Resultados da busca - Aurore Morlon

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  1. 1
    The LIM-only protein FHL2 is a serum-inducible transcriptional coactivator of AP-1

    The LIM-only protein FHL2 is a serum-inducible transcriptional coactivator of AP-1 por Aurore Morlon, Paolo Sassone–Corsi

    Publicado em 2003
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  2. 2
    TAB2, TRAF6 and TAK1 are involved in NF-κB activation induced by the TNF-receptor, Edar and its adaptator Edaradd

    TAB2, TRAF6 and TAK1 are involved in NF-κB activation induced by the TNF-receptor, Edar and its adaptator Edaradd por Aurore Morlon, Arnold Münnich, Asma Smahi

    Publicado em 2005
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  3. 3
    Transcription factor TEAD4 regulates expression of Myogenin and the unfolded protein response genes during C2C12 cell differentiation

    Transcription factor TEAD4 regulates expression of Myogenin and the unfolded protein response genes during C2C12 cell differentiation por Ataaillah Benhaddou, Céline Keime, Tao Ye, Aurore Morlon, Isabelle Michel, Bernard Jost, Gabrielle Mengus, Irwin Davidson

    Publicado em 2011
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  4. 4
    The MHC class I MICA gene is a histocompatibility antigen in kidney transplantation

    The MHC class I MICA gene is a histocompatibility antigen in kidney transplantation por Raphaël Carapito, Ismaïl Aouadi, Martin Verniquet, Meiggie Untrau, Angélique Pichot, Thomas Beaudrey, Xavier Bassand, Sébastien Meyer, Loic Faucher, Juliane Posson, Aurore Morlon, И. В. Котова, Florent Delbos, Alexandre Walencik, Alice Aarnink, Anne Kennel, Caroline Suberbielle, Jean‐Luc Taupin, Benedict M. Matern, Eric Spierings, Nicolas Congy‐Jolivet, Arnaud Essaydi, Peggy Perrin, Antoine Blancher, Dominique Charron, Nezih Cereb, Myriam Maumy‐Bertrand, Frédèric Bertrand, Valérie Garrigue, Vincent Pernin, Laurent Weekers, Maarten Naesens, Nassim Kamar, Christophe Legendre, Denis Glotz, Sophie Caillard, Marc Ladrière, Magali Giral, Dany Anglicheau, Caner Süsal, Seiamak Bahram

    Publicado em 2022
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  5. 5
    Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond–like features

    Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond–like features por Raphaël Carapito, Martina Konantz, Catherine Paillard, Zhichao Miao, Angélique Pichot, Magalie S. Leduc, Yaping Yang, Katie Bergstrom, Donald H. Mahoney, Deborah L. Shardy, Ghada Alsaleh, Lydie Naegely, Aline Kolmer, Nicodème Paul, Antoine Hanauer, Véronique Rolli, Joëlle S. Müller, Elisa Alghisi, Loïc Sauteur, Cécile Macquin, Aurore Morlon, Consuelo Sebastia Sancho, Patrizia Amati‐Bonneau, Vincent Procaccio, Anne‐Laure Mosca‐Boidron, Nathalie Marle, Naël Osmani, Olivier Lefèbvre, Jacky G. Goetz, Şule Ünal, Nurten Akarsu, Mirjana Radosavljevic, Marie‐Pierre Chenard, Fanny Rialland, Audrey Grain, Marie C. Béné, Marion Eveillard, Marie Vincent, Julien Guy, Laurence Faivre, Christel Thauvin‐Robinet, Julien Thévenon, Kasiani C. Myers, Mark D. Fleming, Akiko Shimamura, Elodie Bottollier-Lemallaz, Éric Westhof, Claudia Lengerke, Bertrand Isidor, Seiamak Bahram

    Publicado em 2017
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  6. 6
    Matching for the nonconventional MHC-I MICA gene significantly reduces the incidence of acute and chronic GVHD

    Matching for the nonconventional MHC-I MICA gene significantly reduces the incidence of acute and chronic GVHD por Raphaël Carapito, Nicolas Jung, Marius Kwemou, Meiggie Untrau, Sandra Michel, Angélique Pichot, Gaëlle Giacometti, Cécile Macquin, W. Ilias, Aurore Morlon, Irina Kotova, Petya Apostolova, Annette Schmitt‐Graeff, Anne Cesbron, Katia Gagne, Machteld Oudshoorn, Bronno van der Holt, Myriam Labalette, Eric Spierings, Christophe Picard, Pascale Loiseau, Ryad Tamouza, Antoine Toubert, A. Parissiadis, Valérie Dubois, Xavier Lafarge, Myriam Maumy‐Bertrand, Frédèric Bertrand, Luca Vago, Fabio Ciceri, Catherine Paillard, Sergi Querol, Jorge Sierra, Katharina Fleischhauer, Arnon Nagler, Myriam Labopin, Hidetoshi Inoko, Peter A. von dem Borne, Jürgen Kuball, Masao Ôta, Yoshihiko Katsuyama, Mauricette Michallet, Bruno Lioure, Régis Peffault de Latour, Didier Blaise, Jan J. Cornelissen, Ibrahim Yakoub‐Agha, Frans H.J. Claas, Philippe Moreau, Nöel Milpied, Dominique Charron, Mohamad Mohty, Robert Zeiser, Gerard Socié, Seiamak Bahram

    Publicado em 2016
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  7. 7
    ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder

    ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder por Raphaël Carapito, Ekaterina L. Ivanova, Aurore Morlon, Linyan Meng, Anne Molitor, Éva Erdmann, Bruno Kieffer, Angélique Pichot, Lydie Naegely, Aline Kolmer, Nicodème Paul, Antoine Hanauer, Frédéric Tran Mau‐Them, Nolwenn Jean‐Marçais, Susan M. Hiatt, Gregory M. Cooper, Tatiana Tvrdik, Alison M. Muir, Clémantine Dimartino, Maya Chopra, Jeanne Amiel, Christopher T. Gordon, Fabien Dutreux, Aurore Garde, Christel Thauvin‐Robinet, Xia Wang, Magalie S. Leduc, Meredith Phillips, Heather P. Crawford, Mary K. Kukolich, David Hunt, Victoria Harrison, Mira Kharbanda, Robert Śmigiel, Nina B. Gold, Christina Hung, David Viskochil, Sarah Dugan, Pınar Bayrak‐Toydemir, Géraldine Joly‐Helas, Anne‐Marie Guerrot, Caroline Schluth–Bolard, Marlène Rio, Ingrid M. Wentzensen, Kirsty McWalter, Rhonda E. Schnur, Andrea M. Lewis, Seema R. Lalani, Noël Mensah-Bonsu, Jocelyn Céraline, Zijie Sun, Rafał Płoski, Carlos A. Bacino, Heather C. Mefford, Laurence Faivre, Olaf A. Bodamer, Jamel Chelly, Bertrand Isidor, Seiamak Bahram

    Publicado em 2019
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