Výsledky vyhledávání - Matthieu Bouaziz

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  1. 1
    Accounting for Population Stratification in Practice: A Comparison of the Main Strategies Dedicated to Genome-Wide Association Studies

    Accounting for Population Stratification in Practice: A Comparison of the Main Strategies Dedicated to Genome-Wide Association Studies Autor Matthieu Bouaziz, Christophe Ambroise, Mickaël Guedj

    Vydáno 2011
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  2. 2
    IRF4 haploinsufficiency in a family with Whipple’s disease

    IRF4 haploinsufficiency in a family with Whipple’s disease Autor Antoine Guérin, Gaspard Kerner, Nico Marr, Janet Markle, Florence Fenollar, Natalie Sui Miu Wong, Sabri Boughorbel, Danielle T. Avery, S. Cindy, Salim Bougarn, Matthieu Bouaziz, Vivien Béziat, Erika Della Mina, Carmen Oleaga‐Quintas, Tomi Lazarov, Lisa Worley, Tina Nguyen, Étienne Patin, Caroline Deswarte, Rubén Martínez‐Barricarte, Soraya Boucherit, X Ayral, Sophie Edouard, Stéphanie Boisson‐Dupuis, Vimel Rattina, Benedetta Bigio, Guillaume Vogt, Frédéric Geissmann, Lluís Quintana‐Murci, Damien Chaussabel, Stuart G. Tangye, Didier Raoult, Laurent Abel, Jacinta Bustamante, Jean‐Laurent Casanova

    Vydáno 2018
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  3. 3
    The human CIB1–EVER1–EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses

    The human CIB1–EVER1–EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses Autor Sarah Jill de Jong, Amandine Créquer, Irina Matos, David Hum, Vignesh Gunasekharan, Lazaro Lorenzo, Fabienne Jabot‐Hanin, E. Imahorn, Andrés A. Arias, Hassan Vahidnezhad, Leila Youssefian, Janet Markle, Étienne Patin, Aurelia D’amico, Claire Q. Wang, Florian Full, Armin Ensser, Thomas Leisner, Leslie V. Parise, Matthieu Bouaziz, Nataly Portilla Maya, Xavier Rueda Cadena, Bayaki Saka, Amir Hossein Saeidian, Nessa Aghazadeh, Sirous Zeinali, Peter Itin, James G. Krueger, Lou Laimins, Laurent Abel, Elaine Fuchs, Jouni Uitto, José Luis Franco, Bettina Burger, Gérard Orth, Emmanuelle Jouanguy, Jean‐Laurent Casanova

    Vydáno 2018
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  4. 4
    Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 Deficiency

    Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 Deficiency Autor Tom Le Voyer, Sonoko Sakata, Miyuki Tsumura, Taushif Khan, Ana Esteve‐Solé, Bandar Al‐Saud, Hatice Eke Güngör, Prasad Taur, Valentine Jeanne-Julien, Mette Christiansen, Lisa-Maria Köhler, Gehad ElGhazali, Jérémie Rosain, Shiho Nishimura, Fumiaki Sakura, Matthieu Bouaziz, Carmen Oleaga‐Quintas, Alejandro Nieto-Patlán, Àngela Deyà‐Martínez, Yasemin Altuner Torun, Anna‐Lena Neehus, Manon Roynard, Şefika Elmas Bozdemir, Nawal Al Kaabi, Moza Al Hassani, Irina Mersiyanova, Flore Rozenberg, Carsten Speckmann, Ina Hainmann, Fabian Hauck, Mohammed H. Al-Zahrani, Sami Al-Hajjar, Saleh Al‐Muhsen, Theresa Cole, Ramsay Fuleihan, Peter D. Arkwright, Raffaele Badolato, Laia Alsina, Laurent Abel, Mukesh Desai, Hamoud Al‐Mousa, Anna Shcherbina, Nico Marr, Stéphanie Boisson‐Dupuis, Jean‐Laurent Casanova, Satoshi Okada, Jacinta Bustamante

    Vydáno 2021
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  5. 5
    A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity

