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Items: 1 to 20 of 105

1.

Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD.

Knowles JW, Assimes TL, Boerwinkle E, Fortmann SP, Go A, Grove ML, Hlatky M, Iribarren C, Li J, Myers R, Risch N, Sidney S, Southwick A, Volcik KA, Quertermous T.

BMC Med Genet. 2008 Apr 2;9:23. doi: 10.1186/1471-2350-9-23.

2.

The 3'-UTR C>T polymorphism of the oxidized LDL-receptor 1 (OLR1) gene does not associate with coronary artery disease in Italian CAD patients or with the severity of coronary disease.

Sentinelli F, Filippi E, Fallarino M, Romeo S, Fanelli M, Buzzetti R, Berni A, Baroni MG.

Nutr Metab Cardiovasc Dis. 2006 Jul;16(5):345-52. Epub 2005 Nov 3.

PMID:
16829343
3.

On the association of the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction or coronary artery disease.

Trabetti E, Biscuola M, Cavallari U, Malerba G, Girelli D, Olivieri O, Martinelli N, Corrocher R, Pignatti PF.

Eur J Hum Genet. 2006 Jan;14(1):127-30.

4.

Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease.

Assimes TL, Knowles JW, Priest JR, Basu A, Volcik KA, Southwick A, Tabor HK, Hartiala J, Allayee H, Grove ML, Tabibiazar R, Sidney S, Fortmann SP, Go A, Hlatky M, Iribarren C, Boerwinkle E, Myers R, Risch N, Quertermous T.

Hum Genet. 2008 May;123(4):399-408. doi: 10.1007/s00439-008-0489-5. Epub 2008 Mar 28.

5.

Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events.

Predazzi IM, Martínez-Labarga C, Vecchione L, Mango R, Ciccacci C, Amati F, Ottoni C, Crawford MH, Rickards O, Romeo F, Novelli G.

Ann Hum Biol. 2010 Apr;37(2):136-48. doi: 10.3109/03014460903393857.

PMID:
19961348
6.

A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease.

Assimes TL, Knowles JW, Priest JR, Basu A, Borchert A, Volcik KA, Grove ML, Tabor HK, Southwick A, Tabibiazar R, Sidney S, Boerwinkle E, Go AS, Iribarren C, Hlatky MA, Fortmann SP, Myers RM, Kuhn H, Risch N, Quertermous T.

Atherosclerosis. 2008 May;198(1):136-44. Epub 2007 Oct 23.

7.

Is LOX-1 K167N polymorphism protective for coronary artery disease?

Kurnaz O, Aydogan HY, Isbir CS, Tekeli A, Isbir T.

In Vivo. 2009 Nov-Dec;23(6):969-73.

8.

Oxidized LDL receptor gene (OLR1) is associated with the risk of myocardial infarction.

Tatsuguchi M, Furutani M, Hinagata J, Tanaka T, Furutani Y, Imamura S, Kawana M, Masaki T, Kasanuki H, Sawamura T, Matsuoka R.

Biochem Biophys Res Commun. 2003 Mar 28;303(1):247-50.

PMID:
12646194
9.

Association of LOXIN, a new functional splicing isoform of the OLR1 gene, with severity and prognostic localization of critical coronary artery stenoses.

Cappelletti A, Zanussi M, Mazzavillani M, Magni V, Calori G, Godino C, Ferrari M, Margonato A.

J Cardiovasc Med (Hagerstown). 2014 May;15(5):391-6. doi: 10.2459/JCM.0b013e3283624251.

PMID:
24743687
10.

Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease.

Baessler A, Fischer M, Mayer B, Koehler M, Wiedmann S, Stark K, Doering A, Erdmann J, Riegger G, Schunkert H, Kwitek AE, Hengstenberg C.

Hum Mol Genet. 2007 Apr 15;16(8):887-99. Epub 2007 Feb 26.

11.

Association of common polymorphisms in GLUT9 gene with gout but not with coronary artery disease in a large case-control study.

