COQ6 gene

Known as: CGI10, COQ6, coenzyme Q6, monooxygenase 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2008-2017
012320082017

Papers overview

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Review
2017
Review
2017
Objective: To summarize the clinical manifestation and molecular characteristics of COQ6 mutation induced nephrotic syndrome, and… (More)
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2017
2017
In 2010, INF2 mutations were associated with autosomal-dominant focal segmental glomerulosclerosis (FSGS), clinically presenting… (More)
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Review
2016
Review
2016
Schwannome sind Tumoren der Nervenscheide, die sich von den Schwann-Zellen herleiten. Am häufigsten treten sie am VIII. Hirnnerv… (More)
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2015
2015
To the Editor: Schwannomatosis (OMIM 162091) is a lateonset tumor-predisposition syndrome characterized by the development of… (More)
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2014
2014
Human COQ6 encodes a monooxygenase which is responsible for the C5-hydroxylation of the quinone ring of coenzyme Q (CoQ… (More)
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2014
2014
Purpose:Schwannomatosis, a subtype of neurofibromatosis, is characterized by multiple benign, nonvestibular, nonintradermal… (More)
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2014
2014
Coenzyme Q (CoQ) is an essential factor for aerobic growth and oxidative phosphorylation in the electron transport system. The… (More)
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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… (More)
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2008
2008
Gene amplifications and deletions are frequent in head and neck squamous cell carcinomas (SCC) but the association of these… (More)
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