Associated Papers
Association of Polymorphisms of Glutamate Cysteine Ligase Genes GCLC C-129 T and GCLM C-588 T with Risk of Polycystic Ovary Syndrome in Chinese Women.
Yang C et al.
Reproductive Sciences (thousand Oaks, Calif.), 2022
Association of SOD2 A16V and PON2 S311C polymorphisms with polycystic ovary syndrome in Chinese women.
Liu Q et al.
Journal of Endocrinological Investigation, 2019
Association of GPx1 P198L and CAT C-262T Genetic Variations With Polycystic Ovary Syndrome in Chinese Women.
Sun Y et al.
Frontiers in Endocrinology, 2019
Lactonase activity and status of paraoxonase 1 in Chinese women with polycystic ovarian syndrome.
Zhang Y et al.
European Journal of Endocrinology, 2015
[Association between gene polymorphism of CD40 gene and coronary artery lesion in Kawasaki disease].
Cheng SC et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics, 2014
Genetic determinants of on-aspirin platelet reactivity: focus on the influence of PEAR1.
Würtz M et al.
Plos One, 2014
Association between lipoprotein-associated phospholipase A2 gene polymorphism and coronary artery disease in the Chinese Han population.
Li L et al.
Annals of Human Genetics, 2011
Identification of the G994T polymorphism in exon 9 of plasma platelet-activating factor acetylhydrolase gene as a risk factor for polycystic ovary syndrome.
Fan P et al.
Human Reproduction (oxford, England), 2010
Candidate gene association studies in abdominal aortic aneurysm disease: a review and meta-analysis.
Thompson AR et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery, 2008
Recent advances in genetic analysis of multiple sclerosis: genetic associations and therapeutic implications.
Niino M et al.
Expert Review of Neurotherapeutics, 2007
Comprehensive evaluation of genetic and environmental factors influencing the plasma lipoprotein-associated phospholipase A2 activity in a Japanese population.
Zhang SY et al.
Hypertension Research : Official Journal of the Japanese Society of Hypertension, 2007
A single nucleotide polymorphism in the plasma PAF acetylhydrolase gene and risk of atherosclerosis in Japanese patients with peripheral artery occlusive disease.
Unno N et al.
The Journal of Surgical Research, 2006
Association of platelet-activating factor acetylhydrolase gene polymorphism with premature coronary artery disease in Turkish patients.
Sekuri C et al.
Anadolu Kardiyoloji Dergisi : Akd = the Anatolian Journal of Cardiology, 2006
Platelet-activating factor acetylhydrolase gene polymorphism and its activity in Japanese patients with multiple sclerosis.
Osoegawa M et al.
Journal of Neuroimmunology, 2004
Association of gene polymorphisms with coronary artery disease in individuals with or without nonfamilial hypercholesterolemia.
Shimokata K et al.
Atherosclerosis, 2004
The PON1 M55L gene polymorphism is associated with reduced HDL-associated PAF-AH activity.
Kakafika AI et al.
Journal of Lipid Research, 2003
Fenofibrate induces HDL-associated PAF-AH but attenuates enzyme activity associated with apoB-containing lipoproteins.
Tsimihodimos V et al.
Journal of Lipid Research, 2003
Association of plasma PAF acetylhydrolase gene polymorphism with IMT of carotid arteries in Japanese type 2 diabetic patients.
Yamamoto I et al.
Diabetes Research and Clinical Practice, 2003
Prediction of the risk of myocardial infarction from polymorphisms in candidate genes.
Yamada Y et al.
The New England Journal of Medicine, 2002
Single nucleotide polymorphism (G994-->T) in the plasma platelet-activating factor-acetylhydrolase gene is associated with graft patency of femoropopliteal bypass.
Unno N et al.
Surgery, 2002
N-linked glycosylation of macrophage-derived PAF-AH is a major determinant of enzyme association with plasma HDL.
Tselepis AD et al.
Journal of Lipid Research, 2001
Plasma platelet-activating factor acetylhydrolase deficiency is associated with atherosclerotic occlusive disease in japan.
Unno N et al.
Journal of Vascular Surgery, 2000
Platelet-activating factor acetylhydrolase gene mutation in Japanese children with Escherichia coli O157-associated hemolytic uremic syndrome.
Xu H et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation, 2000
The Ile198Thr and Ala379Val variants of plasmatic PAF-acetylhydrolase impair catalytical activities and are associated with atopy and asthma.
Kruse S et al.
American Journal of Human Genetics, 2000
Role of platelet-activating factor acetylhydrolase gene mutation in Japanese childhood IgA nephropathy.
Tanaka R et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation, 1999
Platelet-activating factor acetylhydrolase gene mutation in Japanese nephrotic children.
Xu H et al.
Kidney International, 1998
Identification of the G994--> T missense in exon 9 of the plasma platelet-activating factor acetylhydrolase gene as an independent risk factor for coronary artery disease in Japanese men.
Yamada Y et al.
Metabolism: Clinical and Experimental, 1998