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Alterations of in vivo CA1 network activity in Dp(16)1Yey Down syndrome model mice
Down syndrome, the leading genetic cause of intellectual disability, results from an extra-copy of chromosome 21. Mice engineered to model this aneuploidy exhibit Down syndrome-like memory deficits in spatial and contextual tasks. While abnormal neuronal function has been identified in these models,...
Autores principales: | Raveau, Matthieu, Polygalov, Denis, Boehringer, Roman, Amano, Kenji, Yamakawa, Kazuhiro, McHugh, Thomas J |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841929/ https://www.ncbi.nlm.nih.gov/pubmed/29485402 http://dx.doi.org/10.7554/eLife.31543 |
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