(Q28366638)

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Specific glutaryl-CoA dehydrogenating activity is deficient in cultured fibroblasts from glutaric aciduria patients

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Specific glutaryl-CoA dehydrogenating activity is deficient in cultured fibroblasts from glutaric aciduria patients (English)

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1 reference

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D B Hyman

1

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K Tanaka

series ordinal

2

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language of work or name

English

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publication date

March 1984

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published in

Journal of Clinical Investigation

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volume

73

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issue

3

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page(s)

778-84

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cites work

Inactivation of general acyl-CoA dehydrogenase from pig kidney by a metabolite of hypoglycin A

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Glutaric aciduria: clinical and laboratory findings in two brothers

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20 March 2017

L-Glutaric acidemia: investigation of a patient and his family

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20 March 2017

Demonstration of a specific mitochondrial isovaleryl-CoA dehydrogenase deficiency in fibroblasts from patients with isovaleric acidemia

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20 March 2017

Isovaleryl-CoA dehydrogenase: demonstration in rat liver mitochondria by ion exchange chromatography and isoelectric focusing

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29 September 2017

Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein

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2 June 2018

Mammalian metabolism of glutaric acid

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2 June 2018

Glutaric aciduria: Inherited deficiency of glutaryl-CoA dehydrogenase activity

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2 June 2018

Jamaican vomiting sickness. Biochemical investigation of two cases

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Glutaric aciduria: biochemical and morphologic considerations.

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2 June 2018

Studies on glutaryl-CoA dehydrogenase in leucocytes, fibroblasts and amniotic fluid cells. The normal enzyme and the mutant form in patients with glutaric aciduria

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Glutaric aciduria in progressive choreo-athetosis

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2 June 2018

On the mode of action of hypoglycin A. 3. Isolation and identification of cis-4-decene-1,10-dioic, cis, cis-4,7-decadiene-1,10-dioic, cis-4-octene-1,8-dioic, glutaric, and adipic acids, N-(methylenecyclopropyl)acetylglycine, and N-isovalerylglycine

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retrieved

12 December 2020

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Glutaric aciduria; A “new” disorder of amino acid metabolism

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12 December 2020

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Glutaric aciduria; presence of glutaconic and beta-hydroxyglutaric acids in urine

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6423663

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glutaric aciduria type II: Report on a previously undescribed metabolic disorder

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reference URL

https://pubmed.ncbi.nlm.nih.gov/6423663

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel tritium release assays for isovaleryl-CoA and butyryl-CoA dehydrogenases

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6423663

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glutaric aciduria type II: in vitro studies on substrate oxidation, acyl-CoA dehydrogenases, and electron-transferring flavoprotein in cultured skin fibroblasts

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6423663

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of action of glutaryl-CoA and butyryl-CoA dehydrogenases. Purification of glutaryl-CoA dehydrogenase

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6423663

retrieved

12 December 2020

based on heuristic

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Identifiers

DOI

10.1172/JCI111271

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Fatcat ID

release_ax7psbghnrfpbjkzk6ijqwtfbu

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PMC publication ID

425080

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PubMed publication ID

6423663

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(Q28366638)

Specific glutaryl-CoA dehydrogenating activity is deficient in cultured fibroblasts from glutaric aciduria patients

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