| Title | Date | PubMed ID |
|---|
| Structural insights into ubiquinone biosynthesis in membranes. | 2014 Feb 21 | 24558159 |
| Early myoclonic epilepsy, hypertrophic cardiomyopathy and subsequently a nephrotic syndrome in a patient with CoQ10 deficiency caused by mutations in para-hydroxybenzoate-polyprenyl transferase (COQ2). | 2013 Nov | 23816342 |
| Effects of inhibiting CoQ10 biosynthesis with 4-nitrobenzoate in human fibroblasts. | 2012 | 22359546 |
| 4-Nitrobenzoate inhibits coenzyme Q biosynthesis in mammalian cell cultures. | 2010 Jul | 20526342 |
| Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency. | 2008 Jun | 18230681 |
| A structural model of the membrane-bound aromatic prenyltransferase UbiA from E. coli. | 2008 Apr 14 | 18338424 |
| COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement. | 2007 Oct | 17855635 |
| Endogenous synthesis of coenzyme Q in eukaryotes. | 2007 Jun | 17482885 |
| Missense mutation of the COQ2 gene causes defects of bioenergetics and de novo pyrimidine synthesis. | 2007 May 1 | 17374725 |
| Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders. | 2007 Mar | 17332895 |