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The role of WRNIP1 in genome maintenance
WRNIP1 interacts with WRN helicase, which is defective in the premature aging disease Werner syndrome. WRNIP1 belongs to the AAA+ ATPase family and is conserved from Escherichia coli to human. The protein contains an ubiquitin-binding zinc finger (UBZ) domain at the N terminus and an ATPase domain i...
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| 發表在: | Cell Cycle |
|---|---|
| Main Authors: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Taylor & Francis
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5384577/ https://ncbi.nlm.nih.gov/pubmed/28118071 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15384101.2017.1282585 |
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