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dc.contributor.authorBenvegnú, Stefano-
dc.date.accessioned2020-06-24T10:00:02Z-
dc.date.available2020-06-24T10:00:02Z-
dc.date.issued2019-
dc.identifierdoi: 10.1002/jnr.24446-
dc.identifierissn: 1097-4547-
dc.identifier.citationJournal of Neuroscience Research (2019)-
dc.identifier.urihttp://hdl.handle.net/10261/215103-
dc.description.abstractAging is a primary risk factor for fatal neurodegenerative disorders, yet the mechanisms underlying physiological healthy aging and pathological aging, and how these mechanisms can divert one scenario to the other, are not completely understood. In recent years, reports indicate that alterations in nucleocytoplasmic transport may be a hallmark of both healthy and pathological aging. In this review, I summarize recent evidence supporting this information, specifically focusing on the association between the nucleocytoplasmic transport and aging of the brain, indicating both common and case-specific mechanisms and their interplay, and pointing out alterations of these mechanisms as regulatory “switches” for the fate of the aging brain. Importantly, some of these alterations are intervenable druggable targets, paving the way to a future pharmacotherapeutic intervention.-
dc.languageeng-
dc.publisherJohn Wiley & Sons-
dc.relation.isversionofPublisher's version-
dc.rightsopenAccess-
dc.subjectAging-
dc.subjectAmyotrophic lateral sclerosis-
dc.subjectAlzheimer's disease-
dc.subjectFrontotemporal dementia-
dc.subjectHuntington disease-
dc.subjectNeurodegeneration-
dc.subjectNeurodegenerative diseases-
dc.subjectPrion diseases-
dc.subjectTauopathies-
dc.titleNucleus–cytoplasm cross-talk in the aging brain-
dc.typeartículo-
dc.identifier.doi10.1002/jnr.24446-
dc.relation.publisherversionhttp://dx.doi.org/10.1002/jnr.24446-
dc.date.updated2020-06-24T10:00:03Z-
dc.relation.csic-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.cerifentitytypePublications-
item.grantfulltextopen-
item.openairetypeartículo-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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