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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...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Veröffentlicht in:EMBO J
Hauptverfasser: Stiff, Tom, Reis, Caroline, Alderton, Gemma K, Woodbine, Lisa, O'Driscoll, Mark, Jeggo, Penny A
Format: Artigo
Sprache:Inglês
Veröffentlicht: Nature Publishing Group 2004
Schlagworte:
Online Zugang: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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