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2. Vitamin A is linked to the expression of the AI-CIII-AIV gene cluster in familial combined hyperlipidemia. Ribalta J; Girona J; Vallvé JC; La Ville AE; Heras M; Masana L J Lipid Res; 1999 Mar; 40(3):426-31. PubMed ID: 10064730 [TBL] [Abstract][Full Text] [Related]
3. Intra-individual variations of fasting plasma lipids, apolipoproteins and postprandial lipemia in familial combined hyperlipidemia compared to controls. Delawi D; Meijssen S; Castro Cabezas M Clin Chim Acta; 2003 Feb; 328(1-2):139-45. PubMed ID: 12559610 [TBL] [Abstract][Full Text] [Related]
4. Contribution of mutations in low density lipoprotein receptor (LDLR) and lipoprotein lipase (LPL) genes to familial combined hyperlipidemia (FCHL): a reappraisal by using a resequencing approach. Minicocci I; Prisco C; Montali A; Di Costanzo A; Ceci F; Pigna G; Arca M Atherosclerosis; 2015 Oct; 242(2):618-24. PubMed ID: 26342331 [TBL] [Abstract][Full Text] [Related]
6. Evidence against alterations in Lecithin:cholesterol acyltransferase (LCAT) activity in familial combined hyperlipidemia. Ribalta J; La Ville AE; Vallvé JC; Girona J; Masana L Atherosclerosis; 1998 Jun; 138(2):383-9. PubMed ID: 9690923 [TBL] [Abstract][Full Text] [Related]
7. Two novel apolipoprotein A-IV variants in individuals with familial combined hyperlipidemia and diminished levels of lipoprotein lipase activity. Deeb SS; Nevin DN; Iwasaki L; Brunzell JD Hum Mutat; 1996; 8(4):319-25. PubMed ID: 8956036 [TBL] [Abstract][Full Text] [Related]
8. Nutrition, body weight and deterioration of familial combined hyperlipidemia. Koprovicová J; Kollár J; Petrásová D Coll Antropol; 2006 Dec; 30(4):777-82. PubMed ID: 17243549 [TBL] [Abstract][Full Text] [Related]
9. Genetic evidence from 7 families that the apolipoprotein B gene is not involved in familial combined hyperlipidemia. Rauh G; Schuster H; Müller B; Schewe S; Keller C; Wolfram G; Zöllner N Atherosclerosis; 1990 Jul; 83(1):81-7. PubMed ID: 1975179 [TBL] [Abstract][Full Text] [Related]
10. Identification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemia. Geurts JM; Janssen RG; van Greevenbroek MM; van der Kallen CJ; Cantor RM; Bu X; Aouizerat BE; Allayee H; Rotter JI; de Bruin TW Hum Mol Genet; 2000 Sep; 9(14):2067-74. PubMed ID: 10958645 [TBL] [Abstract][Full Text] [Related]
11. The lipoprotein lipase (Asn291-->Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia. Hoffer MJ; Bredie SJ; Boomsma DI; Reymer PW; Kastelein JJ; de Knijff P; Demacker PN; Stalenhoef AF; Havekes LM; Frants RR Atherosclerosis; 1996 Jan; 119(2):159-67. PubMed ID: 8808493 [TBL] [Abstract][Full Text] [Related]
12. Effects of atorvastatin on fasting plasma and marginated apolipoproteins B48 and B100 in large, triglyceride-rich lipoproteins in familial combined hyperlipidemia. Verseyden C; Meijssen S; Cabezas MC J Clin Endocrinol Metab; 2004 Oct; 89(10):5021-9. PubMed ID: 15472200 [TBL] [Abstract][Full Text] [Related]
14. Common variants in the lipoprotein lipase gene, but not those in the insulin receptor substrate-1, the beta3-adrenergic receptor, and the intestinal fatty acid binding protein-2 genes, influence the lipid phenotypic expression in familial combined hyperlipidemia. Campagna F; Montali A; Baroni MG; Maria AT; Ricci G; Antonini R; Verna R; Arca M Metabolism; 2002 Oct; 51(10):1298-305. PubMed ID: 12370850 [TBL] [Abstract][Full Text] [Related]
15. Impaired activation of adipocyte lipolysis in familial combined hyperlipidemia. Reynisdottir S; Eriksson M; Angelin B; Arner P J Clin Invest; 1995 May; 95(5):2161-9. PubMed ID: 7738184 [TBL] [Abstract][Full Text] [Related]
16. Delayed and exaggerated postprandial complement component 3 response in familial combined hyperlipidemia. Meijssen S; van Dijk H; Verseyden C; Erkelens DW; Cabezas MC Arterioscler Thromb Vasc Biol; 2002 May; 22(5):811-6. PubMed ID: 12006395 [TBL] [Abstract][Full Text] [Related]
17. The V73M mutation in the hepatic lipase gene is associated with elevated cholesterol levels in four Dutch pedigrees with familial combined hyperlipidemia. Hoffer MJ; Snieder H; Bredie SJ; Demacker PN; Kastelein JJ; Frants RR; Stalenhoef AF Atherosclerosis; 2000 Aug; 151(2):443-50. PubMed ID: 10924721 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Two polymorphisms in the apo A-IV gene and familial combined hyperlipidemia. Groenendijk M; De Bruin TW; Dallinga-Thie GM Atherosclerosis; 2001 Oct; 158(2):369-76. PubMed ID: 11583715 [TBL] [Abstract][Full Text] [Related]
20. Subclasses of low-density lipoprotein and very low-density lipoprotein in familial combined hyperlipidemia: relationship to multiple lipoprotein phenotype. Georgieva AM; van Greevenbroek MM; Krauss RM; Brouwers MC; Vermeulen VM; Robertus-Teunissen MG; van der Kallen CJ; de Bruin TW Arterioscler Thromb Vasc Biol; 2004 Apr; 24(4):744-9. PubMed ID: 14751815 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]