40k Game Sizes AML cell lines with RUNX1 mutations OCI AML5 and Mono Mac1 were more resistant to Ara C than wild type wt RUNX1 AML cell line OCI AML2 Figure 2 C To restore
Subsequent preclinical work demonstrated efficacy of HHT and OM 27 against AML cell lines OCI AML5 and Mono Mac 1 and patient derived primary AML BPCs with 28 Abstract RUNX1 is a transcription factor involved in normal and malignant hematopoiesis Somatic mutations in RUNX1 mtRUNX1 have been documented in de novo
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As shown in Figure 6A C and supplemental Figure 6A C cotreatment with relatively low concentrations of HHT and venetoclax for 24 or 48 hours induced more Wesely et al report that AML iPSC derived hematopoietic cells are hierarchically organized and contain cells with hallmark features of LSCs iLSCs Through integrative genomic studies of
We tested the pre clinical efficacy of HHT or OM against AML cell lines OCI AML5 and Mono Mac 1 and patient derived primary AML BPCs expressing somatic mtRUNX1 or Abstract Purpose RUNX1 mutated RUNX1mut acute myeloid leukemia AML is associated with adverse outcome highlighting the urgent need for a better genetic
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We incorporated mutations that have been reported to influence outcome in AML with RUNX1 RUNX1T1 post induction measurable residual disease as measured by Treatment with ARV 771 30 mg kg SQ daily for 3 weeks also inhibited AML growth and improved survival of NSG mice engrafted with luciferase transduced OCI AML5 cells By
RUNX1 mutations are recurrent aberrations in acute myeloid leukemia AML that are either somatically acquired or originate in the germline Monoallelic pathogenic germline The importance and the unique biology of RUNX1 in AML have been recognized by the World Health Organization WHO by adding 2 separate categories of AML with RUNX1
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AML cell lines with RUNX1 mutations OCI AML5 and Mono Mac1 were more resistant to Ara C than wild type wt RUNX1 AML cell line OCI AML2 Figure 2 C To restore

https://www.sciencedirect.com › science › article › pii
Subsequent preclinical work demonstrated efficacy of HHT and OM 27 against AML cell lines OCI AML5 and Mono Mac 1 and patient derived primary AML BPCs with 28

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