Mechanistic basis for LQT1 caused by S3 mutations in the KCNQ1 subunit ofIKs

A KCNQ1 V205M missense mutation causes a high rate of long QT syndrome in a First Nations community of northern British Columbia: a community-based approach to understanding the impact

(2009) Laura Arbour et al.   GENETICS IN MEDICINE

Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation

(2009) Saumya Das et al.   HEART RHYTHM

Identification of an ethnic-specific variant (V207M) of the KCNQ1 cardiac potassium channel gene in sudden unexplained death and implications from a knock-in mouse model

(2009) Hajime Nishio et al.   INTERNATIONAL JOURNAL OF LEGAL MEDICINE

Common variants at ten loci influence QT interval duration in the QTGEN Study

(2009) Christopher Newton-Cheh et al.   NATURE GENETICS

Two Separate Interfaces between the Voltage Sensor and Pore Are Required for the Function of Voltage-Dependent K+ Channels

(2009) Seok-Yong Lee et al.   PLOS BIOLOGY

Macromolecular Modeling with Rosetta

(2008) Rhiju Das et al.   Annual Review of Biochemistry

Cardiomyopathic and Channelopathic Causes of Sudden Unexplained Death in Infants and Children

(2008) David J. Tester et al.   Annual Review of Medicine

Structure of KCNE1 and Implications for How It Modulates the KCNQ1 Potassium Channel†‡

(2008) Congbao Kang et al.   BIOCHEMISTRY

Structure, Function, and Modification of the Voltage Sensor in Voltage-Gated Ion Channels

(2008) Sara I. Börjesson et al.   CELL BIOCHEMISTRY AND BIOPHYSICS

Cooperative Interactions Between R531 and Acidic Residues in the Voltage Sensing Module of hERG1 Channels

(2008) David R. Piper et al.   CELLULAR PHYSIOLOGY AND BIOCHEMISTRY

Role of S3 and S4 Transmembrane Domain Charged Amino Acids in Channel Biogenesis and Gating of KCa2.3 and KCa3.1

(2008) Yajuan Gao et al.   JOURNAL OF BIOLOGICAL CHEMISTRY