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NBS1 cooperates with homologous recombination to counteract chromosome breakage during replication
Nijmegen breakage syndrome (NBS) is characterized by genome instability and cancer predisposition. NBS patients contain a mutation in the NBS1 gene, which encodes the NBS1 component of the DNA double-strand break (DSB) response complex MRE11/RAD50/NBS1. To investigate the NBS phenotype in more detai...
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| Hlavní autoři: | , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2009
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2995292/ https://ncbi.nlm.nih.gov/pubmed/19782649 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.dnarep.2009.09.002 |
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