Rchr
J-GLOBAL ID:201801012045447550   Update date: Apr. 23, 2024

Mori Takayasu

モリ タカヤス | Mori Takayasu
Affiliation and department:
Job title: Assistant Professor
Other affiliations (1):
Research field  (2): Medical biochemistry ,  Nephrology
Research theme for competitive and other funds  (4):
  • 2017 - 2018 網羅的腎臓病診断パネルを生かした新しい疾患原因遺伝子の探索とデータベースの構築
  • 2015 - 2016 次世代シーケンサーを用いた高血圧バイオマーカー・良性腎硬化症新規原因遺伝子の探索
  • ウロモジュリンの生理的制御メカニズムと病態生理学的機序の解明
  • 塩喪失性腎症の新しい原因遺伝子群の発見とその病態メカニズムの解明
Papers (219):
  • Takuya Fujimaru, Takayasu Mori, Motoko Chiga, Shintaro Mandai, Hiroaki Kikuchi, Fumiaki Ando, Yutaro Mori, Koichiro Susa, Yuta Nakano, Takao Shoji, et al. Genetic Diagnosis of Adult Hemodialysis Patients With Unknown Etiology. Kidney International Reports. 2024. 9. 4. 994-1004
  • Ken Ikenouchi, Daiei Takahashi, Shintaro Mandai, Mizuki Watada, Sayumi Koyama, Motoki Hoshino, Naohiro Takahashi, Wakana Shoda, Tamaki Kuyama, Yutaro Mori, et al. Impact of COVID-19 versus other pneumonia on in-hospital mortality and functional decline among Japanese dialysis patients: a retrospective cohort study. Scientific Reports. 2024. 14. 1
  • Yuta Nakano, Shintaro Mandai, Shotaro Naito, Tamami Fujiki, Yutaro Mori, Fumiaki Ando, Takayasu Mori, Koichiro Susa, Soichiro Iimori, Eisei Sohara, et al. Effect of osteosarcopenia on longitudinal mortality risk and chronic kidney disease progression in older adults. Bone. 2024. 179. 116975-116975
  • Hisazumi Matsuki, Shintaro Mandai, Hiroki Shiwaku, Takaaki Koide, Naohiro Takahashi, Tomoki Yanagi, Shunsuke Inaba, Saaya Ida, Tamami Fujiki, Yutaro Mori, et al. Chronic kidney disease causes blood-brain barrier breakdown via urea-activated matrix metalloproteinase-2 and insolubility of tau protein. Aging. 2023
  • Hideki Yanagawa, Yu Hara, Fumiaki Ando, Soichiro Suzuki, Tamami Fujiki, Daisuke Oikawa, Naofumi Yui, Shintaro Mandai, Yutaro Mori, Koichiro Susa, et al. LRBA signalosomes activate vasopressin-induced AQP2 trafficking at recycling endosomes. The Journal of Physiology. 2023
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MISC (18):
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Books (20):
  • 遺伝性尿細管疾患と遺伝子解析. 腎臓内科
    科学評論社 2023
  • 【腎臓病の最新診療】CKDに潜在する遺伝性腎疾患の重要性. 日本内科学会雑誌
    日本内科学会 2023
  • 【Genetics in CKD】基礎編 サンガーシーケンサーと次世代シーケンサー(解説). 腎と透析
    東京医学社 2023
  • 腎臓病の遺伝子診断の現状. 腎疾患・透析最新の治療2023-2025
    南江堂 2023 ISBN:9784524233694
  • 【CKD患者を診たら-最近のCKD診療の知見とその活かし方】CKDに潜む遺伝性腎疾患. 内科
    南江堂 2021
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Lectures and oral presentations  (226):
  • ステロイドおよび血漿交換により透析を離脱し得た細動脈有意のANCA関連血管炎の一例
    (第68回日本透析医学会学術集会・総会)
  • レオカーナにより救肢が得られたCLTIの一例
    (第68回日本透析医学会学術集会・総会)
  • 透析拒否により晩期透析導入となった2例の転帰
    (第68回日本透析医学会学術集会・総会)
  • 成人期に末期腎不全に至った患者の遺伝的背景の検討
    (第66回日本腎臓学会学術総会)
  • IFT140のヘテロ接合性変異は家族歴のない成人多発性腎嚢胞の一因である
    (第66回日本腎臓学会学術総会)
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Education (2):
  • 2010 - 2014 Tokyo Medical and Dental University
  • 1999 - 2005 Tokyo Medical and Dental University Faculty of Medicine
Professional career (1):
  • 博士(医学) (東京医科歯科大学)
Work history (10):
  • 2021/10 - 現在 Tokyo Medical and Dental University Tokyo Medical and Dental University Division of Integrated Facilities Hemopurification Assistant Professor
  • 2017/04 - 現在 Tokyo Medical and Dental University Graduate School of Medical and Dental Sciences Medical and Dental Sciences Systemic Organ Regulation Nephrology
  • 2018/04 - 2021/09 Tokyo Medical and Dental University (Old Organization)Medical Hospital Central Clinical Facilities Hemopurification Assistant Professor
  • 2017/04 - 2018/03 Tokyo Medical and Dental University (Old Organization)Medical Hospital Central Clinical Facilities Hemopurification Assistant Professor
  • 2016/05 - 2017/03 Tokyo Medical and Dental University Graduate School of Medical and Dental Sciences Medical and Dental Sciences Systemic Organ Regulation Nephrology Visiting Lecturer
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Awards (15):
  • 2021/08 - 日本内科学会 森崇寧. 指導医賞. 内科学会第670回関東地方会
  • 2021/08 - 日本内科学会 森崇寧 内科学会第670回関東地方会 指導医賞
  • 2021/07 - 日本内科学会 第670回日本内科学会関東地方会 指導医賞
  • 2018/06 - 第61回日本腎臓学会学術総会 第21回優秀論文賞 Comprehensive genetic testing approach for major inherited kidney diseases, using next-generation sequencing with a custom panel.
  • 2018/06 - 森崇寧 第61回日本腎臓学会学術総会 第21回優秀論文賞 Comprehensive genetic testing approach for major inherited kidney diseases, using next-generation sequencing with a custom panel.
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