Karyotype evolution and acquisition of FLT3 or RAS pathway alterations drive progression of myelodysplastic syndrome to acute myeloid leukemia

Samankaltaisia teoksia

• Refractory anemia with ring sideroblasts and marked thrombocytosis cases harbor mutations in SF3B1 or other spliceosome genes accompanied by JAK2V617F and ASXL1 mutations
  Tekijä: Jeromin, Sabine, et al.
  Julkaistu: (2015)
• The mutational landscape of 18 investigated genes clearly separates four subtypes of myelodysplastic/myeloproliferative neoplasms
  Tekijä: Meggendorfer, Manja, et al.
  Julkaistu: (2018)
• Specific molecular mutation patterns delineate chronic neutrophilic leukemia, atypical chronic myeloid leukemia, and chronic myelomonocytic leukemia
  Tekijä: Meggendorfer, Manja, et al.
  Julkaistu: (2014)
• Molecular characterization of acute myeloid leukemia patients who relapse more than 3 years after diagnosis: an exome sequencing study of 31 patients
  Tekijä: Hartmann, Luise, et al.
  Julkaistu: (2020)
• Serial assessment of suspected myelodysplastic syndromes: significance of flow cytometric findings validated by cytomorphology, cytogenetics, and molecular genetics
  Tekijä: Kern, Wolfgang, et al.
  Julkaistu: (2013)