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Results: 1 to 20 of 108

Similar articles for PubMed (Select 11988495)

1.

Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia.

Allayee H, Krass KL, Pajukanta P, Cantor RM, van der Kallen CJ, Mar R, Rotter JI, de Bruin TW, Peltonen L, Lusis AJ.

Circ Res. 2002 May 3;90(8):926-31.

2.

Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1A.

van der Kallen CJ, Cantor RM, van Greevenbroek MM, Geurts JM, Bouwman FG, Aouizerat BE, Allayee H, Buurman WA, Lusis AJ, Rotter JI, de Bruin TW.

Int J Obes Relat Metab Disord. 2000 Nov;24(11):1381-91.

PMID:
11126332
3.

Families with familial combined hyperlipidemia and families enriched for coronary artery disease share genetic determinants for the atherogenic lipoprotein phenotype.

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

Am J Hum Genet. 1998 Aug;63(2):577-85.

4.

Genome scan for blood pressure in Dutch dyslipidemic families reveals linkage to a locus on chromosome 4p.

Allayee H, de Bruin TW, Michelle Dominguez K, Cheng LS, Ipp E, Cantor RM, Krass KL, Keulen ET, Aouizerat BE, Lusis AJ, Rotter JI.

Hypertension. 2001 Oct;38(4):773-8.

5.

Segregation analysis of plasma apolipoprotein B levels in familial combined hyperlipidemia.

Bredie SJ, van Drongelen J, Kiemeney LA, Demacker PN, Beaty TH, Stalenhoef AF.

Arterioscler Thromb Vasc Biol. 1997 May;17(5):834-40.

6.
7.

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.

8.

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.

9.

Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex.

Wijsman EM, Brunzell JD, Jarvik GP, Austin MA, Motulsky AG, Deeb SS.

Arterioscler Thromb Vasc Biol. 1998 Feb;18(2):215-26.

10.

Two novel quantitative trait loci on mouse chromosomes 6 and 4 independently and synergistically regulate plasma apoB levels.

Ko C, Lee TL, Lau PW, Li J, Davis BT, Voyiaziakis E, Allison DB, Chua SC Jr, Huang LS.

J Lipid Res. 2001 May;42(5):844-55. Erratum in: J Lipid Res 2001 Oct;42(10):1714.

11.

The Gln223Arg polymorphism in the leptin receptor is associated with familial combined hyperlipidemia.

van der Vleuten GM, Kluijtmans LA, Hijmans A, Blom HJ, Stalenhoef AF, de Graaf J.

Int J Obes (Lond). 2006 Jun;30(6):892-8.

PMID:
16432543
12.

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.

PMID:
9537421
13.
14.

Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.

Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.

Br J Dermatol. 2005 Jan;152(1):29-36.

PMID:
15656797
15.

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.

16.

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. Epub 2003 Mar 12.

17.

Evidence of QTLs on chromosomes 1q42 and 8q24 for LDL-cholesterol and apoB levels in the HERITAGE family study.

Feitosa MF, Borecki IB, Rankinen T, Rice T, Després JP, Chagnon YC, Gagnon J, Leon AS, Skinner JS, Bouchard C, Province MA, Rao DC.

J Lipid Res. 2005 Feb;46(2):281-6. Epub 2004 Dec 1.

18.
19.

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.

20.

Major locus inheritance of apolipoprotein B in Utah pedigrees.

Hasstedt SJ, Wu L, Williams RR.

Genet Epidemiol. 1987;4(2):67-76.

PMID:
3108070
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