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Results: 1 to 20 of 84

1.

CYP1A2 is more variable than previously thought: a genomic biography of the gene behind the human drug-metabolizing enzyme.

Browning SL, Tarekegn A, Bekele E, Bradman N, Thomas MG.

Pharmacogenet Genomics. 2010 Nov;20(11):647-64. doi: 10.1097/FPC.0b013e32833e90eb.

PMID:
20881513
[PubMed - indexed for MEDLINE]
2.

Comparison of linkage disequilibrium patterns and haplotype structure of eight single nucleotide polymorphisms across the CYP1A2 gene between the Korean, and other populations registered in the International HapMap database.

Woo SW, Kang TS, Park HJ, Lee JE, Roh J.

J Clin Pharm Ther. 2009 Aug;34(4):429-36. doi: 10.1111/j.1365-2710.2008.01011.x.

PMID:
19583676
[PubMed - indexed for MEDLINE]
3.

Pharmacogenetics of CYP1A2, novel polymorphisms and haplotypes in three distinct Asian populations.

Lim JS, Singh O, Ramasamy RD, Ramasamy S, Subramanian K, Lee EJ, Chowbay B.

Drug Metab Pharmacokinet. 2010;25(6):616-23. Epub 2010 Oct 1.

PMID:
20930417
[PubMed - indexed for MEDLINE]
Free Article
4.

DNA sequence variation in a 3.7-kb noncoding sequence 5' of the CYP1A2 gene: implications for human population history and natural selection.

Wooding SP, Watkins WS, Bamshad MJ, Dunn DM, Weiss RB, Jorde LB.

Am J Hum Genet. 2002 Sep;71(3):528-42. Epub 2002 Aug 9.

PMID:
12181774
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Genetic polymorphism of CYP1A2 in Ethiopians affecting induction and expression: characterization of novel haplotypes with single-nucleotide polymorphisms in intron 1.

Aklillu E, Carrillo JA, Makonnen E, Hellman K, Pitarque M, Bertilsson L, Ingelman-Sundberg M.

Mol Pharmacol. 2003 Sep;64(3):659-69.

PMID:
12920202
[PubMed - indexed for MEDLINE]
Free Article
6.

Single nucleotide polymorphisms and haplotypes of CYP1A2 in a Japanese population.

Soyama A, Saito Y, Hanioka N, Maekawa K, Komamura K, Kamakura S, Kitakaze M, Tomoike H, Ueno K, Goto Y, Kimura H, Katoh M, Sugai K, Saitoh O, Kawai M, Ohnuma T, Ohtsuki T, Suzuki C, Minami N, Kamatani N, Ozawa S, Sawada J.

Drug Metab Pharmacokinet. 2005 Feb;20(1):24-33. Erratum in: Drug Metab Pharmacokinet. 2005 Apr;20(2):152.

PMID:
15770072
[PubMed - indexed for MEDLINE]
Free Article
7.

Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool.

Pagani L, Kivisild T, Tarekegn A, Ekong R, Plaster C, Gallego Romero I, Ayub Q, Mehdi SQ, Thomas MG, Luiselli D, Bekele E, Bradman N, Balding DJ, Tyler-Smith C.

Am J Hum Genet. 2012 Jul 13;91(1):83-96. doi: 10.1016/j.ajhg.2012.05.015. Epub 2012 Jun 21.

PMID:
22726845
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Search for an association between the human CYP1A2 genotype and CYP1A2 metabolic phenotype.

Jiang Z, Dragin N, Jorge-Nebert LF, Martin MV, Guengerich FP, Aklillu E, Ingelman-Sundberg M, Hammons GJ, Lyn-Cook BD, Kadlubar FF, Saldana SN, Sorter M, Vinks AA, Nassr N, von Richter O, Jin L, Nebert DW.

Pharmacogenet Genomics. 2006 May;16(5):359-67.

PMID:
16609368
[PubMed - indexed for MEDLINE]
9.

Toward the evaluation of function in genetic variability: characterizing human SNP frequencies and establishing BAC-transgenic mice carrying the human CYP1A1_CYP1A2 locus.

Jiang Z, Dalton TP, Jin L, Wang B, Tsuneoka Y, Shertzer HG, Deka R, Nebert DW.

Hum Mutat. 2005 Feb;25(2):196-206.

PMID:
15643613
[PubMed - indexed for MEDLINE]
10.

Identification and functional significance of SNPs underlying conserved haplotype frameworks across ethnic populations.

