Search Results - "Boshuizen, Julia"

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    Cancer drug addiction is relayed by an ERK2-dependent phenotype switch by Kong, Xiangjun, Kuilman, Thomas, Shahrabi, Aida, Boshuizen, Julia, Kemper, Kristel, Song, Ji-Ying, Niessen, Hans W. M., Rozeman, Elisa A., Geukes Foppen, Marnix H., Blank, Christian U., Peeper, Daniel S.

    Published in Nature (London) (12-10-2017)
    “…The identification of an ERK2–JUNB–FRA1 signalling pathway that drives addiction to therapeutic drugs in cancer cells, and an ERK2-dependent phenotype switch…”
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    Journal Article
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    Mutationally-activated PI3’-kinase-α promotes de-differentiation of lung tumors initiated by the BRAFV600E oncoprotein kinase by van Veen, J Edward, Scherzer, Michael, Boshuizen, Julia, Chu, Mollee, Liu, Annie, Landman, Allison, Green, Shon, Trejo, Christy, McMahon, Martin

    Published in eLife (27-08-2019)
    “…Human lung adenocarcinoma exhibits a propensity for de-differentiation, complicating diagnosis and treatment, and predicting poorer patient survival. In…”
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    Rational Cancer Treatment Combinations: An Urgent Clinical Need by Boshuizen, Julia, Peeper, Daniel S.

    Published in Molecular cell (18-06-2020)
    “…We are witnessing several revolutionary technological advances in cancer. These innovations have not only contributed to a growing understanding of the tumor…”
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    Abstract 4591: Specific elimination of invasive and multidrug-resistant cancer cells by an antibody-drug conjugate targeting AXL by Boshuizen, Julia, Koopman, Louise A., Breij, Esther C., Satijn, David, Peeper, Daniel, Parren, Paul W.

    Published in Cancer research (Chicago, Ill.) (01-07-2017)
    “…Abstract Upon therapeutic pressure, cancers commonly select for drug-resistant, invasive subpopulations with elevated expression of the receptor tyrosine…”
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    Mutationally-activated PI3'-kinase-α promotes de-differentiation of lung tumors initiated by the BRAF V600E oncoprotein kinase by van Veen, J Edward, Scherzer, Michael, Boshuizen, Julia, Chu, Mollee, Liu, Annie, Landman, Allison, Green, Shon, Trejo, Christy, McMahon, Martin

    Published in eLife (27-08-2019)
    “…Human lung adenocarcinoma exhibits a propensity for de-differentiation, complicating diagnosis and treatment, and predicting poorer patient survival. In…”
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    Journal Article
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    BMN 673, a Novel and Highly Potent PARP1/2 Inhibitor for the Treatment of Human Cancers with DNA Repair Deficiency by YUQIAO SHEN, REHMAN, Farah L, YING FENG, BOSHUIZEN, Julia, BAJRAMI, Ilirjana, ELLIOTT, Richard, BING WANG, LORD, Christopher J, POST, Leonard E, ASHWORTH, Alan

    Published in Clinical cancer research (15-09-2013)
    “…PARP1/2 inhibitors are a class of anticancer agents that target tumor-specific defects in DNA repair. Here, we describe BMN 673, a novel, highly potent PARP1/2…”
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