ASXL1 mutations in primary and secondary myelofibrosis

Br J Haematol. 2012 Feb;156(3):404-7. doi: 10.1111/j.1365-2141.2011.08865.x. Epub 2011 Sep 19.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Alleles
  • DNA Mutational Analysis
  • Disease Progression
  • Female
  • Humans
  • Janus Kinase 2 / genetics
  • Male
  • Middle Aged
  • Mutation
  • Myeloid Cells / chemistry
  • Polycythemia Vera / genetics
  • Polycythemia Vera / pathology
  • Primary Myelofibrosis / etiology
  • Primary Myelofibrosis / genetics*
  • Repressor Proteins / genetics*
  • Repressor Proteins / physiology
  • Thrombocythemia, Essential / genetics
  • Thrombocythemia, Essential / pathology

Substances

  • ASXL1 protein, human
  • Repressor Proteins
  • JAK2 protein, human
  • Janus Kinase 2