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dc.contributor.authorMartínez, Gabriela [Univ Mayor, Ctr Integrat Biol, Santiago, Chile]es_CL
dc.contributor.authorKhatiwada, Sanjeeves_CL
dc.contributor.authorCosta-Mattioli, Mauroes_CL
dc.contributor.authorHetz, Claudioes_CL
dc.date.accessioned2020-04-08T14:11:55Z
dc.date.accessioned2020-04-13T18:12:34Z
dc.date.available2020-04-08T14:11:55Z
dc.date.available2020-04-13T18:12:34Z
dc.date.issued2018es_CL
dc.identifier.citationMartínez, G., Khatiwada, S., Costa-Mattioli, M., & Hetz, C. (2018). ER proteostasis control of neuronal physiology and synaptic function. Trends in neurosciences, 41(9), 610-624.es_CL
dc.identifier.issn0166-2236es_CL
dc.identifier.issn1878-108Xes_CL
dc.identifier.urihttps://doi.org/10.1016/j.tins.2018.05.009es_CL
dc.identifier.urihttp://repositorio.umayor.cl/xmlui/handle/sibum/6096
dc.description.abstractNeuronal proteostasis is maintained by the dynamic integration of different processes that regulate the synthesis, folding, quality control, and localization of proteins. The endoplasmic reticulum (ER) serves as a fundamental pillar of the proteostasis network, and is emerging as a key compartment to sustain normal brain function. The unfolded protein response (UPR), the main mechanism that copes with ER stress, plays a central role in the quality control of many ion channels and receptors, in addition to crosstalk with signaling pathways that regulate connectivity, synapse formation, and neuronal plasticity. We provide here an overview of recent advances in the involvement of the UPR in maintaining neuronal proteostasis, and discuss its emerging role in brain development, neuronal physiology, and behavior, as well as the implications for neurodegenerative diseases involving cognitive decline.es_CL
dc.description.sponsorshipUS Office of Naval Research-Global (ONR-G) [N62909-16-1-2003]; Millennium InstituteTakeda Pharmaceutical Company Ltd [P09-015-F]; FONDEF [ID16I10223, D11E1007]; US Air Force Office of Scientific ResearchUnited States Department of DefenseAir Force Office of Scientific Research (AFOSR) [FA9550-16-1-0384]; CONICYT-Brazil [441921/2016-7]; Leading House for the Latin American Region seed money grant; FONDECYTComision Nacional de Investigacion Cientifica y Tecnologica (CONICYT)CONICYT FONDECYT [3150637, 1180186]; Muscular Dystrophy; National Institutes of HealthUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USA [NIMH 096816, NINDS 076708]; National Institutes of Health (Sammons Foundation)es_CL
dc.description.sponsorshipThis work was funded by US Office of Naval Research-Global (ONR-G) grant N62909-16-1-2003, Millennium Institute P09-015-F, FONDEF ID16I10223, US Air Force Office of Scientific Research FA9550-16-1-0384, CONICYT-Brazil 441921/2016-7, and a Leading House for the Latin American Region seed money grant (C.H.). We also thank FONDECYT 3150637 (GM). In addition, we are grateful for the support from FONDEF D11E1007, Muscular Dystrophy and FONDECYT 1180186 (C.H.), and for grants from the National Institutes of Health to M.C.M. (NIMH 096816, NINDS 076708, and the Sammons Foundation).es_CL
dc.language.isoenes_CL
dc.publisherELSEVIER SCIENCE LONDONes_CL
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceTrends Neurosci., SEP 2018. 41(9): p. 610-624
dc.subjectNeuroscienceses_CL
dc.titleER Proteostasis Control of Neuronal Physiology and Synaptic Functiones_CL
dc.typeRevisiónes_CL
umayor.facultadCIENCIASes_CL
umayor.politicas.sherpa/romeoRoMEO green journal (Se puede archivar el pre-print y el post-print o versión de editor/PDF). Disponible en: http://sherpa.ac.uk/romeo/index.phpes_CL
umayor.indexadoWOS:000442299100012es_CL
umayor.indexadoPMID: 29945734es_CL
dc.identifier.doiDOI: 10.1016/j.tins.2018.05.009es_CL]
umayor.indicadores.wos-(cuartil)Q1es_CL
umayor.indicadores.scopus-(scimago-sjr)SCIMAGO/ INDICE H: 269 Hes_CL


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