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Cited 37 time in webofscience Cited 42 time in scopus
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The Amyloid-beta Pathway in Alzheimer's Disease

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dc.contributor.authorHampel, Harald-
dc.contributor.authorHardy, John-
dc.contributor.authorBlennow, Kaj-
dc.contributor.authorChen, Christopher-
dc.contributor.authorPerry, George-
dc.contributor.authorKim, Seung Hyun-
dc.contributor.authorVillemagne, Victor L.-
dc.contributor.authorAisen, Paul-
dc.contributor.authorVendruscolo, Michele-
dc.contributor.authorIwatsubo, Takeshi-
dc.contributor.authorMasters, Colin L.-
dc.contributor.authorCho, Min-
dc.contributor.authorLannfelt, Lars-
dc.contributor.authorCummings, Jeffrey L.-
dc.contributor.authorVergallo, Andrea-
dc.date.accessioned2022-07-06T12:08:48Z-
dc.date.available2022-07-06T12:08:48Z-
dc.date.created2021-11-22-
dc.date.issued2021-10-
dc.identifier.issn1359-4184-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/140894-
dc.description.abstractBreakthroughs in molecular medicine have positioned the amyloid-beta (A beta) pathway at the center of Alzheimer's disease (AD) pathophysiology. While the detailed molecular mechanisms of the pathway and the spatial-temporal dynamics leading to synaptic failure, neurodegeneration, and clinical onset are still under intense investigation, the established biochemical alterations of the A beta cycle remain the core biological hallmark of AD and are promising targets for the development of disease-modifying therapies. Here, we systematically review and update the vast state-of-the-art literature of A beta science with evidence from basic research studies to human genetic and multi-modal biomarker investigations, which supports a crucial role of A beta pathway dyshomeostasis in AD pathophysiological dynamics. We discuss the evidence highlighting a differentiated interaction of distinct A beta species with other AD-related biological mechanisms, such as tau-mediated, neuroimmune and inflammatory changes, as well as a neurochemical imbalance. Through the lens of the latest development of multimodal in vivo biomarkers of AD, this cross-disciplinary review examines the compelling hypothesis- and data-driven rationale for A beta-targeting therapeutic strategies in development for the early treatment of AD.-
dc.language영어-
dc.language.isoen-
dc.publisherSPRINGERNATURE-
dc.titleThe Amyloid-beta Pathway in Alzheimer's Disease-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Seung Hyun-
dc.identifier.doi10.1038/s41380-021-01249-0-
dc.identifier.scopusid2-s2.0-85113719979-
dc.identifier.wosid000690816100001-
dc.identifier.bibliographicCitationMOLECULAR PSYCHIATRY, v.26, no.10, pp.5481 - 5503-
dc.relation.isPartOfMOLECULAR PSYCHIATRY-
dc.citation.titleMOLECULAR PSYCHIATRY-
dc.citation.volume26-
dc.citation.number10-
dc.citation.startPage5481-
dc.citation.endPage5503-
dc.type.rimsART-
dc.type.docTypeReview; Early Access-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalResearchAreaPsychiatry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.relation.journalWebOfScienceCategoryPsychiatry-
dc.subject.keywordPlusBASAL FOREBRAIN ATROPHY-
dc.subject.keywordPlusAPOLIPOPROTEIN-E GENOTYPE-
dc.subject.keywordPlusBLOOD-BRAIN-BARRIER-
dc.subject.keywordPlusDENSITY-LIPOPROTEIN RECEPTOR-
dc.subject.keywordPlusIMPAIR SYNAPTIC PLASTICITY-
dc.subject.keywordPlusGAMMA-SECRETASE ACTIVITY-
dc.subject.keywordPlusGENOME-WIDE ASSOCIATION-
dc.subject.keywordPlusPRECURSOR PROTEIN GENE-
dc.subject.keywordPlusA-BETA-
dc.subject.keywordPlusCEREBROSPINAL-FLUID-
dc.identifier.urlhttps://www.nature.com/articles/s41380-021-01249-0-
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