Associated Papers
Associations of genetic factors with vascular diabetes complications: an umbrella review.
Zhou X et al.
Journal of Global Health, 2025
Association between p22PHOX gene C242T polymorphism and hypertension in end-stage kidney disease patients.
Buraczynska M et al.
Journal of Human Hypertension, 2021
[Input of genetic analyses in the differential diagnosis of kidney cysts].
Ghuysen C et al.
Revue Medicale De Liege, 2019
Genetic susceptibility to delayed graft function following kidney transplantation: a systematic review of the literature.
Huart J et al.
Clinical Kidney Journal, 2018
Role of Donors and Recipients' Glutathione S-Transferase Gene Polymorphisms in Association of Oxidative Stress With Delayed Graft Function in Kidney Allograft Recipients.
Azmandian J et al.
Iranian Journal of Kidney Diseases, 2017
NADPH Oxidase-2 and Atherothrombosis: Insight From Chronic Granulomatous Disease.
Violi F et al.
Arteriosclerosis, Thrombosis, and Vascular Biology, 2017
Novel identified associations of RGS1 and RASGRP1 variants in IgA Nephropathy.
Zhou XJ et al.
Scientific Reports, 2016
CYBA encoding p22(phox), the cytochrome b558 alpha polypeptide: gene structure, expression, role and physiopathology.
Stasia MJ
Gene, 2016
p22phox C242T Single-Nucleotide Polymorphism Inhibits Inflammatory Oxidative Damage to Endothelial Cells and Vessels.
Meijles DN et al.
Circulation, 2016
NADPH oxidase p22phox C242T polymorphism and ischemic cerebrovascular disease: an updated meta-analysis.
Li P et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 2015
Investigation of association between donors' and recipients' NADPH oxidase p22(phox) C242T polymorphism and acute rejection, delayed graft function and blood pressure in renal allograft recipients.
Mandegary A et al.
Transplant Immunology, 2015
Additive effect of polymorphisms in the β2 -adrenoceptor and NADPH oxidase p22 phox genes contributes to the loss of estimated glomerular filtration rate in Chinese.
Wang T et al.
Clinical and Experimental Pharmacology & Physiology, 2014
Association of the C242T polymorphism in the NAD(P)H oxidase P22 phox gene with type 2 diabetes mellitus risk: a meta-analysis.
Sun Q et al.
Current Medical Research and Opinion, 2014
Association of the -262C/T polymorphism in the catalase gene promoter and the C242T polymorphism of the NADPH oxidase P22phox gene with essential arterial hypertension in patients with diabetes mellitus type 2.
Petrovič D
Clinical and Experimental Hypertension (new York, N.y. : 1993), 2014
Polymorphisms of C242T and A640G in CYBA gene and the risk of coronary artery disease: a meta-analysis.
Xu Q et al.
Plos One, 2014
C242T polymorphism of NADPH oxidase p22phox gene reduces the risk of coronary artery disease in a random sample of Egyptian population.
Hashad IM et al.
Molecular Biology Reports, 2014
Association of NADPH oxidase p22phox gene C242T, A640G and -930A/G polymorphisms with primary knee osteoarthritis in the Greek population.
Lepetsos P et al.
Molecular Biology Reports, 2013
Association between NADPH oxidase p22(phox) C242T polymorphism and ischemic cerebrovascular disease: a meta-analysis.
Li BH et al.
Plos One, 2013
Influence of the C242T polymorphism of the p22-phox gene (CYBA) on the interaction between urinary sodium excretion and blood pressure in an urban Brazilian population.
Schreiber R et al.
Plos One, 2013
Common mutations and polymorphisms predicting adverse cardiovascular events: current view.
Visvikis-Siest S et al.
Pharmacogenomics, 2012
NAD(P)H oxidase p22(phox) polymorphism and cardiovascular function in amateur runners.
Gallina S et al.
Acta Physiologica (oxford, England), 2012
Chemokine receptor 2-V64I and chemokine receptor 5-Delta32 polymorphisms and clinical risk factors of delayed graft function and acute rejection in kidney transplantation.
Azmandian J et al.
Iranian Journal of Kidney Diseases, 2012
Genetic susceptibility to atherosclerosis.
Kovacic S et al.
Stroke Research and Treatment, 2012
The C242T polymorphism of the p22-phox gene (CYBA) is associated with higher left ventricular mass in Brazilian hypertensive patients.
Schreiber R et al.
Bmc Medical Genetics, 2011
The CAREGENE study: genetic variants of the endothelium and aerobic power in patients with coronary artery disease.
Onkelinx S et al.
Acta Cardiologica, 2011
A polymorphism of NADPH oxidase p22 phox is associated with reduced susceptibility to acute rejection in renal allograft recipients.
Bhandary UV et al.
Transplant Immunology, 2011
Serotonin transporter gene polymorphism may be associated with functional dyspepsia in a Japanese population.
