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983 related items for PubMed ID: 17824830

  • 21. Lentiviral gene transfer into primary and secondary NOD/SCID repopulating cells.
    Woods NB, Fahlman C, Mikkola H, Hamaguchi I, Olsson K, Zufferey R, Jacobsen SE, Trono D, Karlsson S.
    Blood; 2000 Dec 01; 96(12):3725-33. PubMed ID: 11090053
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  • 22. 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 01; 6(10):1049-60. PubMed ID: 15386735
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  • 23. Specific and stable gene transfer to human embryonic stem cells using pseudotyped lentiviral vectors.
    Jang JE, Shaw K, Yu XJ, Petersen D, Pepper K, Lutzko C, Kohn DB.
    Stem Cells Dev; 2006 Feb 01; 15(1):109-17. PubMed ID: 16522168
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  • 24. Hybrid HIV/MSCV LTR enhances transgene expression of lentiviral vectors in human CD34(+) hematopoietic cells.
    Choi JK, Hoang N, Vilardi AM, Conrad P, Emerson SG, Gewirtz AM.
    Stem Cells; 2001 Feb 01; 19(3):236-46. PubMed ID: 11359949
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  • 25. Glycoprotein Ibalpha promoter drives megakaryocytic lineage-restricted expression after hematopoietic stem cell transduction using a self-inactivating lentiviral vector.
    Lavenu-Bombled C, Izac B, Legrand F, Cambot M, Vigier A, Massé JM, Dubart-Kupperschmitt A.
    Stem Cells; 2007 Jun 01; 25(6):1571-7. PubMed ID: 17379771
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  • 27. Highly efficient transduction of the green fluorescent protein gene in human umbilical cord blood stem cells capable of cobblestone formation in long-term cultures and multilineage engraftment of immunodeficient mice.
    van Hennik PB, Verstegen MM, Bierhuizen MF, Limón A, Wognum AW, Cancelas JA, Barquinero J, Ploemacher RE, Wagemaker G.
    Blood; 1998 Dec 01; 92(11):4013-22. PubMed ID: 9834203
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  • 30. Expression from second-generation feline immunodeficiency virus vectors is impaired in human hematopoietic cells.
    Price MA, Case SS, Carbonaro DA, Yu XJ, Petersen D, Sabo KM, Curran MA, Engel BC, Margarian H, Abkowitz JL, Nolan GP, Kohn DB, Crooks GM.
    Mol Ther; 2002 Nov 01; 6(5):645-52. PubMed ID: 12409263
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  • 32. Lentiviral vector transduction of NOD/SCID repopulating cells results in multiple vector integrations per transduced cell: risk of insertional mutagenesis.
    Woods NB, Muessig A, Schmidt M, Flygare J, Olsson K, Salmon P, Trono D, von Kalle C, Karlsson S.
    Blood; 2003 Feb 15; 101(4):1284-9. PubMed ID: 12393514
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  • 33. ABC transporter inhibitors that are substrates enhance lentiviral vector transduction into primitive hematopoietic progenitor cells.
    Davis BM, Humeau L, Slepushkin V, Binder G, Korshalla L, Ni Y, Ogunjimi EO, Chang LF, Lu X, Dropulic B.
    Blood; 2004 Jul 15; 104(2):364-73. PubMed ID: 15059841
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  • 36. Potent inhibition of simian immunodeficiency virus (SIV) replication by an SIV-based lentiviral vector expressing antisense Env.
    Braun SE, Lu XV, Wong FE, Connole M, Qiu G, Chen Z, Slepushkina T, Slepushkin V, Humeau LM, Dropulic B, Johnson RP.
    Hum Gene Ther; 2007 Jul 15; 18(7):653-64. PubMed ID: 17600461
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  • 37. Identification of parameters required for efficient lentiviral vector transduction and engraftment of human cord blood CD34(+) NOD/SCID-repopulating cells.
    Liu Y, Hangoc G, Campbell TB, Goodman M, Tao W, Pollok K, Srour EF, Broxmeyer HE.
    Exp Hematol; 2008 Aug 15; 36(8):947-56. PubMed ID: 18640494
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