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Molecular Basis of Hematological Disease Caused by Inherited or Acquired RUNX1 Mutations - Experimental Hematology
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Glucocorticoids Inhibit Oncogenic RUNX1-ETO in Acute Myeloid Leukemia with Chromosome Translocation t(8;21)
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Figure 10, RUNX1 and CBFβ form a DNA-binding, heterodimeric complex, and both genes form fusions by chromosome translocations in human leukemia - Probe Reports from the NIH Molecular Libraries Program - NCBI Bookshelf
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Genomic Landscape of Patients with Germline RUNX1 Variants and Familial Platelet Disorder with Myeloid Malignancy | bioRxiv
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The structure of the RUNX1 gene and protein. (A) Expression of RUNX1 is... | Download Scientific Diagram
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Leukemia Cells are Addicted to a Healthy Gene - Life Sciences | Weizmann Wonder Wander - News, Features and Discoveries
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Dynamic Runx1 chromatin boundaries affect gene expression in hematopoietic development | Nature Communications
RUNX1 mutations in cytogenetically normal acute myeloid leukemia are associated with a poor prognosis and up-regulation of lymphoid genes | Haematologica
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Cells | Free Full-Text | Multiple Roles of the RUNX Gene Family in Hepatocellular Carcinoma and Their Potential Clinical Implications
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RUNX1-ETO and RUNX1-EVI1 Differentially Reprogram the Chromatin Landscape in t(8;21) and t(3;21) AML - ScienceDirect
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linc00174-EZH2-ZNF24/Runx1-VEGFA Regulatory Mechanism Modulates Post-burn Wound Healing: Molecular Therapy - Nucleic Acids
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