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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Pubblicato in:Neurosci Lett
Autori principali: Latchney, Sarah E., Jaramillo, Thomas C., Rivera, Phillip D., Eisch, Amelia J., Powell, Craig M.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2015
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Article
Accesso online: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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