Mark A. Findeis and a panel of active researchers present their best methods not only for preparing, handling, and characterizing gene delivery agents, but also for gene delivery. To help those preparing and characterizing gene transfer agents, the contributors examine a broad range of compounds tha
Viral Vectors for Gene Therapy: Methods and Protocols
โ Scribed by Edward A. Burton, Shaohua Huang, William F. Goins (auth.), Curtis A. Machida (eds.)
- Book ID
- 127435498
- Publisher
- Humana
- Year
- 2003
- Tongue
- English
- Weight
- 9 MB
- Edition
- 1
- Category
- Library
- City
- Totowa, N.J
- ISBN
- 1592593046
No coin nor oath required. For personal study only.
โฆ Synopsis
The promise of gene therapy can be realized only if workable vectors can be found to deliver therapeutic genes. In Viral Vectors for Gene Therapy: Methods and Protocols, leading researchers from academia and biotechnology describe proven molecular methods for the construction, development, and use of virus vectors for gene transfer and gene therapy. Offering detailed step-by-step instructions to ensure successful results, these experts detail the use of herpes viruses, adenoviruses, adeno-associated viruses, simple and complex retroviruses, including lentiviruses, and other virus systems for vector development and gene transfer. Additional chapters demonstrate the use of virus vectors in the brain and central nervous system. Each protocol includes a discussion of the principles involved, numerous charts and tables, ample references, and notes on possible problems, troubleshooting, and alternative procedures.
Comprehensive and highly practical, Viral Vectors for Gene Therapy: Methods and Protocols provides not only researchers with the basic tools needed to design targeted gene delivery vectors, but also clinicians with an understanding of how to apply viral vectors to the treatment of genetic disorders.
โฆ Subjects
Human Genetics
๐ SIMILAR VOLUMES
In a review article Miller [1] reported on the state of the art of human gene therapy as it was summarized in a meeting at the end of December 1991. The human trials in which human genes were successfully transferred in vitro to mark cells of patients and for gene therapy of genetic disorders. The a