Inoue I - Search Results

1

Dysfunctional missense variant of OAT10/SLC22A13 decreases gout risk and serum uric acid levels.

Higashino T, Morimoto K, Nakaoka H, Toyoda Y, Kawamura Y, Shimizu S, Nakamura T, Hosomichi K, Nakayama A, Ooyama K, Ooyama H, Shimizu T, Ueno M, Ito T, Tamura T, Naito M, Nakashima H, Kawaguchi M, Takao M, Kawai Y, Osada N, Ichida K, Yamamoto K, Suzuki H, Shinomiya N, Inoue I, Takada T, Matsuo H. Higashino T, et al. Among authors: inoue i. Ann Rheum Dis. 2020 Jan;79(1):164-166. doi: 10.1136/annrheumdis-2019-216044. Epub 2019 Nov 28. Ann Rheum Dis. 2020. PMID: 31780526 Free PMC article. No abstract available.

2

Serotonin- and catecholamine-related substances in the brain of ornithine transcarbamylase-deficient Sparse-fur mice in the hyperammonemic state: comparison of two procedures for obtaining brain extract, decapitation and microwave irradiation.

Inoue I, Shimizu T, Saheki T, Noda T, Fukuda T. Inoue I, et al. Biochem Med Metab Biol. 1989 Dec;42(3):232-9. doi: 10.1016/0885-4505(89)90061-3. Biochem Med Metab Biol. 1989. PMID: 2597437

3

Meta-analysis of genetic association studies: methodologies, between-study heterogeneity and winner's curse.

Nakaoka H, Inoue I. Nakaoka H, et al. Among authors: inoue i. J Hum Genet. 2009 Nov;54(11):615-23. doi: 10.1038/jhg.2009.95. Epub 2009 Oct 23. J Hum Genet. 2009. PMID: 19851339 Review.

4

Positional effects of polymorphisms in probe-target sequences on genoplot images of oligonucleotide microarrays.

Cui TL, Nakaoka H, Akiyama K, Kamura H, Hosomichi K, Bae J, Cheong H, Shin H, Yada T, Inoue I. Cui TL, et al. Among authors: inoue i. Genet Mol Res. 2010 Mar 23;9(1):524-31. doi: 10.4238/vol9-1gmr737. Genet Mol Res. 2010. PMID: 20391336 Free article.

5

Differential effects of chromosome 9p21 variation on subphenotypes of intracranial aneurysm: site distribution.

Nakaoka H, Takahashi T, Akiyama K, Cui T, Tajima A, Krischek B, Kasuya H, Hata A, Inoue I. Nakaoka H, et al. Among authors: inoue i. Stroke. 2010 Aug;41(8):1593-8. doi: 10.1161/STROKEAHA.110.586529. Epub 2010 Jul 1. Stroke. 2010. PMID: 20595659

6

Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms.

Akiyama K, Narita A, Nakaoka H, Cui T, Takahashi T, Yasuno K, Tajima A, Krischek B, Yamamoto K, Kasuya H, Hata A, Inoue I. Akiyama K, et al. Among authors: inoue i. J Hum Genet. 2010 Oct;55(10):656-61. doi: 10.1038/jhg.2010.82. Epub 2010 Jul 8. J Hum Genet. 2010. PMID: 20613766

7

TRIM39 and RNF39 are associated with Behçet's disease independently of HLA-B∗51 and -A∗26.

Kurata R, Nakaoka H, Tajima A, Hosomichi K, Shiina T, Meguro A, Mizuki N, Ohono S, Inoue I, Inoko H. Kurata R, et al. Among authors: inoue i. Biochem Biophys Res Commun. 2010 Oct 29;401(4):533-7. doi: 10.1016/j.bbrc.2010.09.088. Epub 2010 Sep 27. Biochem Biophys Res Commun. 2010. PMID: 20875797

8

[Genome informatics].

Nakaoka H, Inoue I. Nakaoka H, et al. Among authors: inoue i. Nihon Rinsho. 2010 Aug;68 Suppl 8:93-9. Nihon Rinsho. 2010. PMID: 20979269 Review. Japanese. No abstract available.

9

Exome resequencing combined with linkage analysis identifies novel PTH1R variants in primary failure of tooth eruption in Japanese.

Yamaguchi T, Hosomichi K, Narita A, Shirota T, Tomoyasu Y, Maki K, Inoue I. Yamaguchi T, et al. Among authors: inoue i. J Bone Miner Res. 2011 Jul;26(7):1655-61. doi: 10.1002/jbmr.385. J Bone Miner Res. 2011. PMID: 21404329 Free article.

10

A systems genetics approach provides a bridge from discovered genetic variants to biological pathways in rheumatoid arthritis.

Nakaoka H, Cui T, Tajima A, Oka A, Mitsunaga S, Kashiwase K, Homma Y, Sato S, Suzuki Y, Inoko H, Inoue I. Nakaoka H, et al. Among authors: inoue i. PLoS One. 2011;6(9):e25389. doi: 10.1371/journal.pone.0025389. Epub 2011 Sep 28. PLoS One. 2011. PMID: 21980439 Free PMC article.

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