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Journal Abstract Search

400 related items for PubMed ID: 8867866

  • 1. Bone marrow gene transfer in three patients with adenosine deaminase deficiency.
    Hoogerbrugge PM, van Beusechem VW, Fischer A, Debree M, le Deist F, Perignon JL, Morgan G, Gaspar B, Fairbanks LD, Skeoch CH, Moseley A, Harvey M, Levinsky RJ, Valerio D.
    Gene Ther; 1996 Feb; 3(2):179-83. PubMed ID: 8867866
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  • 4. Retroviral-mediated gene transfer into mammalian cells.
    Kohn DB, Kantoff PW, Eglitis MA, McLachlin JR, Moen RC, Karson E, Zwiebel JA, Nienhuis A, Karlsson S, O'Reilly R.
    Blood Cells; 1987 Feb; 13(1-2):285-98. PubMed ID: 3311223
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  • 5. Expression of human adenosine deaminase in murine haematopoietic progenitor cells following retroviral transfer.
    Belmont JW, Henkel-Tigges J, Chang SM, Wager-Smith K, Kellems RE, Dick JE, Magli MC, Phillips RA, Bernstein A, Caskey CT.
    Nature; 1987 Feb; 322(6077):385-7. PubMed ID: 3016551
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  • 6. Adenosine deaminase deficiency: clinical expression, molecular basis, and therapy.
    Hershfield MS.
    Semin Hematol; 1998 Oct; 35(4):291-8. PubMed ID: 9801258
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  • 9. Persistent low-level engraftment of rhesus peripheral blood progenitor cells transduced with the fanconi anemia C gene after conditioning with low-dose irradiation.
    Kang EM, Hanazano Y, Frare P, Vanin EF, De Witte M, Metzger M, Liu JM, Tisdale JF.
    Mol Ther; 2001 Jun; 3(6):911-9. PubMed ID: 11407905
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  • 10. [Transplantation of genetically modified cells in the treatment of children with SCID: great hopes and recent disappointments].
    Smogorzewska EM, Weinberg KI, Kohn DB.
    Med Wieku Rozwoj; 2003 Jun; 7(1):27-34. PubMed ID: 13130167
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  • 17. In vivo selective expansion of gene-modified hematopoietic cells in a nonhuman primate model.
    Hanazono Y, Nagashima T, Takatoku M, Shibata H, Ageyama N, Asano T, Ueda Y, Dunbar CE, Kume A, Terao K, Hasegawa M, Ozawa K.
    Gene Ther; 2002 Aug; 9(16):1055-64. PubMed ID: 12140733
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