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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: yamane t. Commun Biol. 2020 Aug 21;3(1):465. doi: 10.1038/s42003-020-01185-9. Commun Biol. 2020. PMID: 32826979 Free PMC article.
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: yamane t. PLoS One. 2020 May 21;15(5):e0233464. doi: 10.1371/journal.pone.0233464. eCollection 2020. PLoS One. 2020. PMID: 32437414 Free PMC article.
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: yamane t. Ocul Immunol Inflamm. 2019;27(5):699-705. doi: 10.1080/09273948.2018.1523438. Epub 2018 Nov 5. Ocul Immunol Inflamm. 2019. PMID: 30395750
The association analysis between HLA-A*26 and Behçet's disease.
Nakamura J, Meguro A, Ishii G, Mihara T, Takeuchi M, Mizuki Y, Yuda K, Yamane T, Kawagoe T, Ota M, Mizuki N. Nakamura J, et al. Among authors: yamane t. Sci Rep. 2019 Mar 14;9(1):4426. doi: 10.1038/s41598-019-40824-y. Sci Rep. 2019. PMID: 30872678 Free PMC article.
Genome-Wide Association Study in Asians Identifies Novel Loci for High Myopia and Highlights a Nervous System Role in Its Pathogenesis.
Meguro A, Yamane T, Takeuchi M, Miyake M, Fan Q, Zhao W, Wang IJ, Mizuki Y, Yamada N, Nomura N, Tsujikawa A, Matsuda F, Hosoda Y, Saw SM, Cheng CY, Tsai TH, Yoshida M, Iijima Y, Teshigawara T, Okada E, Ota M, Inoko H, Mizuki N. Meguro A, et al. Among authors: yamane t. Ophthalmology. 2020 Dec;127(12):1612-1624. doi: 10.1016/j.ophtha.2020.05.014. Epub 2020 May 16. Ophthalmology. 2020. PMID: 32428537
High-resolution mapping for essential hypertension using microsatellite markers.
Yatsu K, Mizuki N, Hirawa N, Oka A, Itoh N, Yamane T, Ogawa M, Shiwa T, Tabara Y, Ohno S, Soma M, Hata A, Nakao K, Ueshima H, Ogihara T, Tomoike H, Miki T, Kimura A, Mano S, Kulski JK, Umemura S, Inoko H. Yatsu K, et al. Among authors: yamane t. Hypertension. 2007 Mar;49(3):446-52. doi: 10.1161/01.HYP.0000257256.77680.02. Epub 2007 Jan 22. Hypertension. 2007. PMID: 17242298
SLC1A1 Gene Variants and Normal Tension Glaucoma: An Association Study.
Nishisako M, Meguro A, Nomura E, Yamane T, Takeuchi M, Ota M, Kashiwagi K, Mabuchi F, Iijima H, Kawase K, Yamamoto T, Nakamura M, Negi A, Sagara T, Nishida T, Inatani M, Tanihara H, Aihara M, Araie M, Fukuchi T, Abe H, Higashide T, Sugiyama K, Kanamoto T, Kiuchi Y, Iwase A, Chin S, Ohno S, Inoko H, Mizuki N. Nishisako M, et al. Among authors: yamane t. Ophthalmic Genet. 2016 Jun;37(2):194-200. doi: 10.3109/13816810.2015.1028649. Epub 2016 Jan 15. Ophthalmic Genet. 2016. PMID: 26771863
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: yamane t. 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.
1,595 results