Construction, Rescue, and Characterization of Vectors Derived from Ovine Atadenovirus

Gene transfer vectors derived from ovine atadenovirus type 7 (OAdV) can efficiently infect a variety of mammalian cells in vitro and in vivo to deliver and express transgenes. However, early OAdV vectors were designed on human mastadenovirus principles prior to the complete characterization of OAdV...

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Hlavní autoři: Löser, Peter, Hofmann, Christian, Both, Gerald W., Uckert, Wolfgang, Hillgenberg, Moritz
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society for Microbiology 2003
Témata:
Gene Therapy
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC254277/
https://ncbi.nlm.nih.gov/pubmed/14581531
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/JVI.77.22.11941-11951.2003
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