نتائج البحث - Claire Perret

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  1. 1
    Bariatric Surgery Induces Disruption in Inflammatory Signaling Pathways Mediated by Immune Cells in Adipose Tissue: A RNA-Seq Study

    Bariatric Surgery Induces Disruption in Inflammatory Signaling Pathways Mediated by Immune Cells in Adipose Tissue: A RNA-Seq Study حسب Christine Poitou, Claire Perret, François Mathieu, Vinh Trương, Yuna Blum, Hervé Durand, Rohia Alili, Nadjim Chelghoum, Véronique Pelloux, Judith Aron‐Wisnewsky, Adriana Torcivia, Jean‐Luc Bouillot, Brian W. Parks, Ewa Ninio, Karine Clément, Laurence Tiret

    منشور في 2015
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    Artigo
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  2. 2
    The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts

    The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts حسب Juha Karvanen, Kaisa Silander, Frank Kee, Laurence Tiret, Veikko Salomaa, Kari Kuulasmaa, Per‐Gunnar Wiklund, Jarmo Virtamo, Olli Saarela, Claire Perret, Markus Perola, Leena Peltonen, François Cambien, Jeanette Erdmann, Mark M. Iles, Heribert Schunkert, Alun Evans

    منشور في 2008
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    Artigo
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  3. 3
    Genetic Analysis of the Interleukin-18 System Highlights the Role of the Interleukin-18 Gene in Cardiovascular Disease

    Genetic Analysis of the Interleukin-18 System Highlights the Role of the Interleukin-18 Gene in Cardiovascular Disease حسب Laurence Tiret, Tiphaine Godefroy, Edith Lubos, Viviane Nicaud, David‐Alexandre Trégouët, Sandrine Barbaux, Renate B. Schnabel, Christoph Bickel, Christine Espinola‐Klein, Odette Poirier, Claire Perret, Thomas Münzel, H. J. Rupprecht, Karl J. Lackner, François Cambien, Stefan Blankenberg

    منشور في 2005
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    Artigo
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  4. 4
    <i>FLNC</i> pathogenic variants in patients with cardiomyopathies: Prevalence and genotype‐phenotype correlations

    <i>FLNC</i> pathogenic variants in patients with cardiomyopathies: Prevalence and genotype‐phenotype correlations حسب Flavie Ader, Pascal de Groote, Patricia Réant, Caroline Rooryck, Delphine Dupin‐Deguine, Caroline Rambaud, Diala Khraiche, Claire Perret, Jean François Pruny, Michèle Mathieu‐Dramard, Marion Gérard, Yann Troadec, Laurent Gouya, Xavier Jeunemaı̂tre, Lionel Van Maldergem, Albert Hagège, Eric Villard, Philippe Charron, Pascale Richard

    منشور في 2019
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    Artigo
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  5. 5
    The Relation of Genetic and Environmental Factors to Systemic Inflammatory Biomarker Concentrations

    The Relation of Genetic and Environmental Factors to Systemic Inflammatory Biomarker Concentrations حسب Renate B. Schnabel, Kathryn L. Lunetta, Martin G. Larson, Josée Dupuis, Izabella Lipinska, Jian Rong, Ming‐Huei Chen, Zhenming Zhao, Jennifer F. Yamamoto, James B. Meigs, Viviane Nicaud, Claire Perret, Tanja Zeller, Stefan Blankenberg, Laurence Tiret, John F. Keaney, Ramachandran S. Vasan, Emelia J. Benjamin

    منشور في 2009
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    Artigo
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  6. 6
    Human CalDAG-GEFI gene (<i>RASGRP2</i>) mutation affects platelet function and causes severe bleeding

    Human CalDAG-GEFI gene (<i>RASGRP2</i>) mutation affects platelet function and causes severe bleeding حسب Matthias Canault, Dorsaf Ghalloussi, Charlotte Grosdidier, Marie Guinier, Claire Perret, Nadjim Chelghoum, Marine Germain, Hana Raslová, Franck Peiretti, Pierre‐Emmanuel Morange, Noémie Saut, Xavier Pillois, Alan T. Nurden, François Cambien, Anne Pierrès, Timo K. van den Berg, Taco W. Kuijpers, Marie‐Christine Alessi, David‐Alexandre Trégouët

    منشور في 2014
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    Artigo
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  7. 7
    Genetics of Venous Thrombosis: Insights from a New Genome Wide Association Study

    Genetics of Venous Thrombosis: Insights from a New Genome Wide Association Study حسب Marine Germain, Noémie Saut, Nicolas Greliche, Christian Dina, Jean‐Charles Lambert, Claire Perret, William Cohen, Tiphaine Oudot‐Mellakh, Guillemette Antoni, Marie‐Christine Alessi, Diana Zélénika, François Cambien, Laurence Tiret, Marion Bertrand, Anne‐Marie Dupuy, Luc Letenneur, Mark Lathrop, Joseph Emmerich, Philippe Amouyel, David‐Alexandre Trégouët, Pierre‐Emmanuel Morange

    منشور في 2011
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    Artigo
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  8. 8
    Genetics and Beyond – The Transcriptome of Human Monocytes and Disease Susceptibility

