Buscar
Mostrando ítems 11-20 de 43
The Unique Case of The Niemann-Pick Type C Cholesterol Storage Disorder
(2014)
Niemann-Pick type C disease (NPC) is a neurovisceral lysosomal cholesterol storage disorder that arises from loss-of-f unction mutations in either the NPCI or NPC2 genes. Both genes code for proteins involved in lysosomal ...
Increased copper levels in in vitro and in vivo models of Niemann-Pick C disease
(2012)
Niemann-Pick type C disease (NPC) is a hereditary neurovisceral atypical lipid storage disorder produced by mutations in the NPC1 and NPC2 genes. The disease is characterized by unesterified cholesterol accumulation in ...
Increased copper levels in in vitro and in vivo models of Niemann-Pick C disease
(2012)
Niemann-Pick type C disease (NPC) is a hereditary neurovisceral atypical lipid storage disorder produced by mutations in the NPC1 and NPC2 genes. The disease is characterized by unesterified cholesterol accumulation in ...