Delisle BP - Search Results

1

A molecular mechanism for adrenergic-induced long QT syndrome.

Wu J, Naiki N, Ding WG, Ohno S, Kato K, Zang WJ, Delisle BP, Matsuura H, Horie M. Wu J, et al. Among authors: delisle bp. J Am Coll Cardiol. 2014 Mar 4;63(8):819-27. doi: 10.1016/j.jacc.2013.08.1648. Epub 2013 Oct 30. J Am Coll Cardiol. 2014. PMID: 24184248 Free article.

2

New Insights into Cardiac Ion Channel Regulation 2.0.

Delisle BP, Aromolaran AS. Delisle BP, et al. Int J Mol Sci. 2023 Mar 5;24(5):4999. doi: 10.3390/ijms24054999. Int J Mol Sci. 2023. PMID: 36902430 Free PMC article.

3

A stepwise external cardioversion protocol for atrial fibrillation to maximize acute success rate.

Darrat Y, Leung S, Elayi L, Parrott K, Ogunbayo G, Kotter J, Sorrell V, Gupta V, Anaya P, Morales G, Catanzarro J, Delisle B, Elayi CS. Darrat Y, et al. Europace. 2023 Mar 30;25(3):828-834. doi: 10.1093/europace/euad009. Europace. 2023. PMID: 36748366 Free PMC article.

4

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: delisle bp. 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.

5

Trafficking-deficient hERG K⁺ channels linked to long QT syndrome are regulated by a microtubule-dependent quality control compartment in the ER.

Smith JL, McBride CM, Nataraj PS, Bartos DC, January CT, Delisle BP. Smith JL, et al. Among authors: delisle bp. Am J Physiol Cell Physiol. 2011 Jul;301(1):C75-85. doi: 10.1152/ajpcell.00494.2010. Epub 2011 Apr 13. Am J Physiol Cell Physiol. 2011. PMID: 21490315 Free PMC article.

6

High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation.

Burgess DE, Bartos DC, Reloj AR, Campbell KS, Johnson JN, Tester DJ, Ackerman MJ, Fressart V, Denjoy I, Guicheney P, Moss AJ, Ohno S, Horie M, Delisle BP. Burgess DE, et al. Among authors: delisle bp. Biochemistry. 2012 Nov 13;51(45):9076-85. doi: 10.1021/bi3009449. Epub 2012 Nov 2. Biochemistry. 2012. PMID: 23092362 Free PMC article.

7

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: delisle bp. 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.

8

Mechanistic basis for type 2 long QT syndrome caused by KCNH2 mutations that disrupt conserved arginine residues in the voltage sensor.

McBride CM, Smith AM, Smith JL, Reloj AR, Velasco EJ, Powell J, Elayi CS, Bartos DC, Burgess DE, Delisle BP. McBride CM, et al. Among authors: delisle bp. J Membr Biol. 2013 May;246(5):355-64. doi: 10.1007/s00232-013-9539-6. Epub 2013 Apr 2. J Membr Biol. 2013. PMID: 23546015 Free PMC article.

9

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

Smith JL, Reloj AR, Nataraj PS, Bartos DC, Schroder EA, Moss AJ, Ohno S, Horie M, Anderson CL, January CT, Delisle BP. Smith JL, et al. Among authors: delisle bp. Am J Physiol Cell Physiol. 2013 Nov 1;305(9):C919-30. doi: 10.1152/ajpcell.00406.2012. Epub 2013 Jul 17. Am J Physiol Cell Physiol. 2013. PMID: 23864605 Free PMC article.

10

A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels.

Hasegawa K, Ohno S, Ashihara T, Itoh H, Ding WG, Toyoda F, Makiyama T, Aoki H, Nakamura Y, Delisle BP, Matsuura H, Horie M. Hasegawa K, et al. Among authors: delisle bp. Heart Rhythm. 2014 Jan;11(1):67-75. doi: 10.1016/j.hrthm.2013.09.073. Epub 2013 Oct 1. Heart Rhythm. 2014. PMID: 24096004

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