HuGE Literature Finder
Records 1-23
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Evaluation of single nucleotide polymorphisms in 6 candidate genes and carotid intima-media thickness in community-dwelling residents.
PloS one 2020 15 (3): e0230715. Wu Fang-Yang, Li Chia-Ing, Liao Li-Na, Liu Chiu-Shong, Lin Wen-Yuan, Lin Chih-Hsueh, Yang Chuan-Wei, Li Tsai-Chung, Lin Cheng-Chi |
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Paraoxonase 1 (PON1) promoter (-107T/C) and coding region (192Q/R and 55L/M) genetic variations in pseudoexfoliation syndrome and pseudoexfoliative glaucoma risk.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 2019 Jul . Can Demirdögen Birsen, Koçan Akçin Canan, Göksoy Ezgi, Yakar Gizem, Öztepe Tugçe, Demirkaya-Budak Sinem, Oflaz Sin |
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Paraoxonase 1 gene polymorphisms and enzyme activities in coronary artery disease and its relationship to serum lipids and glycemia.
Archivos de cardiologia de Mexico 2016 Sep . Fridman Osvaldo, Gariglio Luis, Riviere Stephanie, Porcile Rafael, Fuchs Alicia, Potenzoni Migu |
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Sex-Specific Genetic Variants are Associated With Coronary Endothelial Dysfunction.
Journal of the American Heart Association 2016 5 (4): . Yoshino Satoshi, Cilluffo Rebecca, Prasad Megha, Best Patricia J M, Atkinson Elizabeth J, Aoki Tatsuo, Cunningham Julie M, de Andrade Mariza, Lerman Lilach O, Lerman Am |
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Effect of Extended-Release Niacin on High-Density Lipoprotein (HDL) Functionality, Lipoprotein Metabolism, and Mediators of Vascular Inflammation in Statin-Treated Patients.
Journal of the American Heart Association 2015 4 (9): . Yadav Rahul, Liu Yifen, Kwok See, Hama Salam, France Michael, Eatough Ruth, Pemberton Phil, Schofield Jonathan, Siahmansur Tarza J, Malik Rayaz, Ammori Basil A, Issa Basil, Younis Naveed, Donn Rachelle, Stevens Adam, Durrington Paul, Soran Handre |
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The association of PON1 192 Q/R polymorphism and the risk of female infertility.
Cellular and molecular biology (Noisy-le-Grand, France) 2015 61 (2): 74-7. Mashayekhi F, Behrouzi S, Yousefi M, Salehi |
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Synergistic effects of BuChE non-UU phenotype and paraoxonase (PON1) 55 M allele on the risk of systemic lupus erythematosus: influence on lipid and lipoprotein metabolism and oxidative stress, preliminary report.
Lupus 2014 Mar 23 (3): 263-72. Bahrehmand F, Vaisi-Raygani A, Rahimi Z, Ahmadi R, Kiani A, Tavilani H, Vaisi-Raygani H, Pourmotabbed |
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Genetic polymorphisms of paraoxonase1 192 and glutathione peroxidase1 197 enzymes in familial Mediterranean fever.
Genetics and molecular research : GMR 2014 13 (2): 3292-300. Öktem F, An?l H, Sütcü R, Kuybulu A |
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Paraoxonase-1 status in patients with hereditary hemochromatosis.
Journal of lipid research 2013 May 54 (5): 1484-92. Martinelli Nicola, García-Heredia Anabel, Roca Helena, Aranda Núria, Arija Victoria, Mackness Bharti, Mackness Michael, Busti Fabiana, Aragonès Gerard, Pedro-Botet Juan, Pedica Federica, Cataldo Ivana, Marsillach Judit, Joven Jorge, Girelli Domenico, Camps Jor |
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PON1 gene polymorphisms and plasma PON1 activities in Takayasu's arteritis disease.
Immunology letters 2013 Apr 152 (1): 77-82. Huesca-Gómez Claudia, Soto María Elena, Castrejón-Téllez Vicente, Pérez-Méndez Oscar, Gamboa Ricar |
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Novel common and rare genetic determinants of paraoxonase activity: FTO, SERPINA12, and ITGAL.
