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Journal Abstract Search

237 related items for PubMed ID: 15115917

  • 1. Variable expression of P-glycoprotein in the human placenta and its association with mutations of the multidrug resistance 1 gene (MDR1, ABCB1).
    Hitzl M, Schaeffeler E, Hocher B, Slowinski T, Halle H, Eichelbaum M, Kaufmann P, Fritz P, Fromm MF, Schwab M.
    Pharmacogenetics; 2004 May; 14(5):309-18. PubMed ID: 15115917
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  • 2. Modulation of multidrug resistance P-glycoprotein 1 (ABCB1) expression in human heart by hereditary polymorphisms.
    Meissner K, Jedlitschky G, Meyer zu Schwabedissen H, Dazert P, Eckel L, Vogelgesang S, Warzok RW, Böhm M, Lehmann C, Wendt M, Cascorbi I, Kroemer HK.
    Pharmacogenetics; 2004 Jun; 14(6):381-5. PubMed ID: 15247630
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  • 3. Modulation of human placental P-glycoprotein expression and activity by MDR1 gene polymorphisms.
    Hemauer SJ, Nanovskaya TN, Abdel-Rahman SZ, Patrikeeva SL, Hankins GD, Ahmed MS.
    Biochem Pharmacol; 2010 Mar 15; 79(6):921-5. PubMed ID: 19896927
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  • 4. 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.
    Hitzl M, Drescher S, van der Kuip H, Schäffeler E, Fischer J, Schwab M, Eichelbaum M, Fromm MF.
    Pharmacogenetics; 2001 Jun 15; 11(4):293-8. PubMed ID: 11434506
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  • 7. The drug-transporter gene MDR1 C3435T and G2677T/A polymorphisms and the risk of multidrug-resistant epilepsy in Turkish children.
    Seven M, Batar B, Unal S, Yesil G, Yuksel A, Guven M.
    Mol Biol Rep; 2014 Jan 15; 41(1):331-6. PubMed ID: 24213830
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  • 8. Increased risk for congenital heart defects in children carrying the ABCB1 Gene C3435T polymorphism and maternal periconceptional toxicants exposure.
    Wang C, Xie L, Zhou K, Zhan Y, Li Y, Li H, Qiao L, Wang F, Hua Y.
    PLoS One; 2013 Jan 15; 8(7):e68807. PubMed ID: 23874772
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  • 11. C3435T polymorphism in the MDR1 gene affects the enterocyte expression level of CYP3A4 rather than Pgp in recipients of living-donor liver transplantation.
    Goto M, Masuda S, Saito H, Uemoto S, Kiuchi T, Tanaka K, Inui K.
    Pharmacogenetics; 2002 Aug 15; 12(6):451-7. PubMed ID: 12172213
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  • 13. MDR1 genotype is associated with hepatic cytochrome P450 3A4 basal and induction phenotype.
    Lamba J, Strom S, Venkataramanan R, Thummel KE, Lin YS, Liu W, Cheng C, Lamba V, Watkins PB, Schuetz E.
    Clin Pharmacol Ther; 2006 Apr 15; 79(4):325-38. PubMed ID: 16580901
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  • 14. Role of MDR1 C3435T and GABRG2 C588T gene polymorphisms in seizure occurrence and MDR1 effect on anti-epileptic drug (phenytoin) absorption.
    Ponnala S, Chaudhari JR, Jaleel MA, Bhiladvala D, Kaipa PR, Das UN, Hasan Q.
    Genet Test Mol Biomarkers; 2012 Jun 15; 16(6):550-7. PubMed ID: 22239287
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