Identification of aberrant splicing events in myelodysplastic syndrome patients with splicing factor gene mutations
Main Authors: | 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 |
---|---|
Formato: | Conference item |
Publicado em: |
Elsevier
2017
|
Registos relacionados
-
The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes.
Por: Yip, B, et al.
Publicado em: (2017) -
The role of splicing factor mutations in the pathogenesis of the myelodysplastic syndromes.
Por: Boultwood, J, et al.
Publicado em: (2014) -
Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associations
Por: Pellagatti, A, et al.
Publicado em: (2018) -
Splicing factor mutations in the myelodysplastic syndromes: target genes and therapeutic approaches
Por: Armstrong, R, et al.
Publicado em: (2017) -
Cryptic splicing events in the iron transporter ABCB7 and other key target genes in SF3B1 mutant myelodysplastic syndromes
Por: Dolatshad, H, et al.
Publicado em: (2016)