(Q24302033)

hydroxyacid-oxoacid transhydrogenase activity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

E A Struys

1

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N M Verhoeven

2

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H J Ten Brink

3

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W V Wickenhagen

4

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K M Gibson

5

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C Jakobs

Journal of Inherited Metabolic Disease

6

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language of work or name

English

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publication date

2005

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published in

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volume

28

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issue

6

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page(s)

921-30

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exact match

https://scigraph.springernature.com/pub.10.1007/s10545-005-0114-x

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cites work

Developmental time courses in the brain and kidney of two enzymes that oxidize gamma-hydroxybutyrate.

1 reference

12 December 2020

Direct nonisotopic assay of 3-methylglutaconyl-CoA hydratase in cultured human skin fibroblasts to specifically identify patients with 3-methylglutaconic aciduria type I

1 reference

12 December 2020

D-2-hydroxyglutaric aciduria in neonate with seizures and CNS dysfunction.

1 reference

12 December 2020

Oxidation of gamma-hydroxybutyrate to succinic semialdehyde by a mitochondrial pyridine nucleotide-independent enzyme.

1 reference

12 December 2020

Gamma-aminobutyric acid-transaminase deficiency: a newly recognized inborn error of neurotransmitter metabolism

1 reference

12 December 2020

D-2-hydroxyglutaric aciduria in a newborn with neurological abnormalities: a new neurometabolic disorder?

1 reference

12 December 2020

Mutations in the D-2-hydroxyglutarate dehydrogenase gene cause D-2-hydroxyglutaric aciduria

1 reference

12 December 2020

Stable-isotope dilution analysis of D- and L-2-hydroxyglutaric acid: application to the detection and prenatal diagnosis of D- and L-2-hydroxyglutaric acidemias

1 reference

12 December 2020

D-2-hydroxyglutaric aciduria: further clinical delineation.

1 reference

12 December 2020

1 reference

12 December 2020

D-2-Hydroxyglutaric aciduria: biochemical marker or clinical disease entity?

1 reference

12 December 2020

Isolation and characterization of a hydroxyacid-oxoacid transhydrogenase from rat kidney mitochondria

1 reference

12 December 2020