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The Role Of Solute Carrier Family 30 (Zinc Transporter), Member 8 "SLC30A8" Gene Polymorphism In Susceptibility To Type 2 Diabetes In Selected Sudanese Population

المصدر: مجلة الدراسات العليا
الناشر: جامعة النيلين - كلية الدراسات العليا
المؤلف الرئيسي: Ibrahim, Hadeel (Author)
مؤلفين آخرين: Ibrahim, Amir (Co-Author) , Mohamed, Hiba Salah Aldin (Co-Author) , Salih, Mohammed (Co-Author)
المجلد/العدد: مج2, ع5
محكمة: نعم
الدولة: السودان
التاريخ الميلادي: 2014
الصفحات: 58 - 76
ISSN: 1858-6228
رقم MD: 790529
نوع المحتوى: بحوث ومقالات
اللغة: الإنجليزية
قواعد المعلومات: EcoLink, EduSearch, HumanIndex, IslamicInfo
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LEADER 02653nam a22002777a 4500
001 0165978
041 |a eng 
044 |b السودان 
100 |9 420235  |a Ibrahim, Hadeel  |e Author 
245 |a The Role Of Solute Carrier Family 30 (Zinc Transporter), Member 8 "SLC30A8" Gene Polymorphism In Susceptibility To Type 2 Diabetes In Selected Sudanese Population 
260 |b جامعة النيلين - كلية الدراسات العليا  |c 2014 
300 |a 58 - 76 
336 |a بحوث ومقالات 
520 |b Back ground: SLC30A8 rs11558471 (26465A/G SLC30A8) is Single Nucleotide Polymorphism (SNP), which was found to be associated with Diabetes Type 2 in Han Chinese and European population and represents three other SNPS (rs3802177, rs13266634, rs11558471 ). Variation in SLC30A8 may affect zinc accumulation in insulin granules, affecting insulin stability, storage, or secretion. Higher total zinc intake may attenuate the glucose-raising effect of the rs11558471 SLC30A8 (zinc transporter) variant. Objective: To determine the role of 26465A/G SLC30A8 in susceptibility to T2D in selected Sudanese population. Research design and Methods: Pilot case control study was conducted to investigate the role of 26465A/G SLC30A8 in susceptibility to T2D. The target sequence was amplified using PCR with specific primers and the SNP was genotyped using RLFP (Pst1 restriction enzyme) in fifty five Type 2 Diabetic patients, and forty one normoglycaemic subjects from Tuti Island. Result: This SNP is in hardy Weinberg equilibrium (p=0.437). The major allele frequency in the T2D group and the control group was 0.934, and 0.9635 respectively. There was no significant association of this SNP with T2DM in the study population (chi square= 0.0696, P value= 0.404). Conclusion: The present study indicates that the polymorphism rs11558471 in the human SLC30A8 gene was not associated with type 2 diabetes. 
653 |a الامراض المزمنة  |a مرض السكر  |a السودان 
700 |9 420237  |a Ibrahim, Amir  |e Co-Author 
700 |9 420238  |a Mohamed, Hiba Salah Aldin  |e Co-Author 
700 |9 46597  |a Salih, Mohammed  |e Co-Author 
773 |4 العلوم الإنسانية ، متعددة التخصصات  |4 العلوم الاجتماعية ، متعددة التخصصات  |6 Humanities, Multidisciplinary  |6 Social Sciences, Interdisciplinary  |c 004  |l 005  |m مج2, ع5  |o 1382  |s مجلة الدراسات العليا  |t Journal of Graduate Studies  |v 002  |x 1858-6228 
856 |u 1382-002-005-004.pdf 
930 |d y  |p y 
995 |a EcoLink 
995 |a EduSearch 
995 |a HumanIndex 
995 |a IslamicInfo 
999 |c 790529  |d 790529 

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