(Q40402045)

English

Role of flavinylation in a mild variant of multiple acyl-CoA dehydrogenation deficiency: a molecular rationale for the effects of riboflavin supplementation.

scientific article published on 16 December 2008

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scholarly article

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18 January 2020

Role of flavinylation in a mild variant of multiple acyl-CoA dehydrogenation deficiency: a molecular rationale for the effects of riboflavin supplementation (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19088074%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

dehydrogenation

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based on heuristic

inferred from title

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based on heuristic

inferred from title

Bárbara J. Henriques

1

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18 January 2020

João V. Rodrigues

2

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18 January 2020

3

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18 January 2020

4

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18 January 2020

author name string

Cláudio M Gomes

5

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18 January 2020

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publication date

16 December 2008

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18 January 2020

Journal of Biological Chemistry

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18 January 2020

284

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18 January 2020

7

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18 January 2020

4222-4229

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18 January 2020

Three-dimensional structure of human electron transfer flavoprotein to 2.1-A resolution

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Glutaric acidemia type II: gene structure and mutations of the electron transfer flavoprotein:ubiquinone oxidoreductase (ETF:QO) gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Electron transfer flavoprotein deficiency: functional and molecular aspects

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Genetic defects in fatty acid beta-oxidation and acyl-CoA dehydrogenases. Molecular pathogenesis and genotype-phenotype relationships

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Human acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial beta-oxidation of unsaturated fatty acids

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Differential degradation of variant medium-chain acyl-CoA dehydrogenase by the protein quality control proteases Lon and ClpXP.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Multiple acyl-coenzyme A dehydrogenation disorder responsive to riboflavin: substrate oxidation, flavin metabolism, and flavoenzyme activities in fibroblasts

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Treatment of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria). Experience with diet, riboflavin, and GABA analogue

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

PDBsum more: new summaries and analyses of the known 3D structures of proteins and nucleic acids

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Expression and characterization of two pathogenic mutations in human electron transfer flavoprotein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Purification of electron-transferring flavoprotein from Megasphaera elsdenii and binding of additional FAD with an unusual absorption spectrum

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children: an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 years

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Riboflavin-responsive defects of beta-oxidation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Coordinated and reversible reduction of enzymes involved in terminal oxidative metabolism in skeletal muscle mitochondria from a riboflavin-responsive, multiple acyl-CoA dehydrogenase deficiency patient

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Saccharomyces cerevisiae mitochondria can synthesise FMN and FAD from externally added riboflavin and export them to the extramitochondrial phase.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Riboflavin-responsive epilepsy in a patient with SER209 variant form of short-chain acyl-CoA dehydrogenase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M805719200

21 January 2018

Identifiers

10.1074/JBC.M805719200

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19088074%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19088074%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

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