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The Mount Sinai Journal of Medicine, New York|November 16, 2004
AAV vectors for hemophilia B gene therapyHengjun Chao, Christopher E WalshCurrent Opinion in Molecular Therapeutics|November 19, 2002
Hemophilia gene therapy: novel rAAV vectors and RNA repair strategyHengjun Chao, Christopher E WalshExpert Reviews in Molecular Medicine|January 13, 2006
RNA repair for haemophilia AHengjun Chao, Christopher E WalshMolecular Therapy : the Journal of the American Society of Gene Therapy|November 26, 2009
Regulatory T cells and immune tolerance to coagulation factor IX in the context of intramuscular AAV1 gene transferMeagan Kelly, Arpita S Bharadwaj, Frank Tacke, et al.Blood|December 8, 2009
Induction of immune tolerance to FIX by intramuscular AAV gene transfer is independent of the activation status of dendritic cellsArpita S Bharadwaj, Meagan Kelly, Dongsoo Kim, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|February 26, 2009
Induction of immune tolerance to FIX following muscular AAV gene transfer is AAV-dose/FIX-level dependentMeagan E Kelly, Jiacai Zhuo, Arpita S Bharadwaj, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|May 25, 2002
Expression of human factor VIII by splicing between dimerized AAV vectorsHengjun Chao, Liangwu Sun, Andrew Bruce, et al.Nature Medicine|July 9, 2003
Phenotype correction of hemophilia A mice by spliceosome-mediated RNA trans-splicingHengjun Chao, S Gary Mansfield, Robert C Bartel, et al.Pageof 1