Literature DB >> 61546

Immunological detection of phenylalanine hydroxylase in phenylketonuria.

K Bartholomé, E Ertel.   

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Year:  1976        PMID： 61546     DOI： 10.1016/s0140-6736(76)91262-9

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  3 in total

1.  Studies on human phenylalanine Mono-oxygenase. I. Restricted expression.

Authors:  M D Crawfurd; D A Gibbs; D M Sheppard
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

2.  Studies on the molecular defect in phenylketonuria and hyperphenylalaninaemia using antibodies against phenylalanine hydroxylase.

Authors:  K Bartholomé; A Dresel
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

3.  Excretion of phenylpyruvic, 4-hydroxyphenylpyruvic and indolyl-3-acetic acids by the skin fibroblasts from a phenylketonuric child.

Authors:  A G Antoshechkin; L A Zuyeva; L A Maximova
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982
  3 in total

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