Literature DB >> 733941

Studies on a patient with iminodipeptiduria. II. Lack of prolidase activity in blood cells.

S Umemura.   

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Year:  1978        PMID： 733941

Source DB:  PubMed          Journal:  Physiol Chem Phys        ISSN： 0031-9325


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  12 in total

1.  Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypes.

Authors:  F Endo; A Tanoue; A Kitano; J Arata; D M Danks; C M Lapière; Y Sei; S K Wadman; I Matsuda
Journal:  J Clin Invest       Date:  1990-01       Impact factor: 14.808

2.  Expression and molecular analysis of mutations in prolidase deficiency.

Authors:  P Ledoux; C R Scriver; P Hechtman
Journal:  Am J Hum Genet       Date:  1996-11       Impact factor: 11.025

3.  Molecular characterisation of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same family.

Authors:  A Lupi; A Rossi; E Campari; F Pecora; A M Lund; N H Elcioglu; M Gultepe; M Di Rocco; G Cetta; A Forlino
Journal:  J Med Genet       Date:  2006-12       Impact factor: 6.318

4.  Normal hydroxylation of proline in collagen synthesized by skin fibroblasts from a patient with prolidase deficiency.

Authors:  P M Royce; D M Danks
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

5.  Developmental changes in the activities of prolinase and prolidase in rat salivary glands, and the effect of thyroxine administration.

Authors:  K Imai; T Nagatsu; T Yajima; N Maeda; M Kumegawa; T Kato
Journal:  Mol Cell Biochem       Date:  1982-01-16       Impact factor: 3.396

6.  Screening method for prolidase deficiency.

Authors:  F Endo; I Matsuda
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  Four novel PEPD alleles causing prolidase deficiency.

Authors:  P Ledoux; C Scriver; P Hechtman
Journal:  Am J Hum Genet       Date:  1994-06       Impact factor: 11.025

8.  Increased manganese content and reduced arginase activity in erythrocytes of a patient with prolidase deficiency (iminodipeptiduria).

Authors:  I Lombeck; U Wendel; J Versieck; L van Ballenberghe; H J Bremer; R Duran; S Wadman
Journal:  Eur J Pediatr       Date:  1986-04       Impact factor: 3.183

9.  Extracellular Prolidase (PEPD) Induces Anabolic Processes through EGFR, β1-integrin, and IGF-1R Signaling Pathways in an Experimental Model of Wounded Fibroblasts.

Authors:  Weronika Baszanowska; Magdalena Misiura; Ilona Oscilowska; Jerzy Palka; Wojciech Miltyk
Journal:  Int J Mol Sci       Date:  2021-01-19       Impact factor: 5.923

10.  Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases.

Authors:  Francis Rossignol; Marvid S Duarte Moreno; Carlos R Ferreira; Manuel Schiff; Jean-François Benoist; Manfred Boehm; Emmanuelle Bourrat; Aline Cano; Brigitte Chabrol; Claudine Cosson; José Luís Dapena Díaz; Arthur D'Harlingue; David Dimmock; Alexandra F Freeman; María Tallón García; Cheryl Garganta; Tobias Goerge; Sara S Halbach; Jan de Laffolie; Christina T Lam; Ludovic Martin; Esmeralda Martins; Andrea Meinhardt; Isabelle Melki; Amanda K Ombrello; Noémie Pérez; Dulce Quelhas; Anna Scott; Anne M Slavotinek; Ana Rita Soares; Sarah L Stein; Kira Süßmuth; Jenny Thies
Journal:  Genet Med       Date:  2021-05-26       Impact factor: 8.822
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