Identification of aberrant splicing events in myelodysplastic syndrome patients with splicing factor gene mutations

Podobne zapisy

• The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes.
  od: Yip, B, i wsp.
  Wydane: (2017)
• The role of splicing factor mutations in the pathogenesis of the myelodysplastic syndromes.
  od: Boultwood, J, i wsp.
  Wydane: (2014)
• Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associations
  od: Pellagatti, A, i wsp.
  Wydane: (2018)
• Splicing factor mutations in the myelodysplastic syndromes: target genes and therapeutic approaches
  od: Armstrong, R, i wsp.
  Wydane: (2017)
• COMPREHENSIVE ANALYSIS OF MUTATION STATUS, GENE EXPRESSION PROFILES, BLOOD AND BONE MARROW COUNTS AND OUTCOME IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES
  od: Pellagatti, A, i wsp.
  Wydane: (2014)