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