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  • Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D
    [作者:Meeths, M; Chiang, SCC; Wood, SM; Entesarian, M; Schlums, H; Bang, B; Nordenskjold, E; Bjorklund, C; Jakovljevic, G; Jazbec, J; Hasle, H; Holmqvist, BM; Rajic, L; Pfeifer, S; Rosthoj, S; Sabel, M; Salmi, TT; Stokland, T; Winiarski, J; Ljunggren, HG; Fadeel, B; Nordenskjold, M; Henter, JI; Bryceson, YT,期刊:Blood, 页码:5783-5793 , 文章类型: Article,,卷期:2011年118-22]
  • Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive, often-fatal hyperinflammatory disorder. Mutations in PRF1, UNC13D, STX11, and STXBP2 are causative of FHL2, 3, 4, and 5, respectively. In a maj...
  • IL-36R ligands are potent regulators of dendritic and T cells
    [作者:Vigne, S; Palmer, G; Lamacchia, C; Martin, P; Talabot-Ayer, D; Rodriguez, E; Ronchi, F; Sallusto, F; Dinh, H; Sims, JE; Gabay, C,期刊:Blood, 页码:5813-5823 , 文章类型: Article,,卷期:2011年118-22]
  • IL-36 alpha (IL-1F6), IL-36 beta (IL-1F8), and IL-36 gamma (IL-1F9) are members of the IL-1 family of cytokines. These cytokines bind to IL-36R (IL-1Rrp2) and IL-1RAcP, activating similar intracellular signals as IL-1, w...
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