Literature DB >> 5037630

The metabolism of L-pyroglutamic acid in fibroblasts from a patient with pyroglutamic aciduria: the demonstration of an L-pyroglutamate hydrolase system.

J H Strömme, L Eldjarn.   

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Year:  1972        PMID： 5037630     DOI： 10.3109/00365517209080249

Source DB:  PubMed          Journal:  Scand J Clin Lab Invest        ISSN： 0036-5513            Impact factor:   1.713


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  3 in total

1.  Pyroglutamic aciduria (5-oxoprolinuria) without glutathione synthetase deficiency and with decreased pyroglutamate hydrolase activity.

Authors:  R A Roesel; F A Hommes; L Samper
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

2.  Accumulation of 5-oxoproline in mouse tissues after inhibition of 5-oxoprolinase and administration of amino acids: evidence for function of the gamma-glutamyl cycle.

Authors:  P Van Der Werf; R A Stephani; A Meister
Journal:  Proc Natl Acad Sci U S A       Date:  1974-04       Impact factor: 11.205

3.  Glutathione synthetase deficiency, an inborn error of metabolism involving the gamma-glutamyl cycle in patients with 5-oxoprolinuria (pyroglutamic aciduria).

Authors:  V P Wellner; R Sekura; A Meister; A Larsson
Journal:  Proc Natl Acad Sci U S A       Date:  1974-06       Impact factor: 11.205
  3 in total

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