FMRP Regulates Neurogenesis In Vivo in Xenopus laevis Tadpoles(1,2,3)

Fragile X Syndrome (FXS) is the leading known monogenic form of autism and the most common form of inherited intellectual disability. FXS results from silencing the FMR1 gene during embryonic development, leading to loss of Fragile X Mental Retardation Protein (FMRP), an RNA-binding protein that reg...

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Bibliografische gegevens
Gepubliceerd in:eNeuro
Hoofdauteurs: Faulkner, Regina L., Wishard, Tyler J., Thompson, Christopher K., Liu, Han-Hsuan, Cline, Hollis T.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Society for Neuroscience 2014
Onderwerpen:
New Research
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4384423/
https://ncbi.nlm.nih.gov/pubmed/25844398
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/ENEURO.0055-14.2014
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