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PUBMED FOR HANDHELDS

Journal Abstract Search


239 related items for PubMed ID: 24410402

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  • 7. The hepatobiliary disposition of timosaponin b2 is highly dependent on influx/efflux transporters but not metabolism.
    Sheng J, Tian X, Xu G, Wu Z, Chen C, Wang L, Pan L, Huang C, Pan G.
    Drug Metab Dispos; 2015 Jan; 43(1):63-72. PubMed ID: 25336752
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  • 10. In vitro biliary clearance of angiotensin II receptor blockers and 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors in sandwich-cultured rat hepatocytes: comparison with in vivo biliary clearance.
    Abe K, Bridges AS, Yue W, Brouwer KL.
    J Pharmacol Exp Ther; 2008 Sep; 326(3):983-90. PubMed ID: 18574002
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  • 11. Evaluation of the endothelin receptor antagonists ambrisentan, bosentan, macitentan, and sitaxsentan as hepatobiliary transporter inhibitors and substrates in sandwich-cultured human hepatocytes.
    Lepist EI, Gillies H, Smith W, Hao J, Hubert C, St Claire RL, Brouwer KR, Ray AS.
    PLoS One; 2014 Sep; 9(1):e87548. PubMed ID: 24498134
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  • 12. Statins alter the hepatobiliary transport of unconjugated and conjugated bilirubin in sandwich-cultured rat hepatocytes.
    Szabó M, Veres Z, Bátai-Konczos A, Kékesi O, Kis E, Szabó K, Jemnitz K.
    Toxicol In Vitro; 2014 Sep; 28(6):1136-43. PubMed ID: 24909372
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  • 13. Identification of hepatic phospholipidosis inducers in sandwich-cultured rat hepatocytes, a physiologically relevant model, reveals altered basolateral uptake and biliary excretion of anionic probe substrates.
    Ferslew BC, Brouwer KL.
    Toxicol Sci; 2014 May; 139(1):99-107. PubMed ID: 24563379
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  • 14. Involvement of multiple transporters in the hepatobiliary transport of rosuvastatin.
    Kitamura S, Maeda K, Wang Y, Sugiyama Y.
    Drug Metab Dispos; 2008 Oct; 36(10):2014-23. PubMed ID: 18617601
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  • 15. Quantitative expression profile of hepatobiliary transporters in sandwich cultured rat and human hepatocytes.
    Li N, Bi YA, Duignan DB, Lai Y.
    Mol Pharm; 2009 Oct; 6(4):1180-9. PubMed ID: 19545175
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  • 16. Drug and bile acid transporters in rosuvastatin hepatic uptake: function, expression, and pharmacogenetics.
    Ho RH, Tirona RG, Leake BF, Glaeser H, Lee W, Lemke CJ, Wang Y, Kim RB.
    Gastroenterology; 2006 May; 130(6):1793-806. PubMed ID: 16697742
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  • 17. Differential disposition of chenodeoxycholic acid versus taurocholic acid in response to acute troglitazone exposure in rat hepatocytes.
    Marion TL, Perry CH, St Claire RL, Yue W, Brouwer KL.
    Toxicol Sci; 2011 Apr; 120(2):371-80. PubMed ID: 21262925
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  • 18. Understanding the interplay of drug transporters involved in the disposition of rosuvastatin in the isolated perfused rat liver using a physiologically-based pharmacokinetic model.
    Hobbs M, Parker C, Birch H, Kenworthy K.
    Xenobiotica; 2012 Apr; 42(4):327-38. PubMed ID: 22035568
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  • 19. Role of transporters in the disposition of the selective phosphodiesterase-4 inhibitor (+)-2-[4-({[2-(benzo[1,3]dioxol-5-yloxy)-pyridine-3-carbonyl]-amino}-methyl)-3-fluoro-phenoxy]-propionic acid in rat and human.
    Kalgutkar AS, Feng B, Nguyen HT, Frederick KS, Campbell SD, Hatch HL, Bi YA, Kazolias DC, Davidson RE, Mireles RJ, Duignan DB, Choo EF, Zhao SX.
    Drug Metab Dispos; 2007 Nov; 35(11):2111-8. PubMed ID: 17686907
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  • 20. Evaluation of the endothelin receptor antagonists ambrisentan, darusentan, bosentan, and sitaxsentan as substrates and inhibitors of hepatobiliary transporters in sandwich-cultured human hepatocytes.
    Hartman JC, Brouwer K, Mandagere A, Melvin L, Gorczynski R.
    Can J Physiol Pharmacol; 2010 Jun; 88(6):682-91. PubMed ID: 20628435
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