Search Results - "Platt, James T"

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    β-Catenin Signaling Controls Metastasis in Braf-Activated Pten-Deficient Melanomas by Damsky, William E., Curley, David P., Santhanakrishnan, Manjula, Rosenbaum, Lara E., Platt, James T., Gould Rothberg, Bonnie E., Taketo, Makoto M., Dankort, David, Rimm, David L., McMahon, Martin, Bosenberg, Marcus

    Published in Cancer cell (13-12-2011)
    “…Malignant melanoma is characterized by frequent metastasis, however, specific changes that regulate this process have not been clearly delineated. Although it…”
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    Journal Article
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    Genotype-selective combination therapies for melanoma identified by high-throughput drug screening by Held, Matthew A, Langdon, Casey G, Platt, James T, Graham-Steed, Tisheeka, Liu, Zongzhi, Chakraborty, Ashok, Bacchiocchi, Antonella, Koo, Andrew, Haskins, Jonathan W, Bosenberg, Marcus W, Stern, David F

    Published in Cancer discovery (01-01-2013)
    “…Resistance and partial responses to targeted monotherapy are major obstacles in cancer treatment. Systematic approaches to identify efficacious drug…”
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    MERTK controls melanoma cell migration and survival and differentially regulates cell behavior relative to AXL by Tworkoski, Kathryn A., Platt, James T., Bacchiocchi, Antonella, Bosenberg, Marcus, Boggon, Titus J., Stern, David F.

    Published in Pigment cell and melanoma research (01-07-2013)
    “…Summary The receptor tyrosine kinase AXL regulates melanoma cell proliferation and migration. We now demonstrate that AXL and the related kinase MERTK are…”
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    Convergent and divergent cellular responses by ErbB4 isoforms in mammary epithelial cells by Wali, Vikram B, Haskins, Jonathan W, Gilmore-Hebert, Maureen, Platt, James T, Liu, Zongzhi, Stern, David F

    Published in Molecular cancer research (01-08-2014)
    “…Associations of ErbB4 (ERBB4/HER4), the fourth member of the EGFR family, with cancer are variable, possibly as a result of structural diversity of this…”
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    Systematic Drug Screening Identifies Tractable Targeted Combination Therapies in Triple-Negative Breast Cancer by Wali, Vikram B, Langdon, Casey G, Held, Matthew A, Platt, James T, Patwardhan, Gauri A, Safonov, Anton, Aktas, Bilge, Pusztai, Lajos, Stern, David F, Hatzis, Christos

    Published in Cancer research (Chicago, Ill.) (15-01-2017)
    “…Triple-negative breast cancer (TNBC) remains an aggressive disease without effective targeted therapies. In this study, we addressed this challenge by testing…”
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    Combinatorial drug screening of mammary cells with induced mesenchymal transformation to identify drug combinations for triple-negative breast cancer by Colavito, Sierra A, Platt, James T, Held, Matthew A, Liu, Zongzhi, Sokup, Ryan, Stern, David F

    Published in Oncotarget (06-08-2019)
    “…Mesenchymal stem-like (MSL) breast cancers are enriched for cells with tumor reconstituting and mesenchymal characteristics. These cancers are often…”
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    Salmonella pathogenicity island-2 and anticancer activity in mice by Pawelek, John M, Sodi, Stefano, Chakraborty, Ashok K, Platt, James T, Miller, Samuel, Holden, David W, Hensel, Michael, Low, K Brooks

    Published in Cancer gene therapy (01-10-2002)
    “…Salmonella enterica servovar Typhimurium is capable of targeting, colonizing, and eliciting growth suppression of tumors in mice. We examined the effects of…”
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    Polymerization of 5,6‐Dihydroxyindole‐2‐Carboxylic Acid to Melanin by the Pmel 17/Silver Locus Protein by Chakraborty, Ashok K., Platt, James T., Kim, Kack K., Kwon, Byoung, Bennett, Dorothy C., Pawelek, John M.

    Published in European journal of biochemistry (15-02-1996)
    “…Recent advances in melanogenesis have focused on the role of dihydroxyindole‐2‐carboxylic acid [(HO)2IndCOOH]. For example, it has been shown that formation of…”
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    Abstract B275: Dovitinib as a single-agent or in combination with other small molecule inhibitors for mutant BRAF melanomas by Langdon, Casey G., Held, Matthew A., Koo, Andrew B., Klein, Michael, Liu, Zongzhi, Platt, James T., Stern, David F.

    Published in Molecular cancer therapeutics (01-11-2013)
    “…Abstract Background: Receptor tyrosine kinases (RTKs) modulate many oncogenic signaling pathways. RTKs can be activated as a result of feedback loops initiated…”
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