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Using this approach, we readily identify activated signaling pathways downstream of oncogenic mutants of Flt-3 kinase in a model system of human myeloid leukemia.
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As miRNA-based microarray experiments in general are reproducible [ 43– 45], we readily identified 430 mature miRNAs.
We readily identified 57 Basho bands in A. thaliana, but few strong bands in A. lyrata.
We readily identified genomic disparity of potentially high relevance between primary tumors and CTCs.
Using these 66 metabolites, we readily identified all 30 of the blinded duplicates and triplicates.
We readily identified the same changing regions, confirming OCI as a suitable metric to measure changes in local architecture.
As a diverse group, we readily identified numerous environmental factors that contribute to disease, dysfunction, or poor health.
We readily identified the extent of the duplication when the percentage of read support for the lesion was between 70 and 80%.
When pull-down of HB-MSH2Y238F was done by biotin pull-down assay, we readily identified an interaction between NPM-ALK and HB-MSH2Y238F.
Using this procedure, we readily identified and quantified the degree of RIP in all repeated DNA families within the genome of the necrotrophic fungal wheat pathogen S. nodorum.
When restricting the data set to BMP components or transcription factors, we readily identified additional candidate maternal expression differences in both gene groups.
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