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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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Dettagli Bibliografici
Pubblicato in:EMBO J
Autori principali: Stiff, Tom, Reis, Caroline, Alderton, Gemma K, Woodbine, Lisa, O'Driscoll, Mark, Jeggo, Penny A
Natura: Artigo
Lingua:Inglês
Pubblicazione: Nature Publishing Group 2004
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Accesso online: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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