Hexosaminidase B

Known as: Beta-N-acetylhexosaminidase.B, Hex B, Hexosaminidase B [Chemical/Ingredient] 
A mammalian beta-hexosaminidase isoform that is comprized of hexosaminidase beta subunits. Deficiency of hexosaminidase B due to mutations in the… (More)

Topic mentions per year

Topic mentions per year

1973-2016
024619732016

Papers overview

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2005
2005
BACKGROUND The relationship between the progress of tubular damage and renal insufficiency in autosomal-dominant polycystic… (More)
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2003
2003
In humans, two major beta-hexosaminidase isoenzymes exist: Hex A and Hex B. Hex A is a heterodimer of subunits alpha and beta (60… (More)
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2003
2003
Sandhoff disease is a severe inherited neurodegenerative disorder resulting from deficiency of the β-subunit of hexosaminidases A… (More)
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2002
2002
Human lysosomal beta-hexosaminidases remove terminal beta-glycosidically bound N-acetylhexosamine residues from a number of… (More)
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1997
1997
Tay-Sachs and Sandhoff diseases are autosomal recessive neurodegenerative diseases resulting from the inability to catabolize GM2… (More)
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1995
1995
beta-Hexosaminidase B-isoforms (beta-hexosaminidase B, P, and intermediate forms; abbreviated herein as "Hex B") and serum… (More)
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1991
1991
Ganglioside GD1a-GalNAc was isolated from Tay-Sachs brain, tritium-labeled in its sphingosine moiety, and its enzymic degradation… (More)
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1988
1988
Two sisters presented with progressive muscle cramps, as well as wasting and weakness of the legs with onset after age 20. They… (More)
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1985
1985
The major forms of beta-hexosaminidase (2-acetamido-2-deoxy-beta-D-glucoside acetamidodeoxyglucohydrolase, EC 3.2.1.30) occur as… (More)
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1977
1977
A boy with mild hand tremor since age 2 1/2 was found at 4 to have cherry-red spots and mild trucal ataxia without seizures or… (More)
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