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- W2302363217 abstract "Human adenoviruses (HAdVs) are nonenveloped viruses containing double-stranded deoxyribonucleic acid and the biology of species C HAdV serotype 5 (HAdV-C5) is relatively well-characterized. Because HAdV vector effectively transduces cells, it has been widely used as gene delivery vectors of transgenes in the research fields of gene therapy and basic science. Therefore, HAdV vector is a feasible vehicle to deliver noncoding ribonucleic acids (ncRNAs) in mammalian cells. In vitro and in vivo analyses of ncRNAs using HAdV vectors have been reported. However, studies of viral biology including HAdV have shown that viral genomes encode the gene(s) for RNA interference (RNAi) inhibitor(s) and that the gene products interfere with the key molecules in the RNAi machinery during productive infection. In this chapter, we provide an overview of RNAi in adenoviral biology, adenoviral vectors for RNAi-mediated gene silencing delivery, and the advantages and disadvantages of conventional HAdV vectors." @default.
- W2302363217 created "2016-06-24" @default.
- W2302363217 creator A5074722199 @default.
- W2302363217 date "2016-01-01" @default.
- W2302363217 modified "2023-10-14" @default.
- W2302363217 title "Adenoviral Vectors for RNAi Delivery" @default.
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