Stark K, Reinhard W, Neureuther K, Wiedmann S, Sedlacek K, Baessler A, Fischer M, Weber S, Kaess B, Erdmann J, Schunkert H, Hengstenberg C.

PLoS One. 2008 Apr 9;3(4):e1948. doi: 10.1371/journal.pone.0001948.

12.

OLR1, PON1 and MTHFR gene polymorphisms, conventional risk factors and the severity of coronary atherosclerosis in a Chinese Han population.

Gu Y, Liu Z, Li L, Guo CY, Li CJ, Wang LS, Yang ZJ, Ma WZ, Jia EZ.

Cell Physiol Biochem. 2013;31(1):143-52. doi: 10.1159/000343356. Epub 2013 Jan 31.

13.

IVS4-14 A/G and IVS4-73 C/T polymorphisms in OLR1 gene in patients with ischemic cerebrovascular diseases.

Vietri MT, Molinari AM, Boggia M, Parisi M, Cioffi M.

Genet Test Mol Biomarkers. 2010 Feb;14(1):9-11. doi: 10.1089/gtmb.2009.0101.

PMID:
19929426
14.

Minor allele C of chromosome 1p32 single nucleotide polymorphism rs11206510 confers risk of ischemic stroke in the Chinese Han population.

Xu C, Wang F, Wang B, Li X, Li C, Wang D, Xiong X, Wang P, Lu Q, Wang X, Yang Q, Yin D, Huang Y, Ji L, Wang N, Chen S, Cheng X, Liao Y, Ma X, Su D, Chen G, Xia H, Shi L, Tu X, Wang QK.

Stroke. 2010 Aug;41(8):1587-92. doi: 10.1161/STROKEAHA.110.583096. Epub 2010 Jun 24.

15.

The adiponectin gene SNP+276G>T associates with early-onset coronary artery disease and with lower levels of adiponectin in younger coronary artery disease patients (age <or=50 years).

Filippi E, Sentinelli F, Romeo S, Arca M, Berni A, Tiberti C, Verrienti A, Fanelli M, Fallarino M, Sorropago G, Baroni MG.

J Mol Med (Berl). 2005 Sep;83(9):711-9. Epub 2005 May 5.

PMID:
15877215
16.

In vivo and in vitro studies support that a new splicing isoform of OLR1 gene is protective against acute myocardial infarction.

Mango R, Biocca S, del Vecchio F, Clementi F, Sangiuolo F, Amati F, Filareto A, Grelli S, Spitalieri P, Filesi I, Favalli C, Lauro R, Mehta JL, Romeo F, Novelli G.

Circ Res. 2005 Jul 22;97(2):152-8. Epub 2005 Jun 23.

17.

Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease.

Horne BD, Carlquist JF, Muhlestein JB, Bair TL, Anderson JL.

Circ Cardiovasc Genet. 2008 Dec;1(2):85-92. doi: 10.1161/CIRCGENETICS.108.793158.

18.

Role of six single nucleotide polymorphisms, risk factors in coronary disease, in OLR1 alternative splicing.

Tejedor JR, Tilgner H, Iannone C, Guigó R, Valcárcel J.

RNA. 2015 Jun;21(6):1187-202. doi: 10.1261/rna.049890.115. Epub 2015 Apr 22.

19.

Association between OLR1 K167N SNP and intima media thickness of the common carotid artery in the general population.

Predazzi IM, Norata GD, Vecchione L, Garlaschelli K, Amati F, Grigore L, Cutuli L, Pirillo A, Tramontana S, Romeo F, Novelli G, Catapano AL.

PLoS One. 2012;7(2):e31086. doi: 10.1371/journal.pone.0031086. Epub 2012 Feb 9.

20.

Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study.

Assimes TL, Knowles JW, Basu A, Iribarren C, Southwick A, Tang H, Absher D, Li J, Fair JM, Rubin GD, Sidney S, Fortmann SP, Go AS, Hlatky MA, Myers RM, Risch N, Quertermous T.

Hum Mol Genet. 2008 Aug 1;17(15):2320-8. doi: 10.1093/hmg/ddn132. Epub 2008 Apr 28.

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