| Literature DB >> 24506814 |
Eduardo Gascon1, Fen-Biao Gao.
Abstract
Increasing evidence suggests that frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) share some clinical, pathological, and molecular features as part of a common neurodegenerative spectrum disorder. In recent years, enormous progress has been made in identifying both pathological proteins and genetic mutations associated with FTD-ALS. However, the molecular pathogenic mechanisms of disease onset and progression remain largely unknown. Recent studies have uncovered unexpected links between FTD-ALS and multiple aspects of RNA metabolism, setting the stage for further understanding of the disorder. Here, the authors will focus on microRNAs and review the emerging roles of these small RNAs in several aspects of FTD-ALS pathogenesis.Entities:
Keywords: ALS; C9ORF72; CHMP2B; FTD; FUS; MicroRNA; TDP-43; neurodegeneration; progranulin
Mesh:
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Year: 2014 PMID: 24506814 PMCID: PMC4199862 DOI: 10.3109/01677063.2013.876021
Source DB: PubMed Journal: J Neurogenet ISSN: 0167-7063 Impact factor: 1.250