{"_buckets": {"deposit": "992151ec-5aab-49a8-aa0c-d9b677de7e3b"}, "_deposit": {"created_by": 18, "id": "54030", "owners": [18], "pid": {"revision_id": 0, "type": "depid", "value": "54030"}, "status": "published"}, "_oai": {"id": "oai:kanazawa-u.repo.nii.ac.jp:00054030", "sets": ["2846"]}, "author_link": ["48987", "30802"], "item_9_biblio_info_8": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2016-04-21", "bibliographicIssueDateType": "Issued"}, "bibliographicPageStart": "2p.", "bibliographicVolumeNumber": "1986 – 1987", "bibliographic_titles": [{"bibliographic_title": "昭和62(1987)年度 科学研究費補助金 がん特別研究 研究概要"}, {"bibliographic_title": "1987 Research Project Summary", "bibliographic_titleLang": "en"}]}]}, "item_9_creator_33": {"attribute_name": "著者別表示", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "Sasaki, Takuma"}], "nameIdentifiers": [{"nameIdentifier": "48987", "nameIdentifierScheme": 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從って,BFS及びBITは,毒性面からも,またmyeloid選択毒性面から見てもbusulfanに優るCML治療薬となる可能性が強く示唆された.\n4.臨床応用可能な分化誘導物質をめざして,多数の新規核酸関連合成化合物を検討の結果,2,4ーdiethylー7,7,8,8ーtetramethylーcisー2,4ーdiazabicyclo〔4.2,0〕Octaneー3,5ーdioneがヒト前髓球性白血病細胞(HLー60)に対して強い分化誘導効果と増殖抑制効果を示すことを見出した. また,この新規分化誘導物質に,抗白血病剤(daunomycin)やビタミンA誘導体と併用すると,相乘的に作用が増強されることを見出した.", "subitem_description_type": "Abstract"}]}, "item_9_description_22": {"attribute_name": "内容記述", "attribute_value_mlt": [{"subitem_description": "研究課題/領域番号:62010033, 研究期間(年度):1986 – 1987", "subitem_description_type": "Other"}, {"subitem_description": "出典：「新しい合成制癌剤の研究」研究成果報告書　課題番号62010033\n（KAKEN：科学研究費助成事業データベース（国立情報学研究所））\n（https://kaken.nii.ac.jp/ja/grant/KAKENHI-PROJECT-62010033/)を加工して作成", "subitem_description_type": "Other"}]}, "item_9_description_5": {"attribute_name": "提供者所属", "attribute_value_mlt": [{"subitem_description": "金沢大学がん研究所", "subitem_description_type": "Other"}]}, "item_9_identifier_registration": {"attribute_name": "ID登録", "attribute_value_mlt": 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