نتایج جستجو برای: ژن slc30a8

تعداد نتایج: 15995  

2011
Stavroula Kanoni Jennifer A. Nettleton Marie-France Hivert Zheng Ye Frank J.A. van Rooij Dmitry Shungin Emily Sonestedt Julius S. Ngwa Mary K. Wojczynski Rozenn N. Lemaitre Stefan Gustafsson Jennifer S. Anderson Toshiko Tanaka George Hindy Georgia Saylor Frida Renstrom Amanda J. Bennett Cornelia M. van Duijn Jose C. Florez Caroline S. Fox Albert Hofman Ron C. Hoogeveen Denise K. Houston Frank B. Hu Paul F. Jacques Ingegerd Johansson Lars Lind Yongmei Liu Nicola McKeown Jose Ordovas James S. Pankow Eric J.G. Sijbrands Ann-Christine Syvänen André G. Uitterlinden Mary Yannakoulia M. Carola Zillikens Nick J. Wareham Inga Prokopenko Stefania Bandinelli Nita G. Forouhi L. Adrienne Cupples Ruth J. Loos Goran Hallmans Josée Dupuis Claudia Langenberg Luigi Ferrucci Stephen B. Kritchevsky Mark I. McCarthy Erik Ingelsson Ingrid B. Borecki Jacqueline C.M. Witteman Marju Orho-Melander David S. Siscovick James B. Meigs Paul W. Franks George V. Dedoussis

OBJECTIVE Many genetic variants have been associated with glucose homeostasis and type 2 diabetes in genome-wide association studies. Zinc is an essential micronutrient that is important for β-cell function and glucose homeostasis. We tested the hypothesis that zinc intake could influence the glucose-raising effect of specific variants. RESEARCH DESIGN AND METHODS We conducted a 14-cohort met...

Journal: :The Journal of Clinical Endocrinology & Metabolism 2008

2009
Cheng Hu Rong Zhang Congrong Wang Jie Wang Xiaojing Ma Jingyi Lu Wen Qin Xuhong Hou Chen Wang Yuqian Bao Kunsan Xiang Weiping Jia

BACKGROUND Recent advance in genetic studies added the confirmed susceptible loci for type 2 diabetes to eighteen. In this study, we attempt to analyze the independent and joint effect of variants from these loci on type 2 diabetes and clinical phenotypes related to glucose metabolism. METHODS/PRINCIPAL FINDINGS Twenty-one single nucleotide polymorphisms (SNPs) from fourteen loci were success...

2017
Klara Rosta Zahra Al-Aissa Orsolya Hadarits Jürgen Harreiter Ákos Nádasdi Fanni Kelemen Dagmar Bancher-Todesca Zsolt Komlósi László Németh János Rigó István Sziller Anikó Somogyi Alexandra Kautzky-Willer Gábor Firneisz

CONTEXT Genetic variation in human maternal DNA contributes to the susceptibility for development of gestational diabetes mellitus (GDM). OBJECTIVE We assessed 77 maternal single nucleotide gene polymorphisms (SNPs) for associations with GDM or plasma glucose levels at OGTT in pregnancy. METHODS 960 pregnant women (after dropouts 820: case/control: m99'WHO: 303/517, IADPSG: 287/533) were en...

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