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SMCHD1 promotes ATM‐dependent DNA damage signaling and repair of uncapped telomeres
Structural maintenance of chromosomes flexible hinge domain‐containing protein 1 (SMCHD1) has been implicated in X‐chromosome inactivation, imprinting, and DNA damage repair, and mutations in SMCHD1 can cause facioscapulohumeral muscular dystrophy. More recently, SMCHD1 has also been identified as a...
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| Publicado no: | EMBO J |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7110143/ https://ncbi.nlm.nih.gov/pubmed/32080884 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/embj.2019102668 |
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