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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:eNeuro
Prif Awduron: Faulkner, Regina L., Wishard, Tyler J., Thompson, Christopher K., Liu, Han-Hsuan, Cline, Hollis T.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Society for Neuroscience 2014
Pynciau:
New Research
Mynediad Ar-lein: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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