Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures (Q36450898)

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English	Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

223681

retrieved

14 August 2017

title

Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures (English)

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stated in

Europe PubMed Central

PMC publication ID

223681

retrieved

14 August 2017

main subject

metachromatic leukodystrophy

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based on heuristic

inferred from title

author name string

Porter MT

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

223681

retrieved

14 August 2017

Fluharty AL

series ordinal

2

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stated in

Europe PubMed Central

PMC publication ID

223681

retrieved

14 August 2017

Kihara H

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

223681

retrieved

14 August 2017

language of work or name

English

0 references

publication date

1 March 1969

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stated in

Europe PubMed Central

PMC publication ID

223681

retrieved

14 August 2017

number of pages

5

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inferred from page(s)

published in

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

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stated in

Europe PubMed Central

PMC publication ID

223681

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14 August 2017

volume

62

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stated in

Europe PubMed Central

PMC publication ID

223681

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14 August 2017

issue

3

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stated in

Europe PubMed Central

PMC publication ID

223681

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14 August 2017

page(s)

887-891

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Europe PubMed Central

PMC publication ID

223681

retrieved

14 August 2017

cites work

Protein measurement with the Folin phenol reagent

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223681

retrieved

30 September 2017

Studies on sulphatases. 23. The enzymic desulphation of tyrosine O-sulphate

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223681

retrieved

28 June 2018

Isolation of beta-galactosidase and beta-glucosidase from brain

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223681

retrieved

28 June 2018

Acid hydrolases in skin and plasma in gargoylism. Deficiency of beta-galactosidase in skin.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223681

retrieved

28 June 2018

Metachromatic form of diffuse cerebral sclerosis. V. The nature and significance of low sulfatase activity: a controlled study of brain, liver and kidney in four patients with metachromatic leukodystrophy (MLD).

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223681

retrieved

28 June 2018

Metachromatic leukodystrophy (sulfatide lipidoses) cultured in vitro

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223681

retrieved

28 June 2018

EVIDENCE FOR THE GENETIC BLOCK IN METACHROMATIC LEUCODYSTROPHY (ML).

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223681

retrieved

21 September 2018

Metachromatic form of diffuse cerebral sclerosis. III. Significance of sulfatide and other lipid abnormalities in white matter and kidney

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stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223681

retrieved

21 September 2018

Metachromatic Leukodystrophy: Diagnosis with Samples of Venous Blood

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223681

retrieved

21 September 2018

Hurler's syndrome: demonstration of an inherited disorder of connective tissue in cell culture

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223681

retrieved

21 September 2018

Metachromatic form of diffuse cerebral sclerosis. VI. A rapid test for the sulfatase A deficiency in metachromatic leukodystrophy (MLD) urine

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5257010

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of gaucher's disease and niemann-pick disease with small samples of venous blood

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5257010

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebroside 3-sulfate as a physiological substrate of arylsulfatase A

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5257010

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The assay of arylsulphatases A and B in human urine

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5257010

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

METACHROMATIC FORM OF DIFFUSE CEREBRAL SCLEROSIS. IV. LOW SULFATASE ACTIVITY IN THE URINE OF NINE LIVING PATIENTS WITH METACHROMATIC LEUKODYSTROPHY (MLD)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5257010

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nutrition of animal cells in tissue culture; initial studies on a synthetic medium

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5257010

retrieved

12 December 2020

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[Leukodystrophy, Scholz' type, (metachromatic form of diffuse sclerosis) with sphinolipoidosis (cerebroside-sulfuric acid ester storage disease)]

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5257010

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1073/PNAS.62.3.887

1 reference

stated in

Europe PubMed Central

PMC publication ID

223681

retrieved

14 August 2017

ADS bibcode

1969PNAS...62..887P

0 references

PMC publication ID

223681

1 reference

stated in

Europe PubMed Central

PMC publication ID

223681

retrieved

14 August 2017

PubMed publication ID

5257010

1 reference

stated in

Europe PubMed Central

PMC publication ID

223681

retrieved

14 August 2017

ResearchGate publication ID

17912106

0 references

 

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