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100 related items for PubMed ID: 18003638

  • 1. High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project.
    Kato N, Miyata T, Tabara Y, Katsuya T, Yanai K, Hanada H, Kamide K, Nakura J, Kohara K, Takeuchi F, Mano H, Yasunami M, Kimura A, Kita Y, Ueshima H, Nakayama T, Soma M, Hata A, Fujioka A, Kawano Y, Nakao K, Sekine A, Yoshida T, Nakamura Y, Saruta T, Ogihara T, Sugano S, Miki T, Tomoike H.
    Hum Mol Genet; 2008 Feb 15; 17(4):617-27. PubMed ID: 18003638
    [Abstract] [Full Text] [Related]

  • 2. Replication of the Wellcome Trust genome-wide association study on essential hypertension in a Korean population.
    Hong KW, Jin HS, Cho YS, Lee JY, Lee JE, Cho NH, Shin C, Lee SH, Park HK, Oh B.
    Hypertens Res; 2009 Jul 15; 32(7):570-4. PubMed ID: 19424278
    [Abstract] [Full Text] [Related]

  • 3. 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 15; 17(2):311-9. PubMed ID: 18268114
    [Abstract] [Full Text] [Related]

  • 4. Association of TNFRSF4 gene polymorphisms with essential hypertension.
    Mashimo Y, Suzuki Y, Hatori K, Tabara Y, Miki T, Tokunaga K, Katsuya T, Ogihara T, Yamada M, Takahashi N, Makita Y, Nakayama T, Soma M, Hirawa N, Umemura S, Ohkubo T, Imai Y, Hata A.
    J Hypertens; 2008 May 15; 26(5):902-13. PubMed ID: 18398332
    [Abstract] [Full Text] [Related]

  • 5. Association of alpha2A-adrenergic receptor gene polymorphism with susceptibility to suicide in Japanese females.
    Fukutake M, Hishimoto A, Nishiguchi N, Nushida H, Ueno Y, Shirakawa O, Maeda K.
    Prog Neuropsychopharmacol Biol Psychiatry; 2008 Aug 01; 32(6):1428-33. PubMed ID: 18547701
    [Abstract] [Full Text] [Related]

  • 6. Genetic analysis of the atrial natriuretic peptide gene in essential hypertension.
    Kato N, Sugiyama T, Morita H, Nabika T, Kurihara H, Yamori Y, Yazaki Y.
    Clin Sci (Lond); 2000 Mar 01; 98(3):251-8. PubMed ID: 10677382
    [Abstract] [Full Text] [Related]

  • 7. [Implication of single nucleotide polymorphisms in association study: mitochondrial variations as another genetic markers for hypertension].
    Shoji M, Tsutaya S, Kasai T, Yasujima M.
    Rinsho Byori; 2002 May 01; 50(5):497-501. PubMed ID: 12078048
    [Abstract] [Full Text] [Related]

  • 8. Haplotype-based case-control study of the association between the guanylate cyclase activator 2B (GUCA2B, Uroguanylin) gene and essential hypertension.
    Yoshikawa Y, Nakayama T, Saito K, Hui P, Morita A, Sato N, Takahashi T, Tamura M, Sato I, Aoi N, Doba N, Hinohara S, Soma M, Usami R.
    Hypertens Res; 2007 Sep 01; 30(9):789-96. PubMed ID: 18037771
    [Abstract] [Full Text] [Related]

  • 9. Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome.
    Winkelmann J, Lichtner P, Schormair B, Uhr M, Hauk S, Stiasny-Kolster K, Trenkwalder C, Paulus W, Peglau I, Eisensehr I, Illig T, Wichmann HE, Pfister H, Golic J, Bettecken T, Pütz B, Holsboer F, Meitinger T, Müller-Myhsok B.
    Mov Disord; 2008 Feb 15; 23(3):350-8. PubMed ID: 18058820
    [Abstract] [Full Text] [Related]

  • 10. His595Tyr polymorphism in the methionine synthase reductase (MTRR) gene is associated with pancreatic cancer risk.
    Ohnami S, Sato Y, Yoshimura K, Ohnami S, Sakamoto H, Aoki K, Ueno H, Ikeda M, Morizane C, Shimada K, Sakamoto Y, Esaki M, Saito I, Hirose H, Saito D, Sugimura H, Kosuge T, Okusaka T, Yoshida T.
    Gastroenterology; 2008 Aug 15; 135(2):477-88. PubMed ID: 18515090
    [Abstract] [Full Text] [Related]

