Jinx, an MCMV susceptibility phenotype caused by disruption of Unc13d: a mouse model of type 3 familial hemophagocytic lymphohistiocytosis

Lignende værker

• Jinx, an MCMV susceptibility phenotype caused by disruption of Unc13d: a mouse model of type 3 familial hemophagocytic lymphohistiocytosis
  af: Crozat, Karine, et al.
  Udgivet: (2007)
• Disruption of MyD88 signaling suppresses hemophagocytic lymphohistiocytosis in mice
  af: Krebs, Philippe, et al.
  Udgivet: (2011)
• Velvet, a dominant Egfr mutation that causes wavy hair and defective eyelid development in mice.
  af: Du, Xin, et al.
  Udgivet: (2004)
• Toll-like receptors 9 and 3 as essential components of innate immune defense against mouse cytomegalovirus infection
  af: Tabeta, Koichi, et al.
  Udgivet: (2004)
• Familial Hemophagocytic Lymphohistiocytosis due to Mutation of UNC13D Gene
  af: Giri, Prabhas Prasun, et al.
  Udgivet: (2015)