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Items: 1 to 20 of 198

1.

Chromosome 9p21 rs10757278 polymorphism is associated with the risk of metabolic syndrome.

Bayoglu B, Cakmak HA, Yuksel H, Can G, Karadag B, Ulutin T, Vural VA, Cengiz M.

Mol Cell Biochem. 2013 Jul;379(1-2):77-85. doi: 10.1007/s11010-013-1629-3. Epub 2013 Mar 28.

PMID:
23535969
2.

Polymorphisms in the long non-coding RNA CDKN2B-AS1 may contribute to higher systolic blood pressure levels in hypertensive patients.

Bayoglu B, Yuksel H, Cakmak HA, Dirican A, Cengiz M.

Clin Biochem. 2016 Jul;49(10-11):821-7. doi: 10.1016/j.clinbiochem.2016.02.012. Epub 2016 Mar 2.

PMID:
26944720
3.

Association of polymorphisms on chromosome 9p21.3 region with increased susceptibility of abdominal aortic aneurysm in a Chinese Han population.

Wei Y, Xiong J, Zuo S, Chen F, Chen D, Wu T, Guo W, Hu Y.

J Vasc Surg. 2014 Apr;59(4):879-85. doi: 10.1016/j.jvs.2013.10.095. Epub 2013 Dec 22.

4.

Polymorphisms on chromosome 9p21 confer a risk for acute coronary syndrome in a Chinese Han population.

Zeng Q, Yuan Y, Wang S, Sun J, Zhang T, Qi M.

Can J Cardiol. 2013 Aug;29(8):940-4. doi: 10.1016/j.cjca.2012.11.028. Epub 2013 Mar 1.

PMID:
23454037
5.

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.

6.

Association of arterial stiffness with single nucleotide polymorphism rs1333049 and metabolic risk factors.

Phababpha S, Kukongviriyapan U, Pakdeechote P, Senggunprai L, Kukongviriyapan V, Settasatian C, Tatsanavivat P, Intharaphet P, Senthong V, Komanasin N, Settasatian N, Greenwald SE.

Cardiovasc Diabetol. 2013 Jun 21;12:93. doi: 10.1186/1475-2840-12-93.

7.

A common variant on chromosome 9p21 affects the risk of early-onset coronary artery disease.

Chen Z, Qian Q, Ma G, Wang J, Zhang X, Feng Y, Shen C, Yao Y.

Mol Biol Rep. 2009 May;36(5):889-93. doi: 10.1007/s11033-008-9259-7. Epub 2008 May 6.

PMID:
18459066
8.

Evaluation of association between common genetic variants on chromosome 9p21 and coronary artery disease in Turkish population.

Çakmak HA, Bayoğlu B, Durmaz E, Can G, Karadağ B, Cengiz M, Vural VA, Yüksel H.

Anatol J Cardiol. 2015 Mar;15(3):196-203. doi: 10.5152/akd.2014.5285. Epub 2014 Apr 8.

9.

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
10.

Polymorphisms in lipid metabolism related miRNA binding sites and risk of metabolic syndrome.

Ye Q, Zhao X, Xu K, Li Q, Cheng J, Gao Y, Du J, Shi H, Zhou L.

Gene. 2013 Oct 10;528(2):132-8. doi: 10.1016/j.gene.2013.07.036. Epub 2013 Jul 31.

PMID:
23911300
11.

Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry.

Scheffold T, Kullmann S, Huge A, Binner P, Ochs HR, Schöls W, Thale J, Motz W, Hegge FJ, Stellbrink C, Dorsel T, Gülker H, Heuer H, Dinh W, Stoll M, Haltern G; Forschungsverbund Herz-Kreislauf in NRW (Research Consortium Heart and Circulation in North Rhine-Westphalia)..

BMC Cardiovasc Disord. 2011 Mar 7;11:9. doi: 10.1186/1471-2261-11-9.

12.

Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21.

Gioli-Pereira L, Santos PC, Ferreira NE, Hueb WA, Krieger JE, Pereira AC.

BMC Cardiovasc Disord. 2012 Aug 2;12:61. doi: 10.1186/1471-2261-12-61.

13.

Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study.

Smith JG, Melander O, Lövkvist H, Hedblad B, Engström G, Nilsson P, Carlson J, Berglund G, Norrving B, Lindgren A.

Circ Cardiovasc Genet. 2009 Apr;2(2):159-64. doi: 10.1161/CIRCGENETICS.108.835173. Epub 2009 Feb 12.

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.

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
16.

The myocardial infarction associated CDKN2A/CDKN2B locus on chromosome 9p21 is associated with stroke independently of coronary events in patients with hypertension.

Wahlstrand B, Orho-Melander M, Delling L, Kjeldsen S, Narkiewicz K, Almgren P, Hedner T, Melander O.

J Hypertens. 2009 Apr;27(4):769-73. doi: 10.1097/HJH.0b013e328326f7eb.

PMID:
19293724
17.

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.

18.

Independent association of the variant rs1333049 at the 9p21 locus and coronary heart disease.

Mendonça I, dos Reis RP, Pereira A, Café H, Serrão M, Sousa AC, Freitas AI, Guerra G, Freitas S, Freitas C, Ornelas I, Brehm A, Araújo JJ.

Rev Port Cardiol. 2011 Jun;30(6):575-91. English, Portuguese.

19.

Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.

Shen GQ, Rao S, Martinelli N, Li L, Olivieri O, Corrocher R, Abdullah KG, Hazen SL, Smith J, Barnard J, Plow EF, Girelli D, Wang QK.

J Hum Genet. 2008;53(2):144-50. Epub 2007 Dec 8.

PMID:
18066490
20.

Sex differential genetic effect of chromosome 9p21 on subclinical atherosclerosis.

Lin HF, Tsai PC, Lin RT, Khor GT, Sheu SH, Juo SH.

PLoS One. 2010 Nov 30;5(11):e15124. doi: 10.1371/journal.pone.0015124.

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