The Hermansky-Pudlak Syndrome 1 (HPS1) and HPS4 Proteins Are Components of Two Complexes, BLOC-3 and BLOC-4, Involved in the Biogenesis of Lysosome-related Organelles
Open Access
- 1 May 2003
- journal article
- Published by Elsevier BV
- Vol. 278 (22), 20332-20337
- https://doi.org/10.1074/jbc.m300090200
Abstract
No abstract availableThis publication has 29 references indexed in Scilit:
- Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6Nature Genetics, 2003
- BLOC-1, a Novel Complex Containing the Pallidin and Muted Proteins Involved in the Biogenesis of Melanosomes and Platelet-dense GranulesJournal of Biological Chemistry, 2002
- Assembly and function of AP-3 complexes in cells expressing mutant subunitsThe Journal of cell biology, 2002
- The Gene Mutated in Cocoa Mice, Carrying a Defect of Organelle Biogenesis, Is a Homologue of the Human Hermansky–Pudlak Syndrome-3 GeneGenomics, 2001
- Adaptor-related proteinsCurrent Opinion in Cell Biology, 2001
- Mutation in AP-3 δ in the mocha Mouse Links Endosomal Transport to Storage Deficiency in Platelets, Melanosomes, and Synaptic VesiclesNeuron, 1998
- Positional cloning of a gene for Hermansky–Pudlak syndrome, a disorder of cytoplasmic organellesNature Genetics, 1996
- Tamoxifen and Quercetin Interact with Type II Estrogen Binding Sites and Inhibit the Growth of Human Melanoma CellsJournal of Investigative Dermatology, 1995
- Genetics, Development, and Malignancy of MelanocytesInternational Review of Cytology, 1993
- A line of non‐tumorigenic mouse melanocytes, syngeneic with the B16 melanoma and requiring a tumour promoter for growthInternational Journal of Cancer, 1987