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Arylsulfatase A, human

Known as: Cerebroside-Sulfatase, ASA, EC 3.1.6.8 
Arylsulfatase A (507 aa, ~54 kDa) is encoded by the human ARSA gene. This protein is involved in the hydrolysis of cerebroside sulfate.
National Institutes of Health

Papers overview

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2017
2017
(54) INHIBITOR DEVELOPMENT FOR compound of formulas I or II or III or derivatives thereof as 4-HYDROXYPHENYLPYRUVATE follows: R… 
2017
2017
54 FILM-FORMING COMPOSITION SUITABLE O 594068 4/1994 European Pat. Off.. FOR USE ASA MONOCOAT O 594142 4/1994 European Pat. Off… 
2015
2015
Introduction Argininosuccinic aciduria (ASA; OMIM 207900) is an autosomal recessive metabolic disorder caused by… 
2011
2011
The nature of bonding between N, P, and As constituent atoms in ylide systems with the R(3)XYR' formula (X = N, P, As; Y = N, P… 
2010
2010
The electrochemical behavior of triflusal (TRF) and aspirin (ASA), before and after hydrolysis in water and in alkaline medium… 
Highly Cited
1996
Highly Cited
1996
ArsA ATPase activity is allosterically activated by salts of the semimetal arsenic or antimony. Activation is associated with the… 
1983
1983
Argininosuccinate (ASA) synthetase in the liver from a patient with a variant form of citrullinaemia was analysed. Serum… 
1983
1983
Metachromatic leukodystrophy is a hereditary neurodegenerative disorder in man associated with deficient arylsulfatase-A activity…