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Journal Abstract Search

142 related items for PubMed ID: 17885212

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  • 3. Risk alleles of USF1 gene predict cardiovascular disease of women in two prospective studies.
    Komulainen K, Alanne M, Auro K, Kilpikari R, Pajukanta P, Saarela J, Ellonen P, Salminen K, Kulathinal S, Kuulasmaa K, Silander K, Salomaa V, Perola M, Peltonen L.
    PLoS Genet; 2006 May; 2(5):e69. PubMed ID: 16699592
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  • 6. Common coding variants of the HNF1A gene are associated with multiple cardiovascular risk phenotypes in community-based samples of younger and older European-American adults: the Coronary Artery Risk Development in Young Adults Study and The Cardiovascular Health Study.
    Reiner AP, Gross MD, Carlson CS, Bielinski SJ, Lange LA, Fornage M, Jenny NS, Walston J, Tracy RP, Williams OD, Jacobs DR, Nickerson DA.
    Circ Cardiovasc Genet; 2009 Jun; 2(3):244-54. PubMed ID: 20031592
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  • 7. Potential role of upstream stimulatory factor 1 gene variant in familial combined hyperlipidemia and related disorders.
    Auer S, Hahne P, Soyal SM, Felder T, Miller K, Paulmichl M, Krempler F, Oberkofler H, Patsch W.
    Arterioscler Thromb Vasc Biol; 2012 Jun; 32(6):1535-44. PubMed ID: 22460558
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  • 9. Association of USF1 and APOA5 polymorphisms with familial combined hyperlipidemia in an Italian population.
    Di Taranto MD, Staiano A, D'Agostino MN, D'Angelo A, Bloise E, Morgante A, Marotta G, Gentile M, Rubba P, Fortunato G.
    Mol Cell Probes; 2015 Feb; 29(1):19-24. PubMed ID: 25308402
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  • 10. Familial combined hyperlipidemia in Mexicans: association with upstream transcription factor 1 and linkage on chromosome 16q24.1.
    Huertas-Vazquez A, Aguilar-Salinas C, Lusis AJ, Cantor RM, Canizales-Quinteros S, Lee JC, Mariana-Nuñez L, Riba-Ramirez RM, Jokiaho A, Tusie-Luna T, Pajukanta P.
    Arterioscler Thromb Vasc Biol; 2005 Sep; 25(9):1985-91. PubMed ID: 15976322
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  • 11. Genetic risk assessment for cardiovascular disease in Azoreans (Portugal): a general population-based study.
    Correia M, Branco CC, Bruffaerts N, Balagué A, Mota-Vieira L.
    Gene; 2013 Dec 10; 532(1):132-9. PubMed ID: 24042129
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  • 14. A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia.
    Plaisier CL, Horvath S, Huertas-Vazquez A, Cruz-Bautista I, Herrera MF, Tusie-Luna T, Aguilar-Salinas C, Pajukanta P.
    PLoS Genet; 2009 Sep 10; 5(9):e1000642. PubMed ID: 19750004
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  • 15. Genetic variants in the USF1 gene are associated with low-density lipoprotein cholesterol levels and incident type 2 diabetes mellitus in women: results from the MONICA/KORA Augsburg case-cohort study, 1984-2002.
    Holzapfel C, Baumert J, Grallert H, Müller AM, Thorand B, Khuseyinova N, Herder C, Meisinger C, Hauner H, Wichmann HE, Koenig W, Illig T, Klopp N.
    Eur J Endocrinol; 2008 Oct 10; 159(4):407-16. PubMed ID: 18593823
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  • 16. Association analysis of allelic variants of USF1 in coronary atherosclerosis.
    Kristiansson K, Ilveskoski E, Lehtimäki T, Peltonen L, Perola M, Karhunen PJ.
    Arterioscler Thromb Vasc Biol; 2008 May 10; 28(5):983-9. PubMed ID: 18276913
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  • 18. Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides.
    Coon H, Xin Y, Hopkins PN, Cawthon RM, Hasstedt SJ, Hunt SC.
    Hum Genet; 2005 Sep 10; 117(5):444-51. PubMed ID: 15959806
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  • 19. Plasma Levels of Soluble Interleukin-2 Receptor α: Associations With Clinical Cardiovascular Events and Genome-Wide Association Scan.
    Durda P, Sabourin J, Lange EM, Nalls MA, Mychaleckyj JC, Jenny NS, Li J, Walston J, Harris TB, Psaty BM, Valdar W, Liu Y, Cushman M, Reiner AP, Tracy RP, Lange LA.
    Arterioscler Thromb Vasc Biol; 2015 Oct 10; 35(10):2246-53. PubMed ID: 26293465
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  • 20. The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population.
    Ng MC, Miyake K, So WY, Poon EW, Lam VK, Li JK, Cox NJ, Bell GI, Chan JC.
    Diabetologia; 2005 Oct 10; 48(10):2018-24. PubMed ID: 16132950
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