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Whole-exome sequencing studies have identified common mutations affecting genes encoding components of the RNA splicing machinery in hematological malignancies. Here, we sought to determine how mutations affecting the 3' splice site recognition factor U2AF1 altered its normal role in RNA splicing. W...
ORGANISM(S): Homo sapiens 
RNA-Seq data of U2AF1 isoform depletion experiments.
ORGANISM(S): Homo sapiens 
Identification of differentially spliced genes by wild type or S34F mutation of U2AF1 Examination of effects on splicing events by overexpressing wipdtype or S34F mutation of two U2AF1 isoforms in A549 cells. All experimental conditions are performed in duplicate.
ORGANISM(S): Homo sapiens 
Isoform-specific depletion of U2AF1
U2AF1-S34F and U2AF1-Q157R induce distinct RNA splicing and hematopoietic phenotypes in vivo
Effect of U2AF1-S34F mutation in mouse neutrophils
U2AF1 mutations confer resistance to chemotherapy in AML
Functional Significance of U2AF1 S34F Mutation in Lung Adenocarcinomas
To investigate the transcriptome of hematopoietic stem and progenitor cells (Lin-Sca-1+c-kit+) carrying alterations in splicing factors and/or epigenetic regulators related with the pathogenesis of myelodysplastic syndromes.
ORGANISM(S): Mus musculus 
U2AF1 mutations rescue deleterious exon skipping induced by KRAS mutations
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