Ouyang C, Krontiris TG.

Pharmacogenet Genomics. 2006 Sep;16(9):667-82.

PMID:
16906021
[PubMed - indexed for MEDLINE]
11.

A worldwide survey of haplotype variation and linkage disequilibrium in the human genome.

Conrad DF, Jakobsson M, Coop G, Wen X, Wall JD, Rosenberg NA, Pritchard JK.

Nat Genet. 2006 Nov;38(11):1251-60. Epub 2006 Oct 22.

PMID:
17057719
[PubMed - indexed for MEDLINE]
12.

Redefinition of the human kappa opioid receptor gene (OPRK1) structure and association of haplotypes with opiate addiction.

Yuferov V, Fussell D, LaForge KS, Nielsen DA, Gordon D, Ho A, Leal SM, Ott J, Kreek MJ.

Pharmacogenetics. 2004 Dec;14(12):793-804.

PMID:
15608558
[PubMed - indexed for MEDLINE]
13.

The structure of haplotype blocks in the human genome.

Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, Liu-Cordero SN, Rotimi C, Adeyemo A, Cooper R, Ward R, Lander ES, Daly MJ, Altshuler D.

Science. 2002 Jun 21;296(5576):2225-9. Epub 2002 May 23.

PMID:
12029063
[PubMed - indexed for MEDLINE]
Free Article
14.

Haplotype variation and linkage disequilibrium in 313 human genes.

Stephens JC, Schneider JA, Tanguay DA, Choi J, Acharya T, Stanley SE, Jiang R, Messer CJ, Chew A, Han JH, Duan J, Carr JL, Lee MS, Koshy B, Kumar AM, Zhang G, Newell WR, Windemuth A, Xu C, Kalbfleisch TS, Shaner SL, Arnold K, Schulz V, Drysdale CM, Nandabalan K, Judson RS, Ruano G, Vovis GF.

Science. 2001 Jul 20;293(5529):489-93. Epub 2001 Jul 12. Erratum in: Science 2001 Aug 10;293(5532):1048.

PMID:
11452081
[PubMed - indexed for MEDLINE]
Free Article
15.

Different genetic components in the Ethiopian population, identified by mtDNA and Y-chromosome polymorphisms.

Passarino G, Semino O, Quintana-Murci L, Excoffier L, Hammer M, Santachiara-Benerecetti AS.

Am J Hum Genet. 1998 Feb;62(2):420-34.

PMID:
9463310
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Mitochondrial pathogenic mutations are population-specific.

Breen MS, Kondrashov FA.

Biol Direct. 2010 Dec 31;5:68. doi: 10.1186/1745-6150-5-68.

PMID:
21194457
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Allelic variation and haplotype structure of the dopamine receptor gene DRD2 in nine Indian populations.

Bhaskar LV, Thangaraj K, Mulligan CJ, Rao AP, Pardhasaradhi G, Kumar KP, Shah AM, Sabeera B, Reddy AG, Singh L, Rao VR.

Genet Test. 2008 Mar;12(1):153-60. doi: 10.1089/gte.2007.0073.

PMID:
18373412
[PubMed - indexed for MEDLINE]
18.

The G-113A polymorphism in CYP1A2 affects the caffeine metabolic ratio in a Chinese population.

Chen X, Wang L, Zhi L, Zhou G, Wang H, Zhang X, Hao B, Zhu Y, Cheng Z, He F.

Clin Pharmacol Ther. 2005 Sep;78(3):249-59.

PMID:
16153396
[PubMed - indexed for MEDLINE]
19.

Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism.

Fullerton SM, Clark AG, Weiss KM, Nickerson DA, Taylor SL, Stengârd JH, Salomaa V, Vartiainen E, Perola M, Boerwinkle E, Sing CF.

Am J Hum Genet. 2000 Oct;67(4):881-900. Epub 2000 Sep 13.

PMID:
10986041
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Single nucleotide polymorphisms in bone turnover-related genes in Koreans: ethnic differences in linkage disequilibrium and haplotype.

Kim KS, Kim GS, Hwang JY, Lee HJ, Park MH, Kim KJ, Jung J, Cha HS, Shin HD, Kang JH, Park EK, Kim TH, Hong JM, Koh JM, Oh B, Kimm K, Kim SY, Lee JY.

BMC Med Genet. 2007 Nov 26;8:70.

PMID:
18036257
[PubMed - indexed for MEDLINE]
Free PMC Article

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