Molecular defects in chronic myeloproliferative disorders

Mol Med. 2000 Jul;6(7):555-67.
No abstract available

Publication types

  • Review

MeSH terms

  • Chromosomes, Human, Pair 8 / genetics
  • Fusion Proteins, bcr-abl / genetics*
  • Fusion Proteins, bcr-abl / metabolism
  • Humans
  • Hypereosinophilic Syndrome / genetics
  • Hypereosinophilic Syndrome / physiopathology
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / physiopathology
  • Mastocytosis / genetics
  • Mastocytosis / physiopathology
  • Mutation*
  • Myeloproliferative Disorders / genetics*
  • Myeloproliferative Disorders / physiopathology
  • Signal Transduction*

Substances

  • Fusion Proteins, bcr-abl