Myelodysplastic Syndrome-Associated SRSF2 Mutations Cause Splicing Changes by Altering Binding Motif Sequences-Reference-Cited by-同舟云学术

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Myelodysplastic Syndrome-Associated SRSF2 Mutations Cause Splicing Changes by Altering Binding Motif Sequences

Published:2019-04-16 Issue: Volume:10 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Masaki So,Ikeda Shun,Hata Asuka,Shiozawa Yusuke,Kon Ayana,Ogawa Seishi,Suzuki Kenji,Hakuno Fumihiko,Takahashi Shin-Ichiro,Kataoka Naoyuki

Publisher

Frontiers Media SA

Subject

Genetics (clinical),Genetics,Molecular Medicine

Reference46 articles.

1. MEME: discovering and analyzing DNA and protein sequence motifs.;Bailey;Nucleic Acids Res.,2006

2. A pan-cancer analysis of transcriptome changes associated with somatic mutations in U2AF1 reveals commonly altered splicing events.;Brooks;PLoS One,2014

3. The splicing factors 9G8 and SRp20 transactivate splicing through different and specific enhancers.;Cavaloc;RNA,1999

4. The genetic basis of myelodysplasia and its clinical relevance.;Cazzola;Blood,2013

5. The augmented R-loop is a unifying mechanism for myelodysplastic syndromes induced by high-risk splicing factor mutations.;Chen;Mol. Cell.,2018

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