Viral vectors for gene therapy: the art of turning infectious agents into vehicles of therapeuticsMark A. Kay(Stanford Medicine), Joseph C. Glorioso(University of Pittsburgh), Luigi Naldini(University of Turin)Nature MedicineJanuary 1, 200110.1038/83324Cited by 1,335SaveCiteExport RISWatch citationsAbstractRelated PapersDevelopment of a Self-Inactivating Lentivirus VectorHiroyuki Miyoshi, Ulrike Blömer, Masayo Takahashi et al.|Journal of Virology|1998|1.2kUse of Adeno-Associated Virus as a General Transduction Vector for Mammalian CellsNicholas Muzyczka|Current topics in microbiology and immunology|1992|753Transduction with recombinant adeno-associated virus for gene therapy is limited by leading-strand synthesisKrishna J. Fisher, Guang Ping Gao, Matthew D. Weitzman et al.|Journal of Virology|1996|545Persistence and Expression of the Herpes Simplex Virus Genome in the Absence of Immediate-Early ProteinsLorna A. Samaniego, Lisa Neiderhiser, Neal A. DeLuca|Journal of Virology|1998|370Efficient lentiviral transduction of liver requires cell cycling in vivoFrank Park, Kazuo Ohashi, Winnie Chiu et al.|Nature Genetics|2000|325