RORA and autism in Isfahan population: is there an epigenetic relationship
Cell Journal [Yakhteh]. 2017; 18 (4): 540-546
in English
| IMEMR
| ID: emr-185779
ABSTRACT
Objective:
Autism is a neurodevelopmental disorder characterized by difficulty in verbal and non-verbal communication, impaired social interaction, and restricted and repetitive behavior. It has been recently introduced as a multigenic disorder with significant epigenetic effects on its pathology. Recently, epigenetic silencing of retinoic acid receptor-related orphan receptor alpha [ROR alpha] gene [which has an essential role in neural tissue development] was shown to have occurred in autistic children due to methylation of its promoter region. This may thus explain a significant part of the molecular pathogenesis of autism. Therefore, we aimed to confirm this finding by implementing a case-control [experimental] study in the population of Isfahan
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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Case-Control Studies
/
Promoter Regions, Genetic
/
DNA Methylation
/
Genetic Predisposition to Disease
/
Epigenesis, Genetic
/
Nuclear Receptor Subfamily 1, Group F, Member 1
Limits:
Child
/
Female
/
Humans
/
Male
Language:
English
Journal:
Cell J. [Yakhteh]
Year:
2017
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