Association of Genetic Variants of MTHFR, ENPP1, and ADIPOQ with Myocardial Infarction in Egyptian Patients
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[1] H. Benrahma,et al. Association of the C677T polymorphism in the human methylenetetrahydrofolate reductase (MTHFR) gene with the genetic predisposition for type 2 diabetes mellitus in a Moroccan population. , 2012, Genetic testing and molecular biomarkers.
[2] H. Schinzel,et al. Superficial thrombophlebitis in varicose vein disease: the particular role of methylenetetrahydrofolate reductase , 2011, Phlebology.
[3] Q. Hasan,et al. Association of methylene tetrahydrofolate reductase C677T genotype with type 2 diabetes mellitus patients with and without renal complications. , 2011, Genetic testing and molecular biomarkers.
[4] Shumin Deng,et al. Association of adiponectin gene polymorphisms with the risk of ischemic stroke in a Chinese Han population , 2011, Molecular Biology Reports.
[5] L. Salazar,et al. Frequency of prothrombotic risk factors in patients with deep venous thrombosis and controls: their implications for thrombophilia screening in Chilean subjects. , 2010, Genetic testing and molecular biomarkers.
[6] Xue-jian Hu,et al. C-reactive protein, vitamin B12 and C677T polymorphism of N-5,10-methylenetetrahydrofolate reductase gene are related to insulin resistance and risk factors for metabolic syndrome in Chinese population. , 2010, Clinical and investigative medicine. Medecine clinique et experimentale.
[7] M. Marre,et al. Adiponectin Multimers and ADIPOQ T45G in Coronary Artery Disease in Caribbean Type 2 Diabetic Subjects of African Descent , 2010, Obesity.
[8] In-kyu Lee,et al. Impact of ENPP1 and MMP3 gene polymorphisms on aortic calcification in patients with type 2 diabetes in a Korean population. , 2010, Diabetes research and clinical practice.
[9] C. Leitão,et al. [ENPP1 K121Q polymorphism and ischemic heart disease in diabetic patients]. , 2010, Arquivos brasileiros de cardiologia.
[10] M. Abid,et al. Relationship between genetic polymorphisms of angiotensin-converting enzyme and methylenetetrahydrofolate reductase as risk factors for type 2 diabetes in Tunisian patients. , 2010, Clinical biochemistry.
[11] F. Perticone,et al. ENPP1 Q121 Variant, Increased Pulse Pressure and Reduced Insulin Signaling, and Nitric Oxide Synthase Activity in Endothelial Cells , 2009, Arteriosclerosis, thrombosis, and vascular biology.
[12] A. Minenna,et al. Association of the Q121 variant of ENPP1 gene with decreased kidney function among patients with type 2 diabetes. , 2009, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[13] F. Pellegrini,et al. Role of the ENPP1 K121Q Polymorphism in Glucose Homeostasis , 2008, Diabetes.
[14] T. Mueller,et al. The K121Q polymorphism of ENPP1 and peripheral arterial disease , 2008, Heart and Vessels.
[15] E. Kang,et al. Adiponectin gene polymorphism 45T>G is associated with carotid artery plaques in patients with type 2 diabetes mellitus. , 2008, Metabolism: clinical and experimental.
[16] Xiaochun Kang,et al. ASSOCIATIONS BETWEEN 45T/G POLYMORPHISM OF THE ADIPONECTIN GENE AND PLASMA ADIPONECTIN LEVELS WITH TYPE 2 DIABETES , 2007, Clinical and experimental pharmacology & physiology.
[17] M. Yamagishi,et al. Association of genetic variation of the adiponectin gene with body fat distribution and carotid atherosclerosis in Japanese obese subjects. , 2007, Journal of atherosclerosis and thrombosis.
[18] T. Hansen,et al. Studies of the relationship between the ENPP1 K121Q polymorphism and type 2 diabetes, insulin resistance and obesity in 7,333 Danish white subjects , 2006, Diabetologia.
[19] A. Doria,et al. The K121Q polymorphism of the ENPP1/PC-1 gene is associated with insulin resistance/atherogenic phenotypes, including earlier onset of type 2 diabetes and myocardial infarction. , 2005, Diabetes.
[20] R. Clarke,et al. Homocysteine, MTHFR and risk of venous thrombosis: a meta‐analysis of published epidemiological studies , 2005, Journal of thrombosis and haemostasis : JTH.
[21] C. Dina,et al. The adiponectin gene SNP+45 is associated with coronary artery disease in Type 2 (non‐insulin‐dependent) diabetes mellitus , 2004, Diabetic medicine : a journal of the British Diabetic Association.
