Silencing of ASXL1 impairs the granulomonocytic lineage potential of human CD34⁺ progenitor cells.

Míreanna comhchosúla

• Silencing of ASXL1 impairs the granulomonocytic lineage potential of human CD34+ progenitor cells
  de réir: Davies, C, et al.
  Foilsithe / Cruthaithe: (2013)
• Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia
  de réir: Fernandez-Mercado, M, et al.
  Foilsithe / Cruthaithe: (2010)
• Frequent Mutation of the Polycomb-Associated Gene ASXL1 in the Myelodysplastic Syndromes and in Acute Myeloid Leukaemia
  de réir: Boultwood, J, et al.
  Foilsithe / Cruthaithe: (2009)
• Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia.
  de réir: Boultwood, J, et al.
  Foilsithe / Cruthaithe: (2010)
• High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression.
  de réir: Boultwood, J, et al.
  Foilsithe / Cruthaithe: (2010)