Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/43002
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dc.contributor.authorRavikumar, Brindaen_US
dc.contributor.authorSarkar, Sovanen_US
dc.contributor.authorDavies, Janet E.en_US
dc.contributor.authorFutter, Marieen_US
dc.contributor.authorGarcia-Arencibia, Moisesen_US
dc.contributor.authorGreen-Thompson, Zeyn W.en_US
dc.contributor.authorJimenez-Sanchez, Mariaen_US
dc.contributor.authorKorolchuk, Viktor I.en_US
dc.contributor.authorLichtenberg, Maikeen_US
dc.contributor.authorLuo, Shouqingen_US
dc.contributor.authorMassey, Dunecan C.O.en_US
dc.contributor.authorMenzies, Fiona M.en_US
dc.contributor.authorMoreau, Kevinen_US
dc.contributor.authorNarayanan, Ushaen_US
dc.contributor.authorRenna, Maurizioen_US
dc.contributor.authorSiddiqi, Farah H.en_US
dc.contributor.authorUnderwood, Benjamin R.en_US
dc.contributor.authorWinslow And, Ashley R.en_US
dc.contributor.authorRubinsztein, David C.en_US
dc.contributor.otherRubinsztein, David-
dc.contributor.otherGarcia-Arencibia, Moises-
dc.contributor.otherGarcia-Arencibia, Moises-
dc.contributor.otherKorolchuk, Viktor-
dc.contributor.otherJimenez-Sanchez, Maria-
dc.date.accessioned2018-11-21T12:02:34Z-
dc.date.available2018-11-21T12:02:34Z-
dc.date.issued2010en_US
dc.identifier.issn0031-9333en_US
dc.identifier.urihttp://hdl.handle.net/10553/43002-
dc.description.abstract(Macro)autophagy is a bulk degradation process that mediates the clearance of long-lived proteins and organelles. Autophagy is initiated by double-membraned structures, which engulf portions of cytoplasm. The resulting autophagosomes ultimately fuse with lysosomes, where their contents are degraded. Although the term autophagy was first used in 1963, the field has witnessed dramatic growth in the last 5 years, partly as a consequence of the discovery of key components of its cellular machinery. In this review we focus on mammalian autophagy, and we give an overview of the understanding of its machinery and the signaling cascades that regulate it. As recent studies have also shown that autophagy is critical in a range of normal human physiological processes, and defective autophagy is associated with diverse diseases, including neurodegeneration, lysosomal storage diseases, cancers, and Crohn's disease, we discuss the roles of autophagy in health and disease, while trying to critically evaluate if the coincidence between autophagy and these conditions is causal or an epiphenomenon. Finally, we consider the possibility of autophagy upregulation as a therapeutic approach for various conditions.en_US
dc.languageengen_US
dc.publisher0031-9333-
dc.relation.ispartofPhysiological Reviewsen_US
dc.sourcePhysiological Reviews [ISSN 0031-9333], v. 90, p. 1383-1435en_US
dc.subject32 Ciencias médicasen_US
dc.titleRegulation of mammalian autophagy in physiology and pathophysiologyen_US
dc.typeinfo:eu-repo/semantics/reviewen_US
dc.typeArticleen_US
dc.identifier.doi10.1152/physrev.00030.2009en_US
dc.identifier.scopus78149475088-
dc.identifier.isi000283216100004-
dcterms.isPartOfPhysiological Reviews-
dcterms.sourcePhysiological Reviews[ISSN 0031-9333],v. 90 (4), p. 1383-1435-
dc.contributor.authorscopusid7004224895-
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dc.contributor.authorscopusid57202555664-
dc.contributor.authorscopusid22956196500-
dc.contributor.authorscopusid57203103128-
dc.contributor.authorscopusid36164296400-
dc.contributor.authorscopusid36857708500-
dc.contributor.authorscopusid36847225100-
dc.contributor.authorscopusid24073937700-
dc.contributor.authorscopusid12040449700-
dc.contributor.authorscopusid36626756300-
dc.contributor.authorscopusid7006338728-
dc.description.lastpage1435en_US
dc.description.firstpage1383en_US
dc.relation.volume90en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Reseñaen_US
dc.identifier.wosWOS:000283216100004-
dc.contributor.daisngid1317186-
dc.contributor.daisngid1102884-
dc.contributor.daisngid2356423-
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dc.contributor.daisngid37428-
dc.identifier.investigatorRIDC-3472-2011-
dc.identifier.investigatorRIDB-5538-2012-
dc.identifier.investigatorRIDK-9920-2013-
dc.identifier.investigatorRIDNo ID-
dc.identifier.investigatorRIDNo ID-
dc.utils.revisionen_US
dc.identifier.ulpgcen_US
dc.identifier.ulpgcen_US
dc.identifier.ulpgcen_US
dc.identifier.ulpgcen_US
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.orcid0000-0002-1618-4487-
crisitem.author.fullNameGarcía Arencibia, Moisés-
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