Early and extensive alterations of glial connexins, distal oligodendrogliopathy type demyelination,...
Early and extensive alterations of glial connexins, distal oligodendrogliopathy type demyelination, and nodal/paranodal pathology are characteristic of multiple system atrophy
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Publisher
Switzerland: John Wiley & Sons, Inc
Journal title
Language
English
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Publisher
Switzerland: John Wiley & Sons, Inc
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Contents
The pathological hallmark of multiple system atrophy (MSA) is aberrant accumulation of phosphorylated α‐synuclein in oligodendrocytes, forming glial cytoplasmic inclusions (GCIs). Extensive demyelination occurs particularly in the olivopontocerebellar and striatonigral pathways, but its precise mechanism remains elusive. Glial connexins (Cxs), whic...
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Full title
Early and extensive alterations of glial connexins, distal oligodendrogliopathy type demyelination, and nodal/paranodal pathology are characteristic of multiple system atrophy
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10154368
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10154368
Other Identifiers
ISSN
1015-6305
E-ISSN
1750-3639
DOI
10.1111/bpa.13131
