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] Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder
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[PMID 20967855] A genetic variation located in the promoter of the uPAR (CD87) gene is associated with the vascular complications of systemic sclerosis
[PMID 21761413] Genetic polymorphism of the plasminogen activator inhibitor-1 is associated with an increased risk of endometrial cancer
[PMID 19552680] Common hemostasis and inflammation gene variants and venous thrombosis in older adults from the Cardiovascular Health Study.
[PMID 19878584] PLAUR polymorphisms and lung function in UK smokers.
[PMID 20518747] Association of putative functional variants in the PLAU gene and the PLAUR gene with myocardial infarction.