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Items: 1 to 20 of 71

1.

Association of Polymorphisms (rs 1799782, rs25489 and rs25487) in XRCC1 and (rs 13181) XPD genes with Acute Coronary Artery Syndrome in Subjects from Multan, Pakistan.

Hameed H, Faryal M, Aslam MA, Akbar A, Saad AB, Pasha MB, Latif M, Rehan Sadiq Shaikh RR, Ali M, Iqbal F.

Pak J Pharm Sci. 2016 May;29(3):869-76.

PMID:
27166553
2.

Gene mutations of platelet glycoproteins and response to tirofiban in acute coronary syndrome.

Mansur AP, Roggerio A, Takada JY, Caribé PM, Avakian SD, Strunz CM.

Sao Paulo Med J. 2016 Jan 19. pii: S1516-31802016005001103. [Epub ahead of print]

3.

Relation Between Family History of Premature Coronary Artery Disease and the Risk of Death in Patients With Coronary Artery Disease.

Abdi-Ali A, Shaheen A, Southern D, Zhang M, Knudtson M, White J, Graham M, James MT, Wilton SB.

Am J Cardiol. 2016 Feb 1;117(3):353-8. doi: 10.1016/j.amjcard.2015.11.008. Epub 2015 Nov 18.

PMID:
26723106
4.

Utility of a genetic risk score to predict recurrent cardiovascular events 1 year after an acute coronary syndrome: A pooled analysis of the RISCA, PRAXY, and TRIUMPH cohorts.

Labos C, Martinez SC, Leo Wang RH, Lenzini PA, Pilote L, Bogaty P, Brophy JM, Engert JC, Cresci S, Thanassoulis G.

Atherosclerosis. 2015 Sep;242(1):261-7. doi: 10.1016/j.atherosclerosis.2015.07.029. Epub 2015 Jul 17.

PMID:
26232166
5.

Unveiling specific triggers and precipitating factors for fatal cardiac events in inherited arrhythmia syndromes.

Nakajima T, Kaneko Y, Kurabayashi M.

Circ J. 2015;79(6):1185-92. doi: 10.1253/circj.CJ-15-0322. Epub 2015 Apr 30. Review.

6.

Rs6922269 marker at the MTHFD1L gene predict cardiovascular mortality in males after acute coronary syndrome.

Hubacek JA, Staněk V, Gebauerová M, Poledne R, Aschermann M, Skalická H, Matoušková J, Kruger A, Pěnička M, Hrabáková H, Veselka J, Hájek P, Lánská V, Adámková V, Pitˇha J.

Mol Biol Rep. 2015 Aug;42(8):1289-93. doi: 10.1007/s11033-015-3870-1. Epub 2015 Mar 26.

PMID:
25809277
7.

The -844 G>A PAI-1 polymorphism is associated with acute coronary syndrome in Mexican population.

García-González IJ, Valle Y, Sandoval-Pinto E, Valdés-Alvarado E, Valdez-Haro A, Muñoz-Valle JF, Flores-Salinas HE, Figuera-Villanueva LE, Dávalos-Rodríguez NO, Padilla-Gutiérrez JR.

Dis Markers. 2015;2015:460974. doi: 10.1155/2015/460974. Epub 2015 Feb 19.

8.

Impact of gene polymorphisms, platelet reactivity, and the SYNTAX score on 1-year clinical outcomes in patients with non-ST-segment elevation acute coronary syndrome undergoing percutaneous coronary intervention: the GEPRESS study.

Palmerini T, Calabrò P, Piscione F, De Servi S, Cattaneo M, Maffeo D, Toso A, Bartorelli A, Palmieri C, De Carlo M, Capodanno D, Barozzi C, Tomasi L, Della Riva D, Mariani A, Taglieri N, Reggiani LB, Bianchi R, De Rosa R, Mariani M, Podda G, Généreux P, Stone GW, Angiolillo DJ.

JACC Cardiovasc Interv. 2014 Oct;7(10):1117-27. doi: 10.1016/j.jcin.2014.04.020. Epub 2014 Sep 17.

9.

Reply: The importance of genotype variation beyond different antiplatelet therapy in nonresponder patients.

Aradi D, Komócsi A.

