Efficient control of gene expression in the hematopoietic system using a single Tet-on inducible lentiviral vector
Open Access
- 28 February 2006
- journal article
- Published by Elsevier in Molecular Therapy
- Vol. 13 (2) , 382-390
- https://doi.org/10.1016/j.ymthe.2005.09.012
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Regulatable gene expression systems for gene therapy applications: progress and future challengesMolecular Therapy, 2005
- Retroviral DNA Integration: ASLV, HIV, and MLV Show Distinct Target Site PreferencesPLoS Biology, 2004
- Efficient Marking of Murine Long-Term Repopulating Stem Cells Targeting Unseparated Marrow Cells at Low Lentiviral Vector Particle ConcentrationMolecular Therapy, 2004
- Gene therapy progress and prospects: transcription regulatory systemsGene Therapy, 2004
- Performance- and safety-enhanced lentiviral vectors containing the human interferon-β scaffold attachment region and the chicken β-globin insulatorBlood, 2003
- Lentiviral vector transduction of NOD/SCID repopulating cells results in multiple vector integrations per transduced cell: risk of insertional mutagenesisBlood, 2002
- Germline Transmission and Tissue-Specific Expression of Transgenes Delivered by Lentiviral VectorsScience, 2002
- In Vivo Gene Delivery and Stable Transduction of Nondividing Cells by a Lentiviral VectorScience, 1996
- Transcriptional Activation by Tetracyclines in Mammalian CellsScience, 1995
- Tight control of gene expression in mammalian cells by tetracycline-responsive promoters.Proceedings of the National Academy of Sciences, 1992