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CHRONIC P7C3 TREATMENT RESTORES HIPPOCAMPAL NEUROGENESIS IN THE Ts65Dn MOUSE MODEL OF DOWN SYNDROME

Down Syndrome (DS) is the most common genetic cause of intellectual disability and developmental delay. In addition to cognitive dysfunction, DS patients are marked by diminished neurogenesis, a neuropathological feature also found in the Ts65Dn mouse model of DS. Interestingly, manipulations that e...

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Detalhes bibliográficos
Publicado no:Neurosci Lett
Main Authors: Latchney, Sarah E., Jaramillo, Thomas C., Rivera, Phillip D., Eisch, Amelia J., Powell, Craig M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4363293/
https://ncbi.nlm.nih.gov/pubmed/25668489
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2015.02.008
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