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galsulfase

Known as: ARSB, Arylsufatase B, galsulfase [Chemical/Ingredient] 
National Institutes of Health

Papers overview

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2020
2020
BACKGROUND Although LC-MS/MS is preferred as a reliable method, therapeutic enzyme drugs in the blood matrix may lead to false… 
Review
2018
Review
2018
IntroductionMucopolysaccharidosis VI is a rare disease characterized by the arylsulfatase B enzyme deficiency, which is… 
2017
2017
OBJECTIVE Mucopolysaccharidosis type VI (MPS VI; Maroteaux-Lamy syndrome), a rare autosomal recessive lysosomal storage disease… 
2016
2016
Elucidating the intricate relationships between metabolic and transport pathways contributes to improved predictions of in vivo… 
2016
2016
Immunostaining and activity of the enzyme Arylsulfatase B (ARSB; N-acetylgalactosamine 4-sulfatase) were reduced in prostatic… 
2014
2014
Introduction: Mucopolysaccharidosis VI (MPS VI) is an autosomal recessive lysosomal storage disorder caused by a deficiency in… 
2013
2013
Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC N-acetylgalactosamine-4-sulfatase (Arylsulfatase B… 
2012
2012
Who's first? Aldol cyclization occurs before hydrolysis in the resorcinol ring formation catalyzed by the type III polyketide…