(Q37509878)

20 August 2017

Pseudo arylsulfatase-A deficiency in healthy individuals: genetic and biochemical relationship to metachromatic leukodystrophy (English)

1 reference

metachromatic leukodystrophy

20 August 2017

1 reference

Chang PL

1

1 reference

20 August 2017

Davidson RG

series ordinal

2

1 reference

20 August 2017

language of work or name

English

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publication date

1 December 1983

1 reference

Proceedings of the National Academy of Sciences of the United States of America

20 August 2017

1 reference

20 August 2017

80

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20 August 2017

23

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20 August 2017

7323-7327

1 reference

Protein measurement with the Folin phenol reagent

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Two allelic forms of human arylsulfatase A with different numbers of asparagine-linked oligosaccharides

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase Component

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Globoid cell leucodystrophy (Krabbe's disease): deficiency of galactocerebroside beta-galactosidase

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Absence of -N-acetyl-D-hexosaminidase A activity in a healthy woman

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Electrophoresis of arylsulfatase from normal individuals and patients with metachromatic leukodystrophy

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Apparent deficiency of hexosaminidase A in healthy members of a family with Tay-Sachs disease.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Ploidy of living clones of human somatic cells determined by mensuration at metaphase

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Very low arylsulfatase A and cerebroside sulfatase activities in leukocytes of healthy members of metachromatic leukodystrophy family

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Immunologic Studies of Arylsulfatase A in Normal and Metachromatic Leukodystrophy Liver

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Cerebroside sulfate hydrolysis by fibroblasts from a parent with metachromatic leukodystrophy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

A sensitive fluorescence assay for the simultaneous and separate determination of arylsulphatases A and B

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Apparent biochemical homozygosity in two obligatory heterozygotes for metachromatic leukodystrophy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Detection of arylsulfatase A activity after electrophoresis in polyacrylamide gels: Problems and solutions

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

A simple method for decreasing the toxicity of polyethylene glycol in mammalian cell hybridization

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Cerebroside sulfatase determination in cultured human fibroblasts.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Enzyme electrophoresis on cellulose acetate gel: zymogram patterns in mgh-mouse and man--Chinese hamster somatic cell hybrids.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

The nature of the residual arylsulfatase activity in metachromatic leukodystrophy

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Absence of Hexosaminidase a and B in a Normal Adult

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Polyethylene glycol-induced mammalian cell hybridization: effect of polyethylene glycol molecular weight and concentration

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Inheritance of metachromatic leukodystrophy

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Low arylsulphatase A activity in a family without metachromatic leukodystrophy

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

A CONTROLLED STUDY OF ENZYMIC ACTIVITIES IN THREE HUMAN DISORDERS OF GLYCOLIPID METABOLISM

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Impaired Cerebroside Sulfate Hydrolysis in Fibroblasts of Sibs with “Pseudo” Arylsulfatase A Deficiency without Metachromatic Leukodystrophy

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=390047

Absence of ASA Activity in Healthy Father of a Patient with Metachromatic Leukodystrophy

2 September 2018

1 reference

12 December 2020

The occurrence of low α-l-fucosidase activities in normal human serum

1 reference

12 December 2020

Possible misdiagnosis of Krabbe disease

1 reference

12 December 2020

Non-selective isolation of human somatic cell hybrids by unit-gravity sedimentation

1 reference

12 December 2020

Prenatal Diagnosis of Metachromatic Leukodystrophy in a Family with Pseudo Arylsulfatase A Deficiency by the Cerebroside Sulfate Loading Test

1 reference

12 December 2020

Adult GM2 gangliosidosis in association with Tay-Sachs disease: a new phenotype

1 reference

12 December 2020

Differential assay of arylsulfatase A and B activities: A sensitive method for cultured human cells

1 reference

12 December 2020

Problems in the clinical interpretation of arylsulfatase A deficiency

1 reference

12 December 2020

Enhanced breakdown of arylsulfatase A in multiple sulfatase deficiency

1 reference

12 December 2020

Somatic cell hybridization studies on the genetic regulation and allelic mutations in metachromatic leukodystrophy

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.80.23.7323

1 reference

20 August 2017

0 references

1 reference

20 August 2017

PubMed publication ID

6580647

1 reference