Molecular Pathophysiology of Congenital Long QT Syndrome von Bohnen, M S, Peng, G, Robey, S H, Terrenoire, C, Iyer, V, Sampson, K J, Kass, R S

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Effects of flecainide in patients with new SCN5A mutation: Mutation-specific therapy for long-QT syndrome? von BENHORIN, J, TAUB, R, GOLDMIT, M, KEREM, B, KASS, R. S, WINDMAN, I, MEDINA, A

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Proposed Diagnostic Criteria for the Brugada Syndrome von Wilde, A.A.M., Antzelevitch, C., Borggrefe, M., Brugada, J., Brugada, R., Brugada, P., Corrado, D., Hauer, R.N.W., Kass, R.S., Nademanee, K., Priori, S.G., Towbin, J.A.

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Ion channels The voltage-sensor quartet von Bankston, J. R, Kass, R. S

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Dependence of the GABAA receptor gating kinetics on the alpha-subunit isoform: implications for structure-function relations and synaptic transmission von Gingrich, K J, Roberts, W A, Kass, R S

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Arrhythmogenic mechanism of an LQT-3 mutation of the human heart Na+ channel α-subunit: A computational analysis von WEHRENS, X. H. T, ABRIEL, H, CABO, C, BENHORIN, J, KASS, R. S

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Developmental Changes in Ionic Channel Activity in the Embryonic Murine Heart von Davies, M.P, Doevendans, P, Kubalak, S, Chien, K.R

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Molecular pharmacology of the sodium channel mutation D1790G linked to the long-QT syndrome von ABRIEL, H, WEHRENS, X. H. T, BENHORIN, J, KEREM, B, KASS, R. S

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A computational model of Purkinje fibre single cell electrophysiology: implications for the long QT syndrome von Sampson, K. J., Iyer, V., Marks, A. R., Kass, R. S.

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Novel Arrhythmogenic Mechanism Revealed by a Long-QT Syndrome Mutation in the Cardiac Na+ Channel von Abriel, Hugues, Cabo, Candido, Wehrens, Xander H.T, Rivolta, Ilaria, Motoike, Howard K, Memmi, Mirella, Napolitano, Carlo, Priori, Silvia G, Kass, Robert S

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Lidocaine block of LQT-3 mutant human Na+ channels von AN, R.-H, BANGALORE, R, ROSERO, S. Z, KASS, R. S

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Requirement of a Macromolecular Signaling Complex for β Adrenergic Receptor Modulation of the KCNQ1-KCNE1 Potassium Channel von Marx, Steven O., Kurokawa, Junko, Reiken, Steven, Motoike, Howard, D'Armiento, Jeanine, Marks, Andrew R., Kass, Robert S.

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Stimulation of protein kinase C inhibits bursting in disease-linked mutant human cardiac sodium channels von TATEYAMA, M, KUROKAWA, J, TERRENOIRE, C, RIVOLTA, I, KASS, R. S

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Subunit-Dependent Modulation of Recombinant L-Type Calcium Channels: Molecular Basis for Dihydropyridine Tissue Selectivity von Welling, A, Kwan, Y W, Bosse, E, Flockerzi, V, Hofmann, F, Kass, R S

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Voltage-Dependent Block of Calcium Channel Current in the Calf Cardiac Purkinje Fiber by Dihydropyridine Calcium Channel Antagonists von Sanguinetti, Michael C, Kass, Robert S

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Variant of SCN5A Sodium Channel Implicated in Risk of Cardiac Arrhythmia von Splawski, Igor, Timothy, Katherine W., Tateyama, Michihiro, Clancy, Colleen E., Malhotra, Alka, Beggs, Alan H., Cappuccio, Francesco P., Sagnella, Giuseppe A., Kass, Robert S., Keating, Mark T.

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Diastolic transient inward current in long QT syndrome type 3 is caused by Ca2+ overload and inhibited by ranolazine von Lindegger, N, Hagen, B.M, Marks, A.R, Lederer, W.J, Kass, R.S

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Requirement of Subunit Expression for cAMP-Mediated Regulation of a Heart Potassium Channel von Kurokawa, Junko, Chen, Lei, Kass, Robert S.

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Structural Effects of an LQT-3 Mutation on Heart Na + Channel Gating von Tateyama, M., Liu, H., Yang, A-S., Cormier, J.W., Kass, R.S.

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Expression of a Minimal K+ Channel Protein in Mammalian Cells and Immunolocalization in Guinea Pig Heart von Freeman, Lisa C, Kass, Robert S

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