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Human Gene Therapy|January 20, 1996
High-level tissue-specific expression of functional human factor VIII in miceS Connelly, J M Gardner, A McClelland, et al.Blood|June 1, 1996
Sustained expression of therapeutic levels of human factor VIII in miceS Connelly, J M Gardner, R M Lyons, et al.Blood|November 15, 1996
Complete short-term correction of canine hemophilia A by in vivo gene therapyS Connelly, J Mount, A Mauser, et al.Human Gene Therapy|February 1, 1995
In vivo gene delivery and expression of physiological levels of functional human factor VIII in miceS Connelly, T A Smith, G Dhir, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|January 5, 1999
Haemophilia A gene therapyS Connelly, M KalekoGene Therapy|June 1, 1996
Transient immunosuppression permits successful repetitive intravenous administration of an adenovirus vectorT A Smith, B D White, J M Gardner, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|December 3, 1999
In vivo evaluation of a novel epitope-tagged human factor VIII-encoding adenoviral vectorS Roy, P S Shirley, S Connelly, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|August 12, 1999
Efficient adenoviral vector transduction and expression of functional human factor VIII in cultured primary human hepatocytesJ L Andrews, L Weaver, M Kaleko, et al.Journal of Virology|July 11, 1998
Circumvention of immunity to the adenovirus major coat protein hexonS Roy, P S Shirley, A McClelland, et al.Pageof 47