Search Results - "Pharmacogenetics (London)" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

High plasma pravastatin concentrations are associated with single nucleotide polymorphisms and haplotypes of organic anion transporting polypeptide-C (OATP-C, SLCO1B1)

High plasma pravastatin concentrations are associated with single nucleotide polymorphisms and haplotypes of organic anion transporting polypeptide-C (OATP-C, SLCO1B1)

by Niemi, Mikko, Schaeffeler, Elke, Lang, Thomas, Fromm, Martin F, Neuvonen, Mikko, Kyrklund, Carl, Backman, Janne T, Kerb, Reinhold, Schwab, Matthias, Neuvonen, Pertti J, Eichelbaum, Michel, Kivistö, Kari T
Published in Pharmacogenetics (London) (01.07.2004)

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Comprehensive analysis of thiopurine S-methyltransferase phenotype-genotype correlation in a large population of German-Caucasians and identification of novel TPMT variants

Comprehensive analysis of thiopurine S-methyltransferase phenotype-genotype correlation in a large population of German-Caucasians and identification of novel TPMT variants

by Schaeffeler, Elke, Fischer, Christine, Brockmeier, Dierk, Wernet, Dorothee, Moerike, Klaus, Eichelbaum, Michel, Zanger, Ulrich M, Schwab, Matthias
Published in Pharmacogenetics (London) (01.07.2004)

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A 6 bp polymorphism in the thymidylate synthase gene causes message instability and is associated with decreased intratumoral TS mRNA levels

A 6 bp polymorphism in the thymidylate synthase gene causes message instability and is associated with decreased intratumoral TS mRNA levels

by Mandola, Michael V, Stoehlmacher, Jan, Zhang, Wu, Groshen, Susan, Yu, Mimi C, Iqbal, Syma, Lenz, Heinz-Josef, Ladner, Robert D
Published in Pharmacogenetics (London) (01.05.2004)

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Sequence diversity and haplotype structure in the human ABCB1 (MDR1, multidrug resistance transporter) gene

Sequence diversity and haplotype structure in the human ABCB1 (MDR1, multidrug resistance transporter) gene

by Kroetz, Deanna L, Pauli-Magnus, Christiane, Hodges, Laura M, Huang, Conrad C, Kawamoto, Michiko, Johns, Susan J, Stryke, Doug, Ferrin, Thomas E, DeYoung, Joseph, Taylor, Travis, Carlson, Elaine J, Herskowitz, Ira, Giacomini, Kathleen M, Clark, Andrew G
Published in Pharmacogenetics (London) (01.08.2003)

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Comparison of cytochrome P450 (CYP) genes from the mouse and human genomes, including nomenclature recommendations for genes, pseudogenes and alternative-splice variants

Comparison of cytochrome P450 (CYP) genes from the mouse and human genomes, including nomenclature recommendations for genes, pseudogenes and alternative-splice variants

by Nelson, David R, Zeldin, Darryl C, Hoffman, Susan M G, Maltais, Lois J, Wain, Hester M, Nebert, Daniel W
Published in Pharmacogenetics (London) (01.01.2004)

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Adverse drug reactions to azathioprine therapy are associated with polymorphism in the gene encoding inosine triphosphate pyrophosphatase (ITPase)

Adverse drug reactions to azathioprine therapy are associated with polymorphism in the gene encoding inosine triphosphate pyrophosphatase (ITPase)

by Marinaki, Anthony M, Ansari, Azhar, Duley, John A, Arenas, Monica, Sumi, Satoshi, Lewis, Cathryn M, Shobowale-Bakre, El-Monsor, Escuredo, Emilia, Fairbanks, Lynette D, Sanderson, Jeremy D
Published in Pharmacogenetics (London) (01.03.2004)

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A proposed nomenclature system for the cytosolic sulfotransferase (SULT) superfamily

A proposed nomenclature system for the cytosolic sulfotransferase (SULT) superfamily

by Blanchard, Rebecca L, Freimuth, Robert R, Buck, Jochen, Weinshilboum, Richard M, Coughtrie, Michael W H
Published in Pharmacogenetics (London) (01.03.2004)

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Extensive genetic polymorphism in the human CYP2B6 gene with impact on expression and function in human liver

Extensive genetic polymorphism in the human CYP2B6 gene with impact on expression and function in human liver

by Lang, T, Klein, K, Fischer, J, Nüssler, A K, Neuhaus, P, Hofmann, U, Eichelbaum, M, Schwab, M, Zanger, U M
Published in Pharmacogenetics (London) (01.07.2001)

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Sequence analysis of bile salt export pump (ABCB11) and multidrug resistance p-glycoprotein 3 (ABCB4, MDR3) in patients with intrahepatic cholestasis of pregnancy

Sequence analysis of bile salt export pump (ABCB11) and multidrug resistance p-glycoprotein 3 (ABCB4, MDR3) in patients with intrahepatic cholestasis of pregnancy

by Pauli-Magnus, Christiane, Lang, Thomas, Meier, Yvonne, Zodan-Marin, Tina, Jung, Diana, Breymann, Christian, Zimmermann, Roland, Kenngott, Silke, Beuers, Ulrich, Reichel, Christoph, Kerb, Reinhold, Penger, Anja, Meier, Peter J, Kullak-Ublick, Gerd A
Published in Pharmacogenetics (London) (01.02.2004)

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Disposition of debrisoquine in Caucasians with different CYP2D6-genotypes including those with multiple genes

