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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Dades bibliogràfiques
Publicat a:eNeuro
Autors principals: Faulkner, Regina L., Wishard, Tyler J., Thompson, Christopher K., Liu, Han-Hsuan, Cline, Hollis T.
Format: Artigo
Idioma:Inglês
Publicat: Society for Neuroscience 2014
Matèries:
New Research
Accés en línia: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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