Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia.

Παρόμοια τεκμήρια

• Frequent Mutation of the Polycomb-Associated Gene ASXL1 in the Myelodysplastic Syndromes and in Acute Myeloid Leukaemia
  ανά: Boultwood, J, κ.ά.
  Έκδοση: (2009)
• Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia
  ανά: Fernandez-Mercado, M, κ.ά.
  Έκδοση: (2010)
• Deregulated Gene Expression Pathways in Myelodysplastic Syndrome Hematopoietic Stem Cells
  ανά: Pellagatti, A, κ.ά.
  Έκδοση: (2009)
• Identification of Prognostic Markers by Gene Expression Profiling In Myelodysplastic Syndrome Hematopoietic Stem Cells
  ανά: Pellagatti, A, κ.ά.
  Έκδοση: (2010)
• Marked down-regulation of nucleophosmin-1 is associated with advanced del(5q) myelodysplastic syndrome.
  ανά: Pellagatti, A, κ.ά.
  Έκδοση: (2011)