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Fragile x syndrome and autism: from disease model to therapeutic targets
Autism is an umbrella diagnosis with several different etiologies. Fragile X syndrome (FXS), one of the first identified and leading causes of autism, has been modeled in mice using molecular genetic manipulation. These Fmr1 knockout mice have recently been used to identify a new putative therapeuti...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164025/ https://www.ncbi.nlm.nih.gov/pubmed/21547712 http://dx.doi.org/10.1007/s11689-009-9015-x |
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author | Dölen, Gül Bear, Mark F. |
author_facet | Dölen, Gül Bear, Mark F. |
author_sort | Dölen, Gül |
collection | PubMed |
description | Autism is an umbrella diagnosis with several different etiologies. Fragile X syndrome (FXS), one of the first identified and leading causes of autism, has been modeled in mice using molecular genetic manipulation. These Fmr1 knockout mice have recently been used to identify a new putative therapeutic target, the metabotropic glutamate receptor 5 (mGluR5), for the treatment of FXS. Moreover, mGluR5 signaling cascades interact with a number of synaptic proteins, many of which have been implicated in autism, raising the possibility that therapeutic targets identified for FXS may have efficacy in treating multiple other causes of autism. |
format | Online Article Text |
id | pubmed-3164025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-31640252011-10-18 Fragile x syndrome and autism: from disease model to therapeutic targets Dölen, Gül Bear, Mark F. J Neurodev Disord Article Autism is an umbrella diagnosis with several different etiologies. Fragile X syndrome (FXS), one of the first identified and leading causes of autism, has been modeled in mice using molecular genetic manipulation. These Fmr1 knockout mice have recently been used to identify a new putative therapeutic target, the metabotropic glutamate receptor 5 (mGluR5), for the treatment of FXS. Moreover, mGluR5 signaling cascades interact with a number of synaptic proteins, many of which have been implicated in autism, raising the possibility that therapeutic targets identified for FXS may have efficacy in treating multiple other causes of autism. Springer US 2009-05-12 2009-06 /pmc/articles/PMC3164025/ /pubmed/21547712 http://dx.doi.org/10.1007/s11689-009-9015-x Text en © Springer Science+Business Media, LLC 2009 |
spellingShingle | Article Dölen, Gül Bear, Mark F. Fragile x syndrome and autism: from disease model to therapeutic targets |
title | Fragile x syndrome and autism: from disease model to therapeutic targets |
title_full | Fragile x syndrome and autism: from disease model to therapeutic targets |
title_fullStr | Fragile x syndrome and autism: from disease model to therapeutic targets |
title_full_unstemmed | Fragile x syndrome and autism: from disease model to therapeutic targets |
title_short | Fragile x syndrome and autism: from disease model to therapeutic targets |
title_sort | fragile x syndrome and autism: from disease model to therapeutic targets |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3164025/ https://www.ncbi.nlm.nih.gov/pubmed/21547712 http://dx.doi.org/10.1007/s11689-009-9015-x |
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