Ngā hua rapu - Vogt, Guillaume

In vitro differentiation of human macrophages with enhanced antimycobacterial activity mā Vogt, Guillaume, Nathan, Carl

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23andMe: a new two-sided data-banking market model mā Stoeklé, Henri-Corto, Mamzer-Bruneel, Marie-France, Vogt, Guillaume, Hervé, Christian

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IFN-γ Mediates the Rejection of Haematopoietic Stem Cells in IFN-γR1-Deficient Hosts mā Rottman, Martin, Soudais, Claire, Vogt, Guillaume, Renia, Laurent, Emile, Jean-François, Decaluwe, Hélène, Gaillard, Jean-Louis, Casanova, Jean-Laurent

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Molecular Tumor Boards: Ethical Issues in the New Era of Data Medicine mā Stoeklé, Henri-Corto, Mamzer-Bruneel, Marie-France, Frouart, Charles-Henry, Le Tourneau, Christophe, Laurent-Puig, Pierre, Vogt, Guillaume, Hervé, Christian

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The human gene connectome as a map of short cuts for morbid allele discovery mā Itan, Yuval, Zhang, Shen-Ying, Vogt, Guillaume, Abhyankar, Avinash, Herman, Melina, Nitschke, Patrick, Fried, Dror, Quintana-Murci, Lluis, Abel, Laurent, Casanova, Jean-Laurent

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Inhibitors Selective for Mycobacterial versus Human Proteasomes mā Lin, Gang, Li, Dongyang, de Carvalho, Luiz Pedro Sorio, Deng, Haiteng, Tao, Hui, Vogt, Guillaume, Wu, Kangyun, Schneider, Jean, Chidawanyika, Tamutenda, Warren, J. David, Li, Huilin, Nathan, Carl

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A novel X‐linked recessive form of Mendelian susceptibility to mycobaterial disease mā Bustamante, Jacinta, Picard, Capucine, Fieschi, Claire, Filipe‐Santos, Orchidée, Feinberg, Jacqueline, Perronne, Christian, Chapgier, Ariane, de Beaucoudrey, Ludovic, Vogt, Guillaume, Sanlaville, Damien, Lemainque, Arnaud, Emile, Jean‐François, Abel, Laurent, Casanova, Jean‐Laurent

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French‐style genetics v. 2.0: The “e‐CohortE” project mā Stoeklé, Henri‐Corto, Bollet, Marc, Cobat, Aurélie, Charlier, Philippe, Bloch, Oudy Ch., Flatot, Jérôme, Draghi, Clément, Tolyan, Valérie, Hervé, Christian, Desvaux, Pierre, Uzan, Laurent, Grynberg, Michaël, Alcaïs, Alexandre, Tolédano, Alain, Vogt, Guillaume

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A partial form of recessive STAT1 deficiency in humans mā Chapgier, Ariane, Kong, Xiao-Fei, Boisson-Dupuis, Stéphanie, Jouanguy, Emmanuelle, Averbuch, Diana, Feinberg, Jacqueline, Zhang, Shen-Ying, Bustamante, Jacinta, Vogt, Guillaume, Lejeune, Julien, Mayola, Eleonore, de Beaucoudrey, Ludovic, Abel, Laurent, Engelhard, Dan, Casanova, Jean-Laurent

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Complementation of a pathogenic IFNGR2 misfolding mutation with modifiers of N-glycosylation mā Vogt, Guillaume, Bustamante, Jacinta, Chapgier, Ariane, Feinberg, Jacqueline, Boisson Dupuis, Stephanie, Picard, Capucine, Mahlaoui, Nizar, Gineau, Laure, Alcaïs, Alexandre, Lamaze, Christophe, Puck, Jennifer M., de Saint Basile, Geneviève, Khayat, Claudia Djambas, Mikhael, Raymond, Casanova, Jean-Laurent

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A novel form of cell type-specific partial IFN-γR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon mā Kong, Xiao-Fei, Vogt, Guillaume, Chapgier, Ariane, Lamaze, Christophe, Bustamante, Jacinta, Prando, Carolina, Fortin, Anny, Puel, Anne, Feinberg, Jacqueline, Zhang, Xin-Xin, Gonnord, Pauline, Pihkala-Saarinen, Ulla M., Arola, Mikko, Moilanen, Petra, Abel, Laurent, Korppi, Matti, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent

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Mycobacterium simiae infection in two unrelated patients with different forms of inherited IFN-γR2 deficiency mā Martínez-Barricarte, Rubén, Megged, Orli, Stepensky, Polina, Casimir, Pierre, Moncada-Velez, Marcela, Averbuch, Diana, Assous, Marc Victor, Abuzaitoun, Omar, Kong, Xiao-Fei, Pedergnana, Vincent, Deswarte, Caroline, Migaud, Mélanie, Rose-John, Stefan, Itan, Yuval, Boisson, Bertrand, Belkadi, Aziz, Conti, Francesca, Abel, Laurent, Vogt, Guillaume, Boisson-Dupuis, Stephanie, Casanova, Jean-Laurent, Bustamante, Jacinta

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Novel STAT1 Alleles in Otherwise Healthy Patients with Mycobacterial Disease mā Chapgier, Ariane, Boisson-Dupuis, Stéphanie, Jouanguy, Emmanuelle, Vogt, Guillaume, Feinberg, Jacqueline, Prochnicka-Chalufour, Ada, Casrouge, Armanda, Yang, Kun, Soudais, Claire, Fieschi, Claire, Santos, Orchidée Filipe, Bustamante, Jacinta, Picard, Capucine, de Beaucoudrey, Ludovic, Emile, Jean-François, Arkwright, Peter D, Schreiber, Robert D, Rolinck-Werninghaus, Claudia, Rösen-Wolff, Angela, Magdorf, Klaus, Roesler, Joachim, Casanova, Jean-Laurent

