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COQ2 gene

Known as: COQ2, S. CEREVISIAE, HOMOLOG OF, CL640, PARAHYDROXYBENZOATE-POLYPRENYLTRANSFERASE, MITOCHONDRIAL 
National Institutes of Health

Papers overview

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2018
2018
BackgroundNephrotic syndrome can be caused by a subgroup of mitochondrial diseases classified as primary coenzyme Q10 (CoQ10… 
2016
2016
COQ2 (p-hydroxybenzoate polyprenyl transferase) encodes the enzyme required for the second step of the final reaction sequence of… 
Highly Cited
2007
Highly Cited
2007
Coenzyme Q(10) (CoQ(10)) deficiency has been associated with an increasing number of clinical phenotypes that respond to CoQ(10… 
Highly Cited
2007
Highly Cited
2007
Primary coenzyme Q(10) (CoQ(10)) deficiency includes a group of rare autosomal recessive disorders primarily characterized by… 
Highly Cited
2007
Highly Cited
2007
Coenzyme Q10 (CoQ10) plays a pivotal role in oxidative phosphorylation (OXPHOS), as it distributes electrons among the various… 
Highly Cited
2006
Highly Cited
2006
Ubiquinone (coenzyme Q(10) or CoQ(10)) is a lipid-soluble component of virtually all cell membranes, where it functions as a… 
Highly Cited
2004
Highly Cited
2004
Ubiquinone (UQ), an electron carrier in the respiratory chain ranging from bacteria to humans, shows antioxidative activity in… 
Highly Cited
1996
Highly Cited
1996
The reduction kinetics of coenzyme Q (CoQ, ubiquinone) by NADH:ubiquinone oxidoreductase (complex I, EC 1.6.99.3) was… 
Highly Cited
1994
Highly Cited
1994
Highly Cited
1994
The Escherichia coli ubiA gene coding for 4-hydroxy benzoate octaprenyl transferase is thought to be a key enzyme of ubiquinone…