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The HRDC domain of BLM is required for the dissolution of double Holliday junctions
Bloom's syndrome is a hereditary cancer-predisposition disorder resulting from mutations in the BLM gene. In humans, BLM encodes one of five members of the RecQ helicase family. One function of BLM is to act in concert with topoisomerase IIIα (TOPO IIIα) to resolve recombination intermediates c...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1176466/ https://ncbi.nlm.nih.gov/pubmed/15990871 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.emboj.7600740 |
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