نتایج جستجو برای: slc30a8

تعداد نتایج: 228  

M. Mohaddes

Type 2 Diabetes Mellitus (T2D) is the most common metabolic disease demonstrating itself by hyper- glycemia, due to impaired insulin secretion or action. Recently, Whole-Genome Association studies have revealed the role of several new genes responsible for T2D. One of the most studied genes is SLC30A8 (Zn-T8) which is exclusively expressed in pancreatic ?-cells and participates in insulin stora...

Journal: :The Biochemical journal 2009
Lynley D Pound Suparna A Sarkar Richard K P Benninger Yingda Wang Adisak Suwanichkul Melanie K Shadoan Richard L Printz James K Oeser Catherine E Lee David W Piston Owen P McGuinness John C Hutton David R Powell Richard M O'Brien

The Slc30a8 gene encodes the islet-specific zinc transporter ZnT-8, which provides zinc for insulin-hexamer formation. Polymorphic variants in amino acid residue 325 of human ZnT-8 are associated with altered susceptibility to Type 2 diabetes and ZnT-8 autoantibody epitope specificity changes in Type 1 diabetes. To assess the physiological importance of ZnT-8, mice carrying a Slc30a8 exon 3 del...

Journal: :Genetics and molecular research : GMR 2017
A Teleginski M Welter H R Frigeri R R Réa E M Souza D Alberton F G M Rego G Picheth

Leptin (LEP), a protein that plays a fundamental role in the metabolism of energy reserves, and the solute carrier family 30 A8 zinc transporter (SLC30A8) have been consistently associated with diabetes. Women with gestational diabetes are at moderate risk of developing diabetes type 1 and 2 after pregnancy, in addition to complications to the fetus. We investigated the association of the polym...

Journal: :Transplantation 2009
Eun Seok Kang Myoung Soo Kim Chul Hoon Kim Chung Mo Nam Seung Jin Han Kyu Yeon Hur Chul Woo Ahn Bong Soo Cha Soon Il Kim Hyun Chul Lee Yu Seun Kim

BACKGROUND Posttransplantation diabetes mellitus (PTDM) is a major metabolic complication in renal transplant recipients. Recent genome-wide association studies have identified several genes associated with type 2 diabetes. Here, we examined the association between PTDM and 17 single nucleotide polymorphisms (SNPs) located within 15 genes in a cohort of renal allograft recipients in Korea. MA...

2016
Tiange Wang Huikun Liu Leishen Wang Tao Huang Weiqin Li Yan Zheng Yoriko Heianza Dianjianyi Sun Junhong Leng Shuang Zhang Nan Li Gang Hu Lu Qi

Zinc transporter 8 genetic variant SLC30A8 has been associated with postpartum risk of type 2 diabetes among women with gestational diabetes mellitus (GDM). Gestational weight gain is one of the strongest risk factors for postpartum hyperglycemia. We assessed the interaction between type 2 diabetes-associated SLC30A8 rs13266634 and gestational weight gain on 1-5 years of postpartum glycemic cha...

2017
Aleksey G. Nikitin Viktor Y. Potapov Olga I. Brovkina Ekaterina O. Koksharova Dmitry S. Khodyrev Yury I. Philippov Marina S. Michurova Minara S. Shamkhalova Olga K. Vikulova Svetlana A. Smetanina Lyudmila A. Suplotova Irina V. Kononenko Viktor Y. Kalashnikov Olga M. Smirnova Alexander Y. Mayorov Valery V. Nosikov Alexander V. Averyanov Marina V. Shestakova

BACKGROUND The association of type 2 diabetes mellitus (T2DM) with the KCNJ11, CDKAL1, SLC30A8, CDKN2B, and FTO genes in the Russian population has not been well studied. In this study, we analysed the population frequencies of polymorphic markers of these genes. METHODS The study included 862 patients with T2DM and 443 control subjects of Russian origin. All subjects were genotyped for 10 si...

Journal: :PLoS ONE 2009
Yi Fu Wei Tian Emily B. Pratt Lisa B. Dirling Show-Ling Shyng Charles K. Meshul David M. Cohen

The SLC30A8 gene codes for a pancreatic beta-cell-expressed zinc transporter, ZnT8. A polymorphism in the SLC30A8 gene is associated with susceptibility to type 2 diabetes, although the molecular mechanism through which this phenotype is manifest is incompletely understood. Such polymorphisms may exert their effect via impacting expression level of the gene product. We used an shRNA-mediated ap...

2007
Laura Pascoe Andrea Tura Sheila K. Patel Ibrahim M. Ibrahim Ele Ferrannini Eleftheria Zeggini Michael N. Weedon Andrea Mari Andrew T. Hattersley Mark I. McCarthy Timothy M. Frayling

OBJECTIVE— Type 2 diabetes is characterized by impaired pancreatic -cell function and decreased insulin sensitivity. Genome-wide association studies have identified common, novel type 2 diabetes susceptibility loci within the FTO, CDKAL1, CDKN2A/CDKN2B, IGF2BP2, HHEX/IDE, and SLC30A8 gene regions. Our objective was to explore the relationships between the diabetes-associated alleles and measure...

2009
Clara Kelliny Ulf Ekelund Lars Bo Andersen Soren Brage Ruth J.F. Loos Nicholas J. Wareham Claudia Langenberg

OBJECTIVE The goal of this study was to investigate whether the effects of common genetic variants associated with fasting glucose in adults are detectable in healthy children. RESEARCH DESIGN AND METHODS Single nucleotide polymorphisms in MTNR1B (rs10830963), G6PC2 (rs560887), and GCK (rs4607517) were genotyped in 2,025 healthy European children aged 9-11 and 14-16 years. Associations with f...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شهید چمران اهواز - دانشکده علوم 1391

دیابت نوع 2 رایج ترین ناهنجاری متابولیک است که به وسیله هیپرگلیسمی مزمن شناسایی می شود و بروز آن به شیوه هشدار دهنده ای رو به افزایش می باشد. دیابت شیرین نوع 2 یک بیماری چند عاملی است و ژن های مختلف و فاکتورهای محیطی در بروز آن نقش دارند. روی نقش مهمی در ذخیره و ترشح انسولین بازی می کند. انتقال روی توسط پروتئین های انتقال دهنده روی انجام می گیرد و این پروتئین ها روی را به ماتریکس خارج سلولی و ی...

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