Showing 1 - 6 results of 6 for search 'Rodriguez-Gallego, C', query time: 0.04s
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1
A fast procedure for the detection of defects in Toll-like receptor signaling. by von Bernuth, H, Ku, C, Rodriguez-Gallego, C, Zhang, S, Garty, B, Maródi, L, Chapel, H, Chrabieh, M, Miller, R, Picard, C, Puel, A, Casanova, J
Published 2006Journal article -
2
A novel mutatioin in the <it>PSTPIP1</it> gene is associated with an autoinflammatory disease distinct from classical PAPA syndrome by Sampson B, Bernstein J, Tokio S, Isidor B, Fessatou S, Rodríguez-Gallego C, Gattorno M, Holland S, Aksentijevich I, Lohse P, Holzinger D, Austermann J, Sunderkoetter C, Roth J
Published 2011-09-01Article -
3
Human TLR-7-, -8-, and -9-mediated induction of IFN-alpha/beta and -lambda Is IRAK-4 dependent and redundant for protective immunity to viruses. by Yang, K, Puel, A, Zhang, S, Eidenschenk, C, Ku, C, Casrouge, A, Picard, C, von Bernuth, H, Senechal, B, Plancoulaine, S, Al-Hajjar, S, Al-Ghonaium, A, Maródi, L, Davidson, D, Speert, D, Roifman, C, Garty, B, Ozinsky, A, Barrat, F, Coffman, R, Miller, R, Li, X, Lebon, P, Rodriguez-Gallego, C, Chapel, H
Published 2005Journal article -
4
Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency. by Picard, C, von Bernuth, H, Ghandil, P, Chrabieh, M, Levy, O, Arkwright, P, McDonald, D, Geha, R, Takada, H, Krause, J, Creech, C, Ku, C, Ehl, S, Maródi, L, Al-Muhsen, S, Al-Hajjar, S, Al-Ghonaium, A, Day-Good, N, Holland, S, Gallin, J, Chapel, H, Speert, D, Rodriguez-Gallego, C, Colino, E, Garty, B
Published 2010Journal article -
5
Mutations in STAT3 and IL12RB1 impair the development of human IL-17-producing T cells. by de Beaucoudrey, L, Puel, A, Filipe-Santos, O, Cobat, A, Ghandil, P, Chrabieh, M, Feinberg, J, von Bernuth, H, Samarina, A, Jannière, L, Fieschi, C, Stéphan, J, Boileau, C, Lyonnet, S, Jondeau, G, Cormier-Daire, V, Le Merrer, M, Hoarau, C, Lebranchu, Y, Lortholary, O, Chandesris, M, Tron, F, Gambineri, E, Bianchi, L, Rodriguez-Gallego, C
Published 2008Journal article -
6
Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons by Bolze, A, Boisson, B, Bosch, B, Antipenko, A, Bouaziz, M, Sackstein, P, Chaker-Margot, M, Barlogis, V, Briggs, T, Colino, E, Elmore, A, Fischer, A, Genel, F, Hewlett, A, Jedidi, M, Kelecic, J, Krüger, R, Ku, C, Kumararatne, D, Lefevre-Utile, A, Loughlin, S, Mahlaoui, N, Markus, S, Garcia, J, Nizon, M, Oleastro, M, Pac, M, Picard, C, Pollard, A, Rodriguez-Gallego, C, Thomas, C, Von Bernuth, H, Worth, A, Meyts, I, Risolino, M, Selleri, L, Puel, A, Klinge, S, Abel, L, Casanova, J
Published 2018Journal article