Risultati della ricerca - Sophie Demolombe

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  1. 1
    Polyethylenimine but Not Cationic Lipids Promotes Transgene Delivery to the Nucleus in Mammalian Cells

    Polyethylenimine but Not Cationic Lipids Promotes Transgene Delivery to the Nucleus in Mammalian Cells di H. Pollard, Jean-Serge Rémy, Gildas Loussouarn, Sophie Demolombe, Jean‐Paul Behr, Denis Escande

    Pubblicazione 1998
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  2. 2
    Regional and tissue specific transcript signatures of ion channel genes in the non‐diseased human heart

    Regional and tissue specific transcript signatures of ion channel genes in the non‐diseased human heart di Nathalie Gaborit, Sabrina Le Bouter, Viktória Szüts, András Varró, Denis Escande, Stanley Nattel, Sophie Demolombe

    Pubblicazione 2007
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  3. 3
    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 di Céline Marionneau, Sylvain Brunet, Thomas P. Flagg, Thomas K. Pilgram, Sophie Demolombe, Jeanne M. Nerbonne

    Pubblicazione 2008
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  4. 4
    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 di Céline Marionneau, Brigitte Couette, Jie Liu, Huiyu Li, Matteo E. Mangoni, Joël Nargeot, Ming Lei, Denis Escande, Sophie Demolombe

    Pubblicazione 2004
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  5. 5
    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... di Weinong Guo, W. Edward Jung, Céline Marionneau, Franck Aimond, Haodong Xu, Kathryn A. Yamada, Thomas L. Schwarz, Sophie Demolombe, Jeanne M. Nerbonne

    Pubblicazione 2005
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  6. 6
    Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease

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

    Pubblicazione 2003
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  7. 7
    Differential expression of KvLQT1 and its regulator IsK in mouse epithelia

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

    Pubblicazione 2001
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  8. 8
    Piezo1‐dependent stretch‐activated channels are inhibited by Polycystin‐2 in renal tubular epithelial cells

    Piezo1‐dependent stretch‐activated channels are inhibited by Polycystin‐2 in renal tubular epithelial cells di Rémi Peyronnet, Joana Raquel Martins, Fabrice Duprat, Sophie Demolombe, Malika Arhatte, Martine Jodar, Michel Tauc, Christophe Duranton, Marc Paulais, Jacques Teulon, Éric Honoré, Amanda Patel

    Pubblicazione 2013
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  9. 9
    Contrasting Gene Expression Profiles in Two Canine Models of Atrial Fibrillation

    Contrasting Gene Expression Profiles in Two Canine Models of Atrial Fibrillation di Sophie Cardin, Eric Libby, Patricia Pelletier, Sabrina Le Bouter, Akiko Shiroshita-Takeshita, Nolwenn Le Meur, Jean Léger, Sophie Demolombe, André Ponton, Leon Glass, Stanley Nattel

    Pubblicazione 2007
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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 di 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

    Pubblicazione 2001
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  11. 11
    A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product

    A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product di Sophie Demolombe, Isabelle Baró, Yann Péréon, Jet Bliek, Raha Mohammad-Panah, H. Pollard, Shabnam Morid, M. Mannens, Arthur A.M. Wilde, Jacques Barhanin, Flavien Charpentier, Denis Escande

    Pubblicazione 1998
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  12. 12
    Piezo1 in Smooth Muscle Cells Is Involved in Hypertension-Dependent Arterial Remodeling

    Piezo1 in Smooth Muscle Cells Is Involved in Hypertension-Dependent Arterial Remodeling di Kevin Retailleau, Fabrice Duprat, Malika Arhatte, Sanjeev S. Ranade, Rémi Peyronnet, Joana Raquel Martins, Martine Jodar, Céline Moro, Stefan Offermanns, Yuanyi Feng, Sophie Demolombe, Amanda Patel, Éric Honoré

    Pubblicazione 2015
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  13. 13
    Human Atrial Ion Channel and Transporter Subunit Gene-Expression Remodeling Associated With Valvular Heart Disease and Atrial Fibrillation

    Human Atrial Ion Channel and Transporter Subunit Gene-Expression Remodeling Associated With Valvular Heart Disease and Atrial Fibrillation di Nathalie Gaborit, Marja Steenman, Guillaume Lamirault, Nolwenn Le Meur, Sabrina Le Bouter, Gilles Lande, Jean Léger, Flavien Charpentier, Torsten Christ, Dobromir Dobrev, Denis Escande, Stanley Nattel, Sophie Demolombe

    Pubblicazione 2005
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  14. 14
    Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation

    Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation di Mariëlle Alders, Tamara T. Koopmann, Imke Christiaans, Pieter G. Postema, Leander Beekman, Michael W.T. Tanck, Katja Zeppenfeld, Peter Loh, Karel T. Koch, Sophie Demolombe, Marcel M.A.M. Mannens, Connie R. Bezzina, Arthur A.M. Wilde

    Pubblicazione 2009
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  15. 15
    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 di 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

    Pubblicazione 2008
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  16. 16
    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 di 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

    Pubblicazione 2010
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  17. 17
    Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

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

    Pubblicazione 2008
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  18. 18
    Conditional Mineralocorticoid Receptor Expression in the Heart Leads to Life-Threatening Arrhythmias

    Conditional Mineralocorticoid Receptor Expression in the Heart Leads to Life-Threatening Arrhythmias di Antoine Ouvrard‐Pascaud, Yannis Sainte–Marie, Jean‐Pierre Bénitah, Romain Perrier, Christelle Soukaseum, Aurélie Nguyen Dinh Cat, Anne Royer, Khaï Le Quang, Flavien Charpentier, Sophie Demolombe, Fatima Mechta‐Grigoriou, Ahmed Beggah, Pierre Maison‐Blanche, M. E. Oblin, Claude Delcayre, Glenn I. Fishman, Nicolette Farman, Brigitte Escoubet, Frédéric Jaisser

    Pubblicazione 2005
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  19. 19
    Mouse Model of <i>SCN5A</i> -Linked Hereditary Lenègre’s Disease

    Mouse Model of <i>SCN5A</i> -Linked Hereditary Lenègre’s Disease di 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

    Pubblicazione 2005
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