics|July 27, 2021
CRISPR gene editing in pluripotent stem cells reveals the function of MBNL proteins during human in vitro myogenesisAntoine Mérien, Julie Tahraoui-Bories, Michel Cailleret, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 1, 2019
AAV-Mediated Gene Transfer Restores a Normal Muscle Transcriptome in a Canine Model of X-Linked Myotubular MyopathyJean-Baptiste Dupont, Jianjun Guo, Edith Renaud-Gabardos, et al.
Journal of Cachexia, Sarcopenia and Muscle|February 15, 2021
Myogenesis modelled by human pluripotent stem cells: a multi-omic study of Duchenne myopathy early onsetVirginie Mournetas, Emmanuelle Massouridès, Jean-Baptiste Dupont, et al.
Molecular Therapy. Nucleic Acids|October 28, 2015
Advanced Characterization of DNA Molecules in rAAV Vector Preparations by Single-stranded Virus Next-generation SequencingEmilie Lecomte, Benoît Tournaire, Benjamin Cogné, et al.
Biorxiv : the Preprint Server for Biology|December 18, 2023
Dystrophin deficiency impairs cell junction formation during embryonic myogenesisElise Mozin, Emmanuelle Massouridès, Virginie Mournetas, et al.
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