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Association of Asn221Ser mutation in tissue factor pathway inhibitor-beta with plasma total tissue factor pathway inhibitor level.
Ishikawa J, Okada H, Kato H, Takeshita S, Honda S, Kawasaki T, Suehisa E, Tsuji H, Madoiwa S, Sakata Y, Kojima T, Murata M, Ikeda Y, Kokubo Y, Okamura T, Tomoike H, Miyata T. Ishikawa J, et al. Among authors: ikeda y. Blood Coagul Fibrinolysis. 2009 Jan;20(1):22-6. doi: 10.1097/MBC.0b013e328304e0b9. Blood Coagul Fibrinolysis. 2009. PMID: 20523161
Prevalence of genetic mutations in protein S, protein C and antithrombin genes in Japanese patients with deep vein thrombosis.
Miyata T, Sato Y, Ishikawa J, Okada H, Takeshita S, Sakata T, Kokame K, Kimura R, Honda S, Kawasaki T, Suehisa E, Tsuji H, Madoiwa S, Sakata Y, Kojima T, Murata M, Ikeda Y. Miyata T, et al. Among authors: ikeda y. Thromb Res. 2009 May;124(1):14-8. doi: 10.1016/j.thromres.2008.08.020. Epub 2008 Oct 26. Thromb Res. 2009. PMID: 18954896
Genetic analysis of hereditary factor X deficiency in a French patient of Sri Lankan ancestry: in vitro expression study identified Gly366Ser substitution as the molecular basis of the dysfunctional factor X.
Isshiki I, Favier R, Moriki T, Uchida T, Ishihara H, Van Dreden P, Murata M, Ikeda Y. Isshiki I, et al. Among authors: ikeda y. Blood Coagul Fibrinolysis. 2005 Jan;16(1):9-16. doi: 10.1097/00001721-200501000-00002. Blood Coagul Fibrinolysis. 2005. PMID: 15650540
Genetic risk factors for thrombophilia in Japanese.
Miyata T, Okada H, Kawasaki T, Tsuji H, Madoiwa S, Sakata Y, Kojima T, Murata M, Ikeda Y. Miyata T, et al. Among authors: ikeda y. Rinsho Ketsueki. 2009 May;50(5):381-8. Rinsho Ketsueki. 2009. PMID: 19483398 Review. No abstract available.
5,484 results