| Literature DB >> 9420292 |
V N Kim1, K Mitrophanous, S M Kingsman, A J Kingsman.
Abstract
The use of human immunodeficiency virus vectors for gene therapy is hampered by concern over their safety. This concern might be ameliorated, in part, if the viral accessory genes and proteins could be eliminated from the vector genomes and particles. Here we describe a minimal vector system that is capable of transducing nondividing cells and which does not contain tat, vif, vpr, vpu, and nef.Entities:
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Year: 1998 PMID: 9420292 PMCID: PMC109441
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103