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Current Gene Therapy|May 24, 2003
The pyruvate dehydrogenase complex as a target for gene therapyPeter W Stacpoole, Renius Owen, Terence R FlotteHuman Gene Therapy|March 21, 2017
Retro-Orbital Venous Sinus Delivery of rAAV9 Mediates High-Level Transduction of Brain and Retina Compared with Temporal Vein Delivery in Neonatal Mouse PupsAlisha M Gruntman, Lin Su, Terence R FlotteHuman Gene Therapy Methods|March 24, 2017
CAR T-Cell Therapy: Progress and ProspectsOlivia Wilkins, Allison M Keeler, Terence R FlotteMethods in Molecular Biology (Clifton, N.J.)|December 18, 2023
Approaches to Therapeutic Gene Editing in Alpha-1 Antitrypsin DeficiencyAlisha M Gruntman, Wen Xue, Terence R FlotteProceedings of the National Academy of Sciences of the United States of America|February 1, 2017
Class I-restricted T-cell responses to a polymorphic peptide in a gene therapy clinical trial for α-1-antitrypsin deficiencyRoberto Calcedo, Suryanarayan Somanathan, Qiuyue Qin, et al.Expert Opinion on Biological Therapy|February 24, 2023
Gene therapy for alpha-1 antitrypsin deficiency: an updateDebora Pires Ferreira, Alisha M Gruntman, Terence R FlotteThe Journal of Continuing Education in the Health Professions|February 2, 2023
Defining Scholarship for Today and TomorrowRobert J Milner, Terence R Flotte, Luanne E ThorndykeHuman Gene Therapy Methods|February 20, 2016
Development of rAAV2-CFTR: History of the First rAAV Vector Product to be Used in HumansHeather S Loring, Mai K ElMallah, Terence R FlotteHuman Gene Therapy|January 27, 2026
Advances in Precision Editing Therapies for Alpha-1 Antitrypsin DeficiencyJenny Gao, Erik Sontheimer, Terence R Flotte, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|March 8, 2012
Long-term correction of very long-chain acyl-coA dehydrogenase deficiency in mice using AAV9 gene therapyAllison M Keeler, Thomas Conlon, Glenn Walter, et al.Pageof 90