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Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiency.
Fan X, Kremer Hovinga JA, Shirotani-Ikejima H, Eura Y, Hirai H, Honda S, Kokame K, Taleghani MM, von Krogh AS, Yoshida Y, Fujimura Y, Lämmle B, Miyata T. Fan X, et al. Among authors: honda s. Int J Hematol. 2016 Mar;103(3):283-91. doi: 10.1007/s12185-015-1933-7. Epub 2016 Feb 1. Int J Hematol. 2016. PMID: 26830967 Free article.
Analysis of genetic and predisposing factors in Japanese patients with atypical hemolytic uremic syndrome.
Fan X, Yoshida Y, Honda S, Matsumoto M, Sawada Y, Hattori M, Hisanaga S, Hiwa R, Nakamura F, Tomomori M, Miyagawa S, Fujimaru R, Yamada H, Sawai T, Ikeda Y, Iwata N, Uemura O, Matsukuma E, Aizawa Y, Harada H, Wada H, Ishikawa E, Ashida A, Nangaku M, Miyata T, Fujimura Y. Fan X, et al. Among authors: honda s. Mol Immunol. 2013 Jun;54(2):238-46. doi: 10.1016/j.molimm.2012.12.006. Epub 2013 Jan 8. Mol Immunol. 2013. PMID: 23314101
Polymorphisms in vitamin K-dependent gamma-carboxylation-related genes influence interindividual variability in plasma protein C and protein S activities in the general population.
Kimura R, Kokubo Y, Miyashita K, Otsubo R, Nagatsuka K, Otsuki T, Sakata T, Nagura J, Okayama A, Minematsu K, Naritomi H, Honda S, Sato K, Tomoike H, Miyata T. Kimura R, et al. Among authors: honda s. Int J Hematol. 2006 Dec;84(5):387-97. doi: 10.1532/IJH97.06082. Int J Hematol. 2006. PMID: 17189218 Clinical Trial.
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: honda s. 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
Integrin-linked kinase associated with integrin activation.
Honda S, Shirotani-Ikejima H, Tadokoro S, Maeda Y, Kinoshita T, Tomiyama Y, Miyata T. Honda S, et al. Blood. 2009 May 21;113(21):5304-13. doi: 10.1182/blood-2008-07-169136. Epub 2009 Mar 18. Blood. 2009. PMID: 19299337 Free article.
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: honda s. Blood Coagul Fibrinolysis. 2009 Jan;20(1):22-6. doi: 10.1097/MBC.0b013e328304e0b9. Blood Coagul Fibrinolysis. 2009. PMID: 20523161
Genotypes of vitamin K epoxide reductase, gamma-glutamyl carboxylase, and cytochrome P450 2C9 as determinants of daily warfarin dose in Japanese patients.
Kimura R, Miyashita K, Kokubo Y, Akaiwa Y, Otsubo R, Nagatsuka K, Otsuki T, Okayama A, Minematsu K, Naritomi H, Honda S, Tomoike H, Miyata T. Kimura R, et al. Among authors: honda s. Thromb Res. 2007;120(2):181-6. doi: 10.1016/j.thromres.2006.09.007. Epub 2006 Oct 17. Thromb Res. 2007. PMID: 17049586
1,941 results