Investigation of the mechanism of the dominant negative effect of mutations in the tyrosine kinase domain of the insulin receptor.

Lignende værker

• Mutations in the Extracellular Domain Cause RET Loss of Function by a Dominant Negative Mechanism
  af: Cosma, Maria Pia, et al.
  Udgivet: (1998)
• Mutational analysis of Lck in CD45-negative T cells: dominant role of tyrosine 394 phosphorylation in kinase activity.
  af: D'Oro, U, et al.
  Udgivet: (1996)
• A Computational Study of the Phosphorylation Mechanism of the Insulin Receptor Tyrosine Kinase
  af: Zhou, Baojing, et al.
  Udgivet: (2009)
• Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome
  af: Hong, Sungkook, et al.
  Udgivet: (2016)
• Investigating Molecular Mechanisms of Activation and Mutation of the HER2 Receptor Tyrosine Kinase through Computational Modeling and Simulation
  af: Telesco, Shannon E., et al.
  Udgivet: (2011)