Literature DB >> 1149286

Assay of galactose-1-phosphate uridyl transferase in cultured amniotic cells for prenatal diagnosis of galactosaemia.

A H Fensom, P F Benson.   

Abstract

We report studies designed to establish optimal conditions for the assay of amniotic cell galactose 1-phosphate uridyl transferase (Gal-PUT) for early prenatal diagnosis of galactosaemia. Methods based on linkage of the reaction to cause of non-specific reactions occurring even in the absence of Gal-1-P. In the final method, sonicates of confluent cultures are incubated with (14-C) Gal-1-P is degraded by treatment with alkaline phosphatase. Gal-PUT specific activities of both control and galactosaemic amniotic cells are higher in non-confluent that confluent cultures.

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Year:  1975        PMID: 1149286     DOI: 10.1016/0009-8981(75)90227-2

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


  3 in total

1.  Prenatal diagnosis of a galactosaemia heterozygote by fetal blood enzyme assay.

Authors:  A H Fensom; P F Benson; C H Rodeck; S Campbell; J D Gould
Journal:  Br Med J       Date:  1979-01-06

2.  Prenatal and postnatal diagnostic difficulties in a family with rare alleles of the galactose-1-phosphate uridyl transferase locus.

Authors:  E Christensen; N J Brandt
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

3.  Biochemical studies of a human low-activity galactose-1-phosphate uridyl transferase variant.

Authors:  W G Ng; F Kline; J Lin; R Koch; G N Donnell
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

  3 in total

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