| Literature DB >> 16775218 |
Sherif F El-Khamisy1, Keith W Caldecott.
Abstract
DNA single-strand breaks (SSBs) are the commonest DNA lesions that arise spontaneously in living cells. Cells employ efficient processes for the rapid repair of these breaks and defects in these processes appear to preferentially impact on the nervous system, causing human ataxia. Spinocerebellar ataxia with axonal neuropathy (SCAN1) is a human disease that is associated with a defect in repairing certain types of SSBs. Although it is a rare neurodegenerative disease, understanding the molecular basis of SCAN1 will lead to better understanding of the mechanisms that underpin not only neurodegeneration but also cancer.Entities:
Mesh:
Substances:
Year: 2006 PMID: 16775218 DOI: 10.1093/mutage/gel024
Source DB: PubMed Journal: Mutagenesis ISSN: 0267-8357 Impact factor: 3.000