Polymorphisms of Drug Transporters and Clinical Relevance

作者: Aparna Chhibber , Janine Micheli , Deanna L. Kroetz

DOI: 10.1002/9781118705308.CH20

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参考文章(169)
Monika Hitzl, Siegfried Drescher, Heiko van der Kuip, Elke Schäffeler, Joachim Fischer, Matthias Schwab, Michel Eichelbaum, Martin F. Fromm, The C3435T mutation in the human MDR1 gene is associated with altered efflux of the P-glycoprotein substrate rhodamine 123 from CD56+ natural killer cells. Pharmacogenetics. ,vol. 11, pp. 293- 298 ,(2001) , 10.1097/00008571-200106000-00003
S. Saito, A. Iida, A. Sekine, Y. Miura, C. Ogawa, S. Kawauchi, S. Higuchi, Y. Nakamura, Identification of 779 genetic variations in eight genes encoding members of the ATP-binding cassette, subfamily C (ABCC/MRP/CFTR. Journal of Human Genetics. ,vol. 47, pp. 147- 171 ,(2002) , 10.1007/S100380200018
SLCO1B1 variants and statin-induced myopathy--a genomewide study The New England Journal of Medicine. ,vol. 359, pp. 789- 799 ,(2008) , 10.1056/NEJMOA0801936
Arthur A.B. Bergen, Astrid S. Plomp, Ellen J. Schuurman, Sharon Terry, Martijn Breuning, Hans Dauwerse, Jaap Swart, Marcel Kool, Simone van Soest, Frank Baas, Jacoline B. ten Brink, Paulus T.V.M. de Jong, Mutations in ABCC6 cause pseudoxanthoma elasticum. Nature Genetics. ,vol. 25, pp. 228- 231 ,(2000) , 10.1038/76109
Sandra S. Strautnieks, Laura N. Bull, Alexander S. Knisely, Samuel A. Kocoshis, Niklas Dahl, Henrik Arnell, Etienne Sokal, Karine Dahan, Sarah Childs, Victor Ling, M. Stuart Tanner, Amir F. Kagalwalla, Antal Németh, Joanna Pawlowska, Alastair Baker, Giorgina Mieli-Vergani, Nelson B. Freimer, R. Mark Gardiner, Richard J. Thompson, A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis Nature Genetics. ,vol. 20, pp. 233- 238 ,(1998) , 10.1038/3034
M. Axel Wollmer, Elisabeth Kapaki, Martin Hersberger, Jörg Muntwyler, Fabienne Brunner, Magdalini Tsolaki, Hiroyasu Akatsu, Kenji Kosaka, Makoto Michikawa, Dimitra Molyva, Giorgos P. Paraskevas, Dieter Lütjohann, Arnold von Eckardstein, Christoph Hock, Roger M. Nitsch, Andreas Papassotiropoulos, Ethnicity-dependent genetic association of ABCA2 with sporadic Alzheimer's disease. American Journal of Medical Genetics. ,vol. 141, pp. 534- 536 ,(2006) , 10.1002/AJMG.B.30345
Angela Brooks-Wilson, Michel Marcil, Susanne M. Clee, Lin-Hua Zhang, Kirsten Roomp, Marjel van Dam, Lu Yu, Carl Brewer, Jennifer A. Collins, Henri O.F. Molhuizen, Odell Loubser, B.F. Francis Ouelette, Keith Fichter, Katherine J.D. Ashbourne-Excoffon, Christoph W. Sensen, Stephen Scherer, Stephanie Mott, Maxime Denis, Duane Martindale, Jiri Frohlich, Kenneth Morgan, Ben Koop, Simon Pimstone, John J.P. Kastelein, Jacques Genest, Michael R. Hayden, Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency Nature Genetics. ,vol. 22, pp. 336- 345 ,(1999) , 10.1038/11905
Harunobu Tahara, Sook Wah Yee, Thomas J. Urban, Stephanie Hesselson, Richard A. Castro, Michiko Kawamoto, Doug Stryke, Susan J. Johns, Thomas E. Ferrin, Pui-Yan Kwok, Kathleen M. Giacomini, Functional Genetic Variation in the Basal Promoter of the Organic Cation/Carnitine Transporters OCTN1 (SLC22A4) and OCTN2 (SLC22A5) Journal of Pharmacology and Experimental Therapeutics. ,vol. 329, pp. 262- 271 ,(2009) , 10.1124/JPET.108.146449
Richard H. Ho, Rommel G. Tirona, Brenda F. Leake, Hartmut Glaeser, Wooin Lee, Christopher J. Lemke, Yi Wang, Richard B. Kim, Drug and Bile Acid Transporters in Rosuvastatin Hepatic Uptake: Function, Expression, and Pharmacogenetics Gastroenterology. ,vol. 130, pp. 1793- 1806 ,(2006) , 10.1053/J.GASTRO.2006.02.034