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Journal Abstract Search

162 related items for PubMed ID: 14599813

  • 21. Multiple modifications allow high-titer production of retroviral vectors carrying heterologous regulatory elements.
    Hlavaty J, Stracke A, Klein D, Salmons B, Günzburg WH, Renner M.
    J Virol; 2004 Feb; 78(3):1384-92. PubMed ID: 14722293
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  • 23. Transfer of single gene-containing long terminal repeats into the genome of mammalian cells by a retroviral vector carrying the cre gene and the loxP site.
    Choulika A, Guyot V, Nicolas JF.
    J Virol; 1996 Mar; 70(3):1792-8. PubMed ID: 8627702
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  • 26. Increased probability of expression from modified retroviral vectors in embryonal stem cells and embryonal carcinoma cells.
    Robbins PB, Yu XJ, Skelton DM, Pepper KA, Wasserman RM, Zhu L, Kohn DB.
    J Virol; 1997 Dec; 71(12):9466-74. PubMed ID: 9371608
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  • 27. Retroviral vectors encoding a reverse transcription-activated transgene efficiently limit expression of the gene to target cells.
    Burke JD, Morris JC.
    Mol Ther; 2007 Mar; 15(3):552-9. PubMed ID: 17191073
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  • 29. The woodchuck hepatitis virus post-transcriptional regulatory element reduces readthrough transcription from retroviral vectors.
    Higashimoto T, Urbinati F, Perumbeti A, Jiang G, Zarzuela A, Chang LJ, Kohn DB, Malik P.
    Gene Ther; 2007 Sep; 14(17):1298-304. PubMed ID: 17597793
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  • 30. Human immunodeficiency virus type 1 long terminal repeat quasispecies differ in basal transcription and nuclear factor recruitment in human glial cells and lymphocytes.
    Krebs FC, Mehrens D, Pomeroy S, Goodenow MM, Wigdahl B.
    J Biomed Sci; 1998 Sep; 5(1):31-44. PubMed ID: 9570512
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  • 31. 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
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  • 32. Inhibition of human immunodeficiency virus type-1 by retroviral vectors expressing antisense-TAR.
    Chuah MK, VandenDriessche T, Chang HK, Ensoli B, Morgan RA.
    Hum Gene Ther; 1994 Dec 01; 5(12):1467-75. PubMed ID: 7711139
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  • 33. cis-Active elements of Friend spleen focus-forming virus: from disease induction to disease prevention.
    Baum C, Hunt N, Hildinger M, Eckert HG, Zaehres H, Richters A, John J, Löhler J, Ostertag W.
    Acta Haematol; 1998 Dec 01; 99(3):156-64. PubMed ID: 9587397
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  • 36. Improving transcriptional termination of self-inactivating gamma-retroviral and lentiviral vectors.
    Schambach A, Galla M, Maetzig T, Loew R, Baum C.
    Mol Ther; 2007 Jun 01; 15(6):1167-73. PubMed ID: 17406345
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  • 37. FMEV vectors: both retroviral long terminal repeat and leader are important for high expression in transduced hematopoietic cells.
    Hildinger M, Eckert HG, Schilz AJ, John J, Ostertag W, Baum C.
    Gene Ther; 1998 Nov 01; 5(11):1575-9. PubMed ID: 9930313
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  • 38. 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
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