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Rayleigh SAW-Assisted SH-SAW Immunosensor on X-Cut 148-Y LiTaO3.
Kogai T, Yatsuda H, Kondoh J. Kogai T, et al. IEEE Trans Ultrason Ferroelectr Freq Control. 2017 Sep;64(9):1375-1381. doi: 10.1109/TUFFC.2017.2734282. Epub 2017 Jul 31. IEEE Trans Ultrason Ferroelectr Freq Control. 2017. PMID: 28783630
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities.
Narumi S, Nagasaki K, Kiriya M, Uehara E, Akiba K, Tanase-Nakao K, Shimura K, Abe K, Sugisawa C, Ishii T, Miyako K, Hasegawa Y, Maruo Y, Muroya K, Watanabe N, Nishihara E, Ito Y, Kogai T, Kameyama K, Nakabayashi K, Hata K, Fukami M, Shima H, Kikuchi A, Takayama J, Tamiya G, Hasegawa T. Narumi S, et al. Among authors: kogai t. Nat Genet. 2024 May 7. doi: 10.1038/s41588-024-01735-5. Online ahead of print. Nat Genet. 2024. PMID: 38714868
Inhibition of IL-33 signaling ameliorate hepatic fibrosis with decreasing MCP-1 in a mouse model of diabetes and non-alcoholic steatohepatitis; comparison for luseogliflozin, an SGLT2 inhibitor.
Wakamatsu S, Jojima T, Hashiguchi M, Kishi H, Niitani T, Sakurai S, Iijima T, Kogai T, Tomaru T, Usui I, Aso Y. Wakamatsu S, et al. Among authors: kogai t. J Diabetes Complications. 2024 Jan;38(1):108650. doi: 10.1016/j.jdiacomp.2023.108650. Epub 2023 Nov 23. J Diabetes Complications. 2024. PMID: 38035640
Symptomatic hypocalcemia after treatment for hyperthyroidism in a woman with chromosome 22q11.2 deletion syndrome complicated by Graves' disease: longitudinal changes in the number of subsets of CD4 and CD8 lymphocytes after thyroidectomy.
Iijima T, Jojima T, Hosonuma S, Ohhira E, Tomaru T, Kogai T, Usui I, Aso Y. Iijima T, et al. Among authors: kogai t. Endocr J. 2021 Oct 28;68(10):1187-1195. doi: 10.1507/endocrj.EJ20-0717. Epub 2021 May 11. Endocr J. 2021. PMID: 33980771 Free article.
Empagliflozin increases plasma levels of campesterol, a marker of cholesterol absorption, in patients with type 2 diabetes: Association with a slight increase in high-density lipoprotein cholesterol.
Jojima T, Sakurai S, Wakamatsu S, Iijima T, Saito M, Tomaru T, Kogai T, Usui I, Aso Y. Jojima T, et al. Among authors: kogai t. Int J Cardiol. 2021 May 15;331:243-248. doi: 10.1016/j.ijcard.2021.01.063. Epub 2021 Feb 5. Int J Cardiol. 2021. PMID: 33556413 Clinical Trial.
A case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with a novel frameshift variant in GATA3, p.W10Cfs40, lacks kidney malformation.
Kishi H, Jojima T, Kogai T, Iijima T, Ohira E, Tanuma D, Konno S, Kato K, Kezuka A, Akimoto K, Sakumoto J, Hishinuma A, Tomaru T, Makita N, Usui I, Aso Y. Kishi H, et al. Among authors: kogai t. Clin Case Rep. 2020 Aug 14;8(12):2619-2624. doi: 10.1002/ccr3.3186. eCollection 2020 Dec. Clin Case Rep. 2020. PMID: 33363791 Free PMC article.
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