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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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Detalhes bibliográficos
Main Authors: Stiff, Tom, Reis, Caroline, Alderton, Gemma K, Woodbine, Lisa, O'Driscoll, Mark, Jeggo, Penny A
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2005
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC544916/
https://ncbi.nlm.nih.gov/pubmed/15616588
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.emboj.7600504
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