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https://hdl.handle.net/11499/9740
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Çetin Gökhan Ozan | - |
dc.contributor.author | Barış, İkbal Cansu | - |
dc.contributor.author | Caner, Vildan | - |
dc.contributor.author | Sarıkepe, Bilge | - |
dc.contributor.author | Şen Türk, Nilay | - |
dc.contributor.author | Tepeli, Emre | - |
dc.contributor.author | Hacıoglu, Sibel | - |
dc.date.accessioned | 2019-08-16T13:05:18Z | - |
dc.date.available | 2019-08-16T13:05:18Z | - |
dc.date.issued | 2016 | - |
dc.identifier.issn | 1128-3602 | - |
dc.identifier.uri | https://hdl.handle.net/11499/9740 | - |
dc.description.abstract | OBJECTIVE: We aimed to determine the hot spot mutational frequencies of Enhancer of Zeste homolog 2 (EZH2) and cluster of differentiation 79B (CD79B) genes in a cohort of mature B-cell non-Hodgkin's lymphomas. PATIENTS AND METHODS: DNA samples from formalin-fixed and paraffin embedded (FFPE) tissues from a total of 37 patients with mature B-cell non-Hodgkin lymphomas were included in the study. Molecular genetic analysis was performed by direct sequencing of the DNA samples. RESULTS: We analyzed formaldehyde fixed-paraffin embedded (FFPE) tumor tissue samples from 17 female and 20 male patients with a median age of 63.7 years at the time of diagnosis. None of the patients had previously reported hot spot mutations in EZH2 and CD79B, but previously unreported single nucleotide variations of CD79B were present in nine patients. rs779833118 was the most frequent variation (7/37 patients, 18.9%). A non-synonymous variation rs757407417, which could have a potentially damaging outcome, was detected in two patients. CONCLUSIONS: None of the patients had well-known hot spot mutations in EZH2 and CD79B. However, we detected novel CD79B variations in mature B-cell non-Hodgkin's lymphoma patients. © 2016, Verduci Editore. All rights reserved. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Verduci Editore | en_US |
dc.relation.ispartof | European Review for Medical and Pharmacological Sciences | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | CD79B | en_US |
dc.subject | EZH2 | en_US |
dc.subject | Mature B-cell non-Hodgkin lymphoma | en_US |
dc.subject | Mutation | en_US |
dc.subject | CD79b antigen | en_US |
dc.subject | transcription factor EZH2 | en_US |
dc.subject | CD79 antigen | en_US |
dc.subject | CD79B protein, human | en_US |
dc.subject | EZH2 protein, human | en_US |
dc.subject | adult | en_US |
dc.subject | Article | en_US |
dc.subject | B cell lymphoma | en_US |
dc.subject | cancer staging | en_US |
dc.subject | carcinogenesis | en_US |
dc.subject | CD79B gene | en_US |
dc.subject | clinical article | en_US |
dc.subject | controlled study | en_US |
dc.subject | DNA sequence | en_US |
dc.subject | EZH2 gene | en_US |
dc.subject | female | en_US |
dc.subject | gene frequency | en_US |
dc.subject | gene mutation | en_US |
dc.subject | genetic association | en_US |
dc.subject | genetic variation | en_US |
dc.subject | high risk patient | en_US |
dc.subject | human | en_US |
dc.subject | human tissue | en_US |
dc.subject | male | en_US |
dc.subject | mutational analysis | en_US |
dc.subject | nonhodgkin lymphoma | en_US |
dc.subject | single nucleotide variation | en_US |
dc.subject | aged | en_US |
dc.subject | cohort analysis | en_US |
dc.subject | genetics | en_US |
dc.subject | Lymphoma, B-Cell | en_US |
dc.subject | middle aged | en_US |
dc.subject | mutation | en_US |
dc.subject | pathology | en_US |
dc.subject | very elderly | en_US |
dc.subject | Adult | en_US |
dc.subject | Aged | en_US |
dc.subject | Aged, 80 and over | en_US |
dc.subject | Antigens, CD79 | en_US |
dc.subject | Cohort Studies | en_US |
dc.subject | Enhancer of Zeste Homolog 2 Protein | en_US |
dc.subject | Female | en_US |
dc.subject | Genetic Variation | en_US |
dc.subject | Humans | en_US |
dc.subject | Male | en_US |
dc.subject | Middle Aged | en_US |
dc.title | Mutational status of EZH2 and CD79B hot spots in mature B-cell non-Hodgkin's lymphomas: Novel CD79B variations have been revealed | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 20 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.startpage | 830 | - |
dc.identifier.startpage | 830 | en_US |
dc.identifier.endpage | 836 | en_US |
dc.authorid | 0000000261007973 | - |
dc.authorid | 0000000309809335 | - |
dc.authorid | 0000-0002-8294-558X | - |
dc.authorid | 0000-0003-0757-9206 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 27010137 | en_US |
dc.identifier.scopus | 2-s2.0-85016969196 | en_US |
dc.identifier.wos | WOS:000373350100010 | en_US |
dc.identifier.scopusquality | Q2 | - |
dc.owner | Pamukkale University | - |
dc.snmz | updated | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.languageiso639-1 | en | - |
item.grantfulltext | none | - |
item.openairetype | Article | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.01. Surgical Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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