Search Results - "Wright, William C"

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  1. 1

    Drivers of heritage value: A meta-analysis of monetary valuation studies of cultural heritage by Wright, William C.C., Eppink, Florian V.

    Published in Ecological economics (01-10-2016)
    “…Decisions about cultural and historical heritage conservation can be contentious. Improved insight into the economic benefits derived from preservation could…”
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  2. 2

    Differential Regulation of CYP3A4 and CYP3A5 and its Implication in Drug Discovery by Lolodi, Ogheneochukome, Wang, Yue-Ming, Wright, William C, Chen, Taosheng

    Published in Current drug metabolism (01-01-2017)
    “…Cancer cells use several mechanisms to resist the cytotoxic effects of drugs, resulting in tumor progression and invasion. One such mechanism capitalizes on…”
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  3. 3

    Building a Chemical Toolbox for Human Pregnane X Receptor Research: Discovery of Agonists, Inverse Agonists, and Antagonists Among Analogs Based on the Unique Chemical Scaffold of SPA70 by Li, Yongtao, Lin, Wenwei, Wright, William C, Chai, Sergio C, Wu, Jing, Chen, Taosheng

    Published in Journal of medicinal chemistry (11-02-2021)
    “…Pregnane X receptor (PXR) plays roles in detoxification and other physiological processes. PXR activation may enhance drug metabolism (leading to adverse drug…”
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    Mutation of a single amino acid of pregnane X receptor switches an antagonist to agonist by altering AF-2 helix positioning by Huber, Andrew D., Wright, William C., Lin, Wenwei, Majumder, Kinjal, Low, Jonathan A., Wu, Jing, Buchman, Cameron D., Pintel, David J., Chen, Taosheng

    “…Pregnane X receptor (PXR) is activated by chemicals to transcriptionally regulate drug disposition and possibly decrease drug efficacy and increase resistance,…”
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    Clobetasol Propionate Is a Heme-Mediated Selective Inhibitor of Human Cytochrome P450 3A5 by Wright, William C, Chenge, Jude, Wang, Jingheng, Girvan, Hazel M, Yang, Lei, Chai, Sergio C, Huber, Andrew D, Wu, Jing, Oladimeji, Peter O, Munro, Andrew W, Chen, Taosheng

    Published in Journal of medicinal chemistry (13-02-2020)
    “…The human cytochrome P450 (CYP) enzymes CYP3A4 and CYP3A5 metabolize most drugs and have high similarities in their structure and substrate preference. Whereas…”
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    Genome-wide CRISPR screen reveals PSMA6 to be an essential gene in pancreatic cancer cells by Bakke, Jesse, Wright, William C, Zamora, Anthony E, Oladimeji, Peter, Crawford, Jeremy Chase, Brewer, Christopher T, Autry, Robert J, Evans, William E, Thomas, Paul G, Chen, Taosheng

    Published in BMC cancer (21-03-2019)
    “…Despite its relatively low incidence, pancreatic ductal adenocarcinoma (PDAC) is a leading cause of cancer deaths because of the aggressive growth/metastasis…”
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    CINPA1 binds directly to constitutive androstane receptor and inhibits its activity by Cherian, Milu T., Chai, Sergio C., Wright, William C., Singh, Aman, Alexandra Casal, Morgan, Zheng, Jie, Wu, Jing, Lee, Richard E., Griffin, Patrick R., Chen, Taosheng

    Published in Biochemical pharmacology (01-06-2018)
    “…[Display omitted] The constitutive androstane receptor (CAR) and pregnane X receptor (PXR) are xenobiotic sensors that regulate the expression of…”
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    Structural perspectives of the CYP3A family and their small molecule modulators in drug metabolism by Wright, William C., Chenge, Jude, Chen, Taosheng

    Published in Liver research (01-12-2019)
    “…Cytochrome P450 (CYP) enzymes function to catalyze a wide range of reactions, many of which are critically important for drug response. Members of the human…”
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  14. 14

    CYP3A5 unexpectedly regulates glucose metabolism through the AKT–TXNIP–GLUT1 axis in pancreatic cancer by Shao, Ming, Pan, Qingfei, Tan, Haiyan, Wu, Jing, Lee, Ha Won, Huber, Andrew D., Wright, William C., Cho, Ji-Hoon, Yu, Jiyang, Peng, Junmin, Chen, Taosheng

    Published in Genes & diseases (01-07-2024)
    “…CYP3A5 is a cytochrome P450 (CYP) enzyme that metabolizes drugs and contributes to drug resistance in cancer. However, it remains unclear whether CYP3A5…”
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  15. 15

    Transcription factor ZNF148 is a negative regulator of human muscle differentiation by Bakke, Jesse, Wright, William C., Zamora, Anthony E., Ong, Su Sien, Wang, Yue-Ming, Hoyer, Jessica D., Brewer, Christopher T., Thomas, Paul G., Chen, Taosheng

    Published in Scientific reports (15-08-2017)
    “…Muscle differentiation is a complex process in which muscle progenitor cells undergo determination and eventually cellular fusion. This process is heavily…”
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  16. 16

    Strategies for developing pregnane X receptor antagonists: Implications from metabolism to cancer by Chai, Sergio C., Wright, William C., Chen, Taosheng

    Published in Medicinal research reviews (01-05-2020)
    “…Pregnane X receptor (PXR) is a ligand‐activated nuclear receptor (NR) that was originally identified as a master regulator of xenobiotic detoxification. It…”
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  17. 17

    RNA interference screen identifies NAA10 as a regulator of PXR transcription by Oladimeji, Peter O., Wright, William C., Wu, Jing, Chen, Taosheng

    Published in Biochemical pharmacology (01-02-2019)
    “…[Display omitted] The pregnane X receptor (PXR) is a principal xenobiotic receptor crucial in the detection, detoxification, and clearance of toxic substances…”
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    KANSL2 and MBNL3 are regulators of pancreatic ductal adenocarcinoma invasion by Oladimeji, Peter O., Bakke, Jesse, Wright, William C., Chen, Taosheng

    Published in Scientific reports (30-01-2020)
    “…Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal forms of cancer. One major reason for this is that PDAC quickly metastasizes to other organs,…”
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    Unraveling the Structural Basis of Selective Inhibition of Human Cytochrome P450 3A5 by Wang, Jingheng, Buchman, Cameron D, Seetharaman, Jayaraman, Miller, Darcie J, Huber, Andrew D, Wu, Jing, Chai, Sergio C, Garcia-Maldonado, Efren, Wright, William C, Chenge, Jude, Chen, Taosheng

    Published in Journal of the American Chemical Society (10-11-2021)
    “…The human cytochrome P450 (CYP) CYP3A4 and CYP3A5 enzymes metabolize more than one-half of marketed drugs. They share high structural and substrate similarity…”
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