131 related articles for article (PubMed ID: 21511257)
1. The chromosome 9p21 region and myocardial infarction in a European population.
Koch W; Türk S; Erl A; Hoppmann P; Pfeufer A; King L; Schömig A; Kastrati A
Atherosclerosis; 2011 Jul; 217(1):220-6. PubMed ID: 21511257
[TBL] [Abstract][Full Text] [Related]
2. Extended evidence for association between the melanoma inhibitory activity 3 gene and myocardial infarction.
Koch W; Schatke A; Wolferstetter H; Mueller JC; Schömig A; Kastrati A
Thromb Haemost; 2011 Apr; 105(4):670-5. PubMed ID: 21264445
[TBL] [Abstract][Full Text] [Related]
3. [Genetic predictors of myocardial infarction in subjects of young age].
Shesternia PA; Nikulina SIu; Shul'man VA; Martynova EA; Demkina AI; Orlov PS; Maksimov VN; Voevoda MI
Kardiologiia; 2013; 53(7):4-8. PubMed ID: 24087953
[TBL] [Abstract][Full Text] [Related]
4. Polymorphisms of the NOS3 gene and risk of myocardial infarction in the Tunisian population.
Kallel A; Sbaï MH; Sediri Y; Abdessalem S; Mourali MS; Feki M; Mechmeche R; Jemaa R; Kaabachi N
Cytokine; 2013 Dec; 64(3):646-51. PubMed ID: 24095258
[TBL] [Abstract][Full Text] [Related]
5. Two chromosome 9p21 haplotype blocks distinguish between coronary artery disease and myocardial infarction risk.
Fan M; Dandona S; McPherson R; Allayee H; Hazen SL; Wells GA; Roberts R; Stewart AF
Circ Cardiovasc Genet; 2013 Aug; 6(4):372-80. PubMed ID: 23729007
[TBL] [Abstract][Full Text] [Related]
6. A common variant on chromosome 9p21 affects the risk of myocardial infarction.
Helgadottir A; Thorleifsson G; Manolescu A; Gretarsdottir S; Blondal T; Jonasdottir A; Jonasdottir A; Sigurdsson A; Baker A; Palsson A; Masson G; Gudbjartsson DF; Magnusson KP; Andersen K; Levey AI; Backman VM; Matthiasdottir S; Jonsdottir T; Palsson S; Einarsdottir H; Gunnarsdottir S; Gylfason A; Vaccarino V; Hooper WC; Reilly MP; Granger CB; Austin H; Rader DJ; Shah SH; Quyyumi AA; Gulcher JR; Thorgeirsson G; Thorsteinsdottir U; Kong A; Stefansson K
Science; 2007 Jun; 316(5830):1491-3. PubMed ID: 17478679
[TBL] [Abstract][Full Text] [Related]
7. Chromosome 9p21 genetic variants are associated with myocardial infarction but not with ischemic stroke in a Taiwanese population.
Lin HF; Tsai PC; Liao YC; Lin TH; Tai CT; Juo SH; Lin RT
J Investig Med; 2011 Aug; 59(6):926-30. PubMed ID: 21415773
[TBL] [Abstract][Full Text] [Related]
8. 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; 16(8):887-99. PubMed ID: 17324965
[TBL] [Abstract][Full Text] [Related]
9. Plasma fibrinogen concentration predicts the risk of myocardial infarction differently in various parts of Europe: effects of beta-fibrinogen genotype and environmental factors. The HIFMECH Study.
Mannila MN; Silveira A; Hawe E; Eriksson P; Aillaud MF; Juhan-Vague I; Yudkin J; Margaglione M; di Minno G; Mussoni L; Tremoli E; Humphries S; Hamsten A;
Thromb Haemost; 2004 Dec; 92(6):1240-9. PubMed ID: 15583729
[TBL] [Abstract][Full Text] [Related]
10. Chromosome 9p21 polymorphism is associated with myocardial infarction but not with clinical outcome in Han Chinese.
Peng WH; Lu L; Zhang Q; Zhang RY; Wang LJ; Yan XX; Chen QJ; Shen WF
Clin Chem Lab Med; 2009; 47(8):917-22. PubMed ID: 19548844
[TBL] [Abstract][Full Text] [Related]
11. CDKN2B gene expression is affected by 9p21.3 rs10757278 in CAD patients, six months after the MI.
Zivotić I; Djurić T; Stanković A; Milasinovic D; Stankovic G; Dekleva M; Marković Nikolić N; Alavantić D; Zivković M
Clin Biochem; 2019 Nov; 73():70-76. PubMed ID: 31386834
[TBL] [Abstract][Full Text] [Related]
12. 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):144-150. PubMed ID: 18066490
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 24365123
[TBL] [Abstract][Full Text] [Related]
14. Association study of ACE2 (angiotensin I-converting enzyme 2) gene polymorphisms with coronary heart disease and myocardial infarction in a Chinese Han population.
Yang W; Huang W; Su S; Li B; Zhao W; Chen S; Gu D
Clin Sci (Lond); 2006 Nov; 111(5):333-40. PubMed ID: 16822235
[TBL] [Abstract][Full Text] [Related]
15. 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;
BMC Cardiovasc Disord; 2011 Mar; 11():9. PubMed ID: 21385355
[TBL] [Abstract][Full Text] [Related]
16. Influence of fibrinogen beta-chain gene variations on risk of myocardial infarction in a Chinese Han population.
Lu XF; Yu HJ; Zhou XY; Wang LY; Huang JF; Gu DF
Chin Med J (Engl); 2008 Aug; 121(16):1549-53. PubMed ID: 18982866
[TBL] [Abstract][Full Text] [Related]
17. Expression pattern in human macrophages dependent on 9p21.3 coronary artery disease risk locus.
Zollbrecht C; Grassl M; Fenk S; Höcherl R; Hubauer U; Reinhard W; Esslinger UB; Ebert S; Langmann T; Stark K; Hengstenberg C
Atherosclerosis; 2013 Apr; 227(2):244-9. PubMed ID: 23375685
[TBL] [Abstract][Full Text] [Related]
18. Association between polymorphisms rs1333040 and rs7865618 of chromosome 9p21 and sporadic brain arteriovenous malformations.
Sturiale CL; Fontanella MM; Gatto I; Puca A; Giarretta I; D'Arrigo S; Lofrese G; Rainero I; Gallone S; Pinessi L; Ducati A; Maira G; Pola R
Cerebrovasc Dis; 2014; 37(4):290-5. PubMed ID: 24820060
[TBL] [Abstract][Full Text] [Related]
19. Do allelic variants of the connexin37 1019 gene polymorphism differentially predict for coronary artery disease and myocardial infarction?
Wong CW; Christen T; Pfenniger A; James RW; Kwak BR
Atherosclerosis; 2007 Apr; 191(2):355-61. PubMed ID: 16677656
[TBL] [Abstract][Full Text] [Related]
20. Lack of association of two common polymorphisms on 9p21 with risk of coronary heart disease and myocardial infarction; results from a prospective cohort study.
Dehghan A; van Hoek M; Sijbrands EJ; Oostra BA; Hofman A; van Duijn CM; Witteman JC
BMC Med; 2008 Oct; 6():30. PubMed ID: 18925945
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
