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

Ítems similars

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