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    A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency by Fornes, Oriol, Jia, Alicia, Kuehn, Hye Sun, Min, Qing, Pannicke, Ulrich, Schleussner, Nikolai, Thouenon, Romane, Yu, Zhijia, de Los Angeles Astbury, María, Biggs, Catherine M, Galicchio, Miguel, Garcia-Campos, Jorge Alberto, Gismondi, Silvina, Gonzalez Villarreal, Guadalupe, Hildebrand, Kyla J, Hönig, Manfred, Hou, Jia, Moshous, Despina, Pittaluga, Stefania, Qian, Xiaowen, Rozmus, Jacob, Schulz, Ansgar S, Staines-Boone, Aidé Tamara, Sun, Bijun, Sun, Jinqiao, Uwe, Schauer, Venegas-Montoya, Edna, Wang, Wenjie, Wang, Xiaochuan, Ying, Wenjing, Zhai, Xiaowen, Zhou, Qinhua, Akalin, Altuna, André, Isabelle, Barth, Thomas F E, Baumann, Bernd, Brüstle, Anne, Burgio, Gaetan, Bustamante, Jacinta C, Casanova, Jean-Laurent, Casarotto, Marco G, Cavazzana, Marina, Chentout, Loïc, Cockburn, Ian A, Costanza, Mariantonia, Cui, Chaoqun, Daumke, Oliver, Del Bel, Kate L, Eibel, Hermann, Feng, Xiaoqian, Franke, Vedran, Gebhardt, J Christof M, Götz, Andrea, Grunwald, Stephan, Hoareau, Bénédicte, Hughes, Timothy R, Jacobsen, Eva-Maria, Janz, Martin, Jolma, Arttu, Lagresle-Peyrou, Chantal, Lai, Nannan, Li, Yaxuan, Lin, Susan, Lu, Henry Y, Lugo-Reyes, Saul O, Meng, Xin, Möller, Peter, Moreno-Corona, Nidia, Niemela, Julie E, Novakovsky, Gherman, Perez-Caraballo, Jareb J, Picard, Capucine, Poggi, Lucie, Puig-Lombardi, Maria-Emilia, Randall, Katrina L, Reisser, Anja, Schmitt, Yohann, Seneviratne, Sandali, Sharma, Mehul, Stoddard, Jennifer, Sundararaj, Srinivasan, Sutton, Harry, Tran, Linh Q, Wang, Ying, Wasserman, Wyeth W, Wen, Zichao, Winkler, Wiebke, Xiong, Ermeng, Yang, Ally W H, Yu, Meiping, Zhang, Lumin, Zhang, Hai, Zhao, Qian, Zhen, Xin, Enders, Anselm, Kracker, Sven, Martinez-Barricarte, Ruben, Mathas, Stephan, Rosenzweig, Sergio D, Schwarz, Klaus

    Published in Science immunology
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