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Circadian Regulation of Cardiac Arrhythmias and Electrophysiology.
Delisle BP, Prabhat A, Burgess DE, Ono M, Esser KA, Schroder EA. Delisle BP, et al. Among authors: burgess de. Circ Res. 2024 Mar 15;134(6):659-674. doi: 10.1161/CIRCRESAHA.123.323513. Epub 2024 Mar 14. Circ Res. 2024. PMID: 38484028 Review.
Chronic verapamil treatment remodels ICa,L in mouse ventricle.
Schroder E, Magyar J, Burgess D, Andres D, Satin J. Schroder E, et al. Am J Physiol Heart Circ Physiol. 2007 Apr;292(4):H1906-16. doi: 10.1152/ajpheart.00793.2006. Epub 2006 Dec 8. Am J Physiol Heart Circ Physiol. 2007. PMID: 17158651 Free article.
R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation.
Bartos DC, Duchatelet S, Burgess DE, Klug D, Denjoy I, Peat R, Lupoglazoff JM, Fressart V, Berthet M, Ackerman MJ, January CT, Guicheney P, Delisle BP. Bartos DC, et al. Among authors: burgess de. Heart Rhythm. 2011 Jan;8(1):48-55. doi: 10.1016/j.hrthm.2010.09.010. Epub 2010 Sep 17. Heart Rhythm. 2011. PMID: 20850564 Free PMC article.
A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation.
Bartos DC, Anderson JB, Bastiaenen R, Johnson JN, Gollob MH, Tester DJ, Burgess DE, Homfray T, Behr ER, Ackerman MJ, Guicheney P, Delisle BP. Bartos DC, et al. Among authors: burgess de. J Cardiovasc Electrophysiol. 2013 May;24(5):562-9. doi: 10.1111/jce.12068. Epub 2013 Jan 25. J Cardiovasc Electrophysiol. 2013. PMID: 23350853 Free PMC article.
A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation.
Bartos DC, Giudicessi JR, Tester DJ, Ackerman MJ, Ohno S, Horie M, Gollob MH, Burgess DE, Delisle BP. Bartos DC, et al. Among authors: burgess de. Heart Rhythm. 2014 Mar;11(3):459-68. doi: 10.1016/j.hrthm.2013.11.021. Epub 2013 Nov 21. Heart Rhythm. 2014. PMID: 24269949 Free PMC article.
64 results