2020-09-16T18:30:33Z
2020-09-16T18:30:33Z
2020-09
Niemann-Pick type C (NPC) disease is a childhood autosomal recessive inherited rare neurodegenerative disease characterized by accumulation of cholesterol and glycosphingolipids and where the autophagy-lysosome system and inflammatory processes are implicated in the pathogenesis of the disease. We follow a novel approach to deal with NPC disease, by modulating key features of the disease such as inflammation and autophagy, through inhibition of soluble epoxide hydrolase (sEH).
Object of conference
English
Malalties de Niemann-Pick; Trastorns del metabolisme; Cognició; Niemann-Pick diseases; Disorders of metabolism; Cognition
Reproducció del document publicat a: https://ecnp33-ecnp.ipostersessions.com/default.aspx?s=D7-E7-A0-5B-12-E1-80-A8-97-EE-37-30-9D-AC-5E-71&guestview=true
Pòster presentat a: 33rd European College of Neuropsychopharmacology (ECNP) Congress. 12-15 September 2020
cc by-nc-nd (c) Companys Alemany, Júlia et al., 2020
http://creativecommons.org/licenses/by-nc-nd/3.0/es/