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dc.contributor.author Bödör, Csaba
dc.contributor.author Grossmann, V
dc.contributor.author Popov, N
dc.contributor.author Okosun, J
dc.contributor.author O'Riain, C
dc.contributor.author King, Tan
dc.contributor.author Jacek, Marzec
dc.contributor.author Shamzah, Araf
dc.contributor.author Jun, Wang
dc.contributor.author Abigail, Lee
dc.contributor.author Andrew, Clear
dc.contributor.author Silvia, Montoto
dc.contributor.author Janet, Matthews
dc.contributor.author Sameena, Iqbal
dc.contributor.author Rajnai, Hajnalka
dc.contributor.author Andreas, Rosenwald
dc.contributor.author German, Ott
dc.contributor.author Elias, Campo
dc.contributor.author Lisa, Rimsza
dc.contributor.author Erlend, Smeland
dc.contributor.author Wing, Chan
dc.contributor.author Rita, Braziel
dc.contributor.author Louis, Staudt
dc.contributor.author George, Wright
dc.contributor.author Andrew, Lister
dc.contributor.author Olivier, Elemento
dc.contributor.author Robert, Hills
dc.contributor.author John, Gribben
dc.contributor.author Claude, Chelala
dc.contributor.author Matolcsy, András
dc.contributor.author Alexander, Kohlmann
dc.contributor.author Torsten, Haferlach
dc.contributor.author Randy, Gascoyne
dc.contributor.author Jude, Fitzgibbon
dc.date.accessioned 2016-06-30T11:18:59Z
dc.date.available 2016-06-30T11:18:59Z
dc.date.issued 2013
dc.identifier.citation pagination=3165-3168; journalVolume=122; journalIssueNumber=18; journalTitle=BLOOD;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2887
dc.identifier.uri doi:10.1182/blood-2013-04-496893
dc.description.abstract Gain of function mutations in the H3K27 methyltransferase EZH2 represent a promising therapeutic target in germinal center lymphomas. In this study, we assessed the frequency and distribution of EZH2 mutations in a large cohort of patients with follicular lymphoma (FL) (n = 366) and performed a longitudinal analysis of mutation during the disease progression from FL to transformed FL (tFL) (n = 33). Mutations were detected at 3 recurrent mutation hot spots (Y646, A682, and A692) in 27% of FL cases with variant allele frequencies (VAF) ranging from 2% to 61%. By comparing VAF of EZH2 with other mutation targets (CREBBP, MLL2, TNFRSF14, and MEF2B), we were able to distinguish patients harboring clonal EZH2 mutation from rarer cases with subclonal mutations. Overall, the high incidence of EZH2 mutations in FL and their stability during disease progression makes FL an appropriate disease to evaluate EZH2 targeted therapy.
dc.relation.ispartof urn:issn:0006-4971
dc.title EZH2 mutations are frequent and represent an early event in follicular lymphoma.
dc.type Journal Article
dc.date.updated 2015-11-30T10:35:48Z
dc.language.rfc3066 en
dc.identifier.mtmt 2448880
dc.identifier.wos 000326503200016
dc.identifier.pubmed 24052547
dc.contributor.department SE/AOK/I/I. Sz. Patológiai és Kísérleti Rákkutató Intézet
dc.contributor.institution Semmelweis Egyetem


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