A common renal transport system for lysine, ornithine, arginine and cysteine
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference9 articles.
1. Amino acid clearances in cystinuria
2. Crawhall, J.C., and Segal, S. submitted.
3. Evidence against a Single Renal Transport Defect in Cystinuria
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1. Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuria;Pediatric Nephrology;2000-04
2. Mendelian Phenotypes as “Probes” of Renal Transport Systems for Amino Acids and Phosphate;Comprehensive Physiology;1992-12
3. Genetics of Urolithiasis;Inheritance of Kidney and Urinary Tract Diseases;1990
4. Cystine Fluxes Across the Isolated Jejunal Epithelium in Cystinuria: Increased Efflux Permeability at the Luminal Membrane;Pediatric Research;1987-05
5. Renal Tubular Defects in Phosphate and Amino Acid Transport;Clinical Disorders of Membrane Transport Processes;1987
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