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pubmed-article:1713390pubmed:abstractTextChronic wasting disease (CWD), a progressive neurological disorder of captive mule deer, black-tailed deer, hybrids of mule deer and white-tailed deer and Rocky Mountain elk, is characterized neuropathologically by widespread spongiform change of the neuropil, intracytoplasmic vacuolation in neuronal perikarya and astrocytic hypertrophy and hyperplasia. We report the topographic distribution of amyloid plaques reactive to antibodies prepared against scrapie amyloid in CWD-affected captive mule deer (Odocoileus hemionus hemionus). Scrapie amyloid-immunoreactive plaques were found in the cerebral gray and white matter, in deep subcortical nuclei, in isolation or in clusters in areas of vacuolation, and perivascularly, in subpial and subependymal regions. In the cerebellum, immunoreactive amyloid plaques were observed in the molecular, pyramidal and granular layers. Scrapie amyloid-immunoreactive deposits were also seen in neuronal perikarya. Furthermore, amyloid plaques in CWD-affected captive mule deer were alcianophilic at 0.3 M magnesium chloride indicating the presence of weakly to moderately sulfated glycosaminoglycans. Our data corroborate that CWD in captive mule deer belongs to the subacute virus spongiform encephalopathies.lld:pubmed
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pubmed-article:1713390pubmed:authorpubmed-author:WilliamsE SESlld:pubmed
pubmed-article:1713390pubmed:authorpubmed-author:GajdusekD CDClld:pubmed
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pubmed-article:1713390pubmed:authorpubmed-author:GuiroyD CDClld:pubmed
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pubmed-article:1713390pubmed:pagination475-8lld:pubmed
pubmed-article:1713390pubmed:dateRevised2007-11-9lld:pubmed
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pubmed-article:1713390pubmed:year1991lld:pubmed
pubmed-article:1713390pubmed:articleTitleTopographic distribution of scrapie amyloid-immunoreactive plaques in chronic wasting disease in captive mule deer (Odocoileus hemionus hemionus).lld:pubmed
pubmed-article:1713390pubmed:affiliationLaboratory of Central Nervous System Studies, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892.lld:pubmed
pubmed-article:1713390pubmed:publicationTypeJournal Articlelld:pubmed
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