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Mdm2 and p53 codon 72 polymorphisms in acute myeloid leukemia / Safa Nabil Abdelfattah Mohamed ; Supervised Nabil Mohsen Eldanasouri , Shadia Hassan Ragab , Zainab Ali Hassan Elsaadany

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Safa Nabil Abdelfattah Mohamed , 2012Description: 200P. : charts , facsimiles ; 25cmOther title:
  • فى حالات سرطان الدم الميلودى الحادP53 وشفرة 72 للجينMDM2 المظاهرة المتعددة للجين [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology Summary: 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
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Item type Current library Home library Call number Copy number Status Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.M.Sc.2012.Sa.M (Browse shelf(Opens below)) Not for loan 01010110060342000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.M.Sc.2012.Sa.M (Browse shelf(Opens below)) 60342.CD Not for loan 01020110060342000

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

Issued also as CD

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