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ARSA gene

Known as: CEREBROSIDE-SULFATASE, ARSA, CEREBROSIDE 3-SULFATASE 
This gene is involved in the metabolism of cerebroside sulfate.
National Institutes of Health

Related topics

Related topics

5 relations
Arylsulfatase A, humanCerebroside-SulfataseHydrolysisLeukodystrophy, Metachromatic

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2004
2004
Lipomucopolysaccharidose
SummaryTwo own and several observations of the literatur suggest the existence of an apparently new type of storage disease to be… 
2000
2000
The linker peptide of the ArsA ATPase
Plasmid R773 encodes an As(III)/Sb(III)‐translocating ATPase that confers resistance to those metalloids in Escherichia coli. The… 
Highly Cited
1991
Highly Cited
1991
Two new arylsulfatase A (ARSA) mutations in a juvenile metachromatic leukodystrophy (MLD) patient.
Fragments of the arylsulfatase A (ARSA) gene from a patient with juvenile-onset metachromatic leukodystrophy (MLD) were amplified… 
1988
1988
Leucodystrophy with pigmented glial and scavenger cells (pigmentary type of orthochromatic leucodystrophy).
A 38-year-old man with progressive psychiatric disturbances, dysarthria, myoclonus, rigidity and terminal generalized seizures… 
1983
1983
Pseudo arylsulfatase-A deficiency in healthy individuals: genetic and biochemical relationship to metachromatic leukodystrophy.
Metachromatic leukodystrophy is a hereditary neurodegenerative disorder in man associated with deficient arylsulfatase-A activity… 
Highly Cited
1982
Highly Cited
1982
Enhanced breakdown of arylsulfatase A in multiple sulfatase deficiency.
Multiple sulfatase deficiency (mucosulfatidosis) is a lysosomal storage disorder characterized by the decrease in activities of… 
1980
1980
Regional localization of the genes coding for human ACO2, ARSA, and NAGA on chromosome 22.
The segregation of the chromosome 22 markers ACO2, ARSA, and NAGA was studied in somatic cell hybrid clones. These hybrids were… 
1979
1979
Arylsulphatases A and B in human diploid fibroblasts: differential assay with 4-methylumbelliferylsulphate and AgNO3.
Highly Cited
1971
Highly Cited
1971
THE INCIDENCE AND GENETICS OF METACHROMATIC LEUCODYSTROPHY IN NORTHERN SWEDEN
The purpose of this study was to investigate the incidence and genetics of metachromatic leuco‐dystrophy (MLD). A series of 13… 
1966
1966
Kidney Glycolipids in Late Infantile Metachromatic Leucodystrophy
1. Micropreparations from kidneys of children with metachromatic leucodystrophy were analyzed for neutral glyco‐lipid and… 
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