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Biochemical Pharmacology|July 16, 2019
High-content analysis of constitutive androstane receptor (CAR) translocation identifies mosapride citrate as a CAR agonist that represses gluconeogenesisBryan Mackowiak, Linhao Li, Caitlin Lynch, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|September 25, 2018
Identification of Modulators That Activate the Constitutive Androstane Receptor From the Tox21 10K Compound LibraryCaitlin Lynch, Bryan Mackowiak, Ruili Huang, et al.
Biochemical Pharmacology|August 16, 2015
Genome-wide analysis of human constitutive androstane receptor (CAR) transcriptome in wild-type and CAR-knockout HepaRG cellsDaochuan Li, Bryan Mackowiak, Timothy G Brayman, et al.
Molecular Pharmacology|August 23, 2019
Mechanistic Insights of Phenobarbital-Mediated Activation of Human but Not Mouse Pregnane X ReceptorLinhao Li, Matthew A Welch, Zhihui Li, et al.
Alcohol, Clinical & Experimental Research|April 6, 2026
Aquaporin 9 regulates acetaldehyde uptake, alcohol-induced liver injury, and drinking behaviorCheng Chen, Bryan Mackowiak, Dechun Feng, et al.
Alcoholism, Clinical and Experimental Research|October 13, 2022
Hepatic CYP2B10 is highly induced by binge ethanol and contributes to acute-on-chronic alcohol-induced liver injuryBryan Mackowiak, Mingjiang Xu, Yuhong Lin, et al.
Gut|January 2, 2023
MicroRNA-223 attenuates hepatocarcinogenesis by blocking hypoxia-driven angiogenesis and immunosuppressionYaojie Fu, Bryan Mackowiak, Dechun Feng, et al.
Molecular Pharmacology|April 27, 2017
Molecular Basis of Metabolism-Mediated Conversion of PK11195 from an Antagonist to an Agonist of the Constitutive Androstane ReceptorBryan Mackowiak, Linhao Li, Matthew A Welch, et al.
European Journal of Medicinal Chemistry|June 28, 2019
Human constitutive androstane receptor agonist DL5016: A novel sensitizer for cyclophosphamide-based chemotherapiesDongdong Liang, Linhao Li, Caitlin Lynch, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 28, 2020
Mechanistic Analysis of an Extracellular Signal-Regulated Kinase 2-Interacting Compound that Inhibits Mutant BRAF-Expressing Melanoma Cells by Inducing Oxidative StressRamon Martinez, Weiliang Huang, Ramin Samadani, et al.
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