Gender-related differences in ion-channel and transporter subunit expression in non-diseased human hearts by 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 by 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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Piezo1-dependent regulation of urinary osmolarity by Martins, Joana Raquel, Penton, David, Peyronnet, Rémi, Arhatte, Malika, Moro, Céline, Picard, Nicolas, Kurt, Birgül, Patel, Amanda, Honoré, Eric, Demolombe, Sophie

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

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A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product by 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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Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans by 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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Ion-channel mRNA-expression profiling: Insights into cardiac remodeling and arrhythmic substrates by Nattel, Stanley, Frelin, Yves, Gaborit, Nathalie, Louault, Claire, Demolombe, Sophie

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Smooth muscle filamin A is a major determinant of conduit artery structure and function at the adult stage by Retailleau, Kevin, Arhatte, Malika, Demolombe, Sophie, Jodar, Martine, Baudrie, Véronique, Offermanns, Stefan, Feng, Yuanyi, Patel, Amanda, Honoré, Eric, Duprat, Fabrice

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Distinct Cellular and Molecular Mechanisms Underlie Functional Remodeling of Repolarizing K+ Currents With Left Ventricular Hypertrophy by Marionneau, Céline, Brunet, Sylvain, Flagg, Thomas P, Pilgram, Thomas K, Demolombe, Sophie, Nerbonne, Jeanne M

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Human atrial ion channel and transporter subunit gene-expression remodeling associated with valvular heart disease and atrial fibrillation by 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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β3-Adrenoceptor Control the Cystic Fibrosis Transmembrane Conductance Regulator through a cAMP/Protein Kinase A-independent Pathway by Leblais, Véronique, Demolombe, Sophie, Vallette, Geneviève, Langin, Dominique, Baró, Isabelle, Escande, Denis, Gauthier, Chantal

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In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart by BENDAHHOU, Saïd, MARIONNEAU, Céline, HAUROGNE, Karinne, LARROQUE, Marie-Madeleine, DERAND, Renaud, SZUTS, Viktoria, ESCANDE, Denis, DEMOLOMBE, Sophie, BARHANIN, Jacques

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Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large french family by KYNDT, Florence, PROBST, Vincent, LE MAREC, Hervé, POTET, Franck, DEMOLOMBE, Sophie, CHEVALLIER, Jean-Christophe, BARO, Isabelle, MOISAN, Jean-Paul, BOISSEAU, Pierre, SCHOTT, Jean-Jacques, ESCANDE, Denis

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Lonesome Kv4.2 channels by Demolombe, Sophie

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Targeted Deletion of Kv4.2 Eliminates Ito,f and Results in Electrical and Molecular Remodeling, With No Evidence of Ventricular Hypertrophy or Myocardial Dysfunction by Guo, Weinong, Jung, W Edward, Marionneau, Céline, Aimond, Franck, Xu, Haodong, Yamada, Kathryn A, Schwarz, Thomas L, Demolombe, Sophie, Nerbonne, Jeanne M

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Transcriptional profiling of ion channel genes in Brugada syndrome and other right ventricular arrhythmogenic diseases by Gaborit, Nathalie, Wichter, Thomas, Varro, Andras, Szuts, Viktoria, Lamirault, Guillaume, Eckardt, Lars, Paul, Matthias, Breithardt, Günter, Schulze-Bahr, Eric, Escande, Denis, Nattel, Stanley, Demolombe, Sophie

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Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease by Probst, Vincent, Kyndt, Florence, Potet, Franck, Trochu, Jean-Noel, Mialet, Guy, Demolombe, Sophie, Schott, Jean-Jacques, Baró, Isabelle, Escande, Denis, Le Marec, Hervé

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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 by 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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Marked differences between atrial and ventricular gene-expression remodeling in dogs with experimental heart failure by Cardin, Sophie, Pelletier, Patricia, Libby, Eric, Le Bouter, Sabrina, Xiao, Ling, Kääb, Stefan, Demolombe, Sophie, Glass, Leon, Nattel, Stanley

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Erratum to “Ion-channel mRNA-expression profiling: Insights into cardiac remodeling and arrhythmic substrates” [J. Mol. Cell. Cardiol. 48 (2010) 96–105] by Nattel, Stanley, Frelin, Yves, Gaborit, Nathalie, Louault, Claire, Demolombe, Sophie

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