Detection and Characterization of a Transport System Mediating Cysteamine Entry into Human Fibroblast Lysosomes
Open Access
- 1 January 1995
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 270 (3), 1179-1184
- https://doi.org/10.1074/jbc.270.3.1179
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- Defective glucuronic acid transport from lysosomes of infantile free sialic acid storage disease fibroblastsBiochemical Journal, 1990
- A cysteine-specific lysosomal transport system provides a major route for the delivery of thiol to human fibroblast lysosomes: possible role in supporting lysosomal proteolysis.The Journal of cell biology, 1990
- Separate and shared lysosomal transport of branched and aromatic dipolar amino acidsBiochimica et Biophysica Acta (BBA) - Biomembranes, 1989
- Characterization of a transport system for anionic amino acids in human fibroblast lysosomesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1989
- Characterization of a proton-driven carrier for sialic acid in the lysosomal membranePublished by Elsevier ,1989
- Cystine exodus from normal leucocytes is stimulated by MgATPBiochemical Journal, 1987
- Defective Sialic Acid Egress from Isolated Fibroblast Lysosomes of Patients with Salla DiseaseScience, 1986
- Characteristics of cystine counter-transport in normal and cystinotic lysosome-rich leucocyte granular fractionsBiochemical Journal, 1983
- Cystine Transport Is Defective in Isolated Leukocyte Lysosomes from Patients with CystinosisScience, 1982
- Cystine accumulation and loss in normal, heterozygous, and cystinotic fibroblasts.Proceedings of the National Academy of Sciences, 1982