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ADCK3 gene

Known as: CHAPERONE-ACTIVITY OF BC1 COMPLEX-LIKE, COENZYME Q8A, ADCK3 
National Institutes of Health

Related topics

Related topics

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SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9

Papers overview

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2020
2020
A novel COQ8A missense variant associated with a mild form of primary coenzyme Q10 deficiency type 4.
2019
2019
Haut taux de diagnostic identifié par séquençage de l’exome dans les pathologies neurologiques associant déficience intellectuelle et dystonie
2018
2018
Suppression of respiratory growth defect of mutant deficient in mitochondrial phospholipase A1 by overexpression of genes involved in coenzyme Q synthesis in Saccharomyces cerevisiae
ABSTRACT DDL1 encodes a mitochondrial phospholipase A1 involved in acyl chain remodeling of mitochondrial phospholipids and… 
2016
2016
Cloning and characterization of decaprenyl diphosphate synthase from three different fungi
Coenzyme Q (CoQ) is composed of a benzoquinone moiety and an isoprenoid side chain of varying lengths. The length of the side… 
2016
2016
Programming Saposin-Mediated Compensatory Metabolic Sinks for Enhanced Ubiquinone Production.
Microbial synthesis of ubiquinone by fermentation processes has been emerging in recent years. However, as ubiquinone is a… 
2015
2015
Ataxie cérébelleuse autosomique récessive 2 (ARCA2) : nouvelle mutation ADCK3 chez un patient algérien
2015
2015
Structure and function of ADCK3, an ancient mitochondrial protein involved in coenzyme Q biosynthesis
Coenzyme Q (Q) is an essential lipid best known for its role as an electron carrier in the electron transport chain. Although… 
2014
2014
Improving coenzyme Q8 production in Escherichia coli employing multiple strategies
Coenzyme Q (CoQ) is a medically valuable compound and a high yielding strain for CoQ will have several benefits for the… 
2014
2014
Cerebellar Ataxia with CoQ10 Deficiency Due to a Novel Mutation in ADCK3 (P6.057)
OBJECTIVE: To report a novel homozygous mutation in ADCK3 in a patient with adult onset cerebellar ataxia BACKGROUND: Inherited… 
2013
2013
Pathophysiological and molecular characterization of a mouse model of ARCA2, a recessive cerebellar ataxia associated to Coenzyme Q10 deficiency
ARCA2 is a form of recessive ataxia characterized by a slow progression of the ataxic phenotype, cerebellar atrophy and mild… 
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