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dc.contributor.authorOnomoto, Kojien
dc.contributor.authorMorimoto, Shihoen
dc.contributor.authorKawaguchi, Takahisaen
dc.contributor.authorToyoda, Hidenorien
dc.contributor.authorTanaka, Masamien
dc.contributor.authorKuroda, Masahikoen
dc.contributor.authorUno, Kazukoen
dc.contributor.authorKumada, Takashien
dc.contributor.authorMatsuda, Fumihikoen
dc.contributor.authorShimotohno, Kunitadaen
dc.contributor.authorFujita, Takashien
dc.contributor.authorMurakami, Yoshikien
dc.contributor.alternative村上, 善基ja
dc.date.accessioned2011-06-07T00:33:56Z-
dc.date.available2011-06-07T00:33:56Z-
dc.date.issued2011-
dc.identifier.issn1932-6203-
dc.identifier.urihttp://hdl.handle.net/2433/141816-
dc.description.abstractDespite being expensive, the standard combination of pegylated interferon (Peg-IFN)- α and ribavirin used to treat chronic hepatitis C (CH) results in a moderate clearance rate and a plethora of side effects. This makes it necessary to predict patient outcome so as to improve the accuracy of treatment. Although the antiviral mechanism of genetically altered IL28B is unknown, IL28B polymorphism is considered a good predictor of IFN combination treatment outcome.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherPublic Library of Scienceen
dc.rights© 2011 Onomoto et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.titleDysregulation of IFN system can lead to poor response to pegylated interferon and ribavirin therapy in chronic hepatitis C.en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitlePloS oneen
dc.identifier.volume6-
dc.identifier.issue5-
dc.relation.doi10.1371/journal.pone.0019799-
dc.textversionpublisher-
dc.identifier.artnume19799-
dc.identifier.pmid21603632-
dcterms.accessRightsopen access-
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