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Bibliography

  • 1
    Kohn D. Gene therapy for hematopoietic and lymphoid disorders. Clin Exp Immunol 1997; 107(Suppl. 1):547.
  • 2
    Richter J. Gene transfer to hematopoietic cells – the clinical experience. Eur J Haematol 1997; 59 : 6775.
  • 3
    Miller D, Adam M, Miller A. Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection. Mol Cell Biol 1990; 10 : 423942.
  • 4
    Lewis P & Emerman M. Passage through mitosis is required for oncoretroviruses but not for the human immunodeficiency virus. J Virol 1994; 68 : 5106.
  • 5
    Naldini L, Blomer U, Gallay P et al. In vivo delivery and stable transduction of nondividing cells by a lentiviral vector. Science 1996; 272 : 2637.
  • 6
    Zufferey R, Nagy D, Mandel R, Naldini L, Trono D. Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo. Nat Biotechnol 1997; 15 : 87157.
  • 7
    Dull T, Zufferey R, Kelly M et al. A third-generation lentivirus vector with a conditional packaging system. J Virol 1998; 72 : 846371.
  • 8
    Akkina R, Walton R, Chen M, Li Q, Planelles V, Chen I. High-efficiency gene transfer into CD34+ cells with a human immunodeficiency virus type 1-based retroviral vector pseudotyped with vesicular stomatitis virus envelope glycoprotein G. J Virol 1996; 70 : 25815.
  • 9
    Reiser J, Harmison G, Kluepfel-Stahl S, Brady R, Karlsson S, Schubert M. Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particles. Proc Natl Acad Sci USA 1996; 93 : 1526671.DOI: 10.1073/pnas.93.26.15266
  • 10
    Uchida N, Sutton R, Friera A et al. HIV, but not murine leukemia virus, vectors mediate high efficiency gene transfer into freshly isolated G0/G1 human hematopoietic stem cells. Proc Natl Acad Sci USA 1998; 95 : 1193944.DOI: 10.1073/pnas.95.20.11939
  • 11
    Case S, Price M, Jordan C et al. Stable transduction of quiescent CD34+CD38– human hematopoietic cells by HIV-1-based lentiviral vectors. Proc Natl Acad Sci USA 1999; 96 : 298893.DOI: 10.1073/pnas.96.6.2988
  • 12
    Miyoshi H, Smith K, Mosier D, Verma I, Torbett B. Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors. Science 1999; 283 : 6826.DOI: 10.1126/science.283.5402.682
  • 13
    Sutton R, Reitsma M, Uchida N, Brown P. Transduction of human progenitor hematopoietic stem cells by human immunodeficiency virus type 1-based vectors is cell cycle dependent. J Virol 1999; 73 : 364960.
  • 14
    Larochelle A, Vormoor J, Hanenberg H et al. Identification of primitive human hematopoietic cells capable of repopulating NOD/SCID mouse bone marrow: implications for gene therapy. Nature Med 1996; 2 : 132937.
  • 15
    Cashman J & Eaves C. Human growth factor-enhanced regeneration of transplantable human hematopoietic stem cells in nonobese diabetic/severe combined immunodeficient mice. Blood 1999; 93 : 4817.
  • 16
    Woods N-B, Fahlmann C, Mikkola H et al. Lentiviral gene transfer into primary and secondary NOD/SCID repopulating cells. Blood 2000; 96 : 37253733.
  • 17
    Zufferey R, Donello J, Trono D, Hope T. Woodchuck hepatitis virus posttranscriptional regulatory element enhances expression of transgenes delivered by retroviral vectors. J Virol 1999; 73 : 288692.
  • 18
    Zufferey R, Dull T, Mandel RJ et al. Self-inactivating lentivirus vector for safe and efficient in vivo gene delivery. J Virol 1998; 72 : 987380.