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308 related items for PubMed ID: 18336366

  • 1. 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; 115(10):301-8. PubMed ID: 18336366
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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 15; 111(5):333-40. PubMed ID: 16822235
    [Abstract] [Full Text] [Related]

  • 4. Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction.
    Ozaki K, Ohnishi Y, Iida A, Sekine A, Yamada R, Tsunoda T, Sato H, Sato H, Hori M, Nakamura Y, Tanaka T.
    Nat Genet; 2002 Dec 15; 32(4):650-4. PubMed ID: 12426569
    [Abstract] [Full Text] [Related]

  • 5. Fibrinogen genes and myocardial infarction: a haplotype analysis.
    Koch W, Hoppmann P, Biele J, Mueller JC, Schömig A, Kastrati A.
    Arterioscler Thromb Vasc Biol; 2008 Apr 15; 28(4):758-63. PubMed ID: 18202324
    [Abstract] [Full Text] [Related]

  • 6. Association of PPARalpha gene polymorphisms and lipid serum levels in a Brazilian elderly population.
    Chen ES, Mazzotti DR, Furuya TK, Cendoroglo MS, Ramos LR, Araujo LQ, Burbano RR, Smith Mde A.
    Exp Mol Pathol; 2010 Feb 15; 88(1):197-201. PubMed ID: 19822141
    [Abstract] [Full Text] [Related]

  • 7. Association of transforming growth factor-beta1 gene polymorphisms with myocardial infarction in patients with angiographically proven coronary heart disease.
    Koch W, Hoppmann P, Mueller JC, Schömig A, Kastrati A.
    Arterioscler Thromb Vasc Biol; 2006 May 15; 26(5):1114-9. PubMed ID: 16543493
    [Abstract] [Full Text] [Related]

  • 8. Common polymorphisms in the cannabinoid CB2 receptor gene (CNR2) are not associated with myocardial infarction and cardiovascular risk factors.
    Reinhard W, Stark K, Neureuther K, Sedlacek K, Fischer M, Baessler A, Weber S, Kaess B, Wiedmann S, Erdmann J, Lieb W, Jeron A, Riegger G, Hengstenberg C.
    Int J Mol Med; 2008 Aug 15; 22(2):165-74. PubMed ID: 18636169
    [Abstract] [Full Text] [Related]

  • 9. Multiple less common genetic variants explain the association of the cholesteryl ester transfer protein gene with coronary artery disease.
    Horne BD, Camp NJ, Anderson JL, Mower CP, Clarke JL, Kolek MJ, Carlquist JF, Intermountain Heart Collaborative Study Group.
    J Am Coll Cardiol; 2007 May 22; 49(20):2053-60. PubMed ID: 17512363
    [Abstract] [Full Text] [Related]

  • 10. Inflammatory cytokine gene variants in coronary artery disease patients in Greece.
    Manginas A, Tsiavou A, Chaidaroglou A, Giamouzis G, Degiannis D, Panagiotakos D, Cokkinos DV.
    Coron Artery Dis; 2008 Dec 22; 19(8):575-82. PubMed ID: 19005292
    [Abstract] [Full Text] [Related]

  • 11. Common variation in cytochrome P450 epoxygenase genes and the risk of incident nonfatal myocardial infarction and ischemic stroke.
    Marciante KD, Totah RA, Heckbert SR, Smith NL, Lemaitre RN, Lumley T, Rice KM, Hindorff LA, Bis JC, Hartman B, Psaty BM.
    Pharmacogenet Genomics; 2008 Jun 22; 18(6):535-43. PubMed ID: 18496133
    [Abstract] [Full Text] [Related]

  • 12. Extensive genotyping of the BDNF and NTRK2 genes define protective haplotypes against obsessive-compulsive disorder.
    Alonso P, Gratacòs M, Menchón JM, Saiz-Ruiz J, Segalàs C, Baca-García E, Labad J, Fernández-Piqueras J, Real E, Vaquero C, Pérez M, Dolengevich H, González JR, Bayés M, de Cid R, Vallejo J, Estivill X.
    Biol Psychiatry; 2008 Mar 15; 63(6):619-28. PubMed ID: 17884018
    [Abstract] [Full Text] [Related]

  • 13. Single nucleotide polymorphisms at the adiponectin locus and risk of coronary heart disease in men and women.
    Pischon T, Pai JK, Manson JE, Hu FB, Rexrode KM, Hunter D, Rimm EB.
    Obesity (Silver Spring); 2007 Aug 15; 15(8):2051-60. PubMed ID: 17712123
    [Abstract] [Full Text] [Related]

  • 14. Genotypes and haplotypes predisposing to myocardial infarction: a multilocus case-control study.
    Tobin MD, Braund PS, Burton PR, Thompson JR, Steeds R, Channer K, Cheng S, Lindpaintner K, Samani NJ.
    Eur Heart J; 2004 Mar 15; 25(6):459-67. PubMed ID: 15039125
    [Abstract] [Full Text] [Related]

  • 15. Association between C1019T polymorphism of connexin37 and acute myocardial infarction: a study in patients from Sicily.
    Listì F, Candore G, Lio D, Russo M, Colonna-Romano G, Caruso M, Hoffmann E, Caruso C.
    Int J Cardiol; 2005 Jul 10; 102(2):269-71. PubMed ID: 15982495
    [Abstract] [Full Text] [Related]

  • 16. Lack of association between a common polymorphism near the INSIG2 gene and BMI, myocardial infarction, and cardiovascular risk factors.
    Wiedmann S, Neureuther K, Stark K, Reinhard W, Kallmünzer B, Baessler A, Fischer M, Linsel-Nitschke P, Erdmann J, Schunkert H, Hengstenberg C.
    Obesity (Silver Spring); 2009 Jul 10; 17(7):1390-5. PubMed ID: 19197259
    [Abstract] [Full Text] [Related]

  • 17. Germline variations of the MALT1 gene as risk factors in the development of primary gastric B-cell lymphoma.
    Hellmig S, Bartscht T, Fischbach W, Ott SJ, Rosenstiel P, Klapper W, Fölsch UR, Schreiber S.
    Eur J Cancer; 2009 Jul 10; 45(10):1865-70. PubMed ID: 19394813
    [Abstract] [Full Text] [Related]

  • 18. Associations with myocardial infarction of six polymorphisms selected from a three-stage genome-wide association study.
    Horne BD, Carlquist JF, Muhlestein JB, Nicholas ZP, Anderson JL, Intermountain Heart Collaborative Study Group.
    Am Heart J; 2007 Nov 10; 154(5):969-75. PubMed ID: 17967605
    [Abstract] [Full Text] [Related]

  • 19. Variants in the coagulation factor 2 receptor (F2R) gene influence the risk of myocardial infarction in men through an interaction with interleukin 6 serum levels.
    Gigante B, Vikström M, Meuzelaar LS, Chernogubova E, Silveira A, Hooft FV, Hamsten A, de Faire U.
    Thromb Haemost; 2009 May 10; 101(5):943-53. PubMed ID: 19404549
    [Abstract] [Full Text] [Related]

  • 20. Large-scale evaluation of genetic variants in candidate genes for colorectal cancer risk in the Nurses' Health Study and the Health Professionals' Follow-up Study.
    Hazra A, Chanock S, Giovannucci E, Cox DG, Niu T, Fuchs C, Willett WC, Hunter DJ.
    Cancer Epidemiol Biomarkers Prev; 2008 Feb 10; 17(2):311-9. PubMed ID: 18268114
    [Abstract] [Full Text] [Related]

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