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Neuronal Ca(2+) dyshomeostasis in Huntington disease

The expansion of the N-terminal poly-glutamine tract of the huntingtin (Htt) protein is responsible for Huntington disease (HD). A large number of studies have explored the neuronal phenotype of HD, but the molecular aethiology of the disease is still very poorly understood. This has hampered the de...

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Hlavní autoři: Giacomello, Marta, Oliveros, Juan C., Naranjo, Jose R., Carafoli, Ernesto
Médium: Artigo
Jazyk:Inglês
Vydáno: Landes Bioscience 2013
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3609054/
https://ncbi.nlm.nih.gov/pubmed/23324594
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/pri.23581
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