Dysregulation of Galectin-3 causes neurotoxic phenotypes in the microglia of Huntington’s disease
博士 === 國立陽明大學 === 分子醫學博士學位學程 === 107 === Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder that manifests with movement dysfunction and cognitive decline. The disease-causing mutation is an expansion of CAG repeats in the Huntingtin gene. The resultant mutant Huntingtin (...
| Main Authors: | , |
|---|---|
| Other Authors: | |
| Format: | Others |
| Language: | en_US |
| Published: |
2019
|
| Online Access: | http://ndltd.ncl.edu.tw/handle/m5yw6n |