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...
Uloženo v:
| Vydáno v: | J Virol |
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| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society for Microbiology (ASM)
2002
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC136579/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12239326/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/JVI.76.20.10497-10502.2002 |
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