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Tonic mGluR5/CB1-dependent suppression of inhibition as a pathophysiological hallmark in the striatum of mice carrying a mutant form of huntingtin

Changes in the activity of striatal output neurons (SONs) have been implicated in the pathogenesis of Huntington's disease (HD). In this inherited polyglutamine disorder, accumulation of intracellular toxins causes a variety of deficits, including synaptic dysfunction, but it is still unclear t...

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Detaylı Bibliyografya
Asıl Yazarlar: Dvorzhak, Anton, Semtner, Marcus, Faber, Donald S, Grantyn, Rosemarie
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Blackwell Science Inc 2013
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3591720/
https://ncbi.nlm.nih.gov/pubmed/23230231
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2012.241018
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