Use of Mutant-Specific Ion Channel Characteristics for Risk Stratification of Long QT Syndrome Patients

Protein kinase A-dependent phosphorylation of ryanodine receptors increases Ca2+ leak in mouse heart

(2009) Satoshi Morimoto et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

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

Mutations in Conserved Amino Acids in the KCNQ1 Channel and Risk of Cardiac Events in Type-1 Long-QT Syndrome

(2009) CHRISTIAN JONS et al.   JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY

PKC activation and PIP2 depletion underlie biphasic regulation of IKs by Gq-coupled receptors

(2009) Alessandra Matavel et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

Modeling of the adrenergic response of the human IKs current (hKCNQ1/hKCNE1) stably expressed in HEK-293 cells

(2008) John P. Imredy et al.   AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY

Risk Factors for Aborted Cardiac Arrest and Sudden Cardiac Death in Children With the Congenital Long-QT Syndrome

(2008) Ilan Goldenberg et al.   CIRCULATION

Mechanisms by which atrial fibrillation-associated mutations in the S1 domain of KCNQ1 slow deactivation of IKs channels

(2008) Lioara Restier et al.   JOURNAL OF PHYSIOLOGY-LONDON

Physiological modulation of voltage-dependent inactivation in the cardiac muscle L-type calcium channel: A modelling study

(2007) Ian Findlay et al.   PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY