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Biorxiv : the Preprint Server for Biology|March 31, 2025
Muscle-specific increased expression of JAG1 improves skeletal muscle phenotype in dystrophin-deficient miceFelipe de Souza Leite, Matthias R Lambert, Tracy Yuanfan Zhang, et al.Proceedings of the National Academy of Sciences of the United States of America|September 23, 2025
Muscle-specific increased expression of JAG1 improves the skeletal muscle phenotype in dystrophin-deficient miceFelipe de Souza Leite, Matthias R Lambert, Tracy Yuanfan Zhang, et al.Science Translational Medicine|March 28, 2020
Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophyAngela Lek, Yuanfan Zhang, Keryn G Woodman, et al.Cell Reports|May 31, 2016
Concordant but Varied Phenotypes among Duchenne Muscular Dystrophy Patient-Specific Myoblasts Derived using a Human iPSC-Based ModelIn Young Choi, HoTae Lim, Kenneth Estrellas, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|April 28, 2016
In Vivo Selection Yields AAV-B1 Capsid for Central Nervous System and Muscle Gene TherapySourav R Choudhury, Zachary Fitzpatrick, Anne F Harris, et al.Pageof 3