    Genetics and Beyond – The Transcriptome of Human Monocytes and Disease Susceptibility حسب Tanja Zeller, Philipp S. Wild, Silke Szymczak, Maxime Rotival, Arne Schillert, Raphaële Castagné, Seraya Maouche, Marine Germain, Karl J. Lackner, Heidi Rossmann, Medea Eleftheriadis, Christoph Sinning, Renate B. Schnabel, Edith Lubos, Detlev Mennerich, Werner Rust, Claire Perret, Carole Proust, Viviane Nicaud, Joseph Loscalzo, Norbert Hübner, David‐Alexandre Trégouët, Thomas Münzel, Andreas Ziegler, Laurence Tiret, Stefan Blankenberg, François Cambien

    منشور في 2010
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    Artigo
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  9. 9
    Integrating Genome-Wide Genetic Variations and Monocyte Expression Data Reveals Trans-Regulated Gene Modules in Humans

    Integrating Genome-Wide Genetic Variations and Monocyte Expression Data Reveals Trans-Regulated Gene Modules in Humans حسب Maxime Rotival, Tanja Zeller, Philipp S. Wild, Seraya Maouche, Silke Szymczak, Arne Schillert, Raphaële Castagné, Arne Deiseroth, Carole Proust, Jessy Brocheton, Tiphaine Godefroy, Claire Perret, Marine Germain, Medea Eleftheriadis, Christoph Sinning, Renate B. Schnabel, Edith Lubos, Karl J. Lackner, Heidi Rossmann, Thomas Münzel, Augusto Rendon, Cardiogenics Consortium, Jeanette Erdmann, Panos Deloukas, Christian Hengstenberg, Patrick Diemert, Gilles Montalescot, Willem H. Ouwehand, Nilesh J. Samani, Heribert Schunkert, David‐Alexandre Trégouët, Andreas Ziegler, Alison H. Goodall, François Cambien, Laurence Tiret, Stefan Blankenberg

    منشور في 2011
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    Artigo
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  10. 10
    Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy

    Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy حسب Ulrike Esslinger, Sophie Garnier, Agathe Korniat, Carole Proust, Georgios Kararigas, Martina Müller‐Nurasyid, Jean‐Philippe Empana, Michael P. Morley, Claire Perret, Klaus Stark, Alexander G. Bick, Sanjay Prasad, Jennifer Kriebel, Jin Li, Laurence Tiret, Konstantin Strauch, Declan P. O’Regan, Kenneth B. Marguiles, J. G. Seidman, Pierre Boutouyrie, Patrick Lacolley, Xavier Jouven, Christian Hengstenberg, Michel Komajda, Hákon Hákonarson, Richard Isnard, Eloisa Arbustini, Harald Grallert, Stuart A. Cook, Christine E. Seidman, Vera Regitz‐Zagrosek, Thomas P. Cappola, Philippe Charron, François Cambien, Eric Villard

    منشور في 2017
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    Artigo
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  11. 11
    A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

    A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy حسب Eric Villard, Claire Perret, Françoise Gary, Carole Proust, Gilles Dilanian, Christian Hengstenberg, Volker Ruppert, Eloisa Arbustini, Thomas Wichter, Marine Germain, Olivier Dubourg, Luigi Tavazzi, Marie-Claude Aumont, Pascal de Groote, Laurent Fauchier, Jean‐Noël Trochu, Pierre Gibelin, Jean‐François Aupetit, Klaus Stark, Jeanette Erdmann, Roland Hetzer, Angharad M. Roberts, Paul J.R. Barton, Vera Regitz‐Zagrosek, Uzma Aslam, Laëtitia Duboscq-Bidot, Matthias Meyborg, Bernhard Maisch, Hugo Madeira, Anders Waldenström, Enrique Galve, John G.F. Cleland, Richard Dorent, Gérard Roizès, Tanja Zeller, Stefan Blankenberg, Alison H. Goodall, Stuart A. Cook, David‐Alexandre Trégouët, Laurence Tiret, Richard Isnard, Michel Komajda, Philippe Charron, François Cambien

    منشور في 2011
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    Artigo
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  12. 12
    New susceptibility locus for coronary artery disease on chromosome 3q22.3

    New susceptibility locus for coronary artery disease on chromosome 3q22.3 حسب Jeanette Erdmann, Anika Großhennig, Peter S. Braund, Inke R. König, Christian Hengstenberg, Alistair S. Hall, Patrick Linsel‐Nitschke, Sekar Kathiresan, Ben Wright, David‐Alexandre Trégouët, François Cambien, Petra Bruse, Zouhair Aherrahrou, Arnika Kathleen Wagner, Klaus Stark, Stephen M. Schwartz, Veikko Salomaa, Roberto Elosúa, Olle Melander, Benjamin F. Voight, Christopher J. O’Donnell, Leena Peltonen, David S. Siscovick, David Altshuler, Piera Angelica Merlini, Flora Peyvandi, Luisa Bernardinelli, Diego Ardissino, Arne Schillert, Stefan Blankenberg, Tanja Zeller, Philipp S. Wild, Dániel Schwarz, Laurence Tiret, Claire Perret, Stefan Schreiber, Nour Eddine El Mokhtari, Arne Schäfer, Winfried März, Wilfried Renner, Peter Bugert, Harald Klüter, Jürgen Schrezenmeir, Deborah C. Rubin, Stephen G. Ball, Anthony J. Balmforth, H‐Erich Wichmann, Thomas Meitinger, Marcus Fischer, Christa Meisinger, Jens Baumert, Annette Peters, Willem H. Ouwehand, Panos Deloukas, John R. Thompson, Andreas Ziegler, Nilesh J. Samani, Heribert Schunkert

