BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 16936202)

  • 1. Variation within the gene encoding the upstream stimulatory factor 1 does not influence susceptibility to type 2 diabetes in samples from populations with replicated evidence of linkage to chromosome 1q.
    Zeggini E; Damcott CM; Hanson RL; Karim MA; Rayner NW; Groves CJ; Baier LJ; Hale TC; Hattersley AT; Hitman GA; Hunt SE; Knowler WC; Mitchell BD; Ng MC; O'Connell JR; Pollin TI; Vaxillaire M; Walker M; Wang X; Whittaker P; Xiang K; Jia W; Chan JC; Froguel P; Deloukas P; Shuldiner AR; Elbein SC; McCarthy MI;
    Diabetes; 2006 Sep; 55(9):2541-8. PubMed ID: 16936202
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 48(10):2018-24. PubMed ID: 16132950
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 5(9):e1000642. PubMed ID: 19750004
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Upstream transcription factor 1 (USF1) in risk of type 2 diabetes: association study in 2000 Dutch Caucasians.
    Meex SJ; van Vliet-Ostaptchouk JV; van der Kallen CJ; van Greevenbroek MM; Schalkwijk CG; Feskens EJ; Blaak EE; Wijmenga C; Hofker MH; Stehouwer CD; de Bruin TW
    Mol Genet Metab; 2008 Jul; 94(3):352-5. PubMed ID: 18445538
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Common polymorphisms in the USF1 gene are not associated with type 2 diabetes in French Caucasians.
    Gibson F; Hercberg S; Froguel P
    Diabetes; 2005 Oct; 54(10):3040-2. PubMed ID: 16186412
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).
    Pajukanta P; Lilja HE; Sinsheimer JS; Cantor RM; Lusis AJ; Gentile M; Duan XJ; Soro-Paavonen A; Naukkarinen J; Saarela J; Laakso M; Ehnholm C; Taskinen MR; Peltonen L
    Nat Genet; 2004 Apr; 36(4):371-6. PubMed ID: 14991056
    [TBL] [Abstract][Full Text] [Related]  

  • 8. USF1 contributes to high serum lipid levels in Dutch FCHL families and U.S. whites with coronary artery disease.
    Lee JC; Weissglas-Volkov D; Kyttälä M; Sinsheimer JS; Jokiaho A; de Bruin TW; Lusis AJ; Brennan ML; van Greevenbroek MM; van der Kallen CJ; Hazen SL; Pajukanta P
    Arterioscler Thromb Vasc Biol; 2007 Oct; 27(10):2222-7. PubMed ID: 17673701
    [TBL] [Abstract][Full Text] [Related]  

  • 9. USF1 gene variants, cardiovascular risk, and mortality in European Americans: analysis of two US cohort studies.
    Reiner AP; Carlson CS; Jenny NS; Durda JP; Siscovick DS; Nickerson DA; Tracy RP
    Arterioscler Thromb Vasc Biol; 2007 Dec; 27(12):2736-42. PubMed ID: 17885212
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Unraveling the complex genetics of familial combined hyperlipidemia.
    Suviolahti E; Lilja HE; Pajukanta P
    Ann Med; 2006; 38(5):337-51. PubMed ID: 16938803
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Variants in ARHGEF11, a candidate gene for the linkage to type 2 diabetes on chromosome 1q, are nominally associated with insulin resistance and type 2 diabetes in Pima Indians.
    Ma L; Hanson RL; Que LN; Cali AM; Fu M; Mack JL; Infante AM; Kobes S; ; Bogardus C; Shuldiner AR; Baier LJ
    Diabetes; 2007 May; 56(5):1454-9. PubMed ID: 17287471
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Linkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1q.
    Prokopenko I; Zeggini E; Hanson RL; Mitchell BD; Rayner NW; Akan P; Baier L; Das SK; Elliott KS; Fu M; Frayling TM; Groves CJ; Gwilliam R; Scott LJ; Voight BF; Hattersley AT; Hu C; Morris AD; Ng M; Palmer CN; Tello-Ruiz M; Vaxillaire M; Wang CR; Stein L; Chan J; Jia W; Froguel P; Elbein SC; Deloukas P; Bogardus C; Shuldiner AR; McCarthy MI;
    Diabetes; 2009 Jul; 58(7):1704-9. PubMed ID: 19389826
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 159(4):407-16. PubMed ID: 18593823
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 117(5):444-51. PubMed ID: 15959806
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Variants in the Ca V 2.3 (alpha 1E) subunit of voltage-activated Ca2+ channels are associated with insulin resistance and type 2 diabetes in Pima Indians.
    Muller YL; Hanson RL; Zimmerman C; Harper I; Sutherland J; Kobes S; ; Knowler WC; Bogardus C; Baier LJ
    Diabetes; 2007 Dec; 56(12):3089-94. PubMed ID: 17720895
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular analysis of KCNJ10 on 1q as a candidate gene for Type 2 diabetes in Pima Indians.
    Farook VS; Hanson RL; Wolford JK; Bogardus C; Prochazka M
    Diabetes; 2002 Nov; 51(11):3342-6. PubMed ID: 12401729
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Polymorphisms in the glucokinase-associated, dual-specificity phosphatase 12 (DUSP12) gene under chromosome 1q21 linkage peak are associated with type 2 diabetes.
    Das SK; Chu WS; Hale TC; Wang X; Craig RL; Wang H; Shuldiner AR; Froguel P; Deloukas P; McCarthy MI; Zeggini E; Hasstedt SJ; Elbein SC
    Diabetes; 2006 Sep; 55(9):2631-9. PubMed ID: 16936214
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetics of familial combined hyperlipidemia.
    Naukkarinen J; Ehnholm C; Peltonen L
    Curr Opin Lipidol; 2006 Jun; 17(3):285-90. PubMed ID: 16680034
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.