NADPH oxidase modulates MHC class II antigen presentation by B cells

Por Crotzer, Victoria L., Matute, Juan D., Arias, Andrés A., Zhao, Heng, Quilliam, Lawrence A., Dinauer, Mary C., Blum, Janice S.
Publicado em 2012

A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40(phox) and selective defects in neutrophil NADPH oxidase activity

Por Matute, Juan D., Arias, Andres A., Wright, Nicola A. M., Wrobel, Iwona, Waterhouse, Christopher C. M., Li, Xing Jun, Marchal, Christophe C., Stull, Natalie D., Lewis, David B., Steele, MacGregor, Kellner, James D., Yu, Weiming, Meroueh, Samy O., Nauseef, William M., Dinauer, Mary C.
Publicado em 2009

Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease

Por 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
Publicado em 2011

The human CIB1–EVER1–EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses

Por de Jong, Sarah Jill, Créquer, Amandine, Matos, Irina, Hum, David, Gunasekharan, Vignesh, Lorenzo, Lazaro, Jabot-Hanin, Fabienne, Imahorn, Elias, Arias, Andres A., Vahidnezhad, Hassan, Youssefian, Leila, Markle, Janet G., Patin, Etienne, D’Amico, Aurelia, Wang, Claire Q.F., Full, Florian, Ensser, Armin, Leisner, Tina M., Parise, Leslie V., Bouaziz, Matthieu, Maya, Nataly Portilla, Cadena, Xavier Rueda, Saka, Bayaki, Saeidian, Amir Hossein, Aghazadeh, Nessa, Zeinali, Sirous, Itin, Peter, Krueger, James G., Laimins, Lou, Abel, Laurent, Fuchs, Elaine, Uitto, Jouni, Franco, Jose Luis, Burger, Bettina, Orth, Gérard, Jouanguy, Emmanuelle, Casanova, Jean-Laurent
Publicado no J Exp Med (2018)

Inherited p40(phox) deficiency differs from classic chronic granulomatous disease

Por van de Geer, Annemarie, Nieto-Patlán, Alejandro, Kuhns, Douglas B., Tool, Anton T.J., Arias, Andrés A., Bouaziz, Matthieu, de Boer, Martin, Franco, José Luis, Gazendam, Roel P., van Hamme, John L., van Houdt, Michel, van Leeuwen, Karin, Verkuijlen, Paul J.H., van den Berg, Timo K., Alzate, Juan F., Arango-Franco, Carlos A., Batura, Vritika, Bernasconi, Andrea R., Boardman, Barbara, Booth, Claire, Burns, Siobhan O., Cabarcas, Felipe, Bensussan, Nadine Cerf, Charbit-Henrion, Fabienne, Corveleyn, Anniek, Deswarte, Caroline, Azcoiti, María Esnaola, Foell, Dirk, Gallin, John I., Garcés, Carlos, Guedes, Margarida, Hinze, Claas H., Holland, Steven M., Hughes, Stephen M., Ibañez, Patricio, Malech, Harry L., Meyts, Isabelle, Moncada-Velez, Marcela, Moriya, Kunihiko, Neves, Esmeralda, Oleastro, Matias, Perez, Laura, Rattina, Vimel, Oleaga-Quintas, Carmen, Warner, Neil, Muise, Aleixo M., López, Jeanet Serafín, Trindade, Eunice, Vasconcelos, Julia, Vermeire, Séverine, Wittkowski, Helmut, Worth, Austen, Abel, Laurent, Dinauer, Mary C., Arkwright, Peter D., Roos, Dirk, Casanova, Jean-Laurent, Kuijpers, Taco W., Bustamante, Jacinta
Publicado no J Clin Invest (2018)