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J-GLOBAL ID:201601011762460322   Update date: Feb. 03, 2025

Watanabe Sachiko

ワタナベ サチコ | Watanabe Sachiko
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Affiliation and department:
Homepage URL  (1): https://kaken.nii.ac.jp/ja/search/?qm=80770619
Research field  (1): Immunology
Research theme for competitive and other funds  (10):
  • 2019 - 2022 Mechanism of NLRP3 inflammasome in CAWS-induced vasculitis
  • 2018 - 2022 Role of ARIH2 in the inflammasome-related cardiovascular disease
  • 2018 - 2022 Neutrophils in inflammatory response induced by lipid crystals
  • 2017 - 2021 Study of the role of the immunoproteasome in glucose- or lipid-metabolism
  • 2018 - 2020 ASC contributes to thrombus formation independent of NLRP3
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Papers (27):
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MISC (6):
  • 善家孝介, 善家孝介, 瀬田玲奈, 辻悠人, 渡邊幸子, 渡邊幸子, 室井正志, 室井正志. Regualtion of TRIF-dependent TLR sginaling by PPM family phosphatases. 日本薬学会年会要旨集(Web). 2024. 144th
  • 渡邊幸子, 渡邊幸子, 寺牛あゆみ, 古川憂菜, 善家孝介, 善家孝介, 室井正志, 室井正志. STAT1 N-terminal domain is required for the formation of parallel dimeric structure of activated STAT1. 日本薬学会年会要旨集(Web). 2024. 144th
  • 善家孝介, 善家孝介, 杉本梨乃, 渡邊幸子, 渡邊幸子, 室井正志, 室井正志. NF-κB p105 is necessary for IFNγ-induced iNOS expression. 日本薬学会年会要旨集(Web). 2023. 143rd
  • 渡邊幸子, 渡邊幸子, 善家孝介, 善家孝介, 室井正志, 室井正志. Lipoteichoic acid inhibits TLR4 signaling by forming an inactive TLR4/MD-2 complex dimer under serum-free conditions. 日本薬学会年会要旨集(Web). 2023. 143rd
  • 渡邊幸子, 善家孝介, 室井正志. Lipoteichoic acidはTLR4/MD-2複合体の非活性化型二量体を形成することでTLR4シグナリングを抑制する. 日本エンドトキシン・自然免疫研究会プログラム・抄録集. 2022. 27th (Web)
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Education (1):
  • 2008 - 2013 Kitasato University Graduate School of Science
Professional career (1):
  • 理学博士 (北里大学)
Work history (3):
  • 2021/04 - 現在 Musashino University Faculty of Pharmacy Department of Pharmaceutical Sciences
  • 2016/03 - 2019/09 Jichi Medical University
  • - 2016/02 Kyoto University
※ Researcher’s information displayed in J-GLOBAL is based on the information registered in researchmap. For details, see here.

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