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Blood advances
04 14, 2020;4 (7): 1192-1196.

The K666N mutation in SF3B1 is associated with increased progression of MDS and distinct RNA splicing.

W Brian Dalton, Eric Helmenstine, Lisa Pieterse, Bing Li, Christopher D Gocke, Joshua Donaldson, Zhijian Xiao, Lukasz P Gondek, Gabriel Ghiaur, Ivana Gojo, B Douglas Smith, Mark J Levis, Amy E DeZern
Author Information
  1. W Brian Dalton: The Sidney Kimmel Comprehensive Cancer Center and.
  2. Eric Helmenstine: The Sidney Kimmel Comprehensive Cancer Center and.
  3. Lisa Pieterse: Department of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
  4. Bing Li: MDS and MPN Centre and.
  5. Christopher D Gocke: Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD; and.
  6. Joshua Donaldson: Division of Hematology/Oncology, Department of Medicine, Vanderbilt-Ingram Cancer Center, Nashville, TN.
  7. Zhijian Xiao: MDS and MPN Centre and.
  8. Lukasz P Gondek: The Sidney Kimmel Comprehensive Cancer Center and.
  9. Gabriel Ghiaur: The Sidney Kimmel Comprehensive Cancer Center and.
  10. Ivana Gojo: The Sidney Kimmel Comprehensive Cancer Center and.
  11. B Douglas Smith: The Sidney Kimmel Comprehensive Cancer Center and.
  12. Mark J Levis: The Sidney Kimmel Comprehensive Cancer Center and.
  13. Amy E DeZern: The Sidney Kimmel Comprehensive Cancer Center and.
PMID: 32211880 DOI: 10.1182/bloodadvances.2019001127

Abstract

No abstract text available.

References

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Grants

  1. K08 HL127269/NHLBI NIH HHS
  2. K08 HL136894/NHLBI NIH HHS
  3. K12 CA090625/NCI NIH HHS

MeSH Term

Mutation
RNA Splicing
RNA Splicing Factors

Chemicals

RNA Splicing Factors
Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

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