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dc.contributor.authorCatal, Suzin
dc.contributor.authorEskazan, Ahmet Emre
dc.contributor.authorHatirnaz, Ozden
dc.contributor.authorOzbek, Ugur
dc.contributor.authorErbilgin, Yücel
dc.contributor.authorSoysal, Teoman
dc.date.accessioned2021-03-06T11:45:14Z
dc.date.available2021-03-06T11:45:14Z
dc.date.issued2011
dc.identifier.citationErbilgin Y., Catal S., Eskazan A. E. , Hatirnaz O., Soysal T., Ozbek U., "ABL gene kinase domain mutation scanning by denaturing high performance liquid chromatography sequencing method", TURKISH JOURNAL OF HEMATOLOGY, cilt.28, ss.97-102, 2011
dc.identifier.issn1300-7777
dc.identifier.otherav_f08a6165-ff0a-4db5-b97d-eb5751adf926
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/157847
dc.identifier.urihttps://doi.org/10.5152/tjh.2011.24
dc.description.abstractObjective: Despite the efficacy of the BCR-ABL tyrosine kinase inhibitor imatinib, the development of resistance against imatinib has been observed. The most important mechanisms known to cause resistance are point mutations in the ABL tyrosine kinase and the ATP domain. This study describes the use of denaturing high performance liquid chromatography (dHPLC) as a method to screen for mutations of the ABL gene.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectHematoloji
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectKlinik Tıp
dc.subjectHEMATOLOJİ
dc.titleABL gene kinase domain mutation scanning by denaturing high performance liquid chromatography sequencing method
dc.typeMakale
dc.relation.journalTURKISH JOURNAL OF HEMATOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume28
dc.identifier.issue2
dc.identifier.startpage97
dc.identifier.endpage102
dc.contributor.firstauthorID100121


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