Amino acid transport systems of lysosomes: Possible substitute utility of a surviving transport system for one congenitally defective or absent
Author:
Affiliation:
1. Department of Biological Chemistry, The University of Michigan Medical School, Ann Arbor, Michigan 48109, USA
Abstract
Publisher
Portland Press Ltd.
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Link
https://portlandpress.com/bioscirep/article-pdf/8/2/121/472221/bsr0080121.pdf
Reference28 articles.
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3. Christensen, H. N. (1984).Biochim. Biophys. Acta 779:255?269.
4. Reeves, J. P. (1979).J. Biol. Chem. 254:8914?8921.
5. Gahl, W. A., Reed, G. F., Thoene, J. G., Schulman, J. d., Rizzo, W. B., Jonas, A. J., Denman, D. W., Schlesselman, J. J., Corden, B. J. and Schneider J. A. (1987).N. Engl. J. Med. 316:971?977.
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1. Lysosomal transport of small molecules;Biochemical Medicine and Metabolic Biology;1992-12
2. Incorporation of [32P]orthophosphate into long chains of inorganic polyphosphate within lysosomes of human fibroblasts.;Journal of Biological Chemistry;1992-02
3. Amino Acid Transporters: Systematic Approach and Principles of Control;Mammalian Amino Acid Transport;1992
4. The transport systems of mammalian lysosomes;Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes;1991-12
5. Characteristics of taurine transport in rat liver lysosomes;Journal of Cellular Physiology;1991-06
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