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dc.contributor.authorCatherine Rabouille*
dc.contributor.authorGeorg Haase*
dc.date.accessioned2021-02-11T14:44:18Z
dc.date.available2021-02-11T14:44:18Z
dc.date.issued2016*
dc.date.submitted2016-04-07 11:22:02*
dc.identifier18877*
dc.identifier.issn16648714*
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/48746
dc.description.abstractThe Golgi apparatus is a central organelle that lies at the heart of the secretory pathway. It ensures post-translational protein modifications such as glycosylation and cleavage as well as protein sorting to neuronal axons and dendrites. Structural and functional alterations of the Golgi apparatus (fragmentation and atrophy), which are collectively termed Golgi pathology, are now recognized as a constant feature of many neuro-degenerative diseases. However, the molecular mechanisms underlying these changes and their precise relevance to neurodegeneration have not yet been completely elucidated. This eBook contains 13 reviews that address the molecular mechanisms of Golgi pathology in Parkinson and Alzheimer diseases, amyotrophic lateral sclerosis (ALS) and spinal muscular atrophies, and discuss their potential relevance to the pathological loss of neuronal cell bodies, axons and synapses.*
dc.languageEnglish*
dc.relation.ispartofseriesFrontiers Research Topics*
dc.subjectRC321-571*
dc.subjectQ1-390*
dc.subject.classificationthema EDItEUR::P Mathematics and Science::PS Biology, life sciences::PSA Life sciences: general issues::PSAN Neurosciencesen_US
dc.subject.otherNeurodegenerative Diseases*
dc.subject.otherIntracellular membrane traffic*
dc.subject.otherAmyotrophic Lateral Sclerosis*
dc.subject.othersignaling*
dc.subject.otherGolgi fragmentation*
dc.subject.otherMicrotubules*
dc.subject.otherCell Death*
dc.subject.otherTethers*
dc.subject.othermolecular motors*
dc.subject.othervesicles*
dc.titleGolgi Pathology in Neurodegenerative Diseases*
dc.typebook
oapen.identifier.doi10.3389/978-2-88919-757-6*
oapen.relation.isPublishedBybf5ce210-e72e-4860-ba9b-c305640ff3ae*
oapen.relation.isbn9782889197576*
oapen.pages119*


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