Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes risk

Sulfonylurea receptors regulate the channel pore in ATP-sensitive potassium channels via an intersubunit salt bridge

(2014) David Lodwick et al.   BIOCHEMICAL JOURNAL

Mutations in KCNJ11 are associated with the development of autosomal dominant, early-onset type 2 diabetes

(2013) Limei Liu et al.   DIABETOLOGIA

The ATP-Sensitive K+ Channel ABCC8 S1369A Type 2 Diabetes Risk Variant Increases MgATPase Activity

(2011) M. Fatehi et al.   DIABETES

Coexpression of the Type 2 Diabetes Susceptibility Gene Variants KCNJ11 E23K and ABCC8 S1369A Alter the ATP and Sulfonylurea Sensitivities of the ATP-Sensitive K+ Channel

(2009) K. S.C. Hamming et al.   DIABETES

Kir6.2 Variant E23K Increases ATP-Sensitive K+ Channel Activity and Is Associated With Impaired Insulin Release and Enhanced Insulin Sensitivity in Adults With Normal Glucose Tolerance

(2009) D. T. Villareal et al.   DIABETES

Variable phenotypic spectrum of diabetes mellitus in a family carrying a novelKCNJ11gene mutation

(2008) E. DAmato et al.   DIABETIC MEDICINE

Update of mutations in the genes encoding the pancreatic beta-cell KATPchannel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism

(2008) Sarah E. Flanagan et al.   HUMAN MUTATION