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Search life-sciences literature (45,103,589 articles, preprints and more)

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Mutation-Specific Differences in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) Channel Dysfunction and Long QT Syndrome Phenotypes.
Kekenes-Huskey PM, Burgess DE, Sun B, Bartos DC, Rozmus ER, Anderson CL, January CT, Eckhardt LL, Delisle BP
Int J Mol Sci, 23(13):7389, 02 Jul 2022
Cited by: 7 articles | PMID: 35806392 | PMCID: PMC9266926
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This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
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Quantitative analysis of the Ca²⁺ -dependent regulation of delayed rectifier K⁺ current I_Ks in rabbit ventricular myocytes.
Bartos DC, Morotti S, Ginsburg KS, Grandi E, Bers DM
J Physiol, 595(7):2253-2268, 28 Mar 2017
Cited by: 26 articles | PMID: 28008618
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Potassium channels in the heart: structure, function and regulation.
Grandi E, Sanguinetti MC, Bartos DC, Bers DM, Chen-Izu Y, Chiamvimonvat N, Colecraft HM, Delisle BP, Heijman J, Navedo MF, Noskov S, Proenza C, Vandenberg JI, Yarov-Yarovoy V
J Physiol, 595(7):2209-2228, 13 Nov 2016
Cited by: 51 articles | PMID: 27861921
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The Promise and Peril of Precision Medicine: Phenotyping Still Matters Most.
Ackerman JP, Bartos DC, Kapplinger JD, Tester DJ, Delisle BP, Ackerman MJ
Mayo Clin Proc, S0025-6196(16)30463-3, 08 Oct 2016
Cited by: 43 articles | PMID: 27810088 | PMCID: PMC6365209
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Ion Channels in the Heart.
Bartos DC, Grandi E, Ripplinger CM
Compr Physiol, 5(3):1423-1464, 01 Jul 2015
Cited by: 90 articles | PMID: 26140724 | PMCID: PMC4516287
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The cardiomyocyte molecular clock regulates the circadian expression of Kcnh2 and contributes to ventricular repolarization.
Schroder EA, Burgess DE, Zhang X, Lefta M, Smith JL, Patwardhan A, Bartos DC, Elayi CS, Esser KA, Delisle BP
Heart Rhythm, 12(6):1306-1314, 19 Feb 2015
Cited by: 52 articles | PMID: 25701773 | PMCID: PMC4541807
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Depolarization of cardiac membrane potential synchronizes calcium sparks and waves in tissue.
Sato D, Bartos DC, Ginsburg KS, Bers DM
Biophys J, 107(6):1313-1317, 01 Sep 2014
Cited by: 14 articles | PMID: 25229139 | PMCID: PMC4167289
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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
Heart Rhythm, 11(3):459-468, 21 Nov 2013
Cited by: 16 articles | PMID: 24269949 | PMCID: PMC4333640
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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
Am J Physiol Cell Physiol, 305(9):C919-30, 17 Jul 2013
Cited by: 24 articles | PMID: 23864605 | PMCID: PMC4042535
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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
J Membr Biol, 246(5):355-364, 02 Apr 2013
Cited by: 10 articles | PMID: 23546015 | PMCID: PMC3706098
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Long QT syndrome-associated mutations in intrauterine fetal death.
Crotti L, Tester DJ, White WM, Bartos DC, Insolia R, Besana A, Kunic JD, Will ML, Velasco EJ, Bair JJ, Ghidoni A, Cetin I, Van Dyke DL, Wick MJ, Brost B, Delisle BP, Facchinetti F, George AL, Schwartz PJ, Ackerman MJ
JAMA, 309(14):1473-1482, 01 Apr 2013
Cited by: 78 articles | PMID: 23571586 | PMCID: PMC3852902
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The cardiomyocyte molecular clock, regulation of Scn5a, and arrhythmia susceptibility.
Schroder EA, Lefta M, Zhang X, Bartos DC, Feng HZ, Zhao Y, Patwardhan A, Jin JP, Esser KA, Delisle BP
Am J Physiol Cell Physiol, 304(10):C954-65, 30 Jan 2013
Cited by: 91 articles | PMID: 23364267 | PMCID: PMC3651636
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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
J Cardiovasc Electrophysiol, 24(5):562-569, 25 Jan 2013
Cited by: 34 articles | PMID: 23350853 | PMCID: PMC3640728
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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
Biochemistry, 51(45):9076-9085, 02 Nov 2012
Cited by: 14 articles | PMID: 23092362 | PMCID: PMC3613984
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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
Am J Physiol Cell Physiol, 301(1):C75-85, 13 Apr 2011
Cited by: 22 articles | PMID: 21490315 | PMCID: PMC3129823
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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
Heart Rhythm, 8(1):48-55, 17 Sep 2010
Cited by: 47 articles | PMID: 20850564 | PMCID: PMC3706092
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1-16 of 16 results

Search life-sciences literature (45,103,589 articles, preprints and more)

Search results

Mutation-Specific Differences in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) Channel Dysfunction and Long QT Syndrome Phenotypes.

Quantitative analysis of the Ca²⁺ -dependent regulation of delayed rectifier K⁺ current I_Ks in rabbit ventricular myocytes.

Potassium channels in the heart: structure, function and regulation.

The Promise and Peril of Precision Medicine: Phenotyping Still Matters Most.

Ion Channels in the Heart.

The cardiomyocyte molecular clock regulates the circadian expression of Kcnh2 and contributes to ventricular repolarization.

Depolarization of cardiac membrane potential synchronizes calcium sparks and waves in tissue.

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.

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

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

Long QT syndrome-associated mutations in intrauterine fetal death.

The cardiomyocyte molecular clock, regulation of Scn5a, and arrhythmia susceptibility.

A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation.

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

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

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation.

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