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Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.
Kirino Y, Bertsias G, Ishigatsubo Y, Mizuki N, Tugal-Tutkun I, Seyahi E, Ozyazgan Y, Sacli FS, Erer B, Inoko H, Emrence Z, Cakar A, Abaci N, Ustek D, Satorius C, Ueda A, Takeno M, Kim Y, Wood GM, Ombrello MJ, Meguro A, Gül A, Remmers EF, Kastner DL. Kirino Y, et al. Among authors: inoko h. Nat Genet. 2013 Feb;45(2):202-7. doi: 10.1038/ng.2520. Epub 2013 Jan 6. Nat Genet. 2013. PMID: 23291587 Free PMC article.
Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease.
Kirino Y, Zhou Q, Ishigatsubo Y, Mizuki N, Tugal-Tutkun I, Seyahi E, Özyazgan Y, Ugurlu S, Erer B, Abaci N, Ustek D, Meguro A, Ueda A, Takeno M, Inoko H, Ombrello MJ, Satorius CL, Maskeri B, Mullikin JC, Sun HW, Gutierrez-Cruz G, Kim Y, Wilson AF, Kastner DL, Gül A, Remmers EF. Kirino Y, et al. Among authors: inoko h. Proc Natl Acad Sci U S A. 2013 May 14;110(20):8134-9. doi: 10.1073/pnas.1306352110. Epub 2013 Apr 30. Proc Natl Acad Sci U S A. 2013. PMID: 23633568 Free PMC article.
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: inoko h. Ophthalmic Genet. 2016 Jun;37(2):194-200. doi: 10.3109/13816810.2015.1028649. Epub 2016 Jan 15. Ophthalmic Genet. 2016. PMID: 26771863
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: inoko h. Commun Biol. 2020 Aug 21;3(1):465. doi: 10.1038/s42003-020-01185-9. Commun Biol. 2020. PMID: 32826979 Free PMC article.
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
624 results