Prolidase deficiency and the biochemical assays used in its diagnosis
- 1 February 2006
- journal article
- review article
- Published by Elsevier BV in Analytical Biochemistry
- Vol. 349 (2), 165-175
- https://doi.org/10.1016/j.ab.2005.10.018
Abstract
No abstract availableThis publication has 62 references indexed in Scilit:
- A nonsense mutation of PEPD in four Amish children with prolidase deficiencyAmerican Journal of Medical Genetics Part A, 2006
- Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure–function relationshipJournal of Human Genetics, 2004
- Mechanized Syringe Homogenization of Human and Animal TissuesASSAY and Drug Development Technologies, 2004
- Prolidase deficiency: A multisystemic hereditary disorderJournal of the American Academy of Dermatology, 1993
- Prolidase and prolidase deficiencyLife Sciences, 1984
- 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
- Über proteolytische Enzyme, II. Mitteil.: Bindungsart des Prolins in der GelatineBerichte der deutschen chemischen Gesellschaft (A and B Series), 1932
- Über Dipeptidase und Polypeptidase aus Darm‐Schleimhaut. (XVI. Mitteilung zur Spezifität tierischer Proteasen.)Berichte der deutschen chemischen Gesellschaft (A and B Series), 1929