Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele

Lignende værker

• RUNX1 haploinsufficiency results in granulocyte colony-stimulating factor hypersensitivity
  af: Chin, D W L, et al.
  Udgivet: (2016)
• An acute myeloid leukemia gene, AML1, regulates hemopoietic myeloid cell differentiation and transcriptional activation antagonistically by two alternative spliced forms.
  af: Tanaka, T, et al.
  Udgivet: (1995)
• Frequent somatic mutations in epigenetic regulators in newly diagnosed chronic myeloid leukemia
  af: Togasaki, E, et al.
  Udgivet: (2017)
• Runx2 Haploinsufficiency Ameliorates the Development of Ossification of the Posterior Longitudinal Ligament
  af: Iwasaki, Makiko, et al.
  Udgivet: (2012)
• Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles
  af: Matheny, Christina J, et al.
  Udgivet: (2007)