Torthaí cuardaigh - Jean‐Jacques Schott

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  1. 1
    Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease

    Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease de réir Hideko Kasahara, Bora Lee, Jean‐Jacques Schott, D. Woodrow Benson, J.G. Seidman, Christine E. Seidman, Seigo Izumo

    Foilsithe / Cruthaithe 2000
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  2. 2
    The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance

    The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance de réir Jean‐Baptiste Gourraud, Julien Barc, Aurélie Thollet, Solena Le Scouarnec, Hervé Le Marec, Jean‐Jacques Schott, Richard Redon, Vincent Probst

    Foilsithe / Cruthaithe 2016
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  3. 3
    Genetics of syndromic and non-syndromic mitral valve prolapse

    Genetics of syndromic and non-syndromic mitral valve prolapse de réir Thierry Le Tourneau, Jean Mérot, Antoine Rimbert, Solena Le Scouarnec, Vincent Probst, Hervé Le Marec, Robert A. Levine, Jean‐Jacques Schott

    Foilsithe / Cruthaithe 2018
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  4. 4
    Familial Aggregation of Calcific Aortic Valve Stenosis in the Western Part of France

    Familial Aggregation of Calcific Aortic Valve Stenosis in the Western Part of France de réir Vincent Probst, Solena Le Scouarnec, Antoine Legendre, Valérie Jousseaume, P. Jaafar, Jean-Michel Nguyen, André Chaventré, Hervé Le Marec, Jean‐Jacques Schott

    Foilsithe / Cruthaithe 2006
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  5. 5
    Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains.

    Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains. de réir Michal Pravenec, Dominique Gauguier, Jean‐Jacques Schott, Jérôme Buard, Vladimı́r Křen, V Bı́lá, Claude Szpirer, Josiane Szpirer, J M Wang, He Huang

    Foilsithe / Cruthaithe 1995
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  6. 6
    Cardiac Expression of the Ventricle-Specific Homeobox Gene Irx4 Is Modulated by Nkx2-5 and dHand

    Cardiac Expression of the Ventricle-Specific Homeobox Gene Irx4 Is Modulated by Nkx2-5 and dHand de réir Benoit G. Bruneau, Zheng‐Zheng Bao, Makoto Tanaka, Jean‐Jacques Schott, Seigo Izumo, Constance L. Cepko, J.G. Seidman, Christine E. Seidman

    Foilsithe / Cruthaithe 2000
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  7. 7
    14-3-3 Is a Regulator of the Cardiac Voltage-Gated Sodium Channel Nav1.5

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

    Foilsithe / Cruthaithe 2006
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  8. 8
    Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

    Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease de réir Vincent Probst, Florence Kyndt, F Potet, Jean‐Noël Trochu, G Mialet, Sophie Demolombe, Jean‐Jacques Schott, Isabelle Baró, Denis Escande, Hervé Le Marec

    Foilsithe / Cruthaithe 2003
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  9. 9
    0268 : Involvement of LRRFip1 gene and canonical Wnt pathway in Mitral Valve Prolapse (MVP)

    0268 : Involvement of LRRFip1 gene and canonical Wnt pathway in Mitral Valve Prolapse (MVP) de réir Pauline Labbé, Emilie Faure, Simon Lecointe, Florence Kyndt, Thierry Le Tourneau, José Luís de la Pompa, Cécile Duplàa, Stéphane Zaffran, Jean‐Jacques Schott, Jean Mérot

    Foilsithe / Cruthaithe 2015
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  10. 10
    Novel <i>SCN5A</i> Mutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family

    Novel <i>SCN5A</i> Mutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family de réir Florence Kyndt, Vincent Probst, F Potet, Sophie Demolombe, Jean-Christophe Chevallier, Isabelle Baró, Jean-Paul Moisan, Pierre Boisseau, Jean‐Jacques Schott, Denis Escande, Hervé Le Marec

    Foilsithe / Cruthaithe 2001
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  11. 11
    Molecular Genetics and Functional Anomalies in a Series of 248 Brugada Cases with 11 Mutations in the TRPM4 Channel

    Molecular Genetics and Functional Anomalies in a Series of 248 Brugada Cases with 11 Mutations in the TRPM4 Channel de réir Hui Liu, Stéphanie Chatel, Christophe Simard, Ninda Syam, Laurent Sallé, Vincent Probst, Julie Morel, Gilles Millat, M. Álvarez López, Hugues Abriel, Jean‐Jacques Schott, Romain Guinamard, Patrice Bouvagnet

