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Mutations in the BRCT binding site of BRCA1 result in hyper-recombination
We introduced a K1702M mutation in the BRCA1 BRCT domain known to prevent the binding of proteins harboring pS-X-X-F motifs such as Abraxas-RAP80, BRIP1, and CtIP. Surprisingly, rather than impairing homologous recombination repair (HRR), expression of K1702M resulted in hyper-recombination coincidi...
Autores principales: | Dever, Seth M., Golding, Sarah E., Rosenberg, Elizabeth, Adams, Bret R., Idowu, Michael O., Quillin, John M., Valerie, Nicholas, Xu, Bo, Povirk, Lawrence F., Valerie, Kristoffer |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3156602/ https://www.ncbi.nlm.nih.gov/pubmed/21666281 |
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