Characterization of carrier-mediated transport systems for small neutral amino acids in human fibroblast lysosomes.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference39 articles.
1. Defective cystine exodus from isolated lysosome-rich fractions of cystinotic leucocytes.
2. Cystine Transport Is Defective in Isolated Leukocyte Lysosomes from Patients with Cystinosis
3. Characteristics of cystine counter-transport in normal and cystinotic lysosome-rich leucocyte granular fractions
4. ATP-dependent lysosomal cystine efflux is defective in cystinosis.
5. Detection and characterization of carrier-mediated cationic amino acid transport in lysosomes of normal and cystinotic human fibroblasts. Role in therapeutic cystine removal?
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1. Non-physiological amino acid (NPAA) therapy targeting brain phenylalanine reduction: pilot studies in PAH ENU2 mice;Journal of Inherited Metabolic Disease;2012-09-14
2. Molecular physiology and pathophysiology of lysosomal membrane transporters;Journal of Inherited Metabolic Disease;2008-04
3. Lysosomal Membrane Transport in the Central Nervous System;Handbook of Neurochemistry and Molecular Neurobiology;2007
4. Biochemical and Genetic Analysis of ANK in Arthritis and Bone Disease;The American Journal of Human Genetics;2006-12
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