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261 related items for PubMed ID: 12558785

  • 1. 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; 9(1):94-103. PubMed ID: 12558785
    [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 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]

  • 4. Recombinant factor VIII expression in hematopoietic cells following lentiviral transduction.
    Tiede A, Eder M, von Depka M, Battmer K, Luther S, Kiem HP, Ganser A, Scherr M.
    Gene Ther; 2003 Oct 10; 10(22):1917-25. PubMed ID: 14502221
    [Abstract] [Full Text] [Related]

  • 5. Therapeutic levels of human factor VIII in mice implanted with encapsulated cells: potential for gene therapy of haemophilia A.
    García-Martín C, Chuah MK, Van Damme A, Robinson KE, Vanzieleghem B, Saint-Remy JM, Gallardo D, Ofosu FA, Vandendriessche T, Hortelano G.
    J Gene Med; 2002 Oct 10; 4(2):215-23. PubMed ID: 11933222
    [Abstract] [Full Text] [Related]

  • 6. Sustained transgene expression by human cord blood derived CD34+ cells transduced with simian immunodeficiency virus agmTYO1-based vectors carrying the human coagulation factor VIII gene in NOD/SCID mice.
    Kikuchi J, Mimuro J, Ogata K, Tabata T, Ueda Y, Ishiwata A, Kimura K, Takano K, Madoiwa S, Mizukami H, Hanazono Y, Kume A, Hasegawa M, Ozawa K, Sakata Y.
    J Gene Med; 2004 Oct 10; 6(10):1049-60. PubMed ID: 15386735
    [Abstract] [Full Text] [Related]

  • 7. Efficient lentiviral transduction and improved engraftment of human bone marrow mesenchymal cells.
    Van Damme A, Thorrez L, Ma L, Vandenburgh H, Eyckmans J, Dell'Accio F, De Bari C, Luyten F, Lillicrap D, Collen D, VandenDriessche T, Chuah MK.
    Stem Cells; 2006 Apr 10; 24(4):896-907. PubMed ID: 16339997
    [Abstract] [Full Text] [Related]

  • 8. 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 10; 6(11):1363-77. PubMed ID: 8573610
    [Abstract] [Full Text] [Related]

  • 9. Sustaining expression of B domain-deleted human factor VIII mediated by using lentiviral vectors in NOD/SCID mouse.
    Li YJ, Chen C, Zeng LY, Cao J, Xu KL.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2012 Jun 10; 20(3):658-63. PubMed ID: 22739177
    [Abstract] [Full Text] [Related]

  • 10. Simplified retroviral vector gcsap with murine stem cell virus long terminal repeat allows high and continued expression of enhanced green fluorescent protein by human hematopoietic progenitors engrafted in nonobese diabetic/severe combined immunodeficient mice.
    Kaneko S, Onodera M, Fujiki Y, Nagasawa T, Nakauchi H.
    Hum Gene Ther; 2001 Jan 01; 12(1):35-44. PubMed ID: 11177540
    [Abstract] [Full Text] [Related]

  • 11. Ex vivo gene therapy for hemophilia A that enhances safe delivery and sustained in vivo factor VIII expression from lentivirally engineered endothelial progenitors.
    Matsui H, Shibata M, Brown B, Labelle A, Hegadorn C, Andrews C, Hebbel RP, Galipeau J, Hough C, Lillicrap D.
    Stem Cells; 2007 Oct 01; 25(10):2660-9. PubMed ID: 17615271
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. High-level expression of porcine factor VIII from genetically modified bone marrow-derived stem cells.
    Gangadharan B, Parker ET, Ide LM, Spencer HT, Doering CB.
    Blood; 2006 May 15; 107(10):3859-64. PubMed ID: 16449528
    [Abstract] [Full Text] [Related]

  • 14. Sustained phenotypic correction of hemophilia a mice following oncoretroviral-mediated expression of a bioengineered human factor VIII gene in long-term hematopoietic repopulating cells.
    Moayeri M, Ramezani A, Morgan RA, Hawley TS, Hawley RG.
    Mol Ther; 2004 Nov 15; 10(5):892-902. PubMed ID: 15509507
    [Abstract] [Full Text] [Related]

  • 15. Quantitative assessment of retroviral transfer of the human multidrug resistance 1 gene to human mobilized peripheral blood progenitor cells engrafted in nonobese diabetic/severe combined immunodeficient mice.
    Schiedlmeier B, Kühlcke K, Eckert HG, Baum C, Zeller WJ, Fruehauf S.
    Blood; 2000 Feb 15; 95(4):1237-48. PubMed ID: 10666196
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. Factor VIII delivered by haematopoietic stem cell-derived B cells corrects the phenotype of haemophilia A mice.
    Ramezani A, Zweier-Renn LA, Hawley RG.
    Thromb Haemost; 2011 Apr 01; 105(4):676-87. PubMed ID: 21264447
    [Abstract] [Full Text] [Related]

  • 18. Efficient adenoviral vector transduction and expression of functional human factor VIII in cultured primary human hepatocytes.
    Andrews JL, Weaver L, Kaleko M, Connelly S.
    Haemophilia; 1999 May 01; 5(3):160-8. PubMed ID: 10444282
    [Abstract] [Full Text] [Related]

  • 19. Lentivirus-mediated platelet-derived factor VIII gene therapy in murine haemophilia A.
    Shi Q, Wilcox DA, Fahs SA, Fang J, Johnson BD, DU LM, Desai D, Montgomery RR.
    J Thromb Haemost; 2007 Feb 01; 5(2):352-61. PubMed ID: 17269937
    [Abstract] [Full Text] [Related]

  • 20. [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]

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