P-glycoprotein is responsible for the poor intestinal absorption and low toxicity of oral aconitine: In vitro, in situ, in vivo and in silico studies.

MLA

Yang, Cuiping, et al. “P-Glycoprotein Is Responsible for the Poor Intestinal Absorption and Low Toxicity of Oral Aconitine: In Vitro, in Situ, in Vivo and in Silico Studies.” Toxicology & Applied Pharmacology, vol. 273, no. 3, Dec. 2013, pp. 561–68. EBSCOhost, https://doi.org/10.1016/j.taap.2013.09.030.

APA

Yang, C., Zhang, T., Li, Z., Xu, L., Liu, F., Ruan, J., Liu, K., & Zhang, Z. (2013). P-glycoprotein is responsible for the poor intestinal absorption and low toxicity of oral aconitine: In vitro, in situ, in vivo and in silico studies. Toxicology & Applied Pharmacology, 273(3), 561–568. https://doi.org/10.1016/j.taap.2013.09.030

Chicago

Yang, Cuiping, Tianhong Zhang, Zheng Li, Liang Xu, Fei Liu, Jinxiu Ruan, Keliang Liu, and Zhenqing Zhang. 2013. “P-Glycoprotein Is Responsible for the Poor Intestinal Absorption and Low Toxicity of Oral Aconitine: In Vitro, in Situ, in Vivo and in Silico Studies.” Toxicology & Applied Pharmacology 273 (3): 561–68. doi:10.1016/j.taap.2013.09.030.