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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Giacomello, Marta, Oliveros, Juan C., Naranjo, Jose R., Carafoli, Ernesto
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Landes Bioscience 2013
Gaiak:
Sarrera elektronikoa: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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