177 related articles for article (PubMed ID: 15976322)
1. 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]
2. 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]
3. Contribution of chromosome 1q21-q23 to familial combined hyperlipidemia in Mexican families.
Huertas-Vázquez A; del Rincón JP; Canizales-Quinteros S; Riba L; Vega-Hernández G; Ramírez-Jiménez S; Aurón-Gómez M; Gómez-Pérez FJ; Aguilar-Salinas CA; Tusié-Luna MT
Ann Hum Genet; 2004 Sep; 68(Pt 5):419-27. PubMed ID: 15469419
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
8. Quantitative trait loci for apolipoprotein B, cholesterol, and triglycerides in familial combined hyperlipidemia pedigrees.
Cantor RM; de Bruin T; Kono N; Napier S; van Nas A; Allayee H; Lusis AJ
Arterioscler Thromb Vasc Biol; 2004 Oct; 24(10):1935-41. PubMed ID: 15308552
[TBL] [Abstract][Full Text] [Related]
9. Familial combined hyperlipidemia: upstream transcription factor 1 and beyond.
Lee JC; Lusis AJ; Pajukanta P
Curr Opin Lipidol; 2006 Apr; 17(2):101-9. PubMed ID: 16531745
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Low-density lipoprotein particle size loci in familial combined hyperlipidemia: evidence for multiple loci from a genome scan.
Badzioch MD; Igo RP; Gagnon F; Brunzell JD; Krauss RM; Motulsky AG; Wijsman EM; Jarvik GP
Arterioscler Thromb Vasc Biol; 2004 Oct; 24(10):1942-50. PubMed ID: 15331429
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II.
Putt W; Palmen J; Nicaud V; Tregouet DA; Tahri-Daizadeh N; Flavell DM; Humphries SE; Talmud PJ;
Hum Mol Genet; 2004 Aug; 13(15):1587-97. PubMed ID: 15175273
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Familial combined hyperlipidaemia linked to the apolipoprotein AI-CII-AIV gene cluster on chromosome 11q23-q24.
Wojciechowski AP; Farrall M; Cullen P; Wilson TM; Bayliss JD; Farren B; Griffin BA; Caslake MJ; Packard CJ; Shepherd J
Nature; 1991 Jan; 349(6305):161-4. PubMed ID: 1670899
[TBL] [Abstract][Full Text] [Related]
16. Confirmed locus on chromosome 11p and candidate loci on 6q and 8p for the triglyceride and cholesterol traits of combined hyperlipidemia.
Naoumova RP; Bonney SA; Eichenbaum-Voline S; Patel HN; Jones B; Jones EL; Amey J; Colilla S; Neuwirth CK; Allotey R; Seed M; Betteridge DJ; Galton DJ; Cox NJ; Bell GI; Scott J; Shoulders CC
Arterioscler Thromb Vasc Biol; 2003 Nov; 23(11):2070-7. PubMed ID: 14500288
[TBL] [Abstract][Full Text] [Related]
17. Genetic variants in adipose triglyceride lipase influence lipid levels in familial combined hyperlipidemia.
Nanni L; Quagliarini F; Megiorni F; Montali A; Minicocci I; Campagna F; Pizzuti A; Arca M
Atherosclerosis; 2010 Nov; 213(1):206-11. PubMed ID: 20832801
[TBL] [Abstract][Full Text] [Related]
18. Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23.
Pajukanta P; Nuotio I; Terwilliger JD; Porkka KV; Ylitalo K; Pihlajamäki J; Suomalainen AJ; Syvänen AC; Lehtimäki T; Viikari JS; Laakso M; Taskinen MR; Ehnholm C; Peltonen L
Nat Genet; 1998 Apr; 18(4):369-73. PubMed ID: 9537421
[TBL] [Abstract][Full Text] [Related]
19. Genetic dissection of familial combined hyperlipidemia.
Eurlings PM; van der Kallen CJ; Geurts JM; van Greevenbroek MM; de Bruin TW
Mol Genet Metab; 2001; 74(1-2):98-104. PubMed ID: 11592807
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
