Single copy of variant CYP2A6 alleles does not confer susceptibility to liver dysfunction in patients treated with coumarinBURIAN, M; FREUDENSTEIN, J; TEGTMEIER, M et al.International journal of clinical pharmacology and therapeutics. 2003, Vol 41, Num 4, pp 141-147, issn 0946-1965, 7 p.Article

Possible increased risk for Alzheimer's disease associated with neprilysin geneCLARIMON, J; MUNOZ, F. J; BOADA, M et al.Journal of neural transmission. 2003, Vol 110, Num 6, pp 651-657, issn 0300-9564, 7 p.Article

Genetic polymorphism of drug-metabolizing enzymes and styrene-induced DNA damageBUSCHINI, Annamaria; DE PALMA, Giuseppe; POLI, Paola et al.Environmental and molecular mutagenesis (Print). 2003, Vol 41, Num 4, pp 243-252, issn 0893-6692, 10 p.Article

Study on the distribution of the MSY2 polymorphism in 9 Chinese populationsXIANGNING MENG; YALI XUE; DONGLIN SUN et al.Anthropologischer Anzeiger. 2005, Vol 63, Num 1, pp 23-27, issn 0003-5548, 5 p.Article

CYP2S1 gene polymorphisms in a Korean populationJANG, Yin-Jin; CHA, Eun-Young; KIM, Woo-Young et al.Therapeutic drug monitoring. 2007, Vol 29, Num 3, pp 292-298, issn 0163-4356, 7 p.Article

Limitation of cigarette consumption by CYP2A6*4, *7 and *9 polymorphismsMINEMATSU, N; NAKAMURA, H; FURUUCHI, M et al.The European respiratory journal. 2006, Vol 27, Num 2, pp 289-292, issn 0903-1936, 4 p.Article

Genotyping for polymorphic drug metabolizing enzymes from paraffin-embedded and immunohistochemically stained tumor samplesRAE, James M; CORDERO, Kevin E; SCHEYS, Joshua O et al.Pharmacogenetics (London). 2003, Vol 13, Num 8, pp 501-507, issn 0960-314X, 7 p.Article

Association of genetic polymorphisms in CYP19A1 and blood levels of sex hormones among postmenopausal Chinese womenHUI CAI; XIAO OU SHU; EGAN, Kathleen M et al.Pharmacogenetics and genomics (Print). 2008, Vol 18, Num 8, pp 657-664, issn 1744-6872, 8 p.Article

Short Communication : Characterization of a κ-Casein Genetic Variant in the Chinese Yak, Bos grunniensBAI, W. L; YIN, R. H; ZHAO, S. J et al.Journal of dairy science. 2008, Vol 91, Num 3, pp 1204-1208, issn 0022-0302, 5 p.Article

Interaction between β2 adrenergic receptor polymorphisms determines the extent of isoproterenol-induced vasodilatation ex vivoKHALAILA, Jawad M; ELAMI, Amir; CARACO, Yoseph et al.Pharmacogenetics and genomics (Print). 2007, Vol 17, Num 10, pp 803-811, issn 1744-6872, 9 p.Article

Characterization of hepatobiliary transport systems of a novel α4β1/α4β7 dual antagonist, TR-14035TSUDA-TSUKIMOTO, Minoru; MAEDA, Tomoji; IWANAGA, Takashi et al.Pharmaceutical research. 2006, Vol 23, Num 11, pp 2646-2656, issn 0724-8741, 11 p.Article

Oxidative enzymopathies and vascular diseaseLEOPOLD, Jane A; LOSCALZO, Joseph.Arteriosclerosis, thrombosis, and vascular biology. 2005, Vol 25, Num 7, pp 1332-1340, issn 1079-5642, 9 p.Article

Angiotensinogen promoter haplotypes are associated with blood pressure in untreated hypertensives. Editorial commentBRAND-HERRMANN, Stefan-Martin; KÖPKE, Karla; REICHENBERGER, Florian et al.Journal of hypertension. 2004, Vol 22, Num 7, pp 1255-1258, issn 0263-6352, 13 p.Article

