プレスリリース一覧
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脂肪肝・肥満の治療作用を有するシグナル経路の発見 -未開拓の受容体シグナルを標的とした治療薬の開発に貢献-
(2024年11月12日, Biochimica et Biophysica Acta誌掲載)
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受容体1分子の動きを4色の蛍光色素で同時に観察 薬効評価を加速する蛍光・発光マルチモード標識法の開発
(2024年10月12日, Biophysics and Physicobiology誌掲載)
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日本人の薬剤標的遺伝子の多様性の解析 5万4千人のデータからGPCRにおける多様性を探索
(2024年09月23日, Genes to Cells誌掲載)
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免疫制御に関わる生理活性脂質リゾ PS 受容体の立体構造とシグナル選択性の解明
(2024年9月17日, Cell Chemical Biology誌掲載)
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代謝や食欲を制御するQRFP受容体の構造を解明
(2024年5月29日, Nature Communications誌掲載)
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先天性腎性尿崩症の治療候補薬の性状解析 – 疾患変異に応じた個別化治療アプローチの重要性 –
(2024年5月29日, PLoS One誌掲載)
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シグナル欠損細胞を用いて解き明かされる複雑な細胞内シグナル伝達の全容
(2024年5月22日, Pharmacological Reviews誌掲載)
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カモノハシ由来の改変型受容体を用いたバソプレシン測定法の開発 細胞センサー法による簡便かつ迅速な血中の抗利尿ホルモンの測定
(2024年5月13日, Scientific Reports誌掲載)
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脂質代謝や炎症反応に関わるタンパク質の構造を解明~副作用の少ない新薬の開発の糸口に~
(2023年11月10日, Nature Communications誌掲載)
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第一世代抗うつ薬のリゾホスファチジ酸受容体を介した新たな薬理作用を解明~新しい治療薬の創薬標的として期待~
(2023年10月6日, Neuropsychopharmacology誌掲載)
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脂肪燃焼を促進する人工受容体の開発 -細胞の情報伝達に立脚した創薬手法論の開拓へ-
(2023年8月21日, Signal Transduction and Targeted Therapy誌掲載)
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バセドウ病の鑑別診断のための体外診断用医薬品の共同開発
(2023年6月19日)
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GPCR作動薬による新規の受容体活性化機構の解明
(2023年6月08日, Nature誌掲載)
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COVID-19治療薬の副作用の仕組みを解明 -受容体経路を抑制することで副作用改善の可能性-
(2023年5月16日, Communications Biology誌掲載)
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自己免疫疾患に関わるシグナル複合体の立体構造を解明 ~ 脂質受容体に対する創薬開発に貢献 ~
(2023年2月28日, Nature Communication誌掲載)
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受容体のシグナル伝達機構の多様性に迫る―シグナル伝達を緻密に制御した薬の開発に期待 ―
(2023年2月13日, Communication Biology誌掲載)
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温度・化学刺激を感知するタンパク質の測定技術の開発―TRP チャネルを標的とした創薬に貢献―
(2023年2月08日, PLoS ONE誌掲載)
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細胞の情報伝達のオンオフを切り替える脂質分子 ―細胞内取り込み因子アレスチンが受容体に結合する第二の機構の発見―
(2022年11月11日, Cell誌掲載)
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神経ペプチドの受容体 GPCR の立体構造の解明
(2022年8月17日, PLOS BIOLOGY誌掲載)
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骨代謝に関わるPTH1受容体のシグナル伝達複合体を可視化 ―安全性の高い効果的な骨粗しょう症治療薬の合理的設計に貢献―
(2022年8月09日, Molecular Cell誌(オンライン版)掲載)
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シグナル伝達の「偏り」を生み出すリン酸化機構の解明
〜副作用を切り分けた GPCR 作動薬の開発に貢献〜
(2022年2月10日, Nature Communications誌掲載)
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多発性硬化症治療薬が作用する受容体の構造基盤を解明 〜副作用の少ない安全性の高い薬剤の開発に貢献〜
(2021年12月24日, Nature Chemical Biology誌掲載)
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振動分光法を駆使した薬剤効能測定法の開発 ~アセチルコリン受容体を標的とした神経疾患の治療薬開発への期待~
(2021年12月01日, Communications Biology誌掲載)
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非典型的な7回膜貫通型受容体のシグナル伝達経路を解明
(2021年10月01日, Molecular Cell誌掲載)
