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Circulation|July 19, 2019
Disruption of Ca<sup>2+</sup><sub>i</sub> Homeostasis and Connexin 43 Hemichannel Function in the Right Ventricle Precedes Overt Arrhythmogenic Cardiomyopathy in Plakophilin-2-Deficient MiceJoon-Chul Kim, Marta Pérez-Hernández, Francisco J Alvarado, et al.
Circulation Research|February 27, 2013
Super-resolution scanning patch clamp reveals clustering of functional ion channels in adult ventricular myocyteAnamika Bhargava, Xianming Lin, Pavel Novak, et al.
Circulation Research|August 4, 2007
Connexin43 remodeling caused by inhibition of plakophilin-2 expression in cardiac cellsEva M Oxford, Hassan Musa, Karen Maass, et al.
The Journal of Biological Chemistry|October 20, 2004
Structural changes in the carboxyl terminus of the gap junction protein connexin43 indicates signaling between binding domains for c-Src and zonula occludens-1Paul L Sorgen, Heather S Duffy, Prangya Sahoo, et al.
Cell Communication & Adhesion|December 19, 2003
Kinetics of protein-protein interactions of connexins: use of enzyme linked sorbent assaysHeather S Duffy, Phyllis O'Donnell, Wanda Coombs, et al.
Physiological Reviews|February 2, 2023
The intercalated disc: a unique organelle for electromechanical synchrony in cardiomyocytesMorten S Nielsen, Chantal J M van Opbergen, Toon A B van Veen, et al.
Circulation. Arrhythmia and Electrophysiology|June 16, 2020
Single-Molecule Localization of the Cardiac Voltage-Gated Sodium Channel Reveals Different Modes of Reorganization at Cardiomyocyte Membrane DomainsSarah H Vermij, Jean-Sébastien Rougier, Esperanza Agulló-Pascual, et al.
Circulation Research|July 31, 2004
Modifications in the biophysical properties of connexin43 channels by a peptide of the cytoplasmic loop regionAkiko Seki, Heather S Duffy, Wanda Coombs, et al.
Frontiers in Physiology|January 11, 2020
Mitochondrial Dysfunction as Substrate for Arrhythmogenic Cardiomyopathy: A Search for New Disease MechanismsChantal J M van Opbergen, Lyanne den Braven, Mario Delmar, et al.
Circulation Research|May 10, 2005
Functional characterization of connexin43 mutations found in patients with oculodentodigital dysplasiaJunko Shibayama, William Paznekas, Akiko Seki, et al.
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