COQ2 gene

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

Topic mentions per year

Topic mentions per year

1980-2018
012319802018

Papers overview

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2017
2017
We report a 3-year follow-up of high-dose ubiquinol supplementation in a case of familial multiple system atrophy (MSA) with… (More)
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2015
2015
Multiple-system atrophy (MSA) is a fatal neurodegenerative disorder with unknown etiology. It is widely considered to be a… (More)
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2015
2015
A recent collaborative study that combined linkage analysis with whole-genome sequencing of family members of multiplex families… (More)
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2015
2015
Recent studies in Japan have associated multiple system atrophy (MSA), a neurodegenerative disease of uncertain etiology, with… (More)
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Highly Cited
2007
Highly Cited
2007
Primary coenzyme Q(10) (CoQ(10)) deficiency includes a group of rare autosomal recessive disorders primarily characterized by… (More)
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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… (More)
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2006
2006
Coenzyme Q (CoQ) is an isoprenoid quinine that functions as an electron carrier in the mitochondrial respiratory chain in… (More)
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2005
2005
Coenzyme Q functions as an electron carrier and reversibly changes to either an oxidized (CoQ), intermediate (CoQ.-), or reduced… (More)
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1994
1994
Polyprenyldiphosphate: 4-hydroxybenzoate polyprenyltransferase (4-HB polyprenyltransferase) is a key enzyme in ubiquinone… (More)
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Highly Cited
1992
Highly Cited
1992
Coenzyme Q functions as a lipid-soluble electron carrier in eukaryotes. In Saccharomyces cerevisiae, the enzymes responsible for… (More)
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