[New insight into pathogenesis of idiopathic myelofibrosis--review]

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2007 Dec;15(6):1330-4.
[Article in Chinese]

Abstract

Idiopathic myelofibrosis is a type of chronic myeloproliferative disorders characterized by splenomegaly, a leukoerythroblastic blood picture, teardrop poikilocytosis, in various degrees of bone marrow fibrosis and extramedullary hematopoiesis. In this paper, the biological characters and pathogenesis of idiopathic myelofibrosis such as mutation of tyrosine kinase receptor, mutation of GABA transporter 1, JAK2 mutation and c-MPl mutation, as well as other pathogenesis related with idiopathic myelofibrosis were reviewed.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • GABA Plasma Membrane Transport Proteins / genetics
  • Humans
  • Janus Kinase 2 / genetics
  • Mutation
  • Primary Myelofibrosis / etiology*
  • Primary Myelofibrosis / genetics*
  • Receptor Protein-Tyrosine Kinases / genetics
  • Receptors, Thrombopoietin / genetics

Substances

  • GABA Plasma Membrane Transport Proteins
  • Receptors, Thrombopoietin
  • MPL protein, human
  • Receptor Protein-Tyrosine Kinases
  • JAK2 protein, human
  • Janus Kinase 2