Mannose 6-phosphate receptors, Niemann-Pick C2 protein, and lysosomal cholesterol accumulation
Open Access
- 1 December 2005
- journal article
- Published by Elsevier in Journal of Lipid Research
- Vol. 46 (12), 2559-2569
- https://doi.org/10.1194/jlr.m500131-jlr200
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Structure and function of the NPC2 proteinBiochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, 2004
- Niemann–Pick type C disease: importance of N-glycosylation sites for function and cellular location of the NPC2 proteinMolecular Genetics and Metabolism, 2004
- Disturbed Cholesterol Traffic but Normal Proteolytic Function in LAMP-1/LAMP-2 Double-deficient FibroblastsMolecular Biology of the Cell, 2004
- Sterol-modulated Glycolipid Sorting Occurs in Niemann-Pick C1 Late EndosomesPublished by Elsevier ,2001
- Transmembrane Molecular Pump Activity of Niemann-Pick C1 ProteinScience, 2000
- Neither type of mannose 6-phosphate receptor is sufficient for targeting of lysosomal enzymes along intracellular routes.The Journal of cell biology, 1996
- Re-expression of the Mannose 6-Phosphate Receptors in Receptor-deficient FibroblastsJournal of Biological Chemistry, 1996
- The Two Mannose 6-Phosphate Receptors Transport Distinct Complements of Lysosomal ProteinsJournal of Biological Chemistry, 1995
- Differences in the endosomal distributions of the two mannose 6-phosphate receptors.The Journal of cell biology, 1993
- Deglycosylation of asparagine-linked glycans by peptide:N-glycosidase FBiochemistry, 1985