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Items: 8


Inherited disorders of bilirubin clearance.

Memon N, Weinberger BI, Hegyi T, Aleksunes LM.

Pediatr Res. 2016 Mar;79(3):378-86. doi: 10.1038/pr.2015.247. Epub 2015 Nov 23. Review.


PharmGKB summary: very important pharmacogene information for UGT1A1.

Barbarino JM, Haidar CE, Klein TE, Altman RB.

Pharmacogenet Genomics. 2014 Mar;24(3):177-83. doi: 10.1097/FPC.0000000000000024. Review. No abstract available.


UGT1A1 is a major locus influencing bilirubin levels in African Americans.

Chen G, Ramos E, Adeyemo A, Shriner D, Zhou J, Doumatey AP, Huang H, Erdos MR, Gerry NP, Herbert A, Bentley AR, Xu H, Charles BA, Christman MF, Rotimi CN.

Eur J Hum Genet. 2012 Apr;20(4):463-8. doi: 10.1038/ejhg.2011.206. Epub 2011 Nov 16.


Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.

Sanna S, Busonero F, Maschio A, McArdle PF, Usala G, Dei M, Lai S, Mulas A, Piras MG, Perseu L, Masala M, Marongiu M, Crisponi L, Naitza S, Galanello R, Abecasis GR, Shuldiner AR, Schlessinger D, Cao A, Uda M.

Hum Mol Genet. 2009 Jul 15;18(14):2711-8. doi: 10.1093/hmg/ddp203. Epub 2009 May 6.


Genome-wide linkage of cotinine pharmacokinetics suggests candidate regions on chromosomes 9 and 11.

He Y, Bergen AW, Hops H, Andrews JA, Tildesley E, Lessov-Schlaggar CN, Webster C, Benowitz N, Swan GE.

Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 5;150B(4):554-9. doi: 10.1002/ajmg.b.30859.


Pharmacogenomics in colorectal cancer: the first step for individualized-therapy.

Bandrés E, Zárate R, Ramirez N, Abajo A, Bitarte N, Garíia-Foncillas J.

World J Gastroenterol. 2007 Nov 28;13(44):5888-901. Review.


Role of cysteine residues in the function of human UDP glucuronosyltransferase isoform 1A1 (UGT1A1).

Ghosh SS, Lu Y, Lee SW, Wang X, Guha C, Roy-Chowdhury J, Roy-Chowdhury N.

Biochem J. 2005 Dec 15;392(Pt 3):685-92.


Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility.

de Jong MM, Nolte IM, te Meerman GJ, van der Graaf WT, Oosterwijk JC, Kleibeuker JH, Schaapveld M, de Vries EG.

J Med Genet. 2002 Apr;39(4):225-42. Review.

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