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メラトニン受容体のシグナル伝達複合体の構造を解明 〜 睡眠や概日リズムの構造基盤の理解と睡眠薬の開発に貢献 〜
(2021年8月16日, Nature Structural & Molecular Biology誌掲載)
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最後に残された β アドレナリン受容体の立体構造を解明 〜副作用の少ない β アドレナリン受容体標的薬の創製に貢献へ〜
(2021年7月27日, Molecular Cell誌掲載)
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脂質受容体の新たな活性化機構を解明 ―脂質がまっすぐ伸びて活性化―
(2021年6月10日, Science Advances誌掲載)
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シグナル情報伝達を担うRNA由来の液性因子を発見 -炎症疾患の新たな核酸医薬開発に期待-
(2021年1月20日, Molecular Cell誌掲載)
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統合失調症に関わるドパミン受容体の構造解明 ―副作用を抑えた薬の迅速な探索・設計が可能に―
(2020年12月23日, Nature Structural & Molecular Biology誌掲載)
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精神疾患に関わるPAC1受容体のシグナル伝達複合体を可視化
(2020年3月10日, Nature Structural & Molecular Biology誌掲載)
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分子の立体構造が明らかにする血圧調節の仕組み ―少しの違いで大違い―
(2020年1月17日, Structure誌掲載)
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痛覚制御や血圧制御、薬物依存等に関与する受容体膜タンパク質、 ニューロテンシン受容体による G タンパク質活性化機構の解明
(2019年6月27日, Nature誌掲載)
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細胞表面の情報センサーの基本原理を解明 ―センサータンパク質に作用するくすりの開発に貢献―
(2019年5月31日, Cell誌掲載)
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統合失調症やパーキンソン病の治療薬の標的の構造解明 ―副作用を抑えた薬の合理的な探索・設計が可能に―
(2019年1月31日, Nature Structural & Molecular Biology誌掲載)
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腸内細菌がつくる乳酸・ピルビン酸により免疫が活性化される仕組みを解明
(2019年1月24日, Nature誌掲載)
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肺動脈性肺高血圧症の治療薬ボセンタンの作用機構を解明
(2017年8月17日, Nature Structural & Molecular Biology誌掲載)
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脂質分子LPAを受容する膜受容体の構造を解明 ―乏毛症やがん治療薬の創出につながる基盤情報が明らかに―
(2017年8月10日, Nature誌掲載)
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神経回路構築を制御する脂質を発見-異なる種類の感覚を伝える神経突起を脂質で誘導-
(2015年8月28日, Science誌掲載)
Signal profiles and spatial regulation of β-arrestin recruitment through Gβ(5) and GRK3 at the μ-opioid receptor
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The repertoire of G-protein-coupled receptor variations in the Japanese population 54KJPN
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Cell swelling enhances ligand-driven β-adrenergic signaling
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A molecular mechanism to diversify Ca(2+) signaling downstream of Gs protein-coupled receptors
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Molecular mechanism of distinct chemokine engagement and functional divergence of the human Duffy antigen receptor
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Molecular mechanism of the endothelin receptor type B interactions with Gs, Gi, and Gq
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Engineered mini-G proteins block the internalization of cognate GPCRs and disrupt downstream intracellular signaling
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A single-domain intrabody targeting the follicle-stimulating hormone receptor impacts FSH-induced G protein-dependent signalling
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G protein-biased LPAR1 agonism of prototypic antidepressants: Implication in the identification of novel therapeutic target for depression
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