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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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Bibliografiske detaljer
Main Authors: Dvorzhak, Anton, Semtner, Marcus, Faber, Donald S, Grantyn, Rosemarie
Format: Artigo
Sprog:Inglês
Udgivet: Blackwell Science Inc 2013
Fag:
Online adgang: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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