190 related articles for article (PubMed ID: 34313925)
1. Association between rs3088440 (G > A) polymorphism at 9p21.3 locus with the occurrence and severity of coronary artery disease in an Iranian population.
Pourgholi M; Abazari O; Pourgholi L; Ghasemi-Kasman M; Boroumand M
Mol Biol Rep; 2021 Aug; 48(8):5905-5912. PubMed ID: 34313925
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 19956784
[TBL] [Abstract][Full Text] [Related]
3. Association of rs10811656 on 9P21.3 with the risk of coronary artery disease in a Chinese population.
Yan J; Zeng J; Xie Z; Liu D; Wang L; Chen Z
Lipids Health Dis; 2016 Aug; 15(1):126. PubMed ID: 27507036
[TBL] [Abstract][Full Text] [Related]
4. Variants in 9p21 Predicts Severity of Coronary Artery Disease in a Chinese Han Population.
Jing J; Su L; Zeng Y; Tang X; Wei J; Wang L; Zhou L
Ann Hum Genet; 2016 Sep; 80(5):274-81. PubMed ID: 27461153
[TBL] [Abstract][Full Text] [Related]
5. Genetic mechanisms mediating atherosclerosis susceptibility at the chromosome 9p21 locus.
Cunnington MS; Keavney B
Curr Atheroscler Rep; 2011 Jun; 13(3):193-201. PubMed ID: 21487702
[TBL] [Abstract][Full Text] [Related]
6. The association of polymorphic variants, rs2267788, rs1333049 and rs2383207 with coronary artery disease, its severity and presentation in North Indian population.
Kashyap S; Kumar S; Agarwal V; Misra DP; Rai MK; Kapoor A
Gene; 2018 Mar; 648():89-96. PubMed ID: 29309886
[TBL] [Abstract][Full Text] [Related]
7. 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; 61(2):143-7. PubMed ID: 23199516
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 25333979
[TBL] [Abstract][Full Text] [Related]
9. The SNP rs7865618 of 9p21.3 locus emerges as the most promising marker of coronary artery disease in the southern Indian population.
Manjula G; Pranavchand R; Kumuda I; Reddy BS; Reddy BM
Sci Rep; 2020 Dec; 10(1):21511. PubMed ID: 33298998
[TBL] [Abstract][Full Text] [Related]
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; 127(7):799-810. PubMed ID: 23315372
[TBL] [Abstract][Full Text] [Related]
11. Common SNP-based haplotype analysis of the 9p21.3 gene locus as predictor coronary artery disease in Tanzanian population.
Akan G; Kisenge P; Sanga TS; Mbugi E; Adolf I; Turkcan MK; Janabi M; Atalar F
Cell Mol Biol (Noisy-le-grand); 2019 Jul; 65(6):33-43. PubMed ID: 31472045
[TBL] [Abstract][Full Text] [Related]
12. Association Study of rs1333040 and rs1004638 Polymorphisms in the 9p21 Locus with Coronary Artery Disease in Southwest of Iran.
Golabgir Khademi K; Foroughmand AM; Galehdari H; Yazdankhah S; Pourmahdi Borujeni M; Shahbazi Z; Dinarvand P
Iran Biomed J; 2016; 20(2):122-7. PubMed ID: 26597055
[TBL] [Abstract][Full Text] [Related]
13. Association Study Between Coronary Artery Disease and rs1333049 Polymorphism at 9p21.3 Locus in Italian Population.
Pignataro P; Pezone L; Di Gioia G; Franco D; Iaccarino G; Iolascon A; Ciccarelli M; Capasso M
J Cardiovasc Transl Res; 2017 Dec; 10(5-6):455-458. PubMed ID: 28639227
[TBL] [Abstract][Full Text] [Related]
14. 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; 21(18):4021-9. PubMed ID: 22706276
[TBL] [Abstract][Full Text] [Related]
15. Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility.
Anderson JL; Horne BD; Kolek MJ; Muhlestein JB; Mower CP; Park JJ; May HT; Camp NJ; Carlquist JF
Am Heart J; 2008 Dec; 156(6):1155-1162.e2. PubMed ID: 19033013
[TBL] [Abstract][Full Text] [Related]
16. Genetic variants of chromosome 9p21.3 region associated with coronary artery disease and premature coronary artery disease in an Asian Indian population.
Kalpana B; Murthy DK; Balakrishna N; Aiyengar MT
Indian Heart J; 2019; 71(3):263-271. PubMed ID: 31543200
[TBL] [Abstract][Full Text] [Related]
17. Disease-associated polymorphisms in 9p21 are not associated with extreme longevity.
Congrains A; Kamide K; Hirose N; Arai Y; Oguro R; Nakama C; Imaizumi Y; Kawai T; Kusunoki H; Yamamoto H; Onishi-Takeya M; Takeya Y; Yamamoto K; Sugimoto K; Akasaka H; Saitoh S; Miura T; Awata N; Kato N; Katsuya T; Ikebe K; Gondo Y; Rakugi H
Geriatr Gerontol Int; 2015 Jun; 15(6):797-803. PubMed ID: 25257646
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 23091611
[TBL] [Abstract][Full Text] [Related]
19. 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; 470(7333):264-8. PubMed ID: 21307941
[TBL] [Abstract][Full Text] [Related]
20. The 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosis.
Chen SN; Ballantyne CM; Gotto AM; Marian AJ
BMC Cardiovasc Disord; 2009 Jan; 9():3. PubMed ID: 19173706
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]