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SGSH gene

Known as: N-sulfoglucosamine sulfohydrolase, HEPARAN SULFATE SULFATASE, SGSH 
 
National Institutes of Health

Papers overview

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Review
2018
Review
2018
BackgroundNeurodevelopmental disorders, as a class of diseases, have been particularly difficult to treat even when the… Expand
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2015
2015
AIMS For the standardization of flow-mediated vasodilatation (FMD) assessment as a clinical tool, validation of its reliability… Expand
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2014
2014
Mucopolysaccharidosis IIIA is a fatal neurodegenerative disease that typically manifests itself in childhood and is caused by… Expand
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2012
2012
Mucopolysaccharidosis type IIIA (MPSIIIA) is an inherited lysosomal storage disease caused by deficiency of sulfamidase… Expand
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Highly Cited
2009
Highly Cited
2009
Mucopolysaccharidosis type IIIA (MPS IIIA) results from lack of functional sulfamidase (SGSH), a lysosomal enzyme. Its substrate… Expand
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2009
2009
The biosynthesis study of antibiotics saframycin (SFM) in Streptomyces lavendulae and safracin (SAC) in Pseudomonas fluorescens… Expand
Highly Cited
2008
Highly Cited
2008
Mucopolysaccharidosis type IIIA (MPS IIIA), which is a lysosomal storage disorder (LSD) caused by inherited deficiency of… Expand
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Highly Cited
2007
Highly Cited
2007
At present, there is no widely available, safe and effective treatment for lysosomal storage disorders (LSD) that affect the… Expand
Highly Cited
2004
Highly Cited
2004
Lysosomal storage disorders (LSD) are rare inherited metabolic diseases in which genetic alterations affect lysosomal proteins… Expand
1972
1972
Abstract Suspensions of various rat tissues were treated with Triton X-100 and then assayed for sulfate releasing activity using… Expand