Renal iminoglycinuria without intestinal malabsorption of glycine and imino acids
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference20 articles.
1. Renal tubular transport of proline, hydroxyproline and glycine in health and in familial hyperprolinemia;Scriver;J. Clin. Invest.,1964
2. Possible locations for common gene product in membrane transport of iminoacids and glycine;Scriver;Nature,1964
3. Renal tubular transport of proline, hydroxyproline and glycine. II. Hydroxy-L-proline as substrate and as inhibitor in vivo;Scriver;J. Clin. Invest.,1966
4. Specificity of transport of neutral and basic amino acids in rat kidney;Wilson;Amer. J. Physiol.,1967
5. Prolinuria: a new renal tubular defect in transport of proline and glycine;Tada;Tohoku J. Exp. Med.,1965
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2. The Multifaceted Roles of Proline in Cell Behavior;Frontiers in Cell and Developmental Biology;2021-08-12
3. Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters;Journal of Clinical Investigation;2008-12-01
4. The transport and metabolism of l-proline-14C in the rat in vivo;Metabolism;1978-08
5. Renal transport of amino acids;Reviews of Physiology, Biochemistry and Pharmacology;1975
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