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dc.contributor.authorAkçay, Arzu
dc.contributor.authorTürkkan, Emine
dc.contributor.authorOztunc, Ceren
dc.contributor.authorYildiz, Inci
dc.contributor.authorAnak, Sema
dc.contributor.authorDevecioglu, Omer
dc.contributor.authorHatirnaz, Ozden
dc.contributor.authorCelkan, Tiraje
dc.contributor.authorUnuvar, Aysegul
dc.contributor.authorSayitoglu, Müge
dc.contributor.authorKaraman, SERAP
dc.contributor.authorCinar, Suzan
dc.contributor.authorTimur, Cetin
dc.contributor.authorAYDOGAN, Gonul
dc.contributor.authorAtay, Didem
dc.contributor.authorORHANER, Betul
dc.contributor.authorSarper, Nazan
dc.contributor.authorDeniz, Gunnur
dc.contributor.authorOzbek, Ugur
dc.contributor.authorFirtina, Sinem
dc.contributor.authorErbilgin, Yucel
dc.date.accessioned2021-03-04T10:36:41Z
dc.date.available2021-03-04T10:36:41Z
dc.date.issued2012
dc.identifier.citationFirtina S., Sayitoglu M., Hatirnaz O., Erbilgin Y., Oztunc C., Cinar S., Yildiz I., Celkan T., Anak S., Unuvar A., et al., "Evaluation of PAX5 gene in the early stages of leukemic B cells in the childhood B cell acute lymphoblastic leukemia", LEUKEMIA RESEARCH, cilt.36, sa.1, ss.87-92, 2012
dc.identifier.issn0145-2126
dc.identifier.othervv_1032021
dc.identifier.otherav_6e11a041-8d7b-4e86-a38c-762ebe9ff8a2
dc.identifier.urihttp://hdl.handle.net/20.500.12627/76006
dc.identifier.urihttps://doi.org/10.1016/j.leukres.2011.07.017
dc.description.abstractB-lineage acute lymphoblastic leukemia (B-ALL) is a common subtype of acute leukemia in children. PAX5 plays a central role in B-cell development and differentiation. In this study, we analyzed PAX5 expression levels, transactivation domain mutations/deletions in B-ALL patients (n = 115) and healthy controls (n = 10). Relative PAX5 mRNA levels were significantly increased in B-ALL patients (p < 0.0001). PAX5 expression was also evaluated in three different B-ALL subgroups (pro B, Common B and Pre B ALL) and showed stage specific expression levels. Pro B (p = 0.04) and pre B (p = 0.04) patients showed significantly high PAX5 mRNA levels compared to stage specific controls. At least one deletion of exons 7-8 or 9 has been identified in the 41% of the patients. CD34 positivity in patients and presence of large deletions (Delta 7/8/9) showed a significant correlation (p = 0.05). None of our patients showed PAX5 point mutations, but two previously identified SNPs (rs3780135 and rs35469494) were detected. Our results support that PAX5 is a critical factor in B-ALL development and aberrant PAX5 expression especially at early stages may leads to leukemic transformation. (C) 2011 Elsevier Ltd. All rights reserved.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectONKOLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectHEMATOLOJİ
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectHematoloji
dc.subjectOnkoloji
dc.titleEvaluation of PAX5 gene in the early stages of leukemic B cells in the childhood B cell acute lymphoblastic leukemia
dc.typeMakale
dc.relation.journalLEUKEMIA RESEARCH
dc.contributor.departmentİstanbul Medeniyet Üniversitesi , ,
dc.identifier.volume36
dc.identifier.issue1
dc.identifier.startpage87
dc.identifier.endpage92
dc.contributor.firstauthorID505


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