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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Detalles Bibliográficos
Autores principales: Faulkner, Regina L., Wishard, Tyler J., Thompson, Christopher K., Liu, Han-Hsuan, Cline, Hollis T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2014
Materias:
New Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384423/
https://www.ncbi.nlm.nih.gov/pubmed/25844398
http://dx.doi.org/10.1523/ENEURO.0055-14.2014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384423/
https://www.ncbi.nlm.nih.gov/pubmed/25844398
http://dx.doi.org/10.1523/ENEURO.0055-14.2014

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