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Pubmed for Handhelds

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Journal Abstract Search

112 related items for PubMed ID: 7606840

  • 21. A missense mutation in exon 6 of the CYP2D6 gene leading to a histidine 324 to proline exchange is associated with the poor metabolizer phenotype of sparteine.
    Evert B, Griese EU, Eichelbaum M.
    Naunyn Schmiedebergs Arch Pharmacol; 1994 Oct; 350(4):434-9. PubMed ID: 7845481
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  • 22. CYP2D6 genotype determination in the Danish population.
    Brøsen K, Nielsen PN, Brusgaard K, Gram LF, Skjødt K.
    Eur J Clin Pharmacol; 1994 Oct; 47(3):221-5. PubMed ID: 7867674
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  • 23. Debrisoquine polymorphism: novel CYP2D6 gene Bam HI restriction fragment length polymorphism in the Ngawbé Guaymí Indian of Panama.
    Petersen DD, Kong AN, Jorge LF, Nebert DW, Arias TD.
    Pharmacogenetics; 1991 Dec; 1(3):136-42. PubMed ID: 1688244
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  • 29. Molecular genetic analysis of the cytochrome P450-debrisoquine hydroxylase locus and association with cancer susceptibility.
    Smith CA, Moss JE, Gough AC, Spurr NK, Wolf CR.
    Environ Health Perspect; 1992 Nov; 98():107-12. PubMed ID: 1486838
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  • 31. CYP2D6 genes and risk of liver cancer.
    Agúndez JA, Ledesma MC, Benítez J, Ladero JM, Rodríguez-Lescure A, Díaz-Rubio E, Díaz-Rubio M.
    Lancet; 1995 Apr 01; 345(8953):830-1. PubMed ID: 7898230
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  • 32. The human cytochrome P450 CYP3 locus: assignment to chromosome 7q22-qter.
    Spurr NK, Gough AC, Stevenson K, Wolf CR.
    Hum Genet; 1989 Jan 01; 81(2):171-4. PubMed ID: 2563251
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  • 36. A new CYP2D6 allele with a nine base insertion in exon 9 in a Japanese population associated with poor metabolizer phenotype.
    Yokoi T, Kosaka Y, Chida M, Chiba K, Nakamura H, Ishizaki T, Kinoshita M, Sato K, Gonzalez FJ, Kamataki T.
    Pharmacogenetics; 1996 Oct 01; 6(5):395-401. PubMed ID: 8946471
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  • 38. Mutant debrisoquine hydroxylation genes in Parkinson's disease.
    Armstrong M, Daly AK, Cholerton S, Bateman DN, Idle JR.
    Lancet; 1992 Apr 25; 339(8800):1017-8. PubMed ID: 1349052
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