Caldag-Gefi Down-Regulation in the Striatum as a Neuroprotective Change in Huntington's Disease.
Huntingtin protein (Htt) is ubiquitously expressed, yet Huntington’s disease (HD), a fatal neurologic disorder produced by expansion of an Htt polyglutamine tract, is characterized by neurodegeneration that occurs primarily in the striatum and cerebral cortex. Such discrepancies between sites of...
Main Authors: | , , , , , , , , , , |
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Other Authors: | |
Format: | Article |
Language: | en_US |
Published: |
IRL Press at Oxford University Press
2011
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Online Access: | http://hdl.handle.net/1721.1/64695 https://orcid.org/0000-0001-5016-0756 https://orcid.org/0000-0002-4326-7720 |