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Volumn 95, Issue 6, 2014, Pages 583-585

CYP2C9, SLCO1B1, SLCO1B3, and ABCB11 polymorphisms in patients with bosentan-induced liver toxicity

Author keywords

[No Author keywords available]

Indexed keywords

BILE ACID; BILE SALT EXPORT PUMP; BOSENTAN; CYTOCHROME P450 2C9; SOLUTE CARRIER ORGANIC ANION TRANSPORTER 1B1; SOLUTE CARRIER ORGANIC ANION TRANSPORTER 1B3;

EID: 84901020332     PISSN: 00099236     EISSN: 15326535     Source Type: Journal    
DOI: 10.1038/clpt.2014.42     Document Type: Review
Times cited : (14)

References (10)
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  • 2
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  • 3
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    • Bosentan is a substrate of human oatp1b1 and oatp1b3: Inhibition of hepatic uptake as the common mechanism of its interactions with cyclosporin a, rifampicin, and sildenafil
    • Treiber, A., Schneiter, R., Hausler, S. & Stieger, B. Bosentan is a substrate of human OATP1B1 and OATP1B3: Inhibition of hepatic uptake as the common mechanism of its interactions with cyclosporin A, rifampicin, and sildenafil. Drug Metab. Dispos. 35, 1400-1407 (2007
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    • Treiber, A.1    Schneiter, R.2    Hausler, S.3    Stieger, B.4
  • 4
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    • The endothelin antagonist bosentan inhibits the canalicular bile salt export pump: A potential mechanism for hepatic adverse reactions
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    • Fattinger, K.1
  • 5
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    • Association of CYP2C9 2 with bosentan-induced liver injury
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    • Markova, S.M.1
  • 6
    • 84894486504 scopus 로고    scopus 로고
    • CYP2C9 polymorphism is not a major determinant of bosentan exposure in healthy volunteers
    • Markert, C., Burhenne, J., Weiss, J., Mikus, G. & Haefeli, W.E. CYP2C9 polymorphism is not a major determinant of bosentan exposure in healthy volunteers. Clin. Pharmacol. Ther. 95, 250-251 (2013
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    • Markert, C.1    Burhenne, J.2    Weiss, J.3    Mikus, G.4    Haefeli, W.E.5
  • 7
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    • Evaluation of the endothelin receptor antagonists ambrisentan, darusentan, bosentan, and sitaxsentan as substrates and inhibitors of hepatobiliary transporters in sandwich-cultured human hepatocytes
    • Hartman, J.C., Brouwer, K., Mandagere, A., Melvin, L. & Gorczynski, R. Evaluation of the endothelin receptor antagonists ambrisentan, darusentan, bosentan, and sitaxsentan as substrates and inhibitors of hepatobiliary transporters in sandwich-cultured human hepatocytes. Can. J. Physiol. Pharmacol. 88, 682-691 (2010
    • (2010) Can. J. Physiol. Pharmacol , vol.88 , pp. 682-691
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  • 8
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  • 9
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    • Contribution of MRP2 in alterations of canalicular bile formation by the endothelin antagonist bosentan
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  • 10
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    • Fahrmayr, C. et al. Phase I and II metabolism and MRP2-mediated export of bosentan in a MDCKIIOATP1B1-CYP3A4-UGT1A1-MRP2 quadrupletransfected cell line. Br. J. Pharmacol. 169, 21-33 (2013
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    • Fahrmayr, C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.