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Cystathionine γ-lyase deficiency mediates neurodegeneration in Huntington’s disease

Huntington’s disease is an autosomal dominant disease associated with a mutation in the gene encoding huntingtin (Htt) leading to expanded polyglutamine repeats of mutant Htt (mHtt) that elicit oxidative stress, neurotoxicity, and motor and behavioural changes(1). Huntington’s disease is characteriz...

詳細記述

保存先:
書誌詳細
出版年:Nature
主要な著者: Paul, Bindu D., Sbodio, Juan I., Xu, Risheng, Vandiver, M. Scott, Cha, Jiyoung Y., Snowman, Adele M., Snyder, Solomon H.
フォーマット: Artigo
言語:Inglês
出版事項: 2014
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4349202/
https://ncbi.nlm.nih.gov/pubmed/24670645
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature13136
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