Study of the association of protein tyrosine phoshatase non receptor 22 gene (PTPN22) C1858T gene polymorphism with Graves' / Maysa Ibrahim Mohamed Farghly ; Supervised Dina Mohamed Elabd , Safaa Algabarty , Mahassen Abogabl

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Maysa Ibrahim Mohamed Farghly

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TextLanguage: English Publication details: Cairo : Maysa Ibrahim Mohamed Farghly , 2012Description: 94P. : charts , facsimiles ; 25cmOther title:

دراسة العلاقة بين الأشكال المتعددة لجين البروتين تيروزين فوسفاتيز ت/ت 1858 ومرض الجريفز [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 : The protein tyrosin phoshatase non receptor 22 gene (PTPN22) is an important negative regulator of signal transduction through the T- cell receptors (TCR). A single - nucleotide polymorphism (SNP) C1858T within this gene was shown to be a risk factor for several autoimmune diseases as Graves` disease . Conclusion : No staisticall significant association was found between the PTPN22 C1858T polymorphism and Graves' disease

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Item type	Current library	Home library	Call number	Copy number	Status	Date due	Barcode
Thesis	قاعة الرسائل الجامعية - الدور الاول	المكتبة المركزبة الجديدة - جامعة القاهرة	Cai01.11.07.M.Sc.2012.Ma.S (Browse shelf(Opens below))		Not for loan		01010110059821000
CD - Rom	مخـــزن الرســائل الجـــامعية - البدروم	المكتبة المركزبة الجديدة - جامعة القاهرة	Cai01.11.07.M.Sc.2012.Ma.S (Browse shelf(Opens below))	59821.CD	Not for loan		01020110059821000

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

Background : The protein tyrosin phoshatase non receptor 22 gene (PTPN22) is an important negative regulator of signal transduction through the T- cell receptors (TCR). A single - nucleotide polymorphism (SNP) C1858T within this gene was shown to be a risk factor for several autoimmune diseases as Graves` disease . Conclusion : No staisticall significant association was found between the PTPN22 C1858T polymorphism and Graves' disease

Issued also as CD

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