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          <dc:title>脳脊髄液中のアミロイドβオリゴマー化抑制物質解明と早期診断・治療法開発の展開</dc:title>
          <dc:title xml:lang="en">Inhibitors of amyloid beta oligomerization in human cerebrospinal fluid</dc:title>
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            <jpcoar:nameIdentifier nameIdentifierURI="https://kaken.nii.ac.jp/ja/search/?qm=30755773" nameIdentifierScheme="e-Rad">30755773</jpcoar:nameIdentifier>
            <jpcoar:creatorName>池田, 篤平</jpcoar:creatorName>
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          <datacite:description descriptionType="Abstract">ヒト脳脊髄液のAmyloidβ蛋白に対するオリゴマー化抑制作用の原因物質の解明を行った。脳脊髄液を液体クロマトグラフィー(Size-exclusion column)で分注し、MS/MSで評価し、Angiotensin I、II、IIIの他、既知の蛋白の断片などの16種のペプチドの合成を行った。オリゴマー化の抑制力をPICUP法で評価し、AngiotensinI-IIIを含む11種のペプチドで抑制力をみとめ、Aβの線維化に対する抑制力をThioflavin T法を用いて評価し、9種のペプチドで抑制力を認めた。これらの蛋白はAlzheimer病の発生機序の究明、治療法の開発に寄与する。</datacite:description>
          <datacite:description descriptionType="Abstract">The purpose of this research was to identify inhibitors of amyloid β (Aβ) oligomerization in human cerebrospinal fluid (CSF). CSF was fractionated using centrifugation through a column and size-exclusion high-performance liquid chromatography. Two CSF fractions had inhibitory effects on Aβ oligomerization, as determined using tandem mass spectrometry. We identified 16 peptides with the desired activity: Angiotensins I, II, and III, and known fragments of these peptides. Using photo-induced cross-linking of unmodified proteins (PICUP), we identified 11 peptides with Aβ oligomerization inhibitory activity, including Angiotensins I-III. Thioflavin T fluorescence was used to identify 9 peptides with Aβ fibrillation inhibitory activity, including Angiotensins I-III. The discovery of these peptides contributes to the investigation of the mechanism underlying Alzheimer's disease pathology and the development of therapeutic strategies for Alzheimer’s disease.</datacite:description>
          <datacite:description descriptionType="Other">研究課題/領域番号:16K19506, 研究期間(年度):2016-04-01 – 2018-03-31</datacite:description>
          <datacite:description descriptionType="Other">出典：研究課題「脳脊髄液中のアミロイドβオリゴマー化抑制物質解明と早期診断・治療法開発の展開」課題番号16K19506
（KAKEN：科学研究費助成事業データベース（国立情報学研究所）） 
（https://kaken.nii.ac.jp/ja/report/KAKENHI-PROJECT-16K19506/16K19506seika/）を加工して作成</datacite:description>
          <datacite:description descriptionType="Other">金沢大学医薬保健研究域医学系</datacite:description>
          <datacite:date dateType="Issued">2018-06-06</datacite:date>
          <dc:language>jpn</dc:language>
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          <jpcoar:identifier identifierType="DOI">https://doi.org/10.24517/00059329</jpcoar:identifier>
          <jpcoar:identifier identifierType="HDL">http://hdl.handle.net/2297/00059329</jpcoar:identifier>
          <jpcoar:identifier identifierType="URI">https://kanazawa-u.repo.nii.ac.jp/records/53045</jpcoar:identifier>
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            <jpcoar:relatedIdentifier identifierType="URI">https://kaken.nii.ac.jp/ja/grant/KAKENHI-PROJECT-16K19506/</jpcoar:relatedIdentifier>
            <jpcoar:relatedTitle>https://kaken.nii.ac.jp/ja/grant/KAKENHI-PROJECT-16K19506/</jpcoar:relatedTitle>
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            <jpcoar:relatedIdentifier identifierType="URI">https://kaken.nii.ac.jp/ja/report/KAKENHI-PROJECT-16K19506/16K19506seika/</jpcoar:relatedIdentifier>
            <jpcoar:relatedTitle>https://kaken.nii.ac.jp/ja/report/KAKENHI-PROJECT-16K19506/16K19506seika/</jpcoar:relatedTitle>
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          <jpcoar:sourceTitle>平成29(2017)年度 科学研究費補助金 若手研究(B) 研究成果報告書</jpcoar:sourceTitle>
          <jpcoar:sourceTitle xml:lang="en">2017 Fiscal Year Final Research Report</jpcoar:sourceTitle>
          <jpcoar:volume>2016-04-01 – 2018-03-31</jpcoar:volume>
          <jpcoar:pageStart>4p.</jpcoar:pageStart>
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            <datacite:date dateType="Available">2020-10-19</datacite:date>
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