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MPS III B

Known as: Mucopolysaccharidosis Type IIIBs, Deficiency, NAGLU, N Acetyl alpha D Glucosaminidase Deficiency 
A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme N-acetyl-alpha-D-glucosaminidase. It is characterized by… 
National Institutes of Health

Papers overview

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1993
1993
ZusammenfassungUm die biochemischen Veränderungen in Fischmuskel während der Lagerung auf Eis und während des Einfrier- und… 
1984
1984
The biosynthesis of alpha-N-acetylglucosaminidase in normal and Sanfilippo B fibroblasts was studied by labeling cells with [35S… 
1982
1982
Compared to values obtained in healthy normotensive control subjects, serum activity of the lysosomal enzyme N-acetyl-β-D… 
1981
1981
The phospholipid acyl-chain dependence of the membrane-bound lysosomal beta-N-acetyl-D-glucosaminidase has been examined on… 
1979
1979
Cultured mouse peritoneal macrophages were shown to secrete the lysosomal enzyme N-acetyl-glucosaminidase (N-ac-Glu) in response… 
1978
1978
Beta-N-acetyl glucosaminidase (NAG) is a lyosomal enzyme found in high concentrations in the epithelial cells of renal tubules… 
1974
1974
The distribution of some hydrolytic enzymes in fowl semen was studied. Washed spermatozoa and seminal plasma were examined for… 
1971
1971
carcinogenic activity. It may be that oxidation of the nitrogen enhances the ease of hydrolysis, as suggested by Irving (1966… 
1971
1971
The enzymes al-fucosidase, β-galactosidase, β-glucosidase, β-acetylglucosaminidase, β-glucuronidase and L-mannosidase were… 
1968
1968
Ockerman, P. A. & Kohlin, P. Tissue Acid Hydrolase Activities in Gaucher's Disease. Scand. J. clin. Lab. Invest. 22, 62-64, 1968…