Literature DB >> 4336165

Steric, chiral and conformational aspects of the 3-hydroxy- and 20-hydroxysteroid dehydrogenase activities of cortisone reductase preparations.

W Gibb, J Jeffery.   

Abstract

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Year:  1972        PMID： 4336165     DOI： 10.1016/0005-2744(72)90191-x

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN： 0006-3002


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  5 in total

1.  [A method for quantitative dertermination of 20-keto steroids in urine during the use of a 3 alpha-, 20 beta-hydroxysteroid: NAD oxidoreductase (author's transl)].

Authors:  R Allner; M Eggstein; H Kujawski
Journal:  Klin Wochenschr       Date:  1975-09-15

2.  Influence of a 17 beta-sulphate group on reduction of a steroid 3-oxo group by cortisone reductase.

Authors:  W Gibb; J Jeffery
Journal:  Biochem J       Date:  1972-11       Impact factor: 3.857

3.  Radio-enzymic assay of oxo steroids by their reduction with the tritiated form of reduced nicotinamide--adenine dinucleotide.

Authors:  J K Norymberski; N Stoddart; J B Wolstenholme
Journal:  Biochem J       Date:  1975-01       Impact factor: 3.857

4.  Structural features of ring C of 20-oxo steroids and the interaction with cortisone reductase.

Authors:  I H White; J Jeffery
Journal:  Biochem J       Date:  1974-02       Impact factor: 3.857

5.  3-Hydroxy steroid dehydrogenase activities of cortisone reductase.

Authors:  W Gibb; J Jeffery
Journal:  Biochem J       Date:  1973-12       Impact factor: 3.857
  5 in total

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