Результати пошуку - Frédéric Torès

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  1. 1
    Antitumour activity of an inhibitor of miR-34a in liver cancer with β-catenin-mutations

    Antitumour activity of an inhibitor of miR-34a in liver cancer with β-catenin-mutations за авторством Angélique Gougèlet, Chiara Sartor, Laura Bachelot, Cécile Godard, Carmen Marchiol, Gilles Renault, Frédéric Torès, Patrick Nitschké, Catherine Cavard, Benoît Terris, Christine Perret, Sabine Colnot

    Опубліковано 2015
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  2. 2
    SLY regulates genes involved in chromatin remodeling and interacts with TBL1XR1 during sperm differentiation

    SLY regulates genes involved in chromatin remodeling and interacts with TBL1XR1 during sperm differentiation за авторством C. Moretti, Maria‐Elisabetta Serrentino, Côme Ialy‐Radio, Marion Delessard, Tatiana Soboleva, Frédéric Torès, Marjorie Leduc, Patrick Nitschké, Joël R. Drevet, David J. Tremethick, Daniel Vaiman, Ayhan Kocer, Julie Cocquet

    Опубліковано 2017
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    Artigo
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  3. 3
    RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects

    RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects за авторством Marc Jeanpierre, G. Macé, Mélanie Parisot, Vincent Morinière, A. Pawtowsky, Max E. Benabou, Jéléna Martinovic, Jeanne Amiel, Tania Attié‐Bitach, Anne‐Lise Delezoide, Philippe Loget, Patricia Blanchet, Dominique Gaillard, M. Gonzalés, Wassila Carpentier, Patrick Nitschké, Frédéric Torès, Laurence Heidet, Corinne Antignac, Rémi Salomon

    Опубліковано 2011
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  4. 4
    Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans

    Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans за авторством Camille Humbert, Flora Silbermann, Bharti Morar, Mélanie Parisot, Mohammed Zarhrate, Cécile Masson, Frédéric Torès, Patricia Blanchet, Marie-José Perez, Yuliya Petrov, Philippe Khau Van Kien, J. Roume, Brigitte Leroy, Olivier Gribouval, Luba Kalaydjieva, Laurence Heidet, Rémi Salomon, Corinne Antignac, Alexandre Benmerah, Sophie Saunier, Marc Jeanpierre

    Опубліковано 2014
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  5. 5
    <scp>TUBB</scp> 1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology

    <scp>TUBB</scp> 1 mutations cause thyroid dysgenesis associated with abnormal platelet physiology за авторством Athanasia Stoupa, Frédéric Adam, Dulanjalee Kariyawasam, Catherine Strassel, Sanjay Gawade, Gabor Szinnai, Alexandre Kauskot, Dominique Lasne, Carsten Janke, Kathiresan Natarajan, Alain Schmitt, Christine Bôle‐Feysot, Patrick Nitschké, Juliane Léger, Fabienne Jabot‐Hanin, Frédéric Torès, Anita Michel, Arnold Münnich, Claude Besmond, Raphaël Scharfmann, François Lanza, Delphine Borgel, Michel Polak, Aurore Carré

    Опубліковано 2018
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  6. 6
    Mutations in Endothelin 1 Cause Recessive Auriculocondylar Syndrome and Dominant Isolated Question-Mark Ears

    Mutations in Endothelin 1 Cause Recessive Auriculocondylar Syndrome and Dominant Isolated Question-Mark Ears за авторством Christopher T. Gordon, Florence Petit, Peter M. Kroisel, Linda P. Jakobsen, Roseli Maria Zechi‐Ceide, Myriam Oufadem, Christine Bôle‐Feysot, Solenn Pruvost, Cécile Masson, Frédéric Torès, Thierry Hieu, Patrick Nitschké, Pernille Lindholm, P. Pellerin, Maria Leine Guion‐Almeida, Nancy Mizue Kokitsu‐Nakata, Siulan Vendramini‐Pittoli, Arnold Münnich, Stanislas Lyonnet, Muriel Holder‐Espinasse, Jeanne Amiel

