Zheng, Y.F.; Min, J.S.; Kim, D.; Park, J.B.; Choi, S.-W.; Lee, E.S.; Na, K.; Bae, S.K.
In Vitro Inhibition of Human UDP-Glucuronosyl-Transferase (UGT) Isoforms by Astaxanthin, β-Cryptoxanthin, Canthaxanthin, Lutein, and Zeaxanthin: Prediction of in Vivo Dietary Supplement-Drug Interactions. Molecules 2016, 21, 1052.
https://doi.org/10.3390/molecules21081052
AMA Style
Zheng YF, Min JS, Kim D, Park JB, Choi S-W, Lee ES, Na K, Bae SK.
In Vitro Inhibition of Human UDP-Glucuronosyl-Transferase (UGT) Isoforms by Astaxanthin, β-Cryptoxanthin, Canthaxanthin, Lutein, and Zeaxanthin: Prediction of in Vivo Dietary Supplement-Drug Interactions. Molecules. 2016; 21(8):1052.
https://doi.org/10.3390/molecules21081052
Chicago/Turabian Style
Zheng, Yu Fen, Jee Sun Min, Doyun Kim, Jung Bae Park, Sung-Wook Choi, Eun Seong Lee, Kun Na, and Soo Kyung Bae.
2016. "In Vitro Inhibition of Human UDP-Glucuronosyl-Transferase (UGT) Isoforms by Astaxanthin, β-Cryptoxanthin, Canthaxanthin, Lutein, and Zeaxanthin: Prediction of in Vivo Dietary Supplement-Drug Interactions" Molecules 21, no. 8: 1052.
https://doi.org/10.3390/molecules21081052
APA Style
Zheng, Y. F., Min, J. S., Kim, D., Park, J. B., Choi, S.-W., Lee, E. S., Na, K., & Bae, S. K.
(2016). In Vitro Inhibition of Human UDP-Glucuronosyl-Transferase (UGT) Isoforms by Astaxanthin, β-Cryptoxanthin, Canthaxanthin, Lutein, and Zeaxanthin: Prediction of in Vivo Dietary Supplement-Drug Interactions. Molecules, 21(8), 1052.
https://doi.org/10.3390/molecules21081052
