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All grants tagged with "Acute Myeloid Leukemia (AML)"

Translational Utility of New Models of Human AML - Benjamin Kleeman (2017)
Benjamin Kleeman
Cincinnati Children's Hospital Medical Center
POST Program Grants, Awarded 2017
Establishing the Function of Novel MicroRNAs Associated with Resistance and Relapse in Pediatric AML
Vivian Oehler, MD, Soheil Meshinchi, MD/PhD
Fred Hutchinson Cancer Research Center
Innovation Grants, Awarded 2017
Phase I Study of Lentivirus Engineered Autologous AML Cells Expressing IL-12 in Children and Young Adults with Relapsed AML
Michael Burke, MD, Jeffrey Medin, MD/PhD
Children’s Hospital of Wisconsin - Milwaukee
Reach Grants, Awarded 2017
Novel Approaches to AML Differentiation Therapy
Andrew Lane, MD/PhD
Dana-Farber Cancer Institute
'A' Award Grants, Awarded 2017
Drug Screen for FPD/AML Therapeutics
Mortimer Poncz, MD
Children’s Hospital of Philadelphia
RARE Grant Program (Research Accelerating RUNX1 Exploration), Awarded 2017
Role of Inflammatory Microenvironment in Clonal evolution and Progression from FPD to AML
Anupriya Agarwal, PhD
Oregon Health & Science University
RARE Grant Program (Research Accelerating RUNX1 Exploration), Awarded 2017
Pharmacologic Enhancement of Residual Wild Type RUNX1 Protein Activity in FPD/AML
Alan Cantor, MD/PhD
Boston Children’s Hospital
RARE Grant Program (Research Accelerating RUNX1 Exploration), Awarded 2016
Identifying Therapeutic Targets to Prevent Progression of Familial RUNX1 Disorder to AML Using Novel iPSC Models
Eirini Papapetrou, MD/PhD
Icahn School of Medicine at Mount Sinai
RARE Grant Program (Research Accelerating RUNX1 Exploration), Awarded 2016
Characterization of Pre-Leukemia Associated with Familial RUNX1 Mutations
Ravi Majeti, MD/PhD
Stanford University
RARE Grant Program (Research Accelerating RUNX1 Exploration), Awarded 2016
Restoring RUNX1 Levels in FPD/AML
Marshall Horwitz, MD/PhD
University of Washington, Seattle
RARE Grant Program (Research Accelerating RUNX1 Exploration), Awarded 2016

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