Reversal of Fragile X Phenotypes by Manipulation of AβPP/Aβ Levels in Fmr1(KO) Mice

Fragile X syndrome (FXS) is the most common form of inherited intellectual disability and the leading known genetic cause of autism. Fragile X mental retardation protein (FMRP), which is absent or expressed at substantially reduced levels in FXS, binds to and controls the postsynaptic translation of...

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Detalles Bibliográficos
Autores principales: Westmark, Cara J., Westmark, Pamela R., O'Riordan, Kenneth J., Ray, Brian C., Hervey, Crystal M., Salamat, M. Shahriar, Abozeid, Sara H., Stein, Kelsey M., Stodola, Levi A., Tranfaglia, Michael, Burger, Corinna, Berry-Kravis, Elizabeth M., Malter, James S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3202540/
https://www.ncbi.nlm.nih.gov/pubmed/22046307
http://dx.doi.org/10.1371/journal.pone.0026549

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3202540/
https://www.ncbi.nlm.nih.gov/pubmed/22046307
http://dx.doi.org/10.1371/journal.pone.0026549

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