  • 11. Association of hypertension with single nucleotide polymorphisms in the quantitative trait locus for abdominal obesity-metabolic syndrome on chromosome 17.
    Cheung BM, Leung RY, Man YB, Ong KL, Wong LY, Lau CP, Lam KS.
    J Hum Hypertens; 2006 Jun 15; 20(6):419-25. PubMed ID: 16511504
    [Abstract] [Full Text] [Related]

  • 12. Association of novel promoter single nucleotide polymorphisms in vasopressin V1a receptor gene with essential hypertension in nonobese Japanese.
    Hasan KN, Shoji M, Sugimoto K, Tsutaya S, Matsuda E, Kudo R, Nakaji S, Suda T, Yasujima M.
    J Hum Hypertens; 2007 Oct 15; 21(10):825-7. PubMed ID: 17653244
    [Abstract] [Full Text] [Related]

  • 13. Verification of 525 coding SNPs in 179 hypertension candidate genes in the Japanese population: identification of 159 SNPs in 93 genes.
    Okuda T, Fujioka Y, Kamide K, Kawano Y, Goto Y, Yoshimasa Y, Tomoike H, Iwai N, Hanai S, Miyata T.
    J Hum Genet; 2002 Oct 15; 47(8):387-94. PubMed ID: 12181638
    [Abstract] [Full Text] [Related]

  • 14. Association study of calcitonin-receptor-like receptor gene in essential hypertension.
    Sano M, Kuroi N, Nakayama T, Sato N, Izumi Y, Soma M, Kokubun S.
    Am J Hypertens; 2005 Mar 15; 18(3):403-8. PubMed ID: 15797661
    [Abstract] [Full Text] [Related]

  • 15. The microsatellite alleles on chromosome 1 associated with essential hypertension and blood pressure levels.
    Nakayama T, Soma M, Kanmatsuse K, Kokubun S.
    J Hum Hypertens; 2004 Nov 15; 18(11):823-8. PubMed ID: 15190264
    [Abstract] [Full Text] [Related]

  • 16. Identification of hypertension-susceptibility genes and pathways by a systemic multiple candidate gene approach: the millennium genome project for hypertension.
    Kohara K, Tabara Y, Nakura J, Imai Y, Ohkubo T, Hata A, Soma M, Nakayama T, Umemura S, Hirawa N, Ueshima H, Kita Y, Ogihara T, Katsuya T, Takahashi N, Tokunaga K, Miki T.
    Hypertens Res; 2008 Feb 15; 31(2):203-12. PubMed ID: 18360038
    [Abstract] [Full Text] [Related]

  • 17. [Linkage analysis of the polymorphism at D17S1878 site with essential hypertension].
    Fu LY, Zhao YY, Shi JP, Li H, Wang WL, Lu JY, Liu H.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2006 Apr 15; 28(2):129-33. PubMed ID: 16733890
    [Abstract] [Full Text] [Related]

  • 18. High-resolution whole-genome association study of Parkinson disease.
    Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PV, Frazer KA, Cox DR, Ballinger DG.
    Am J Hum Genet; 2005 Nov 15; 77(5):685-93. PubMed ID: 16252231
    [Abstract] [Full Text] [Related]

  • 19. Nonsynonymous coding single-nucleotide polymorphisms spanning the genome in relation to glioblastoma survival and age at diagnosis.
    Wrensch M, McMillan A, Wiencke J, Wiemels J, Kelsey K, Patoka J, Jones H, Carlton V, Miike R, Sison J, Moghadassi M, Prados M.
    Clin Cancer Res; 2007 Jan 01; 13(1):197-205. PubMed ID: 17200355
    [Abstract] [Full Text] [Related]

  • 20. A new measure of the effective number of tests, a practical tool for comparing families of non-independent significance tests.
    Galwey NW.
    Genet Epidemiol; 2009 Nov 01; 33(7):559-68. PubMed ID: 19217024
    [Abstract] [Full Text] [Related]

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