Toyoshima F et al.
Bmc Medical Genetics, 2011
First survey of the three gene polymorphisms (PON1 Q192R, eNOS E298D and eNOS C-786T) potentially associated with coronary artery spasm in African populations and comparison with worldwide data.
Fujihara J et al.
Cell Biochemistry and Function, 2011
Variant angina and coronary artery spasm: the clinical spectrum, pathophysiology, and management.
Kusama Y et al.
Journal of Nippon Medical School = Nippon Ika Daigaku Zasshi, 2011
Effects of six functional SNPs on the urinary 8-isoprostane level in a general Japanese population; Shimane COHRE Study.
Suyama Y et al.
Disease Markers, 2011
The effect of p22(phox) -930A/G, A640G and C242T polymorphisms of NADPH oxidase on peripheral and central pressures in healthy, normotensive individuals.
Xaplanteris P et al.
Hypertension Research : Official Journal of the Japanese Society of Hypertension, 2010
Genetic variants associated with neutrophil function in aggressive periodontitis and healthy controls.
Nibali L et al.
Journal of Periodontology, 2010
Influence of genetic polymorphisms in oxidative stress related genes and smoking on plasma MDA-LDL, soluble CD40 ligand, E-selectin and soluble ICAM1 levels in patients with coronary artery disease.
Ueno T et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 2009
Genetic variation of myeloperoxidase gene contributes to atopic asthma susceptibility: a preliminary association study in Russian population.
Polonikov AV et al.
The Journal of Asthma : Official Journal of the Association for the Care of Asthma, 2009
Haplotype analysis of the NADPH oxidase p22 phox gene in patients with bronchial asthma.
Izakovicova Holla L et al.
International Archives of Allergy and Immunology, 2009
Association of polymorphism of the p22PHOX component of NADPH oxidase in gastroduodenal diseases in Japan.
Tahara T et al.
Scandinavian Journal of Gastroenterology, 2009
The C242T polymorphism of the p22phox component of NAD(P)H oxidase and vascular risk. Two case-control studies and a meta-analysis.
Di Castelnuovo A et al.
Thrombosis and Haemostasis, 2008
Polymorphisms in the lymphotoxin alpha gene and the risk of ischemic stroke in the Japanese population. The Fukuoka Stroke Registry and the Hisayama Study.
Hagiwara N et al.
Cerebrovascular Diseases (basel, Switzerland), 2008
[Influence of polymorphism's of endothelial nitric oxide synthase gene and polymorphism of NADPH oxidase gene on development of complications of arterial hypertension].
Kuznetsova TIu et al.
Kardiologiia, 2008
The C242T polymorphism of the NAD(P)H oxidase p22phox subunit is associated with an enhanced risk for cerebrovascular disease at a young age.
Genius J et al.
Cerebrovascular Diseases (basel, Switzerland), 2008
NAD(P)H oxidase p22phox C242T polymorphism and ischemic stroke in Japan: the Fukuoka Stroke Registry and the Hisayama study.
Kuroda J et al.
European Journal of Neurology, 2007
The 242T variant of the CYBA gene polymorphism increases the risk of coronary artery disease associated with cigarette smoking and hypercholesterolemia.
Niemiec P et al.
Coronary Artery Disease, 2007
Association of gene polymorphism with genetic susceptibility to stroke in Asian populations: a meta-analysis.
Banerjee I et al.
Journal of Human Genetics, 2007
NADPH oxidase polymorphisms in cerebral small vessel disease.
Khan U et al.
Cerebrovascular Diseases (basel, Switzerland), 2007
NAD(P)H oxidase p22phox gene C242T polymorphism, nitric oxide production, salt sensitivity and cardiovascular risk factors in Hispanics.
Castejon AM et al.
Journal of Human Hypertension, 2006
Relationship between common functional polymorphisms of the p22phox gene (-930A > G and +242C > T) and nephropathy as a result of Type 2 diabetes in a Chinese population.
Lim SC et al.
Diabetic Medicine : a Journal of the British Diabetic Association, 2006
Hemorheologic profile in systemic sclerosis: role of NOS3 -786T > C and 894G >T polymorphisms in modulating both the hemorheologic parameters and the susceptibility to the disease.
Fatini C et al.
Arthritis and Rheumatism, 2006
C242T polymorphism in CYBA gene (p22phox) and risk of coronary artery disease in a population of Caucasian Italians.
Nasti S et al.
Disease Markers, 2006
Haplotype analysis of NAD(P)H oxidase p22 phox polymorphisms in end-stage renal disease.
Doi K et al.
Journal of Human Genetics, 2005
Lack of association of eNOS (G894T) and p22phox NADPH oxidase subunit (C242T) polymorphisms with systemic sclerosis in a cohort of French Caucasian patients.
Allanore Y et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2004