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Journal Abstract Search

209 related items for PubMed ID: 8525635

  • 21. 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; 74(8):3668-81. PubMed ID: 10729143
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  • 23. Self-inactivating retroviral vector-mediated gene transfer induces oncogene activation and immortalization of primary murine bone marrow cells.
    Bosticardo M, Ghosh A, Du Y, Jenkins NA, Copeland NG, Candotti F.
    Mol Ther; 2009 Nov; 17(11):1910-8. PubMed ID: 19638958
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  • 28. Liver-directed gene therapy: a retroviral vector with a complete LTR and the ApoE enhancer-alpha 1-antitrypsin promoter dramatically increases expression of human alpha 1-antitrypsin in vivo.
    Okuyama T, Huber RM, Bowling W, Pearline R, Kennedy SC, Flye MW, Ponder KP.
    Hum Gene Ther; 1996 Mar 20; 7(5):637-45. PubMed ID: 8845389
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  • 29. Insertion of two independent enhancers in the long terminal repeat of a self-inactivating vector results in high-titer retroviral vectors with tissue-specific expression.
    Fassati A, Bardoni A, Sironi M, Wells DJ, Bresolin N, Scarlato G, Hatanaka M, Yamaoka S, Dickson G.
    Hum Gene Ther; 1998 Nov 20; 9(17):2459-68. PubMed ID: 9853513
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  • 31. Construction of human factor IX expression vectors in retroviral vector frames optimized for muscle cells.
    Wang JM, Zheng H, Sugahara Y, Tan J, Yao SN, Olson E, Kurachi K.
    Hum Gene Ther; 1996 Sep 10; 7(14):1743-56. PubMed ID: 8886845
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  • 32. Two blocks in Moloney murine leukemia virus expression in undifferentiated F9 embryonal carcinoma cells as determined by transient expression assays.
    Feuer G, Taketo M, Hanecak RC, Fan H.
    J Virol; 1989 May 10; 63(5):2317-24. PubMed ID: 2704078
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  • 34. Leukemogenicity of Moloney murine leukemia viruses carrying polyoma enhancer sequences in the long terminal repeat is dependent on the nature of the inserted polyoma sequences.
    Fan H, Chute H, Chao E, Pattengale PK.
    Virology; 1988 Sep 10; 166(1):58-65. PubMed ID: 2842957
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  • 36. Analysis of adenovirus trans-complementation-mediated gene expression controlled by melanoma-specific TETP promoter in vitro.
    Fontecedro AC, Lutschg V, Eichhoff O, Dummer R, Greber UF, Hemmi S.
    Virol J; 2010 Jul 29; 7():175. PubMed ID: 20670430
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  • 37. Self-inactivating retroviral vectors designed for transfer of whole genes into mammalian cells.
    Yu SF, von Rüden T, Kantoff PW, Garber C, Seiberg M, Rüther U, Anderson WF, Wagner EF, Gilboa E.
    Proc Natl Acad Sci U S A; 1986 May 29; 83(10):3194-8. PubMed ID: 3458176
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  • 39. Endothelial cell-specific transcriptional targeting from a hybrid long terminal repeat retrovirus vector containing human prepro-endothelin-1 promoter sequences.
    Jäger U, Zhao Y, Porter CD.
    J Virol; 1999 Dec 29; 73(12):9702-9. PubMed ID: 10559279
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