Luis Garcia
Université De Versailles St Quentin
Montigny-sur-loing, 20261, France
Montigny-sur-loing, 20261, France
Last Updated: 09/26/2026
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Found 24 publications
Antisense oligonucleotide selection scheme for rare Duchenne muscular dystrophy mutations: Application to DMD exon 16 skipping.
Journal: Molecular therapy. Nucleic acids
Published: February 05, 2026
Systemic distribution of tricyclo-DNA antisense oligonucleotide following intratracheal instillation in the mouse.
Journal: NAR molecular medicine
Published: October 07, 2025
Givinostat enhances antisense oligonucleotide efficacy in the mdx52 model of Duchenne muscular dystrophy.
Journal: Molecular therapy. Nucleic acids
Published: August 22, 2025
Improving angiogenesis ameliorates the efficacy of ASO-based exon skipping for the treatment of Duchenne muscular dystrophy.
Journal: Molecular therapy. Nucleic acids
Published: July 15, 2025
Combined 20-Hydroxyecdysone and Antisense-Mediated Exon Skipping Improve Functional Outcomes in a Mouse Model of Duchenne Muscular Dystrophy.
Journal: Nucleic acid therapeutics
Published: February 17, 2025
Valproic Acid Improves Antisense-Mediated Exon-Skipping Efficacy in mdx Mice.
Journal: International journal of molecular sciences
Published: January 13, 2025
Impact of the Inhibition of Organic Anion Transporter on Tricyclo-DNA-Mediated Exon Skipping in the mdx Mouse Model.
Journal: Nucleic acid therapeutics
Published: November 15, 2023
Networking to Optimize Dmd exon 53 Skipping in the Brain of mdx52 Mouse Model.
Journal: Biomedicines
Published: September 19, 2023
Dystrophin myonuclear domain restoration governs treatment efficacy in dystrophic muscle.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: January 03, 2023
Partial restoration of brain dystrophin by tricyclo-DNA antisense oligonucleotides alleviates emotional deficits in mdx52 mice.
Journal: Molecular therapy. Nucleic acids
Published: October 20, 2022
Last Updated: 09/26/2026