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Human Molecular Genetics|June 26, 2019
AAV-based gene therapies for the muscular dystrophiesJulie M Crudele, Jeffrey S ChamberlainMolecular Therapy : the Journal of the American Society of Gene Therapy|April 19, 2017
Progress toward Gene Therapy for Duchenne Muscular DystrophyJoel R Chamberlain, Jeffrey S ChamberlainCurrent Topics in Developmental Biology|February 3, 2009
The value of mammalian models for duchenne muscular dystrophy in developing therapeutic strategiesGlen B Banks, Jeffrey S ChamberlainMolecular Therapy. Nucleic Acids|December 2, 2025
Genetic strategies for therapy of Duchenne muscular dystrophyAgnieszka Łoboda, Jeffrey S Chamberlain, Józef DulakMolecular Therapy : the Journal of the American Society of Gene Therapy|May 28, 2009
Evaluation of vascular delivery methodologies to enhance rAAV6-mediated gene transfer to canine striated musculaturePaul Gregorevic, Brian R Schultz, James M Allen, et al.Muscle & Nerve|April 5, 2013
Gene and cell-mediated therapies for muscular dystrophyPatryk Konieczny, Kristy Swiderski, Jeffrey S ChamberlainBiochimica Et Biophysica Acta|October 27, 2006
Viral-mediated gene therapy for the muscular dystrophies: successes, limitations and recent advancesGuy L Odom, Paul Gregorevic, Jeffrey S ChamberlainMolecular Therapy : the Journal of the American Society of Gene Therapy|December 20, 2005
Gene therapy strategies for Duchenne muscular dystrophy utilizing recombinant adeno-associated virus vectorsMichael J Blankinship, Paul Gregorevic, Jeffrey S ChamberlainCurrent Opinion in Molecular Therapeutics|November 13, 2004
Viral vectors for gene transfer to striated musclePaul Gregorevic, Michael J Blankinship, Jeffrey S ChamberlainMolecular Therapy : the Journal of the American Society of Gene Therapy|April 4, 2025
The road toward AAV-mediated gene therapy of Duchenne muscular dystrophyNiclas E Bengtsson, Hichem Tasfaout, Jeffrey S ChamberlainPageof 16