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

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

Bibliográfalaš dieđut
Váldodahkkit: Boultwood, J, Perry, J, Pellagatti, A, Fernandez-Mercado, M, Fernandez-Santamaria, C, Calasanz, M, Larrayoz, M, Garcia-Delgado, M, Giagounidis, A, Malcovati, L, Della Porta, MG, Jädersten, M, Killick, S, Hellström-Lindberg, E, Cazzola, M, Wainscoat, J
Materiálatiipa: Journal article
Giella:English
Almmustuhtton: 2010
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  • Frequent Mutation of the Polycomb-Associated Gene ASXL1 in the Myelodysplastic Syndromes and in Acute Myeloid Leukaemia
    Dahkki: Boultwood, J, et al.
    Almmustuhtton: (2009)
  • Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia
    Dahkki: Fernandez-Mercado, M, et al.
    Almmustuhtton: (2010)
  • Deregulated Gene Expression Pathways in Myelodysplastic Syndrome Hematopoietic Stem Cells
    Dahkki: Pellagatti, A, et al.
    Almmustuhtton: (2009)
  • Identification of Prognostic Markers by Gene Expression Profiling In Myelodysplastic Syndrome Hematopoietic Stem Cells
    Dahkki: Pellagatti, A, et al.
    Almmustuhtton: (2010)
  • Marked down-regulation of nucleophosmin-1 is associated with advanced del(5q) myelodysplastic syndrome.
    Dahkki: Pellagatti, A, et al.
    Almmustuhtton: (2011)

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