Year |
Citation |
Score |
2022 |
Kekenes-Huskey PM, Burgess DE, Sun B, Bartos DC, Rozmus ER, Anderson CL, January CT, Eckhardt LL, Delisle BP. Mutation-Specific Differences in Kv7.1 () and Kv11.1 () Channel Dysfunction and Long QT Syndrome Phenotypes. International Journal of Molecular Sciences. 23. PMID 35806392 DOI: 10.3390/ijms23137389 |
0.753 |
|
2017 |
Liao Z, Ginsburg KS, Bartos DC, Jiang Y, Despa S, Bers DM. High Diastolic Sodium Influx in Heart Failure has Drug-Sensitivities Like Late Sodium Current, but Produces Inward Current at Diastolic Potentials Biophysical Journal. 112: 333a. DOI: 10.1016/J.Bpj.2016.11.1802 |
0.37 |
|
2016 |
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. Potassium channels in the heart: structure, function and regulation. The Journal of Physiology. PMID 27861921 DOI: 10.1113/Jp272864 |
0.671 |
|
2016 |
Ackerman JP, Bartos DC, Kapplinger JD, Tester DJ, Delisle BP, Ackerman MJ. The Promise and Peril of Precision Medicine: Phenotyping Still Matters Most. Mayo Clinic Proceedings. PMID 27810088 DOI: 10.1016/j.mayocp.2016.08.008 |
0.587 |
|
2015 |
Bartos DC, Grandi E, Ripplinger CM. Ion Channels in the Heart. Comprehensive Physiology. 5: 1423-64. PMID 26140724 DOI: 10.1002/Cphy.C140069 |
0.337 |
|
2015 |
Schroder EA, Burgess DE, Zhang X, Lefta M, Smith JL, Patwardhan A, Bartos DC, Elayi CS, Esser KA, Delisle BP. The cardiomyocyte molecular clock regulates the circadian expression of Kcnh2 and contributes to ventricular repolarization. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 12: 1306-14. PMID 25701773 DOI: 10.1016/J.Hrthm.2015.02.019 |
0.6 |
|
2014 |
Bartos DC, Giudicessi JR, Tester DJ, Ackerman MJ, Ohno S, Horie M, Gollob MH, Burgess DE, Delisle BP. 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. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 459-68. PMID 24269949 DOI: 10.1016/J.Hrthm.2013.11.021 |
0.734 |
|
2013 |
Smith JL, Reloj AR, Nataraj PS, Bartos DC, Schroder EA, Moss AJ, Ohno S, Horie M, Anderson CL, January CT, Delisle BP. Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulum. American Journal of Physiology. Cell Physiology. 305: C919-30. PMID 23864605 DOI: 10.1152/Ajpcell.00406.2012 |
0.763 |
|
2013 |
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, et al. Long QT syndrome-associated mutations in intrauterine fetal death. Jama. 309: 1473-82. PMID 23571586 DOI: 10.1001/Jama.2013.3219 |
0.624 |
|
2013 |
McBride CM, Smith AM, Smith JL, Reloj AR, Velasco EJ, Powell J, Elayi CS, Bartos DC, Burgess DE, Delisle BP. Mechanistic basis for type 2 long QT syndrome caused by KCNH2 mutations that disrupt conserved arginine residues in the voltage sensor. The Journal of Membrane Biology. 246: 355-64. PMID 23546015 DOI: 10.1007/S00232-013-9539-6 |
0.748 |
|
2013 |
Schroder EA, Lefta M, Zhang X, Bartos DC, Feng HZ, Zhao Y, Patwardhan A, Jin JP, Esser KA, Delisle BP. The cardiomyocyte molecular clock, regulation of Scn5a, and arrhythmia susceptibility. American Journal of Physiology. Cell Physiology. 304: C954-65. PMID 23364267 DOI: 10.1152/Ajpcell.00383.2012 |
0.645 |
|
2013 |
Bartos DC, Anderson JB, Bastiaenen R, Johnson JN, Gollob MH, Tester DJ, Burgess DE, Homfray T, Behr ER, Ackerman MJ, Guicheney P, Delisle BP. A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation. Journal of Cardiovascular Electrophysiology. 24: 562-9. PMID 23350853 DOI: 10.1111/Jce.12068 |
