Refractory anemia with ring sideroblasts and marked thrombocytosis cases harbor mutations in SF3B1 or other spliceosome genes accompanied by JAK2V617F and ASXL1 mutations

Podobne zapisy

• High frequencies of SF3B1 and JAK2 mutations in refractory anemia with ring sideroblasts associated with marked thrombocytosis strengthen the assignment to the category of myelodysplastic/myeloproliferative neoplasms
  od: Jeromin, Sabine, i wsp.
  Wydane: (2013)
• Mutations of JAK2 and TET2, but not CBL are detectable in a high portion of patients with refractory anemia with ring sideroblasts and thrombocytosis
  od: Flach, Johanna, i wsp.
  Wydane: (2010)
• Specific molecular mutation patterns delineate chronic neutrophilic leukemia, atypical chronic myeloid leukemia, and chronic myelomonocytic leukemia
  od: Meggendorfer, Manja, i wsp.
  Wydane: (2014)
• Molecular characterization of AML with RUNX1-RUNX1T1 at diagnosis and relapse reveals net loss of co-mutations
  od: Alexander Höllein, i wsp.
  Wydane: (2019-02-01)
• Molecular characterization of AML with RUNX1-RUNX1T1 at diagnosis and relapse reveals net loss of co-mutations
  od: Höllein, Alexander, i wsp.
  Wydane: (2019)