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Flecainide ameliorates arrhythmogenicity through NCX flux in Andersen-Tawil syndrome-iPS cell-derived cardiomyocytes.
Kuroda Y, Yuasa S, Watanabe Y, Ito S, Egashira T, Seki T, Hattori T, Ohno S, Kodaira M, Suzuki T, Hashimoto H, Okata S, Tanaka A, Aizawa Y, Murata M, Aiba T, Makita N, Furukawa T, Shimizu W, Kodama I, Ogawa S, Kokubun N, Horigome H, Horie M, Kamiya K, Fukuda K. Kuroda Y, et al. Among authors: ito s. Biochem Biophys Rep. 2017 Jan 11;9:245-256. doi: 10.1016/j.bbrep.2017.01.002. eCollection 2017 Mar. Biochem Biophys Rep. 2017. PMID: 28956012 Free PMC article.
Embryonic type Na+ channel β-subunit, SCN3B masks the disease phenotype of Brugada syndrome.
Okata S, Yuasa S, Suzuki T, Ito S, Makita N, Yoshida T, Li M, Kurokawa J, Seki T, Egashira T, Aizawa Y, Kodaira M, Motoda C, Yozu G, Shimojima M, Hayashiji N, Hashimoto H, Kuroda Y, Tanaka A, Murata M, Aiba T, Shimizu W, Horie M, Kamiya K, Furukawa T, Fukuda K. Okata S, et al. Among authors: ito s. Sci Rep. 2016 Sep 28;6:34198. doi: 10.1038/srep34198. Sci Rep. 2016. PMID: 27677334 Free PMC article.
Emerin plays a crucial role in nuclear invagination and in the nuclear calcium transient.
Shimojima M, Yuasa S, Motoda C, Yozu G, Nagai T, Ito S, Lachmann M, Kashimura S, Takei M, Kusumoto D, Kunitomi A, Hayashiji N, Seki T, Tohyama S, Hashimoto H, Kodaira M, Egashira T, Hayashi K, Nakanishi C, Sakata K, Yamagishi M, Fukuda K. Shimojima M, et al. Among authors: ito s. Sci Rep. 2017 Mar 14;7:44312. doi: 10.1038/srep44312. Sci Rep. 2017. PMID: 28290476 Free PMC article.
Authors' reply to Ozeke et al.
Ito S, Inage T, Aizawa Y, Fukuda K, Fukumoto Y. Ito S, et al. Europace. 2015 Sep;17(9):1455. doi: 10.1093/europace/euv029. Europace. 2015. PMID: 26443793 No abstract available.
Sex-Dependent Phenotypic Variability of an SCN5A Mutation: Brugada Syndrome and Sick Sinus Syndrome.
Aizawa Y, Fujisawa T, Katsumata Y, Kohsaka S, Kunitomi A, Ohno S, Sonoda K, Hayashi H, Hojo R, Fukamizu S, Nagase S, Ito S, Nakajima K, Nishiyama T, Kimura T, Kurita Y, Furukawa Y, Takatsuki S, Ogawa S, Nakazato Y, Sumiyoshi M, Kosaki K, Horie M, Fukuda K. Aizawa Y, et al. Among authors: ito s. J Am Heart Assoc. 2018 Sep 18;7(18):e009387. doi: 10.1161/JAHA.118.009387. J Am Heart Assoc. 2018. PMID: 30371189 Free PMC article.
An RyR2 mutation found in a family with a short-coupled variant of torsade de pointes.
Kimura M, Fujisawa T, Aizawa Y, Matsuhashi N, Ito S, Nakajima K, Kashimura S, Kunitomi A, Katsumata Y, Nishiyama T, Kimura T, Nishiyama N, Yuasa S, Takatsuki S, Kosaki K, Fukuda K. Kimura M, et al. Among authors: ito s. Int J Cardiol. 2017 Jan 15;227:367-369. doi: 10.1016/j.ijcard.2016.11.052. Epub 2016 Nov 8. Int J Cardiol. 2017. PMID: 27839804 No abstract available.
A Homozygous CASQ2 Mutation in a Japanese Patient with Catecholaminergic Polymorphic Ventricular Tachycardia.
Fujisawa T, Aizawa Y, Katsumata Y, Udo A, Ito S, Hatakeyama K, Hirose M, Miyama H, Nakajima K, Nishiyama T, Kimura T, Nitta M, Misumi K, Takatsuki S, Kosaki K, Fukuda K. Fujisawa T, et al. Among authors: ito s. Case Rep Genet. 2019 Jan 8;2019:9056596. doi: 10.1155/2019/9056596. eCollection 2019. Case Rep Genet. 2019. PMID: 30729048 Free PMC article.
Development of monomorphic ventricular tachycardia in a patient with fever-induced Brugada syndrome.
Sato Y, Aizawa Y, Fujisawa T, Ito S, Katano K, Fuse N, Miyabe A, Osada K, Ishihara R, Tosaka A, Tamamura T, Mizumura T, Sugimura Y, Nakajima K, Katsumata Y, Nishiyama T, Kimura T, Furukawa Y, Takatsuki S, Kosaki K, Fukuda K. Sato Y, et al. Among authors: ito s. J Arrhythm. 2018 Jun 4;34(4):465-468. doi: 10.1002/joa3.12068. eCollection 2018 Aug. J Arrhythm. 2018. PMID: 30167021 Free PMC article.
9,475 results