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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...

詳細記述

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書誌詳細
主要な著者: Dvorzhak, Anton, Semtner, Marcus, Faber, Donald S, Grantyn, Rosemarie
フォーマット: Artigo
言語:Inglês
出版事項: Blackwell Science Inc 2013
主題:
オンライン・アクセス: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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