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Herpes simplex virus encephalitis in a patient with complete TLR3 deficiency: TLR3 is otherwise redundant in protective immunity mā Guo, Yiqi, Audry, Magali, Ciancanelli, Michael, Alsina, Laia, Azevedo, Joana, Herman, Melina, Anguiano, Esperanza, Sancho-Shimizu, Vanessa, Lorenzo, Lazaro, Pauwels, Elodie, Philippe, Paul Bastard, Pérez de Diego, Rebeca, Cardon, Annabelle, Vogt, Guillaume, Picard, Capucine, Andrianirina, Zafitsara Zo, Rozenberg, Flore, Lebon, Pierre, Plancoulaine, Sabine, Tardieu, Marc, Valérie Doireau, Jouanguy, Emmanuelle, Chaussabel, Damien, Geissmann, Frederic, Abel, Laurent, Casanova, Jean-Laurent, Zhang, Shen-Ying

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Haploinsufficiency at the human IFNGR2 locus contributes to mycobacterial disease mā Kong, Xiao-Fei, Vogt, Guillaume, Itan, Yuval, Macura-Biegun, Anna, Szaflarska, Anna, Kowalczyk, Danuta, Chapgier, Ariane, Abhyankar, Avinash, Furthner, Dieter, Djambas Khayat, Claudia, Okada, Satoshi, Bryant, Vanessa L., Bogunovic, Dusan, Kreins, Alexandra, Moncada-Vélez, Marcela, Migaud, Mélanie, Al-Ajaji, Sulaiman, Al-Muhsen, Saleh, Holland, Steven M., Abel, Laurent, Picard, Capucine, Chaussabel, Damien, Bustamante, Jacinta, Casanova, Jean-Laurent, Boisson-Dupuis, Stéphanie

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Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation mā Moncada-Vélez, Marcela, Martinez-Barricarte, Rubén, Bogunovic, Dusan, Kong, Xiao-Fei, Blancas-Galicia, Lizbeth, Tirpan, Cengiz, Aksu, Guzide, Vincent, Quentin B., Boisson, Bertrand, Itan, Yuval, Ramírez-Alejo, Noé, Okada, Satoshi, Kreins, Alexandra Y., Bryant, Vanessa L., Franco, Jose Luis, Migaud, Mélanie, Espinosa-Padilla, Sara, Yamazaki-Nakashimada, Marco, Espinosa-Rosales, Francisco, Kutukculer, Necil, Abel, Laurent, Bustamante, Jacinta, Vogt, Guillaume, Casanova, Jean-Laurent, Boisson-Dupuis, Stéphanie

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Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease mā Bustamante, Jacinta, Arias, Andres A, Vogt, Guillaume, Picard, Capucine, Galicia, Lizbeth Blancas, Prando, Carolina, Grant, Audrey V, Marchal, Christophe C, Hubeau, Marjorie, Chapgier, Ariane, de Beaucoudrey, Ludovic, Puel, Anne, Feinberg, Jacqueline, Valinetz, Ethan, Jannière, Lucile, Besse, Céline, Boland, Anne, Brisseau, Jean-Marie, Blanche, Stéphane, Lortholary, Olivier, Fieschi, Claire, Emile, Jean-François, Boisson-Dupuis, Stéphanie, Al-Muhsen, Saleh, Woda, Bruce, Newburger, Peter E, Condino-Neto, Antonio, Dinauer, Mary C, Abel, Laurent, Casanova, Jean-Laurent

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Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency mā Bogunovic, Dusan, Byun, Minji, Durfee, Larissa A., Abhyankar, Avinash, Sanal, Ozden, Mansouri, Davood, Salem, Sandra, Radovanovic, Irena, Grant, Audrey V., Adimi, Parisa, Mansouri, Nahal, Okada, Satoshi, Bryant, Vanessa L., Kong, Xiao-Fei, Kreins, Alexandra, Velez, Marcela Moncada, Boisson, Bertrand, Khalilzadeh, Soheila, Ozcelik, Ugur, Darazam, Ilad Alavi, Schoggins, John W., Rice, Charles M., Al-Muhsen, Saleh, Behr, Marcel, Vogt, Guillaume, Puel, Anne, Bustamante, Jacinta, Gros, Philippe, Huibregtse, Jon M., Abel, Laurent, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent

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

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X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production mā Filipe-Santos, Orchidée, Bustamante, Jacinta, Haverkamp, Margje H., Vinolo, Emilie, Ku, Cheng-Lung, Puel, Anne, Frucht, David M., Christel, Karin, von Bernuth, Horst, Jouanguy, Emmanuelle, Feinberg, Jacqueline, Durandy, Anne, Senechal, Brigitte, Chapgier, Ariane, Vogt, Guillaume, de Beaucoudrey, Ludovic, Fieschi, Claire, Picard, Capucine, Garfa, Meriem, Chemli, Jalel, Bejaoui, Mohamed, Tsolia, Maria N., Kutukculer, Necil, Plebani, Alessandro, Notarangelo, Luigi, Bodemer, Christine, Geissmann, Frédéric, Israël, Alain, Véron, Michel, Knackstedt, Maike, Barbouche, Ridha, Abel, Laurent, Magdorf, Klaus, Gendrel, Dominique, Agou, Fabrice, Holland, Steven M., Casanova, Jean-Laurent

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