A bile acid protects against motor and cognitive deficits and reduces striatal degeneration in the 3-nitropropionic acid model of Huntington's disease

There is currently no effective treatment for Huntington's disease (HD), a progressive, fatal, neurodegenerative disorder characterized by motor and cognitive deterioration. It is well established that HD is associated with perturbation of mitochondrial e

Detalhes bibliográficos
Autor principal: Keene, CD (author)
Outros Autores: Rodrigues, CMP (author), Eich, T (author), Linehan-Stieers, C (author), Abt, A (author), Kren, BT (author), Steer, CJ (author), Low, WC (author)
Formato: article
Idioma:eng
Publicado em: 2015
Assuntos:
Neurosciences
Texto completo:http://hdl.handle.net/10451/21050
País:Portugal
Oai:oai:repositorio.ul.pt:10451/21050

Texto Completo

http://hdl.handle.net/10451/21050

Registos relacionados