"Steryl-Sulfatase" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An arylsulfatase with high specificity towards sulfated steroids. Defects in this enzyme are the cause of ICHTHYOSIS, X-LINKED.
| Descriptor ID |
D043266
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| MeSH Number(s) |
D08.811.277.352.827.070.625
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| Concept/Terms |
Steryl-Sulfatase- Steryl-Sulfatase
- Steryl Sulfatase
- Arylsulfatase C
- Arylsulphatase C
- Cholesterol Sulfatase
- Sulfatase, Cholesterol
- Cholesterol Sulfate Sulfatase
- Sulfatase, Cholesterol Sulfate
- Sulfate Sulfatase, Cholesterol
- Dehydroepiandrosterone Sulfate Sulfatase
- Sulfatase, Dehydroepiandrosterone Sulfate
- Sulfate Sulfatase, Dehydroepiandrosterone
- DHEA Sulfatase
- Sulfatase, DHEA
- Estrone Sulfate Sulfatase
- Sulfatase, Estrone Sulfate
- Sulfate Sulfatase, Estrone
- Estrone Sulfate Sulfohydrolase
- Sulfate Sulfohydrolase, Estrone
- Sulfohydrolase, Estrone Sulfate
- Steroid Sulfatase
- Sulfatase, Steroid
- Steroid Sulfohydrolase
- Sulfohydrolase, Steroid
- Steroid Sulphatase
- Sulphatase, Steroid
- Sterol Sulfatase
- Sulfatase, Sterol
- Sterylsulfatase
- 3 Beta-Hydroxysteroid Sulfate Sulfatase
- 3 Beta Hydroxysteroid Sulfate Sulfatase
|
Below are MeSH descriptors whose meaning is more general than "Steryl-Sulfatase".
Below are MeSH descriptors whose meaning is more specific than "Steryl-Sulfatase".
This graph shows the total number of publications written about "Steryl-Sulfatase" by people in this website by year, and whether "Steryl-Sulfatase" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 0 | 1 | 1 |
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Below are the most recent publications written about "Steryl-Sulfatase" by people in Profiles.
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Low or absent unconjugated estriol in pregnancy: an indicator for steroid sulfatase deficiency detectable by fluorescence in situ hybridization and biochemical analysis. Prenat Diagn. 2002 Nov; 22(11):1028-32.
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Characterization of the deletion breakpoints in a patient with steroid sulfatase deficiency. Hum Mutat. 1994; 4(1):76-8.
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Correction of steroid sulfatase deficiency by gene transfer into basal cells of tissue-cultured epidermis from patients with recessive X-linked ichthyosis. Exp Cell Res. 1993 Dec; 209(2):392-7.
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A yeast artificial chromosome contig linking the steroid sulfatase and Kallmann syndrome loci on the human X chromosome short arm. Genomics. 1993 Oct; 18(1):1-6.
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Sequence analysis of a partial deletion of the human steroid sulfatase gene reveals 3 bp of homology at deletion breakpoints. Genomics. 1992 Jul; 13(3):892-3.
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Identification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosis. Am J Hum Genet. 1992 Mar; 50(3):483-91.
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Isolation and characterization of a yeast artificial chromosome (YAC) contig around the human steroid sulfatase gene. Genomics. 1992 Jan; 12(1):7-12.
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Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiency. Am J Med Genet. 1991 Nov 01; 41(2):184-7.
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Screening for steroid sulfatase (STS) gene deletions by multiplex DNA amplification. Hum Genet. 1990 May; 84(6):571-3.
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Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels. Genomics. 1989 Jan; 4(1):36-40.