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Journal Abstract Search

711 related items for PubMed ID: 11319904

  • 1. 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; 3(4):438-48. PubMed ID: 11319904
    [Abstract] [Full Text] [Related]

  • 2. High levels of transgene expression following transduction of long-term NOD/SCID-repopulating human cells with a modified lentiviral vector.
    Gao Z, Golob J, Tanavde VM, Civin CI, Hawley RG, Cheng L.
    Stem Cells; 2001 Apr; 19(3):247-59. PubMed ID: 11359950
    [Abstract] [Full Text] [Related]

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

  • 4. Lentiviral vectors for enhanced gene expression in human hematopoietic cells.
    Ramezani A, Hawley TS, Hawley RG.
    Mol Ther; 2000 Nov; 2(5):458-69. PubMed ID: 11082319
    [Abstract] [Full Text] [Related]

  • 5. 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; 2(1):71-80. PubMed ID: 10899830
    [Abstract] [Full Text] [Related]

  • 6. 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; 6(10):1049-60. PubMed ID: 15386735
    [Abstract] [Full Text] [Related]

  • 7. Comparison of HIV- and EIAV-based vectors on their efficiency in transducing murine and human hematopoietic repopulating cells.
    Siapati EK, Bigger BW, Miskin J, Chipchase D, Parsley KL, Mitrophanous K, Themis M, Thrasher AJ, Bonnet D.
    Mol Ther; 2005 Sep; 12(3):537-46. PubMed ID: 16099415
    [Abstract] [Full Text] [Related]

  • 8. Molecular evidence of lentiviral vector-mediated gene transfer into human self-renewing, multi-potent, long-term NOD/SCID repopulating hematopoietic cells.
    Ailles L, Schmidt M, Santoni de Sio FR, Glimm H, Cavalieri S, Bruno S, Piacibello W, Von Kalle C, Naldini L.
    Mol Ther; 2002 Nov; 6(5):615-26. PubMed ID: 12409260
    [Abstract] [Full Text] [Related]

  • 9. Optimization of adenovirus serotype 35 vectors for efficient transduction in human hematopoietic progenitors: comparison of promoter activities.
    Sakurai F, Kawabata K, Yamaguchi T, Hayakawa T, Mizuguchi H.
    Gene Ther; 2005 Oct; 12(19):1424-33. PubMed ID: 15944730
    [Abstract] [Full Text] [Related]

  • 10. Lentiviral transduction of human hematopoietic cells by HIV-1- and SIV-based vectors containing a bicistronic cassette driven by various internal promoters.
    Dupuy FP, Mouly E, Mesel-Lemoine M, Morel C, Abriol J, Cherai M, Baillou C, Nègre D, Cosset FL, Klatzmann D, Lemoine FM.
    J Gene Med; 2005 Sep; 7(9):1158-71. PubMed ID: 15880619
    [Abstract] [Full Text] [Related]

  • 11. 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; 25(6):1571-7. PubMed ID: 17379771
    [Abstract] [Full Text] [Related]

  • 12. Transduction of human CD34+ CD38- bone marrow and cord blood-derived SCID-repopulating cells with third-generation lentiviral vectors.
    Guenechea G, Gan OI, Inamitsu T, Dorrell C, Pereira DS, Kelly M, Naldini L, Dick JE.
    Mol Ther; 2000 Jun; 1(6):566-73. PubMed ID: 10933981
    [Abstract] [Full Text] [Related]

  • 13. Highly efficient lentiviral gene transfer in CD34+ and CD34+/38-/lin- cells from mobilized peripheral blood after cytokine prestimulation.
    Géronimi F, Richard E, Redonnet-Vernhet I, Lamrissi-Garcia I, Lalanne M, Ged C, Moreau-Gaudry F, De Verneuil H.
    Stem Cells; 2003 Jun; 21(4):472-80. PubMed ID: 12832700
    [Abstract] [Full Text] [Related]

  • 14. Lentivirus-mediated gene transfer in primary T cells is enhanced by a central DNA flap.
    Dardalhon V, Herpers B, Noraz N, Pflumio F, Guetard D, Leveau C, Dubart-Kupperschmitt A, Charneau P, Taylor N.
    Gene Ther; 2001 Feb; 8(3):190-8. PubMed ID: 11313790
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Expression of human factor IX gene in murine plasma through lentiviral vector-infected haematopoietic stem cells.
    Chen H, Yao H, Huang L, Shen Q, Jia W, Xue J.
    Clin Exp Pharmacol Physiol; 2006 Dec 01; 33(12):1196-201. PubMed ID: 17184501
    [Abstract] [Full Text] [Related]

  • 17. Development of an enhanced B-specific lentiviral vector expressing BTK: a tool for gene therapy of XLA.
    Moreau T, Barlogis V, Bardin F, Nunes JA, Calmels B, Chabannon C, Tonnelle C.
    Gene Ther; 2008 Jun 01; 15(12):942-52. PubMed ID: 18323795
    [Abstract] [Full Text] [Related]

  • 18. Elongation factor 1 (EF1alpha) promoter in a lentiviral backbone improves expression of the CD20 suicide gene in primary T lymphocytes allowing efficient rituximab-mediated lysis.
    Serafini M, Bonamino M, Golay J, Introna M.
    Haematologica; 2004 Jan 01; 89(1):86-95. PubMed ID: 14754610
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. Inhibition of simian/human immunodeficiency virus replication in CD4+ T cells derived from lentiviral-transduced CD34+ hematopoietic cells.
    Braun SE, Wong FE, Connole M, Qiu G, Lee L, Gillis J, Lu X, Humeau L, Slepushkin V, Binder GK, Dropulic B, Johnson RP.
    Mol Ther; 2005 Dec 01; 12(6):1157-67. PubMed ID: 16168713
    [Abstract] [Full Text] [Related]

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