Yüklüyor......

Corticostriatal dysfunction underlies diminished striatal ascorbate release in the R6/2 mouse model of Huntington’s disease

A behavior-related deficit in the release of ascorbate (AA), an antioxidant vitamin, occurs in the striatum of R6/2 mice expressing the human mutation for Huntington’s disease (HD), a dominantly inherited condition characterized by striatal dysfunction. To determine the role of corticostriatal fiber...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Dorner, Jenelle L., Miller, Benjamin R., Klein, Emma L., Murphy-Nakhnikian, Alexander, Andrews, Rachel L., Barton, Scott J., Rebec, George V.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2009
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2745264/
https://ncbi.nlm.nih.gov/pubmed/19616518
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainres.2009.07.019
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!