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Authordc.contributor.authorTaylor, Rebecca C. 
Authordc.contributor.authorHetz Flores, Claudio
Admission datedc.date.accessioned2021-03-30T18:55:25Z
Available datedc.date.available2021-03-30T18:55:25Z
Publication datedc.date.issued2020
Cita de ítemdc.identifier.citationAging Cell. 2020;19:e13265.es_ES
Identifierdc.identifier.other10.1111/acel.13265
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/178868
Abstractdc.description.abstractThe aging process is characterized by a progressive decline in the function of most tissues, representing the main risk factor in the development of a variety of human diseases. Studies in multiple animal models have demonstrated that interventions that improve the capacity to maintain endoplasmic reticulum (ER) proteostasis prolong life and healthspan. ER stress is monitored by the unfolded protein response (UPR), a signaling pathway that mediates adaptive processes to restore proteostasis or the elimination of damaged cells by apoptosis. Here, we discuss recent advances in understanding the significance of the UPR to aging and its implications for the maintenance of cell physiology of various cell types and organs. The possible benefits of targeting the UPR to extend healthspan and reduce the risk of developing age-related diseases are also discussed.es_ES
Patrocinadordc.description.sponsorshipANID/FONDAP program 15150012 Takeda Pharmaceutical Company Ltd P09015-F FONDEF ID16I10223 D11E1007 Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT) CONICYT FONDECYT 1180186 Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT) C17S02 Michael J Fox For Parkinson's research target validation 12473.01 Office of Naval Research 20RT0419 UK Research & Innovation (UKRI) Medical Research Council UK (MRC) European Commissiones_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherWileyes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceAging Celles_ES
Keywordsdc.subjectAginges_ES
Keywordsdc.subjectAutophagyes_ES
Keywordsdc.subjectCell&#8208es_ES
Keywordsdc.subjectNonautonomouses_ES
Keywordsdc.subjectER stresses_ES
Keywordsdc.subjectProtein misfoldinges_ES
Keywordsdc.subjectProteostasises_ES
Títulodc.titleMastering organismal aging through the endoplasmic reticulum proteostasis networkes_ES
Document typedc.typeArtículo de revistaes_ES
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorcrbes_ES
Indexationuchile.indexArtículo de publicación ISI
Indexationuchile.indexArtículo de publicación SCOPUS


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile