dc.date.accessioned2020-03-11T20:30:09Z
dc.date.accessioned2022-10-18T22:48:29Z
dc.date.available2020-03-11T20:30:09Z
dc.date.available2022-10-18T22:48:29Z
dc.date.created2020-03-11T20:30:09Z
dc.date.issued2008
dc.identifierhttp://hdl.handle.net/10533/239026
dc.identifier13980001
dc.identifierWOS:000260110500028
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4470365
dc.description.abstractThe major protein constituent of amyloid deposits in Alzheimer's disease (AD) is the amyloid-beta-peptide (Abeta). Amyloid deposits contain "chaperone molecules" which play critical roles in amyloid formation and toxicity. In the present work, we test an
dc.languageeng
dc.relation10.1016/j.cbi.2008.05.026
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.titleRelease of Acetylcholinesterase (AChE) from β-Amyloid plaques assemblies improves the spatial memory impairments in APP-transgenic mice
dc.typeArticulo


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