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Journal Abstract Search

79 related items for PubMed ID: 7980640

  • 1. pNAT and CYP2D6 gene polymorphism in epileptic patients.
    Borlak JT, Harsany V, Schneble H, Haegele KD.
    Biochem Pharmacol; 1994 Nov 01; 48(9):1717-20. PubMed ID: 7980640
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  • 2. Mutant genes of cytochrome P-450IID6, glutathione S-transferase class Mu, and arylamine N-acetyltransferase in lung cancer patients.
    Roots I, Brockmöller J, Drakoulis N, Loddenkemper R.
    Clin Investig; 1992 Nov 01; 70(3-4):307-19. PubMed ID: 1355678
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  • 3. Debrisoquine hydroxylation phenotype, acetylation phenotype, and ABO blood groups as genetic host factors of lung cancer risk.
    Roots I, Drakoulis N, Ploch M, Heinemeyer G, Loddenkemper R, Minks T, Nitz M, Otte F, Koch M.
    Klin Wochenschr; 1988 Nov 01; 66 Suppl 11():87-97. PubMed ID: 2846954
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  • 5. Concordance of P450 2D6 (debrisoquine hydroxylase) phenotype and genotype: inability of dextromethorphan metabolic ratio to discriminate reliably heterozygous and homozygous extensive metabolizers.
    Evans WE, Relling MV.
    Pharmacogenetics; 1991 Dec 01; 1(3):143-8. PubMed ID: 1688245
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  • 8. Frequent distribution of ultrarapid metabolizers of debrisoquine in an ethiopian population carrying duplicated and multiduplicated functional CYP2D6 alleles.
    Aklillu E, Persson I, Bertilsson L, Johansson I, Rodrigues F, Ingelman-Sundberg M.
    J Pharmacol Exp Ther; 1996 Jul 01; 278(1):441-6. PubMed ID: 8764380
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  • 10. CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy.
    Planté-Bordeneuve V, Bandmann O, Wenning G, Quinn NP, Daniel SE, Harding AE.
    Mov Disord; 1995 May 01; 10(3):277-8. PubMed ID: 7651442
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  • 11. Debrisoquine hydroxylase gene polymorphism in meningioma.
    Wundrack I, Meese E, Müllenbach R, Blin N.
    Acta Neuropathol; 1994 May 01; 88(5):472-4. PubMed ID: 7847077
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  • 12. Genetic polymorphisms of cytochromes P450: CYP2C9, CYP2C19, and CYP2D6 in Croatian population.
    Bozina N, Granić P, Lalić Z, Tramisak I, Lovrić M, Stavljenić-Rukavina A.
    Croat Med J; 2003 Aug 01; 44(4):425-8. PubMed ID: 12950145
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  • 13. N-acetyltransferase polymorphism. Comparison of phenotype and genotype in humans.
    Hickman D, Sim E.
    Biochem Pharmacol; 1991 Aug 08; 42(5):1007-14. PubMed ID: 1872889
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  • 17. 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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