Glutathione synthetase deficiency, an inborn error of metabolism involving the gamma-glutamyl cycle in patients with 5-oxoprolinuria (pyroglutamic aciduria). (Q37449843)

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scientific article published on June 1974

Language	Label	Description	Also known as
English	Glutathione synthetase deficiency, an inborn error of metabolism involving the gamma-glutamyl cycle in patients with 5-oxoprolinuria (pyroglutamic aciduria).	scientific article published on June 1974

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Glutathione synthetase deficiency, an inborn error of metabolism involving the gamma-glutamyl cycle in patients with 5-oxoprolinuria (pyroglutamic aciduria). (English)

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

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glutathione synthetase deficiency

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Wellner VP

1

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Sekura R

2

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Meister A

3

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Larsson A

4

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

language of work or name

0 references

publication date

1 June 1974

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

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

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Europe PubMed Central

PMC publication ID

20 August 2017

71

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Europe PubMed Central

PMC publication ID

20 August 2017

6

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Europe PubMed Central

PMC publication ID

20 August 2017

2505-2509

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Protein measurement with the Folin phenol reagent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=388488

23 August 2017

THE OPTICALLY-SPECIFIC ENZYMATIC CYCLIZATION OF D-GLUTAMATE

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=388488

23 August 2017

Enzymatic Conversion of 5-Oxo-L-Proline (L-Pyrrolidone Carboxylate) to L-Glutamate Coupled with Cleavage of Adenosine Triphosphate to Adenosine Diphosphate, a Reaction in the γ-Glutamyl Cycle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=388488

23 August 2017

The gamma-glutamyl cycle: a possible transport system for amino acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=388488

23 August 2017

Glutathione biosynthesis in human erythrocytes. I. Identification of the enzymes of glutathione synthesis in hemolysates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=388488

14 September 2017

On the enzymology of amino acid transport

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=388488

14 September 2017

Pyroglutamic aciduria--a new inborn error of metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=388488

26 June 2018

Esophageal hiatus hernia and mental retardation: life-threatening postoperative metabolic acidosis and potassium deficiency linked with a new inborn error of nitrogen metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=388488

26 June 2018

Pyroglutamic aciduria. Studies in an infant with chronic metabolic acidosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=388488

26 June 2018

Partial reactions catalyzed by -glutamylcysteine synthetase and evidence for an activated glutamate intermediate.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=388488

26 June 2018

Glutathione Synthetase Deficiency as a Cause of Hereditary Hemolytic Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=388488

2 September 2018

[Glutathione synthesis during congenital hemolytic anemia with reduced glutathione deficiency. Congenital erythrocytic glutathione-synthetase deficiency?]

1 reference

https://pubmed.ncbi.nlm.nih.gov/4152248

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tripeptide (Glutathione) Synthetase. Purification, Properties, and Mechanism of Action*

1 reference

https://pubmed.ncbi.nlm.nih.gov/4152248

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disulfide and sulfhydryl compounds in TCA extracts of human blood and plasma

1 reference

https://pubmed.ncbi.nlm.nih.gov/4152248

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Metabolism of L-Pyroglutamic Acid in Fibroblasts from a Patient with Pyroglutamic Aciduria: The Demonstration of an L-Pyroglutamate Hydrolase System

1 reference

https://pubmed.ncbi.nlm.nih.gov/4152248

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pyroglutamic aciduria: studies on the enzymic block and on the metabolic origin of pyroglutamic acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/4152248

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary absence of reduced glutathione in the erythrocytes - a new clinical and biochemical entity? (Preliminary communication)

1 reference

https://pubmed.ncbi.nlm.nih.gov/4152248

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital nonspherocytic hemolytic anemia, associated with glutathione deficiency of the erythrocytes. Hematologic, biochemical and genetic studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/4152248

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.71.6.2505

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

1974PNAS...71.2505W

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release_zmug2ymcwbappf7ezgocnsd5va

1 reference

https://api.fatcat.wiki/v0/release/zmug2ymcwbappf7ezgocnsd5va

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

ResearchGate publication ID

0 references

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