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

The K666N mutation of SF3B1 has distinct clinicopathologic features in MDS. The K666N mutation of SF3B1 has a distinct RNA splicing profile.

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Detalhes bibliográficos
Publicado no:Blood Adv
Main Authors: Dalton, W. Brian, Helmenstine, Eric, Pieterse, Lisa, Li, Bing, Gocke, Christopher D., Donaldson, Joshua, Xiao, Zhijian, Gondek, Lukasz P., Ghiaur, Gabriel, Gojo, Ivana, Smith, B. Douglas, Levis, Mark J., DeZern, Amy E.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2020
Assuntos:
Stimulus Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7160262/
https://ncbi.nlm.nih.gov/pubmed/32211880
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2019001127
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