Production and concentration of pseudotyped HIV-1-based gene transfer vectors
- 25 May 2000
- journal article
- Published by Springer Nature in Gene Therapy
- Vol. 7 (11) , 910-913
- https://doi.org/10.1038/sj.gt.3301188
Abstract
At the forefront of medicine, Gene Therapy brings you the latest research into genetic and cell-based technologies to treat disease. It also publishes Progress & Prospects reviews and News and Commentary articles, which highlight the cutting edge of the field.Keywords
This publication has 15 references indexed in Scilit:
- Lentiviruses as gene transfer agents for delivery to non-dividing cellsCurrent Opinion in Biotechnology, 1998
- Toward highly efficient cell-type-specific gene transfer with retroviral vectors displaying single-chain antibodiesJournal of Virology, 1997
- Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particlesProceedings of the National Academy of Sciences, 1996
- In Vivo Gene Delivery and Stable Transduction of Nondividing Cells by a Lentiviral VectorScience, 1996
- Human immunodeficiency virus type 1 cell cycle control: Vpr is cytostatic and mediates G2 accumulation by a mechanism which differs from DNA damage checkpoint controlJournal of Virology, 1996
- High-titer packaging cells producing recombinant retroviruses resistant to human serumJournal of Virology, 1995
- HIV-1 Reverse Transcription A Termination Step at the Center of the GenomeJournal of Molecular Biology, 1994
- Production of high-titer helper-free retroviruses by transient transfection.Proceedings of the National Academy of Sciences, 1993
- Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: concentration to very high titer and efficient gene transfer into mammalian and nonmammalian cells.Proceedings of the National Academy of Sciences, 1993
- Analysis of mutation in human cells by using an Epstein-Barr virus shuttle system.Molecular and Cellular Biology, 1987