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Design and Packaging of Adeno-Associated Virus Gene Targeting Vectors

Adeno-associated virus (AAV) vectors can transduce cells by several mechanisms, including (i) gene addition by chromosomal integration or episomal transgene expression or (ii) gene targeting by modification of homologous chromosomal sequences. The latter process can be used to correct a variety of m...

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Main Authors: Hirata, Roli K., Russell, David W.
Formáid: Artigo
Teanga:Inglês
Foilsithe: American Society for Microbiology 2000
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC111981/
https://ncbi.nlm.nih.gov/pubmed/10775597
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