E. Pratt

Molecular defects of ATP-sensitive potassium channels in congenital hyperinsulinism

S. Shyng, Jeremy D. Bushman, E. Pratt, 2012 .

N-terminal transmembrane domain of SUR1 controls gating of Kir6.2 by modulating channel sensitivity to PIP2

S. Shyng, W. Skach, Cathrin E. Bruederle, 2011, The Journal of general physiology.

Engineered Kir6.2 mutations that correct the trafficking defect of KATP channels caused by specific SUR1 mutations

S. Shyng, E. Pratt, Qing Zhou, 2013, Channels.

Engineered interaction between SUR1 and Kir6.2 that enhances ATP sensitivity in KATP channels

S. Shyng, E. Pratt, Qing Zhou, 2012, The Journal of general physiology.

Sulfonylurea Receptor 1 Mutations That Cause Opposite Insulin Secretion Defects with Chemical Chaperone Exposure*

C. Stanley, S. Shyng, E. Pratt, 2009, Journal of Biological Chemistry.

Kir6.2 Mutations Associated With Neonatal Diabetes Reduce Expression of ATP-Sensitive K+ channels

S. Shyng, E. Pratt, Yu‐Wen Lin, 2006, Diabetes.