    Foilsithe / Cruthaithe 2013
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  12. 12
    Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block

    Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block de réir Ninda Syam, Stéphanie Chatel, Lijo Cherian Ozhathil, Valentin Sottas, Jean‐Sébastien Rougier, Alban‐Elouen Baruteau, Estelle Baron, Mohamed‐Yassine Amarouch, Xavier Daumy, Vincent Probst, Jean‐Jacques Schott, Hugues Abriel

    Foilsithe / Cruthaithe 2016
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  13. 13
    Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome

    Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome de réir Julien Barc, François Briec, Sébastien Schmitt, Florence Kyndt, Martine Le Cunff, Estelle Baron, C Vieyres, Frédéric Sacher, Richard Redon, Cédric Le Caignec, Hervé Le Marec, Vincent Probst, Jean‐Jacques Schott

    Foilsithe / Cruthaithe 2010
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  14. 14
    Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28

    Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28 de réir Florence Kyndt, Jean‐Jacques Schott, Jean‐Noël Trochu, Florence Baranger, O. Herbert, Valerie E. Scott, Édith Fressinaud, Albert David, Jean‐Paul Moisan, Jean-Brieuc Bouhour, Hervé Le Marec, Bernard Bénichou

    Foilsithe / Cruthaithe 1998
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  15. 15
    Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients

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

    Foilsithe / Cruthaithe 2002
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  16. 16
    Defining the Cellular Phenotype of “Ankyrin-B Syndrome” Variants

    Defining the Cellular Phenotype of “Ankyrin-B Syndrome” Variants de réir Peter J. Mohler, Solena Le Scouarnec, Isabelle Denjoy, J. S. Lowe, Pascale Guicheney, Lise Caron, Iwona M. Driskell, Jean‐Jacques Schott, Kris Norris, Antoine Leenhardt, Richard B. Kim, Denis Escande, Dan M. Roden

    Foilsithe / Cruthaithe 2007
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  17. 17
    Genetics and pathophysiology of mitral valve prolapse

    Genetics and pathophysiology of mitral valve prolapse de réir Constance Delwarde, Romain Capoulade, Jean Mérot, Solena Le Scouarnec, Nabila Bouatia‐Naji, Mengyao Yu, Olivier Huttin, Christine Selton‐Suty, Jean‐Marc Sellal, Nicolas Piriou, Jean‐Jacques Schott, Christian Dina, Thierry Le Tourneau

    Foilsithe / Cruthaithe 2023
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  18. 18
    Identification of Large Families in Early Repolarization Syndrome

    Identification of Large Families in Early Repolarization Syndrome de réir Jean‐Baptiste Gourraud, Solena Le Scouarnec, Frédéric Sacher, Stéphanie Chatel, Nicolas Derval, Vincent Portero, Pascal Chavernac, Juan E. Sandoval, Philippe Mabo, Richard Redon, Jean‐Jacques Schott, Hervé Le Marec, Michel Haı̈ssaguerre, Vincent Probst

    Foilsithe / Cruthaithe 2013
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  19. 19
    Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease

    Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease de réir Solena Le Scouarnec, Naina Bhasin, C Vieyres, Thomas J. Hund, Shane R. Cunha, Olha M. Koval, Céline Marionneau, Biyi Chen, Yuejin Wu, Sophie Demolombe, Long‐Sheng Song, Hervé Le Marec, Vincent Probst, Jean‐Jacques Schott, Mark E. Anderson, Peter J. Mohler

    Foilsithe / Cruthaithe 2008
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  20. 20
    Mutations in the Gene Encoding Filamin A as a Cause for Familial Cardiac Valvular Dystrophy

    Mutations in the Gene Encoding Filamin A as a Cause for Familial Cardiac Valvular Dystrophy de réir Florence Kyndt, Jean-Pierre Gueffet, Vincent Probst, Philippe Jaafar, Antoine Legendre, Françoise Le Bouffant, Claire Toquet, Estelle Roy, Lesley McGregor, Sally Ann Lynch, Ruth Newbury-Ecob, Vinh Tran, Ian Young, Jean‐Noël Trochu, Hervé Le Marec, Jean‐Jacques Schott

    Foilsithe / Cruthaithe 2006
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