Allison R. Reloj

Pharmacological correction of long QT-linked mutations in <i>KCNH2</i> (<i>hERG</i>) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulum

Jennifer L. Smith, Allison R. Reloj, Parvathi Nataraj et al. · American Journal of Physiology-Cell Physiology · 2013 · 34 citations · Full text

Natural Sciences, Pharmacology, Physiology +17

Mechanistic Basis for Type 2 Long QT Syndrome Caused by KCNH2 Mutations that Disrupt Conserved Arginine Residues in the Voltage Sensor

Christie M. McBride, Ashley M. Smith, Jennifer L. Smith et al. · The Journal of Membrane Biology · 2013 · 23 citations

Natural Sciences, Genetics, Molecular Genetics +17

High-Risk Long QT Syndrome Mutations in the Kv7.1 (KCNQ1) Pore Disrupt the Molecular Basis for Rapid K⁺ Permeation

Don E. Burgess, Daniel C. Bartos, Allison R. Reloj et al. · Biochemistry · 2012 · 16 citations

Life Sciences, Cardiology, Genetics +17