NMD abnormalities during brain development in the Fmr1-knockout mouse model of fragile X syndrome

Abstract Background Fragile X syndrome (FXS) is an intellectual disability attributable to loss of fragile X protein (FMRP). We previously demonstrated that FMRP binds mRNAs targeted for nonsense-mediated mRNA decay (NMD) and that FMRP loss results in hyperactivated NMD and inhibition of neuronal di...

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Auteurs principaux: Tatsuaki Kurosaki, Hitomi Sakano, Christoph Pröschel, Jason Wheeler, Alexander Hewko, Lynne E. Maquat
Format: article
Langue:EN
Publié: BMC 2021
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Accès en ligne:https://doaj.org/article/a0a799aab3524b98be9f5f34a7a8b37c
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