Tomoike H - Search Results

1

BMPR2 mutations found in Japanese patients with familial and sporadic primary pulmonary hypertension.

Morisaki H, Nakanishi N, Kyotani S, Takashima A, Tomoike H, Morisaki T. Morisaki H, et al. Among authors: tomoike h. Hum Mutat. 2004 Jun;23(6):632. doi: 10.1002/humu.9251. Hum Mutat. 2004. PMID: 15146475

2

Leptin gene and leptin receptor gene polymorphisms are associated with sweet preference and obesity.

Mizuta E, Kokubo Y, Yamanaka I, Miyamoto Y, Okayama A, Yoshimasa Y, Tomoike H, Morisaki H, Morisaki T. Mizuta E, et al. Among authors: tomoike h. Hypertens Res. 2008 Jun;31(6):1069-77. doi: 10.1291/hypres.31.1069. Hypertens Res. 2008. PMID: 18716353

3

Association study of 11beta-hydroxysteroid dehydrogenase type 1 gene polymorphisms and metabolic syndrome in urban Japanese cohort.

Miyamoto Y, Morisaki H, Yamanaka I, Kokubo Y, Masuzaki H, Okayama A, Tomoike H, Nakao K, Okamura T, Yoshimasa Y, Morisaki T. Miyamoto Y, et al. Among authors: tomoike h. Diabetes Res Clin Pract. 2009 Aug;85(2):132-8. doi: 10.1016/j.diabres.2009.05.017. Epub 2009 Jun 16. Diabetes Res Clin Pract. 2009. PMID: 19535162

4

A novel Thr56Met mutation of the autosomal recessive hypercholesterolemia gene associated with hypercholesterolemia.

Harada K, Miyamoto Y, Morisaki H, Ohta N, Yamanaka I, Kokubo Y, Makino H, Harada-Shiba M, Okayama A, Tomoike H, Okamura T, Saito Y, Yoshimasa Y, Morisaki T. Harada K, et al. Among authors: tomoike h. J Atheroscler Thromb. 2010 Feb 26;17(2):131-40. doi: 10.5551/jat.2873. Epub 2010 Feb 3. J Atheroscler Thromb. 2010. PMID: 20124734 Free article.

5

Resistin gene variations are associated with the metabolic syndrome in Japanese men.

Miyamoto Y, Morisaki H, Kokubo Y, Yamanaka I, Tomoike H, Okayama A, Yoshimasa Y, Morisaki T. Miyamoto Y, et al. Among authors: tomoike h. Obes Res Clin Pract. 2009 May;3(2):I-II. doi: 10.1016/j.orcp.2008.11.003. Obes Res Clin Pract. 2009. PMID: 24345560

6

The role of a common TNNT2 polymorphism in cardiac hypertrophy.

Komamura K, Iwai N, Kokame K, Yasumura Y, Kim J, Yamagishi M, Morisaki T, Kimura A, Tomoike H, Kitakaze M, Miyatake K. Komamura K, et al. Among authors: tomoike h. J Hum Genet. 2004;49(3):129-133. doi: 10.1007/s10038-003-0121-4. Epub 2004 Feb 24. J Hum Genet. 2004. PMID: 14986170

7

Identification of genetic markers associated with high-density lipoprotein-cholesterol by genome-wide screening in a Japanese population: the Suita study.

Hiura Y, Shen CS, Kokubo Y, Okamura T, Morisaki T, Tomoike H, Yoshida T, Sakamoto H, Goto Y, Nonogi H, Iwai N. Hiura Y, et al. Among authors: tomoike h. Circ J. 2009 Jun;73(6):1119-26. doi: 10.1253/circj.cj-08-1101. Epub 2009 Apr 10. Circ J. 2009. PMID: 19359809 Free article.

8

Association of four genetic loci with uric acid levels and reduced renal function: the J-SHIPP Suita study.

Tabara Y, Kohara K, Kawamoto R, Hiura Y, Nishimura K, Morisaki T, Kokubo Y, Okamura T, Tomoike H, Iwai N, Miki T. Tabara Y, et al. Among authors: tomoike h. Am J Nephrol. 2010;32(3):279-286. doi: 10.1159/000318943. Epub 2010 Aug 13. Am J Nephrol. 2010. PMID: 20714133

9

Common variants in the ATP2B1 gene are associated with susceptibility to hypertension: the Japanese Millennium Genome Project.

Tabara Y, Kohara K, Kita Y, Hirawa N, Katsuya T, Ohkubo T, Hiura Y, Tajima A, Morisaki T, Miyata T, Nakayama T, Takashima N, Nakura J, Kawamoto R, Takahashi N, Hata A, Soma M, Imai Y, Kokubo Y, Okamura T, Tomoike H, Iwai N, Ogihara T, Inoue I, Tokunaga K, Johnson T, Caulfield M, Munroe P; Global Blood Pressure Genetics Consortium; Umemura S, Ueshima H, Miki T. Tabara Y, et al. Among authors: tomoike h. Hypertension. 2010 Nov;56(5):973-80. doi: 10.1161/HYPERTENSIONAHA.110.153429. Epub 2010 Oct 4. Hypertension. 2010. PMID: 20921432 Free PMC article.

10

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. Okuda T, et al. Among authors: tomoike h. J Hum Genet. 2002;47(8):387-94. doi: 10.1007/s100380200056. J Hum Genet. 2002. PMID: 12181638

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