Parkin regulates kainate receptors by interacting with the GluK2 subunit

Although loss-of-function mutations in the PARK2 gene, the gene that encodes the protein parkin, cause autosomal recessive juvenile parkinsonism, the responsible molecular mechanisms remain unclear. Evidence suggests that a loss of parkin dysregulates excitatory synapses. Here we show that parkin in...

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Detalles Bibliográficos
Autores principales: Maraschi, AnnaMaria, Ciammola, Andrea, Folci, Alessandra, Sassone, Francesca, Ronzitti, Giuseppe, Cappelletti, Graziella, Silani, Vincenzo, Sato, Shigeto, Hattori, Nobutaka, Mazzanti, Michele, Chieregatti, Evelina, Mulle, Christophe, Passafaro, Maria, Sassone, Jenny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4218952/
https://www.ncbi.nlm.nih.gov/pubmed/25316086
http://dx.doi.org/10.1038/ncomms6182

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