Multiple forms of iduronate 2-sulphate sulphatase in human tissues and body fluids
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Biophysics,Structural Biology
Reference9 articles.
1. Identification and partial characterization of two enzyme forms of iduronate sulfatase from human placenta
2. Iduronate sulfatase in amniotic fluid: An aid in the prenatal diagnosis of the Hunter syndrome
3. Iduronate Sulfatase Activity in Serum, Lymphocytes, and Fibroblasts—Simplified Diagnosis of the Hunter Syndrome
4. An improved assay for iduronate 2-sulphate sulphatase in serum and its use in the detection of carriers of the Hunter syndrome
5. Purification and Some Properties of Human Liver Iduronate Sulfatase1
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1. Characterization of a HIR-Fab-IDS, Novel Iduronate 2-Sulfatase Fusion Protein for the Treatment of Neuropathic Mucopolysaccharidosis Type II (Hunter Syndrome);BioDrugs;2023-04-04
2. The Enzymatic Degradation of Heparan Sulfate;Protein & Peptide Letters;2017-10-24
3. Dynamic changes of the luminal and mucosa-associated gut microbiota during and after antibiotic therapy with paromomycin;Gut Microbes;2015-07-04
4. Absence of α-galactosidase cross-correction in Fabry heterozygote cultured skin fibroblasts;Molecular Genetics and Metabolism;2015-02
5. A biochemical and physicochemical comparison of two recombinant enzymes used for enzyme replacement therapies of hunter syndrome;Glycoconjugate Journal;2014-04-30
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