Abstract
Many kinds of vectors for gene transfer have been developed in the last 20 yr. These include viral vectors such retroviruses (1,2), adenoviruses (3,4), and adeno-associated viruses (5); nonviral vectors utilizing cell-specific recognizing components (6,7); and lipid-mediated liposomes (8). Some of these gene-transfer methods have reached Phase I and II clinical trials, while others are still in the laboratory. This chapter focuses on protocols for the use of asialoglycoprotein receptor-based carriers to alter hepatitis B virus (HBV) viral replication in cell culture and animal models.
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Konishi, M., Wu, C.H., Wu, G.Y. (2004). Delivery of Hepatitis B Virus Therapeutic Agents Using Asialoglycoprotein Receptor-Based Liver-Specific Targeting. In: Hamatake, R.K., Lau, J.Y.N. (eds) Hepatitis B and D Protocols. Methods in Molecular Medicine™, vol 96. Humana Press. https://doi.org/10.1385/1-59259-670-3:163
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DOI: https://doi.org/10.1385/1-59259-670-3:163
Publisher Name: Humana Press
Print ISBN: 978-1-58829-108-0
Online ISBN: 978-1-59259-670-6
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