Regional and tissue specific transcript signatures of ion channel genes in the non-diseased human heart von Gaborit, Nathalie, Le Bouter, Sabrina, Szuts, Viktoria, Varro, Andras, Escande, Denis, Nattel, Stanley, Demolombe, Sophie

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Specific pattern of ionic channel gene expression associated with pacemaker activity in the mouse heart von Marionneau, Céline, Couette, Brigitte, Liu, Jie, Li, Huiyu, Mangoni, Matteo E., Nargeot, Joël, Lei, Ming, Escande, Denis, Demolombe, Sophie

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Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients von Smits, Jeroen P.P, Eckardt, Lars, Probst, Vincent, Bezzina, Connie R, Schott, Jean Jacques, Remme, Carol Ann, Haverkamp, Wilhelm, Breithardt, Günter, Escande, Denis, Schulze-Bahr, Eric, LeMarec, Hervé, Wilde, Arthur A.M

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Polyethylenimine but Not Cationic Lipids Promotes Transgene Delivery to the Nucleus in Mammalian Cells von Pollard, H, Remy, J S, Loussouarn, G, Demolombe, S, Behr, J P, Escande, D

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Variable Nav1.5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn5a+/− Mouse Model von Leoni, Anne-Laure, Gavillet, Bruno, Rougier, Jean-Sébastien, Marionneau, Céline, Probst, Vincent, Le Scouarnec, Solena, Schott, Jean-Jacques, Demolombe, Sophie, Bruneval, Patrick, Huang, Christopher L. H., Colledge, William H., Grace, Andrew A., Le Marec, Hervé, Wilde, Arthur A., Mohler, Peter J., Escande, Denis, Abriel, Hugues, Charpentier, Flavien

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Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model von Leoni, Anne-Laure, Gavillet, Bruno, Rougier, Jean-Sébastien, Marionneau, Céline, Probst, Vincent, Le Scouarnec, Solena, Schott, Jean-Jacques, Demolombe, Sophie, Bruneval, Patrick, Huang, Christopher L H, Colledge, William H, Grace, Andrew A, Le Marec, Hervé, Wilde, Arthur A, Mohler, Peter J, Escande, Denis, Abriel, Hugues, Charpentier, Flavien

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Impaired KCNQ1–KCNE1 and Phosphatidylinositol-4,5-Bisphosphate Interaction Underlies the Long QT Syndrome von Park, Kyu-Ho, Piron, Julien, Dahimene, Shehrazade, Mérot, Jean, Baró, Isabelle, Escande, Denis, Loussouarn, Gildas

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Progressive Cardiac Conduction Defect is the Prevailing Phenotype in Carriers of a Brugada Syndrome SCN5A Mutation von PROBST, VINCENT, ALLOUIS, MARIE, SACHER, FREDERIC, PATTIER, SABINE, BABUTY, DOMINIQUE, MABO, PHILIPE, MANSOURATI, JACQUES, VICTOR, JACQUES, NGUYEN, JEAN-MICHEL, SCHOTT, JEAN-JACQUES, BOISSEAU, PIERRE, ESCANDE, DENIS, LE MAREC, HERVÉ

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14-3-3 Is a Regulator of the Cardiac Voltage-Gated Sodium Channel Nav1.5 von Allouis, Marie, Le Bouffant, Françoise, Wilders, Ronald, Péroz, David, Schott, Jean-Jacques, Noireaud, Jacques, Le Marec, Hervé, Mérot, Jean, Escande, Denis, Baró, Isabelle

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Novel Brugada SCN5A Mutation Leading to ST Segment Elevation in the Inferior or the Right Precordial Leads von POTET, FRANCK, MABO, PHILIPPE, LE COQ, GUILLAUME, PROBST, VINCENT, SCHOTT, JEAN-JACQUES, AIRAUD, FABRICE, GUIHARD, GILLES, DAUBERT, JEAN-CLAUDE, ESCANDE, DENIS, LE MAREC, HERVÉ

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Differential expression of KvLQT1 and its regulator IsK in mouse epithelia von Demolombe, Sophie, Franco, Diego, de Boer, Piet, Kuperschmidt, Sabina, Roden, Dan, Pereon, Yann, Jarry, Anne, Moorman, Antoon F. M, Escande, Denis

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A Common Antitussive Drug, Clobutinol, Precipitates the Long QT Syndrome 2 von Bellocq, Chloe, Wilders, Ronald, Schott, Jean-Jacques, Louerat-Oriou, Benedicte, Boisseau, Pierre, Le Marec, Herve, Escande, Denis, Baro, Isabelle

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Gender-related differences in ion-channel and transporter subunit expression in non-diseased human hearts von Gaborit, Nathalie, Varro, Andras, Le Bouter, Sabrina, Szuts, Viktoria, Escande, Denis, Nattel, Stanley, Demolombe, Sophie

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Long-term amiodarone administration remodels expression of ion channel transcripts in the mouse heart von Le Bouter, Sabrina, El Harchi, Aziza, Marionneau, Céline, Bellocq, Chloé, Chambellan, Arnaud, van Veen, Toon, Boixel, Christophe, Gavillet, Bruno, Abriel, Hugues, Le Quang, Khai, Chevalier, Jean-Christophe, Lande, Gilles, Léger, Jean J, Charpentier, Flavien, Escande, Denis, Demolombe, Sophie

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AKAP proteins anchor cAMP-dependent protein kinase to KvLQT1/IsK channel complex von Potet, Franck, Scott, John D, Mohammad-Panah, Raha, Escande, Denis, Baro, Isabelle

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Differential expression of KvLQT1 isoforms across the human ventricular wall von Pereon, Yann, Demolombe, Sophie, Baro, Isabelle, Drouin, Emmanuel, Charpentier, Flavien, Escande, Denis

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Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans von Watanabe, Hiroshi, Koopmann, Tamara T, Le Scouarnec, Solena, Yang, Tao, Ingram, Christiana R, Schott, Jean-Jacques, Demolombe, Sophie, Probst, Vincent, Anselme, Frédéric, Escande, Denis, Wiesfeld, Ans C P, Pfeufer, Arne, Kääb, Stefan, Wichmann, H-Erich, Hasdemir, Can, Aizawa, Yoshifusa, Wilde, Arthur A M, Roden, Dan M, Bezzina, Connie R

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Mutation in the KCNQ1 gene leading to the short QT-interval syndrome von BELLOCQ, Chloé, VAN GINNEKEN, Antoni C. G, BEZZINA, Connie R, ALDERS, Mariel, ESCANDE, Denis, MANNENS, Marcel M. A. M, BARO, Isabelle, WILDE, Arthur A. M

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A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product von Demolombe, S, Baró, I, Péréon, Y, Bliek, J, Mohammad-Panah, R, Pollard, H, Morid, S, Mannens, M, Wilde, A, Barhanin, J, Charpentier, F, Escande, D

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Human atrial ion channel and transporter subunit gene-expression remodeling associated with valvular heart disease and atrial fibrillation von GABORIT, Nathalie, STEENMAN, Marja, ESCANDE, Denis, NATTEL, Stanley, DEMOLOMBE, Sophie, LAMIRAULT, Guillaume, LE MEUR, Nolwenn, LE BOUTER, Sabrina, LANDE, Gilles, LEGER, Jean, CHARPENTIER, Flavien, CHRIST, Torsten, DOBREV, Dobromir

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