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Page 1
Genetic control of CCL24, POR, and IL23R contributes to the pathogenesis of sarcoidosis.
Meguro A, Ishihara M, Petrek M, Yamamoto K, Takeuchi M, Mrazek F, Kolek V, Benicka A, Yamane T, Shibuya E, Yoshino A, Isomoto A, Ota M, Yatsu K, Shijubo N, Nagai S, Yamaguchi E, Yamaguchi T, Namba K, Kaburaki T, Takase H, Morimoto SI, Hori J, Kono K, Goto H, Suda T, Ikushima S, Ando Y, Takenaka S, Takeuchi M, Yuasa T, Sugisaki K, Ohguro N, Hiraoka M, Kitaichi N, Sugiyama Y, Horita N, Asukata Y, Kawagoe T, Kimura I, Ishido M, Inoko H, Mochizuki M, Ohno S, Bahram S, Remmers EF, Kastner DL, Mizuki N. Meguro A, et al. Among authors: ohguro n. Commun Biol. 2020 Aug 21;3(1):465. doi: 10.1038/s42003-020-01185-9. Commun Biol. 2020. PMID: 32826979 Free PMC article.
Acute retinal necrosis: factors associated with anatomic and visual outcomes.
Iwahashi-Shima C, Azumi A, Ohguro N, Okada AA, Kaburaki T, Goto H, Sonoda KH, Namba K, Mizuki N, Mochizuki M. Iwahashi-Shima C, et al. Among authors: ohguro n. Jpn J Ophthalmol. 2013 Jan;57(1):98-103. doi: 10.1007/s10384-012-0211-y. Epub 2012 Nov 2. Jpn J Ophthalmol. 2013. PMID: 23117419
Evaluation of the long-term efficacy and safety of infliximab treatment for uveitis in Behçet's disease: a multicenter study.
Takeuchi M, Kezuka T, Sugita S, Keino H, Namba K, Kaburaki T, Maruyama K, Nakai K, Hijioka K, Shibuya E, Komae K, Hori J, Ohguro N, Sonoda KH, Mizuki N, Okada AA, Ishibashi T, Goto H, Mochizuki M. Takeuchi M, et al. Among authors: ohguro n. Ophthalmology. 2014 Oct;121(10):1877-84. doi: 10.1016/j.ophtha.2014.04.042. Epub 2014 Jun 18. Ophthalmology. 2014. PMID: 24950593
Development and validation of new diagnostic criteria for acute retinal necrosis.
Takase H, Okada AA, Goto H, Mizuki N, Namba K, Ohguro N, Sonoda KH, Tomita M, Keino H, Kezuka T, Kubono R, Mizuuchi K, Shibuya E, Takahashi H, Yanai R, Mochizuki M. Takase H, et al. Among authors: ohguro n. Jpn J Ophthalmol. 2015 Jan;59(1):14-20. doi: 10.1007/s10384-014-0362-0. Epub 2014 Dec 10. Jpn J Ophthalmol. 2015. PMID: 25492579
Investigation of the association between IL10 gene polymorphisms and Vogt-Koyanagi-Harada disease in a Japanese population.
Higashi K, Meguro A, Takeuchi M, Yamane T, Kitaichi N, Horie Y, Namba K, Ohno S, Nakao K, Sakamoto T, Sakai T, Tsuneoka H, Keino H, Okada AA, Takeda A, Fukuhara T, Mashimo H, Ohguro N, Oono S, Enaida H, Okinami S, Mizuki N. Higashi K, et al. Among authors: ohguro n. Ophthalmic Genet. 2017 Mar-Apr;38(2):187-189. doi: 10.3109/13816810.2016.1145698. Epub 2016 Apr 4. Ophthalmic Genet. 2017. PMID: 27046676 No abstract available.
Association Study of ARMC9 Gene Variants with Vogt-Koyanagi-Harada Disease in Japanese Patients.
Ohno T, Meguro A, Takeuchi M, Yamane T, Teshigawara T, Kitaichi N, Horie Y, Namba K, Ohno S, Nakao K, Sakamoto T, Sakai T, Nakano T, Keino H, Okada AA, Takeda A, Fukuhara T, Mashimo H, Ohguro N, Oono S, Enaida H, Okinami S, Mizuki N. Ohno T, et al. Among authors: ohguro n. Ocul Immunol Inflamm. 2019;27(5):699-705. doi: 10.1080/09273948.2018.1523438. Epub 2018 Nov 5. Ocul Immunol Inflamm. 2019. PMID: 30395750
Variants in IL23R-C1orf141 and ADO-ZNF365-EGR2 are associated with susceptibility to Vogt-Koyanagi-Harada disease in Japanese population.
Sakono T, Meguro A, Takeuchi M, Yamane T, Teshigawara T, Kitaichi N, Horie Y, Namba K, Ohno S, Nakao K, Sakamoto T, Sakai T, Nakano T, Keino H, Okada AA, Takeda A, Ito T, Mashimo H, Ohguro N, Oono S, Enaida H, Okinami S, Horita N, Ota M, Mizuki N. Sakono T, et al. Among authors: ohguro n. PLoS One. 2020 May 21;15(5):e0233464. doi: 10.1371/journal.pone.0233464. eCollection 2020. PLoS One. 2020. PMID: 32437414 Free PMC article.
94 results