Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors.

Gene transfer vectors based on adeno-associated virus (AAV) are emerging as highly promising for use in human gene therapy by virtue of their characteristics of wide host range, high transduction efficiencies, and lack of cytopathogenicity. To better define the biology of AAV-mediated gene transfer,...

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izdano v:	J Virol
Principais autores:	Podsakoff, G, Wong, K K, Chatterjee, S
Format:	Artigo
Jezik:	Inglês
Izdano:	American Society for Microbiology (ASM) 1994
Teme:	Research Article
Online dostop:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC236967/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8057446/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.68.9.5656-5666.1994
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