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pro vyhledávání: '"Paine, M. F."'
Akademický článek
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Autor:
Paine, M. F., Cherrington, N. J., Hargraves, T. L., Vanderah, T. W., Dzierlenga, A. L., Clarke, J. D., Ainslie, G. R.
Morphine is metabolized in humans to morphine-3-glucuronide (M3G) and the pharmacologically active morphine-6-glucuronide (M6G). The hepatobiliary disposition of both metabolites relies upon multidrug resistance-associated proteins Mrp3 and Mrp2, loc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0583ac827fe56f4520fb2458252afca
Altered morphine glucuronide and bile acid disposition in patients with nonalcoholic steatohepatitis
Autor:
Stewart, P. W., Johnston, C. K., Ferslew, B. C., Jia, W., Brouwer, K. L.R., Tsakalozou, E., Barritt, A. S., Paine, M. F., Bridges, A. S.
The functional impact of altered drug transport protein expression on the systemic pharmacokinetics of morphine, hepatically-derived morphine glucuronide (morphine-3- and morphine-6-glucuronide), and fasting bile acids was evaluated in patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e36b648da52ce7612607122aee60084a
Akademický článek
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Akademický článek
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Supported by a usage history that predates written records and the perception that “natural” ensures safety, herbal products have increasingly been incorporated into Western health care. Consumers often self-administer these products concomitantl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac750ab0c10db22ddc5d84222f6e45ff
Autor:
Li, Y., Paine, M. F., Scarlett, Y. V., Ainslie, G. R., Hull, J. H., Wolf, K. K., Connolly, E. A.
Dietary substances, including herbal products and citrus juices, can perpetrate interactions with conventional medications. Regulatory guidances for dietary substance–drug interaction assessment are lacking. This deficiency is due in part to challe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f3fa5f2a45320b76dda466e897e7471
(S)-Warfarin 7-hydroxylation and midazolam 1′-hydroxylation are among the preferred probe substrate reactions for CYP2C9 and CYP3A4/5, respectively. The impact of solvents on enzyme activity, kinetic parameters, and predicted in vivo hepatic cleara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f12a06f39cde320466b2a7265ecb700
Autor:
Hall, J. E., Generaux, C. N., Goldsmith, R. B., Tidwell, R. R., Olson, C. A., Paine, M. F., Clewell, H. J., Brouwer, K. L. R., Yan, G. Z., Yoon, M.
Dose selection during antiparasitic drug development in animal models and humans traditionally has relied on correlations between plasma concentrations obtained at or below maximally tolerated doses that are efficacious. The objective of this study w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::babb181e77abea70e43a9b0df81b74be
Autor:
Paine, M. F., Tidwell, R. R., Wang, M. Z., Brouwer, K. L. R., Pollack, G. M., Yan, G. Z., Hall, J. E.
Selection of in vitro models that accurately characterize metabolite systemic and hepatobiliary exposure remains a challenge in drug development. In the present study, mechanisms underlying differences in systemic exposure of two active metabolites,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be12405749fe9b0c747eb575444df9d5