The association between kir6.2 mutation and type 1 diabetes / Alaa Afif Abdelraouf ; Supervised Nadida Abdelhamid Gohar , Shereen Abdelghaffar Taha , Nahla Aly Fawzy Fayek
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TextLanguage: English Publication details: Cairo : Alaa Afif Abdelraouf , 2012Description: 81Leaves : charts , facsimiles ; 25cmOther title: - العلاقة بين التحور الجينى للجين ( كير 2و6 ) والنوع الاول من البول السكرى [Added title page title]
- Issued also as CD
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Thesis
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.07.Ph.D.2012.Al.A (Browse shelf(Opens below)) | Not for loan | 01010110058249000 | ||
CD - Rom
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.07.Ph.D.2012.Al.A (Browse shelf(Opens below)) | 58249.CD | Not for loan | 01020110058249000 |
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Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology
The pancreatic ATP - sensitive potassium ( Katp ) channel is a critical regulator of beta - cell insulin secretion . Heterozygous activating mutations in the KCNJ11 gene , which encodes the Kir 6.2 subunit of the Katp channel , have been found to cause diabetes in the neonatal period or early infancy . This molecular study hypothesized that KCNJ11 mutations could present clinically as type 1 diabetes
Issued also as CD
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