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Purpose We used recombinant adenoviral vectors for gene therapy in liver transplantation, and investigated the efficacy of gene transfer and expression on the grafts and genetic heterogeneity, with two exogenous gene transfer methods in three different syngeneic rat strains. Methods We transferred adenoviral vector encoding Escherichia coli β-galactosidase via a donor tail vein 3 days before transplantation;...
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