Adeno-Associated Virus Vector-Mediated Transgene Integration into Neurons and Other Nondividing Cell Targets

The site-specific integration of wild-type adeno-associated virus (wtAAV) into the human genome is a very attractive feature for the development of AAV-based gene therapy vectors. However, knowledge about integration of wtAAV, as well as currently configured recombinant AAV (rAAV) vectors, is limite...

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Dades bibliogràfiques

Publicat a:	J Virol
Autors principals:	Wu, Ping, Phillips, M. Ian, Bui, John, Terwilliger, Ernest F.
Format:	Artigo
Idioma:	Inglês
Publicat:	American Society for Microbiology (ASM) 1998
Matèries:	Gene Therapy
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC110396/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9621054/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.72.7.5919-5926.1998
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