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Dendritic cells require STAT-1 phosphorylated at its transactivating domain for the induction of peptide-specific CTL, , , , , , , , , and 16 other author(s). J Immunol, 183 (4): 2286-2293 (2009)Collagen VII in severe recessive dystrophic epidermolysis bullosa: expression of mRNA but lack of intact protein product in skin and cutaneous cells in vitro, , , , , , , and . J Invest Dermatol, 102 (2): 260-262 (1994)A combination of a common splice site mutation and a frameshift mutation in the COL7A1 gene: absence of functional collagen VII in keratinocytes and skin, , , , , , , , , and . J Invest Dermatol, 109 (3): 384-389 (1997)Cell entry, efficient RNA replication, and production of infectious hepatitis C virus progeny in mouse liver-derived cells, , , , , , , , , and 4 other author(s). Hepatology, 59 (1): 78-88 (2014)Conditional IFNAR1 ablation reveals distinct requirements of Type I IFN signaling for NK cell maturation and tumor surveillance, , , , , , , , , and 7 other author(s). Oncoimmunology, 1 (7): 1027-1037 (2012)Myeloid type I interferon signaling promotes atherosclerosis by stimulating macrophage recruitment to lesions, , , , , , , , , and 4 other author(s). Cell Metab, 12 (2): 142-153 (August 2010)N1L is an ectromelia virus virulence factor and essential for in vivo spread upon respiratory infection., , , , , , , , and . J Virol, 85 (7): 3557-3569 (2011)Thogoto virus infection induces sustained type I interferon responses that depend on RIG-I-like helicase signaling of conventional dendritic cells., , , , , , and . J Virol, 84 (23): 12344-12350 (2010)Concomitant type I IFN receptor-triggering of T cells and of DC is required to promote maximal modified vaccinia virus Ankara-induced T-cell expansion, , , , , , , , , and . Eur J Immunol, 40 (10): 2769-2777 (October 2010)The role of antibody concentration and avidity in antiviral protection, , , , , , , , and . Science, 276 (5321): 2024-2027 (1997)