    منشور في 2009
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    Artigo
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  13. 13
    Genome-wide association study of intracranial aneurysm identifies three new risk loci

    Genome-wide association study of intracranial aneurysm identifies three new risk loci حسب Katsuhito Yasuno, Kaya Bilgüvar, Philippe Bijlenga, Siew‐Kee Low, Boris Krischek, Georg Auburger, Matthias Simon, Dietmar Krex, Zülfikar Arlıer, Nikhil R. Nayak, Ynte M. Ruigrok, Mika Niemelä, Atsushi Tajima, Mikael von und zu Fraunberg, Tamás Dóczi, Florentina Wirjatijasa, Akira Hata, Jordi Blasco, Ági Oszvald, Hidetoshi Kasuya, Gulam Zilani, Beate Schoch, Pankaj Kumar Singh, Carsten Stüer, Roelof Risselada, Jürgen Beck, Teresa Solá, Filomena Ricciardi, Arpo Aromaa, Thomas Illig, Stefan Schreiber, Cornelia M. van Duijn, Leonard H. van den Berg, Claire Perret, Carole Proust, Constantin Roder, Ali Öztürk, Emília Ilona Gaál, Daniela Berg, Christof Geisen, Christoph M. Friedrich, Paul Summers, Alejandro F. Frangi, Matthew W. State, H.‐Erich Wichmann, Monique M.B. Breteler, Cisca Wijmenga, Shrikant Mane, Leena Peltonen, Elío Vivas, Miriam Sturkenboom, Patricia V. Lawford, James V. Byrne, Juan Macho, Erol I. Sandalcioglu, Bernhard Meyer, Andreas Raabe, Helmuth Steinmetz, Daniel A. Rüfenacht, Juha E. Jääskeläinen, Juha Hernesniemi, Gabriël J.E. Rinkel, Hitoshi Zembutsu, Ituro Inoue, Aarno Palotie, François Cambien, Yusuke Nakamura, Richard P. Lifton, Murat Günel

    منشور في 2010
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    Artigo
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  14. 14
    A Genome-Wide Association Study Identifies <i>LIPA</i> as a Susceptibility Gene for Coronary Artery Disease

    A Genome-Wide Association Study Identifies <i>LIPA</i> as a Susceptibility Gene for Coronary Artery Disease حسب Philipp S. Wild, Tanja Zeller, Arne Schillert, Silke Szymczak, Christoph Sinning, Arne Deiseroth, Renate B. Schnabel, Edith Lubos, Till Keller, Medea Eleftheriadis, Christoph Bickel, Hans J. Rupprecht, Sandra Wilde, Heidi Rossmann, Patrick Diemert, L. Adrienne Cupples, Claire Perret, Jeanette Erdmann, Klaus Stark, Marcus E. Kleber, Stephen E. Epstein, Benjamin F. Voight, Kari Kuulasmaa, Mingyao Li, Arne Schäfer, Norman Klopp, Peter S. Braund, Hendrik B. Sager, Serkalem Demissie, Carole Proust, Inke R. König, H.-Erich Wichmann, Wibke Reinhard, Michael M. Hoffmann, Jarmo Virtamo, Mary Susan Burnett, David S. Siscovick, Per Wiklund, Liming Qu, Nour Eddine El Mokthari, John R. Thompson, Annette Peters, Albert V. Smith, Emmanuelle Yon, Jens Baumert, Christian Hengstenberg, Winfried März, Philippe Amouyel, Joseph M. Devaney, Stephen M. Schwartz, Olli Saarela, Nehal N. Mehta, Deborah C. Rubin, Kaisa Silander, Alistair S. Hall, Jean Ferrières, Tamara B. Harris, Olle Melander, Frank Kee, Hákon Hákonarson, Juergen Schrezenmeir, Vilmundur Guðnason, Roberto Elosúa, Dominique Arveiler, Alun Evans, Daniel J. Rader, Thomas Illig, Stefan Schreiber, Joshua C. Bis, David Altshuler, Maryam Kavousi, J. C. M. Witteman, André G. Uitterlinden, Albert Hofman, Aaron R. Folsom, Maja Barbalić, Eric Boerwinkle, Sekar Kathiresan, Muredach P. Reilly, Christopher J. O’Donnell, Nilesh J. Samani, Heribert Schunkert, François Cambien, Karl J. Lackner, Laurence Tiret, Veikko Salomaa, Thomas Münzel, Andreas Ziegler, Stefan Blankenberg

    منشور في 2011
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    Revisão
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