Resultados de procura - Céline Marionneau

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  1. 1
    RhoA Expression Is Controlled by Nitric Oxide through cGMP-dependent Protein Kinase Activation

    RhoA Expression Is Controlled by Nitric Oxide through cGMP-dependent Protein Kinase Activation por Vincent Sauzeau, Malvyne Rolli‐Derkinderen, Céline Marionneau, Gervaise Loirand, Pierre Pacaud

    Publicado 2003
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  2. 2
    Distinct Cellular and Molecular Mechanisms Underlie Functional Remodeling of Repolarizing K <sup>+</sup> Currents With Left Ventricular Hypertrophy

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

    Publicado 2008
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  3. 3
    Calmodulin Kinase II Inhibition Shortens Action Potential Duration by Upregulation of K <sup>+</sup> Currents

    Calmodulin Kinase II Inhibition Shortens Action Potential Duration by Upregulation of K <sup>+</sup> Currents por Jingdong Li, Céline Marionneau, Rong Zhang, Vaibhavi Shah, Johannes Hell, Jeanne M. Nerbonne, Mark E. Anderson

    Publicado 2006
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  4. 4
    Homeostatic regulation of electrical excitability in physiological cardiac hypertrophy

    Homeostatic regulation of electrical excitability in physiological cardiac hypertrophy por Kai‐Chien Yang, Nicholas C. Foeger, Céline Marionneau, Patrick Y. Jay, Julie R. McMullen, Jeanne M. Nerbonne

    Publicado 2010
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  5. 5
    Specific pattern of ionic channel gene expression associated with pacemaker activity in the mouse heart

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

    Publicado 2004
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  6. 6
    The Sodium Channel Accessory Subunit Navβ1 Regulates Neuronal Excitability through Modulation of Repolarizing Voltage-Gated K<sup>+</sup>Channels

    The Sodium Channel Accessory Subunit Navβ1 Regulates Neuronal Excitability through Modulation of Repolarizing Voltage-Gated K<sup>+</sup>Channels por Céline Marionneau, Yarimar Carrasquillo, Aaron J. Norris, R. Reid Townsend, Lori L. Isom, Andrew J. Link, Jeanne M. Nerbonne

    Publicado 2012
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  7. 7
    Voltage-gated sodium channels assemble and gate as dimers

    Voltage-gated sodium channels assemble and gate as dimers por Jérôme Clatot, Malcolm Hoshi, Xiaoping Wan, Haiyan Liu, Ankur Jain, Krekwit Shinlapawittayatorn, Céline Marionneau, Eckhard Ficker, Taekjip Ha, Isabelle Deschênes

    Publicado 2017
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  8. 8
    Targeted Deletion of Kv4.2 Eliminates <i>I</i> <sub>to,f</sub> and Results in Electrical and Molecular Remodeling, With No Evidence of Ventricular Hypertrophy or Myocardial Dysfunction

    Targeted Deletion of Kv4.2 Eliminates <i>I</i> <sub>to,f</sub> and Results in Electrical and Molecular Remodeling, With No Evidence of Ventricular Hypertrophy or Myocardial Dysfunc... por Weinong Guo, W. Edward Jung, Céline Marionneau, Franck Aimond, Haodong Xu, Kathryn A. Yamada, Thomas L. Schwarz, Sophie Demolombe, Jeanne M. Nerbonne

    Publicado 2005
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  9. 9
    Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison

    Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison por Gildas Loussouarn, Damien Sternberg, Sophie Nicole, Céline Marionneau, Françoise Le Bouffant, Gilles Toumaniantz, Julien Barc, Olfat A. Malak, Véronique Fressart, Yann Péréon, Isabelle Baró, Flavien Charpentier

    Publicado 2016
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  10. 10
    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 por 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

    Publicado 2008
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  11. 11
    Variable Nav1.5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn5a+/− Mouse Model

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

    Publicado 2010
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  12. 12
    Mouse Model of <i>SCN5A</i> -Linked Hereditary Lenègre’s Disease

    Mouse Model of <i>SCN5A</i> -Linked Hereditary Lenègre’s Disease por Anne Royer, Toon A.B. van Veen, Sabrina Le Bouter, Céline Marionneau, Violaine Griol‐Charhbili, Anne‐Laure Léoni, Marja Steenman, Harold V.M. van Rijen, Sophie Demolombe, Catharine A. Goddard, Christine Richer, Brigitte Escoubet, T. Jarry‐Guichard, William H Colledge, Daniel Gros, Jacques M.T. de Bakker, Andrew A. Grace, Denis Escande, Flavien Charpentier

    Publicado 2005
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  13. 13
    Na<sup>+</sup> channel function, regulation, structure, trafficking and sequestration

    Na<sup>+</sup> channel function, regulation, structure, trafficking and sequestration por Ye Chen‐Izu, Robin M. Shaw, Geoffrey S. Pitt, Vladimir Yarov‐Yarovoy, Jon T. Sack, Hugues Abriel, Richard W. Aldrich, Luiz Belardinelli, Mark B. Cannell, William A. Catterall, Walter Chazin, Nipavan Chiamvimonvat, Isabelle Deschênes, Eleonora Grandi, Thomas J. Hund, Leighton T. Izu, Lars S. Maier, Victor A. Maltsev, Céline Marionneau, Peter J. Mohler, Sridharan Rajamani, Randall L. Rasmusson, Eric A. Sobie, Colleen E. Clancy, Donald M. Bers

    Publicado 2015
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  14. 14
    <i>RRAD</i> mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome

    <i>RRAD</i> mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome por Nadjet Belbachir, Vincent Portero, Zeina R. Al Sayed, Jean‐Baptiste Gourraud, Florian Dilasser, Laurence Jesel, Hongchao Guo, Haodi Wu, Nathalie Gaborit, Christophe Guilluy, Aurore Girardeau, Stéphanie Bonnaud, Floriane Simonet, Matilde Karakachoff, S. Pattier, Clare L. Scott, Sophie Burel, Céline Marionneau, Caroline Chariau, Anne Gaignerie, Laurent David, Emmanuelle Génin, Jean‐François Deleuze, Christian Dina, Vincent Sauzeau, Gervaise Loirand, Isabelle Baró, Jean‐Jacques Schott, Vincent Probst, Joseph C. Wu, Richard Redon, Flavien Charpentier, Solena Le Scouarnec

    Publicado 2019
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