| Literature DB >> 19640594 |
Rosa Rademakers1, Anne Rovelet-Lecrux.
Abstract
Our understanding of the molecular genetic basis of two common neurodegenerative dementias, Alzheimer's disease (AD) and frontotemporal lobar degeneration (FTLD), has greatly advanced in recent years. Progranulin mutations were identified as a major cause of FTLD and a potential susceptibility factor for other forms of dementia. In addition, through copy-number analyses of previously identified disease genes and the study of microRNA regulation in dementia, new evidence emerged to support the view that subtle variability in the expression of known disease proteins could increase the risk for sporadic forms of dementia. Finally, in late-onset AD populations, the first genome-wide association studies were performed and novel potential AD susceptibility genes reported. These exciting findings provide novel insights into the disease mechanisms underlying dementia and hold promise for the development of potential treatments.Entities:
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Year: 2009 PMID: 19640594 PMCID: PMC2864783 DOI: 10.1016/j.tins.2009.05.005
Source DB: PubMed Journal: Trends Neurosci ISSN: 0166-2236 Impact factor: 13.837