Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Misato Nishikawa"'
Autor:
Misato Nakanishi-Koakutsu, Kenji Miki, Yuki Naka, Masako Sasaki, Takayuki Wakimizu, Stephanie C. Napier, Chikako Okubo, Megumi Narita, Misato Nishikawa, Reo Hata, Kazuhisa Chonabayashi, Akitsu Hotta, Kenichi Imahashi, Tomoyuki Nishimoto, Yoshinori Yoshida
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-14 (2024)
Abstract Current differentiation protocols for human induced pluripotent stem cells (hiPSCs) produce heterogeneous cardiomyocytes (CMs). Although chamber-specific CM selection using cell surface antigens enhances biomedical applications, a cell surfa
Externí odkaz:
https://doaj.org/article/73e8538871d040e3ae7023f2f88a2a49
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:
Ryuji Okamoto, Itaru Goto, Yuhei Nishimura, Issei Kobayashi, Ryotaro Hashizume, Yoshinori Yoshida, Rie Ito, Yuhko Kobayashi, Misato Nishikawa, Yusuf Ali, Shunsuke Saito, Toshio Tanaka, Yoshiki Sawa, Masaaki Ito, Kaoru Dohi
Publikováno v:
PLoS ONE, Vol 15, Iss 10, p e0240129 (2020)
AimsGJB4 encodes a transmembrane connexin protein (Cx30.3) that is a component of gap junctions. This study investigated whether GJB4 plays an important role in human heart disease and function.Methods and resultsWe examined a patient and her older b
Externí odkaz:
https://doaj.org/article/294e16dd3291414e871dbbd752693a2a
Autor:
Asami Kashiwa, Takeru Makiyama, Hirohiko Kohjitani, Thomas L. Maurissen, Taisuke Ishikawa, Yuta Yamamoto, Yimin Wuriyanghai, Jingshan Gao, Hai Huang, Tomohiko Imamura, Takanori Aizawa, Misato Nishikawa, Kazuhisa Chonabayashi, Hiroyuki Mishima, Seiko Ohno, Futoshi Toyoda, Seiichi Sato, Koh-Ichiro Yoshiura, Kazuhiro Takahashi, Yoshinori Yoshida, Knut Woltjen, Minoru Horie, Naomasa Makita, Takeshi Kimura
Publikováno v:
Heart Rhythm. 20:89-99
Autor:
Jingshan Gao, Takeru Makiyama, Yuta Yamamoto, Takuya Kobayashi, Hisaaki Aoki, Thomas L. Maurissen, Yimin Wuriyanghai, Asami Kashiwa, Tomohiko Imamura, Takanori Aizawa, Hai Huang, Hirohiko Kohjitani, Misato Nishikawa, Kazuhisa Chonabayashi, Megumi Fukuyama, Hiromi Manabe, Kouichi Nakau, Tsutomu Wada, Koichi Kato, Futoshi Toyoda, Yoshinori Yoshida, Naomasa Makita, Knut Woltjen, Seiko Ohno, Nagomi Kurebayashi, Takashi Murayama, Takashi Sakurai, Minoru Horie, Takeshi Kimura
Publikováno v:
Circulation: Arrhythmia and Electrophysiology. 16
Background: CaM (calmodulin) is a ubiquitously expressed, multifunctional Ca 2+ sensor protein that regulates numerous proteins. Recently, CaM missense variants have been identified in patients with malignant inherited arrhythmias, such as long QT sy
Autor:
Akitsu Hotta, Misato Nishikawa, Megumi Narita, Yoshinori Yoshida, Azusa Inagaki, Chikako Okubo, Shinya Yamanaka
Publikováno v:
Stem Cell Reports
Summary Hand1 and Hand2 are transcriptional factors, and knockout mice of these genes show left and right ventricular hypoplasia, respectively. However, their function and expression in human cardiogenesis are not well studied. To delineate their exp
Autor:
Asami, Kashiwa, Takeru, Makiyama, Hirohiko, Kohjitani, Thomas L, Maurissen, Taisuke, Ishikawa, Yuta, Yamamoto, Yimin, Wuriyanghai, Jingshan, Gao, Hai, Huang, Tomohiko, Imamura, Takanori, Aizawa, Misato, Nishikawa, Kazuhisa, Chonabayashi, Hiroyuki, Mishima, Seiko, Ohno, Futoshi, Toyoda, Seiichi, Sato, Koh-Ichiro, Yoshiura, Kazuhiro, Takahashi, Yoshinori, Yoshida, Knut, Woltjen, Minoru, Horie, Naomasa, Makita, Takeshi, Kimura
Publikováno v:
Heart rhythm. 20(1)
A missense mutation in the α1c subunit of voltage-gated L-type CaWe aimed to investigate the electrophysiological features and pathophysiological mechanisms of CACNA1C-E1115K in patient-specific induced pluripotent stem cell (iPSC)-derived cardiomyo
Autor:
Yoshinori Yoshida, Azusa Inagaki, Misato Nishikawa, Akifumi Takaori-Kondo, Hiroshi Kawabata, Makiko Yamasaki-Morita, Yuki Morimoto, Miki Nagao, Chikako Okubo, Megumi Narita, Kayoko Nakanishi, Kazuhisa Chonabayashi
Publikováno v:
Blood advances. 6(4)
X-linked sideroblastic anemia (XLSA) is associated with mutations in the erythroid-specific δ-aminolevulinic acid synthase (ALAS2) gene. Treatment for XLSA is mainly supportive, except in pyridoxine-responsive patients. Female XLSA often represents
Publikováno v:
IEEJ Transactions on Electronics, Information and Systems. 138:1566-1572
Autor:
Masaaki Ito, Issei Kobayashi, Kaoru Dohi, Yusuf Ali, Rie Ito, Yoshiki Sawa, Yoshinori Yoshida, Toshio Tanaka, Shunsuke Saito, Ryuji Okamoto, Ryotaro Hashizume, Misato Nishikawa, Itaru Goto, Yuhei Nishimura, Yuhko Kobayashi
Publikováno v:
PLoS ONE, Vol 15, Iss 10, p e0240129 (2020)
PLoS ONE
PLoS ONE
AimsGJB4 encodes a transmembrane connexin protein (Cx30.3) that is a component of gap junctions. This study investigated whether GJB4 plays an important role in human heart disease and function.Methods and resultsWe examined a patient and her older b