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Peer-reviewed veterinary case report

Embryonic Mutant Huntingtin Aggregate Formation in Mouse Models of Huntington's Disease.

Journal:
Journal of Huntington's disease
Year:
2016
Authors:
Osmand, Alexander P et al.
Affiliation:
Department of Biochemistry and Cellular and Molecular Biology · United States

Abstract

The role of aggregate formation in the pathophysiology of Huntington's disease (HD) remains uncertain. However, the temporal appearance of aggregates tends to correlate with the onset of symptoms and the numbers of neuropil aggregates correlate with the progression of clinical disease. Using highly sensitive immunohistochemical methods we have detected the appearance of diffuse aggregates during embryonic development in the R6/2 and YAC128 mouse models of HD. These are initially seen in developing axonal tracts and appear to spread throughout the cerebrum in the early neonate.

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Original publication: https://pubmed.ncbi.nlm.nih.gov/27886014/