Genetic variation in the cholesterol transporter NPC1L1, ischaemic vascular disease, and gallstone disease.
第一作者:
Bo Kobberø,Lauridsen
第一单位:
Department of Clinical Biochemistry, Rigshospitalet, Copenhagen University Hospitals and Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 9, Copenhagen, Denmark.
作者:
主题词
ATP结合匣式转运子(ATP-Binding Cassette Transporters);老年人(Aged);抗胆固醇血症药(Anticholesteremic Agents);胆固醇, LDL(Cholesterol, LDL);药物疗法, 联合(Drug Therapy, Combination);女(雌)性(Female);胆石(Gallstones);遗传变异(Genetic Variation);基因型(Genotype);人类(Humans);羟甲基戊二酰基CoA还原酶抑制剂(Hydroxymethylglutaryl-CoA Reductase Inhibitors);高胆固醇血症(Hypercholesterolemia);缺血(Ischemia);脂类代谢(Lipid Metabolism);男(雄)性(Male);膜蛋白质类(Membrane Proteins);膜转运蛋白质类(Membrane Transport Proteins);孟德尔随机化分析(Mendelian Randomization Analysis);中年人(Middle Aged);心肌梗死(Myocardial Infarction);危险因素(Risk Factors);卒中(Stroke)
DOI
10.1093/eurheartj/ehv108
PMID
25841872
发布时间
2022-03-18
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European heart journal
1601-8页
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