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Journal Abstract Search

202 related items for PubMed ID: 9508053

  • 1. Bone marrow stromal cells as targets for gene therapy of hemophilia A.
    Chuah MK, Brems H, Vanslembrouck V, Collen D, VandenDriessche T.
    Hum Gene Ther; 1998 Feb 10; 9(3):353-65. PubMed ID: 9508053
    [Abstract] [Full Text] [Related]

  • 2. Long-term persistence of human bone marrow stromal cells transduced with factor VIII-retroviral vectors and transient production of therapeutic levels of human factor VIII in nonmyeloablated immunodeficient mice.
    Chuah MK, Van Damme A, Zwinnen H, Goovaerts I, Vanslembrouck V, Collen D, VandenDriessche T.
    Hum Gene Ther; 2000 Mar 20; 11(5):729-38. PubMed ID: 10757352
    [Abstract] [Full Text] [Related]

  • 3. Bone marrow mesenchymal cells for haemophilia A gene therapy using retroviral vectors with modified long-terminal repeats.
    Van Damme A, Chuah MK, Dell'accio F, De Bari C, Luyten F, Collen D, VandenDriessche T.
    Haemophilia; 2003 Jan 20; 9(1):94-103. PubMed ID: 12558785
    [Abstract] [Full Text] [Related]

  • 4. Improved gene transfer into human lymphocytes using retroviruses with the gibbon ape leukemia virus envelope.
    Lam JS, Reeves ME, Cowherd R, Rosenberg SA, Hwu P.
    Hum Gene Ther; 1996 Aug 01; 7(12):1415-22. PubMed ID: 8844200
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  • 5. [Human factor VIII expression in retrovirus vector-transduced bone marrow stromal cells].
    Guo X, Wang H, Chu H.
    Zhonghua Xue Ye Xue Za Zhi; 2001 Sep 01; 22(9):461-3. PubMed ID: 11758224
    [Abstract] [Full Text] [Related]

  • 6. Development and analysis of retroviral vectors expressing human factor VIII as a potential gene therapy for hemophilia A.
    Chuah MK, VandenDriessche T, Morgan RA.
    Hum Gene Ther; 1995 Nov 01; 6(11):1363-77. PubMed ID: 8573610
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  • 8. Bone marrow stromal cell-mediated gene therapy for hemophilia A: in vitro expression of human factor VIII with high biological activity requires the inclusion of the proteolytic site at amino acid 1648.
    Chiang GG, Rubin HL, Cherington V, Wang T, Sobolewski J, McGrath CA, Gaffney A, Emami S, Sarver N, Levine PH, Greenberger JS, Hurwitz DR.
    Hum Gene Ther; 1999 Jan 01; 10(1):61-76. PubMed ID: 10022531
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  • 10. Transduction of human hematopoietic progenitor cells with retroviral vectors based on the gibbon ape leukemia virus.
    Eglitis MA, Schneiderman RD.
    Biochem Biophys Res Commun; 1997 Feb 13; 231(2):477-80. PubMed ID: 9070304
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  • 13. Gene transfer into marrow repopulating cells: comparison between amphotropic and gibbon ape leukemia virus pseudotyped retroviral vectors in a competitive repopulation assay in baboons.
    Kiem HP, Heyward S, Winkler A, Potter J, Allen JM, Miller AD, Andrews RG.
    Blood; 1997 Dec 01; 90(11):4638-45. PubMed ID: 9373277
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  • 14. Increased gene transfer into human hematopoietic progenitor cells by extended in vitro exposure to a pseudotyped retroviral vector.
    von Kalle C, Kiem HP, Goehle S, Darovsky B, Heimfeld S, Torok-Storb B, Storb R, Schuening FG.
    Blood; 1994 Nov 01; 84(9):2890-7. PubMed ID: 7524756
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  • 15. Extracellular inorganic phosphate regulates gibbon ape leukemia virus receptor-2/phosphate transporter mRNA expression in rat bone marrow stromal cells.
    Wada K, Mizuno M, Komori T, Tamura M.
    J Cell Physiol; 2004 Jan 01; 198(1):40-7. PubMed ID: 14584042
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  • 16. Expression of human coagulation factor VIII in adipocytes transduced with the simian immunodeficiency virus agmTYO1-based vector for hemophilia A gene therapy.
    Ogata K, Mimuro J, Kikuchi J, Tabata T, Ueda Y, Naito M, Madoiwa S, Takano K, Hasegawa M, Ozawa K, Sakata Y.
    Gene Ther; 2004 Feb 01; 11(3):253-9. PubMed ID: 14737084
    [Abstract] [Full Text] [Related]

  • 17. Correction of murine hemophilia A by hematopoietic stem cell gene therapy.
    Moayeri M, Hawley TS, Hawley RG.
    Mol Ther; 2005 Dec 01; 12(6):1034-42. PubMed ID: 16226058
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  • 18. Efficient production of human FVIII in hemophilic mice using lentiviral vectors.
    Kootstra NA, Matsumura R, Verma IM.
    Mol Ther; 2003 May 01; 7(5 Pt 1):623-31. PubMed ID: 12718905
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  • 19. Lentiviral vectors pseudotyped with envelope glycoproteins derived from gibbon ape leukemia virus and murine leukemia virus 10A1.
    Stitz J, Buchholz CJ, Engelstädter M, Uckert W, Bloemer U, Schmitt I, Cichutek K.
    Virology; 2000 Jul 20; 273(1):16-20. PubMed ID: 10891403
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  • 20. Gene therapy for hemophilia A: production of therapeutic levels of human factor VIII in vivo in mice.
    Dwarki VJ, Belloni P, Nijjar T, Smith J, Couto L, Rabier M, Clift S, Berns A, Cohen LK.
    Proc Natl Acad Sci U S A; 1995 Feb 14; 92(4):1023-7. PubMed ID: 7862626
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