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分子病態部

研究業績

  • No association between dysplasminogenemia with p.Ala620Thr mutation and atypical hemolytic uremic syndrome.
    Toshiyuki Miyata, Yumiko Uchida, Yoko Yoshida, Hideki Kato, Masanori Matsumoto, Koichi Kokame, Yoshihiro Fujimura, and Masaomi Nangaku.
    Int. J. Hematol., In press.
  • Deletion of Herpud1 enhances heme oxygenase-1 expression in a mouse model of Parkinson's disease.
    Thuong Manh Le, Koji Hashida, Hieu Minh Ta, Mika Takarada-Iemata, Koichi Kokame, Yasuko Kitao, and Osamu Hori.
    Parkinsons. Dis. 2016, 6163934 (2016)
  • Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiency.
    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 Lammle, and Toshiyuki Miyata.
    Int. J. Hematol. 103, 283-291 (2016)
  • Influence of a rotational speed modulation system used with an implantable continuous-flow left ventricular assist device (EVAHEART) on von Willebrand factor dynamics.
    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.
    Artif. Organs, In press.

過去の業績

最終更新日 2016年11月08日

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