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dc.contributor.authorXiao, Han
dc.contributor.authorKillip, Marian Jane
dc.contributor.authorStaeheli, Peter
dc.contributor.authorRandall, Richard Edward
dc.contributor.authorJackson, David
dc.date.accessioned2013-12-09T15:01:01Z
dc.date.available2013-12-09T15:01:01Z
dc.date.issued2013-12
dc.identifier.citationXiao , H , Killip , M J , Staeheli , P , Randall , R E & Jackson , D 2013 , ' The human interferon-induced MxA protein inhibits early stages of influenza A virus infection by retaining the incoming viral genome in the cytoplasm ' , Journal of Virology , vol. 87 , no. 23 , pp. 13053-13058 . https://doi.org/10.1128/JVI.02220-13en
dc.identifier.issn0022-538X
dc.identifier.otherPURE: 20574668
dc.identifier.otherPURE UUID: 7f40be1b-2b43-4392-bb6b-aba0bed8c188
dc.identifier.otherScopus: 84887131870
dc.identifier.otherORCID: /0000-0002-9304-6678/work/60427009
dc.identifier.urihttps://hdl.handle.net/10023/4280
dc.description.abstractThe induction of an interferon-induced antiviral state is a powerful cellular response against viral infection that limits viral spread. Here we show that a pre-existing antiviral state inhibits replication of influenza A viruses in human A549 cells by preventing transport of the viral genome to the nucleus and the interferon-induced MxA protein is necessary but not sufficient for this process. This represents a previously unreported antiviral function of MxA against influenza A virus infection.
dc.language.isoeng
dc.relation.ispartofJournal of Virologyen
dc.rightsCopyright © 2013 Xiao et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 Unported license.en
dc.subjectQR355 Virologyen
dc.subject.lccQR355en
dc.titleThe human interferon-induced MxA protein inhibits early stages of influenza A virus infection by retaining the incoming viral genome in the cytoplasmen
dc.typeJournal articleen
dc.contributor.sponsorThe Wellcome Trusten
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.identifier.doihttps://doi.org/10.1128/JVI.02220-13
dc.description.statusPeer revieweden
dc.identifier.grantnumber087751/A/08/Zen


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