    A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity Autor Vivien Béziat, Juan Li, Jian‐Xin Lin, S. Cindy, Peng Li, Aziz Bousfiha, Isabelle Pellier, Samaneh Zoghi, Safa Barış, Sevgi Keleş, Paul Gray, Ning Du, Yi Wang, Yoann Zerbib, Romain Lévy, Thibaut Leclercq, Frédégonde About, Ai Ing Lim, Geetha Rao, Kathryn Payne, Simon J. Pelham, Danielle T. Avery, Elissa K. Deenick, Bethany Pillay, Janet Chou, Romain Guéry, Aziz Belkadi, Antoine Guérin, Mélanie Migaud, Vimel Rattina, Fatima Ailal, Ibtihal Benhsaien, Matthieu Bouaziz, Tanwir Habib, Damien Chaussabel, Nico Marr, Jamel El‐Benna, Bodo Grimbacher, Orli Wargon, Jacinta Bustamante, Bertrand Boisson, Ingrid Müller‐Fleckenstein, Bernhard Fleckenstein, Marie‐Olivia Chandesris, Matthias Titeux, Sylvie Fraïtag, Marie‐Alexandra Alyanakian, Marianne Leruez‐Ville, Capucine Pïcard, Isabelle Meyts, James P. Di Santo, Alain Hovnanian, Ayper Somer, Ahmet Özen, Nima Rezaei, Talal A. Chatila, Laurent Abel, Warren J. Leonard, Stuart G. Tangye, Anne Puel, Jean‐Laurent Casanova

    Vydáno 2018
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  6. 6
    Inherited p40phox deficiency differs from classic chronic granulomatous disease

    Inherited p40phox deficiency differs from classic chronic granulomatous disease Autor Annemarie van de Geer, Alejandro Nieto-Patlán, Douglas B. Kuhns, Anton T. J. Tool, Andrés A. Arias, Matthieu Bouaziz, Martin de Boer, José Luis Franco, Roel P. Gazendam, John L. van Hamme, Michel van Houdt, Karin van Leeuwen, Paul Verkuijlen, Timo K. van den Berg, Juan F. Álzate, Carlos A. Arango-Franco, Vritika Batura, Andrea Bernasconi, Barbara Boardman, Claire Booth, Siobhán O. Burns, Felipe Cabarcas, Nadine Cerf‐Bensussan, Fabienne Charbit‐Henrion, Anniek Corveleyn, Caroline Deswarte, María Esnaola Azcoiti, Dirk Foell, John I. Gallin, Carlos Garcés, Margarida Guedes, Claas Hinze, Steven M. Holland, Stephen Hughes, Patricio Ibáñez, Harry L. Malech, Isabelle Meyts, Marcela Moncada‐Vélez, Kunihiko Moriya, Esmeralda Neves, Matías Oleastro, Laura Pérez, Vimel Rattina, Carmen Oleaga‐Quintas, Neil Warner, Aleixo M. Muise, Jeanet Serafín‐López, Eunice Trindade, Júlia Vasconcelos, Séverine Vermeire, Helmut Wittkowski, Austen Worth, Laurent Abel, Mary C. Dinauer, Peter D. Arkwright, Dirk Roos, Jean‐Laurent Casanova, Taco W. Kuijpers, Jacinta Bustamante

    Vydáno 2018
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  7. 7
    Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common <i>TYK2</i> missense variant

    Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common <i>TYK2</i> missense variant Autor Stéphanie Boisson‐Dupuis, Noé Ramírez-Alejo, Zhi Li, Étienne Patin, Geetha Rao, Gaspard Kerner, Che Kang Lim, Dimitry N. Krementsov, Nicholas Hernandez, S. Cindy, Qian Zhang, Janet Markle, Rubén Martínez‐Barricarte, Kathryn Payne, Robert O. Fisch, Caroline Deswarte, Joshua Halpern, Matthieu Bouaziz, Jeanette Mulwa, Durga Sivanesan, Tomi Lazarov, Rodrigo Naves, Patricia García, Yuval Itan, Bertrand Boisson, Alix Checchi, Fabienne Jabot‐Hanin, Aurélie Cobat, Andrea Guennoun, Carolyn C. Jackson, Sevgi Pekcan, Zafer Çalışkaner, Jaime Inostroza, Beatriz Tavares Costa‐Carvalho, José Antônio Tavares de Albuquerque, Humberto Garcia‐Ortíz, Lorena Orozco, Tayfun Özçelık, A. Abid, Ismail Abderahmani Rhorfi, Hicham Souhi, Hicham Naji Amrani, Adil Zegmout, Frédéric Geissmann, Stephen W. Michnick, Ingrid Müller‐Fleckenstein, Bernhard Fleckenstein, Anne Puel, Michael J. Ciancanelli, Nico Marr, Hassan Abolhassani, María Elvira Balcells, Antônio Condino‐Neto, Alexis Strickler, Katia Abarca, Cory Teuscher, Hans D. Ochs, İsmail Reisli, Esra Hazar Sayar, Jamila El Baghdadi, Jacinta Bustamante, Lennart Hammarström, Stuart G. Tangye, Sandra Pellegrini, Lluís Quintana‐Murci, Laurent Abel, Jean‐Laurent Casanova

    Vydáno 2018
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