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COQ2 gene

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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Author response: A genome-wide association study in multiple system atrophy
We thank Drs. Tsuji and Mitsui for the comment about COQ2 variants and risk for MSA. While our study of European ancestry… 
2014
2014
No excess of loss-of-function variants in COQ2 in pathologically confirmed multiple system atrophy
2013
2013
Mutações no Gene COQ2 na Atrofia de Múltiplos Sistemas Familiar e Esporádica
2012
2012
Next generation sequencing (NGS) in the UK steroid resistant nephrotic syndrome (SRNS) study reveals complex genetic heterogeneity
This national cohort was developed within the rare renal disease registry (RaDaR) with detailed clinical phenotyping. Sequencing… 
2008
2008
Tacrolimus effective in steroid-dependent minimal change nephrotic syndrome
They propose that inherited mutations in COQ2 cause a primary glomerular disease— “COQ2 nephropathy”—characterized by renal… 
2008
2008
New treatment algorithms for idiopathic glomerular disease
They propose that inherited mutations in COQ2 cause a primary glomerular disease— “COQ2 nephropathy”—characterized by renal… 
2006
2006
Thévenod life-and-death decisions ? A role for mitochondrial aquaporins in cellular
[PDF] [Full Text] [Abstract] , January 1, 2007; 292 (1): C157-C163. Am J Physiol Cell Physiol A. Kaasik, D. Safiulina, A… 
1968
1968
Hepatic content of coenzyme Q in rats after administration of various coenzyme Q compounds and 14C-labeled coenzyme Q.
1. The CoQ content of whole rat liver increased significantly as compared with the control after the intramuscular administration…