[HTML][HTML] The time-dependent effects of St John's wort on cytochrome P450, uridine diphosphate-glucuronosyltransferase, glutathione S-transferase, and NAD (P) H …

JF Yang, YR Liu, CC Huang, YF Ueng - journal of food and drug analysis, 2018 - Elsevier
Abstract Hypericum perforatum [St. John's wort (SJW)] is known to cause a drug interaction
with the substrates of cytochrome P450 (P450, CYP) isoforms, mainly CYP3A. This study …

The time-dependent effects of St John's wort on cytochrome P450, uridine diphosphate-glucuronosyltransferase, glutathione S-transferase, and NAD (P) H-quinone …

JF Yang, YR Liu, CC Huang, YF Ueng - Journal of Food and Drug …, 2018 - hero.epa.gov
Abstract Hypericum perforatum [St. John's wort (SJW)] is known to cause a drug interaction
with the substrates of cytochrome P450 (P450, CYP) isoforms, mainly CYP3A. This study …

[HTML][HTML] The time-dependent effects of St John's wort on cytochrome P450, uridine diphosphate-glucuronosyltransferase, glutathione S-transferase, and NAD (P) H …

JF Yang, YR Liu, CC Huang… - Journal of Food and Drug …, 2018 - ncbi.nlm.nih.gov
Abstract Hypericum perforatum [St. John's wort (SJW)] is known to cause a drug interaction
with the substrates of cytochrome P450 (P450, CYP) isoforms, mainly CYP3A. This study …

The time-dependent effects of St John's wort on cytochrome P450, uridine diphosphate-glucuronosyltransferase, glutathione S-transferase, and NAD (P) H-quinone …

JF Yang, YR Liu, CC Huang, YF Ueng - Journal of Food and Drug …, 2017 - europepmc.org
Abstract Hypericum perforatum [St. John's wort (SJW)] is known to cause a drug interaction
with the substrates of cytochrome P450 (P450, CYP) isoforms, mainly CYP3A. This study …

The time-dependent effects of St John's wort on cytochrome P450, uridine diphosphate-glucuronosyltransferase, glutathione S-transferase, and NAD (P) H-quinone …

Y Jin-Fu, L Yue-Rong, CC Huang… - Journal of Food and …, 2018 - search.proquest.com
Abstract Hypericum perforatum [St. John's wort (SJW)] is known to cause a drug interaction
with the substrates of cytochrome P450 (P450, CYP) isoforms, mainly CYP3A. This study …

The time-dependent effects of St John's wort on cytochrome P450, uridine diphosphate-glucuronosyltransferase, glutathione S-transferase, and NAD (P) H-quinone …

JF Yang, YR Liu, CC Huang, YF Ueng - 2018 - agris.fao.org
Hypericum perforatum [St. John's wort (SJW)] is known to cause a drug interaction with the
substrates of cytochrome P450 (P450, CYP) isoforms, mainly CYP3A. This study aims to …

The time-dependent effects of St John's wort on cytochrome P450, uridine diphosphate-glucuronosyltransferase, glutathione S-transferase, and NAD (P) H-quinone …

JF Yang, YR Liu, CC Huang, YF Ueng - Journal of Food and Drug …, 2018 - jfda-online.com
Abstract Hypericum perforatum [St. John's wort (SJW)] is known to cause a drug interaction
with the substrates of cytochrome P450 (P450, CYP) isoforms, mainly CYP3A. This study …

The time-dependent effects of St John's wort on cytochrome P450, uridine diphosphateglucuronosyltransferase, glutathione S-transferase, and NAD (P) H-quinone …

JF Yang, YR Liu, CC Huang… - Journal of Food & Drug …, 2018 - search.ebscohost.com
Abstract Hypericum perforatum [St. John's wort (SJW)] is known to cause a drug interaction
with the substrates of cytochrome P450 (P450, CYP) isoforms, mainly CYP3A. This study …

[PDF][PDF] The time-dependent effects of St John's wort on cytochrome P450, uridine diphosphate-glucuronosyltransferase, glutathione S-transferase, and NAD (P) H …

JF Yang, YR Liu, CC Huang, YF Ueng - cyberleninka.org
The drug-metabolizing cytochrome P450 (P450, CYP)-dependent monooxygenase system
primarily localizes at the membranes of endoplasmic reticulum and participates in the …

The time-dependent effects of St John's wort on cytochrome P450, uridine diphosphate-glucuronosyltransferase, glutathione S-transferase, and NAD (P) H-quinone …

JF Yang, YR Liu, CC Huang… - Journal of food and …, 2018 - pubmed.ncbi.nlm.nih.gov
Hypericum perforatum [St. John's wort (SJW)] is known to cause a drug interaction with the
substrates of cytochrome P450 (P450, CYP) isoforms, mainly CYP3A. This study aims to …