Associated Papers
Effect of donor GSTM3 rs7483 genetic variant on tacrolimus elimination in the early period after liver transplantation.
Zhang T et al.
Peerj, 2024
39465171 (PubMed )
Supplement: peerj-12-18360-s002.7z › drug-metabolizing_enzymes_and_transporter__DMET__microarray › markerlist.xlsx › markerlist.TXT
Pharmacogenetics of human sulfotransferases and impact of amino acid exchange on Phase II drug metabolism.
Isvoran A et al.
Drug Discovery Today, 2022
Fine Mapping of a GWAS-Derived Obesity Candidate Region on Chromosome 16p11.2.
Volckmar AL et al.
Plos One, 2015
A G613A missense in the Hutchinson's progeria lamin A/C gene causes a lone, autosomal dominant atrioventricular block.
Villa F et al.
Immunity & Ageing : I & A, 2014
25469153 (PubMed )
Supplement: 12979_2014_19_MOESM2_ESM.xls › Sheet1
Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes.
Christodoulou K et al.
Gut, 2013
22543157 (PubMed )
Supplement: gutjnl-2011-301833-s1.pdf
Genetic polymorphism in metabolism and host defense enzymes: implications for human health risk assessment.
Ginsberg G et al.
Critical Reviews in Toxicology, 2010
Inherited variation in carcinogen-metabolizing enzymes and risk of colorectal polyps.
Goode EL et al.
Carcinogenesis, 2007
Human cytosolic sulphotransferases: genetics, characteristics, toxicological aspects.
Glatt H et al.
Mutation Research, 2001
Select a paper to view details