ロード中...
A Huntingtin Peptide Inhibits PolyQ-Huntingtin Associated Defects
BACKGROUND: Huntington’s disease (HD) is caused by the abnormal expansion of the polyglutamine tract in the human Huntingtin protein (polyQ-hHtt). Although this mutation behaves dominantly, huntingtin loss of function also contributes to HD pathogenesis. Indeed, wild-type Huntingtin plays a protecti...
保存先:
| 主要な著者: | , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Public Library of Science
2013
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3701666/ https://ncbi.nlm.nih.gov/pubmed/23861941 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0068775 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|