0.626 |
|
2013 |
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 B. Malignant Long QT Syndrome KCNQ1 Mutations in the Pore Disrupt the Molecular Basis for Rapid K+ Permeation Biophysical Journal. 104: 268a. DOI: 10.1016/J.Bpj.2012.11.1503 |
0.729 |
|
2013 |
Bartos DC, Burgess DE, Reloj AR, Giudicessi J, Tester DJ, Ackerman MJ, Delisle BP. A Mutation in the Voltage-Sensor of Kv7.1 Prevents PKA Activation of IKs to Elicit Concealed Type 1 Long QT Syndrome during Stress Biophysical Journal. 104: 267a-268a. DOI: 10.1016/J.Bpj.2012.11.1502 |
0.701 |
|
2013 |
Smith JL, Reloj AR, Nataraj PS, Bartos DC, January CT, Delisle BP. Cellular Mechanism for the Pharmacological Correction of hERG Mutations Linked to the Long QT Syndrome Biophysical Journal. 104: 266a. DOI: 10.1016/J.Bpj.2012.11.1496 |
0.78 |
|
2012 |
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. High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation. Biochemistry. 51: 9076-85. PMID 23092362 DOI: 10.1021/Bi3009449 |
0.735 |
|
2012 |
Bartos D, Giudicessi J, Tester D, Ackerman M, Delisle B. Protracted QTc Prolongation following Treadmill Testing Identifies a Type 1 Long QT Mutation that is Resistant to PKA Activation Heart Rhythm. 9: 1916. DOI: 10.1016/J.Hrthm.2012.09.109 |
0.703 |
|
2011 |
Smith JL, McBride CM, Nataraj PS, Bartos DC, January CT, Delisle BP. Trafficking-deficient hERG K⺠channels linked to long QT syndrome are regulated by a microtubule-dependent quality control compartment in the ER. American Journal of Physiology. Cell Physiology. 301: C75-85. PMID 21490315 DOI: 10.1152/Ajpcell.00494.2010 |
0.771 |
|
2011 |
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. R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 8: 48-55. PMID 20850564 DOI: 10.1016/J.Hrthm.2010.09.010 |
0.769 |
|
2011 |
Burgess D, Bartos D, Schmidt E, Johnson J, Tester D, Ohno S, Horie M, Ackerman M, Delisle B. Atomic-Scale Modeling Predicts a Mechanism for Long QT Type 1 Dysfunction Associated With Pore Mutations Heart Rhythm. 8: 1821-1822. DOI: 10.1016/J.Hrthm.2011.09.034 |
0.642 |
|
2011 |
Burgess DE, Bartos DC, Schmidt ES, Delisle B. A Computational Model for the Effect that a KCNQ1 Mutation Linked to Jervell and Lange-Nielson Syndrome has on Human Cardiac Action Potential Duration Biophysical Journal. 100: 436a-437a. DOI: 10.1016/J.Bpj.2010.12.2573 |
0.691 |
|
2011 |
Bartos DC, Schmidt ES, Burgess DE, Delisle BP. A Spectrum of Functional Phenotypes Associated with LQT1 Mutations Identified in Patients with Early-Onset Atrial Fibrillation Biophysical Journal. 100: 427a. DOI: 10.1016/J.Bpj.2010.12.2524 |
0.734 |
|
2010 |
Smith JL, McBride CM, Bartos DC, January CT, Delisle B. Microtubule Dependent Mechanisms Regulate the Trafficking Deficient Phenotype of hERG Mutations Linked to Long QT Syndrome Biophysical Journal. 98: 118a-119a. DOI: 10.1016/J.Bpj.2009.12.647 |
0.783 |
|
2009 |
Smith JL, Bartos DC, January CT, Delisle BP. Trafficking-deficient LQT2 Mutations Disrupt Different Steps of hERG Channel Transport Biophysical Journal. 96: 190a. DOI: 10.1016/J.Bpj.2008.12.894 |
0.778 |
|
2009 |
Bartos DC, Smith JL, Kilby JA, January CT, Delisle BP. Wild-Type KCNQ1 Modulates the Gating of the LQT1 Mutation R231C Biophysical Journal. 96: 380a. DOI: 10.1016/J.Bpj.2008.12.2847 |
0.773 |
|
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