Disposition of debrisoquine in Caucasians with different CYP2D6-genotypes including those with multiple genes

by Dalén, P, Dahl, M L, Eichelbaum, M, Bertilsson, L, Wilkinson, G R
Published in Pharmacogenetics (London) (01.12.1999)

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Deposition of Alzheimer's beta-amyloid is inversely correlated with P-glycoprotein expression in the brains of elderly non-demented humans

Deposition of Alzheimer's beta-amyloid is inversely correlated with P-glycoprotein expression in the brains of elderly non-demented humans

by Vogelgesang, Silke, Cascorbi, Ingolf, Schroeder, Eike, Pahnke, Jens, Kroemer, Heyo K, Siegmund, Werner, Kunert-Keil, Christiane, Walker, Lary C, Warzok, Rolf W
Published in Pharmacogenetics (London) (01.10.2002)

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Identification of common polymorphisms in the promoter of the UGT1A9 gene: evidence that UGT1A9 protein and activity levels are strongly genetically controlled in the liver

Identification of common polymorphisms in the promoter of the UGT1A9 gene: evidence that UGT1A9 protein and activity levels are strongly genetically controlled in the liver

by Girard, Hugo, Court, Michael H, Bernard, Olivier, Fortier, Louis-Charles, Villeneuve, Lyne, Hao, Qin, Greenblatt, David J, von Moltke, Lisa L, Perussed, Louis, Guillemette, Chantal
Published in Pharmacogenetics (London) (01.08.2004)

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Natural allelic variants of breast cancer resistance protein (BCRP) and their relationship to BCRP expression in human intestine

Natural allelic variants of breast cancer resistance protein (BCRP) and their relationship to BCRP expression in human intestine

by Zamber, Charis P, Lamba, Jatinder K, Yasuda, Kazuto, Farnum, Jennifer, Thummel, Kenneth, Schuetz, John D, Schuetz, Erin G
Published in Pharmacogenetics (London) (01.01.2003)

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Ivermectin sensitivity in collies is associated with a deletion mutation of the mdr1 gene

Ivermectin sensitivity in collies is associated with a deletion mutation of the mdr1 gene

by Mealey, K L, Bentjen, S A, Gay, J M, Cantor, G H
Published in Pharmacogenetics (London) (01.11.2001)

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Common allelic variants of cytochrome P4503A4 and their prevalence in different populations

Common allelic variants of cytochrome P4503A4 and their prevalence in different populations

by Lamba, Jatinder K, Lin, Yvonne S, Thummel, Kenneth, Daly, Ann, Watkins, Paul B, Strom, Stephen, Zhang, Jiong, Schuetz, Erin G
Published in Pharmacogenetics (London) (01.03.2002)

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Pharmacogenetics and herb-drug interactions: experience with Ginkgo biloba and omeprazole

Pharmacogenetics and herb-drug interactions: experience with Ginkgo biloba and omeprazole

by Yin, Ophelia Q P, Tomlinson, Brian, Waye, Mary M Y, Chow, Albert H L, Chow, Moses S S
Published in Pharmacogenetics (London) (01.12.2004)

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Contribution of common polymorphisms in reduced folate carrier and gamma-glutamylhydrolase to methotrexate polyglutamate levels in patients with rheumatoid arthritis

Contribution of common polymorphisms in reduced folate carrier and gamma-glutamylhydrolase to methotrexate polyglutamate levels in patients with rheumatoid arthritis

by Dervieux, Thierry, Kremer, Joel, Lein, Diana Orentas, Capps, Robert, Barham, Robert, Meyer, Gary, Smith, Katie, Caldwell, Jacques, Furst, Daniel E
Published in Pharmacogenetics (London) (01.11.2004)

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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

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

by Hitzl, M, Drescher, S, van der Kuip, H, Schäffeler, E, Fischer, J, Schwab, M, Eichelbaum, M, Fromm, M F
Published in Pharmacogenetics (London) (01.06.2001)

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The effect of CYP3A5 and MDR1 (ABCB1) polymorphisms on cyclosporine and tacrolimus dose requirements and trough blood levels in stable renal transplant patients

The effect of CYP3A5 and MDR1 (ABCB1) polymorphisms on cyclosporine and tacrolimus dose requirements and trough blood levels in stable renal transplant patients

by Haufroid, Vincent, Mourad, Michel, Van Kerckhove, Valérie, Wawrzyniak, Jeremie, De Meyer, Martine, Eddour, Djamila Chaib, Malaise, Jacques, Lison, Dominique, Squifflet, Jean-Paul, Wallemacq, Pierre
Published in Pharmacogenetics (London) (01.03.2004)

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Polymorphisms in the methylenetetrahydrofolate reductase gene were associated with both the efficacy and the toxicity of methotrexate used for the treatment of rheumatoid arthritis, as evidenced by single locus and haplotype analyses

Polymorphisms in the methylenetetrahydrofolate reductase gene were associated with both the efficacy and the toxicity of methotrexate used for the treatment of rheumatoid arthritis, as evidenced by single locus and haplotype analyses

by Urano, Wako, Taniguchi, Atsuo, Yamanaka, Hisashi, Tanaka, Eiichi, Nakajima, Hiroshi, Matsuda, Yuko, Akama, Hideto, Kitamura, Yutaka, Kamatani, Naoyuki
Published in Pharmacogenetics (London) (01.04.2002)

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