Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice

Lack of fragile X mental retardation protein (FMRP) causes Fragile X Syndrome, the most common form of inherited mental retardation. FMRP is an RNA-binding protein and is a component of messenger ribonucleoprotein complexes, associated with brain polyribosomes, including dendritic polysomes. FMRP is...

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Autors principals: de Vrij, Femke M.S., Levenga, Josien, van der Linde, Herma C., Koekkoek, Sebastiaan K., De Zeeuw, Chris I., Nelson, David L., Oostra, Ben A., Willemsen, Rob
Format: Artigo
Idioma:Inglês
Publicat: 2008
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2481236/
https://ncbi.nlm.nih.gov/pubmed/18571098
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2008.04.002
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