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Cited 59 time in webofscience Cited 61 time in scopus
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dc.contributor.authorJung, JH-
dc.contributor.authorPark, JH-
dc.contributor.authorJee, MH-
dc.contributor.authorKeum, SJ-
dc.contributor.authorCho, MS-
dc.contributor.authorYoon, SK-
dc.contributor.authorJang, SK-
dc.date.accessioned2015-06-25T02:37:21Z-
dc.date.available2015-06-25T02:37:21Z-
dc.date.created2011-09-20-
dc.date.issued2011-09-
dc.identifier.issn0022-538X-
dc.identifier.other2015-OAK-0000024092en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/11316-
dc.description.abstractHigh-mobility group box 1 (HMGB1), an abundant nuclear protein that triggers host immune responses, is an endogenous danger signal involved in the pathogenesis of various infectious agents. However, its role in hepatitis C virus (HCV) infection is not known. Here, we show that HMGB1 protein is translocated from the nucleus to cytoplasm and subsequently is released into the extracellular milieu by HCV infection. Secreted HMGB1 triggers antiviral responses and blocks HCV infection, a mechanism that may limit HCV propagation in HCV patients. Secreted HMGB1 also may have a role in liver cirrhosis, which is a common comorbidity in HCV patients. Further investigations into the roles of HMGB1 in the diseases caused by HCV infection will shed light on and potentially help prevent these serious and prevalent HCV-related diseases.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherAMER SOC MICROBIOLOGY-
dc.relation.isPartOfJOURNAL OF VIROLOGY-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleHepatitis C Virus Infection Is Blocked by HMGB1 Released from Virus-Infected Cells-
dc.typeArticle-
dc.contributor.college융합생명공학부en_US
dc.identifier.doi10.1128/JVI.00682-11-
dc.author.googleJung, JHen_US
dc.author.googlePark, JHen_US
dc.author.googleJang, SKen_US
dc.author.googleYoon, SKen_US
dc.author.googleCho, MSen_US
dc.author.googleKeum, SJen_US
dc.author.googleJee, MHen_US
dc.relation.volume85en_US
dc.relation.issue18en_US
dc.relation.startpage9359en_US
dc.relation.lastpage9368en_US
dc.contributor.id10088382en_US
dc.relation.journalJOURNAL OF VIROLOGYen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF VIROLOGY, v.85, no.18, pp.9359 - 9368-
dc.identifier.wosid000293956400010-
dc.date.tcdate2019-01-01-
dc.citation.endPage9368-
dc.citation.number18-
dc.citation.startPage9359-
dc.citation.titleJOURNAL OF VIROLOGY-
dc.citation.volume85-
dc.contributor.affiliatedAuthorJang, SK-
dc.identifier.scopusid2-s2.0-80052489035-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc35-
dc.description.scptc35*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusMOBILITY GROUP BOX-1-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlus1 PROTEIN-
dc.subject.keywordPlusINJURY-
dc.subject.keywordPlusHCV-
dc.subject.keywordPlusINTERFERON-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusAUTOPHAGY-
dc.subject.keywordPlusCIRRHOSIS-
dc.subject.keywordPlusBINDING-
dc.relation.journalWebOfScienceCategoryVirology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaVirology-

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장승기JANG, SUNG KEY
Dept of Life Sciences
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