中文

Journal Publications

[1]Drug-microbiota interactions: an emerging priority for precision medicine.Signal Transduct Target Ther, 2023, 8 (1) : 386.
[2]Resveratrol in Liquor Exacerbates Alcoholic Liver Injury with a Reduced Therapeutic Effect in Mice: An Unsupervised Herbal Wine Habit Is Risky.Nutrients, 2022, 14 (22) : 4752.
[3]A Joint Technology Combining the Advantages of Capillary Micro-sampling with Mass Spectrometry and Applied to the Trans-resveratrol Pharmacokinetic Study in Mice.J Anal Methods Chem, 2022, 2022 (2022) : 5952436.
[4]Gut Microbiota and Host Cyp450s Co-contribute to Pharmacokinetic Variability in Mice with Non-Alcoholic Steatohepatitis: Effects Vary From Drug to Drug.J Adv Res, 2021, 39: 319-332.
[5]Lrp6 Genotype affects Individual Susceptibility to Nonalcoholic Fatty Liver Disease and Silibinin Therapeutic Response via Wnt/β-catenin-Cyp2e1 Signaling.Int J Biol Sci, 2021, 17 (14) : 3936-3953.
[6]Sirtuin3 rs28365927 functional variant confers to the high risk of non-alcoholic fatty liver disease in Chinese Han population. Lipids Health Dis.Lipids Health Dis, 2021, 20 (1) : 92.
[7]The LRP6 functional mutation rs2302685 contributes to individual susceptibility to alcoholic liver injury related to the Wnt/β-catenin-TCF1-CYP2E1 signaling pathway.Arch Toxicol, 2019, 93 (6) : 1679-1695.
[8]Increased expression of SLC46A3 to oppose the progression of hepatocellular carcinoma and its effect on sorafenib therapy.Biomed Pharmacother, 2019, 114 (114) : 108864.
[9]Reversing Epigenetic Alterations Caused by Alcohol: A Promising Therapeutic Direction for Alcoholic Liver Disease.Alcohol Clin Exp Res, 2018, 42 (10) : 1863-1873.
[10]The potent mechanism-based inactivation of CYP2D6 and CYP3A4 with fusidic acid in in vivo bioaccumulation.Xenobiotica, 2017, 48 (10) : 999-1005.
[11]Screening of drug metabolizing enzymes for fusidic acid and its interactions with isoform-selective substrates in vitro.Xenobiotica, 2016, 47 (9) : 778-784.
[12]Screening of Drug Metabolizing Enzymes for the Ginsenoside Compound K in vitro: An Efficient Anti-cancer Substance Originating from Panax Ginseng.PLoS One, 2016, 11 (2) : e0147183.
[13]Kinetics of cytochrome P450 enzymes for metabolism of sodium tanshinone IIA sulfonate in vitro.Chin Med, 2016, 22 (11) : 11.
[14]Quantification of Meranzin Hydrate in Rat Hippocampus and Plasma by LC–MS/MS: A Compound Derived from Chaihu–Shugan–San Displays Antidepressant Potential.Chromatographia, 2015, 78 (3-4) : 221-229.
[15]Quercetin significantly inhibits the metabolism of caffeine-a substrate of cytochrome P450 1A2 unrelated to CYP1A2*1C (-2964G>A) and *1F (734C>A) gene polymorphisms.Biomed Res Int, 2014, 2014 (2014) : 405071.
[16]Searching the cytochrome p450 enzymes for the metabolism of meranzin hydrate: a prospective antidepressant originating from chaihu-shugan-san..PLoS One, 2014, 9 (11) : e113819.
[17]Effect of a single-dose rifampin on the pharmacokinetics of pitavastatin in healthy volunteers.Eur J Clin Pharmacol, 2013, 69 (11) : 1933-8.
[18]Genistein alters caffeine exposure in healthy female volunteers.Eur J Clin Pharmacol, 2010, 67 (4) : 347-53.
[19]Liu Wei Di Huang Wan, a well-known traditional Chinese medicine, induces CYP1A2 while suppressing CYP2A6 and N-acetyltransferase 2 activities in man.J Ethnopharmacol, 2010, 132 (1) : 213-8.
[20]Plant polyphenol curcumin significantly affects CYP1A2 and CYP2A6 activity in healthy, male Chinese volunteers.Ann Pharmacother, 2010, 44 (6) : 1038-45.

total22 1/2

firstpreviousnext last Page

Yao Chen

Zip Code:
Postal Address:
Mobile:
Email:

Central South University All rights reserved 湘ICP备05005659号-1

Click:

The Last Update Time:..