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Creating an Infrastructure for Collaborative Clinical Research and Publication of Consensus Guidelines for RUNX1 Familial Platelet Disorder |
The Cleveland Clinic Foundation |
The RUNX1 Research Program |
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Mutagenesis and disease progression in RUNX1 mutant blood stem cells is caused by inflammation-induced hyperactive signaling and supraphysiological mitochondrial ROS |
St. Jude Children’s Research Hospital |
The RUNX1 Research Program |
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Delivering on the Promise of Germline Genetic Testing for RUNX1 Variants |
University of Washington, Seattle |
The RUNX1 Research Program |
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Using Chemical Genetics to Define the Precise Role of RUNX1 in Transcription and Beyond |
Albert Einstein College of Medicine |
The RUNX1 Research Program |
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Characterizing Inflammatory Phenotypes Associated with RUNX1 Deficiency |
Dana-Farber Cancer Institute |
The RUNX1 Research Program |
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Role of PHF6 Mutations in Germline RUNX1 Deficiency Associated Hematopoietic Disorders |
The Regents of the University of California San Francisco |
The RUNX1 Research Program |
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Assessing Clonal Fitness and Mechanisms of Clonal Evolution in FPD-MN |
Memorial Sloan-Kettering Cancer Center |
The RUNX1 Research Program |
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Modeling familial platelet disorder associated RUNX1 mutations in mice |
University of Massachusetts Medical School |
The RUNX1 Research Program |
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Restoring RUNX1 Levels in FPD/AML |
University of Washington, Seattle |
The RUNX1 Research Program |
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Characterization of Pre-Leukemia Associated with Familial RUNX1 Mutations |
Stanford University |
The RUNX1 Research Program |
