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Oxidative metabolism and Ca(2+) handling in striatal mitochondria from YAC128 mice, a model of Huntington’s disease
The mechanisms implicated in the pathology of Huntington’s disease (HD) remain not completely understood, although dysfunction of mitochondrial oxidative metabolism and Ca(2+) handling have been suggested as contributing factors. However, in our previous studies with mitochondria isolated from the w...
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| 出版年: | Neurochem Int |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5495615/ https://ncbi.nlm.nih.gov/pubmed/28062223 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuint.2017.01.001 |
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