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dc.contributor.author Tapia-Rojas, Cheril
dc.contributor.author Cabezas-Opazo, Fabian
dc.contributor.author Deaton, Carol A.
dc.contributor.author Vergara, Erick H.
dc.contributor.author Johnson, Gail V.W.
dc.contributor.author Quintanilla, Rodrigo A.
dc.date.accessioned 2024-09-26T00:27:21Z
dc.date.available 2024-09-26T00:27:21Z
dc.date.issued 2019-04
dc.identifier.issn 0301-0082
dc.identifier.uri https://repositorio.uss.cl/handle/uss/12211
dc.description Publisher Copyright: © 2018 Elsevier Ltd
dc.description.abstract Tau is a protein that is highly enriched in neurons and was originally defined by its ability to bind and stabilize microtubules. However, it is now becoming evident that the functions of tau extend beyond its ability to modulate microtubule dynamics. Tau plays a role in mediating axonal transport, synaptic structure and function, and neuronal signaling pathways. Although tau plays important physiological roles in neurons, its involvement in neurodegenerative diseases, and most prominently in the pathogenesis of Alzheimer disease (AD), has directed the majority of tau studies. However, a thorough knowledge of the physiological functions of tau and its post-translational modifications under normal conditions are necessary to provide the foundation for understanding its role in pathological settings. In this review, we will focus on human tau, summarizing tau structure and organization, as well as its posttranslational modifications associated with physiological processes. We will highlight possible mechanisms involved in mediating the turnover of tau and finally discuss newly elucidated tau functions in a physiological context. en
dc.language.iso eng
dc.relation.ispartof vol. 175 Issue: Pages: 54-76
dc.source Progress in Neurobiology
dc.title It's all about tau en
dc.type Artículo de revisión
dc.identifier.doi 10.1016/j.pneurobio.2018.12.005
dc.publisher.department Facultad de Medicina y Ciencia


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