Literature DB >> 171772

Phosphoribosylpyrophosphate overproduction, a new metabolic abnormality in the Lesch Nyhan syndrome.

G H Reem.   

Abstract

The activity of phosphoribosylpyrophosphate synthetase and the rate of phosphoribosylpyrophosphate accumulation are significantly increased in cultured lymphocytes of Lesch Nyhan patients deficient in hypoxanthine guanine phosphoribosyltransferase and in a clone of mutagen-induced, hypoxanthine guanine phosphoribosyltransferase deficient human lymphocytes. The increase in phosphoribosylpyrophosphate synthetase activity is the cause of the abnormally high cellular phosphoribosylpyrophosphate content and possibly of the purine overproduction described in this syndrome.

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Year:  1975        PMID: 171772     DOI: 10.1126/science.171772

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  4 in total

1.  Electrophoretic heterogeneity of 5-phosphoribosyl-1-pyrophosphate synthetase within and among humans.

Authors:  R V Lebo; D W Martin
Journal:  Biochem Genet       Date:  1978-10       Impact factor: 1.890

2.  Role of adenine phosphoribosyltransferase in adenine uptake in wild-type and APRT- mutants of CHO.

Authors:  F R Witney; M W Taylor
Journal:  Biochem Genet       Date:  1978-10       Impact factor: 1.890

3.  The mode of genetic transmission of gouty family with increased phosphoribosylpyrophosphate synthetase activity.

Authors:  F Takeuchi; F Hanaoka; E Yano; M Yamada; Y Horiuchi; I Akaoka
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

4.  Isolation of a Chinese hamster cell mutant with low intracellular phosphoribosylpyrophosphate concentration.

Authors:  C R Crawford; R E Bryant
Journal:  Mol Cell Biol       Date:  1982-12       Impact factor: 4.272

  4 in total

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