Bridgett Knox
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Researcher
Also affiliated: Qingdao University (2020); United States Food and Drug Administration (2015–2025)
Faculty Researcher
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Bridgett Knox's research focuses on the pharmacological effects of drugs and their mechanisms of action, particularly involving microRNA regulation. Her work investigates how substances like ketoconazole can suppress steroidogenesis through CYP17A1 inhibition, with a potential role for microRNAs in these processes. Knox also explores the application of microphysiological systems as an in vitro method for evaluating drug absorption, distribution, metabolism, excretion, and toxicity. She has published 17 papers with 416 citations and an h-index of 12. Key collaborators include Dongying Li and Baitang Ning, with whom she shares multiple publications.
Metrics
- h-index: 12
- Publications: 17
- Citations: 418
Selected Publications
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SARS-CoV-2 Spike Protein’s Structural Dynamics Affect the Activity of the Bebtelovimab Antibody (2026)
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Microphysiological systems as an emerging in vitro approach for the evaluation of drug absorption, distribution, metabolism, and excretion and toxicity (2025)
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Pharmacological Effects of Ketoconazole in the Treatment of Steroidogenesis Suppression via CYP17A1 Inhibition May Involve MicroRNA Regulation (2023)
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Identification of Translational microRNA Biomarker Candidates for Ketoconazole-Induced Liver Injury Using Next-Generation Sequencing (2020)
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Long noncoding RNA LINC00844-mediated molecular network regulates expression of drug metabolizing enzymes and nuclear receptors in human liver cells (2020)
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Coordinated Regulation of UGT2B15 Expression by Long Noncoding RNA LINC00574 and hsa-miR-129-5p in HepaRG Cells (2020)
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FREMSA: A Method That Provides Direct Evidence of the Interaction between microRNA and mRNA (2020)
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MicroRNAs hsa-miR-495-3p and hsa-miR-486-5p suppress basal and rifampicin-induced expression of human sulfotransferase 2A1 (SULT2A1) by facilitating mRNA degradation (2019)
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A functional SNP in the 3′‐UTR of TAP2 gene interacts with microRNA hsa‐miR‐1270 to suppress the gene expression (2017)
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Multiple microRNAs function as self-protective modules in acetaminophen-induced hepatotoxicity in humans (2017)
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The expression, induction and pharmacological activity of CYP1A2 are post-transcriptionally regulated by microRNA hsa-miR-132-5p (2017)
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MicroRNA hsa-miR-370-3p suppresses the expression and induction of CYP2D6 by facilitating mRNA degradation (2017)
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Systems view of adipogenesis via novel omics-driven and tissue-specific activity scoring of network functional modules (2016)
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MicroRNA hsa-miR-25-3p suppresses the expression and drug induction of CYP2B6 in human hepatocytes (2016)
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Modulation of ALDH5A1 and SLC22A7 by microRNA hsa-miR-29a-3p in human liver cells (2015)
Collaboration Network
Top Collaborators
- Pharmacological Effects of Ketoconazole in the Treatment of Steroidogenesis Suppression via CYP17A1 Inhibition May Involve MicroRNA Regulation
- Microphysiological systems as an emerging in vitro approach for the evaluation of drug absorption, distribution, metabolism, and excretion and toxicity
- Pharmacological Effects of Ketoconazole in the Treatment of Steroidogenesis Suppression via CYP17A1 Inhibition May Involve MicroRNA Regulation
- Microphysiological systems as an emerging in vitro approach for the evaluation of drug absorption, distribution, metabolism, and excretion and toxicity
- Pharmacological Effects of Ketoconazole in the Treatment of Steroidogenesis Suppression via CYP17A1 Inhibition May Involve MicroRNA Regulation
- Microphysiological systems as an emerging in vitro approach for the evaluation of drug absorption, distribution, metabolism, and excretion and toxicity
- Microphysiological systems as an emerging in vitro approach for the evaluation of drug absorption, distribution, metabolism, and excretion and toxicity
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