    Опубліковано 2013
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  7. 7
    Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract

    Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract за авторством Laurence Heidet, Vincent Morinière, C. Henry, Lara De Tomasi, Madeline Louise Reilly, Camille Humbert, Olivier Alibeu, Cécile Fourrage, Christine Bôle‐Feysot, Patrick Nitschké, Frédéric Torès, Marc Bras, Marc Jeanpierre, Christine Piétrement, Dominique Gaillard, Marie Gonzalès, Robert Novo, Élise Schaefer, J. Roume, Jéléna Martinovic, Valérie Malan, Rémi Salomon, Sophie Saunier, Corinne Antignac, Marc Jeanpierre

    Опубліковано 2017
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  8. 8
    Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice

    Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice за авторством Lara De Tomasi, Pierre David, Camille Humbert, Flora Silbermann, Christelle Arrondel, Frédéric Torès, Stéphane Fouquet, Audrey Desgrange, Olivier Niel, Christine Bôle‐Feysot, Patrick Nitschké, J. Roume, Marie‐Pierre Cordier, Christine Piétrement, Bertrand Isidor, Philippe Khau Van Kien, Marie Gonzalès, Marie‐Hélène Saint‐Frison, Jéléna Martinovic, Robert Novo, Juliette Piard, Christelle Cabrol, Ishwar C. Verma, Ratna Dua Puri, Hubert Journel, Jacqueline Aziza, Laurent Gavard, Marie-Hélène Saïd-Menthon, Laurence Heidet, Sophie Saunier, Marc Jeanpierre

    Опубліковано 2017
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  9. 9
    Somatic genetic rescue of a germline ribosome assembly defect

    Somatic genetic rescue of a germline ribosome assembly defect за авторством Shengjiang Tan, Laëtitia Kermasson, Christine Hilcenko, Vasileios Kargas, David Traynor, Ahmed Z. Boukerrou, Norberto Escudero-Urquijo, Alexandre Faille, Alexis Bertrand, Maxim Rossmann, Beatriz Goyenechea, Jin Li, Jonathan Moreil, Olivier Alibeu, Blandine Beaupain, Christine Bôle‐Feysot, Stefano Fumagalli, Sophie Kaltenbach, Jean-Alain Martignoles, Cécile Masson, Patrick Nitschké, Mélanie Parisot, Aurore Pouliet, Isabelle Radford‐Weiss, Frédéric Torès, Jean‐Pierre de Villartay, Mohammed Zarhrate, Ai Ling Koh, Kong Boo Phua, Bruno Reversade, Peter J. Bond, Christine Bellanné‐Chantelot, Isabelle Callebaut, François Delhommeau, Jean Donadieu, Alan J. Warren, Patrick Revy

    Опубліковано 2021
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  10. 10
    A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency

    A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency за авторством Jérémie Rosain, Carmen Oleaga‐Quintas, Caroline Deswarte, Hannah Verdin, Stéphane Marot, Garyfallia Syridou, Mahboubeh Mansouri, Seyed Alireza Mahdaviani, Edna Venegas‐Montoya, Μαρία Τσολιά, Mehrnaz Mesdaghi, Л.И. Чернышова, Yuriy Stepanovskiy, Nima Parvaneh, Davood Mansouri, Sigifredo Pedraza‐Sánchez, Анастасія Бондаренко, Sara Elva Espinosa‐Padilla, Marco Antonio Yamazaki‐Nakashimada, Alejandro Nieto-Patlán, Gaspard Kerner, Nathalie Lambert, Corinne Jacques, Emilie Corvilain, Mélanie Migaud, Virginie Grandin, María Teresa Herrera, Fabienne Jabot‐Hanin, Stéphanie Boisson‐Dupuis, Capucine Pïcard, Patrick Nitschké, Anne Puel, Frédéric Torès, Laurent Abel, Lizbeth Blancas‐Galicia, Elfride De Baere, Christine Bôle‐Feysot, Jean‐Laurent Casanova, Jacinta Bustamante

    Опубліковано 2018
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