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dc.contributor.authorLang-Rollin, I.es
dc.contributor.authorRideout, H.J.es
dc.contributor.authorStefanis, L.-
dc.date.accessioned2011-06-08T09:02:39Z-
dc.date.available2011-06-08T09:02:39Z-
dc.date.issued2003-
dc.identifier.issn0213-3911es
dc.identifier.urihttp://hdl.handle.net/10201/21414-
dc.description.abstractSummary. Ubiquitinated inclusions and selective neuronal cell death are considered the pathological hallmarks of Parkinson’s disease and other neurodegenerative diseases. Recent genetic, pathological and biochemical evidence suggests that dysfunction of ubiquitin-dependent protein degradation by the proteasome might be a contributing, if not initiating factor in the pathogenesis of these diseases. In neuronal cell culture models inhibition of the proteasome leads to cell death and formation of fibrillar ubiquitin and a- synuclein-positive inclusions, thus modeling some aspects of Lewy body diseases. The processes of inclusion formation and neuronal cell death share some common mechanisms, but can also be dissociated at a certain level.es
dc.formatapplication/pdfes
dc.format.extent9es
dc.languageenges
dc.publisherMurcia : F. Hernándezes
dc.relation.ispartofHistology and histopathologyes
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectNeurodegenerativees
dc.subjectApoptosises
dc.subject.otherCDU::6 - Ciencias aplicadas::61 - Medicinaes
dc.titleUbiquitinated inclusions and neuronal cell deathes
dc.typeinfo:eu-repo/semantics/articlees
Aparece en las colecciones:Vol.18, nº 2 (2003)

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