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

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

Manylion Llyfryddiaeth
Prif Awduron: Pellagatti, A, Steeples, V, Sharma, E, Repapi, E, Yip, B, Armstrong, R, Dolatshad, H, Lockstone, H, Taylor, S, Giagounidis, A, Vyas, P, Papaemmanuil, E, Woll, P, Killick, S, Malcovati, L, Hellstrom-Lindberg, E, Cazzola, M, Smith, C, Boultwood, J
Fformat: Conference item
Cyhoeddwyd: Elsevier 2017
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Eitemau Tebyg

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

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