Cardiac Arrhythmias - New Considerations by F. Breijo-Marquez

By F. Breijo-Marquez

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Genetically defined therapy of inherited longQT syndrome. Correction of abnormal repolarization by potassium. Circulation 94(5): 1018-1022. , Dagradi, F. & Schwartz, P. J. (2008). Congenital long QT syndrome. Orphanet journal of rare diseases 3: 18. , Fishman, G. I. & McDonald, T. V. (2000). Cyclic AMP regulates the HERG K(+) channel by dual pathways. Curr Biol 10(11): 671-674. , Vincent, G. , Green, E. D. & Keating, M. T. (1995). A Molecular Basis for Cardiac Arrhythmia: HERG Mutations Cause Long QT Syndrome.

Proc Natl Acad Sci U S A 98(5): 2526-2531. , Le Marec, H. & Escande, D. (1998). Adult KCNE1knockout mice exhibit a mild cardiac cellular phenotype. Biochem Biophys Res Commun 251(3): 806-810. , Bian, J. & McDonald, T. V. (2009). PKA phosphorylation of HERG protein regulates the rate of channel synthesis. Am J Physiol Heart Circ Physiol 296(5): H1244-1254. , Wu, Z. , Bian, J. S. & McDonald, T. V. (2010). Post-transcriptional control of human ether-a-go-go-related gene potassium channel protein by alpha-adrenergic receptor stimulation.

Bian, J. S. & McDonald, T. V. (2010). Post-transcriptional control of human ether-a-go-go-related gene potassium channel protein by alpha-adrenergic receptor stimulation. Mol Pharmacol 78(2): 186197. , Um, S. , Walsh, C. , Tang, Y. & McDonald, T. V. (2011). A Dual Mechanism for IKs Current Reduction bu the Pathogenic Mutation KCNQ1-S277L. Pacing Clin Electrophysiol In Press. Cheng, S. , Gregory, R. , Souza, D. , White, G. , O'Riordan, C. R. & Smith, A. E. (1990). Defective intracellular transport and processing of CFTR is the molecular basis of most Cystic Fibrosis.

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