Mutation in glycerol-3-phosphate dehydrogenase 1-like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias von LONDON, Barry, MICHALEC, Michael, BATY, Catherine J, LAGANA, Stephen, ALEONG, Ryan, GUTMANN, Rebecca, ACKERMAN, Michael J, MCNAMARA, Dennis M, WEISS, Raul, DUDLEY, Samuel C, MEHDI, Haider, XIAODONG ZHU, KERCHNER, Laurie, SANYAL, Shamarendra, VISWANATHAN, Prakash C, PFAHNL, Arnold E, SHANG, Lijuan L, MADHUSUDANAN, Mohan

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A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation von Viswanathan, Prakash C, Benson, D Woodrow, Balser, Jeffrey R

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Functional Interactions between Distinct Sodium Channel Cytoplasmic Domains through the Action of Calmodulin von Potet, Franck, Chagot, Benjamin, Anghelescu, Mircea, Viswanathan, Prakash C., Stepanovic, Svetlana Z., Kupershmidt, Sabina, Chazin, Walter J., Balser, Jeffrey R.

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Two Distinct Congenital Arrhythmias Evoked by a Multidysfunctional Na+ Channel von Veldkamp, Marieke W, Viswanathan, Prakash C, Bezzina, Connie, Baartscheer, Antonius, Wilde, Arthur A. M, Balser, Jeffrey R

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Oxidative Mediated Lipid Peroxidation Recapitulates Proarrhythmic Effects on Cardiac Sodium Channels von Fukuda, Koji, Davies, Sean S, Nakajima, Tadashi, Ong, Boon-Hooi, Kupershmidt, Sabina, Fessel, Joshua, Amarnath, Venkataraman, Anderson, Mark E, Boyden, Penelope A, Viswanathan, Prakash C, Roberts, L Jackson, Balser, Jeffrey R

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Cellular arrhythmogenic effects of congenital and acquired long-QT syndrome in the heterogeneous myocardium von VISWANATHAN, P. C, RUDY, Y

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Genetics of acquired long QT syndrome von Roden, Dan M, Viswanathan, Prakash C

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A sodium channel pore mutation causing Brugada syndrome von Pfahnl, Arnold E., MD, PhD, Viswanathan, Prakash C., PhD, Weiss, Raul, MD, Shang, Lijuan L., PhD, Sanyal, Shamarendra, MD, PhD, Shusterman, Vladimir, MD, PhD, Kornblit, Cari, BS, London, Barry, MD, PhD, Dudley, Samuel C., MD, PhD

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Sex, Age, and Regional Differences in L-Type Calcium Current Are Important Determinants of Arrhythmia Phenotype in Rabbit Hearts With Drug-Induced Long QT Type 2 von Sims, Carl, Reisenweber, Steven, Viswanathan, Prakash C, Choi, Bum-Rak, Walker, William H, Salama, Guy

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Effects of I(Kr) and I(Ks) heterogeneity on action potential duration and its rate dependence: A simulation study von Viswanathan, Prakash C, Shaw, Robin M, Rudy, Yoram

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Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome von Ficker, Eckhard, Thomas, Dierk, Viswanathan, Prakash C, Dennis, Adrienne T, Priori, Silvia G, Napolitano, Carlo, Memmi, Mirella, Wible, Barbara A, Kaufman, Elizabeth S, Iyengar, Sudha, Schwartz, Peter J, Rudy, Yoram, Brown, Arthur M

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Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes von Yang, Ping, Kanki, Hideaki, Drolet, Benoit, Yang, Tao, Wei, Jian, Viswanathan, Prakash C, Hohnloser, Stefan H, Shimizu, Wataru, Schwartz, Peter J, Stanton, Marshall, Murray, Katherine T, Norris, Kris, George, Jr, Alfred L, Roden, Dan M

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Compound-specific Na+ channel pore conformational changes induced by local anaesthetics von Fukuda, Koji, Nakajima, Tadashi, Viswanathan, Prakash C., Balser, Jeffrey R.

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Recreating an artificial biological pacemaker: Insights from a theoretical model von Viswanathan, Prakash C., Coles, James A., Sharma, Vinod, Sigg, Daniel C.

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A sodium-channel mutation causes isolated cardiac conduction disease von Balser, Jeffrey R, Tan, Hanno L, Bink-Boelkens, Margreet T. E, Bezzina, Connie R, Viswanathan, Prakash C, Beaufort-Krol, Gertie C. M, van Tintelen, Peter J, van den Berg, Maarten P, Wilde, Arthur A. M

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Clinical, genetic, and biophysical characterization of SCN5A mutations associated with atrioventricular conduction block von WANG, Dao W, VISWANATHAN, Prakash C, BALSER, Jeffrey R, GEORGE, Alfred L, BENSON, D. Woodrow

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Quantitation of protein kinase A-mediated trafficking of cardiac sodium channels in living cells von HALLAQ, Haifa, ZHENJIANG YANG, VISWANATHAN, Prakash C, FUKUDA, Koji, WANGZHEN SHEN, WANG, Dao W, WELLS, K. Sam, JINGSONG ZHOU, JIANXUN YI, MURRAY, Katherine T

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Inherited Sodium Channelopathies A Continuum of Channel Dysfunction von Viswanathan, Prakash C, Balser, Jeffrey R

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New mechanism contributing to drug-induced arrhythmia : Rescue of a misprocessed LQT3 mutant von KAI LIU, TAO YANG, VISWANATHAN, Prakash C, RODEN, Dan M

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HERG Is Protected from Pharmacological Block by α-1,2-Glucosyltransferase Function von Nakajima, Tadashi, Hayashi, Kenshi, Viswanathan, Prakash C., Kim, Min-Young, Anghelescu, Mircea, Barksdale, Kate A., Shuai, Wen, Balser, Jeffrey R., Kupershmidt, Sabina

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