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Cited by 757

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Selective Sparing of a Class of Striatal Neurons in Huntington's Disease

Ferrante, R. J., Kowall, N. W., Beal, M. F., Richardson, E. P., Bird, E. D., Martin, J. B.·1985·Science

Abstract

A distinct subpopulation of striatal aspiny neurons, containing the enzyme nicotinamide adenine dinucleotide phosphate diaphorase, is preserved in the caudate nucleus in Huntington's disease. Biochemical assays confirmed a significant increase in the activity of this enzyme in both the caudate nucleus and putamen in postmortem brain tissue from patients with this disease. The resistance of these neurons suggests that the gene defect in Huntington's disease may be modifiable by the local biochemical environment. This finding may provide insight into the nature of the genetically programmed cell death that is a characteristic of the disease.

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Metadata

Authors
Ferrante, R. J., Kowall, N. W., Beal, M. F., Richardson, E. P., Bird, E. D., & Martin, J. B.
Venue
Science
Published
1985-11
Volume
230
Issue
4725
Pages
561-563
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2013063789
Cited by
757
References
0
FWCI
8.52
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Selective Sparing of a Class of Striatal Neurons in Huntington's Disease. https://app.cochat.ai/papers/10.1126/science.2931802
The paper
Ferrante, R. J., Kowall, N. W., Beal, M. F., Richardson, E. P., Bird, E. D., & Martin, J. B. (1985). Selective Sparing of a Class of Striatal Neurons in Huntington's Disease. Science. https://doi.org/10.1126/science.2931802

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.