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dc.contributor.authorCox, Sarah J-
dc.contributor.authorLam, Brian-
dc.contributor.authorPrasad, Ajay-
dc.date.accessioned2024-05-29T09:04:52Z-
dc.date.available2024-05-29T09:04:52Z-
dc.date.issued2019-
dc.identifier.otherOER000004045vi
dc.identifier.urihttp://dlib.hust.edu.vn/handle/HUST/24895-
dc.descriptionTài liệu này được phát hành theo giấy phép CC-BY-NC-ND 4.0vi
dc.description.abstractAmyloid-β aggregation at the cell-membrane of neruonal cells is implicated as a source of toxicity for Alzheimer’s disease. Small molecules have been studied for their ability to supress amyloid aggregation and toxicity, but the presence of membranes negate their activity. Here, we have identified 5 small molecules that are active at the membrane interface.vi
dc.description.urihttps://www.biorxiv.org/content/10.1101/853499v1vi
dc.formatPDFvi
dc.language.isoenvi
dc.publisherBiochemical Journalvi
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Vietnam*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/vn/*
dc.subjectAlzheimervi
dc.subjectAmyloid-βvi
dc.subject.lccQD405vi
dc.titleHigh Throughput Screening at the Membrane Interface Reveals New Inhibitors of Amyloid-βvi
dc.typeJournal articlevi
Appears in Collections:OER - Kỹ thuật hóa học; Công nghệ sinh học - Thực phẩm; Công nghệ môi trường

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