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Human Gene Therapy|May 31, 2012
Cell and gene therapy for genetic diseases: inherited disorders affecting the lung and those mimicking sudden infant death syndromeAllison M Keeler, Terence R FlotteMethods in Molecular Biology (Clifton, N.J.)|July 29, 2017
Therapeutics: Gene Therapy for Alpha-1 Antitrypsin DeficiencyAlisha M Gruntman, Terence R FlotteClinical Pharmacology and Therapeutics|February 1, 2022
Gene Therapy for Rare Neurological DisordersTerence R Flotte, Dominic J GesslerHuman Gene Therapy Methods|June 13, 2015
Progress with Recombinant Adeno-Associated Virus Vectors for Gene Therapy of Alpha-1 Antitrypsin DeficiencyAlisha M Gruntman, Terence R FlotteHuman Gene Therapy. Clinical Development|September 11, 2015
Delivery of Adeno-Associated Virus Gene Therapy by Intravascular Limb Infusion MethodsAlisha M Gruntman, Terence R FlotteExpert Opinion on Biological Therapy|November 4, 2014
Current status of gene therapy for α-1 antitrypsin deficiencyHeather S Loring, Terence R FlotteExpert Opinion on Biological Therapy|July 23, 2004
Recombinant adeno-associated virus vectors for gene therapyThomas J Conlon, Terence R FlotteCurrent Opinion in Biotechnology|December 3, 2002
Production of clinical-grade recombinant adeno-associated virus vectorsRichard O Snyder, Terence R FlotteFASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 9, 2019
The rapidly evolving state of gene therapyAlisha M Gruntman, Terence R FlotteAnnual Review of Virology|July 9, 2019
Recombinant Adeno-Associated Virus Gene Therapy in Light of Luxturna (and Zolgensma and Glybera): Where Are We, and How Did We Get Here?Allison M Keeler, Terence R FlottePageof 21