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dc.contributor.author Himer, Leonóra
dc.contributor.author Balog, Attila
dc.contributor.author Szebeni, Beáta
dc.contributor.author Nagy-Szakál, Dorottya
dc.contributor.author Sziksz, Erna
dc.contributor.author Reusz, György
dc.contributor.author Tulassay, Tivadar
dc.contributor.author Vannay, Ádám
dc.date.accessioned 2015-04-30T11:19:00Z
dc.date.available 2015-04-30T11:19:00Z
dc.date.issued 2010
dc.identifier 77953177481
dc.identifier.citation pagination=1003-1010; journalVolume=151; journalIssueNumber=25; journalTitle=ORVOSI HETILAP;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/1578
dc.identifier.uri doi:10.1556/OH.2010.28880
dc.description.abstract Th17 cells are the newly described subset of the CD4 <sup>+ </sup> T lymphocytes. Activated Th17 cells are characterized by their ability to produce IL-17A and other pro-inflammatory cytokines. IL-17A regulates immune function through its cell- surface receptor expressed on epithelial-and endothelial cells, fibroblasts and leukocytes by promoting neutrophil recruitment and releasing further pro-inflammatory mediators. Failures of the susceptible balance of the immunoregulation may lead to unchecked immune response and autoimmune diseases. The central role of Th17 cells and cytokines produced by Th17 cells were confirmed in a wide variety of human autoimmune diseases, including rheumatoid arthritis. Recently Th17 cells and its cytokines come into the focus of immunological research as potential therapeutic targets.
dc.relation.ispartof urn:issn:0030-6002
dc.title A Th17 sejtek szerepe rheumatoid arthritisben
dc.type Journal Article
dc.date.updated 2015-03-13T10:12:54Z
dc.language.rfc3066 hu
dc.identifier.mtmt 1384931
dc.identifier.pubmed 20519185
dc.contributor.department SE/AOK/K/ISZGYK/MTA-SE Gyermekgyógyászati és Nephrológiai Kutatócsoport
dc.contributor.department SE/AOK/K/I. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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