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Calpain and STriatal-Enriched protein tyrosine Phosphatase (STEP) activation contribute to extrasynaptic NMDA receptor localization in a Huntington's disease mouse model

In Huntington's disease (HD), the mutant huntingtin (mhtt) protein is associated with striatal dysfunction and degeneration. Excitotoxicity and early synaptic defects are attributed, in part, to altered NMDA receptor (NMDAR) trafficking and function. Deleterious extrasynaptic NMDAR localization...

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Dettagli Bibliografici
Autori principali: Gladding, Clare M., Sepers, Marja D., Xu, Jian, Zhang, Lily Y.J., Milnerwood, Austen J., Lombroso, Paul J., Raymond, Lynn A.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2012
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3412376/
https://ncbi.nlm.nih.gov/pubmed/22523092
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/dds154
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