BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 16680034)

  • 21. The involvement of upstream stimulatory factor 1 in Dutch patients with familial combined hyperlipidemia.
    van der Vleuten GM; Isaacs A; Hijmans A; van Duijn CM; Stalenhoef AF; de Graaf J
    J Lipid Res; 2007 Jan; 48(1):193-200. PubMed ID: 17065663
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. High frequency of a retinoid X receptor gamma gene variant in familial combined hyperlipidemia that associates with atherogenic dyslipidemia.
    Nohara A; Kawashiri MA; Claudel T; Mizuno M; Tsuchida M; Takata M; Katsuda S; Miwa K; Inazu A; Kuipers F; Kobayashi J; Koizumi J; Yamagishi M; Mabuchi H
    Arterioscler Thromb Vasc Biol; 2007 Apr; 27(4):923-8. PubMed ID: 17272748
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels.
    Pajukanta P; Terwilliger JD; Perola M; Hiekkalinna T; Nuotio I; Ellonen P; Parkkonen M; Hartiala J; Ylitalo K; Pihlajamäki J; Porkka K; Laakso M; Viikari J; Ehnholm C; Taskinen MR; Peltonen L
    Am J Hum Genet; 1999 May; 64(5):1453-63. PubMed ID: 10205279
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Secondary disorders of lipid metabolism, metabolic syndrome and familial combined hyperlipidemia].
    Steinmetz A; Schäfer JR
    Wien Med Wochenschr; 1994; 144(12-13):299-307. PubMed ID: 8650933
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Disorder of lipid metabolism in visceral fat syndrome--relation to familial combined hyperlipidemia].
    Ishigami M; Nakamura T; Matsuzawa Y
    Nihon Rinsho; 2002 May; 60(5):868-74. PubMed ID: 12029987
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Upstream transcription factor 1 influences plasma lipid and metabolic traits in mice.
    Wu S; Mar-Heyming R; Dugum EZ; Kolaitis NA; Qi H; Pajukanta P; Castellani LW; Lusis AJ; Drake TA
    Hum Mol Genet; 2010 Feb; 19(4):597-608. PubMed ID: 19995791
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q.
    Pajukanta P; Allayee H; Krass KL; Kuraishy A; Soro A; Lilja HE; Mar R; Taskinen MR; Nuotio I; Laakso M; Rotter JI; de Bruin TW; Cantor RM; Lusis AJ; Peltonen L
    Am J Hum Genet; 2003 Apr; 72(4):903-17. PubMed ID: 12638083
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Relationship between familial combined hyperlipidemia and insulin resistance.
    Jackuliaková D; Vaverková H; Karásek D
    Vnitr Lek; 2008 Nov; 54(11):1045-53. PubMed ID: 19069677
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Whole-genome maps of USF1 and USF2 binding and histone H3 acetylation reveal new aspects of promoter structure and candidate genes for common human disorders.
    Rada-Iglesias A; Ameur A; Kapranov P; Enroth S; Komorowski J; Gingeras TR; Wadelius C
    Genome Res; 2008 Mar; 18(3):380-92. PubMed ID: 18230803
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prediction of genetic risk for dyslipidemia.
    Yamada Y; Matsuo H; Warita S; Watanabe S; Kato K; Oguri M; Yokoi K; Metoki N; Yoshida H; Satoh K; Ichihara S; Aoyagi Y; Yasunaga A; Park H; Tanaka M; Nozawa Y
    Genomics; 2007 Nov; 90(5):551-8. PubMed ID: 17919884
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel mutation in USF1 gene is associated with familial combined hyperlipidemia.
    Taghizadeh E; Mirzaei F; Jalilian N; Ghayour Mobarhan M; Ferns GA; Pasdar A
    IUBMB Life; 2020 Apr; 72(4):616-623. PubMed ID: 31725952
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Familial combined hyperlipidemia; solution on the horizon?].
    Porkka K; Taskinen MR
    Duodecim; 1995; 111(18):1755-62. PubMed ID: 9340268
    [No Abstract]   [Full Text] [Related]  

  • 39. 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]  

  • 40. Combined hyperlipidemia: familial but not (usually) monogenic.
    Brahm AJ; Hegele RA
    Curr Opin Lipidol; 2016 Apr; 27(2):131-40. PubMed ID: 26709473
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.