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Items: 1 to 20 of 109

1.

Heritability and genetic loci of fatty liver in familial combined hyperlipidemia.

Brouwers MC, Cantor RM, Kono N, Yoon JL, van der Kallen CJ, Bilderbeek-Beckers MA, van Greevenbroek MM, Lusis AJ, de Bruin TW.

J Lipid Res. 2006 Dec;47(12):2799-807. Epub 2006 Sep 13.

2.

Fatty liver is an integral feature of familial combined hyperlipidaemia: relationship with fat distribution and plasma lipids.

Brouwers MC, Bilderbeek-Beckers MA, Georgieva AM, van der Kallen CJ, van Greevenbroek MM, de Bruin TW.

Clin Sci (Lond). 2007 Jan;112(2):123-30.

PMID:
16958621
3.

Five-year follow-up of waist circumference, insulin and ALT levels in familial combined hyperlipidaemia.

Brouwers MC, van Greevenbroek MM, Vermeulen VM, van Lin JM, van der Kallen CJ, de Bruin TW.

Clin Sci (Lond). 2007 Nov;113(9):375-81.

PMID:
17564583
4.

Fatty liver--based identification of two distinct hypertriglyceridemic subgroups in familial combined hyperlipidemia.

Brouwers MC, van Greevenbroek MM, Bilderbeek-Beckers MA, Robertus-Teunissen MG, van der Kallen CJ, Stehouwer CD, de Bruin TW.

Metabolism. 2007 Oct;56(10):1311-7.

PMID:
17884438
5.

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. Epub 2004 Aug 12.

6.

Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart Study.

Coon H, Myers RH, Borecki IB, Arnett DK, Hunt SC, Province MA, Djousse L, Leppert MF.

Arterioscler Thromb Vasc Biol. 2000 Oct;20(10):2275-80.

7.

Variants in the PPARgamma gene affect fatty acid and glycerol metabolism in familial combined hyperlipidemia.

Eurlings PM, van der Kallen CJ, Vermeulen VM, de Bruin TW.

Mol Genet Metab. 2003 Nov;80(3):296-301.

PMID:
14680975
8.

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.

9.

A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.

Aouizerat BE, Allayee H, Cantor RM, Davis RC, Lanning CD, Wen PZ, Dallinga-Thie GM, de Bruin TW, Rotter JI, Lusis AJ.

Am J Hum Genet. 1999 Aug;65(2):397-412.

10.

Plasma PAI-1 levels are independently related to fatty liver and hypertriglyceridemia in familial combined hyperlipidemia, involvement of apolipoprotein E.

Brouwers MC, Govers-Riemslag J, Schalkwijk CG, van Greevenbroek MM, van der Kallen CJ, Bekers O, van Dieijen-Visser MP, Ten Oever J, Bilderbeek-Beckers MA, de Bruin TW, Ten Cate H, Stehouwer CD.

Thromb Res. 2008;122(4):466-72. doi: 10.1016/j.thromres.2007.12.009. Epub 2008 Feb 8.

PMID:
18262228
11.

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.

12.

Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin:cholesterol acyltransferase on 16q.

Aouizerat BE, Allayee H, Cantor RM, Dallinga-Thie GM, Lanning CD, de Bruin TW, Lusis AJ, Rotter JI.

Arterioscler Thromb Vasc Biol. 1999 Nov;19(11):2730-6.

13.

Increased arterial stiffness in familial combined hyperlipidemia.

Brouwers MC, Reesink KD, van Greevenbroek MM, Meinders JM, van der Kallen CJ, Schaper N, Hoeks AP, Stehouwer CD.

J Hypertens. 2009 May;27(5):1009-16. Erratum in: J Hypertens. 2009 Aug;27(8):1718.

PMID:
19402225
14.

Familial dyslipidemic hypertension syndrome: familial combined hyperlipidemia, and the role of abdominal fat mass.

Keulen ET, Voors-Pette C, de Bruin TW.

Am J Hypertens. 2001 Apr;14(4 Pt 1):357-63.

PMID:
11336182
15.
16.

Plasma proprotein convertase subtilisin kexin type 9 is a heritable trait of familial combined hyperlipidaemia.

Brouwers MC, van Greevenbroek MM, Troutt JS, Bonner Freeman A, Lu A, Schaper NC, Konrad RJ, Stehouwer CD.

Clin Sci (Lond). 2011 Nov;121(9):397-403. doi: 10.1042/CS20110129.

PMID:
21539517
17.

Abdominal obesity and expression of familial combined hyperlipidemia.

van der Kallen CJ, Voors-Pette C, de Bruin TW.

Obes Res. 2004 Dec;12(12):2054-61.

PMID:
15687407
18.

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. Epub 2005 Jun 23.

19.

Haplotypes of the ApoA-I/C-III/A-IV gene cluster and familial combined hyperlipidemia.

Tahvanainen E, Pajukanta P, Porkka K, Nieminen S, Ikävalko L, Nuotio I, Taskinen MR, Peltonen L, Ehnholm C.

Arterioscler Thromb Vasc Biol. 1998 Nov;18(11):1810-7.

20.

Identification of the PPARA locus on chromosome 22q13.3 as a modifier gene in familial combined hyperlipidemia.

Eurlings PM, van der Kallen CJ, Geurts JM, Flavell DM, de Bruin TW.

Mol Genet Metab. 2002 Dec;77(4):274-81.

PMID:
12468272
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