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23. Major role of local immune responses in antibody formation to factor IX in AAV gene transfer. Wang L; Cao O; Swalm B; Dobrzynski E; Mingozzi F; Herzog RW Gene Ther; 2005 Oct; 12(19):1453-64. PubMed ID: 15889137 [TBL] [Abstract][Full Text] [Related]
24. Theodore E. Woodward Award. AAV-mediated gene transfer for hemophilia. High KA Trans Am Clin Climatol Assoc; 2003; 114():337-51; discussion 351-2. PubMed ID: 12813929 [TBL] [Abstract][Full Text] [Related]
25. Hemophilia Gene Therapy: Caught Between a Cure and an Immune Response. Herzog RW Mol Ther; 2015 Sep; 23(9):1411-2. PubMed ID: 26321180 [No Abstract] [Full Text] [Related]
26. Therapeutic plasma concentrations of human factor IX in mice after gene delivery into the amniotic cavity: a model for the prenatal treatment of haemophilia B. Schneider H; Adebakin S; Themis M; Cook T; Douar AM; Pavirani A; Coutelle C J Gene Med; 1999; 1(6):424-32. PubMed ID: 10753068 [TBL] [Abstract][Full Text] [Related]
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29. Platelets: a new target for gene therapy of haemophilia B. Brown MA Thromb Haemost; 2002 Mar; 87(3):362-3. PubMed ID: 11916064 [No Abstract] [Full Text] [Related]
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31. Genetic Targeting of the Albumin Locus to Treat Hemophilia. Davidoff AM; Nathwani AC N Engl J Med; 2016 Mar; 374(13):1288-90. PubMed ID: 27028920 [No Abstract] [Full Text] [Related]
32. Current therapeutic relevance of liver gene transfer. Heard JM Hepatology; 1994 Jul; 20(1 Pt 1):253-4. PubMed ID: 8020896 [No Abstract] [Full Text] [Related]
34. New approaches to treating haemophilia. Habeck M Mol Med Today; 2000 Jun; 6(6):214-5. PubMed ID: 10840378 [No Abstract] [Full Text] [Related]
35. Recombinant adeno-associated virus delivers human factor IX in mice. Stewart A Mol Med Today; 1997 Sep; 3(9):368. PubMed ID: 9302683 [No Abstract] [Full Text] [Related]
36. Mutant macaque factor IX T262A: a tool for hemophilia B gene therapy studies in macaques. Ishiwata A; Mimuro J; Mizukami H; Kashiwakura Y; Yasumoto A; Sakata A; Ohmori T; Madoiwa S; Ono F; Shima M; Yoshioka A; Ozawa K; Sakata Y Thromb Res; 2010 Jun; 125(6):533-7. PubMed ID: 20170943 [TBL] [Abstract][Full Text] [Related]
37. Muscle-directed gene transfer and transient immune suppression result in sustained partial correction of canine hemophilia B caused by a null mutation. Herzog RW; Mount JD; Arruda VR; High KA; Lothrop CD Mol Ther; 2001 Sep; 4(3):192-200. PubMed ID: 11545609 [TBL] [Abstract][Full Text] [Related]