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426 related items for PubMed ID: 11264344

  • 1. 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; 75(8):3547-55. PubMed ID: 11264344
    [Abstract] [Full Text] [Related]

  • 2. Marking and gene expression by a lentivirus vector in transplanted human and nonhuman primate CD34(+) cells.
    An DS, Wersto RP, Agricola BA, Metzger ME, Lu S, Amado RG, Chen IS, Donahue RE.
    J Virol; 2000 Feb; 74(3):1286-95. PubMed ID: 10627539
    [Abstract] [Full Text] [Related]

  • 3. Efficient human immunodeficiency virus-based vector transduction of unstimulated human mobilized peripheral blood CD34+ cells in the SCID-hu Thy/Liv model of human T cell lymphopoiesis.
    Douglas JL, Lin WY, Panis ML, Veres G.
    Hum Gene Ther; 2001 Mar 01; 12(4):401-13. PubMed ID: 11242532
    [Abstract] [Full Text] [Related]

  • 4. Rhesus monkey model for fetal gene transfer: studies with retroviral- based vector systems.
    Tarantal AF, O'Rourke JP, Case SS, Newbound GC, Li J, Lee CI, Baskin CR, Kohn DB, Bunnell BA.
    Mol Ther; 2001 Feb 01; 3(2):128-38. PubMed ID: 11237669
    [Abstract] [Full Text] [Related]

  • 5. Efficient detection and selection of immature rhesus monkey and human CD34+ hematopoietic cells expressing the enhanced green fluorescent protein (EGFP).
    Bierhuizen MF, Westerman Y, Hartong SC, Visser TP, Wognum AW, Wagemaker G.
    Leukemia; 1999 Apr 01; 13(4):605-13. PubMed ID: 10214869
    [Abstract] [Full Text] [Related]

  • 6. A murine leukemia virus (MuLV) long terminal repeat derived from rhesus macaques in the context of a lentivirus vector and MuLV gag sequence results in high-level gene expression in human T lymphocytes.
    Kung SK, An DS, Chen IS.
    J Virol; 2000 Apr 01; 74(8):3668-81. PubMed ID: 10729143
    [Abstract] [Full Text] [Related]

  • 7. Critical factors influencing stable transduction of human CD34(+) cells with HIV-1-derived lentiviral vectors.
    Haas DL, Case SS, Crooks GM, Kohn DB.
    Mol Ther; 2000 Jul 01; 2(1):71-80. PubMed ID: 10899830
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. 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 Jan 01; 19(3):236-46. PubMed ID: 11359949
    [Abstract] [Full Text] [Related]

  • 10. Transient in vivo beta-globin production after lentiviral gene transfer to hematopoietic stem cells in the nonhuman primate.
    Hayakawa J, Ueda T, Lisowski L, Hsieh MM, Washington K, Phang O, Metzger M, Krouse A, Donahue RE, Sadelain M, Tisdale JF.
    Hum Gene Ther; 2009 Jun 01; 20(6):563-72. PubMed ID: 19222366
    [Abstract] [Full Text] [Related]

  • 11. High-level transduction and gene expression in hematopoietic repopulating cells using a human immunodeficiency [correction of imunodeficiency] virus type 1-based lentiviral vector containing an internal spleen focus forming virus promoter.
    Demaison C, Parsley K, Brouns G, Scherr M, Battmer K, Kinnon C, Grez M, Thrasher AJ.
    Hum Gene Ther; 2002 May 01; 13(7):803-13. PubMed ID: 11975847
    [Abstract] [Full Text] [Related]

  • 12. Highly efficient gene transfer into preterm CD34 hematopoietic progenitor cells.
    Shields LE, Kiem HP, Andrews RG.
    Am J Obstet Gynecol; 2000 Sep 01; 183(3):732-7. PubMed ID: 10992201
    [Abstract] [Full Text] [Related]

  • 13. Long-term engraftment of nonobese diabetic/severe combined immunodeficient mice with human CD34+ cells transduced by a self-inactivating human immunodeficiency virus type 1 vector.
    Gatlin J, Padgett A, Melkus MW, Kelly PF, Garcia JV.
    Hum Gene Ther; 2001 Jun 10; 12(9):1079-89. PubMed ID: 11399229
    [Abstract] [Full Text] [Related]

  • 14. Transplantation of transduced nonhuman primate CD34+ cells using a gibbon ape leukemia virus vector: restricted expression of the gibbon ape leukemia virus receptor to a subset of CD34+ cells.
    Bunnell BA, Kluge KA, Lee-Lin SQ, Byrne ER, Orlic D, Metzger ME, Agricola BA, Wersto RP, Bodine DM, Morgan RA, Donahue RE.
    Gene Ther; 1999 Jan 10; 6(1):48-56. PubMed ID: 10341875
    [Abstract] [Full Text] [Related]

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  • 18. Enhanced transgene expression in cord blood CD34(+)-derived hematopoietic cells, including developing T cells and NOD/SCID mouse repopulating cells, following transduction with modified trip lentiviral vectors.
    Sirven A, Ravet E, Charneau P, Zennou V, Coulombel L, Guétard D, Pflumio F, Dubart-Kupperschmitt A.
    Mol Ther; 2001 Apr 10; 3(4):438-48. PubMed ID: 11319904
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  • 20. Lentiviral vectors for enhanced gene expression in human hematopoietic cells.
    Ramezani A, Hawley TS, Hawley RG.
    Mol Ther; 2000 Nov 10; 2(5):458-69. PubMed ID: 11082319
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