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Arylsulfatase B

Known as: N-Acetylgalactosamine-4-sulfate Sulfatase, Sulfatase, N-Acetylgalactosamine-4-sulfate, N Acetylgalactosamine 4 sulfate Sulfatase 
An arylsulfatase that catalyzes the hydrolysis of the 4-sulfate groups of the N-acetyl-D-galactosamine 4-sulfate units of chondroitin sulfate and… Expand
National Institutes of Health

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2007
2007
BACKGROUND The genetic disorder cystic fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance… Expand
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Highly Cited
2005
Highly Cited
2005
SummaryA dual staining method has been developed to identify two types of mucous secreting cells in the gastric mucosa of human… Expand
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Highly Cited
2005
Highly Cited
2005
Entamoeba histolytica, an intestinal protozoan parasite, is a major cause of morbidity and mortality in developing countries. The… Expand
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2005
2005
SummaryA new lysosomal storage disease with autosomal recessive inheritance is described in two male siblings of 5 1/2 and 4… Expand
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2002
2002
Abstract. The aim of this work was to show differences in the terminal and subterminal sugar composition of carbohydrate chains… Expand
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1996
1996
Mucopolysaccharidosis VI (MPS VI) is a lysosomal storage disease with autosomal recessive inheritance caused by a deficiency of… Expand
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1994
1994
Mucopolysaccharidosis type VI, or Maroteaux-Lamy syndrome, is a lysosomal storage disorder caused by a deficiency of the enzyme… Expand
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1979
1979
Summary: This report gives a more complete description of pathologic and enzymologic findings in the feline Maroteaux-Lamy… Expand
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1977
1977
A Siamese cat that presented clinical signs similar to those seen in humans with mucopolysaccharidoses was studied. The animal… Expand
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1974
1974
Summary Fibroblasts derived from patients with Maroteaux-Lamy syndrome (mucopolysaccharidosis VI) contained about 10% of normal… Expand
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