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dc.contributor.author Szondy, Klára
dc.contributor.author Rusai, Krisztina
dc.contributor.author Szabó, Attila
dc.contributor.author Nagy A
dc.contributor.author Gál, Krisztina
dc.contributor.author Fekete, Andrea
dc.contributor.author Kováts, Zsuzsanna
dc.contributor.author Losonczy, György
dc.contributor.author Lukácsovits, József
dc.contributor.author Müller, Veronika
dc.date.accessioned 2016-05-10T13:32:20Z
dc.date.available 2016-05-10T13:32:20Z
dc.date.issued 2012
dc.identifier 84860121190
dc.identifier.citation pagination=317-322; journalVolume=30; journalIssueNumber=4; journalTitle=CANCER INVESTIGATION;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2262
dc.identifier.uri doi:10.3109/07357907.2012.657815
dc.description.abstract The inducible heat shock protein (HSP)72 plays a central role in antitumor immunomodulation. HSP72 expression was assessed on tumor samples of 43 patients with advanced and metastatic small cell lung cancer (SCLC) by immunohistochemistry and HSP72 [HSPA1B A(1267)G] polymorphism was determined. HSP72 expression of SCLC cells was significantly decreased in GG as compared to cells of AA or AG genotype patients, and was associated with significantly shorter survival in GG patients as compared to carriers of the A allele. Decreased HSP72 expression of SCLC cells associated with HSP72 GG genotype is a negative prognostic factor for survival in SCLC patients. © 2012 Informa Healthcare USA, Inc.
dc.relation.ispartof urn:issn:0735-7907
dc.title Tumor cell expression of Heat Shock Protein (HSP) 72 is influenced by HSP72 [HSPA1B A(1267)G] polymorphism and predicts Survival in Small Cell Lung Cancer (SCLC) patients
dc.type Journal Article
dc.date.updated 2015-11-03T11:37:43Z
dc.language.rfc3066 en
dc.identifier.mtmt 1953782
dc.identifier.wos 000303249200009
dc.identifier.pubmed 22468780
dc.contributor.department SE/AOK/K/I. Sz. Gyermekgyógyászati Klinika
dc.contributor.department SE/AOK/K/Pulmonológiai Klinika
dc.contributor.institution Semmelweis Egyetem


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