Inoko H - Search Results

1

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: inoko h. 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

2

The HLA genomic loci map: expression, interaction, diversity and disease.

Shiina T, Hosomichi K, Inoko H, Kulski JK. Shiina T, et al. Among authors: inoko h. J Hum Genet. 2009 Jan;54(1):15-39. doi: 10.1038/jhg.2008.5. Epub 2009 Jan 9. J Hum Genet. 2009. PMID: 19158813 Review.

3

TRIM39R, but not TRIM39B, regulates type I interferon response.

Kurata R, Tajima A, Yonezawa T, Inoko H. Kurata R, et al. Among authors: inoko h. Biochem Biophys Res Commun. 2013 Jun 21;436(1):90-5. doi: 10.1016/j.bbrc.2013.05.064. Epub 2013 May 23. Biochem Biophys Res Commun. 2013. PMID: 23707810

4

HLA-B51 Carriers are Susceptible to Ocular Symptoms of Behçet Disease and the Association between the Two Becomes Stronger towards the East along the Silk Road: A Literature Survey.

Horie Y, Meguro A, Ohta T, Lee EB, Namba K, Mizuuchi K, Iwata D, Mizuki N, Ota M, Inoko H, Ishida S, Ohno S, Kitaichi N. Horie Y, et al. Among authors: inoko h. Ocul Immunol Inflamm. 2017 Feb;25(1):37-40. doi: 10.3109/09273948.2015.1136422. Epub 2016 Mar 8. Ocul Immunol Inflamm. 2017. PMID: 26954704 Review.

5

[HLA gene region and its diversity].

Shiina T, Inoko H. Shiina T, et al. Among authors: inoko h. Nihon Rinsho. 2005 Apr;63 Suppl 4:293-8. Nihon Rinsho. 2005. PMID: 15861671 Review. Japanese. No abstract available.

6

[Four-digit allele genotyping of HLA-A and HLA-B genes in Japanese patients with Behçet's disease (BD) by a PCR-SSOP-luminex method and stratification analysis according to each major symptom of BD].

Kamiishi T, Itoh Y, Meguro A, Nishida T, Sasaki S, Nanba K, Ohno S, Inoko H, Mizuki N. Kamiishi T, et al. Among authors: inoko h. Nippon Ganka Gakkai Zasshi. 2008 May;112(5):451-8. Nippon Ganka Gakkai Zasshi. 2008. PMID: 18517005 Japanese.

7

Investigation of the association between Toll-like receptor 2 gene polymorphisms and Behçet's disease in Japanese patients.

Tomiyama R, Meguro A, Ota M, Katsuyama Y, Nishide T, Uemoto R, Iijima Y, Ohno S, Inoko H, Mizuki N. Tomiyama R, et al. Among authors: inoko h. Hum Immunol. 2009 Jan;70(1):41-4. doi: 10.1016/j.humimm.2008.10.014. Epub 2008 Nov 17. Hum Immunol. 2009. PMID: 19014987

8

Genetics of Behçet disease inside and outside the MHC.

Meguro A, Inoko H, Ota M, Katsuyama Y, Oka A, Okada E, Yamakawa R, Yuasa T, Fujioka T, Ohno S, Bahram S, Mizuki N. Meguro A, et al. Among authors: inoko h. Ann Rheum Dis. 2010 Apr;69(4):747-54. doi: 10.1136/ard.2009.108571. Epub 2009 Aug 13. Ann Rheum Dis. 2010. PMID: 19684014

9

Lack of association between toll-like receptor 4 gene polymorphisms and sarcoidosis-related uveitis in Japan.

Asukata Y, Ota M, Meguro A, Katsuyama Y, Ishihara M, Namba K, Kitaichi N, Morimoto S, Kaburaki T, Ando Y, Takenaka S, Inoko H, Ohno S, Mizuki N. Asukata Y, et al. Among authors: inoko h. Mol Vis. 2009 Dec 10;15:2673-82. Mol Vis. 2009. PMID: 20011079 Free PMC article.

10

Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility.

Writing Committee for the Normal Tension Glaucoma Genetic Study Group of Japan Glaucoma Society; Meguro A, Inoko H, Ota M, Mizuki N, Bahram S. Writing Committee for the Normal Tension Glaucoma Genetic Study Group of Japan Glaucoma Society, et al. Among authors: inoko h. Ophthalmology. 2010 Jul;117(7):1331-8.e5. doi: 10.1016/j.ophtha.2009.12.001. Epub 2010 Apr 3. Ophthalmology. 2010. PMID: 20363506

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