Potassium channels in the heart: structure, function and regulation von Grandi, Eleonora, Sanguinetti, Michael C., Bartos, Daniel C., Bers, Donald M., Chen‐Izu, Ye, Chiamvimonvat, Nipavan, Colecraft, Henry M., Delisle, Brian P., Heijman, Jordi, Navedo, Manuel F., Noskov, Sergei, Proenza, Catherine, Vandenberg, Jamie I., Yarov‐Yarovoy, Vladimir

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The cardiomyocyte molecular clock, regulation of Scn5a, and arrhythmia susceptibility von Schroder, Elizabeth A, Lefta, Mellani, Zhang, Xiping, Bartos, Daniel C, Feng, Han-Zhong, Zhao, Yihua, Patwardhan, Abhijit, Jin, Jian-Ping, Esser, Karyn A, Delisle, Brian P

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The cardiomyocyte molecular clock regulates the circadian expression of Kcnh2 and contributes to ventricular repolarization von Schroder, Elizabeth A., PhD, Burgess, Don E., PhD, Zhang, Xiping, PhD, Lefta, Mellani, PhD, MD, Smith, Jennifer L., BS, Patwardhan, Abhijit, PhD, Bartos, Daniel C., PhD, Elayi, Claude S., MD, Esser, Karyn A., PhD, Delisle, Brian P., PhD

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Long QT Syndrome–Associated Mutations in Intrauterine Fetal Death von Crotti, Lia, Tester, David J, White, Wendy M, Bartos, Daniel C, Insolia, Roberto, Besana, Alessandra, Kunic, Jennifer D, Will, Melissa L, Velasco, Ellyn J, Bair, Jennifer J, Ghidoni, Alice, Cetin, Irene, Van Dyke, Daniel L, Wick, Myra J, Brost, Brian, Delisle, Brian P, Facchinetti, Fabio, George, Alfred L, Schwartz, Peter J, Ackerman, Michael J

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Depolarization of Cardiac Membrane Potential Synchronizes Calcium Sparks and Waves in Tissue von Sato, Daisuke, Bartos, Daniel C., Ginsburg, Kenneth S., Bers, Donald M.

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A KCNQ1 Mutation Causes a High Penetrance for Familial Atrial Fibrillation von BARTOS, DANIEL C., ANDERSON, JEFFREY B., BASTIAENEN, RACHEL, JOHNSON, JONATHAN N., GOLLOB, MICHAEL H., TESTER, DAVID J., BURGESS, DON E., HOMFRAY, TESSA, BEHR, ELIJAH R., ACKERMAN, MICHAEL J., GUICHENEY, PASCALE, DELISLE, BRIAN P.

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R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation von Bartos, Daniel C., BS, Duchatelet, Sabine, PhD, Burgess, Don E., PhD, Klug, Didier, MD, Denjoy, Isabelle, MD, Peat, Rachel, PhD, Lupoglazoff, Jean-Marc, MD, PhD, Fressart, Véronique, MD, PhD, Berthet, Myriam, BA, Ackerman, Michael J., MD, PhD, January, Craig T., MD, PhD, Guicheney, Pascale, PhD, Delisle, Brian P., PhD

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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 von Smith, Jennifer L, Reloj, Allison R, Nataraj, Parvathi S, Bartos, Daniel C, Schroder, Elizabeth A, Moss, Arthur J, Ohno, Seiko, Horie, Minoru, Anderson, Corey L, January, Craig T, Delisle, Brian P

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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 von Smith, Jennifer L, McBride, Christie M, Nataraj, Parvathi S, Bartos, Daniel C, January, Craig T, Delisle, Brian P

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The Promise and Peril of Precision Medicine von Ackerman, Jaeger P., BA, Bartos, Daniel C., PhD, Kapplinger, Jamie D., BS, Tester, David J., BS, Delisle, Brian P., PhD, Ackerman, Michael J., MD, PhD

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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 von Bartos, Daniel C., PhD, Giudicessi, John R., BA, Tester, David J., BS, Ackerman, Michael J., MD, PhD, Ohno, Seiko, MD, PhD, Horie, Minoru, MD, PhD, Gollob, Michael H., MD, Burgess, Don E., PhD, Delisle, Brian P., PhD

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The Promise and Peril of Precision Medicine: Phenotyping Still Matters Most von Ackerman, Jaeger P, Bartos, Daniel C, Kapplinger, Jamie D, Tester, David J, Delisle, Brian P, Ackerman, Michael J

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Quantitative analysis of the Ca2+‐dependent regulation of delayed rectifier K+ current IKs in rabbit ventricular myocytes von Bartos, Daniel C., Morotti, Stefano, Ginsburg, Kenneth S., Grandi, Eleonora, Bers, Donald M.

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High-Risk Long QT Syndrome Mutations in the Kv7.1 (KCNQ1) Pore Disrupt the Molecular Basis for Rapid K+ Permeation von Burgess, Don E, Bartos, Daniel C, Reloj, Allison R, Campbell, Kenneth S, Johnson, Jonathan N, Tester, David J, Ackerman, Michael J, Fressart, Véronique, Denjoy, Isabelle, Guicheney, Pascale, Moss, Arthur J, Ohno, Seiko, Horie, Minoru, Delisle, Brian P

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Mutation-Specific Differences in Kv7.1 ( KCNQ1 ) and Kv11.1 ( KCNH2 ) Channel Dysfunction and Long QT Syndrome Phenotypes von Kekenes-Huskey, Peter M, Burgess, Don E, Sun, Bin, Bartos, Daniel C, Rozmus, Ezekiel R, Anderson, Corey L, January, Craig T, Eckhardt, Lee L, Delisle, Brian P

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Quantitative analysis of the Ca 2+ -dependent regulation of delayed rectifier K + current I Ks in rabbit ventricular myocytes von Bartos, Daniel C, Morotti, Stefano, Ginsburg, Kenneth S, Grandi, Eleonora, Bers, Donald M

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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 von McBride, Christie M., Smith, Ashley M., Smith, Jennifer L., Reloj, Allison R., Velasco, Ellyn J., Powell, Jonathan, Elayi, Claude S., Bartos, Daniel C., Burgess, Don E., Delisle, Brian P.

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Diastolic Sodium Current in Cardiomyocytes Assessed with Lithium von Ginsburg, Kenneth S., Jiang, Yanyan, Bartos, Daniel C., Despa, Sanda I., Bers, Donald M.

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Quantitative analysis of the Ca super(2+)-dependent regulation of delayed rectifier K super(+) current I sub(Ks) in rabbit ventricular myocytes von Bartos, Daniel C, Morotti, Stefano, Ginsburg, Kenneth S, Grandi, Eleonora, Bers, Donald M

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Quantitative analysis of the Ca2+‐dependent regulation of delayed rectifier K+ current I Ks in rabbit ventricular myocytes von Bartos, Daniel C., Morotti, Stefano, Ginsburg, Kenneth S., Grandi, Eleonora, Bers, Donald M.

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