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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.

Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Journal article
Hizkuntza:English
Argitaratua: 2010
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Antzeko izenburuak

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

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