72 related articles for article (PubMed ID: 20031629)
1. Functional variant disrupts insulin induction of USF1: mechanism for USF1-associated dyslipidemias.
Naukkarinen J; Nilsson E; Koistinen HA; Söderlund S; Lyssenko V; Vaag A; Poulsen P; Groop L; Taskinen MR; Peltonen L
Circ Cardiovasc Genet; 2009 Oct; 2(5):522-9. PubMed ID: 20031629
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. USF1 and dyslipidemias: converging evidence for a functional intronic variant.
Naukkarinen J; Gentile M; Soro-Paavonen A; Saarela J; Koistinen HA; Pajukanta P; Taskinen MR; Peltonen L
Hum Mol Genet; 2005 Sep; 14(17):2595-605. PubMed ID: 16076849
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. USF1 deficiency activates brown adipose tissue and improves cardiometabolic health.
Laurila PP; Soronen J; Kooijman S; Forsström S; Boon MR; Surakka I; Kaiharju E; Coomans CP; Van Den Berg SA; Autio A; Sarin AP; Kettunen J; Tikkanen E; Manninen T; Metso J; Silvennoinen R; Merikanto K; Ruuth M; Perttilä J; Mäkelä A; Isomi A; Tuomainen AM; Tikka A; Ramadan UA; Seppälä I; Lehtimäki T; Eriksson J; Havulinna A; Jula A; Karhunen PJ; Salomaa V; Perola M; Ehnholm C; Lee-Rueckert M; Van Eck M; Roivainen A; Taskinen MR; Peltonen L; Mervaala E; Jalanko A; Hohtola E; Olkkonen VM; Ripatti S; Kovanen PT; Rensen PC; Suomalainen A; Jauhiainen M
Sci Transl Med; 2016 Jan; 8(323):323ra13. PubMed ID: 26819196
[TBL] [Abstract][Full Text] [Related]
7. Associations between USF1 gene variants and cardiovascular risk factors in the Quebec Family Study.
Choquette AC; Bouchard L; Houde A; Bouchard C; Pérusse L; Vohl MC
Clin Genet; 2007 Mar; 71(3):245-53. PubMed ID: 17309647
[TBL] [Abstract][Full Text] [Related]
8. Genetic association and interaction analysis of USF1 and APOA5 on lipid levels and atherosclerosis.
Laurila PP; Naukkarinen J; Kristiansson K; Ripatti S; Kauttu T; Silander K; Salomaa V; Perola M; Karhunen PJ; Barter PJ; Ehnholm C; Peltonen L
Arterioscler Thromb Vasc Biol; 2010 Feb; 30(2):346-52. PubMed ID: 19910639
[TBL] [Abstract][Full Text] [Related]
9. Molecular characterization, expression patterns, and association analysis with carcass traits of porcine USF1 gene.
Wu H; Qiao M; Peng X; Wu J; Liu G; Sun H; Li L; Mei S
Appl Biochem Biotechnol; 2013 Jul; 170(6):1310-9. PubMed ID: 23666615
[TBL] [Abstract][Full Text] [Related]
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
[TBL] [Abstract][Full Text] [Related]
11. Upstream transcription factor 1 gene polymorphisms are associated with high antilipolytic insulin sensitivity and show gene-gene interactions.
Kantartzis K; Fritsche A; Machicao F; Stumvoll M; Machann J; Schick F; Häring HU; Stefan N
J Mol Med (Berl); 2007 Jan; 85(1):55-61. PubMed ID: 17016691
[TBL] [Abstract][Full Text] [Related]
12. Chronic ethanol-induced insulin resistance is associated with macrophage infiltration into adipose tissue and altered expression of adipocytokines.
Kang L; Sebastian BM; Pritchard MT; Pratt BT; Previs SF; Nagy LE
Alcohol Clin Exp Res; 2007 Sep; 31(9):1581-8. PubMed ID: 17624994
[TBL] [Abstract][Full Text] [Related]
13. A common polymorphism in the 5' region of the human protein c gene binds USF1.
Thain KR; Nakada TA; Boyd JH; Russell JA; Walley KR
Thromb Res; 2012 Sep; 130(3):451-7. PubMed ID: 22425321
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Multiple environmental and genetic factors influence skeletal muscle PGC-1alpha and PGC-1beta gene expression in twins.
Ling C; Poulsen P; Carlsson E; Ridderstråle M; Almgren P; Wojtaszewski J; Beck-Nielsen H; Groop L; Vaag A
J Clin Invest; 2004 Nov; 114(10):1518-26. PubMed ID: 15546003
[TBL] [Abstract][Full Text] [Related]
17. Cooperative activation of lipocalin-type prostaglandin D synthase gene expression by activator protein-2beta in proximal promoter and upstream stimulatory factor 1 within intron 4 in human brain-derived TE671 cells.
Fujimori K; Urade Y
Gene; 2007 Aug; 397(1-2):143-52. PubMed ID: 17574780
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Insulin stimulates interleukin-6 and tumor necrosis factor-alpha gene expression in human subcutaneous adipose tissue.
Krogh-Madsen R; Plomgaard P; Keller P; Keller C; Pedersen BK
Am J Physiol Endocrinol Metab; 2004 Feb; 286(2):E234-8. PubMed ID: 14532168
[TBL] [Abstract][Full Text] [Related]
20. The intron 6 G/T polymorphism of c-myb oncogene and the risk for coronary in-stent restenosis.
Gross CM; Krämer J; Pfeufer A; Dietz R; Gessner R; Praus M
Basic Res Cardiol; 2004 Jul; 99(4):309-14. PubMed ID: 15221349
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
