Safa Nabil Abdelfattah Mohamed

Mdm2 and p53 codon 72 polymorphisms in acute myeloid leukemia / فى حالات سرطان الدم الميلودى الحادP53 وشفرة 72 للجينMDM2 المظاهرة المتعددة للجين Safa Nabil Abdelfattah Mohamed ; Supervised Nabil Mohsen Eldanasouri , Shadia Hassan Ragab , Zainab Ali Hassan Elsaadany - Cairo : Safa Nabil Abdelfattah Mohamed , 2012 - 200P. : charts , facsimiles ; 25cm

Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology

Acute myeloid leukemia (AML) is a heterogeneous disease with numerous genetic abnormalities . Among them , functional SNPs in both , the tumor suppressor protein , p53 and its key cellular regulator Mdm2 . We investigated the risk of Mdm 2 SNP309 alone or in combination with the p53 codon 72 polymorphism in AML patients in a study that included 50 de novo AML patients and 50 healthy control subjects



Acute myeloid leukemia Mdm2 P53