نتایج جستجو برای: like 2 rs7903146

تعداد نتایج: 3019731  

2009
Ludmila Prokunina-Olsson Cullan Welch Ola Hansson Neeta Adhikari Laura J. Scott Nicolle Usher Maurine Tong Andrew Sprau Amy Swift Lori L. Bonnycastle Michael R. Erdos Zhi He Richa Saxena Brennan Harmon Olga Kotova Eric P. Hoffman David Altshuler Leif Groop Michael Boehnke Francis S. Collins Jennifer L. Hall

Common variants in the transcription factor 7-like 2 (TCF7L2) gene have been identified as the strongest genetic risk factors for type 2 diabetes (T2D). However, the mechanisms by which these non-coding variants increase risk for T2D are not well-established. We used 13 expression assays to survey mRNA expression of multiple TCF7L2 splicing forms in up to 380 samples from eight types of human t...

Journal: :BMC Medicine 2006
David Melzer Anna Murray Alison J Hurst Michael N Weedon Stefania Bandinelli Anna Maria Corsi Luigi Ferrucci Guiseppe Paolisso Jack M Guralnik Timothy M Frayling

BACKGROUND A polymorphism in the transcription factor 7-like 2 (TCF7L2) gene has been found to be associated with type 2 diabetes in case-control studies. We aimed to estimate associations of the marker rs7903146 (C/T) polymorphism with fasting glucose, lipids, diabetes prevalence and complications in an older general population. METHODS In total, 944 subjects aged > or = 65 years from the po...

Journal: :Diabetes 2006
Laura J Scott Lori L Bonnycastle Cristen J Willer Andrew G Sprau Anne U Jackson Narisu Narisu William L Duren Peter S Chines Heather M Stringham Michael R Erdos Timo T Valle Jaakko Tuomilehto Richard N Bergman Karen L Mohlke Francis S Collins Michael Boehnke

Transcription factor 7-like 2 (TCF7L2) is part of the Wnt signaling pathway. Genetic variants within TCF7L2 on chromosome 10q were recently reported to be associated with type 2 diabetes in Icelandic, Danish, and American (U.S.) samples. We previously observed a modest logarithm of odds score of 0.61 on chromosome 10q, approximately 1 Mb from TCF7L2, in the Finland-United States Investigation o...

2016
Riobaldo Cintra Filipe A. Moura Luiz S.F. Carvalho Mauricio Daher Simone N. Santos Ana P.R. Costa Valeria N. Figueiredo Joalbo M. Andrade Francisco A.R. Neves Jose C. Quinaglia e Silva Andrei C. Sposito

BACKGOUND The favorable effects of insulin during myocardial infarction (MI) remain unclear due to the divergence between mechanistic studies and clinical trials of exogenous insulin administration. The rs7903146 polymorphism of the transcription factor 7-like 2 (TCF7L2) gene is associated with attenuated insulin secretion. METHODS In non-diabetic patients with ST-elevation MI (STEMI), using ...

Journal: :Diabetology and Metabolic Syndrome 2009
Edmond K Kabagambe Stephen P Glasser Jose M Ordovas Daruneewan Warodomwichit Michael Y Tsai Paul N Hopkins Ingrid B Borecki Mary Wojczynski Donna K Arnett

BACKGROUND Inflammation is implicated in causing diabetes. We tested whether transcription factor 7 like-2 (TCF7L2) gene polymorphisms (rs12255372 and rs7903146), consistently associated with type 2 diabetes, are associated with plasma concentrations of inflammatory markers before and after three weeks of daily treatment with fenofibrate. METHODS Men and women in the Genetics of Lipid-Lowerin...

Background and Objective: Ecto-nucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) is a class II membrane glycoprotein that binds to insulin α receptor and can interfere in insulin signaling pathway. Transcription factor-7-like 2 (TCF7L2) is a transcription factor which plays a critical role in pancreatic β cell activity. ENPP1 and TCF7L2 gene polymorphisms may have functional role in suscep...

Journal: :Genetics and molecular research : GMR 2014
C M A R Barros A P Araujo-Neto T R Lopes M A L Barros F J N Motta R Canalle L C C Nunes J A Rey R R Burbano M A Lima-Barros F K N Yoshioka G R Pinto

Approximately 200 million people suffer from type 2 diabetes (T2D) worldwide, and the rapid increase in the prevalence of this disease is likely a result of multiple environmental factors, such as increased food intake and decreased physical activity in genetically predisposed individuals. Different population studies have demonstrated a strong association of two polymorphic variations in the T...

2012
Galina Smushkin Matheni Sathananthan Airani Sathananthan Chiara Dalla Man Francesco Micheletto Alan R. Zinsmeister Claudio Cobelli Adrian Vella

The mechanisms by which common genetic variation predisposes to type 2 diabetes remain unclear. The disease-associated variants in TCF7L2 (rs7903146) and WFS1 (rs10010131) have been shown to affect response to exogenous glucagon-like peptide 1 (GLP-1), while variants in KCNQ1 (rs151290, rs2237892, and rs2237895) alter endogenous GLP-1 secretion. We set out to validate these observations using a...

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