J Am Coll Cardiol. 2014 Jul 22;64(3):334. doi: 10.1016/j.jacc.2014.04.037. No abstract available. Erratum in: J Am Coll Cardiol. 2014 Jul 22:64(3):335.

10.

The importance of genotype variation beyond different antiplatelet therapy in nonresponder patients.

Sardella G, Calcagno S.

J Am Coll Cardiol. 2014 Jul 22;64(3):333-4. doi: 10.1016/j.jacc.2014.02.613. No abstract available.

11.

Strategies to reduce bleeding risk in acute coronary syndromes and percutaneous coronary intervention: new and emerging pharmacotherapeutic considerations.

Coons JC, Miller T.

Pharmacotherapy. 2014 Sep;34(9):973-90. doi: 10.1002/phar.1447. Epub 2014 Jun 5. Review.

PMID:
24898316
12.

The SNP rs1883832 in CD40 gene and risk of atherosclerosis in Chinese population: a meta-analysis.

Yun Y, Ma C, Ma X.

PLoS One. 2014 May 14;9(5):e97289. doi: 10.1371/journal.pone.0097289. eCollection 2014.

13.

Cys327Cys polymorphism of the PAPP-A gene (pregnancy associated plasma protein A) is related to mortality of long term hemodialysis patients.

Kalousová M, Jáchymová M, Muravská A, Kuběna AA, Dusilová-Sulková S, Tesař V, Zima T.

Clin Biochem. 2014 May;47(7-8):578-83. doi: 10.1016/j.clinbiochem.2014.03.006. Epub 2014 Mar 22.

PMID:
24667032
14.

Genetic polymorphism rs6922269 in the MTHFD1L gene is associated with survival and baseline active vitamin B12 levels in post-acute coronary syndromes patients.

Palmer BR, Slow S, Ellis KL, Pilbrow AP, Skelton L, Frampton CM, Palmer SC, Troughton RW, Yandle TG, Doughty RN, Whalley GA, Lever M, George PM, Chambers ST, Ellis C, Richards AM, Cameron VA.

PLoS One. 2014 Mar 11;9(3):e89029. doi: 10.1371/journal.pone.0089029. eCollection 2014.

15.

Association of endothelial nitric oxide synthase (eNOS) gene polymorphism (Glu 298 Asp) with coronary artery disease in subjects from Multan, Pakistan.

Taqddus A, Saad AB, Pasha B, Latif M, Safdar S, Shaikh RS, Ali M, Iqbal F.

Pak J Pharm Sci. 2014 Mar;27(2):357-63.

PMID:
24577926
16.

Relation between K469E gene polymorphism of ICAM-1 and recurrence of ACS and cardiovascular mortality.

Liu LZ, Wu EP, Liu HL.

Asian Pac J Trop Med. 2013 Nov;6(11):916-20. doi: 10.1016/S1995-7645(13)60164-9.

17.

Cytochrome CYP2C19 polymorphism and risk of adverse clinical events in clopidogrel-treated patients: a meta-analysis based on 23,035 subjects.

Mao L, Jian C, Changzhi L, Dan H, Suihua H, Wenyi T, Wei W.

Arch Cardiovasc Dis. 2013 Oct;106(10):517-27. doi: 10.1016/j.acvd.2013.06.055. Epub 2013 Sep 27. Review.

18.

Single nucleotide polymorphisms in cholesteryl ester transfer protein gene and recurrent coronary heart disease or mortality in patients with established atherosclerosis.

Virani SS, Lee VV, Brautbar A, Grove ML, Nambi V, Alam M, Elayda M, Wilson JM, Willerson JT, Boerwinkle E, Ballantyne CM.

Am J Cardiol. 2013 Nov 1;112(9):1287-92. doi: 10.1016/j.amjcard.2013.05.073. Epub 2013 Jul 25.

19.
20.

[Relevance of CYP2C19 2 regarding platelet reactivity in patients with acute coronary syndrome treated with clopidogrel].

Cano P, Consuegra-Sánchez L, Conesa P, Torres-Moreno D, Jaulent L, Dau D, Picó F, Villegas M.

Med Clin (Barc). 2014 Jul 7;143(1):6-12. doi: 10.1016/j.medcli.2013.04.042. Epub 2013 Jul 10. Spanish.

PMID:
23850044
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