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Results: 1 to 20 of 174

Similar articles for PubMed (Select 22419126)

1.

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
2.

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

3.

Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients.

Kyriakou T, Pontefract DE, Viturro E, Hodgkinson CP, Laxton RC, Bogari N, Cooper G, Davies M, Giblett J, Day IN, Simpson IA, Albrecht C, Ye S.

Hum Mol Genet. 2007 Jun 15;16(12):1412-22. Epub 2007 Apr 5.

4.

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
5.

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
6.

[Significance of -191G/C single nucleotide polymorphisms in the promoter region of ATP-binding cassette transporter gene in coronary artery disease].

Liu L, Guo ZG, Wang QG, Liu SL, Lai WY, Tu Y.

Di Yi Jun Yi Da Xue Xue Bao. 2005 Jun;25(6):660-2, 666. Chinese.

7.

Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease.

Clee SM, Zwinderman AH, Engert JC, Zwarts KY, Molhuizen HO, Roomp K, Jukema JW, van Wijland M, van Dam M, Hudson TJ, Brooks-Wilson A, Genest J Jr, Kastelein JJ, Hayden MR.

Circulation. 2001 Mar 6;103(9):1198-205.

8.

Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes.

Clee SM, Kastelein JJ, van Dam M, Marcil M, Roomp K, Zwarts KY, Collins JA, Roelants R, Tamasawa N, Stulc T, Suda T, Ceska R, Boucher B, Rondeau C, DeSouich C, Brooks-Wilson A, Molhuizen HO, Frohlich J, Genest J Jr, Hayden MR.

J Clin Invest. 2000 Nov;106(10):1263-70.

9.

A frequent variant in the ABCA1 gene is associated with increased coronary heart disease risk and a better response to statin treatment in familial hypercholesterolemia patients.

Versmissen J, Oosterveer DM, Yazdanpanah M, Mulder M, Dehghan A, Defesche JC, Kastelein JJ, Sijbrands EJ.

Eur Heart J. 2011 Feb;32(4):469-75. doi: 10.1093/eurheartj/ehq208. Epub 2010 Jul 1.

10.

Impact of LDL apheresis on atheroprotective reverse cholesterol transport pathway in familial hypercholesterolemia.

Orsoni A, Villard EF, Bruckert E, Robillard P, Carrie A, Bonnefont-Rousselot D, Chapman MJ, Dallinga-Thie GM, Le Goff W, Guerin M.

J Lipid Res. 2012 Apr;53(4):767-75. doi: 10.1194/jlr.M024141. Epub 2012 Feb 15.

12.

Increased risk of coronary artery disease in Caucasians with extremely low HDL cholesterol due to mutations in ABCA1, APOA1, and LCAT.

Tietjen I, Hovingh GK, Singaraja R, Radomski C, McEwen J, Chan E, Mattice M, Legendre A, Kastelein JJ, Hayden MR.

Biochim Biophys Acta. 2012 Mar;1821(3):416-24. doi: 10.1016/j.bbalip.2011.08.006. Epub 2011 Aug 19.

PMID:
21875686
14.

Common variants in the ATP-binding cassette transporter 1 gene with decreased HDL-cholesterol levels and coronary artery disease.

Catakoglu AB, Duman BS, Kurtoğlu H, Ersöz M, Sener M, Celebi H, Cağatay P, Aytekin V, Aytekin S.

Arch Med Res. 2008 Nov;39(8):735-42. doi: 10.1016/j.arcmed.2008.07.008.

PMID:
18996286
15.
16.

Familial hypercholesterolemia: molecular, biochemical, and clinical characterization of a French-Canadian pediatric population.

Assouline L, Levy E, Feoli-Fonseca JC, Godbout C, Lambert M.

Pediatrics. 1995 Aug;96(2 Pt 1):239-46.

PMID:
7630677
17.

A common variant in the ABCA1 gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia.

Cenarro A, Artieda M, Castillo S, Mozas P, Reyes G, Tejedor D, Alonso R, Mata P, Pocoví M, Civeira F; Spanish FH group.

J Med Genet. 2003 Mar;40(3):163-8.

18.

ABCA1 gene polymorphisms and their associations with coronary artery disease and plasma lipids in males from three ethnic populations in Singapore.

Tan JH, Low PS, Tan YS, Tong MC, Saha N, Yang H, Heng CK.

Hum Genet. 2003 Jul;113(2):106-17. Epub 2003 Apr 23.

PMID:
12709788
19.

A promoter variant of the ATP-binding cassette transporter A1 gene alters the HDL cholesterol level in the general Japanese population.

Shioji K, Nishioka J, Naraba H, Kokubo Y, Mannami T, Inamoto N, Kamide K, Takiuchi S, Yoshii M, Miwa Y, Kawano Y, Miyata T, Miyazaki S, Goto Y, Nonogi H, Tago N, Iwai N.

J Hum Genet. 2004;49(3):141-7. Epub 2004 Feb 21.

PMID:
14986172
20.

Genotypic effect of the -565C>T polymorphism in the ABCA1 gene promoter on ABCA1 expression and severity of atherosclerosis.

Kyriakou T, Hodgkinson C, Pontefract DE, Iyengar S, Howell WM, Wong YK, Eriksson P, Ye S.

Arterioscler Thromb Vasc Biol. 2005 Feb;25(2):418-23. Epub 2004 Nov 4.

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