[22] S. Hadjadj,et al. Adiponectin gene polymorphisms and adiponectin levels are independently associated with the development of hyperglycemia during a 3-year period: the epidemiologic data on the insulin resistance syndrome prospective study. , 2004, Diabetes.
[23] R. Terkeltaub,et al. Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification , 2003, Nature Genetics.
[24] H. Markus,et al. Early Carotid Atherosclerosis and Family History of Vascular Disease: Specific Effects on Arterial Sites Have Implications for Genetic Studies , 2003, Arteriosclerosis, thrombosis, and vascular biology.
[25] D. Wald,et al. Homocysteine and cardiovascular disease: evidence on causality from a meta-analysis , 2002, BMJ : British Medical Journal.
[26] P. Cugini,et al. Higher blood pressure load (baric impact) in normotensives with endothelial dysfunction: a paraphysiological status of "pre-hypertension". , 2002, La Clinica terapeutica.
[27] C. Bogardus,et al. Plasma adiponectin concentration is associated with skeletal muscle insulin receptor tyrosine phosphorylation, and low plasma concentration precedes a decrease in whole-body insulin sensitivity in humans. , 2002, Diabetes.
[28] M. Pfeffer,et al. Cardiovascular Risk Assessment Using Pulse Pressure in the First National Health and Nutrition Examination Survey (NHANES I) , 2001, Hypertension.
[29] A. Pizzuti,et al. The Q allele variant (GLN121) of membrane glycoprotein PC-1 interacts with the insulin receptor and inhibits insulin signaling more effectively than the common K allele variant (LYS121). , 2001, Diabetes.
[30] S. Kihara,et al. Adipocyte-Derived Plasma Protein, Adiponectin, Suppresses Lipid Accumulation and Class A Scavenger Receptor Expression in Human Monocyte-Derived Macrophages , 2001, Circulation.
[31] Bruce M. Spiegelman,et al. Obesity and the Regulation of Energy Balance , 2001, Cell.
[32] H. Lodish,et al. Proteolytic cleavage product of 30-kDa adipocyte complement-related protein increases fatty acid oxidation in muscle and causes weight loss in mice. , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[33] H. Mangge,et al. Insulin is an independent correlate of plasma homocysteine levels in obese children and adolescents. , 2000, Diabetes care.
[34] G Scarlato,et al. A polymorphism (K121Q) of the human glycoprotein PC-1 gene coding region is strongly associated with insulin resistance. , 1999, Diabetes.
[35] D. Wilcken,et al. Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: the result of a meta-analysis. , 1998, Circulation.
[36] G. Andrews,et al. Burden of disease , 1998, British Journal of Psychiatry.
[37] S. Vollset,et al. Plasma homocysteine levels and mortality in patients with coronary artery disease. , 1997, The New England journal of medicine.
[38] W. Willett,et al. Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians. , 1996, Circulation.
[39] R. Rozen. Annotation Molecular genetics of methylenetetrahydrofolate reductase deficiency , 1996, Journal of Inherited Metabolic Disease.
[40] I. Pabinger,et al. Thrombotic risk in hereditary antithrombin III, protein C, or protein S deficiency. A cooperative, retrospective study. Gesellschaft fur Thrombose- und Hamostaseforschung (GTH) Study Group on Natural Inhibitors. , 1996, Arteriosclerosis, thrombosis, and vascular biology.
[41] M. Shichiri,et al. Insulinlike Growth Factor‐I Induces Hypertrophy With Enhanced Expression of Muscle Specific Genes in Cultured Rat Cardiomyocytes , 1993, Circulation.
[42] M. Norusis,et al. Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease. , 1991, American journal of human genetics.
[43] W. Garvey,et al. Adiponectin multimeric complexes and the metabolic syndrome trait cluster. , 2006, Diabetes.
[44] Fu-Mei Chung,et al. ENPP1 K121Q polymorphism is not related to type 2 diabetes mellitus, features of metabolic syndrome, and diabetic cardiovascular complications in a Chinese population. , 2006, The review of diabetic studies : RDS.
[45] I. Goldfine,et al. Membrane glycoprotein PC-1 inhibition of insulin receptor function occurs via direct interaction with the receptor alpha-subunit. , 2000, Diabetes.
[46] B. Maddux,et al. Membrane Glycoprotein PC1 Inhibition of Insulin Receptor Function Occurs Via Direct Interaction With the Receptor-Subunit , 1999 .
[47] R. Rozen. Molecular genetics of methylenetetrahydrofolate reductase deficiency. , 1996, Journal of inherited metabolic disease.
[48] R. Matthews,et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase , 1995, Nature Genetics.
[49] Diabetes mellitus. Report of a WHO Study Group. , 1985, World Health Organization technical report series.
[50] Patrick Murphy,et al. What Is Statistics , 2014 .