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Journal of Thrombosis and Haemostasis : JTH|August 17, 2005
Gene transfer for hemophilia: can therapeutic efficacy in large animals be safely translated to patients?K HighAir Medical Journal|February 22, 2001
Airway obstruction induced by angiotensin-converting enzymes inhibitorsR K High, V W HighHaemophilia : the Official Journal of the World Federation of Hemophilia|May 11, 2006
Cellular and genetic therapies for haemophiliaD Lillicrap, T VandenDriessche, K HighHaemophilia : the Official Journal of the World Federation of Hemophilia|January 5, 1999
Hepatic gene therapy for haemophilia BM A KayJournal of Anaesthesiology, Clinical Pharmacology|February 21, 2012
Perioperative management of a patient with an axial-flow rotary ventricular assist device for laparoscopic ileo-colectomySubramanian Sathishkumar, R Kodavatiganti, S Plummer, et al.Human Gene Therapy|August 31, 1999
A simple method for constructing E1- and E1/E4-deleted recombinant adenoviral vectorsH Mizuguchi, M A KayMethods in Molecular Medicine|February 5, 2014
Methods for delivery of genes to hepatocytes in vivo using recombinant adenovirus vectorsD Barr, M A KayCurrent Gene Therapy|July 23, 2003
From virus evolution to vector revolution: use of naturally occurring serotypes of adeno-associated virus (AAV) as novel vectors for human gene therapyD Grimm, M A KayMolecular Therapy : the Journal of the American Society of Gene Therapy|September 8, 2001
Modified HIV-1 based lentiviral vectors have an effect on viral transduction efficiency and gene expression in vitro and in vivoF Park, M A KayPageof 11