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Journal Abstract Search

151 related items for PubMed ID: 19404551

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  • 9. Association of genetic variants with chronic kidney disease in Japanese individuals.
    Yoshida T, Kato K, Fujimaki T, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Tanaka M, Nozawa Y, Kimura G, Yamada Y.
    Clin J Am Soc Nephrol; 2009 May; 4(5):883-90. PubMed ID: 19406964
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  • 11. Association of gene polymorphisms with chronic kidney disease in Japanese individuals.
    Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y.
    Int J Mol Med; 2009 Oct; 24(4):539-47. PubMed ID: 19724895
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  • 13. Association of polymorphisms of BTN2A1 and ILF3 with myocardial infarction in Japanese individuals with or without hypertension, diabetes mellitus or chronic kidney disease.
    Yoshida T, Kato K, Oguri M, Horibe H, Kawamiya T, Yokoi K, Fujimaki T, Watanabe S, Satoh K, Aoyagi Y, Tanaka M, Yoshida H, Shinkai S, Nozawa Y, Yamada Y.
    Int J Mol Med; 2011 May; 27(5):745-52. PubMed ID: 21347509
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  • 17. Association of gene polymorphisms with chronic kidney disease in high- or low-risk subjects defined by conventional risk factors.
    Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Nozawa Y, Yamada Y.
    Int J Mol Med; 2009 Jun; 23(6):785-92. PubMed ID: 19424605
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  • 18. Association of a polymorphism of BCHE with ischemic stroke in Japanese individuals with chronic kidney disease.
    Oguri M, Kato K, Yokoi K, Yoshida T, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Tanaka M, Nozawa Y, Yamada Y.
    Mol Med Rep; 2009 Jun; 2(5):779-85. PubMed ID: 21475901
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  • 19. Association of a polymorphism of the interleukin 6 receptor gene with chronic kidney disease in Japanese individuals.
    Horibe H, Fujimaki T, Oguri M, Kato K, Matsuoka R, Abe S, Tokoro F, Arai M, Noda T, Watanabe S, Yamada Y.
    Nephrology (Carlton); 2015 Apr; 20(4):273-8. PubMed ID: 25524550
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  • 20. Identification of a glutamic acid repeat polymorphism of ALMS1 as a novel genetic risk marker for early-onset myocardial infarction by genome-wide linkage analysis.
    Ichihara S, Yamamoto K, Asano H, Nakatochi M, Sukegawa M, Ichihara G, Izawa H, Hirashiki A, Takatsu F, Umeda H, Iwase M, Inagaki H, Hirayama H, Sone T, Nishigaki K, Minatoguchi S, Cho MC, Jang Y, Kim HS, Park JE, Tada-Oikawa S, Kitajima H, Matsubara T, Sunagawa K, Shimokawa H, Kimura A, Lee JY, Murohara T, Inoue I, Yokota M.
    Circ Cardiovasc Genet; 2013 Dec; 6(6):569-78. PubMed ID: 24122612
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