Literature DB >> 95907

Two-dimensional thin-layer chromatography for the screening of disorders of purine and pyrimidine metabolism.

A H van Gennip, D Y van Noordenburg-Huistra, P K de Bree, S K Wadman.   

Abstract

A method is presented for the two-dimensional thin-layer chromatographic screening of purines, pyrimidines and their nucleosides in the urine. Prior to chromatography, isolation of these substances from the urine is performed by anion-exchange column chromatography. Purines and pyramidines are quantitatively eluted with formic acid 0.01 M and 4 M respectively. The results of recovery and stability experiments are given. Normal excretory patterns are presented. Also results in patients with various diseases are shown: ornithine transcarbamylase deficiency, adenosine deaminase deficiency, purine nucleoside phosphorylase deficiency, adenine phosphoribosyltransferase deficiency, xanthine oxidase deficiency and hypoxanthine-guanine phosphoribosyltransferase deficiency. Finally the pattern of a patient on treatment with allopurinol is given.

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Year:  1978        PMID: 95907     DOI: 10.1016/0009-8981(78)90452-7

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  5 in total

1.  Combined deficiency of xanthine oxidase and sulphite oxidase: a defect of molybdenum metabolism or transport?

Authors:  M Duran; F A Beemer; C van de Heiden; J Korteland; P K de Bree; M Brink; S K Wadman; I Lombeck
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

2.  The effect of molybdenum cofactor deficiency on the purine pattern of cerebrospinal fluid.

Authors:  A H van Gennip; A Stroomer; W G Plandsoen; N G Abeling
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

3.  Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism.

Authors:  S K Wadman; R Berger; M Duran; P K de Bree; S A Stoker-de Vries; F A Beemer; J J Weits-Binnerts; T J Penders; J K van der Woude
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

4.  Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor.

Authors:  J L Johnson; W R Waud; K V Rajagopalan; M Duran; F A Beemer; S K Wadman
Journal:  Proc Natl Acad Sci U S A       Date:  1980-06       Impact factor: 11.205

5.  A case of formiminoglutamic aciduria. Clinical and biochemical studies.

Authors:  M Duran; D Ketting; P K de Bree; F J van Sprang; S K Wadman; T J Penders; R H Wilms
Journal:  Eur J Pediatr       Date:  1981-07       Impact factor: 3.183

  5 in total

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