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Journal Abstract Search

283 related items for PubMed ID: 18679625

  • 1. Retroviral modification of mesenchymal stem cells for gene therapy of hemophilia.
    Doering CB.
    Methods Mol Biol; 2008; 433():203-12. PubMed ID: 18679625
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  • 4. Heterogeneity of the immune response to adenovirus-mediated factor VIII gene therapy in different inbred hemophilic mouse strains.
    Rawle FE, Shi CX, Brown B, McKinven A, Tinlin S, Graham FL, Hough C, Lillicrap D.
    J Gene Med; 2004 Dec; 6(12):1358-68. PubMed ID: 15493040
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  • 9. Gene therapy strategies for hemophilia: benefits versus risks.
    Petrus I, Chuah M, VandenDriessche T.
    J Gene Med; 2010 Oct; 12(10):797-809. PubMed ID: 20848668
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  • 11. Sustained FVIII expression and phenotypic correction of hemophilia A in neonatal mice using an endothelial-targeted sleeping beauty transposon.
    Liu L, Mah C, Fletcher BS.
    Mol Ther; 2006 May; 13(5):1006-15. PubMed ID: 16464640
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  • 17. Biosynthesis of FVIII in megakaryocytic cells: improved production and biochemical characterization.
    Rodriguez MH, Plantier JL, Enjolras N, Réa M, Leboeuf M, Uzan G, Négrier C.
    Br J Haematol; 2004 Dec; 127(5):568-75. PubMed ID: 15566360
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  • 18. Gene transfer as an approach to treating hemophilia.
    High KA.
    Semin Thromb Hemost; 2003 Feb; 29(1):107-20. PubMed ID: 12640573
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