Common polymorphisms of Fibulin-5 and the risk of abdominal aortic aneurysm developmentBADGER, Stephen A; SOONG, Chee V; O'DONNELL, Mark E et al.Vascular medicine (London). 2010, Vol 15, Num 2, pp 113-117, issn 1358-863X, 5 p.Article

The association of Fcγ receptor IIIb genetic polymorphism and susceptibility to periodontitis in Taiwanese individualsHO, Ya-Ping; YANG, Yi-Hsin; HO, Kun-Yen et al.Journal of clinical periodontology. 2010, Vol 37, Num 2, pp 145-151, issn 0303-6979, 7 p.Article

Association of IL-1B genetic polymorphisms with an increased risk of opioid and alcohol dependenceLIANG LIU; HUTCHINSON, Mark R; WHITE, Jason M et al.Pharmacogenetics and genomics (Print). 2009, Vol 19, Num 11, pp 869-876, issn 1744-6872, 8 p.Article

The effect of SLCΟ1B1*15 on the disposition of pravastatin and pitavastatin is substrate dependent : the contribution of transporting activity changes by SLCΟ1B1 15JIAN WEI DENG; SONG, Im-Sook; HO JUNG SHIN et al.Pharmacogenetics and genomics (Print). 2008, Vol 18, Num 5, pp 424-433, issn 1744-6872, 10 p.Article

Analysis of Single Nucleotide Polymorphisms in the Melanocortin-4 Receptor Promoter in Infantile SpasmsLIU, Z.-L; HE, B; FANG, F et al.Neuropediatrics. 2007, Vol 38, Num 6, pp 304-309, issn 0174-304X, 6 p.Article

Association study of the CNR1 gene exon 3 alternative promoter region polymorphisms and substance dependenceHERMAN, Aryeh I; KRANZLER, Henry R; CUBELLS, Joseph F et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2006, Vol 141, Num 5, pp 499-503, issn 1552-4841, 5 p.Article

Three haplotypes associated with CYP2A6 phenotypes in CaucasiansHABERL, Michael; ANWALD, Birgit; KLEIN, Kathrin et al.Pharmacogenetics and genomics (Print). 2005, Vol 15, Num 9, pp 609-624, issn 1744-6872, 16 p.Article

Sources of polycyclic aromatic hydrocarbon exposure in non-occupationally exposed KoreansYANG, Mihi; KIM, Soyeon; LEE, Eunil et al.Environmental and molecular mutagenesis (Print). 2003, Vol 42, Num 4, pp 250-257, issn 0893-6692, 8 p.Article

The genetic basis of the endocannabinoid system and drug addiction in humansLOPEZ-MORENO, Jose Antonio; ECHEVERRY-ALZATE, Victor; BÜHLER, Kora-Mareen et al.Journal of psychopharmacology (Oxford). 2012, Vol 26, Num 1, pp 133-143, issn 0269-8811, 11 p.Article

A Functional Variant Provided Further Evidence for the Association of ARVCF With SchizophreniaMAS, Sergi; BERNARDO, Miquel; GASSO, Patricia et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 5, pp 1052-1059, issn 1552-4841, 8 p.Article

CYP2C9 polymorphism: prevalence in healthy and warfarin-treated Malay and Chinese in MalaysiaNGOW, H. A; WAN KHAIRINA, W. M. N; TEH, L. K et al.Singapore medical journal. 2009, Vol 50, Num 5, pp 490-493, issn 0037-5675, 4 p.Article

APOE genotype makes a small contribution to warfarin dose requirementsSCONCE, Elizabeth A; DALY, Ann K; KHAN, Tayyaba I et al.Pharmacogenetics and genomics (Print). 2006, Vol 16, Num 8, pp 609-611, issn 1744-6872, 3 p.Article