Associated Papers
Harnessing the paradoxical phenotypes of APOE ɛ2 and APOE ɛ4 to identify genetic modifiers in Alzheimer's disease.
Kim YW et al.
Alzheimer's & Dementia : the Journal of the Alzheimer's Association, 2021
33576571 (PubMed )
Supplement: ALZ-17-831-s002.xlsx › Table_S4
PRKAG3 polymorphisms associated with sporadic Wolff-Parkinson-White syndrome among a Taiwanese population.
Weng KP et al.
Journal of the Chinese Medical Association : Jcma, 2016
Association study of AMP-activated protein kinase subunit genes in polycystic ovary syndrome.
Sproul K et al.
European Journal of Endocrinology, 2009
Role of AMP-activated protein kinase gamma 3 genetic variability in glucose and lipid metabolism in non-diabetic whites.
Weyrich P et al.
Diabetologia, 2007
Gain-of-function R225W mutation in human AMPKgamma(3) causing increased glycogen and decreased triglyceride in skeletal muscle.
Costford SR et al.
Plos One, 2007
Mutation analysis of AMP-activated protein kinase subunits in inherited cardiomyopathies: implications for kinase function and disease pathogenesis.
Oliveira SM et al.
Journal of Molecular and Cellular Cardiology, 2003
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