Skip to main content

and
  1. No Access

    Article

    c-CBL is not required for leukemia induction by Bcr-Abl in mice

    Bcr-Abl tyrosine kinase activity is essential for the pathogenesis of chronic myeloid leukemia (CML). A number of Bcr-Abl substrates have been identified, but it is not clear which of these substrates are require...

    Daniela M Dinulescu, Lisa J Wood, Lei Shen, Marc Loriaux, Christopher L Corless in Oncogene (2003)

  2. No Access

    Article

    Gastrointestinal stromal tumors (GISTs) with KIT and PDGFRA mutations have distinct gene expression profiles

    Most GISTs require oncogenic activation of the KIT or PDGFRA receptor tyrosine kinase proteins, and the genomic mechanisms of oncogene activation are heterogeneous. Notably, the kinase mutation type correlates wi...

    Subbaya Subramanian, Robert B West, Christopher L Corless, Wenbin Ou in Oncogene (2004)

  3. No Access

    Article

    Does tumor mutational status correlate with clinical response to imatinib?

    Michael C Heinrich, Christopher L Corless in Nature Clinical Practice Oncology (2006)

  4. Article

    Open Access

    Integrated genomic study of quadruple-WT GIST (KIT/PDGFRA/SDH/RAS pathway wild-type GIST)

    About 10-15% of adult gastrointestinal stromal tumors (GIST) and the vast majority of pediatric GIST do not harbour KIT or platelet-derived growth factor receptor alpha (PDGFRA) mutations (J Clin Oncol 22:3813–38...

    Margherita Nannini, Annalisa Astolfi, Milena Urbini, Valentina Indio in BMC Cancer (2014)

  5. Article

    Open Access

    FGFR1 and NTRK3 actionable alterations in “Wild-Type” gastrointestinal stromal tumors

    About 10–15% of adult, and most pediatric, gastrointestinal stromal tumors (GIST) lack mutations in KIT, PDGFRA, SDHx, or RAS pathway components (KRAS, BRAF, NF1). The identification of additional mutated gene...

    Eileen Shi, Juliann Chmielecki, Chih-Min Tang in Journal of Translational Medicine (2016)

  6. Article

    Open Access

    Implementing a comprehensive translational oncology platform: from molecular testing to actionability

    In order to establish the workflows required to implement a real-time process involving multi-omic analysis of patient samples to support precision-guided therapeutic intervention, a tissue acquisition and ana...

    Zahi I. Mitri, Swapnil Parmar, Brett Johnson in Journal of Translational Medicine (2018)

  7. Article

    Open Access

    Loss of the PTCH1 tumor suppressor defines a new subset of plexiform fibromyxoma

    Plexiform fibromyxoma (PF) is a rare gastric tumor often confused with gastrointestinal stromal tumor. These so-called “benign” tumors often present with upper GI bleeding and gastric outlet obstruction. It wa...

    Sudeep Banerjee, Christopher L. Corless in Journal of Translational Medicine (2019)

  8. Article

    Open Access

    Characterizing advanced breast cancer heterogeneity and treatment resistance through serial biopsies and comprehensive analytics

    Molecular heterogeneity in metastatic breast cancer presents multiple clinical challenges in accurately characterizing and treating the disease. Current diagnostic approaches offer limited ability to assess he...

    Allen Li, Jamie M. Keck, Swapnil Parmar, Janice Patterson in npj Precision Oncology (2021)

  9. Article

    Open Access

    Multiomics analysis of serial PARP inhibitor treated metastatic TNBC inform on rational combination therapies

    In a pilot study, we evaluated the feasibility of real-time deep analysis of serial tumor samples from triple negative breast cancer patients to identify mechanisms of resistance and treatment opportunities as...

    Marilyne Labrie, Allen Li, Allison Creason, Courtney Betts in npj Precision Oncology (2021)