Kawata S - Search Results

1

Association of an intronic haplotype of the LIPC gene with hyperalphalipoproteinemia in two independent populations.

Iijima H, Emi M, Wada M, Daimon M, Toriyama S, Koyano S, Sato H, Hopkins PN, Hunt SC, Kubota I, Kawata S, Kato T. Iijima H, et al. Among authors: kawata s. J Hum Genet. 2008;53(3):193-200. doi: 10.1007/s10038-007-0236-0. Epub 2007 Dec 27. J Hum Genet. 2008. PMID: 18160998

2

Linkage disequilibrium analyses of natriuretic peptide precursor B locus reveal risk haplotype conferring high plasma BNP levels.

Takeishi Y, Toriyama S, Takabatake N, Shibata Y, Konta T, Emi M, Kato T, Kawata S, Kubota I. Takeishi Y, et al. Among authors: kawata s. Biochem Biophys Res Commun. 2007 Oct 19;362(2):480-4. doi: 10.1016/j.bbrc.2007.08.028. Epub 2007 Aug 13. Biochem Biophys Res Commun. 2007. PMID: 17719005

3

Association of CC chemokine ligand 5 genotype with urinary albumin excretion in the non-diabetic Japanese general population: the Takahata study.

Konta T, Emi M, Toriyama S, Ariumi H, Ishii M, Takasaki S, Ikeda A, Ichikawa K, Shibata Y, Takabatake N, Takeishi Y, Kato T, Kawata S, Kubota I. Konta T, et al. Among authors: kawata s. J Hum Genet. 2008;53(3):267. doi: 10.1007/s10038-008-0246-6. Epub 2008 Jan 24. J Hum Genet. 2008. PMID: 18217191

4

Genetic association between aldehyde dehydrogenase 2 (ALDH2) variation and high-density lipoprotein cholesterol (HDL-C) among non-drinkers in two large population samples in Japan.

Wada M, Daimon M, Emi M, Iijima H, Sato H, Koyano S, Tajima K, Kawanami T, Kurita K, Hunt SC, Hopkins PN, Kubota I, Kawata S, Kato T. Wada M, et al. Among authors: kawata s. J Atheroscler Thromb. 2008 Aug;15(4):179-84. doi: 10.5551/jat.e542. J Atheroscler Thromb. 2008. PMID: 18776700 Free article.

5

The novel and independent association between single-point SNP of NPHP4 gene and renal function in non-diabetic Japanese population: the Takahata study.

Konta T, Takasaki S, Ichikawa K, Emi M, Toriyama S, Satoh H, Ikeda A, Suzuki K, Mashima Y, Shibata Y, Watanabe T, Kato T, Kawata S, Kubota I. Konta T, et al. Among authors: kawata s. J Hum Genet. 2010 Dec;55(12):791-5. doi: 10.1038/jhg.2010.113. Epub 2010 Sep 16. J Hum Genet. 2010. PMID: 20844548

6

A nonfunctioning single nucleotide polymorphism in olfactory receptor gene family is associated with the forced expiratory volume in the first second/the forced vital capacity values of pulmonary function test in a Japanese population.

Takabatake N, Toriyama S, Takeishi Y, Shibata Y, Konta T, Inoue S, Abe S, Igarashi A, Tokairin Y, Ishii M, Koyano S, Emi M, Kato T, Kawata S, Kubota I. Takabatake N, et al. Among authors: kawata s. Biochem Biophys Res Commun. 2007 Dec 21;364(3):662-7. doi: 10.1016/j.bbrc.2007.10.068. Epub 2007 Oct 22. Biochem Biophys Res Commun. 2007. PMID: 17964544

7

Association of the PIK3C2G gene polymorphisms with type 2 DM in a Japanese population.

Daimon M, Sato H, Oizumi T, Toriyama S, Saito T, Karasawa S, Jimbu Y, Wada K, Kameda W, Susa S, Yamaguchi H, Emi M, Muramatsu M, Kubota I, Kawata S, Kato T. Daimon M, et al. Among authors: kawata s. Biochem Biophys Res Commun. 2008 Jan 18;365(3):466-71. doi: 10.1016/j.bbrc.2007.10.180. Epub 2007 Nov 6. Biochem Biophys Res Commun. 2008. PMID: 17991425

8

Common null variant, Arg192Stop, in a G-protein coupled receptor, olfactory receptor 1B1, associated with decreased serum cholinesterase activity.

Koyano S, Emi M, Saito T, Makino N, Toriyama S, Ishii M, Kubota I, Kato T, Kawata S. Koyano S, et al. Among authors: kawata s. Hepatol Res. 2008 Jul;38(7):696-703. doi: 10.1111/j.1872-034X.2008.00327.x. Epub 2008 Mar 4. Hepatol Res. 2008. PMID: 18328065

9

Salt consumption-dependent association of the GNB3 gene polymorphism with type 2 DM.

Daimon M, Sato H, Sasaki S, Toriyama S, Emi M, Muramatsu M, Hunt SC, Hopkins PN, Karasawa S, Wada K, Jimbu Y, Kameda W, Susa S, Oizumi T, Fukao A, Kubota I, Kawata S, Kato T. Daimon M, et al. Among authors: kawata s. Biochem Biophys Res Commun. 2008 Sep 26;374(3):576-80. doi: 10.1016/j.bbrc.2008.07.065. Epub 2008 Jul 24. Biochem Biophys Res Commun. 2008. PMID: 18656447

10

Genetic polymorphisms of paraoxonase-1 are associated with chronic kidney disease in Japanese women.

Ichikawa K, Konta T, Emi M, Toriyama S, Takasaki S, Ikeda A, Shibata Y, Takabatake N, Takeishi Y, Kato T, Kawata S, Kubota I. Ichikawa K, et al. Among authors: kawata s. Kidney Int. 2009 Jul;76(2):183-9. doi: 10.1038/ki.2009.97. Epub 2009 Apr 8. Kidney Int. 2009. PMID: 19357718 Free article.

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