The EIF4G1 gene and Parkinson's disease.
Identifieur interne : 000015 ( PubMed/Corpus ); précédent : 000014; suivant : 000016The EIF4G1 gene and Parkinson's disease.
Auteurs : H. Deng ; Y. Wu ; J. JankovicSource :
- Acta neurologica Scandinavica ; 2015.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Eukaryotic Initiation Factor-4G.
- genetics : Parkinson Disease.
- Humans, Mutation.
Abstract
Variants in the EIF4G1 gene have been recently identified to be responsible for autosomal dominant PD (PARK18), but its role in the PD-related neurodegeneration is unclear. Several EIF4G1 mutation/variants were found to be associated with PD, and functional studies have suggested that these variants may impair the ability of cells to rapidly and dynamically respond to stress, thus probably participating in the development of PD, and these indicated that EIF4G1 variants may play an important role in pathogenicity of PD, although the frequency is low. Further studies involving large sample size of patients with PD from diverse populations, as well as studies of EIF4G1 expression and in scaffold function, are warranted.
DOI: 10.1111/ane.12397
PubMed: 25765080
Links to Exploration step
pubmed:25765080Le document en format XML
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<front><div type="abstract" xml:lang="en">Variants in the EIF4G1 gene have been recently identified to be responsible for autosomal dominant PD (PARK18), but its role in the PD-related neurodegeneration is unclear. Several EIF4G1 mutation/variants were found to be associated with PD, and functional studies have suggested that these variants may impair the ability of cells to rapidly and dynamically respond to stress, thus probably participating in the development of PD, and these indicated that EIF4G1 variants may play an important role in pathogenicity of PD, although the frequency is low. Further studies involving large sample size of patients with PD from diverse populations, as well as studies of EIF4G1 expression and in scaffold function, are warranted.</div>
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