Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Sayako Hirose"'
Autor:
Sayako Hirose, Takeru Makiyama, Dario Melgari, Yuta Yamamoto, Yimin Wuriyanghai, Fumika Yokoi, Suguru Nishiuchi, Takeshi Harita, Mamoru Hayano, Hirohiko Kohjitani, Jingshan Gao, Asami Kashiwa, Misato Nishikawa, Jie Wu, Jun Yoshimoto, Kazuhisa Chonabayashi, Seiko Ohno, Yoshinori Yoshida, Minoru Horie, Takeshi Kimura
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
BackgroundLong QT syndrome type 3 (LQT3) is caused by gain-of-function mutations in the SCN5A gene, which encodes the α subunit of the cardiac voltage-gated sodium channel. LQT3 patients present bradycardia and lethal arrhythmias during rest or slee
Externí odkaz:
https://doaj.org/article/781b014fbf9f4ada9153e2489cb7d3b1
Autor:
Kenichi Sasaki, Takeru Makiyama, Yoshinori Yoshida, Yimin Wuriyanghai, Tsukasa Kamakura, Suguru Nishiuchi, Mamoru Hayano, Takeshi Harita, Yuta Yamamoto, Hirohiko Kohjitani, Sayako Hirose, Jiarong Chen, Mihoko Kawamura, Seiko Ohno, Hideki Itoh, Ayako Takeuchi, Satoshi Matsuoka, Masaru Miura, Naokata Sumitomo, Minoru Horie, Shinya Yamanaka, Takeshi Kimura
Publikováno v:
PLoS ONE, Vol 11, Iss 10, p e0164795 (2016)
INTRODUCTION:Human induced pluripotent stem cells (hiPSCs) offer a unique opportunity for disease modeling. However, it is not invariably successful to recapitulate the disease phenotype because of the immaturity of hiPSC-derived cardiomyocytes (hiPS
Externí odkaz:
https://doaj.org/article/5f9aff9cb1e5483da6488741c61c808b
Autor:
Takashi Sakurai, Yimin Wuriyanghai, Naoyuki Tetsuo, Koichi Kato, Nagomi Kurebayashi, Takashi Murayama, Seiko Ohno, Takeru Makiyama, Masao Yoshinaga, Takeshi Kimura, Hisaaki Aoki, Minoru Horie, Minako Hoshiai, Hiroaki Kise, Megumi Fukuyama, Yuko Wada, Sayako Hirose
Publikováno v:
EP Europace. 24:497-510
Aims:Gain-of-function mutations in RYR2, encoding the cardiac ryanodine receptor channel (RyR2), cause catecholaminergic polymorphic ventricular tachycardia (CPVT). Whereas, genotype-phenotype correlations of loss-of-function mutations remains unknow
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2320
Electrophysiological analysis of human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) using a patch-clamp technique enables the most precise evaluation of electrophysiological properties in single cells. Compared to multielectrode a
Publikováno v:
Methods in Molecular Biology ISBN: 9781071614839
Electrophysiological analysis of human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) using a patch-clamp technique enables the most precise evaluation of electrophysiological properties in single cells. Compared to multielectrode a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e7df4bbdb08cb5e807ae5da2e365d74
https://doi.org/10.1007/978-1-0716-1484-6_13
https://doi.org/10.1007/978-1-0716-1484-6_13
Autor:
Nagomi Kurebayashi, Takashi Murayama, Naoyuki Tetsuo, Sayako Hirose, Minoru Horie, Seiko Ohno, Takashi Sakurai
Publikováno v:
Biophysical Journal. 121:175a
Autor:
Nagomi Kurebayashi, Takashi Murayama, Naoyuki Tetsuo, Sayako Hirose, Minoru Horie, Seiko Ohno, Takashi Sakurai
Publikováno v:
Proceedings for Annual Meeting of The Japanese Pharmacological Society. 95:3-O
Autor:
Fumika Yokoi, Takeru Makiyama, Minoru Horie, Yoshinori Yoshida, Takeshi Harita, Yimin Wuriyanghai, Kazuhisa Chonabayashi, Hirohiko Kohjitani, Jingshan Gao, Kenichi Sasaki, Suguru Nishiuchi, Yuta Yamamoto, Takeshi Kimura, Jiarong Chen, Ken Watanabe, Sayako Hirose, T Kamakura, Seiko Ohno, Mamoru Hayano
Publikováno v:
Heart Rhythm. 15:1566-1574
Background Long QT syndrome type 1 (LQT1) is caused by mutations in KCNQ1, which encodes the α subunit of the slow delayed rectifier potassium current channel. We previously reported that a synonymous mutation, c.1032G>A, p.A344Aspl, in KCNQ1 is mos
Autor:
Fumika Yokoi, Takeru Makiyama, Hideki Motomura, Takeshi Kimura, Seiko Ohno, Hirohiko Kohjitani, Minoru Horie, Jiarong Chen, Kenichi Sasaki, Yimin Wuriyanghai, Takeshi Harita, Yoshinori Yoshida, Taisuke Ishikawa, Naomasa Makita, Sayako Hirose, Kazuhisa Chonabayashi, Mamoru Hayano, Suguru Nishiuchi, Yuta Yamamoto
Publikováno v:
Human Molecular Genetics. 26:1670-1677
Calmodulin is a ubiquitous Ca2+ sensor molecule encoded by three distinct calmodulin genes, CALM1-3. Recently, mutations in CALM1-3 have been reported to be associated with severe early-onset long-QT syndrome (LQTS). However, the underlying mechanism
Publikováno v:
BioMed Research International, Vol 2016 (2016)
BioMed Research International
BioMed Research International
Introduction. Cardiac involvement of myasthenia gravis (MG) accompanies a poor prognosis. In the present study, we aimed to investigate the relationship between ECG abnormality and cardiac involvement.Methods. Of 178 patients diagnosed with MG betwee