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Journal Abstract Search

298 related items for PubMed ID: 19110623

  • 21. Applications of Sleeping Beauty transposons for nonviral gene therapy.
    Liu H, Visner GA.
    IUBMB Life; 2007 Jun; 59(6):374-9. PubMed ID: 17613167
    [Abstract] [Full Text] [Related]

  • 22. Targeted gene modification in mouse ES cells using integrase-defective lentiviral vectors.
    Okada Y, Ueshin Y, Hasuwa H, Takumi K, Okabe M, Ikawa M.
    Genesis; 2009 Apr; 47(4):217-23. PubMed ID: 19208434
    [Abstract] [Full Text] [Related]

  • 23. Applying a "double-feature" promoter to identify cardiomyocytes differentiated from human embryonic stem cells following transposon-based gene delivery.
    Orbán TI, Apáti A, Németh A, Varga N, Krizsik V, Schamberger A, Szebényi K, Erdei Z, Várady G, Karászi E, Homolya L, Német K, Gócza E, Miskey C, Mátés L, Ivics Z, Izsvák Z, Sarkadi B.
    Stem Cells; 2009 May; 27(5):1077-87. PubMed ID: 19415778
    [Abstract] [Full Text] [Related]

  • 24. Somatic integration and long-term transgene expression in normal and haemophilic mice using a DNA transposon system.
    Yant SR, Meuse L, Chiu W, Ivics Z, Izsvak Z, Kay MA.
    Nat Genet; 2000 May; 25(1):35-41. PubMed ID: 10802653
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  • 26. Lentiviral transduction of immune cells.
    Swainson L, Mongellaz C, Adjali O, Vicente R, Taylor N.
    Methods Mol Biol; 2008 May; 415():301-20. PubMed ID: 18370162
    [Abstract] [Full Text] [Related]

  • 27. Generation of efficient human blood progenitor-targeted recombinant adeno-associated viral vectors (AAV) by applying an AAV random peptide library on primary human hematopoietic progenitor cells.
    Sellner L, Stiefelhagen M, Kleinschmidt JA, Laufs S, Wenz F, Fruehauf S, Zeller WJ, Veldwijk MR.
    Exp Hematol; 2008 Aug; 36(8):957-64. PubMed ID: 18495326
    [Abstract] [Full Text] [Related]

  • 28. Transposon vectors for gene-trap insertional mutagenesis in vertebrates.
    Clark KJ, Geurts AM, Bell JB, Hackett PB.
    Genesis; 2004 Aug; 39(4):225-33. PubMed ID: 15286994
    [Abstract] [Full Text] [Related]

  • 29. Insertional mutagenesis and development of malignancies induced by integrating gene delivery systems: implications for the design of safer gene-based interventions in patients.
    Romano G, Marino IR, Pentimalli F, Adamo V, Giordano A.
    Drug News Perspect; 2009 May; 22(4):185-96. PubMed ID: 19536363
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  • 31. Transposable elements for transgenesis and insertional mutagenesis in vertebrates: a contemporary review of experimental strategies.
    Ivics Z, Izsvák Z.
    Methods Mol Biol; 2004 May; 260():255-76. PubMed ID: 15020812
    [Abstract] [Full Text] [Related]

  • 32. Current development of lentiviral-mediated gene transfer.
    Romano G.
    Drug News Perspect; 2005 Mar; 18(2):128-34. PubMed ID: 15883621
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  • 35. Oncogenesis following delivery of a nonprimate lentiviral gene therapy vector to fetal and neonatal mice.
    Themis M, Waddington SN, Schmidt M, von Kalle C, Wang Y, Al-Allaf F, Gregory LG, Nivsarkar M, Themis M, Holder MV, Buckley SM, Dighe N, Ruthe AT, Mistry A, Bigger B, Rahim A, Nguyen TH, Trono D, Thrasher AJ, Coutelle C.
    Mol Ther; 2005 Oct; 12(4):763-71. PubMed ID: 16084128
    [Abstract] [Full Text] [Related]

  • 36. Spleen necrosis virus-derived C-type retroviral vectors for gene transfer to quiescent cells.
    Parveen Z, Krupetsky A, Engelstädter M, Cichutek K, Pomerantz RJ, Dornburg R.
    Nat Biotechnol; 2000 Jun; 18(6):623-9. PubMed ID: 10835599
    [Abstract] [Full Text] [Related]

  • 37. Capture of antigen-specific T lymphocytes from human blood by selective immortalization to establish long-term T-cell lines maintaining primary cell characteristics.
    Barsov EV, Andersen H, Coalter VJ, Carrington M, Lifson JD, Ott DE.
    Immunol Lett; 2006 May 15; 105(1):26-37. PubMed ID: 16442639
    [Abstract] [Full Text] [Related]

  • 38. Efficient gene transfer into human monocyte-derived macrophages using defective lentiviral vectors.
    Lu Y, Liu C, Zeng L, Lin Z, Dewhurst S, Gartner S, Planelles V.
    Cell Mol Biol (Noisy-le-grand); 2003 Nov 15; 49(7):1151-6. PubMed ID: 14682398
    [Abstract] [Full Text] [Related]

  • 39. Design of a nonviral vector for site-selective, efficient integration into the human genome.
    Kaminski JM, Huber MR, Summers JB, Ward MB.
    FASEB J; 2002 Aug 15; 16(10):1242-7. PubMed ID: 12153992
    [Abstract] [Full Text] [Related]

  • 40. Evaluation of safety and efficacy of RNAi against HIV-1 in the human immune system (Rag-2(-/-)gammac(-/-)) mouse model.
    ter Brake O, Legrand N, von Eije KJ, Centlivre M, Spits H, Weijer K, Blom B, Berkhout B.
    Gene Ther; 2009 Jan 15; 16(1):148-53. PubMed ID: 18668146
    [Abstract] [Full Text] [Related]

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