Human COQ9 Rescues a coq9 Yeast Mutant by Enhancing Coenzyme Q Biosynthesis from 4-Hydroxybenzoic Acid and Stabilizing the CoQ-Synthome - Test2 - elhamkhani - TriplyDB

Human COQ9 Rescues a coq9 Yeast Mutant by Enhancing Coenzyme Q Biosynthesis from 4-Hydroxybenzoic Acid and Stabilizing the CoQ-Synthome

Human COQ9 Rescues a coq9 Yeast Mutant by Enhancing Coenzyme Q Biosynthesis from 4-Hydroxybenzoic Acid and Stabilizing the CoQ-Synthome

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Coenzyme Q10 Supplementation in Aging and Disease.

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Human COQ9 Rescues a coq9 Yeast Mutant by Enhancing Coenzyme Q Biosynthesis from 4-Hydroxybenzoic Acid and Stabilizing the CoQ-Synthome

http://www.wikidata.org/entity/Q33881708

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2017 nî lūn-bûn

@nan

2017 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2017 թվականի հուլիսին հրատարակված գիտական հոդված

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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name

Human COQ9 Rescues a coq9 Yeas ...... d Stabilizing the CoQ-Synthome

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Human COQ9 Rescues a coq9 Yeas ...... d Stabilizing the CoQ-Synthome

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label

Human COQ9 Rescues a coq9 Yeas ...... d Stabilizing the CoQ-Synthome

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Human COQ9 Rescues a coq9 Yeas ...... d Stabilizing the CoQ-Synthome

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prefLabel

Human COQ9 Rescues a coq9 Yeas ...... d Stabilizing the CoQ-Synthome

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Human COQ9 Rescues a coq9 Yeas ...... d Stabilizing the CoQ-Synthome

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FPHYS.2017.00463

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Frontiers in Physiology

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Human COQ9 Rescues a coq9 Yeas ...... d Stabilizing the CoQ-Synthome

@en

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Brigitte Meunier

http://www.w3.org/2001/XMLSchema#string

Catherine F Clarke

http://www.w3.org/2001/XMLSchema#string

Christopher M Allan

http://www.w3.org/2001/XMLSchema#string

Cuiwen H He

http://www.w3.org/2001/XMLSchema#string

Dylan S Black

http://www.w3.org/2001/XMLSchema#string

Shamima Rahman

http://www.w3.org/2001/XMLSchema#string

P2860

Mitochondrial COQ9 is a lipid-binding protein that associates with COQ7 to enable coenzyme Q biosynthesis

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.

A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease

Functional characterization of the S. cerevisiae genome by gene deletion and parallel analysis

Yeast COQ4 encodes a mitochondrial protein required for coenzyme Q synthesis.

Genetic evidence for a multi-subunit complex in the O-methyltransferase steps of coenzyme Q biosynthesis.

A conserved START domain coenzyme Q-binding polypeptide is required for efficient Q biosynthesis, respiratory electron transport, and antioxidant function in Saccharomyces cerevisiae.

Saccharomyces cerevisiae Coq9 polypeptide is a subunit of the mitochondrial coenzyme Q biosynthetic complex

The Saccharomyces cerevisiae COQ6 gene encodes a mitochondrial flavin-dependent monooxygenase required for coenzyme Q biosynthesis.

Characterization of the COQ5 gene from Saccharomyces cerevisiae. Evidence for a C-methyltransferase in ubiquinone biosynthesis.

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463

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scholarly article

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10.3389/FPHYS.2017.00463

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8

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2017-07-07T00:00:00Z

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28736527

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5500610

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