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Blood Cells, Molecules & Diseases|June 27, 1998
An improved method for generating retroviral producer clones for vectors lacking a selectable marker geneD A Persons, M G Mehaffey, M Kaleko, et al.Journal of Bacteriology|September 1, 1971
Location and orientation of the phoA locus on the Escherichia coli K-12 linkage mapA Nakata, G R Peterson, E L Brooks, et al.Gene Therapy|July 29, 2003
Synthesis of adenoviral targeting molecules by intein-mediated protein ligationO Nyanguile, C Dancik, J Blakemore, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|March 29, 2001
Generation and characterization of E1/E2a/E3/E4-deficient adenoviral vectors encoding human factor VIIIJ L Andrews, M J Kadan, M I Gorziglia, et al.Gene 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.Journal of Virology|November 1, 1988
Design of retrovirus vectors for transfer and expression of the human beta-globin geneA D Miller, M A Bender, E A Harris, et al.Human Gene Therapy|September 6, 2001
Adenovirus-mediated factor VIII gene expression results in attenuated anti-factor VIII-specific immunity in hemophilia A mice compared with factor VIII protein infusionJ A Bristol, A Gallo-Penn, J Andrews, et al.Human Gene Therapy|December 28, 1999
Adenoviral vector-mediated expression of physiologic levels of human factor VIII in nonhuman primatesT Brann, D Kayda, R M Lyons, et al.Thrombosis and Haemostasis|March 4, 1999
Evaluation of an adenoviral vector encoding full-length human factor VIII in hemophiliac miceS Connelly, J L Andrews, A M Gallo-Penn, 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.Pageof 5