Contribution of deletion in angiotensin-converting enzyme but not A1166C angiotensin II type-1 receptor gene polymorphisms to clinical outcomes in atherothrombotic disease.
作者:
主题词
老年人(Aged);主动脉疾病(Aortic Diseases);动脉闭塞性疾病(Arterial Occlusive Diseases);DNA突变分析(DNA Mutational Analysis);女(雌)性(Female);遗传关联研究(Genetic Association Studies);人类(Humans);INDEL突变(INDEL Mutation);Kaplan-Meiers评估(Kaplan-Meier Estimate);男(雄)性(Male);中年人(Middle Aged);多元分析(Multivariate Analysis);肽基二肽酶A(Peptidyl-Dipeptidase A);外周动脉疾病(Peripheral Arterial Disease);多态性, 单核苷酸(Polymorphism, Single Nucleotide);比例危险度模型(Proportional Hazards Models);前瞻性研究(Prospective Studies);受体, 血管紧张素, 1型(Receptor, Angiotensin, Type 1);血管疾病(Vascular Diseases);血管移植术(Vascular Grafting)
DOI
10.1016/j.arcmed.2011.05.003
PMID
21722816
发布时间
2022-03-11
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