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High-Throughput Tyrosine Kinase Activity Profiling Identifies FAK as a Candidate Therapeutic Target in Ewing Sarcoma. Cancer research, 2013/05/01, Volume 73, Issue 9, p.2873-83, (2013)
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Targeting MYCN in Neuroblastoma by BET Bromodomain Inhibition. Cancer discovery, 2013/03/01, Volume 3, Issue 3, p.308-323, (2013)
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Integrative Analysis Reveals an Outcome-Associated and Targetable Pattern of p53 and Cell Cycle Deregulation in Diffuse Large B Cell Lymphoma. Cancer cell, 2012/09/11, Volume 22, Issue 3, p.359-72, (2012)
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Chemical Genomics Identifies Small-Molecule MCL1 Repressors and BCL-xL as a Predictor of MCL1 Dependency. Cancer cell, 2012/04/17, Volume 21, Issue 4, p.547-62, (2012)
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Proteomic and genetic approaches identify Syk as an AML target. Cancer cell, 2009/10/06, Volume 16, Issue 4, p.281-94, (2009)
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Identification of AML1-ETO modulators by chemical genomics. Blood, 2009/06/11, Volume 113, Issue 24, p.6193-205, (2009)
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Bead-based profiling of tyrosine kinase phosphorylation identifies SRC as a potential target for glioblastoma therapy. Nature biotechnology, 2009/01/01, Volume 27, Issue 1, p.77-83, (2009)
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Expression-based screening identifies the combination of histone deacetylase inhibitors and retinoids for neuroblastoma differentiation. Proceedings of the National Academy of Sciences of the United States of America, 2008/07/15, Volume 105, Issue 28, p.9751-6, (2008)
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Signature-based small molecule screening identifies cytosine arabinoside as an EWS/FLI modulator in Ewing sarcoma. PLoS medicine, 2007/04/01, Volume 4, Issue 4, p.e122, (2007)
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