Journal of lipid research 2012 Nov . Kim DS, Burt AA, Crosslin DR, Robertson PD, Ranchalis JE, Boyko EJ, Nickerson DA, Furlong CE, Jarvik GP |
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Predictive role of multilocus genetic polymorphisms in cardiovascular disease and inflammation-related genes on chronic kidney disease in Type 2 diabetes--an 8-year prospective cohort analysis of 1163 patients.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2012 Jan 27 (1): 190-6. Wang Ying, Luk Andrea O Y, Ma Ronald C W, So Wing-Yee, Tam Claudia H T, Ng Maggie C Y, Yang Xilin, Lam Vincent, Tong Peter C Y, Chan Juliana C |
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Main determinants of PON1 activity in hemodialysis patients.
American journal of nephrology 2012 36 (4): 317-23. Ribeiro Sandra, do Sameiro Faria Maria, Mascarenhas-Melo Filipa, Freitas Isabel, Mendonça Maria Isabel, Nascimento Henrique, Rocha-Pereira Petronila, Miranda Vasco, Mendonça Denisa, Quintanilha Alexandre, Belo Luís, Costa Elísio, Reis Flávio, Santos-Silva Ali |
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C-reactive protein levels are associated with paraoxonase polymorphism L55M in patients undergoing cardiac SPECT imaging.
Scandinavian journal of clinical and laboratory investigation 2011 May 71 (3): 179-84. Acampa Wanda, Di Taranto Maria D, Morgante Alberto, Salvatore Barbara, Evangelista Laura, Ricci Francesca, Costanzo Pierluigi, de Sisto Emma, Filardi Pasquale P, Petretta Mario, Fortunato Giuliana, Cuocolo Alber |
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Association of anti-oxidized LDL and candidate genes with severity of coronary stenosis in the Women's Ischemia Syndrome Evaluation study.
Journal of lipid research 2011 Apr 52 (4): 801-7. Chen Qi, Reis Steven E, Kammerer Candace, Craig Wendy, McNamara Dennis M, Holubkov Richard, Sharaf Barry L, Sopko George, Pauly Daniel F, Merz C Noel Bairey, Kamboh M Ilyas, |
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Paraoxonase 1 polymorphism Q192R affects the pro-inflammatory cytokine TNF-alpha in healthy males.
BMC research notes 2011 4 (1): 141. Lüersen Kai, Schmelzer Constance, Boesch-Saadatmandi Christine, Kohl Christine, Rimbach Gerald, Döring Fra |
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The role of chronic inflammation and Leu55Met PON1 polymorphism in the pathogenesis of polycystic ovary syndrome.
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2010 Sep 26 (9): 673-83. Lenarcik Agnieszka, Bidzi?ska-Speichert Bozena, Tworowska-Bardzi?ska Urszu |
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PON1 is a longevity gene: results of a meta-analysis.
Ageing research reviews 2009 Oct 8 (4): 277-84. Lescai Francesco, Marchegiani Francesca, Franceschi Claud |
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Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.
Clinica chimica acta; international journal of clinical chemistry 2009 Apr 402 (1-2): 189-92. Zee Robert Y L, Bubes Vadim, Shrivastava Sanjay, Ridker Paul M, Glynn Robert |
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Genetic variation in the paraoxonase-3 (PON3) gene is associated with serum PON1 activity.
Annals of human genetics 2008 Jan 72 (Pt 1): 72-81. Sanghera Dharambir K, Manzi Susan, Minster Ryan L, Shaw Penny, Kao Amy, Bontempo Franklin, Kamboh M Ily |
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Glyoxalase I A111E, paraoxonase 1 Q192R and L55M polymorphisms: susceptibility factors of multiple sclerosis?
Multiple sclerosis (Houndmills, Basingstoke, England) 2007 May 13 (4): 446-53. Sidoti A, Antognelli C, Rinaldi C, D'Angelo R, Dattola V, Girlanda P, Talesa V, Amato |
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The genetics of human longevity.
Annals of the New York Academy of Sciences 2006 May 1067 (): 252-63. Capri Miriam, Salvioli Stefano, Sevini Federica, Valensin Silvana, Celani Laura, Monti Daniela, Pawelec Graham, De Benedictis Giovanna, Gonos Efstathios S, Franceschi Claud |
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Indications that paraoxonase-1 contributes to plasma high density lipoprotein levels in familial hypercholesterolemia.
Journal of lipid research 2005 Mar 46 (3): 445-51. van Himbergen Thomas M, Roest Mark, de Graaf Jacqueline, Jansen Eugène H J M, Hattori Hiroaki, Kastelein John J P, Voorbij Hieronymus A M, Stalenhoef Anton F H, van Tits Lambertus J |
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- Page last updated:Feb 24, 2021
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