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747 related items for PubMed ID: 11177540

  • 21. Addition of the human interferon beta scaffold attachment region to retroviral vector backbones increases the level of in vivo transgene expression among progeny of engrafted human hematopoietic stem cells.
    Murray L, Travis M, Luens-Abitorabi K, Olsson K, Plavec I, Forestell S, Hanania EG, Hill B.
    Hum Gene Ther; 2000 Sep 20; 11(14):2039-50. PubMed ID: 11020802
    [Abstract] [Full Text] [Related]

  • 22. Characterization of retroviral gene transfer into highly purified human CD34(-) cells with primitive hematopoietic capacity.
    Murdoch B, Gallacher L, Chadwick K, Bhatia M.
    Mol Ther; 2002 May 20; 5(5 Pt 1):635-43. PubMed ID: 11991755
    [Abstract] [Full Text] [Related]

  • 23. Retrovirus-mediated gene transfer into human CD34+38low primitive cells capable of reconstituting long-term cultures in vitro and nonobese diabetic-severe combined immunodeficiency mice in vivo.
    Marandin A, Dubart A, Pflumio F, Cosset FL, Cordette V, Chapel-Fernandes S, Coulombel L, Vainchenker W, Louache F.
    Hum Gene Ther; 1998 Jul 01; 9(10):1497-511. PubMed ID: 9681421
    [Abstract] [Full Text] [Related]

  • 24. Lentivirus vector-mediated hematopoietic stem cell gene transfer of common gamma-chain cytokine receptor in rhesus macaques.
    An DS, Kung SK, Bonifacino A, Wersto RP, Metzger ME, Agricola BA, Mao SH, Chen IS, Donahue RE.
    J Virol; 2001 Apr 01; 75(8):3547-55. PubMed ID: 11264344
    [Abstract] [Full Text] [Related]

  • 25. The late dividing population of gamma-retroviral vector transduced human mobilized peripheral blood progenitor cells contributes most to gene-marked cell engraftment in nonobese diabetic/severe combined immunodeficient mice.
    Brenner S, Ryser MF, Whiting-Theobald NL, Gentsch M, Linton GF, Malech HL.
    Stem Cells; 2007 Jul 01; 25(7):1807-13. PubMed ID: 17464090
    [Abstract] [Full Text] [Related]

  • 26. MDR1 gene expression in NOD/SCID repopulating cells after retroviral gene transfer under clinically relevant conditions.
    Schilz AJ, Schiedlmeier B, Kühlcke K, Fruehauf S, Lindemann C, Zeller WJ, Grez M, Fauser AA, Baum C, Eckert HG.
    Mol Ther; 2000 Dec 01; 2(6):609-18. PubMed ID: 11124062
    [Abstract] [Full Text] [Related]

  • 27. Retroviral transduction of human CD34+ cells on fibronectin fragment CH-296 is inhibited by high concentrations of vector containing medium.
    Relander T, Brun A, Hawley RG, Karlsson S, Richter J.
    J Gene Med; 2001 Dec 01; 3(3):207-18. PubMed ID: 11437326
    [Abstract] [Full Text] [Related]

  • 28.
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  • 29. Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors.
    Miyoshi H, Smith KA, Mosier DE, Verma IM, Torbett BE.
    Science; 1999 Jan 29; 283(5402):682-6. PubMed ID: 9924027
    [Abstract] [Full Text] [Related]

  • 30. Stimulation of mouse bone marrow cells with kit ligand, FLT3 ligand, and thrombopoietin leads to efficient retrovirus-mediated gene transfer to stem cells, whereas interleukin 3 and interleukin 11 reduce transduction of short- and long-term repopulating cells.
    Wognum AW, Visser TP, Peters K, Bierhuizen MF, Wagemaker G.
    Hum Gene Ther; 2000 Oct 10; 11(15):2129-41. PubMed ID: 11044914
    [Abstract] [Full Text] [Related]

  • 31. 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
    [Abstract] [Full Text] [Related]

  • 32. Transduction of human NOD/SCID-repopulating cells with both lymphoid and myeloid potential by foamy virus vectors.
    Josephson NC, Vassilopoulos G, Trobridge GD, Priestley GV, Wood BL, Papayannopoulou T, Russell DW.
    Proc Natl Acad Sci U S A; 2002 Jun 11; 99(12):8295-300. PubMed ID: 12060773
    [Abstract] [Full Text] [Related]

  • 33. Retroviral vectors for high-level transgene expression in T lymphocytes.
    Engels B, Cam H, Schüler T, Indraccolo S, Gladow M, Baum C, Blankenstein T, Uckert W.
    Hum Gene Ther; 2003 Aug 10; 14(12):1155-68. PubMed ID: 12908967
    [Abstract] [Full Text] [Related]

  • 34. A new red fluorescent protein that allows efficient marking of murine hematopoietic stem cells.
    Sanuki S, Hamanaka S, Kaneko S, Otsu M, Karasawa S, Miyawaki A, Nakauchi H, Nagasawa T, Onodera M.
    J Gene Med; 2008 Sep 10; 10(9):965-71. PubMed ID: 18613301
    [Abstract] [Full Text] [Related]

  • 35. A comparison of targeting performance of oncoretroviral versus lentiviral vectors on human keratinocytes.
    Serrano F, Del Rio M, Larcher F, Garcia M, Muñoz E, Escamez MJ, Muñoz M, Meana A, Bernad A, Jorcano JL.
    Hum Gene Ther; 2003 Nov 01; 14(16):1579-85. PubMed ID: 14577919
    [Abstract] [Full Text] [Related]

  • 36. Retrovirus-mediated gene expression in hematopoietic cells correlates inversely with growth factor stimulation.
    Lu M, Zhang N, Maruyama M, Hawley RG, Ho AD.
    Hum Gene Ther; 1996 Dec 01; 7(18):2263-71. PubMed ID: 8953317
    [Abstract] [Full Text] [Related]

  • 37. In vivo persistence of retrovirally transduced murine long-term repopulating cells is not limited by expression of foreign gene products in the fully or minimally myeloablated setting.
    Kang E, Giri N, Wu T, Sellers S, Kirby M, Hanazono Y, Tisdale J, Dunbar CE.
    Hum Gene Ther; 2001 Sep 01; 12(13):1663-72. PubMed ID: 11535169
    [Abstract] [Full Text] [Related]

  • 38. Efficient retrovirus-mediated gene transfer to transplantable human bone marrow cells in the absence of fibronectin.
    Hennemann B, Oh IH, Chuo JY, Kalberer CP, Schley PD, Rose-John S, Humphries RK, Eaves CJ.
    Blood; 2000 Oct 01; 96(7):2432-9. PubMed ID: 11001895
    [Abstract] [Full Text] [Related]

  • 39. Sustained retroviral gene marking and expression in lymphoid and myeloid cells derived from transduced hematopoietic progenitor cells.
    Plavec I, Voytovich A, Moss K, Webster D, Hanley MB, Escaich S, Ho KE, Böhnlein E, DiGiusto DL.
    Gene Ther; 1996 Aug 01; 3(8):717-24. PubMed ID: 8854097
    [Abstract] [Full Text] [Related]

  • 40. Optimization of retroviral-mediated gene transfer to human NOD/SCID mouse repopulating cord blood cells through a systematic analysis of protocol variables.
    Hennemann B, Conneally E, Pawliuk R, Leboulch P, Rose-John S, Reid D, Chuo JY, Humphries RK, Eaves CJ.
    Exp Hematol; 1999 May 01; 27(5):817-25. PubMed ID: 10340397
    [Abstract] [Full Text] [Related]

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