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Results: 1 to 20 of 64

1.

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, Piťha J.

Mol Biol Rep. 2015 Mar 26. [Epub ahead of print]

PMID:
25809277
2.

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, Francisco Muñoz-Valle J, 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.

3.

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.

PMID:
25034076
4.

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.

PMID:
25034075
5.

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.

PMID:
24898316
6.

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.

7.

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
8.

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
9.

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.

10.

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.

11.

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.

12.
13.

[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
14.

[Elevated coronary mortality in Mauritius: risk factors and genetic analyses].

Baligadoo S.

Bull Acad Natl Med. 2012 Oct;196(7):1381-94; discussion 1394-6. French.

PMID:
23815022
15.

Update on Kawasaki disease: epidemiology, aetiology and pathogenesis.

Yim D, Curtis N, Cheung M, Burgner D.

J Paediatr Child Health. 2013 Sep;49(9):704-8. doi: 10.1111/jpc.12172. Epub 2013 Apr 7. Review.

PMID:
23560706
16.

FOXP3 genetic variant and risk of acute coronary syndrome in Chinese Han population.

Yang Q, Chen Y, Yong W.

Cell Biochem Funct. 2013 Oct;31(7):599-602. doi: 10.1002/cbf.2945. Epub 2013 Jan 9.

PMID:
23299803
17.

Influence of 23 coronary artery disease variants on recurrent myocardial infarction or cardiac death: the GRACE Genetics Study.

Wauters E, Carruthers KF, Buysschaert I, Dunbar DR, Peuteman G, Belmans A, Budaj A, Van de Werf F, Lambrechts D, Fox KA.

Eur Heart J. 2013 Apr;34(13):993-1001. doi: 10.1093/eurheartj/ehs389. Epub 2012 Nov 15.

18.

Near patient anti-platelet response testing over time and gene analysis in patients admitted with acute coronary syndromes.

Amoah V, Storey RF, Worrall AP, Goodridge K, Lovatt T, Smallwood A, Armesilla AL, Nevill AM, Cotton JM.

Platelets. 2013;24(8):643-8. doi: 10.3109/09537104.2012.733046. Epub 2012 Nov 13.

PMID:
23148794
19.

Genetic testing in patients with acute coronary syndrome undergoing percutaneous coronary intervention: a cost-effectiveness analysis.

Lala A, Berger JS, Sharma G, Hochman JS, Scott Braithwaite R, Ladapo JA.

J Thromb Haemost. 2013 Jan;11(1):81-91. doi: 10.1111/jth.12059.

PMID:
23137413
20.

Clinical and genetic association of serum paraoxonase and arylesterase activities with cardiovascular risk.

Tang WH, Hartiala J, Fan Y, Wu Y, Stewart AF, Erdmann J, Kathiresan S; CARDIoGRAM Consortium, Roberts R, McPherson R, Allayee H, Hazen SL.

Arterioscler Thromb Vasc Biol. 2012 Nov;32(11):2803-12. doi: 10.1161/ATVBAHA.112.253930. Epub 2012 Sep 13.

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