MPL W515 and JAK2 V617 mutation analysis in patients with refractory anemia with ringed sideroblasts and an elevated platelet count

Haematologica. 2006 Dec;91(12 Suppl):ECR57.

Abstract

Discovery of a constitutively activating point mutation of the Janus kinase 2 (JAK2) receptor-associated tyrosine kinase in patients with polycythemia vera (PV) and other BCR/ABL-negative myeloproliferative disorders prompted many groups around the world to examine diverse subsets of patients with myeloid diseases for the prevalence of the JAK2 V617F mutation and its clinical and pathological associations.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged, 80 and over
  • Anemia, Refractory / blood
  • Anemia, Refractory / classification
  • Anemia, Refractory / genetics*
  • Anemia, Sideroblastic / blood
  • Anemia, Sideroblastic / genetics*
  • Animals
  • DNA Mutational Analysis
  • Enzyme Activation / genetics
  • Female
  • Humans
  • Janus Kinase 2 / genetics*
  • Male
  • Middle Aged
  • Mutation, Missense*
  • Platelet Count
  • Point Mutation*
  • Receptors, Thrombopoietin / genetics*

Substances

  • Receptors, Thrombopoietin
  • MPL protein, human
  • JAK2 protein, human
  • Janus Kinase 2