Prolidase and prolidase deficiency
- 21 May 1984
- journal article
- review article
- Published by Elsevier in Life Sciences
- Vol. 34 (21) , 1985-1998
- https://doi.org/10.1016/0024-3205(84)90363-1
Abstract
No abstract availableKeywords
This publication has 49 references indexed in Scilit:
- Normal hydroxylation of proline in collagen synthesized by skin fibroblasts from a patient with prolidase deficiencyJournal of Inherited Metabolic Disease, 1981
- Assignment of the gene for peptidase S (PEPS) to chromosome 4 in man and confirmation of peptidase D (PEPD) assignment to chromosome 19Cytogenetic and Genome Research, 1978
- Iminopeptiduria, skin ulcerations, and edema in a boy with prolidase deficiencyThe Journal of Pediatrics, 1977
- Prolidase deficiency: Report of a second case with quantitation of the excessively excreted amino acidsThe Journal of Pediatrics, 1977
- Covalent coupling of calf brain prolidaseJournal of Neuroscience Research, 1977
- Assignment of the peptidase D gene locus (PEPD) to chromosome 19 in manCytogenetic and Genome Research, 1976
- Peptiduria in polyostotic fibrous dysplasiaBiochemical Medicine, 1971
- Peptidase D (prolidase) variants in manAnnals of Human Genetics, 1969
- GLYCYL-PROLINE IN URINE OF HUMANS WITH BONE DISEASECanadian Journal of Physiology and Pharmacology, 1964
- Peptiduria in an Unusual Bone Disorder: Isolation of Two PeptidesArchives of Disease in Childhood, 1963