Improved Hepatic Gene Transfer by Using an Adeno-Associated Virus Serotype 5 Vector

Adeno-associated viral (AAV) vectors have been shown to direct stable gene transfer and expression in hepatocytes, which makes them attractive tools for treatment of inherited disorders such as hemophilia B. While substantial levels of coagulation factor IX (F.IX) have been achieved using AAV seroty...

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Detalhes bibliográficos
Main Authors: Mingozzi, Federico, Schüttrumpf, Jörg, Arruda, Valder R., Liu, Yuhong, Liu, Yi-Lin, High, Katherine A., Xiao, Weidong, Herzog, Roland W.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Microbiology 2002
Assuntos:
Gene Therapy
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC136579/
https://ncbi.nlm.nih.gov/pubmed/12239326
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/JVI.76.20.10497-10502.2002
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