Lipid trafficking defects in Niemann-Pick type C disease
Descrição
Elevation of plasma lysosphingomyelin-509 and urinary bile acid
TPC2 rescues lysosomal storage in mucolipidosis type IV, Niemann
Niemann-Pick type C disease: molecular mechanisms and potential
Niemann-Pick type C proteins promote microautophagy by expanding
Consensus clinical management guidelines for Niemann-Pick disease
PDF) Niemann–Pick C1 Is a Late Endosome-Resident Protein That
Understanding the phenotypic variability in Niemann-Pick disease
Lipid-mediated motor-adaptor sequestration impairs axonal lysosome
Miglustat in Niemann-Pick disease type C patients: a review
Cessation of rapid late endosomal tubulovesicular trafficking in
Juvenile CLN3 disease is a lysosomal cholesterol storage disorder
Niemann-Pick disease type C – topic of research paper in
Niemann–Pick type C disease: cellular pathology and
The pathogenesis of Niemann–Pick type C disease: a role for
de
por adulto (o preço varia de acordo com o tamanho do grupo)
