1. Buckley, David B, Klaassen, Curtis D. 2006. Tissue- and gender-specific mRNA expression of UDP-glucuronosyltransferases (UGTs) in mice. In Drug metabolism and disposition: the biological fate of chemicals, 35, 121-7. doi:. https://pubmed.ncbi.nlm.nih.gov/17050650/
2. Zhang, Tianpeng, Guo, Lianxia, Yu, Fangjun, Chen, Min, Wu, Baojian. 2019. The nuclear receptor Rev-erbα participates in circadian regulation of Ugt2b enzymes in mice. In Biochemical pharmacology, 161, 89-97. doi:10.1016/j.bcp.2019.01.010. https://pubmed.ncbi.nlm.nih.gov/30639455/
3. Chik, Mazzura Wan, Hazalin, Nurul Aqmar Mohd Nor, Singh, Gurmeet Kaur Surindar. 2022. Regulation of phase I and phase II neurosteroid enzymes in the hippocampus of an Alzheimer's disease rat model: A focus on sulphotransferases and UDP-glucuronosyltransferases. In Steroids, 184, 109035. doi:10.1016/j.steroids.2022.109035. https://pubmed.ncbi.nlm.nih.gov/35405201/
4. Lu, Hong, Cui, Wei, Klaassen, Curtis D. 2011. Nrf2 protects against 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-induced oxidative injury and steatohepatitis. In Toxicology and applied pharmacology, 256, 122-35. doi:10.1016/j.taap.2011.07.019. https://pubmed.ncbi.nlm.nih.gov/21846477/
5. Li, Cindy Yanfei, Renaud, Helen J, Klaassen, Curtis D, Cui, Julia Yue. 2015. Age-Specific Regulation of Drug-Processing Genes in Mouse Liver by Ligands of Xenobiotic-Sensing Transcription Factors. In Drug metabolism and disposition: the biological fate of chemicals, 44, 1038-49. doi:10.1124/dmd.115.066639. https://pubmed.ncbi.nlm.nih.gov/26577535/
6. Aleksunes, Lauren M, Klaassen, Curtis D. 2012. Coordinated regulation of hepatic phase I and II drug-metabolizing genes and transporters using AhR-, CAR-, PXR-, PPARα-, and Nrf2-null mice. In Drug metabolism and disposition: the biological fate of chemicals, 40, 1366-79. doi:10.1124/dmd.112.045112. https://pubmed.ncbi.nlm.nih.gov/22496397/
7. Buckley, David B, Klaassen, Curtis D. 2009. Induction of mouse UDP-glucuronosyltransferase mRNA expression in liver and intestine by activators of aryl-hydrocarbon receptor, constitutive androstane receptor, pregnane X receptor, peroxisome proliferator-activated receptor alpha, and nuclear factor erythroid 2-related factor 2. In Drug metabolism and disposition: the biological fate of chemicals, 37, 847-56. doi:10.1124/dmd.108.024190. https://pubmed.ncbi.nlm.nih.gov/19144771/
智鼠故事 
