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Orphanet Journal of Rare Diseases|November 23, 2024
A Natural History Study of Timothy SyndromeKatherine W Timothy, Rosemary Bauer, Kerry A Larkin, et al.
Circulation. Cardiovascular Genetics|April 19, 2011
The S1103Y cardiac sodium channel variant is associated with implantable cardioverter-defibrillator events in blacks with heart failure and reduced ejection fractionAlbert Y Sun, Jason I Koontz, Svati H Shah, et al.
The Journal of Clinical Investigation|August 29, 2018
The two-pore domain potassium channel TREK-1 mediates cardiac fibrosis and diastolic dysfunctionDennis M Abraham, Teresa E Lee, Lewis J Watson, et al.
The Journal of Clinical Investigation|April 4, 2013
Calcium influx through L-type CaV1.2 Ca2+ channels regulates mandibular developmentKapil V Ramachandran, Jessica A Hennessey, Adam S Barnett, et al.
Heart Rhythm|October 8, 2013
FGF12 is a candidate Brugada syndrome locusJessica A Hennessey, Cherisse A Marcou, Chuan Wang, et al.
American Heart Journal|October 27, 2009
Rationale and design of the Duke Electrophysiology Genetic and Genomic Studies (EPGEN) biorepositoryJason I Koontz, Daniel Haithcock, Valerie Cumbea, et al.
Plos Genetics|December 14, 2012
Dissection of a quantitative trait locus for PR interval duration identifies Tnni3k as a novel modulator of cardiac conductionElisabeth M Lodder, Brendon P Scicluna, Annalisa Milano, et al.
JCI Insight|December 5, 2017
Increased Ca2+ signaling through CaV1.2 promotes bone formation and prevents estrogen deficiency-induced bone lossChike Cao, Yinshi Ren, Adam S Barnett, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 2, 2015
STIM1-Ca2+ signaling modulates automaticity of the mouse sinoatrial nodeHengtao Zhang, Albert Y Sun, Jong J Kim, et al.
The Journal of Clinical Investigation|November 14, 2018
Cardiac CaV1.2 channels require β subunits for β-adrenergic-mediated modulation but not traffickingLin Yang, Alexander Katchman, Jared Kushner, et al.
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