Literature DB >> 7239517

Screening method for prolidase deficiency.

F Endo, I Matsuda.   

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Year:  1981        PMID： 7239517     DOI： 10.1007/bf00274691

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  15 in total

1.  A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS.

Authors:  R GUTHRIE; A SUSI
Journal:  Pediatrics       Date:  1963-09       Impact factor: 7.124

2.  Studies on a patient with iminopeptiduria. I. Identification of urinary iminopeptides.

Authors:  H Kodama; S Umemura; M Shimomura; S Mizuhara; J Arata; Y Yamamoto; A Yasutake; N Izumiya
Journal:  Physiol Chem Phys       Date:  1976

3.  Iminopeptiduria, skin ulcerations, and edema in a boy with prolidase deficiency.

Authors:  L J Sheffield; P Schlesinger; K Faull; B J Halpern; G M Schier; R G Cotton; J Hammond; D M Danks
Journal:  J Pediatr       Date:  1977-10       Impact factor: 4.406

4.  Prolidase deficiency: report of a second case with quantitation of the excessively excreted amino acids.

Authors:  G F Powell; A Kurosky; R M Maniscalco
Journal:  J Pediatr       Date:  1977-08       Impact factor: 4.406

5.  Determination of dipeptides in urine.

Authors:  R A Johnstone; T J Povall; J D Baty; J L Pousset; C Charpentier; A Lemonnier
Journal:  Clin Chim Acta       Date:  1974-04       Impact factor: 3.786

6.  A prolidase deficiency in man with iminopeptiduria.

Authors:  G F Powell; M A Rasco; R M Maniscalco
Journal:  Metabolism       Date:  1974-06       Impact factor: 8.694

7.  Further studies on a patient with iminodipeptiduria: a probable case of prolidase deficiency.

Authors:  N R Buist; J J Strandholm; J F Bellinger; N G Kennaway
Journal:  Metabolism       Date:  1972-12       Impact factor: 8.694

8.  Iminodipeptiduria: a genetic defect in recycling collagen; a method for determining prolidase in erythrocytes.

Authors:  S H Jackson; A W Dennis; M Greenberg
Journal:  Can Med Assoc J       Date:  1975-10-18       Impact factor: 8.262

9.  Prolidase deficiency: its dermatological manifestations and some additional biochemical studies.

Authors:  J Arata; S Umemura; Y Yamamoto; M Hagiyama; N Nohara
Journal:  Arch Dermatol       Date:  1979-01

10.  Prolidase deficiency with imidodipeptiduria. A familial case with and without clinical symptoms.

Authors:  M Isemura; T Hanyu; F Gejyo; R Nakazawa; R Igarashi; S Matsuo; K Ikeda; Y Sato
Journal:  Clin Chim Acta       Date:  1979-05-02       Impact factor: 3.786
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  5 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.  Molecular defect in siblings with prolidase deficiency and absence or presence of clinical symptoms. A 0.8-kb deletion with breakpoints at the short, direct repeat in the PEPD gene and synthesis of abnormal messenger RNA and inactive polypeptide.

Authors:  A Tanoue; F Endo; I Akaboshi; T Oono; J Arata; I Matsuda
Journal:  J Clin Invest       Date:  1991-04       Impact factor: 14.808

3.  Substrate specificity of manganese-activated prolidase in control and prolidase-deficient cultured skin fibroblasts.

Authors:  J Butterworth; D Priestman
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

4.  A single nucleotide change in the prolidase gene in fibroblasts from two patients with polypeptide positive prolidase deficiency. Expression of the mutant enzyme in NIH 3T3 cells.

Authors:  A Tanoue; F Endo; A Kitano; I Matsuda
Journal:  J Clin Invest       Date:  1990-07       Impact factor: 14.808

5.  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
  5 in total

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