ロード中...
Mutations in the Human AAA(+) Chaperone p97 and Related Diseases
A number of neurodegenerative diseases have been linked to mutations in the human protein p97, an abundant cytosolic AAA(+) (ATPase associated with various cellular activities) ATPase, that functions in a large number of cellular pathways. With the assistance of a variety of cofactors and adaptor pr...
保存先:
| 出版年: | Front Mol Biosci |
|---|---|
| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Frontiers Media S.A.
2016
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5131264/ https://ncbi.nlm.nih.gov/pubmed/27990419 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fmolb.2016.00079 |
| 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!
|