Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

ETF dehydrogenase advances in molecular genetics and impact on treatment.

Critical reviews in biochemistry and molecular biology - 1 Aug 2021

Missaglia Sara, Tavian Daniela, Angelini Corrado

Abstract excerpt

Electron transfer flavoprotein dehydrogenase, also called ETF-ubiquinone oxidoreductase (ETF-QO), is a protein localized in the inner membrane of mitochondria, playing a central role in the electron-transfer system. Indeed, ETF-QO mediates electron transport from flavoprotein dehydrogenases to the ubiquinone pool. ETF-QO mutations are often associated with riboflavin-responsive multiple acyl-CoA dehydrogenase...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Carnitine
Share to Electron-Transferring Flavoproteins
Share to Iron-Sulfur Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mitochondria

Share to Multiple Acyl Coenzyme A Dehydrogenase Deficiency

Share to Mutation

Share to Oxidoreductases Acting on CH-NH Group Donors

Share to Ubiquinone

Source

Identifiers

PMID: 33823724
DOI: 10.1080/10409238.2021.1908952

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

ETF dehydrogenase advances in molecular genetics and impact on treatment.PMID 33823724Read ↗

Electron transfer flavoprotein and its role in mitochondrial energy metabolism in health and disease.Semantic proximity Read ↗

ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.Semantic proximity Read ↗

Disorders of flavin adenine dinucleotide metabolism: MADD and related deficiencies.Semantic proximity Read ↗

Electron transfer flavoprotein deficiency: functional and molecular aspects.Semantic proximity Read ↗

Characterization of mitochondrial proteome in a severe case of ETF-QO deficiency.Semantic proximity Read ↗

Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report.Semantic proximity Read ↗

Deep Intronic ETFDH Variants Represent a Recurrent Pathogenic Event in Multiple Acyl-CoA Dehydrogenase Deficiency.Semantic proximity Read ↗

ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.Semantic proximity Read ↗

Novel ETF dehydrogenase mutations in a patient with mild glutaric aciduria type II and complex II-III deficiency in liver and muscle.Semantic proximity Read ↗

Clinical characteristics and gene mutation analysis of an adult patient with ETFDH‑related multiple acyl‑CoA dehydrogenase deficiency.Semantic proximity Read ↗

New insights into the nutritional genomics of adult-onset riboflavin-responsive diseasesSemantic proximity Read ↗

Conformational analysis of the riboflavin-responsive ETF:QO-p.Pro456Leu variant associated with mild multiple acyl-CoA dehydrogenase deficiency.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.