| Literature DB >> 18679616 |
Abstract
Helper-dependent adenoviral vectors (HDAd) are deleted of all viral coding sequences and have demonstrated tremendous potential for gene therapy by providing long-term, high-level transgene expression in the absence of chronic toxicity. Thus, HDAd are superior to early generation Ad for gene therapy of genetic diseases where long-term transgene expression is required. This chapter describes in detail the rescue, amplification, and large-scale production of HDAd.Entities:
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Year: 2008 PMID: 18679616 DOI: 10.1007/978-1-59745-237-3_3
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745