000 | 01777cam a2200313 a 4500 | ||
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003 | EG-GiCUC | ||
008 | 131028s2013 ua dh f m 000 0 eng d | ||
040 |
_aEG-GiCUC _beng _cEG-GiCUC |
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041 | 0 | _aeng | |
049 | _aDeposite | ||
097 | _aM.Sc | ||
099 | _aCai01.08.06.M.Sc.2013.Ma.P | ||
100 | 0 | _aMai Muhammed Ragab | |
245 | 1 | 0 |
_aProtein kinase R (PKR) expression as a predictive factor for interferon response in chronic hepatitis C patients / _cMai Muhammed Ragab ; Supervised Magdy Ali Amin , Amal Ahmed Mohamed |
246 | 1 | 5 | _aنسبة وجود جين بروتين كايناز كدليل على مدى استجابة مرضى الالتهاب الكبدى الوبائى المزمن سى للعلاج بالانترفيرون |
260 |
_aCairo : _bMai Muhammed Ragab , _c2013 |
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300 |
_a99 P. : _bcharts , facsimiles ; _c25cm |
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502 | _aThesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Microbiology and Immunology | ||
520 | _aEgypt has the highest prevalence of hepatitis C virus (HCV) worldwide . Currently combined pegylated interferon and ribavirin therapy are the standard treatment . The biological activity of interferon (IFN) is mediated by the induction of intracellular antiviral proteins, such as 2'-5' oligoadenylate synthetase, and dsRNA - activated protein kinase. IFN inducible double - stranded RNA- activated protein kinase (PKR) is thought to play a key antiviral role against HCV | ||
530 | _aIssued also as CD | ||
653 | 4 | _aChronic hepatitis C | |
653 | 4 | _aPegylated interfern | |
653 | 4 | _aProtein kinase gene | |
700 | 0 |
_aAmal Ahmed Mohamed , _eSupervisor |
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700 | 0 |
_aMagdy Ali Amin , _eSupervisor |
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905 |
_aNazla _eRevisor |
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905 |
_aSoheir _eCataloger |
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942 |
_2ddc _cTH |
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999 |
_c43914 _d43914 |