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MCM10 mediates RECQ4 association with MCM2-7 helicase complex during DNA replication
Mutations in RECQ4, a member of the RecQ family of DNA helicases, have been linked to the progeroid disease Rothmund–Thomson Syndrome. Attempts to understand the complex phenotypes observed in recq4-deficient cells suggest a potential involvement in DNA repair and replication, yet the molecular basi...
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| Hauptverfasser: | , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Nature Publishing Group
2009
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2760112/ https://ncbi.nlm.nih.gov/pubmed/19696745 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/emboj.2009.235 |
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