Gene transduction efficiency in cells of different species by HIV and EIAV vectors
- 27 June 2002
- journal article
- research article
- Published by Springer Nature in Gene Therapy
- Vol. 9 (14), 932-938
- https://doi.org/10.1038/sj.gt.3301708
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.This publication has 28 references indexed in Scilit:
- Rabies virus glycoprotein pseudotyping of lentiviral vectors enables retrograde axonal transport and access to the nervous system after peripheral deliveryHuman Molecular Genetics, 2001
- Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequencesNature Genetics, 2000
- A Rev-Independent Human Immunodeficiency Virus Type 1 (HIV-1)-Based Vector That Exploits a Codon-Optimized HIV-1 gag-pol GeneJournal of Virology, 2000
- Interactions between Equine Cyclin T1, Tat, and TAR Are Disrupted by a Leucine-to-Valine Substitution Found in Human Cyclin T1Journal of Virology, 2000
- Efficient Transduction of Nondividing Cells by Optimized Feline Immunodeficiency Virus VectorsMolecular Therapy, 2000
- Feline immunodeficiency virus vectors persistently transduce nondividing airway epithelia and correct the cystic fibrosis defectJournal of Clinical Investigation, 1999
- Stable gene transfer to the nervous system using a non-primate lentiviral vectorGene Therapy, 1999
- Gene transfer vectors derived from equine infectious anemia virusGene Therapy, 1998
- Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectorsNature Medicine, 1998
- In Vivo Gene Delivery and Stable Transduction of Nondividing Cells by a Lentiviral VectorScience, 1996