Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

34 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Impaired respiratory function in MELAS-induced pluripotent stem cells with high heteroplasmy levels.
Kodaira M, Hatakeyama H, Yuasa S, Seki T, Egashira T, Tohyama S, Kuroda Y, Tanaka A, Okata S, Hashimoto H, Kusumoto D, Kunitomi A, Takei M, Kashimura S, Suzuki T, Yozu G, Shimojima M, Motoda C, Hayashiji N, Saito Y, Goto Y, Fukuda K. Kodaira M, et al. Among authors: motoda c. FEBS Open Bio. 2015 Mar 20;5:219-25. doi: 10.1016/j.fob.2015.03.008. eCollection 2015. FEBS Open Bio. 2015. PMID: 25853038 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: motoda c. 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: motoda c. Sci Rep. 2017 Mar 14;7:44312. doi: 10.1038/srep44312. Sci Rep. 2017. PMID: 28290476 Free PMC article.
Analysis of cardiomyocyte movement in the developing murine heart.
Hashimoto H, Yuasa S, Tabata H, Tohyama S, Seki T, Egashira T, Hayashiji N, Hattori F, Kusumoto D, Kunitomi A, Takei M, Kashimura S, Yozu G, Shimojima M, Motoda C, Muraoka N, Nakajima K, Sakaue-Sawano A, Miyawaki A, Fukuda K. Hashimoto H, et al. Among authors: motoda c. Biochem Biophys Res Commun. 2015 Sep 4;464(4):1000-1007. doi: 10.1016/j.bbrc.2015.07.036. Epub 2015 Jul 10. Biochem Biophys Res Commun. 2015. PMID: 26168730
The complement C3-complement factor D-C3a receptor signalling axis regulates cardiac remodelling in right ventricular failure.
Ito S, Hashimoto H, Yamakawa H, Kusumoto D, Akiba Y, Nakamura T, Momoi M, Komuro J, Katsuki T, Kimura M, Kishino Y, Kashimura S, Kunitomi A, Lachmann M, Shimojima M, Yozu G, Motoda C, Seki T, Yamamoto T, Shinya Y, Hiraide T, Kataoka M, Kawakami T, Suzuki K, Ito K, Yada H, Abe M, Osaka M, Tsuru H, Yoshida M, Sakimura K, Fukumoto Y, Yuzaki M, Fukuda K, Yuasa S. Ito S, et al. Among authors: motoda c. Nat Commun. 2022 Sep 15;13(1):5409. doi: 10.1038/s41467-022-33152-9. Nat Commun. 2022. PMID: 36109509 Free PMC article.
A nonsynonymous polymorphism in semaphorin 3A as a risk factor for human unexplained cardiac arrest with documented ventricular fibrillation.
Nakano Y, Chayama K, Ochi H, Toshishige M, Hayashida Y, Miki D, Hayes CN, Suzuki H, Tokuyama T, Oda N, Suenari K, Uchimura-Makita Y, Kajihara K, Sairaku A, Motoda C, Fujiwara M, Watanabe Y, Yoshida Y, Ohkubo K, Watanabe I, Nogami A, Hasegawa K, Watanabe H, Endo N, Aiba T, Shimizu W, Ohno S, Horie M, Arihiro K, Tashiro S, Makita N, Kihara Y. Nakano Y, et al. Among authors: motoda c. PLoS Genet. 2013 Apr;9(4):e1003364. doi: 10.1371/journal.pgen.1003364. Epub 2013 Apr 11. PLoS Genet. 2013. PMID: 23593010 Free PMC article.
HCN4 Gene Polymorphisms Are Associated With Occurrence of Tachycardia-Induced Cardiomyopathy in Patients With Atrial Fibrillation.
Nakano Y, Ochi H, Sairaku A, Onohara Y, Tokuyama T, Motoda C, Matsumura H, Tomomori S, Amioka M, Hironobe N, Ohkubo Y, Okamura S, Makita N, Yoshida Y, Chayama K, Kihara Y. Nakano Y, et al. Among authors: motoda c. Circ Genom Precis Med. 2018 Jul;11(7):e001980. doi: 10.1161/CIRCGEN.117.001980. Circ Genom Precis Med. 2018. PMID: 29987112
Chromosome 4q25 Variant rs6817105 Bring Sinus Node Dysfunction and Left Atrial Enlargement.
Tomomori S, Nakano Y, Ochi H, Onohara Y, Sairaku A, Tokuyama T, Motoda C, Matsumura H, Amioka M, Hironobe N, Okubo Y, Okamura S, Kawazoe H, Nishiyama Y, Tahara H, Chayama K, Kihara Y. Tomomori S, et al. Among authors: motoda c. Sci Rep. 2018 Oct 1;8(1):14565. doi: 10.1038/s41598-018-32453-8. Sci Rep. 2018. PMID: 30275471 Free PMC article.
H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promoters.
Matsumura H, Nakano Y, Ochi H, Onohara Y, Sairaku A, Tokuyama T, Tomomori S, Motoda C, Amioka M, Hironobe N, Toshishige M, Takahashi S, Imai K, Sueda T, Chayama K, Kihara Y. Matsumura H, et al. Among authors: motoda c. J Biomed Sci. 2017 Dec 4;24(1):91. doi: 10.1186/s12929-017-0397-x. J Biomed Sci. 2017. PMID: 29202755 Free PMC article.
34 results