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Modulation of dADAR-dependent RNA editing by the Drosophila fragile X mental retardation protein

Loss of FMR1 gene function results in fragile X syndrome (FXS), the most common heritable form of intellectual disability. The protein encoded from this locus (FMRP) is an RNA binding protein thought to primarily act as a translational regulator, however recent studies implicate FMRP in other mechan...

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Библиографические подробности
Главные авторы: Bhogal, Balpreet, Jepson, James E., Savva, Yiannis A., Pepper, Anita S.-R., Reenan, Robert A., Jongens, Thomas A.
Формат: Artigo
Язык:Inglês
Опубликовано: 2011
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Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC3225737/
https://ncbi.nlm.nih.gov/pubmed/22037499
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nn.2950
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