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Journal Abstract Search

410 related items for PubMed ID: 9445062

  • 21. Adeno-associated virus type 2-mediated gene transfer: altered endocytic processing enhances transduction efficiency in murine fibroblasts.
    Hansen J, Qing K, Srivastava A.
    J Virol; 2001 May; 75(9):4080-90. PubMed ID: 11287557
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  • 22. Genomic stability of self-complementary adeno-associated virus 2 during early stages of transduction in mouse muscle in vivo.
    Ren C, Kumar S, Shaw DR, Ponnazhagan S.
    Hum Gene Ther; 2005 Sep; 16(9):1047-57. PubMed ID: 16149903
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  • 23. Second-strand synthesis is a rate-limiting step for efficient transduction by recombinant adeno-associated virus vectors.
    Ferrari FK, Samulski T, Shenk T, Samulski RJ.
    J Virol; 1996 May; 70(5):3227-34. PubMed ID: 8627803
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  • 28. Rescue and replication of adeno-associated virus type 2 as well as vector DNA sequences from recombinant plasmids containing deletions in the viral inverted terminal repeats: selective encapsidation of viral genomes in progeny virions.
    Wang XS, Ponnazhagan S, Srivastava A.
    J Virol; 1996 Mar; 70(3):1668-77. PubMed ID: 8627687
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  • 29. Recombinant self-complementary adeno-associated virus serotype vector-mediated hematopoietic stem cell transduction and lineage-restricted, long-term transgene expression in a murine serial bone marrow transplantation model.
    Maina N, Han Z, Li X, Hu Z, Zhong L, Bischof D, Weigel-Van Aken KA, Slayton WB, Yoder MC, Srivastava A.
    Hum Gene Ther; 2008 Apr; 19(4):376-83. PubMed ID: 18370591
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  • 31. Integrating adenovirus-adeno-associated virus hybrid vectors devoid of all viral genes.
    Lieber A, Steinwaerder DS, Carlson CA, Kay MA.
    J Virol; 1999 Nov; 73(11):9314-24. PubMed ID: 10516040
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  • 34. Adeno-associated virus 2-mediated transduction and erythroid lineage-restricted expression from parvovirus B19p6 promoter in primary human hematopoietic progenitor cells.
    Kurpad C, Mukherjee P, Wang XS, Ponnazhagan S, Li L, Yoder MC, Srivastava A.
    J Hematother Stem Cell Res; 1999 Dec; 8(6):585-92. PubMed ID: 10645765
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  • 36. Adeno-associated virus (AAV) vectors achieve prolonged transgene expression in mouse myocardium and arteries in vivo: a comparative study with adenovirus vectors.
    Vassalli G, Büeler H, Dudler J, von Segesser LK, Kappenberger L.
    Int J Cardiol; 2003 Aug; 90(2-3):229-38. PubMed ID: 12957756
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  • 37. Recombinant adeno-associated virus mediates a high level of gene transfer but less efficient integration in the K562 human hematopoietic cell line.
    Malik P, McQuiston SA, Yu XJ, Pepper KA, Krall WJ, Podsakoff GM, Kurtzman GJ, Kohn DB.
    J Virol; 1997 Mar; 71(3):1776-83. PubMed ID: 9032306
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  • 38. Optimizing the transduction efficiency of capsid-modified AAV6 serotype vectors in primary human hematopoietic stem cells in vitro and in a xenograft mouse model in vivo.
    Song L, Kauss MA, Kopin E, Chandra M, Ul-Hasan T, Miller E, Jayandharan GR, Rivers AE, Aslanidi GV, Ling C, Li B, Ma W, Li X, Andino LM, Zhong L, Tarantal AF, Yoder MC, Wong KK, Tan M, Chatterjee S, Srivastava A.
    Cytotherapy; 2013 Aug; 15(8):986-98. PubMed ID: 23830234
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  • 39. Evaluation of recombinant adeno-associated virus as a gene transfer vector for the retina.
    Grant CA, Ponnazhagan S, Wang XS, Srivastava A, Li T.
    Curr Eye Res; 1997 Sep; 16(9):949-56. PubMed ID: 9288458
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