Liver gene therapy and hepatocellular carcinoma: A complex web
Author:
Funder
NHLBI
Publisher
Elsevier BV
Subject
Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine
Reference6 articles.
1. Long-Term Follow-Up of the First in Human Intravascular Delivery of AAV for Gene Transfer: AAV2-hFIX16 for Severe Hemophilia B;George;Mol Ther,2020
2. AAV Joins the Rank of Genotoxic Vectors;Davé;Mol Ther,2021
3. Recurrent AAV2-related insertional mutagenesis in human hepatocellular carcinomas;Nault;Nat. Genet.,2015
4. A long-term study of AAV gene therapy in dogs with hemophilia A identifies clonal expansions of transduced liver cells;Nguyen;Nat Biotechnol,2021
5. Adeno-associated virus in the liver: natural history and consequences in tumour development;La Bella;Gut,2020
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