Recent advances in the application of induced pluripotent stem cell technology to the study of myeloid malignancies
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A miRNA screening identifies miR-192-5p as associated with response to azacitidine and lenalidomide therapy in myelodysplastic syndromes.
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Finding consistency in classifications of myeloid neoplasms: a perspective on behalf of the International Workshop for Myelodysplastic Syndromes.
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An agenda to advance research in MDS: A TOP 10 Priority List from the first international workshop in MDS (iwMDS).
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Splicing factor mutations in the myelodysplastic syndromes: Role of key aberrantly spliced genes in disease pathophysiology and treatment.
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Activation of targetable inflammatory immune signaling is seen in myelodysplastic syndromes with SF3B1 mutations.
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BCL-2 Inhibitor ABT-737 Effectively Targets Leukemia-Initiating Cells with Differential Regulation of Relevant Genes Leading to Extended Survival in a NRAS/BCL-2 Mouse Model of High Risk-Myelodysplastic Syndrome.
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ASXL1 mutations are associated with distinct epigenomic alterations that lead to sensitivity to venetoclax and azacytidine
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MDS DISEASE PROGRESSION: INSIGHTS FROM THE TRANSCRIPTOME
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Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes.
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MDMX acts as a pervasive preleukemic-to-acute myeloid leukemia transition mechanism.
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Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes.
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The utilisation of glutamine and glucose by a 3-D tumour model trapped in quiescence.
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Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples.
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Azacitidine and Lenalidomide in Higher-Risk Myelodysplastic Syndromes. Long-Term Results of a Randomized Phase II Multicenter Study and Impact of Cytogenetic Scores and Mutational Status on Long-Lasting Responses
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Sequential Analysis of miRNA Profiling during Azacitidine and Lenalidomide Therapy in Myelodysplastic Syndromes
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DEFERASIROX TARGETS PHOSPHOLIPASE C BETA1 SIGNALING IN MYELODYSPLASTIC SYNDROMES (MDS)
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Spliceosome mutations: 1 plus 1 does not always equal 2.
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