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Journal Abstract Search

182 related items for PubMed ID: 9157946

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  • 4. 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
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  • 5. 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
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  • 6. Lipoprotein lipase gene mutations D9N and N291S in four pedigrees with familial combined hyperlipidaemia.
    de Bruin TW, Mailly F, van Barlingen HH, Fisher R, Castro Cabezas M, Talmud P, Dallinga-Thie GM, Humphries SE.
    Eur J Clin Invest; 1996 Aug; 26(8):631-9. PubMed ID: 8872057
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  • 7. 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. PubMed ID: 10559018
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  • 8. Adipose tissue lipoprotein lipase and hormone-sensitive lipase. Contrasting findings in familial combined hyperlipidemia and insulin resistance syndrome.
    Reynisdottir S, Angelin B, Langin D, Lithell H, Eriksson M, Holm C, Arner P.
    Arterioscler Thromb Vasc Biol; 1997 Oct; 17(10):2287-92. PubMed ID: 9351402
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  • 9. 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
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  • 15. Lack of association of the apolipoprotein A-I-C-III-A-IV gene XmnI and SstI polymorphisms and of the lipoprotein lipase gene mutations in familial combined hyperlipoproteinemia in French Canadian subjects.
    Marcil M, Boucher B, Gagné E, Davignon J, Hayden M, Genest J.
    J Lipid Res; 1996 Feb; 37(2):309-19. PubMed ID: 9026529
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  • 16. Association between genetic variation at the APO AI-CIII-AIV gene cluster and familial combined hyperlipidaemia.
    Xu CF, Talmud P, Schuster H, Houlston R, Miller G, Humphries S.
    Clin Genet; 1994 Dec; 46(6):385-97. PubMed ID: 7889654
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  • 17. 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. PubMed ID: 10417282
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  • 18. Lack of evidence for linkage between low-density lipoprotein subclass phenotypes and the apolipoprotein B locus in familial combined hyperlipidemia.
    Austin MA, Wijsman E, Guo SW, Krauss RM, Brunzell JD, Deeb S.
    Genet Epidemiol; 1991 Aug; 8(5):287-97. PubMed ID: 1761202
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  • 19. Contribution of the hepatic lipase gene to the atherogenic lipoprotein phenotype in familial combined hyperlipidemia.
    Allayee H, Dominguez KM, Aouizerat BE, Krauss RM, Rotter JI, Lu J, Cantor RM, de Bruin TW, Lusis AJ.
    J Lipid Res; 2000 Feb; 41(2):245-52. PubMed ID: 10681408
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