Chimeric Mice Engrafted With Canine Hepatocytes Exhibits Similar AAV Transduction Efficiency to Hemophilia B Dog
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DOI: 10.3389/fphar.2022.815317
Abstract: Adeno-associated virus (AAV) mediated gene therapy has been successfully applied in clinical trials, including hemophilia. Novel AAV vectors have been developed with enhanced transduction and specific tissue tropism. Considering the difference in efficacy of AAV… read more here.
Keywords: aav transduction; transduction; mice; canine hepatocytes ... See more keywords