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5. Characterization of prolidase activity in erythrocytes from a patient with prolidase deficiency: comparison with prolidase I and II purified from normal human erythrocytes. Liu G, Nakayama K, Sagara Y, Awata S, Yamashita K, Manabe M, Kodama H. Clin Biochem; 2005 Jul; 38(7):625-31. PubMed ID: 16009141 [Abstract] [Full Text] [Related]
11. Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypes. Endo F, Tanoue A, Kitano A, Arata J, Danks DM, Lapière CM, Sei Y, Wadman SK, Matsuda I. J Clin Invest; 1990 Jan; 85(1):162-9. PubMed ID: 1688567 [Abstract] [Full Text] [Related]
13. In situ activation of human erythrocyte prolidase: potential for enzyme replacement therapy in prolidase deficiency. Hechtman P, Richter A, Corman N, Leong YM. Pediatr Res; 1988 Dec; 24(6):709-12. PubMed ID: 3205627 [Abstract] [Full Text] [Related]