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Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations
Ataxia with oculomotor apraxia 2 (AOA-2) and amyotrophic lateral sclerosis (ALS4) are neurological disorders caused by mutations in the gene encoding for senataxin (SETX), a putative RNA:DNA helicase involved in transcription and in the maintenance of genome integrity. Here, using ChIP followed by h...
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| Publicat a: | Nat Commun |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group UK
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5803260/ https://ncbi.nlm.nih.gov/pubmed/29416069 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-018-02894-w |
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