Literature DB >> 6573909

A new method for the determination of steroid sulphatase activity in leukocytes in X-linked recessive ichthyosis.

A C Jöbsis, W P De Groot, A E Meijer, C M Van der Loos.   

Abstract

The diagnosis of X-linked ichthyosis can now be reliably established by using a non-radioactive method to detect steroid sulphatase deficiency in leukocytes. This new method yields the same results with leukocytes as with cultured fibroblasts. The second type of microsomal arylsulphatase previously described in cultured fibroblasts is also present in leukocytes.

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Year:  1983        PMID: 6573909     DOI: 10.1111/j.1365-2133.1983.tb01058.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  4 in total

1.  Partial lyonisation of steroid sulphatase gene in single hair roots.

Authors:  P J Willems; H W de Bruijn; A Groenhuis; B R Mooyaart; R Berger
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

2.  Recognising placental steroid sulphatase deficiency.

Authors:  A C Jöbsis; C M van der Loos; J M Walboomers; W P de Groot
Journal:  Br Med J (Clin Res Ed)       Date:  1984-01-21

3.  Cholesterol sulphate in the microsomal sulphatase deficient placenta.

Authors:  A Marinkovic-Ilsen; M L Williams
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

4.  Tissue-specific expression of human arylsulfatase-C isozymes and steroid sulfatase.

Authors:  D G Munroe; P L Chang
Journal:  Am J Hum Genet       Date:  1987-02       Impact factor: 11.025

  4 in total

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