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Journal Abstract Search

267 related items for PubMed ID: 7501469

  • 1.
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  • 2. 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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  • 3. Cre/loxP-mediated excision of a neomycin resistance expression unit from an integrated retroviral vector increases long terminal repeat-driven transcription in human hematopoietic cells.
    Fernex C, Dubreuil P, Mannoni P, Bagnis C.
    J Virol; 1997 Oct; 71(10):7533-40. PubMed ID: 9311833
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  • 4. Retroviral vectors produced in the cytoplasmic vaccinia virus system transduce intron-containing genes.
    Konetschny C, Holzer GW, Falkner FG.
    J Virol; 2002 Feb; 76(3):1236-43. PubMed ID: 11773399
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  • 5. Unusually high frequency of reconstitution of long terminal repeats in U3-minus retrovirus vectors by DNA recombination or gene conversion.
    Olson P, Temin HM, Dornburg R.
    J Virol; 1992 Mar; 66(3):1336-43. PubMed ID: 1310753
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  • 6. Cre recombinase-mediated site-specific modification of a cellular genome using an integrase-defective retroviral vector.
    Huang S, Kawabe Y, Ito A, Kamihira M.
    Biotechnol Bioeng; 2010 Nov 01; 107(4):717-29. PubMed ID: 20632375
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  • 7. Targeted transgene insertion into the CHO cell genome using Cre recombinase-incorporating integrase-defective retroviral vectors.
    Kawabe Y, Shimomura T, Huang S, Imanishi S, Ito A, Kamihira M.
    Biotechnol Bioeng; 2016 Jul 01; 113(7):1600-10. PubMed ID: 26724679
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  • 8. Novel integrating adenoviral/retroviral hybrid vector for gene therapy.
    Murphy SJ, Chong H, Bell S, Diaz RM, Vile RG.
    Hum Gene Ther; 2002 Apr 10; 13(6):745-60. PubMed ID: 11936973
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  • 9. Removal of the selectable marker gene from transgenic tobacco plants by expression of Cre recombinase from a tobacco mosaic virus vector through agroinfection.
    Jia H, Pang Y, Chen X, Fang R.
    Transgenic Res; 2006 Jun 10; 15(3):375-84. PubMed ID: 16779652
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  • 13. 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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  • 14. 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 20; 78(3):1384-92. PubMed ID: 14722293
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  • 18. 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 20; 83(10):3194-8. PubMed ID: 3458176
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  • 19. Excision of an integrated provirus by the action of FLP recombinase.
    Schübeler D, Mielke C, Bode J.
    In Vitro Cell Dev Biol Anim; 1997 May 20; 33(10):825-30. PubMed ID: 9466689
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  • 20. Retroviral vectors for homologous recombination provide efficient cloning and expression in mammalian cells.
    Kobayashi E, Kishi H, Ozawa T, Horii M, Hamana H, Nagai T, Muraguchi A.
    Biochem Biophys Res Commun; 2014 Feb 14; 444(3):319-24. PubMed ID: 24462869
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