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Journal Abstract Search

310 related items for PubMed ID: 12778174

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  • 3. Targeted transgene integration into transgenic mouse fibroblasts carrying the full-length human AAVS1 locus mediated by HSV/AAV rep(+) hybrid amplicon vector.
    Bakowska JC, Di Maria MV, Camp SM, Wang Y, Allen PD, Breakefield XO.
    Gene Ther; 2003 Sep; 10(19):1691-702. PubMed ID: 12923568
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  • 4. AAV loves an active genome.
    Russell DW.
    Nat Genet; 2003 Jul; 34(3):241-2. PubMed ID: 12833043
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  • 5. Recombinant adeno-associated virus (AAV-CFTR) vectors do not integrate in a site-specific fashion in an immortalized epithelial cell line.
    Kearns WG, Afione SA, Fulmer SB, Pang MC, Erikson D, Egan M, Landrum MJ, Flotte TR, Cutting GR.
    Gene Ther; 1996 Sep; 3(9):748-55. PubMed ID: 8875221
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  • 9. Utility of intraperitoneal administration as a route of AAV serotype 5 vector-mediated neonatal gene transfer.
    Ogura T, Mizukami H, Mimuro J, Madoiwa S, Okada T, Matsushita T, Urabe M, Kume A, Hamada H, Yoshikawa H, Sakata Y, Ozawa K.
    J Gene Med; 2006 Aug; 8(8):990-7. PubMed ID: 16685745
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  • 10. Cardio-specific long-term gene expression in a porcine model after selective pressure-regulated retroinfusion of adeno-associated viral (AAV) vectors.
    Raake PW, Hinkel R, Müller S, Delker S, Kreuzpointner R, Kupatt C, Katus HA, Kleinschmidt JA, Boekstegers P, Müller OJ.
    Gene Ther; 2008 Jan; 15(1):12-7. PubMed ID: 17943147
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  • 11. Integration of active human beta-galactosidase gene (100 kb) into genome using HSV/AAV amplicon vector.
    Oehmig A, Cortés ML, Perry KF, Sena-Esteves M, Fraefel C, Breakefield XO.
    Gene Ther; 2007 Jul; 14(14):1078-91. PubMed ID: 17460718
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  • 12. Injection of a recombinant AAV serotype 2 into canine skeletal muscles evokes strong immune responses against transgene products.
    Yuasa K, Yoshimura M, Urasawa N, Ohshima S, Howell JM, Nakamura A, Hijikata T, Miyagoe-Suzuki Y, Takeda S.
    Gene Ther; 2007 Sep; 14(17):1249-60. PubMed ID: 17581597
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  • 13. Long-term expression and repeated administration of AAV type 1, 2 and 5 vectors in skeletal muscle of immunocompetent adult mice.
    Rivière C, Danos O, Douar AM.
    Gene Ther; 2006 Sep; 13(17):1300-8. PubMed ID: 16688207
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  • 14. 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
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  • 15. Recombinant adeno-associated virus derived vectors (rAAV2) efficiently transduce ovarian and hepatocellular carcinoma cells--implications for cancer gene therapy.
    Małecki M, Swoboda P, Pachecka J.
    Acta Pol Pharm; 2009 Aug; 66(1):93-9. PubMed ID: 19226976
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