(Q33989276)

30 July 2017

title

Genetic complementation studies of multiple sulfatase deficiency (English)

1 reference

30 July 2017

A. L. Horwitz

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A118467

30 April 2022

language of work or name

English

0 references

publication date

1 December 1979

1 reference

full work available at URL

30 July 2017

https://europepmc.org/articles/PMC411892

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A118467

https://europepmc.org/articles/PMC411892?pdf=render

30 April 2022

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A118467

https://pnas.org/doi/pdf/10.1073/pnas.76.12.6496

30 April 2022

1 reference

Crossref

DOI

10.1073/PNAS.76.12.6496

https://api.crossref.org/works/10.1073/PNAS.76.12.6496

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

30 April 2022

published in

1 reference

30 July 2017

volume

76

1 reference

30 July 2017

issue

12

1 reference

30 July 2017

page(s)

6496-6499

1 reference

The specific assay of arylsulphatase C, a rat liver microsomal marker enzyme

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=411892

Electrophoresis of arylsulfatase from normal individuals and patients with metachromatic leukodystrophy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=411892

Multiple sulfatase deficiencies in cultured skin fibroblasts. Occurrence in patients with a variant form of metachromatic leukodystrophy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=411892

Studies in metachromatic leukodystrophy. XII. Multiple sulfatase deficiency

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=411892

Improved techniques for the induction of mammalian cell hybridization by polyethylene glycol

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=411892

Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=411892

The enzymic defect in Morquio's disease: The specificity of N-acetylhexosamine sulfatases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=411892

Lysosomal arylsulfatase deficiencies in humans: Chromosome assignments for arylsulfatase A and B

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=411892

Presence of arylsulfatase A (ARS A) in multiple sulfatase deficiency disorder fibroblasts

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=411892

The biosynthesis of chondroitin sulfate

5 July 2018

1 reference

12 December 2020

Correction of human mucolipidosis II enzyme abnormalities in somatic cell hybrids

1 reference

12 December 2020

The assay of arylsulphatases A and B in human urine

1 reference

12 December 2020

Hurler and Hunter syndromes: mutual correction of the defect in cultured fibroblasts

1 reference

12 December 2020

A monospecific antibody to human sulfatase A. Preparation, characterization and significance

1 reference

12 December 2020

Reduced arylsulfatase B activity of the mutant enzyme protein in Maroteaux-Lamy syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.76.12.6496

1 reference

30 July 2017

0 references

1 reference

30 July 2017

1 reference