Glycogen autophagy

dc.contributor.authorKotoulas, O. B.en
dc.contributor.authorKalamidas, S. A.en
dc.contributor.authorKondomerkos, D. J.en
dc.date.accessioned2015-11-24T19:14:38Z
dc.date.available2015-11-24T19:14:38Z
dc.identifier.issn1059-910X-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/21356
dc.rightsDefault Licence-
dc.subjectAnimalsen
dc.subjectAnimals, Newbornen
dc.subject*Autophagyen
dc.subjectFemaleen
dc.subjectHepatocytes/*metabolism/ultrastructureen
dc.subjectHumansen
dc.subjectLiver Glycogen/*metabolismen
dc.subjectMaleen
dc.subjectRatsen
dc.subjectVacuoles/physiology/ultrastructureen
dc.titleGlycogen autophagyen
heal.abstractGlycogen autophagy, which includes the sequestration and degradation of cell glycogen in the autophagic vacuoles, is a selective process under conditions of demand for the massive hepatic production of glucose, as in the postnatal period. It represents a link between autophagy and glycogen metabolism. The formation of autophagic vacuoles in the hepatocytes of newborn animals is spatially and biochemically related to the degradation of cell glycogen. Many molecular elements and signaling pathways including the cyclic AMP/cyclic AMP-dependent protein kinase and the phosphoinositides/TOR pathways are implicated in the control of this process. These two pathways may converge on the same target to regulate glycogen autophagy.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primary10.1002/jemt.20046-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/15287014-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1002/jemt.20046/asset/20046_ftp.pdf?v=1&t=h1ymhv29&s=6fb96ca32c558de808283d3fa9817c5506de28b2-
heal.journalNameMicrosc Res Techen
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate2004-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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