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811 results

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Page 1
Metabolic syndrome is linked to the incidence of pancreatic cancer.
Miyashita Y, Hitsumoto T, Fukuda H, Kim J, Ito S, Kimoto N, Asakura K, Yata Y, Yabumoto M, Washio T, Kitakaze M. Miyashita Y, et al. EClinicalMedicine. 2023 Dec 12;67:102353. doi: 10.1016/j.eclinm.2023.102353. eCollection 2024 Jan. EClinicalMedicine. 2023. PMID: 38169901 Free PMC article.
The CR9 element is a novel mechanical load-responsive enhancer that regulates natriuretic peptide genes expression.
Miyashita Y, Tsukamoto O, Matsuoka K, Kamikubo K, Kuramoto Y, Ying Fu H, Tsubota T, Hasuike H, Takayama T, Ito H, Hitsumoto T, Okamoto C, Kioka H, Oya R, Shinomiya H, Hakui H, Shintani Y, Kato H, Kitakaze M, Sakata Y, Asano Y, Takashima S. Miyashita Y, et al. FASEB J. 2021 Apr;35(4):e21495. doi: 10.1096/fj.202002111RR. FASEB J. 2021. PMID: 33689182
Aberrant accumulation of TMEM43 accompanied by perturbed transmural gene expression in arrhythmogenic cardiomyopathy.
Shinomiya H, Kato H, Kuramoto Y, Watanabe N, Tsuruda T, Arimura T, Miyashita Y, Miyasaka Y, Mashimo T, Takuwa A, Motooka D, Okuzaki D, Matsuoka K, Tsukamoto O, Hakui H, Yamada N, Lee JK, Kioka H, Kitakaze M, Takashima S, Sakata Y, Asano Y. Shinomiya H, et al. Among authors: miyashita y. FASEB J. 2021 Nov;35(11):e21994. doi: 10.1096/fj.202100800R. FASEB J. 2021. PMID: 34674311
Mutant KCNJ3 and KCNJ5 Potassium Channels as Novel Molecular Targets in Bradyarrhythmias and Atrial Fibrillation.
Yamada N, Asano Y, Fujita M, Yamazaki S, Inanobe A, Matsuura N, Kobayashi H, Ohno S, Ebana Y, Tsukamoto O, Ishino S, Takuwa A, Kioka H, Yamashita T, Hashimoto N, Zankov DP, Shimizu A, Asakura M, Asanuma H, Kato H, Nishida Y, Miyashita Y, Shinomiya H, Naiki N, Hayashi K, Makiyama T, Ogita H, Miura K, Ueshima H, Komuro I, Yamagishi M, Horie M, Kawakami K, Furukawa T, Koizumi A, Kurachi Y, Sakata Y, Minamino T, Kitakaze M, Takashima S. Yamada N, et al. Among authors: miyashita y. Circulation. 2019 Apr 30;139(18):2157-2169. doi: 10.1161/CIRCULATIONAHA.118.036761. Circulation. 2019. PMID: 30764634
Loss-of-function mutations in the co-chaperone protein BAG5 cause dilated cardiomyopathy requiring heart transplantation.
Hakui H, Kioka H, Miyashita Y, Nishimura S, Matsuoka K, Kato H, Tsukamoto O, Kuramoto Y, Takuwa A, Takahashi Y, Saito S, Ohta K, Asanuma H, Fu HY, Shinomiya H, Yamada N, Ohtani T, Sawa Y, Kitakaze M, Takashima S, Sakata Y, Asano Y. Hakui H, et al. Among authors: miyashita y. Sci Transl Med. 2022 Jan 19;14(628):eabf3274. doi: 10.1126/scitranslmed.abf3274. Epub 2022 Jan 19. Sci Transl Med. 2022. PMID: 35044787
Phospholamban p.Arg14del Cardiomyopathy: A Japanese Case Series.
Tabata T, Kuramoto Y, Ohtani T, Miyawaki H, Miyashita Y, Sera F, Kioka H, Higo S, Asano Y, Hikoso S, Sakata Y. Tabata T, et al. Among authors: miyashita y. Intern Med. 2022 Jul 1;61(13):1987-1993. doi: 10.2169/internalmedicine.8594-21. Epub 2021 Dec 18. Intern Med. 2022. PMID: 34924461 Free PMC article.
Clinical Outcomes and Genetic Analyses of Restrictive Cardiomyopathy in Children.
Ishida H, Narita J, Ishii R, Suginobe H, Tsuru H, Wang R, Yoshihara C, Ueyama A, Ueda K, Hirose M, Hashimoto K, Nagano H, Kogaki S, Kuramoto Y, Miyashita Y, Asano Y, Ozono K. Ishida H, et al. Among authors: miyashita y. Circ Genom Precis Med. 2023 Aug;16(4):382-389. doi: 10.1161/CIRCGEN.122.004054. Epub 2023 Jun 28. Circ Genom Precis Med. 2023. PMID: 37377035
811 results