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Study of xeroderma pigmentosum Ccomplemetation group D (XPD) codon 751 polymorphism in hepatocellular carcinoma / Asmaa Mohamed Fteah Abdelaziz ; Supervised Nevine Ezz Eldin Elabd , Mona Mohamed Hassan , Asmaa Mohamed Kamal

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Asmaa Mohamed Fteah Abdelaziz , 2014Description: 141 P. : charts , facsimiles ; 25cmOther title:
  • دراسة الأشكال المتعددة للجين إكس بي دي 751 في حالات سرطان الكبد الخلوي [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: Background: Hepatocellular carcinoma (HCC) is the most common primary tumor of the liver. The molecular determinants of the HCC progression are still under investigation. The Xeroderma Pigmentosum Complementation Group D (XPD) is a major DNA repair gene which plays a vital role in Nucleotide Excision repair (NER) which is reported to be associated with risk of several cancers. Genetic polymorphisms in XPD gene may influence individual variations in DNA repair capacity, which may be associated with increased risk of HCC. OBJECTIVE: The aim of this study was to investigate the association between XPD/ERCC2 Lys751Gln (A/C) gene polymorphism (rs 13181) and the incidence of HCC in Egyptian patients
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.M.Sc.2014.As.S (Browse shelf(Opens below)) Not for loan 01010110065849000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.M.Sc.2014.As.S (Browse shelf(Opens below)) 65849.CD Not for loan 01020110065849000

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

Background: Hepatocellular carcinoma (HCC) is the most common primary tumor of the liver. The molecular determinants of the HCC progression are still under investigation. The Xeroderma Pigmentosum Complementation Group D (XPD) is a major DNA repair gene which plays a vital role in Nucleotide Excision repair (NER) which is reported to be associated with risk of several cancers. Genetic polymorphisms in XPD gene may influence individual variations in DNA repair capacity, which may be associated with increased risk of HCC. OBJECTIVE: The aim of this study was to investigate the association between XPD/ERCC2 Lys751Gln (A/C) gene polymorphism (rs 13181) and the incidence of HCC in Egyptian patients

Issued also as CD

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