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Cockayne Syndrome group B protein interacts with TRF2 and regulates telomere length and stability
The majority of Cockayne syndrome (CS) patients carry a mutation in Cockayne Syndrome group B (CSB), a large nuclear protein implicated in DNA repair, transcription and chromatin remodeling. However, whether CSB may play a role in telomere metabolism has not yet been characterized. Here, we report t...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3479199/ https://ncbi.nlm.nih.gov/pubmed/22904069 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gks745 |
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