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ADCK3 gene

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

Papers overview

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Highly Cited
2016
Highly Cited
2016
Autosomal recessive ataxias are a clinically diverse group of syndromes that in some cases are caused by mutations in genes with… Expand
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Highly Cited
2016
Highly Cited
2016
The UbiB protein kinase-like (PKL) family is widespread, comprising one-quarter of microbial PKLs and five human homologs, yet… Expand
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Review
2016
Review
2016
Coenzyme Q (CoQ, or ubiquinone) is a remarkable lipid that plays an essential role in mitochondria as an electron shuttle between… Expand
Highly Cited
2015
Highly Cited
2015
The ancient UbiB protein kinase-like family is involved in isoprenoid lipid biosynthesis and is implicated in human diseases, but… Expand
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Highly Cited
2013
Highly Cited
2013
Identification of single-gene causes of steroid-resistant nephrotic syndrome (SRNS) has furthered the understanding of the… Expand
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Highly Cited
2011
Highly Cited
2011
Coenzyme Q (ubiquinone or Q) is a lipid electron and proton carrier in the electron transport chain. In yeast Saccharomyces… Expand
Highly Cited
2010
Highly Cited
2010
Hereditary ataxias are genetic disorders characterized by uncoordinated gait and often poor coordination of hands, speech, and… Expand
2009
2009
It has been widely accepted that most coenzyme Q (CoQ) exists freely in the mitochondrial membrane as a CoQ pool. However, the… Expand
Highly Cited
2008
Highly Cited
2008
Coenzyme Q(10) (CoQ(10)) plays a pivotal role in oxidative phosphorylation (OXPHOS) in that it distributes electrons between the… Expand
1996
1996
Effects of various derivatives of alpha-tocopherol (VE) and coenzyme Q (CoQ) on superoxide (O2.-) generation of neutrophils and… Expand