Результати пошуку - Alejandro Nieto-Patlán

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  1. 1
    A partial form of inherited human USP18 deficiency underlies infection and inflammation

    A partial form of inherited human USP18 deficiency underlies infection and inflammation за авторством Marta Martín-Fernández, Sofija Buta, Tom Le Voyer, Zhi Li, Lasse Toftdal Dynesen, Françoise Vuillier, Lina Franklin, Fatima Ailal, Alice Muglia Thomaz da Silva Amancio, Louise Malle, Conor Gruber, Ibtihal Benhsaien, Jennie Altman, Justin Taft, Caroline Deswarte, Manon Roynard, Alejandro Nieto-Patlán, Kunihiko Moriya, Jérémie Rosain, Nathalie Boddaert, Aziz Bousfiha, Yanick J. Crow, Dragana Janković, Alan Sher, Jean‐Laurent Casanova, Sandra Pellegrini, Jacinta Bustamante, Dusan Bogunovic

    Опубліковано 2022
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    Artigo
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  2. 2
    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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    Revisão
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  3. 3
    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 за авторством 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

    Опубліковано 2021
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    Carta
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  4. 4
    Human IFN-γ immunity to mycobacteria is governed by both IL-12 and IL-23

    Human IFN-γ immunity to mycobacteria is governed by both IL-12 and IL-23 за авторством Rubén Martínez‐Barricarte, Janet Markle, S. Cindy, Elissa K. Deenick, Noé Ramírez-Alejo, Federico Mele, Daniela Latorre, Seyed Alireza Mahdaviani, Caner Aytekin, Davood Mansouri, Vanessa L. Bryant, Fabienne Jabot‐Hanin, Caroline Deswarte, Alejandro Nieto-Patlán, Laura Surace, Gaspard Kerner, Yuval Itan, Sandra Jovic, Danielle T. Avery, Natalie Wong, Geetha Rao, Étienne Patin, Satoshi Okada, Benedetta Bigio, Bertrand Boisson, Franck Rapaport, Yoann Seeleuthner, Monika Schmidt, Aydan İkincioğulları, Figen Doğu, Gönül Tanır, Payam Tabarsi, Mohammed Reza Bloursaz, Julia K. Joseph, Avneet Heer, Xiao‐Fei Kong, Mélanie Migaud, Tomi Lazarov, Frédéric Geissmann, Bernhard Fleckenstein, Cecilia S. Lindestam Arlehamn, Alessandro Sette, Anne Puel, Jean‐François Emile, Esther van de Vosse, Lluís Quintana‐Murci, James P. Di Santo, Laurent Abel, Stéphanie Boisson‐Dupuis, Jacinta Bustamante, Stuart G. Tangye, Federica Sallusto, Jean‐Laurent Casanova

    Опубліковано 2018
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    Artigo
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  5. 5
    Inherited p40phox deficiency differs from classic chronic granulomatous disease

    Inherited p40phox deficiency differs from classic chronic granulomatous disease за авторством 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

    Опубліковано 2018
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    Artigo
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