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Iduronate Sulfatase

Known as: Sulfatase, Sulfoiduronate, Hunter Corrective Factor, Sulfatase, Iduronate 
An enzyme that specifically cleaves the ester sulfate of iduronic acid. Its deficiency has been demonstrated in Hunter's syndrome, which is… 
National Institutes of Health

Related topics

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12 relations

Narrower (3)

ElapraseIDS protein, humanidursulfase
IDS geneIn BloodMucopolysaccharidosis IIProcess of secretion

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Conformational selection of the AGA*IA(M) heparin pentasaccharide when bound to the fibroblast growth factor receptor.
The interaction of the synthetic pentasaccharide AGA*IA(M) (GlcNS,6S-GlcA-GlcNS,3S,6S-IdoA2S-GlcNS,6S-Me) with the extracellular… 
Review
2010
Review
2010
Corrective Feedback in L2 Writing: Theoretical Perspectives, Empirical Insights, and Future Directions
The role of (written) corrective feedback (CF) in the process of acquiring a second language (L2) has been an issue of… 
2007
2007
Preclinical dose ranging studies for enzyme replacement therapy with idursulfase in a knock-out mouse model of MPS II.
Highly Cited
1998
Highly Cited
1998
Mutation analysis in 57 unrelated patients with MPS II (Hunter’s disease)
Genomic DNA from 57 unrelated MPS II (Hunter’s disease) patients was analysed for mutations of the iduronate sulphatase (IDS… 
1998
1998
Mutational spectrum of the iduronate-2-sulfatase (IDS) gene in 36 unrelated Russian MPS II patients
Abstract We present a mutational analysis of the iduronate-2-sulfatase (IDS) gene of 36 Russian patients with Hunter syndrome… 
Highly Cited
1984
Highly Cited
1984
Characterization of cholecystokinin receptors on bovine gallbladder membranes.
Cholecystokinin (CCK) binding to its receptors on a muscularis membrane fraction of bovine gallbladder was characterized using a… 
1977
1977
The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency?
Profound iduronate sulfatase deficiency, characteristic of the Hunter syndrome, has been found in cultured fibroblasts, serum… 
Highly Cited
1976
Highly Cited
1976
Iduronate Sulfatase Activity in Serum, Lymphocytes, and Fibroblasts—Simplified Diagnosis of the Hunter Syndrome
Extract: A previously described assay for iduronate sulfatase has been adapted for use with serum, lymphocytes, and fibroblasts… 
Highly Cited
1973
Highly Cited
1973
The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase.
Skin fibroblasts cultured from patients affected with the Hunter syndrome are deficient in the activity of a protein, named the… 
Highly Cited
1951
Highly Cited
1951
A basic study of the chewing forces of a denture wearer.
The problem of thumbsucking should be corrected by the parent and the pedia­ trician. If the habit has not been cor­ rected by… 
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