Miyata T - Search Results

1

Genetic risk factors for deep vein thrombosis among Japanese: importance of protein S K196E mutation.

Miyata T, Kimura R, Kokubo Y, Sakata T. Miyata T, et al. Int J Hematol. 2006 Apr;83(3):217-23. doi: 10.1532/IJH97.A20514. Int J Hematol. 2006. PMID: 16720551 Review.

2

Haplotype of thrombomodulin gene associated with plasma thrombomodulin level and deep vein thrombosis in the Japanese population.

Sugiyama S, Hirota H, Kimura R, Kokubo Y, Kawasaki T, Suehisa E, Okayama A, Tomoike H, Hayashi T, Nishigami K, Kawase I, Miyata T. Sugiyama S, et al. Among authors: miyata t. Thromb Res. 2007;119(1):35-43. doi: 10.1016/j.thromres.2005.12.012. Epub 2006 Feb 28. Thromb Res. 2007. PMID: 16507317

3

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: miyata t. Int J Hematol. 2006 Dec;84(5):387-97. doi: 10.1532/IJH97.06082. Int J Hematol. 2006. PMID: 17189218 Clinical Trial.

4

A large deletion of the PROS1 gene in a deep vein thrombosis patient with protein S deficiency.

Yin T, Takeshita S, Sato Y, Sakata T, Shin Y, Honda S, Kawasaki T, Tsuji H, Kojima T, Madoiwa S, Sakata Y, Murata M, Ikeda Y, Miyata T. Yin T, et al. Among authors: miyata t. Thromb Haemost. 2007 Oct;98(4):783-9. doi: 10.1160/th07-03-0211. Thromb Haemost. 2007. PMID: 17938802

5

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. 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

6

Usefulness of antithrombin deficiency phenotypes for risk assessment of venous thromboembolism: type I deficiency as a strong risk factor for venous thromboembolism.

Mitsuguro M, Sakata T, Okamoto A, Kameda S, Kokubo Y, Tsutsumi Y, Sano M, Miyata T. Mitsuguro M, et al. Among authors: miyata t. Int J Hematol. 2010 Oct;92(3):468-73. doi: 10.1007/s12185-010-0687-5. Epub 2010 Sep 23. Int J Hematol. 2010. PMID: 20859710

7

Plasma protein S activity correlates with protein S genotype but is not sensitive to identify K196E mutant carriers.

Kimura R, Sakata T, Kokubo Y, Okamoto A, Okayama A, Tomoike H, Miyata T. Kimura R, et al. Among authors: miyata t. J Thromb Haemost. 2006 Sep;4(9):2010-3. doi: 10.1111/j.1538-7836.2006.02071.x. J Thromb Haemost. 2006. PMID: 16961608 Free article.

8

Three novel missense mutations of WNK4, a kinase mutated in inherited hypertension, in Japanese hypertensives: implication of clinical phenotypes.

Kamide K, Takiuchi S, Tanaka C, Miwa Y, Yoshii M, Horio T, Mannami T, Kokubo Y, Tomoike H, Kawano Y, Miyata T. Kamide K, et al. Among authors: miyata t. Am J Hypertens. 2004 May;17(5 Pt 1):446-9. doi: 10.1016/j.amjhyper.2003.12.020. Am J Hypertens. 2004. PMID: 15110905

9

Potential of free-form TFPI and PAI-1 to be useful markers of early atherosclerosis in a Japanese general population (the Suita Study): association with the intimal-medial thickness of carotid arteries.

Sakata T, Mannami T, Baba S, Kokubo Y, Kario K, Okamoto A, Kumeda K, Ohkura N, Katayama Y, Miyata T, Tomoike H, Kato H. Sakata T, et al. Among authors: miyata t. Atherosclerosis. 2004 Oct;176(2):355-60. doi: 10.1016/j.atherosclerosis.2004.05.017. Atherosclerosis. 2004. PMID: 15380459

10

Association of genetic polymorphisms of sodium-calcium exchanger 1 gene, NCX1, with hypertension in a Japanese general population.

Kokubo Y, Inamoto N, Tomoike H, Kamide K, Takiuchi S, Kawano Y, Tanaka C, Katanosaka Y, Wakabayashi S, Shigekawa M, Hishikawa O, Miyata T. Kokubo Y, et al. Among authors: miyata t. Hypertens Res. 2004 Oct;27(10):697-702. doi: 10.1291/hypres.27.697. Hypertens Res. 2004. PMID: 15785003 Free article.

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