Cargando...

Rab11 rescues synaptic dysfunction and behavioural deficits in a Drosophila model of Huntington's disease

Synapse abnormalities in Huntington's disease (HD) patients can precede clinical diagnosis and neuron loss by decades. The polyglutamine expansion in the huntingtin (htt) protein that underlies this disorder leads to perturbations in many cellular pathways, including the disruption of Rab11-dep...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Steinert, Joern R., Campesan, Susanna, Richards, Paul, Kyriacou, Charalambos P., Forsythe, Ian D., Giorgini, Flaviano
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3373239/
https://ncbi.nlm.nih.gov/pubmed/22466800
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/dds117
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!