Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Death and UCP2[original query] |
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Association of a common polymorphism in the promoter of UCP2 with susceptibility to multiple sclerosis. Journal of molecular medicine (Berlin, Germany) 2005 Oct 83 (10): 806-11. Vogler Susanne, Goedde René, Miterski Bianca, Gold Ralf, Kroner Antje, Koczan Dirk, Zettl Uwe-Klaus, Rieckmann Peter, Epplen Joerg T, Ibrahim Saleh |
The common -866G>A variant in the promoter of UCP2 is associated with decreased risk of coronary artery disease in type 2 diabetic men. Diabetes 2008 Apr 57 (4): 1063-8. Cheurfa Nadir, Dubois-Laforgue Danièle, Ferrarezi Daniela A F, Reis André F, Brenner Guilherme M, Bouché Clara, Le Feuvre Claude, Fumeron Frédéric, Timsit José, Marre Michel, Velho Gilber |
Interaction between the UCP2 -866 G>A polymorphism, diabetes, and beta-blocker use among patients with acute coronary syndromes. Pharmacogenetics and genomics 2010 Apr 20 (4): 231-8. Beitelshees Amber L, Finck Brian N, Leone Teresa C, Cresci Sharon, Wu Jun, Province Michael A, Fabbrini Elisa, Kirk Erik, Zineh Issam, Klein Samuel, Spertus John A, Kelly Daniel |
Genetic variants in eleven telomere-associated genes and the risk of incident cardio/cerebrovascular disease: The Women's Genome Health Study. Clinica chimica acta; international journal of clinical chemistry 2011 Jan 412 (1-2): 199-202. Zee Robert Y L, Ridker Paul M, Chasman Daniel |
Association of genetic variants of ghrelin, leptin and UCP2 with malnutrition inflammation syndrome and survival in end-stage renal disease patients. Genes & nutrition 2013 Nov 8 (6): 611-21. Sharma Richa, Agrawal Suraksha, Saxena Anita, Pandey Manmohan, Sharma R |
Association between UCP2 A55V polymorphism and risk of cardiovascular events in patients with multi-vessel coronary arterial disease. BMC medical genetics 2013 14 (1): 40. Gioli-Pereira Luciana, Santos Paulo Cjl, Sugaya Luisa S, Ferreira Noely E, Krieger José Eduardo, Pereira Alexandre C, Hueb Whady |
Association of insertion-deletions polymorphisms with colorectal cancer risk and clinical features. World journal of gastroenterology 2017 Oct 23 (37): 6854-6867. Marques Diego, Ferreira-Costa Layse Raynara, Ferreira-Costa Lorenna Larissa, Correa Romualdo da Silva, Borges Aline Maciel Pinheiro, Ito Fernanda Ribeiro, Ramos Carlos Cesar de Oliveira, Bortolin Raul Hernandes, Luchessi André Ducati, Ribeiro-Dos-Santos Ândrea, Santos Sidney, Silbiger Vivian Noguei |
Uncoupling Protein 2 as genetic risk factor for systemic lupus erythematosus: association with malondialdehyde levels and intima media thickness. Minerva cardioangiologica 2020 6 68 (6): 609-618. Gambino Caterina M, Accardi Giulia, Aiello Anna, Caruso Calogero, Carru Ciriaco, Gioia Bruno G, Guggino Giuliana, Rizzo Sergio, Zinellu Angelo, Ciaccio Marcello, Candore Giuseppi |
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- Page last updated:May 06, 2024
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