H. Zhang

A method for the simultaneous evaluation of the activities of seven major human drug-metabolizing cytochrome P450s using an in vitro cocktail of probe substrates and fast gradient liquid chromatography tandem mass spectrometry.

Honglu Zhang, S. Ball, H. Lim, 2001, Drug metabolism and disposition: the biological fate of chemicals.

In vitro hepatic metabolism of a CYP3A-mediated drug, quinine, in Adélie penguins.

L. S. Davis, D. Saville, P. Coville, 1999, Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology.

Effect of the Grapefruit Flavonoid Naringin on Pharmacokinetics of Quinine in Rats

P. Coville, S. Wanwimolruk, C. Wong, 2000, Drug metabolism and drug interactions.

Effects of cigarette smoking on quinine pharmacokinetics in malaria

P. Pitisuttithum, S. Pukrittayakamee, S. Wanwimolruk, 2002, European Journal of Clinical Pharmacology.

Toxicological evaluation of New Zealand deer velvet powder. Part I: acute and subchronic oral toxicity studies in rats.

S. Haines, J. Suttie, P. Coville, 2000, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[The pharmacokinetics and disposition of tetramethylpyrazine phosphate in dogs and rats].

X. Cao, M. L. Chen, H. Zhang, 1986, Yao xue xue bao = Acta pharmaceutica Sinica.

Evidence for involvement of human CYP3A in the 3-hydroxylation of quinine.

J. Miners, R. Walker, P. Coville, 2003, British journal of clinical pharmacology.

[Study on toxicological mechanism of moniliformin].

J. Li, H. Zhang, 1989, Wei sheng wu xue bao = Acta microbiologica Sinica.

Utility of multivariate analysis in support of in vitro metabolite identification studies: retrospective analysis using the antidepressant drug nefazodone

A. Kalgutkar, R. Bonner, R. P. Schneider, 2010, Xenobiotica; the fate of foreign compounds in biological systems.

Mechanism-based inhibition of human cytochrome P4503A4 by domperidone

R. M. Fancher, H. Zhang, S.-Y. Chang, 2010, Xenobiotica; the fate of foreign compounds in biological systems.

High anticancer efficacy of L-proline-m-bis (2-chloroethyl) amino-L-phenylalanyl-L-norvaline ethyl ester hydrochloride (MF13) in vivo.

J. Roboz, J. Holland, G. Bekesi, 2001, Anticancer research.