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Journal Abstract Search

181 related items for PubMed ID: 17192767

  • 21. No effect of MDR1 C3435T variant on loperamide disposition and central nervous system effects.
    Pauli-Magnus C, Feiner J, Brett C, Lin E, Kroetz DL.
    Clin Pharmacol Ther; 2003 Nov; 74(5):487-98. PubMed ID: 14586389
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  • 22. Pharmacogenetics of cyclosporine in children suggests an age-dependent influence of ABCB1 polymorphisms.
    Fanta S, Niemi M, Jönsson S, Karlsson MO, Holmberg C, Neuvonen PJ, Hoppu K, Backman JT.
    Pharmacogenet Genomics; 2008 Feb; 18(2):77-90. PubMed ID: 18192894
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  • 23. Influence of functional haplotypes in the drug transporter gene ABCB1 on central nervous system drug distribution in humans.
    Brunner M, Langer O, Sunder-Plassmann R, Dobrozemsky G, Müller U, Wadsak W, Krcal A, Karch R, Mannhalter C, Dudczak R, Kletter K, Steiner I, Baumgartner C, Müller M.
    Clin Pharmacol Ther; 2005 Aug; 78(2):182-90. PubMed ID: 16084852
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  • 24. Functional evaluation of polymorphisms in the human ABCB1 gene and the impact on clinical responses of antiepileptic drugs.
    Hung CC, Chen CC, Lin CJ, Liou HH.
    Pharmacogenet Genomics; 2008 May; 18(5):390-402. PubMed ID: 18408562
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  • 25. Imatinib disposition and ABCB1 (MDR1, P-glycoprotein) genotype.
    Gurney H, Wong M, Balleine RL, Rivory LP, McLachlan AJ, Hoskins JM, Wilcken N, Clarke CL, Mann GJ, Collins M, Delforce SE, Lynch K, Schran H.
    Clin Pharmacol Ther; 2007 Jul; 82(1):33-40. PubMed ID: 17495881
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  • 27. ABCB1 genetic variability and methadone dosage requirements in opioid-dependent individuals.
    Coller JK, Barratt DT, Dahlen K, Loennechen MH, Somogyi AA.
    Clin Pharmacol Ther; 2006 Dec; 80(6):682-90. PubMed ID: 17178268
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  • 31. ABCB1 Polymorphisms and Cold Pressor Pain Responses: Opioid-Dependent Patients on Methadone Maintenance Therapy.
    Zahari Z, Lee CS, Ibrahim MA, Musa N, Mohd Yasin MA, Lee YY, Tan SC, Mohamad N, Ismail R.
    Nurs Res; 2017 Dec; 66(2):134-144. PubMed ID: 28252574
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  • 32. Association of ABCB1 genetic variants 3435C>T and 2677G>T to ABCB1 mRNA and protein expression in brain tissue from refractory epilepsy patients.
    Mosyagin I, Runge U, Schroeder HW, Dazert E, Vogelgesang S, Siegmund W, Warzok RW, Cascorbi I.
    Epilepsia; 2008 Sep; 49(9):1555-61. PubMed ID: 18494787
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  • 33. Quantitative structure--activity relationship analysis and molecular dynamics simulation to functionally validate nonsynonymous polymorphisms of human ABC transporter ABCB1 (P-glycoprotein/MDR1).
    Sakurai A, Onishi Y, Hirano H, Seigneuret M, Obanayama K, Kim G, Liew EL, Sakaeda T, Yoshiura K, Niikawa N, Sakurai M, Ishikawa T.
    Biochemistry; 2007 Jul 03; 46(26):7678-93. PubMed ID: 17559192
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  • 34. Ethnicity-related polymorphisms and haplotypes in the human ABCB1 gene.
    Kimchi-Sarfaty C, Marple AH, Shinar S, Kimchi AM, Scavo D, Roma MI, Kim IW, Jones A, Arora M, Gribar J, Gurwitz D, Gottesman MM.
    Pharmacogenomics; 2007 Jan 03; 8(1):29-39. PubMed ID: 17187507
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  • 36. Determination of ABCB1 polymorphisms and haplotypes frequencies in a French population.
    Jeannesson E, Albertini L, Siest G, Gomes AM, Ribeiro V, Aslanidis C, Schmitz G, Visvikis-Siest S.
    Fundam Clin Pharmacol; 2007 Aug 03; 21(4):411-8. PubMed ID: 17635180
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