Functional Correction of Fanconi Anemia Group C Hematopoietic Cells by the Use of a Novel Lentiviral Vector
Open Access
- 30 April 2001
- journal article
- Published by Elsevier in Molecular Therapy
- Vol. 3 (4) , 485-490
- https://doi.org/10.1006/mthe.2001.0287
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectorsNature Medicine, 1998
- Sustained expression of genes delivered directly into liver and muscle by lentiviral vectorsNature Genetics, 1997
- Stable and efficient gene transfer into the retina using an HIV-based lentiviral vectorProceedings of the National Academy of Sciences, 1997
- Multiply attenuated lentiviral vector achieves efficient gene delivery in vivoNature Biotechnology, 1997
- Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particlesProceedings of the National Academy of Sciences, 1996
- Efficient transfer, integration, and sustained long-term expression of the transgene in adult rat brains injected with a lentiviral vector.Proceedings of the National Academy of Sciences, 1996
- In Vivo Gene Delivery and Stable Transduction of Nondividing Cells by a Lentiviral VectorScience, 1996
- Molecular basis of the pathobiology of lentivirusesVirus Research, 1994
- 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
- Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection.Molecular and Cellular Biology, 1990