ロード中...
Tafazzin Mutation Affecting Cardiolipin Leads to Increased Mitochondrial Superoxide Anions and Mitophagy Inhibition in Barth Syndrome
Tafazzin is a phospholipid transacylase that catalyzes the remodeling of cardiolipin, a mitochondrial phospholipid required for oxidative phosphorylation. Mutations of the tafazzin gene cause Barth syndrome, which is characterized by mitochondrial dysfunction and dilated cardiomyopathy, leading to p...
保存先:
| 出版年: | Cells |
|---|---|
| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI
2020
|
| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7589545/ https://ncbi.nlm.nih.gov/pubmed/33096711 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells9102333 |
| 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!
|