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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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| Asıl Yazarlar: | , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2012
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| Konular: | |
| Online Erişim: | 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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