| 主要論文・著書 | - Seiko Nakajima-Doi, Osamu Seguchi, Yasuhiro Shintani, Tomoyuki Fujita, Satsuki Fukushima, Yorihiko Matsumoto, Yuka Eura, Koichi Kokame, Shigeki Miyata, Sachi Matsuda, Hiroki Mochizuki, Keiichiro Iwasaki, Yuki Kimura, Koichi Toda, Yuto Kumai, Kensuke Kuroda, Takuya Watanabe, Masanobu Yanase, Junjiro Kobayashi, Norihide Fukushima.
Experience of the use of octreotide for refractory gastrointestinal bleeding in a patient with Jarvik2000® left ventricular assist device.
J Artif Organs, 22, 334-337, 2019 - Mario Navarro-Marquez, Natalia Torrealba, Rodrigo Troncoso, Cesar Vasquez-Trincado, Marcelo Rodriguez, Pablo E Morales, Elisa Villalobos, Yuka Eura, Lorena Garcia, Mario Chiong, Amira Klip, Enrique Jaimovich, Koichi Kokame, and Sergio Lavandero.
Herpud1 impacts insulin-dependent glucose uptake in skeletal muscle cells by controlling the Ca2+-calcineurin-Akt axis.
Biochim Biophys Acta, 1864, 1653-1662, 2018 - Natalia Torrealba, Mario Navarro-Marquez, Valeria Garrido, Zully Pedrozo, Diego Romero, Yuka Eura, Elisa Villalobos, Juan Carlos Roa, Mrio Chiong, Koichi Kokame, and Sergio Lavandero.
Herpud1 negatively regulates pathological cardiac hypertrophy by inducing IP3 receptor degradation.
Sci Rep, 7, e13402, 2017 - Noritsugu Naito, Toshihide Mizuno, Takashi Nishimura, Satoru Kishimoto, Yoshiaki Takewa, Yuka Eura, Koichi Kokame, Toshiyuki Miyata, Kazuma Date, Akihide Umeki, Masahiko Ando, Minoru Ono and Eisuke Tatsumi.
Influence of a rotational speed modulation system used with an implantable continuous-flow left ventricular assist device on von Willebrand factor dynamics.
Artif Organs, 40, 877-883, 2016 - Xinping Fan, Johanna A. Kremer Hovinga, Hiroko Shirotani-Ikejima, Yuka Eura, Hidenori Hirai, Shigenori Honda, Koichi Kokame, Magnus Mansouri Taleghani, Anne-Sophie von Krogh, Yoko Yoshida, Yoshihiro Fujimura, Bernhard Lämmle and Toshiyuki Miyata.
Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiency.
Int J Hematol, 103, 283-291, 2016 - Yuka Eura, Koichi Kokame, Toshiro Takafuta, Ryojiro Tanaka, Hikaru Kobayashi, Fumihiro Ishida, Shuichi Hisanaga, Masanori Matsumoto, Yoshihiro Fujimura, Toshiyuki Miyata.
Genetic gene analysis using genomic quantitative PCR: Identification of ADAMTS13 large deletions in two patients with Upshaw-Schulman Syndrome.
Mol Genet Genomic Med, 2, 240-244, 2014 - Yuka Eura, Hiroji Yanamoto, Yuji Arai, Tomohiko Okuda, Toshiyuki Miyata, Koichi Kokame.
Derlin-1 deficiency is embryonic lethal, Derlin-3 deficiency appears normal, and Herp deficiency is intolerant to glucose load and ischemia in mice.
PLoS ONE, 7(3), e34298, 2012 - Yuka Eura, Naotada Ishihara, Toshihiko Oka, Katsuyoshi Mihara.
Identification of a novel protein that regulates mitochondrial fusion by modulating mitofusin (Mfn) protein function.
J Cell Sci, 119(Pt23), 4913-4925, 2006 - Naotada Ishihara, Yuka Eura, Katsuyoshi Mihara.
Mitofusin 1 and 2 play distinct roles in mitochondrial fusion reactions via GTPase activity.
J Cell Sci, 117(Pt26), 6535-6546, 2004 - Naotada Ishihara, Akihiro Jofuku, Yuka Eura, Katsuyoshi Mihara.
Regulation of mitochondrial morphology by membrane potential, and Drp-1-dependent division and FZO1-dependent fusion reaction in mammalian cells.
Biochem Biophys Res Commun, 301(4), 891-898, 2003 - Yuka Eura, Naotada Ishihara, Sadaki Yokota, Katsuyoshi Mihara.
Two mitofusin proteins, mammalian homologues of FZO, with distinct functions are both required for mitochondrial fusion.
J Biochem, 134(3), 333-344, 2003
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