Components and proteolytic processing sites of arylsulfatase B from human placenta
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Biophysics,Structural Biology
Reference26 articles.
1. Deficiency of chondroitin sulfate N-acetylgalactosamine 4-sulfate sulfatase in Maroteaux-Lamy syndrome
2. Maroteaux-lamy disease (mucopolysaccharidosis VI), subtype A: Deficiency of a N-acetylgalactosamine-4-sulfatase
3. The Enzymatic Desulfation of Sulfated Sugar Nucleotides by a Novel Sulfatase in Hen Oviduct
4. Uridine diphospho-N-acetylgalactosamine-4-sulfate sulfohydrolase activity of human arylsulfatase B and its deficiency in the Maroteaux-Lamy syndrome
5. Diagnosis of Maroteaux—Lamy syndrome by the use of radiolabelled oligosaccharides as substrates for the determination of arylsulphatase B activity
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5. Structural aspects of therapeutic enzymes to treat metabolic disorders;Human Mutation;2009-12
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