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PUBMED FOR HANDHELDS

Journal Abstract Search


104 related items for PubMed ID: 16116695

  • 21. Genetic variation in coagulation factors II, V, VII and fatal MI.
    Mikkelsson J, Karhunen PJ.
    Thromb Haemost; 2002 Feb; 87(2):349-50. PubMed ID: 11858502
    [No Abstract] [Full Text] [Related]

  • 22. Haplotype effect of the matrix metalloproteinase-1 gene on risk of myocardial infarction.
    Pearce E, Tregouet DA, Samnegård A, Morgan AR, Cox C, Hamsten A, Eriksson P, Ye S.
    Circ Res; 2005 Nov 11; 97(10):1070-6. PubMed ID: 16210545
    [Abstract] [Full Text] [Related]

  • 23. A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study.
    Kardys I, Klaver CC, Despriet DD, Bergen AA, Uitterlinden AG, Hofman A, Oostra BA, Van Duijn CM, de Jong PT, Witteman JC.
    J Am Coll Cardiol; 2006 Apr 18; 47(8):1568-75. PubMed ID: 16630992
    [Abstract] [Full Text] [Related]

  • 24. Asp92Asn polymorphism in the myeloid IgA Fc receptor is associated with myocardial infarction in two disparate populations: CARE and WOSCOPS.
    Iakoubova OA, Tong CH, Chokkalingam AP, Rowland CM, Kirchgessner TG, Louie JZ, Ploughman LM, Sabatine MS, Campos H, Catanese JJ, Leong DU, Young BA, Lew D, Tsuchihashi Z, Luke MM, Packard CJ, Zerba KE, Shaw PM, Shepherd J, Devlin JJ, Sacks FM.
    Arterioscler Thromb Vasc Biol; 2006 Dec 18; 26(12):2763-8. PubMed ID: 17008591
    [Abstract] [Full Text] [Related]

  • 25. Apolipoprotein E, CI and B gene polymorphisms in a sample of patients with coronary heart disease in the Kuwaiti population.
    Al-Bustan SA, Alkhalaf M, Al-Rashdan I, Al-Otaibi S, Al-Baker E, Balding D, Alnaqeeb MA.
    Med Princ Pract; 2009 Dec 18; 18(4):294-9. PubMed ID: 19494537
    [Abstract] [Full Text] [Related]

  • 26. Haplotype and genotype effects of the F7 gene on circulating factor VII, coagulation activation markers and incident coronary heart disease in UK men.
    Ken-Dror G, Drenos F, Humphries SE, Talmud PJ, Hingorani AD, Kivimäki M, Kumari M, Bauer KA, Morrissey JH, Ireland HA.
    J Thromb Haemost; 2010 Nov 18; 8(11):2394-403. PubMed ID: 20735728
    [Abstract] [Full Text] [Related]

  • 27. Decreased risk for myocardial infarction and lower tumor necrosis factor-alpha levels in carriers of variants of the PDCD1 gene.
    Bennet AM, Alarcón-Riquelme M, Wiman B, de Faire U, Prokunina-Olsson L.
    Hum Immunol; 2006 Sep 18; 67(9):700-5. PubMed ID: 17002900
    [Abstract] [Full Text] [Related]

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  • 30. Glucocorticoid receptor gene and risk of cardiovascular disease.
    van den Akker EL, Koper JW, van Rossum EF, Dekker MJ, Russcher H, de Jong FH, Uitterlinden AG, Hofman A, Pols HA, Witteman JC, Lamberts SW.
    Arch Intern Med; 2008 Jan 14; 168(1):33-9. PubMed ID: 18195193
    [Abstract] [Full Text] [Related]

  • 31. The decanucleotide insertion/deletion polymorphism in the promoter region of the coagulation factor VII gene and the risk of familial myocardial infarction.
    Di Castelnuovo A, D'Orazio A, Amore C, Falanga A, Donati MB, Iacoviello L.
    Thromb Res; 2000 Apr 01; 98(1):9-17. PubMed ID: 10706929
    [Abstract] [Full Text] [Related]

  • 32. Association between PPARalpha gene polymorphisms and myocardial infarction.
    Reinhard W, Stark K, Sedlacek K, Fischer M, Baessler A, Neureuther K, Weber S, Kaess B, Wiedmann S, Mitsching S, Lieb W, Erdmann J, Meisinger C, Doering A, Tolle R, Jeron A, Riegger G, Hengstenberg C.
    Clin Sci (Lond); 2008 Nov 01; 115(10):301-8. PubMed ID: 18336366
    [Abstract] [Full Text] [Related]

  • 33. 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 15; 16(8):887-99. PubMed ID: 17324965
    [Abstract] [Full Text] [Related]

  • 34. The MCP-1 -2518 (A to G) single nucleotide polymorphism is not associated with myocardial infarction in the Czech population.
    Cermakova Z, Petrkova J, Arakelyan A, Drabek J, Mrazek F, Lukl J, Petrek M.
    Int J Immunogenet; 2005 Oct 15; 32(5):315-8. PubMed ID: 16164699
    [Abstract] [Full Text] [Related]

  • 35. A novel polymorphism in intron 1a of the human factor VII gene (G73A): study of a healthy Italian population and of 190 young survivors of myocardial infarction.
    Peyvandi F, Mannucci PM, Bucciarelli P, Zeinali S, Akhavan S, Sacchi E, Merlini PA, Perry DJ.
    Br J Haematol; 2000 Feb 15; 108(2):247-53. PubMed ID: 10691850
    [Abstract] [Full Text] [Related]

  • 36. Neutrophil elastase gene variation and coronary heart disease.
    Schönfelder J, Telgmann R, Nicaud V, Brand E, Dördelmann C, Rüssmann C, Beining K, Schmidt-Petersen K, Evans A, Kee F, Morrison C, Arveiler D, Cambien F, Paul M, Brand-Herrmann SM.
    Pharmacogenet Genomics; 2007 Aug 15; 17(8):629-37. PubMed ID: 17622939
    [Abstract] [Full Text] [Related]

  • 37. Polymorphisms in the factor VII gene and the risk of myocardial infarction.
    Mannucci PM.
    N Engl J Med; 2001 Feb 08; 344(6):458-9. PubMed ID: 11221609
    [No Abstract] [Full Text] [Related]

  • 38. Matrix metalloproteinase 1 promoter polymorphisms and risk of myocardial infarction: a case-control study in a Spanish population.
    Román-García P, Coto E, Reguero JR, Cannata-Andía JB, Lozano I, Avanzas P, Morís C, Rodríguez I.
    Coron Artery Dis; 2009 Sep 08; 20(6):383-6. PubMed ID: 19620856
    [Abstract] [Full Text] [Related]

  • 39. Common variants in the thrombomodulin gene as a risk for myocardial infarction in the north of Europe (HIFMECH Study).
    Konstantoulas C, Hawe E, Saut N, Yudkin JS, di Minno G, Margaglione M, Hamsten A, Humphries SE, Juhan-Vague I, Ireland H, HIFMECH Study Group.
    Thromb Haemost; 2004 Mar 08; 91(3):628-30. PubMed ID: 14983241
    [No Abstract] [Full Text] [Related]

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