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dc.contributor.authorÖztürk, Fatma
dc.contributor.authorDaloğlu, Cihan
dc.contributor.authorAçık, Leyla
dc.contributor.authorKılıç, Mehmet
dc.contributor.authorKoç, Mahmut
dc.date.accessioned2014-07-15T11:55:33Z
dc.date.available2014-07-15T11:55:33Z
dc.date.issued2008
dc.identifier.issn1307-3923
dc.identifier.urihttp://hdl.handle.net/11413/208
dc.description.abstractMolecula r mutations to proto - oncogene sequences may be involved in the pathogenesis of human thyroid neoplasm. Problems on oncogenes and tumor supressor genes activation in cell circle could cause tumor. Many oncogenes and tumor suppressing genes exist in varying percentages in various types of thyroid cancers. Ras, Gsp, Ret or Trk oncogenes can be involve in thyroid tumors . Members of t h e Ras gene family (H-ras, K-ras, and N-ras) are signal transferring proteins. These genes codes for 21 kDa GTP binding proteins. We studied 24 thyroid cancer and 77 control for ras gene point mutations in two different codons (12 and 13) using a restriction fragment length polymorphism technique. According to enzyme digesting, no c-K-ras gene codon 12/13 and N-ras gene codon 12 point mutation were observed in any of the samples we studied .tr_TR
dc.language.isoen_UStr_TR
dc.publisherİstanbul Kültür Üniversitesitr_TR
dc.subjectras genetr_TR
dc.subjectthyroid cancertr_TR
dc.subjectmutationtr_TR
dc.subjectRFLPtr_TR
dc.titleRas oncogenes polymorphism in Turkish thyroid cancer patientstr_TR
dc.typeArticletr_TR


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