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Results: 1 to 20 of 172

Similar articles for PubMed (Select 21307941)

1.

9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response.

Harismendy O, Notani D, Song X, Rahim NG, Tanasa B, Heintzman N, Ren B, Fu XD, Topol EJ, Rosenfeld MG, Frazer KA.

Nature. 2011 Feb 10;470(7333):264-8. doi: 10.1038/nature09753.

2.

Interferon-γ activates expression of p15 and p16 regardless of 9p21.3 coronary artery disease risk genotype.

Almontashiri NA, Fan M, Cheng BL, Chen HH, Roberts R, Stewart AF.

J Am Coll Cardiol. 2013 Jan 15;61(2):143-7. doi: 10.1016/j.jacc.2012.08.1020. Epub 2012 Nov 28.

3.

Haplotypes on 9p21 modify the risk for coronary artery disease among Indians.

AshokKumar M, Emmanuel C, Dhandapany PS, Rani DS, SaiBabu R, Cherian KM, Thangaraj K.

DNA Cell Biol. 2011 Feb;30(2):105-10. doi: 10.1089/dna.2010.1046. Epub 2010 Sep 21.

PMID:
20858033
4.

Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.

Shen GQ, Li L, Rao S, Abdullah KG, Ban JM, Lee BS, Park JE, Wang QK.

Arterioscler Thromb Vasc Biol. 2008 Feb;28(2):360-5. Epub 2007 Nov 29.

5.

The 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosis.

Chen SN, Ballantyne CM, Gotto AM Jr, Marian AJ.

BMC Cardiovasc Disord. 2009 Jan 27;9:3. doi: 10.1186/1471-2261-9-3.

6.

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

Visel A, Zhu Y, May D, Afzal V, Gong E, Attanasio C, Blow MJ, Cohen JC, Rubin EM, Pennacchio LA.

Nature. 2010 Mar 18;464(7287):409-12. doi: 10.1038/nature08801. Epub 2010 Feb 21.

7.

The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissues.

Pilbrow AP, Folkersen L, Pearson JF, Brown CM, McNoe L, Wang NM, Sweet WE, Tang WH, Black MA, Troughton RW, Richards AM, Franco-Cereceda A, Gabrielsen A, Eriksson P, Moravec CS, Cameron VA.

PLoS One. 2012;7(6):e39574. doi: 10.1371/journal.pone.0039574. Epub 2012 Jun 29.

8.

The 9p21 locus does not affect risk of coronary artery disease through induction of type 1 interferons.

Erridge C, Gracey J, Braund PS, Samani NJ.

J Am Coll Cardiol. 2013 Oct 8;62(15):1376-81. doi: 10.1016/j.jacc.2013.07.031. Epub 2013 Aug 7.

9.

Genetic analysis of the 9p21.3 CAD risk locus in Asian Indians.

Shanker J, Arvind P, Jambunathan S, Nair J, Kakkar V.

Thromb Haemost. 2014 May 5;111(5):960-9. doi: 10.1160/TH13-08-0706. Epub 2014 Jan 23.

PMID:
24452806
10.

Resequencing and clinical associations of the 9p21.3 region: a comprehensive investigation in the Framingham heart study.

Johnson AD, Hwang SJ, Voorman A, Morrison A, Peloso GM, Hsu YH, Thanassoulis G, Newton-Cheh C, Rogers IS, Hoffmann U, Freedman JE, Fox CS, Psaty BM, Boerwinkle E, Cupples LA, O'Donnell CJ.

Circulation. 2013 Feb 19;127(7):799-810. doi: 10.1161/CIRCULATIONAHA.112.111559. Epub 2013 Jan 11.

11.

Functional analyses of coronary artery disease associated variation on chromosome 9p21 in vascular smooth muscle cells.

Motterle A, Pu X, Wood H, Xiao Q, Gor S, Ng FL, Chan K, Cross F, Shohreh B, Poston RN, Tucker AT, Caulfield MJ, Ye S.

Hum Mol Genet. 2012 Sep 15;21(18):4021-9. doi: 10.1093/hmg/dds224. Epub 2012 Jun 15.

12.

The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population.

Cheng X, Shi L, Nie S, Wang F, Li X, Xu C, Wang P, Yang B, Li Q, Pan Z, Li Y, Xia H, Zheng C, Ke Y, Wu Y, Tang T, Yan X, Yang Y, Xia N, Yao R, Wang B, Ma X, Zeng Q, Tu X, Liao Y, Wang QK.

Diabetes. 2011 Feb;60(2):680-4. doi: 10.2337/db10-0185.

13.

A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.

Osman W, Low SK, Takahashi A, Kubo M, Nakamura Y.

Hum Mol Genet. 2012 Jun 15;21(12):2836-42. doi: 10.1093/hmg/dds103. Epub 2012 Mar 13.

14.

9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han population.

Ding H, Xu Y, Wang X, Wang Q, Zhang L, Tu Y, Yan J, Wang W, Hui R, Wang CY, Wang DW.

Circ Cardiovasc Genet. 2009 Aug;2(4):338-46. doi: 10.1161/CIRCGENETICS.108.810226. Epub 2009 May 28.

15.

Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus.

Jarinova O, Stewart AF, Roberts R, Wells G, Lau P, Naing T, Buerki C, McLean BW, Cook RC, Parker JS, McPherson R.

Arterioscler Thromb Vasc Biol. 2009 Oct;29(10):1671-7. doi: 10.1161/ATVBAHA.109.189522. Epub 2009 Jul 10.

16.

Association between 9p21.3 genomic markers and coronary artery disease in East Asians: a meta-analysis involving 9,813 cases and 10,710 controls.

Guo J, Li W, Wu Z, Cheng X, Wang Y, Chen T.

Mol Biol Rep. 2013 Jan;40(1):337-43. doi: 10.1007/s11033-012-2066-1. Epub 2012 Oct 20.

PMID:
23086272
17.

Functional genomics of the 9p21.3 locus for atherosclerosis: clarity or confusion?

Chen HH, Almontashiri NA, Antoine D, Stewart AF.

Curr Cardiol Rep. 2014 Jul;16(7):502. doi: 10.1007/s11886-014-0502-7. Review.

PMID:
24893939
18.

Chromosome 9p21 haplotypes and prognosis in white and black patients with coronary artery disease.

Gong Y, Beitelshees AL, Cooper-DeHoff RM, Lobmeyer MT, Langaee TY, Wu J, Cresci S, Province MA, Spertus JA, Pepine CJ, Johnson JA.

Circ Cardiovasc Genet. 2011 Apr;4(2):169-78. doi: 10.1161/CIRCGENETICS.110.959296. Epub 2011 Mar 3.

19.

Methylation of p15INK4b and expression of ANRIL on chromosome 9p21 are associated with coronary artery disease.

Zhuang J, Peng W, Li H, Wang W, Wei Y, Li W, Xu Y.

PLoS One. 2012;7(10):e47193. doi: 10.1371/journal.pone.0047193. Epub 2012 Oct 16.

20.

The rs10757278 polymorphism of the 9p21.3 locus is associated with premature coronary artery disease in Polish patients.

Niemiec P, Gorczynska-Kosiorz S, Iwanicki T, Krauze J, Trautsolt W, Grzeszczak W, Bochenek A, Zak I.

Genet Test Mol Biomarkers. 2012 Sep;16(9):1080-5. doi: 10.1089/gtmb.2012.0046. Epub 2012 Sep 4.

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