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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...

詳細記述

保存先:
書誌詳細
出版年:Neurochem Int
主要な著者: Hamilton, James, Brustovetsky, Tatiana, Brustovetsky, Nickolay
フォーマット: Artigo
言語:Inglês
出版事項: 2017
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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