N-sulfoglucosamine sulfohydrolase activity
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Mucopolysaccharidosis (MPS) IIIA, also known as Sanfilippo syndrome type A, is a severe, progressive disease that affects the… Expand Mucopolysaccharidoses type IIIA (MPS‐IIIA) is a neurodegenerative lysosomal storage disorder (LSD) caused by inherited defects of… Expand Mucopolysaccharidosis type IIIA (SanÐlippo A; McKusick 25290) is caused by a deÐciency of lysosomal sulphamidase activity (EC 3… Expand Sanfilippo A syndrome, mucopolysaccharidosis type IIIA, is caused by a deficiency of heparan sulphamidase activity, and usually… Expand Summary4-Methylumbelliferyl-α-d-N-sulphoglucosaminide (MU-α-GlcNS) was synthesized and shown to be a substrate for the lysosomal… Expand Early amniocentesis performed at 13 weeks gestation was utilized to obtain amniocytes for culture. Sonicates of cultured… Expand Human sulphamate sulphohydrolase was purified at least 20,000-fold to homogeneity from liver with a three-step four-column… Expand 1. Sulphamidase activity was assayed by incubation of the radiolabelled disaccharide O-(alpha-2-sulphamino-2-deoxy-D… Expand A sulphamidase activity present in rat spleen capable of hydrolysing N-[(35)S]sulphated heparin was studied. This activity was… Expand Abstract A method for the estimation of arylsulphatases A and B (E.C. 18.104.22.168 arylsulphate sulphohydrolase) in serum is presented… Expand