The Cherenkov Telescope Array production system for Monte Carlo simulations and analysis von Arrabito, L, Bernloehr, K, Bregeon, J, Cumani, P, Hassan, T, Haupt, A, Maier, G, Moralejo, A, Neyroud, N, Stagni, F, Tsaregorodtsev, A

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Study of the cardiac sodium channel in a mouse model of Scn5a haploinsufficiency towards a novel approach of therapy von Ferrand, M, Mougenot, N, Laporte, P L, Leclerc, A, Algalarrondo, V, Extramiana, F, Charpentier, F, Neyroud, N

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Notched T waves on Holter recordings enhance detection of patients with LQT2 (HERG) mutations von LUPOGLAZOFF, J. M, DENJOY, I, MAILLARD, G, COUMEL, P, GUICHENEY, P, BERTHET, M, NEYROUD, N, DEMAY, L, RICHARD, P, HAINQUE, B, VAKSMANN, G, KLUG, D, LEENHARDT, A

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Different Atrial and Ventricular Resting Membrane Potentials May Explain the Phenotypical Variability of a Truncating SCN5A Mutation von Clatot, J, Ziyadeh-Isleem, A, Duchatelet, S, Gandjbakhch, E, Denjoy, I, Hidden-Lucet, F, Hatem, S.N, Coulombe, A, Neyroud, N, Deschênes, I, Guicheney, P

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Dominant-Negative Suppression of Nav1.5 Channel by N-Terminal SCN5A Mutations in Brugada Syndrome von Clatot, J, Ziyadeh-Isleem, A, Coulombe, A, Maugenre, S, Denjoy, I, Hatem, S.N, Guicheney, P, Neyroud, N

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Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndrome von Neyroud, N., Maison- Blanche, P., Denjoy, I., Chevret, S., Donger, C., Dausse, E., Fayn, J., Badilini, F., Menhabi, N., Schwartz, K., Guicheney, P., Coumel, P.

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P5713A new scn5a mutation responsible for multifocal ectopic purkinje-related premature contractions von Doisne, N, Waldmann, V, Waintraub, X, Fressart, V, Fosse, L, Hidden-Lucet, F, Redheuil, A, Neyroud, N, Gandjbakhch, E

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279Exploration of the dominant-negative effect of a SCN5A mutation in mice using adeno-associated viruses von Doisne, N, Grauso, Marta, Mougenot, N, Clergue, M, Coulombe, A, Guicheney, P, Neyroud, N

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P128Recovery of Scn5a-deficient mice cardiac conduction using AAVs von Doisne, N, Grauso-Culetto, M, Mougenot, N, Clergue, M, Fosse, L, Coulombe, A, Guicheney, P, Charpentier, F, Neyroud, N

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A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome von Neyroud, Nathalie, Tesson, Frédérique, Denjoy, Isabelle, Leibovici, Michel, Donger, Claire, Barhanin, Jacques, Fauré, Sabine, Gary, Françoise, Coumel, Philippe, Petit, Christine, Schwartz, Ketty, Guicheney, Pascale

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CRISPR/Cas9-mediated generation of cardiomyocytes derived from human induced pluripotent stem cells to model SCN5A deficiency von Gizon, M., Fontaine, V., Duboscq-Bidot, L., Kassa, L. El, Giraud-Triboult, K., Villard, E., Neyroud, N.

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Splicing mutations in KCNQ1 : A mutation hot spot at codon 344 that produces in frame transcripts von MURRAY, A, DONGER, C, SYRRIS, P, AFZAL, A. R, PATTON, M. A, GUICHENEY, P, JEFFERY, S, FENSKE, C, SPILLMAN, I, RICHARD, P, DONG, Y. B, NEYROUND, N, CHEVALIER, P, DENJOY, I, CARTER, N

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P371Role of the N- and distal C-terminal domains in Nav1.5 alpha-subunit interaction von Neyroud, N, Ziyadeh-Isleem, A, Clatot, J, Deschenes, I, Coulombe, A, Guicheney, P

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Isoform-Specific Modulation of Voltage-Gated Na+ Channels by Calmodulin von Deschênes, Isabelle, Neyroud, Nathalie, DiSilvestre, Deborah, Marbán, Eduardo, Yue, David T, Tomaselli, Gordon F

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Control of Rhythm and Rate278Cx43 hemichannels in ventricular cardiomyocytes can be activated by an elevation of cytoplasmic Ca2+ through a CaM-dependent signaling cascade and are... von De Smet, M, Doisne, N, Stillitano, F, Lissoni, A, Wang, N, Leybaert, L, Grauso, M, Mougenot, N, Clergue, M, Coulombe, A, Guicheney, P, Neyroud, N, Kong, CW, Hansen, J, Funck-Brentano, C, Jeziorowska, D, Zahr, N, Li, R, Iyengar, R, Hajjar, RJ, Hulot, JS

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KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome von DONGER, C, DENJOY, I, BERTHET, M, NEYROUD, N, CRUAUD, C, BENNACEUR, M, CHIVORET, G, SCHWARTZ, K, COUMEL, P, GUICHENEY, P

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A new SCN5A mutation responsible for Multifocal Ectopic Purkinje-Related Premature Contractions von Doisne, Nicolas, Waldmann, V., Fressart, V., Redheuil, Alban, Fosse, L., Waintraub, Xavier, Hidden-Lucet, F., Neyroud, N., Gandjbakhch, E.

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Somatic gene transfer of tagged K+ channel fragments to probe trafficking and electrical function in epithelial cells and cardiac myocytes von Neyroud, N, Deschênes, I, Akao, M, Nuss, H B, Marbán, E

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Overexpression of the cardiac Na + channel in Scn5a deficient mice using AAVs von Doisne, N., Grauso, M., Mougenot, N., Clergue, M., Coulombe, A., Charpentier, F., Guicheney, P., Neyroud, N.

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Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias von Chouabe, Christophe, Neyroud, Nathalie, Guicheney, Pascale, Lazdunski, Michel, Romey, Georges, Barhanin, Jacques

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