Targeted transgene integration into transgenic mouse fibroblasts carrying the full-length human AAVS1 locus mediated by HSV/AAV rep+ hybrid amplicon vector
- 18 August 2003
- journal article
- research article
- Published by Springer Science and Business Media LLC in Gene Therapy
- Vol. 10 (19), 1691-1702
- https://doi.org/10.1038/sj.gt.3302061
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- An infectious transfer and expression system for genomic DNA loci in human and mouse cellsNature Biotechnology, 2001
- Extrachromosomal Recombinant Adeno-Associated Virus Vector Genomes Are Primarily Responsible for Stable Liver Transduction In VivoJournal of Virology, 2001
- Improved Helper Virus-Free Packaging System for HSV Amplicon Vectors Using an ICP27-Deleted, Oversized HSV-1 DNA in a Bacterial Artificial ChromosomeMolecular Therapy, 2001
- Delivery of herpes simplex virus amplicon-based vectors to the dentate gyrus does not alter hippocampal synaptic transmission in vivoGene Therapy, 1999
- HSV-1 AmpliconPublished by Springer Science and Business Media LLC ,1998
- Herpes Simplex Virus Type 1 Amplicon Vectors with Glucocorticoid-Inducible Gene ExpressionHuman Gene Therapy, 1995
- Biology of Herpes Simplex Virus (HSV) Defective Viruses and Development of the Amplicon SystemPublished by Elsevier BV ,1995
- Adeno-associated virus (AAV) Rep proteins mediate complex formation between AAV DNA and its integration site in human DNA.Proceedings of the National Academy of Sciences of the United States of America, 1994
- Inhibition of Cellular transformation by the adeno-associated virus rep geneVirology, 1991
- The herpes simplex virus amplicon: A new eucaryotic defective-virus cloning-amplifying vectorCell, 1982