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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Detaylı Bibliyografya
Yayımlandı:Neurosci Lett
Asıl Yazarlar: Latchney, Sarah E., Jaramillo, Thomas C., Rivera, Phillip D., Eisch, Amelia J., Powell, Craig M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2015
Konular:
Article
Online Erişim: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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