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dc.contributor.authorBARIŞ, SAFA
dc.contributor.authorBatar, Bahadir
dc.contributor.authorOzdemir, Nihal
dc.contributor.authorGuven, Mehmet
dc.contributor.authorCelkan, Tiraje
dc.date.accessioned2021-03-02T22:07:16Z
dc.date.available2021-03-02T22:07:16Z
dc.date.issued2012
dc.identifier.citationOzdemir N., Celkan T., BARIŞ S., Batar B., Guven M., "DNA repair gene XPD and XRCC1 polymorphisms and the risk of febrile neutropenia and mucositis in children with leukemia and lymphoma", LEUKEMIA RESEARCH, cilt.36, sa.5, ss.565-569, 2012
dc.identifier.issn0145-2126
dc.identifier.otherav_0add2eec-14e6-4ed4-a5ca-7380892c592f
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/13017
dc.identifier.urihttps://doi.org/10.1016/j.leukres.2011.10.012
dc.description.abstractThe aim of the study is to investigate association between DNA repair gene XPD and XRCC1 polymorphisms and febrile neutropenia (FN) and mucositis. The study population consisted of 29 children with Burkitt lymphoma and 61 children with acute lymphoblastic leukemia. Analysis revealed that XRCC1194Trp allele showed a protective effect against longer FN and mucositis. There was also statistically increased risk for severe mucositis in patients with XRCC1Arg399Gln polymorphism. There are no studies that have examined this relationship before. Further studies with larger cohorts are needed to clarify the association. (C) 2011 Elsevier Ltd. All rights reserved.
dc.language.isoeng
dc.subjectHematoloji
dc.subjectOnkoloji
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectHEMATOLOJİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectONKOLOJİ
dc.titleDNA repair gene XPD and XRCC1 polymorphisms and the risk of febrile neutropenia and mucositis in children with leukemia and lymphoma
dc.typeMakale
dc.relation.journalLEUKEMIA RESEARCH
dc.contributor.department, ,
dc.identifier.volume36
dc.identifier.issue5
dc.identifier.startpage565
dc.identifier.endpage569
dc.contributor.firstauthorID204225


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