Is Parkinson's disease a lysosomal disorder?

dc.contributor.authorKlein, Andrés
dc.contributor.authorMazzulli, Joseph
dc.date.accessioned2022-05-12T21:30:48Z
dc.date.available2022-05-12T21:30:48Z
dc.date.issued2018
dc.description.abstractCommon forms of Parkinson’s disease have long been described as idiopathic, with no single penetrant genetic factor capable of influencing disease aetiology. Recent genetic studies indicate a clear association of variants within several lysosomal genes as risk factors for idiopathic Parkinson’s disease. The emergence of novel variants suggest that the aetiology of idiopathic Parkinson’s disease may be explained by the interaction of several partially penetrant mutations that, while seemingly complex, all appear to converge on cellular clearance pathways. These newly evolving data are consistent with mechanistic studies linking a-synuclein toxicity to lysosomal abnormalities, and indicate that idiopathic Parkinson’s disease resembles features of Mendelian lysosomal storage disorders at a genetic and biochemical level. These findings offer novel pathways to exploit for the development of diseasealtering therapies for idiopathic Parkinson’s disease that target specific components of the lysosomal system.es
dc.description.versionVersión publicadaes
dc.identifier.citationKlein AD, Mazzulli JR. Is Parkinson's disease a lysosomal disorder? Brain. 2018 Aug 1;141(8):2255-2262. doi: 10.1093/brain/awy147.es
dc.identifier.urihttps://doi.org/ 10.1093/brain/awy147es
dc.identifier.urihttp://hdl.handle.net/11447/6085
dc.language.isoenes
dc.subjectNeurodegenerationes
dc.subjectAlpha-synucleines
dc.subjectLysosomal storage diseasees
dc.subjectProtein traffickinges
dc.subjectAutophagyes
dc.titleIs Parkinson's disease a lysosomal disorder?es
dc.typeArticlees
dcterms.sourceBrain : a journal of neurologyes

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