Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.
By V. Lyssenko, R. Lupi, P. Marchetti, S. del Guerra, M. Orho-Melander, P. Almgren, M. Sjögren, C. Ling, K. Eriksson, ÅsaLinda Lethagen and 6 more. Journal of Clinical Investigation, 2007
839 citations recorded by the source corpus.
Subfields: Endocrinology, Diabetes and Metabolism, Genetics, Surgery
View Paper: https://www.semanticscholar.org/paper/511b89dc0f8fdb5f4cd69c6959583688ebab19de
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In Endocrinology, Diabetes and Metabolism
In Genetics
In Surgery
Citations in the corpus
- From the Triumvirate to the Ominous Octet: A New Paradigm for the Treatment of Type 2 Diabetes Mellitus (2009, background): “Studies by Groop and colleagues (63) have shown that the T-allele of single nucleotide polymorphism rs7903146 of the TCF7L2 gene is associated with impaired insulin secretion in vivo and reduced responsiveness to glucagon-like peptide 1 (GLP-1).”
- TCF/LEFs and Wnt signaling in the nucleus. (2012, background): “The strongest diabetes-associated polymorphism identified to date occurs in an intervening sequence of the TCF4/TCF7L2 gene (Grant et al. 2006; Lyssenko et al. 2007; and reviewed in Doria et al. 2008).”
- Pathogenesis of Type 2 Diabetes Mellitus (2015, background): “The risks of alleles in TCF7L2 were associated with hepatic but not peripheral IR and enhanced the rate of hepatic glucose production in human [162].”
- The Role of Incretins in Glucose Homeostasis and Diabetes Treatment (2008, background): “This is very interesting from a clinical standpoint because genetic studies have linked the risk for T2DM to TCF7L2 polymorphisms (Lyssenko et al., 2007).”