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Page 1
t6A and ms2t6A Modified Nucleosides in Serum and Urine as Strong Candidate Biomarkers of COVID-19 Infection and Severity.
Biomolecules. 2022 Sep 3;12(9):1233. doi: 10.3390/biom12091233.
Biomolecules. 2022.
PMID: 36139072
Free PMC article.
Camostat mesilate, a serine protease inhibitor, exerts aquaretic effects and decreases urinary exosomal AQP2 levels.
Kakizoe Y, Nakagawa T, Iwata Y, Deng Q, Adachi M, Miyasato Y, Nakagawa M, Nagayoshi Y, Nishiguchi K, Narita Y, Izumi Y, Kuwabara T, Tomita K, Kitamura K, Mukoyama M.
Kakizoe Y, et al. Among authors: nagayoshi y.
J Pharmacol Sci. 2022 Dec;150(4):204-210. doi: 10.1016/j.jphs.2022.09.003. Epub 2022 Sep 19.
J Pharmacol Sci. 2022.
PMID: 36344042
Free article.
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Efficacy of continuous erythropoietin receptor activator for end-stage renal disease patients with renal anemia before and after peritoneal dialysis initiation.
Fujimoto D, Adachi M, Miyasato Y, Hata Y, Inoue H, Oda A, Kakizoe Y, Nakagawa T, Shimasaki A, Nakamura K, Nagayoshi Y, Mukoyama M.
Fujimoto D, et al. Among authors: nagayoshi y.
Clin Exp Nephrol. 2021 Feb;25(2):191-199. doi: 10.1007/s10157-020-01973-x. Epub 2020 Oct 6.
Clin Exp Nephrol. 2021.
PMID: 33025233
Free PMC article.
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The serine protease plasmin plays detrimental roles in epithelial sodium channel activation and podocyte injury in Dahl salt-sensitive rats.
Deng Q, Kakizoe Y, Iwata Y, Nakagawa T, Miyasato Y, Nakagawa M, Nishiguchi K, Nagayoshi Y, Adachi M, Narita Y, Izumi Y, Kuwabara T, Tsuda Y, Mukoyama M.
Deng Q, et al. Among authors: nagayoshi y.
Hypertens Res. 2023 Jan;46(1):50-62. doi: 10.1038/s41440-022-01064-2. Epub 2022 Oct 15.
Hypertens Res. 2023.
PMID: 36241707
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A Serine Protease Inhibitor, Camostat Mesilate, Suppresses Urinary Plasmin Activity and Alleviates Hypertension and Podocyte Injury in Dahl Salt-Sensitive Rats.
Iwata Y, Deng Q, Kakizoe Y, Nakagawa T, Miyasato Y, Nakagawa M, Nishiguchi K, Nagayoshi Y, Narita Y, Izumi Y, Kuwabara T, Adachi M, Mukoyama M.
Iwata Y, et al. Among authors: nagayoshi y.
Int J Mol Sci. 2023 Oct 30;24(21):15743. doi: 10.3390/ijms242115743.
Int J Mol Sci. 2023.
PMID: 37958726
Free PMC article.
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Autosomal dominant Alport syndrome due to a COL4A4 mutation with an additional ESPN variant detected by whole-exome analysis.
Izumi Y, Hamaguchi A, Miura R, Nakagawa T, Nakagawa M, Saida K, Miyake N, Nagayoshi Y, Kakizoe Y, Miyoshi T, Kohda Y, Misumi Y, Matsumoto N, Ando Y, Mukoyama M.
Izumi Y, et al. Among authors: nagayoshi y.
CEN Case Rep. 2020 Feb;9(1):59-64. doi: 10.1007/s13730-019-00429-w. Epub 2019 Nov 1.
CEN Case Rep. 2020.
PMID: 31677115
Free PMC article.
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