Literature DB >> 509732

Study of a case with severe red-cell pyrimidine 5'-nucleotidase deficiency.

H A Buc, J C Kaplan, A Najman.   

Abstract

A deficiency of erythrocyte pyrimidine 5'-nucleotidase was found in a 23-year-old male suffering from severe congenital hemolytic disease. Results from exhaustive metabolic exploration are given and compared with reticulocyte-rich blood from subjects with auto-immune hemolytic disease. Evidence is given that the 20% apparent P5N residual activity corresponds to a non-specific acid phosphatase.

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Year:  1979        PMID: 509732     DOI: 10.1016/0009-8981(79)90339-5

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


  2 in total

1.  Detection of pyrimidine 5'-nucleotidase deficiency using 1H- or 31P-nuclear magnetic resonance.

Authors:  T Kagimoto; K Shirono; T Higaki; T Oda; H Matsuzaki; K Nagata; T Nakaji; Y Morino; K Takatsuki
Journal:  Experientia       Date:  1986-01-15

2.  Comparative study of effects of lead on the activity of erythrocyte pyrimidine 5'-nucleotidase and delta-aminolevulinate dehydratase in vivo and in vitro.

Authors:  K Tomokuni; M Ogata
Journal:  Arch Toxicol       Date:  1980-09       Impact factor: 5.153

  2 in total

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