Human Hepatocyte Transduction with Adeno-Associated Virus Vector
Author:
Publisher
Springer US
Link
https://link.springer.com/content/pdf/10.1007/978-1-0716-2557-6_5
Reference42 articles.
1. Sobrevals L et al (2012) AAV vectors transduce hepatocytes in vivo as efficiently in cirrhotic as in healthy rat livers. Gene Ther 19(4):411–417
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3. Kattenhorn LM et al (2016) Adeno-associated virus gene therapy for liver disease. Hum Gene Ther 27(12):947–961
4. George LA et al (2020) Long-term follow-up of the first in human intravascular delivery of AAV for gene transfer: AAV2-hFIX16 for severe hemophilia B. Mol Ther 28(9):2073–2082
5. Leng Y et al (2019) Long-term correction of copper metabolism in Wilson’s disease mice with AAV8 vector delivering truncated ATP7B. Hum Gene Ther 30(12):1494–1504
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