Rchr
J-GLOBAL ID:202101012702854271   Update date: May. 20, 2024

Maruyama Keiko

マルヤマ ケイコ | Maruyama Keiko
Affiliation and department:
Research field  (1): Hematology and oncology
Research keywords  (1): 血液凝固
Research theme for competitive and other funds  (8):
  • 2023 - 2026 凝固第V因子改変体を用いた新たなプロテインSおよびプロテインC活性検査法の確立
  • 2023 - 2024 Pros1イントロン1欠失マウスを用いたプロテインS発現調節機構の解明
  • 2022 - 2023 Protein S遺伝子のイントロン1に潜む未知の発現調節機構の解明
  • 2020 - 2023 血液凝固制御因子プロテインSおよびプロテインCの活性測定法の開発
  • 2022 - 血栓形成抑制に重要な働きをするプロテインSの新たな発現調節機構の解明
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Papers (13):
  • Keiko Maruyama, Shigeki Miyata, Koichi Kokame. Alpha-HIT assay: A new assay for heparin-induced thrombocytopenia antibody detection using FcγRIIa-coated beads and Alpha technology. Research and Practice in Thrombosis and Haemostasis. 2022. 6. 7
  • Satomi Nagaya, Keiko Maruyama, Atsushi Watanabe, Makiko Meguro-Horike, Yuta Imai, Yuki Hiroshima, Shin-Ichi Horike, Koichi Kokame, Eriko Morishita. First report of inherited protein S deficiency caused by paternal PROS1 mosaicism. Haematologica. 2021. 107. 1. 330-333
  • Makoto Osada, Keiko Maruyama, Koichi Kokame, Ryunosuke Denda, Kohei Yamazaki, Hisako Kunieda, Maki Hirao, Seiji Madoiwa, Nobuo Okumura, Mitsuru Murata, et al. A novel homozygous variant of the thrombomodulin gene causes a hereditary bleeding disorder. Blood Advances. 2021
  • Keiko Maruyama, Koichi Kokame. Carrier frequencies of antithrombin, protein C, and protein S deficiency variants estimated using a public database and expression experiments. Research and Practice in Thrombosis and Haemostasis. 2021. 5. 1. 179-186
  • Miyu Usui, Tadashi Ozawa, Younhee Kim, Takafumi Mashiko, Kosuke Matsuzono, Keiko Maruyama, Koichi Kokame, Rie Usui, Reiji Koide, Shigeru Fujimoto. Cerebral venous sinus thrombosis associated with protein S deficiency during pregnancy: a case report. Journal of Obstetrics and Gynaecology. 2020. 40. 1. 135-136
more...
MISC (3):
  • Keiko MARUYAMA, Koichi KOKAME. Estimating the frequencies of pathogenic variants of antithrombin, protein C, and protein S using a public database and expression experiments. Japanese Journal of Thrombosis and Hemostasis. 2021. 32. 5. 635-637
  • Keiko MARUYAMA. ELISA-based detection system for Protein S K196E mutation, a genetic risk factor for venous thromboembolism. Japanese Journal of Thrombosis and Hemostasis. 2016. 27. 4. 466-470
  • 宮田敏行, 丸山慶子. 日本人における先天性血栓性素因-欧米との比較-. 臨床血液. 2014. 55. 8. 908-916
Books (3):
  • 臨床に直結する血栓止血学 改訂2版
    中外医学社 2018 ISBN:9784498125797
  • 動脈・静脈の疾患(上)
    日本臨牀社 2017
  • 止血・血栓ハンドブック
    西村書店 2015
Education (3):
  • 2010 - 2013 金沢大学大学院 医学系研究科 博士後期課程(保健学専攻)
  • 2008 - 2010 Kanazawa University
  • 2004 - 2008 Kanazawa University
Work history (5):
  • 2023/12 - 現在 国立研究開発法人国立循環器病研究センター 研究所 分子病態部 上級研究員
  • 2020/04 - 2023/11 National Cerebral and Cardiovascular Center, Research Institute Department of Molecular Pathogenesis
  • 2017/04 - 2020/03 National Cerebral and Cardiovascular Center, Research Institute Department of Molecular Pathogenesis
  • 2016/04 - 2017/03 National Cerebral and Cardiovascular Center, Research Institute Department of Molecular Pathogenesis
  • 2013/04 - 2016/03 National Cerebral and Cardiovascular Center, Research Institute Department of Molecular Pathogenesis
Awards (2):
  • 2022/06 - 日本血栓止血学会 第44回日本血栓止血学会学術集会 優秀ポスター賞
  • 2016/06 - 日本血栓止血学会 第21回日本血栓止血学会学術奨励賞
Association Membership(s) (3):
日本検査血液学会 ,  日本血液学会 ,  日本血栓止血学会
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