The FIP1L1-PDGFRA T674I mutation can be inhibited by the tyrosine kinase inhibitor AMN107 (nilotinib)

Blood. 2006 Jun 15;107(12):4970-1; author reply 4972. doi: 10.1182/blood-2006-01-0285.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Amino Acid Substitution*
  • Benzamides
  • Cells, Cultured
  • Humans
  • Hypereosinophilic Syndrome / drug therapy
  • Hypereosinophilic Syndrome / enzymology*
  • Imatinib Mesylate
  • Oncogene Proteins, Fusion / antagonists & inhibitors*
  • Oncogene Proteins, Fusion / genetics
  • Piperazines / therapeutic use
  • Point Mutation*
  • Protein Kinase Inhibitors / pharmacology*
  • Protein Kinase Inhibitors / therapeutic use
  • Pyrimidines / pharmacology*
  • Pyrimidines / therapeutic use
  • Receptor, Platelet-Derived Growth Factor alpha / antagonists & inhibitors*
  • Receptor, Platelet-Derived Growth Factor alpha / genetics
  • mRNA Cleavage and Polyadenylation Factors / antagonists & inhibitors*
  • mRNA Cleavage and Polyadenylation Factors / genetics

Substances

  • Benzamides
  • Oncogene Proteins, Fusion
  • Piperazines
  • Protein Kinase Inhibitors
  • Pyrimidines
  • mRNA Cleavage and Polyadenylation Factors
  • Imatinib Mesylate
  • FIP1L1-PDGFRA fusion protein, human
  • Receptor, Platelet-Derived Growth Factor alpha
  • nilotinib