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To confirm their role in oncogenesis and gain insight into the mechanism whereby these novel fusions promote disease, we introduced each of them as well as their individual gene counterparts into murine hematopoietic progenitor cells that were assessed in murine syngeneic transplantation models. Accompanying histological, immunophenotypic and genome-wide molecular characterization of resultant tumors delineated common and unique modes of leukemogenesis.
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