Article
IGF-1 intranasal administration rescues Huntington's disease phenotypes in YAC128 mice.
Molecular neurobiology - 1 Jun 2014
Lopes Carla, Ribeiro Márcio, Duarte Ana I, Humbert Sandrine, Saudou Frederic, Pereira de Almeida Luís, Hayden Michael, Rego A Cristina
Abstract excerpt
Huntington's disease (HD) is an autosomal dominant disease caused by an expansion of CAG repeats in the gene encoding for huntingtin. Brain metabolic dysfunction and altered Akt signaling pathways have been associated with disease progression. Nevertheless, conflicting results persist regarding t...
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