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Nbs1 is required for ATR-dependent phosphorylation events
Nijmegen breakage syndrome (NBS) is characterised by microcephaly, developmental delay, characteristic facial features, immunodeficiency and radiosensitivity. Nbs1, the protein defective in NBS, functions in ataxia telangiectasia mutated protein (ATM)-dependent signalling likely facilitating ATM pho...
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| Yayımlandı: | EMBO J |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Nature Publishing Group
2004
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC544916/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/15616588/ https://ncbi.nlm.nih.govhttps://doi.org/10.1038/sj.emboj.7600504 |
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