Impaired Intracellular Trafficking of Adeno-Associated Virus Type 2 Vectors Limits Efficient Transduction of Murine Fibroblasts

Although adeno-associated virus type 2 (AAV) has gained attention as a potentially useful alternative to the more commonly used retrovirus- and adenovirus-based vectors for human gene therapy, efficient gene transfer and transgene expression by AAV vectors require that the following two obstacles be...

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Detalhes bibliográficos

Publicado no:	J Virol
Principais autores:	Hansen, Jonathan, Qing, Keyun, Kwon, Hyung-Joo, Mah, Cathryn, Srivastava, Arun
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Microbiology (ASM) 2000
Assuntos:	Gene Therapy
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC111620/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10623762/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.74.2.992-996.2000
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