The DNA mismatch repair gene hMSH2 is a potent coactivator of oestrogen receptor α

The DNA mismatch repair gene is a key regulator in the elimination of base–base mismatches and insertion/deletion loops (IDLs). Human MutS homologue 2 (hMSH2), originally identified as a human homologue of the bacterial MutS, is a tumour suppressor gene frequently mutated in hereditary nonpolyposis...

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Detalhes bibliográficos
Main Authors: Wada-Hiraike, O, Yano, T, Nei, T, Matsumoto, Y, Nagasaka, K, Takizawa, S, Oishi, H, Arimoto, T, Nakagawa, S, Yasugi, T, Kato, S, Taketani, Y
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2005
Assuntos:
Genetics and Genomics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2361802/
https://ncbi.nlm.nih.gov/pubmed/15886699
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.bjc.6602614
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