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Results: 1 to 20 of 101

1.

Epipolymorphisms within lipoprotein genes contribute independently to plasma lipid levels in familial hypercholesterolemia.

Guay SP, Brisson D, Lamarche B, Gaudet D, Bouchard L.

Epigenetics. 2014 May 1;9(5):718-29. doi: 10.4161/epi.27981. Epub 2014 Feb 6.

PMID:
24504152
[PubMed - in process]
2.

DNA methylation variations at CETP and LPL gene promoter loci: new molecular biomarkers associated with blood lipid profile variability.

Guay SP, Brisson D, Lamarche B, Marceau P, Vohl MC, Gaudet D, Bouchard L.

Atherosclerosis. 2013 Jun;228(2):413-20. doi: 10.1016/j.atherosclerosis.2013.03.033. Epub 2013 Apr 9.

PMID:
23623643
[PubMed - indexed for MEDLINE]
3.

Low-density lipoprotein apheresis: an evidence-based analysis.

Health Quality Ontario.

Ont Health Technol Assess Ser. 2007;7(5):1-101. Epub 2006 Nov 1.

PMID:
23074505
[PubMed]
Free PMC Article
4.

Heterozygous familial hypercholesterolemia in children: low-density lipoprotein receptor mutational analysis and variation in the expression of plasma lipoprotein-lipid concentrations.

Torres AL, Moorjani S, Vohl MC, Gagné C, Lamarche B, Brun LD, Lupien PJ, Després JP.

Atherosclerosis. 1996 Sep 27;126(1):163-71.

PMID:
8879444
[PubMed - indexed for MEDLINE]
5.

ABCA1 gene promoter DNA methylation is associated with HDL particle profile and coronary artery disease in familial hypercholesterolemia.

Guay SP, Brisson D, Munger J, Lamarche B, Gaudet D, Bouchard L.

Epigenetics. 2012 May;7(5):464-72. doi: 10.4161/epi.19633. Epub 2012 May 1.

PMID:
22419126
[PubMed - indexed for MEDLINE]
7.

Relative contribution of low-density lipoprotein receptor and lipoprotein lipase gene mutations to angiographically assessed coronary artery disease among French Canadians.

Gaudet D, Vohl MC, Julien P, Tremblay G, Perron P, Gagné C, Bergeron J, Moorjani S, Després JP.

Am J Cardiol. 1998 Aug 1;82(3):299-305.

PMID:
9708657
[PubMed - indexed for MEDLINE]
8.

Contribution of receptor negative versus receptor defective mutations in the LDL-receptor gene to angiographically assessed coronary artery disease among young (25-49 years) versus middle-aged (50-64 years) men.

Gaudet D, Vohl MC, Couture P, Moorjani S, Tremblay G, Perron P, Gagné C, Després JP.

Atherosclerosis. 1999 Mar;143(1):153-61.

PMID:
10208490
[PubMed - indexed for MEDLINE]
9.

CETP (cholesteryl ester transfer protein) promoter -1337 C>T polymorphism protects against coronary atherosclerosis in Japanese patients with heterozygous familial hypercholesterolaemia.

Takata M, Inazu A, Katsuda S, Miwa K, Kawashiri MA, Nohara A, Higashikata T, Kobayashi J, Mabuchi H, Yamagishi M.

Clin Sci (Lond). 2006 Nov;111(5):325-31.

PMID:
16822236
[PubMed - indexed for MEDLINE]
Free Article
10.

Low-density lipoprotein and high-density lipoprotein cholesterol levels in relation to genetic polymorphisms and menopausal status: the Atherosclerosis Risk in Communities (ARIC) Study.

Chamberlain AM, Folsom AR, Schreiner PJ, Boerwinkle E, Ballantyne CM.

Atherosclerosis. 2008 Oct;200(2):322-8. doi: 10.1016/j.atherosclerosis.2007.12.045. Epub 2008 Feb 13.

PMID:
18275964
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Transfer of lipids to high-density lipoprotein (HDL) is altered in patients with familial hypercholesterolemia.

Martinez LR, Santos RD, Miname MH, Deus DF, Lima ES, Maranhão RC.

Metabolism. 2013 Aug;62(8):1061-4. doi: 10.1016/j.metabol.2013.02.008. Epub 2013 Mar 26.

PMID:
23540443
[PubMed - indexed for MEDLINE]
13.

Association between the TaqIB polymorphism in the cholesteryl ester transfer protein gene locus and plasma lipoprotein levels in familial hypercholesterolemia.

Carmena-Ramón R, Ascaso JF, Real JT, Nájera G, Ordovás JM, Carmena R.

Metabolism. 2001 Jun;50(6):651-6.

PMID:
11398140
[PubMed - indexed for MEDLINE]
14.

Association of polymorphisms in genes involved in lipoprotein metabolism with plasma concentrations of remnant lipoproteins and HDL subpopulations before and after hormone therapy in postmenopausal women.

Lamon-Fava S, Asztalos BF, Howard TD, Reboussin DM, Horvath KV, Schaefer EJ, Herrington DM.

Clin Endocrinol (Oxf). 2010 Feb;72(2):169-75. doi: 10.1111/j.1365-2265.2009.03644.x. Epub 2009 May 29.

PMID:
19489872
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Epigenome-wide analysis in familial hypercholesterolemia identified new loci associated with high-density lipoprotein cholesterol concentration.

Guay SP, Voisin G, Brisson D, Munger J, Lamarche B, Gaudet D, Bouchard L.

Epigenomics. 2012 Dec;4(6):623-39. doi: 10.2217/epi.12.62.

PMID:
23244308
[PubMed - indexed for MEDLINE]
16.

Loci for CETP, LPL, LIPC, and APOC3 affect plasma lipoprotein size and sub-population distribution in Hispanic and non-Hispanic white subjects: the Columbia University BioMarkers Study.

Humphries SE, Berglund L, Isasi CR, Otvos JD, Kaluski D, Deckelbaum RJ, Shea S, Talmud PJ.

Nutr Metab Cardiovasc Dis. 2002 Aug;12(4):163-72.

PMID:
12514935
[PubMed - indexed for MEDLINE]
17.

Metabolic factors clustering, lipoprotein cholesterol, apolipoprotein B, lipoprotein (a) and apolipoprotein E phenotypes in premature coronary artery disease in French Canadians.

Weber M, McNicoll S, Marcil M, Connelly P, Lussier-Cacan S, Davignon J, Latour Y, Genest J Jr.

Can J Cardiol. 1997 Mar;13(3):253-60.

PMID:
9117913
[PubMed - indexed for MEDLINE]
18.

Different genes and polymorphisms affecting high-density lipoprotein cholesterol levels in Greek familial hypercholesterolemia patients.

Dedoussis GV, Maumus S, Choumerianou DM, Skoumas J, Pitsavos C, Stefanadis C, Visvikis-Siest S.

Genet Test. 2006 Fall;10(3):192-9.

PMID:
17020471
[PubMed - indexed for MEDLINE]
19.
20.

Coronary artery disease in heterozygous familial hypercholesterolemia patients with the same LDL receptor gene mutation.

Ferrières J, Lambert J, Lussier-Cacan S, Davignon J.

Circulation. 1995 Aug 1;92(3):290-5.

PMID:
7634440
[PubMed - indexed for MEDLINE]
Free Article

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