Associated Papers
Polymorphisms and disease: hotspots of inactivation in methyltransferases.
Rutherford K et al.
Trends in Biochemical Sciences, 2010
Human phenylethanolamine N-methyltransferase genetic polymorphisms and exercise-induced epinephrine release.
Ji Y et al.
Physiological Genomics, 2008
Resequencing PNMT in European hypertensive and normotensive individuals: no common susceptibilily variants for hypertension and purifying selection on intron 1.
Kepp K et al.
Bmc Medical Genetics, 2007
Human phenylethanolamine N-methyltransferase pharmacogenomics: gene re-sequencing and functional genomics.
Ji Y et al.
Journal of Neurochemistry, 2005
Insights into S-adenosyl-l-methionine (SAM)-dependent methyltransferase related diseases and genetic polymorphisms.
Li J et al.
Mutation Research. Reviews in Mutation Research, 0
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