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iduronate-2-sulfatase activity
Known as:
2-sulfo-L-iduronate 2-sulfatase activity
, L-iduronosulfatase activity
, iduronate-2-sulfate sulfatase activity
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Catalysis of the hydrolysis of the 2-sulfate groups of the L-iduronate 2-sulfate units of dermatan sulfate, heparan sulfate and heparin. [EC:3.1.6.13…
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National Institutes of Health
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Related topics
Related topics
2 relations
IDS gene
Broader (1)
chondroitinsulfatase activity
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
1998
1998
New pathway of heparan sulphate degradation. Iduronate sulphatase and N-sulphoglucosamine 6-sulphatase act on the polymer chain prior to depolymerisation by a N-sulpho-glucosaminidase and…
M. G. Medeiros
,
T. M. Ferreira
,
E. L. Leite
,
L. Toma
,
C. Dietrich
,
H. Nader
Comparative Biochemistry and Physiology Part B…
1998
Corpus ID: 22047374
1998
1998
Mucopolysaccharidosis type II (Hunter's syndrome) in Taiwan.
P. Su
,
W. Hwu
,
+4 authors
T. R. Wang
Journal of the Formosan Medical Association…
1998
Corpus ID: 35454389
The mucopolysaccharidoses are a group of inherited disorders of lysosomal storage of glycosaminoglycans. Among them…
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1992
1992
Fragile X mental retardation and the iduronate sulphatase locus: testing Laird's model of fra(X) inheritance.
A. Clarke
,
D. Bradley
,
K. Gillespie
,
D. Rees
,
A. Holland
,
N. Thomas
American journal of medical genetics
1992
Corpus ID: 10488945
Fragile X [fra(X)] mental retardation syndrome is the most frequent familial cause of mental handicap. The clinical phenotype is…
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1987
1987
Hunter syndrome: presence of material cross-reacting with antibodies against iduronate sulfatase
A. Daniele
,
P. Natale
Human Genetics
1987
Corpus ID: 13349788
SummaryPolyclonal antibodies were obtained from rabbits by injection of iduronate sulfatase purified 35,000-fold from human…
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1982
1982
Administration of iduronate sulfatase by plasma exchange to patients with the Hunter syndrome: a clinical study.
F. R. Brown
,
C. W. Hall
,
+7 authors
H. Moser
American journal of medical genetics
1982
Corpus ID: 24303624
The Hunter syndrome (MPS II) is the only mucopolysaccharidosis in which there is appreciable activity of the deficient enzyme in…
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1980
1980
Interaction between heparan sulphate chains. II. Structural characterization of iduronate- and glucuronate-containing sequences in aggregating chains.
L. Fransson
,
B. Havsmark
,
I. Nieduszynski
,
T. Huckerby
Biochimica et Biophysica Acta
1980
Corpus ID: 38271477
1979
1979
alpha-L-iduronidase, beta-D-glucuronidase, and 2-sulfo-L-iduronate 2-sulfatase: preparation and characterization of radioactive substrates from heparin.
J. Hopwood
Carbohydrate Research
1979
Corpus ID: 21576502
Radioactive disaccharide substrates for alpha-L-iduronidase, beta-D-glucuronidase, and 2-sulfo-L-iduronate 2-sulfatase have been…
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1977
1977
Iduronate sulfatase in amniotic fluid: an aid in the prenatal diagnosis of the hunter syndrome.
Ingeborg Liebaers
,
Paola Di Natale
,
Elizabeth F. Neufeld
Jornal de Pediatria
1977
Corpus ID: 20491913
Highly Cited
1976
Highly Cited
1976
Iduronate Sulfatase Activity in Serum, Lymphocytes, and Fibroblasts—Simplified Diagnosis of the Hunter Syndrome
I. Liebaers
,
E. Neufeld
Pediatric Research
1976
Corpus ID: 19091494
Extract: A previously described assay for iduronate sulfatase has been adapted for use with serum, lymphocytes, and fibroblasts…
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1976
1976
Iduronate sulfatase determination for the diagnosis of the Hunter syndrome and the detection of the carrier state.
E. Neufeld
,
I. Liebaers
,
T. W. Lim
Advances in Experimental Medicine and Biology
1976
Corpus ID: 41402972
The research efforts of the last few years have clarified the biochemical basis of the mucopolysaccharidoses (17). Some practical…
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