| P50 | author | Ta-Yuan Chang | Q40361636 |
| P2093 | author name string | Cruz JC | |
| P2860 | cites work | Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis | Q24315133 |
| | Dissecting the role of the golgi complex and lipid rafts in biosynthetic transport of cholesterol to the cell surface. | Q27863672 |
| | Acyl-coenzyme A:cholesterol acyltransferase | Q28245277 |
| | Sterol resistance in CHO cells traced to point mutation in SREBP cleavage-activating protein | Q28295187 |
| | Prevention of lysosomal storage in Tay-Sachs mice treated with N-butyldeoxynojirimycin | Q28505993 |
| | Cholesterol homeostasis in human brain: evidence for an age-dependent flux of 24S-hydroxycholesterol from the brain into the circulation | Q28613091 |
| | A simplification of the protein assay method of Lowry et al. which is more generally applicable | Q29615220 |
| | A receptor-mediated pathway for cholesterol homeostasis | Q29616158 |
| | A role for caveolin in transport of cholesterol from endoplasmic reticulum to plasma membrane | Q34406843 |
| | Niemann-Pick type II fibroblasts exhibit impaired cholesterol esterification in response to sphingomyelin hydrolysis | Q41643557 |
| | Niemann-pick type C1 (NPC1) overexpression alters cellular cholesterol homeostasis | Q42492641 |
| | Cholesterol modulates membrane traffic along the endocytic pathway in sphingolipid-storage diseases | Q47622411 |
| | Role of Niemann-Pick type C1 protein in intracellular trafficking of low density lipoprotein-derived cholesterol | Q47887125 |
| | Broad screening test for sphingolipid-storage diseases. | Q52174471 |
| | Embryonic Striatal Neurons from Niemann-Pick Type C Mice Exhibit Defects in Cholesterol Metabolism and Neurotrophin Responsiveness | Q57371887 |
| | Transport of cholesterol from the endoplasmic reticulum to the plasma membrane | Q36212465 |
| | The intracellular transport of low density lipoprotein-derived cholesterol is defective in Niemann-Pick type C fibroblasts | Q36220506 |
| | Isolation and characterization of Chinese hamster ovary cell mutants defective in intracellular low density lipoprotein-cholesterol trafficking | Q36222559 |
| | Substantial narrowing of the Niemann-Pick C candidate interval by yeast artificial chromosome complementation. | Q36656106 |
| | A defect in cholesterol esterification in Niemann-Pick disease (type C) patients | Q37558069 |
| | Mammalian cell mutant requiring cholesterol and unsaturated fatty acid for growth | Q37594257 |
| | Cholesterol movement in Niemann-Pick type C cells and in cells treated with amphiphiles | Q40888730 |
| | Recombinant acyl-CoA:cholesterol acyltransferase-1 (ACAT-1) purified to essential homogeneity utilizes cholesterol in mixed micelles or in vesicles in a highly cooperative manner | Q40987614 |
| | Characterization of a cytosolic heat-shock protein-caveolin chaperone complex. Involvement in cholesterol trafficking | Q41052229 |
| | Cellular cholesterol efflux mediated by cyclodextrins | Q41324065 |
| | Translocation of both lysosomal LDL-derived cholesterol and plasma membrane cholesterol to the endoplasmic reticulum for esterification may require common cellular factors involved in cholesterol egress from the acidic compartments (lysosomes/endoso | Q41370531 |
| P433 | issue | 52 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 41309-41316 | |
| P577 | publication date | 2000-12-01 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Fate of endogenously synthesized cholesterol in Niemann-Pick type C1 cells | |
| P478 | volume | 275 | |