Mitochondrial cytochrome c oxidase deficiency - Test2 - elhamkhani - TriplyDB

Mitochondrial cytochrome c oxidase deficiency

Mitochondrial cytochrome c oxidase deficiency

http://www.wikidata.org/entity/Q26769015

about

The effects of indoor and outdoor temperature on metabolic rate and adipose tissue - the Mississippi perspective on the obesity epidemic.Tissue- and Condition-Specific Isoforms of Mammalian Cytochrome c Oxidase Subunits: From Function to Human Disease.The genetics and pathology of mitochondrial disease.Respiratory chain supercomplexes: Structures, function and biogenesis.A CMC1-knockout reveals translation-independent control of human mitochondrial complex IV biogenesis.COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiency Mutation in the COX4I1 gene is associated with short stature, poor weight gain and increased chromosomal breaks, simulating Fanconi anemia.New insights into mitogenomic phylogeny and copy number in eight indigenous sheep populations based on the ATP synthase and cytochrome c oxidase genes.The Complexity of Mitochondrial Complex IV: An Update of Cytochrome c Oxidase Biogenesis in Plants.

P2860

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P2860

Mitochondrial cytochrome c oxidase deficiency

http://www.wikidata.org/entity/Q26769015

description

2016 nî lūn-bûn

@nan

2016 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի մարտին հրատարակված գիտական հոդված

@hy

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

name

Mitochondrial cytochrome c oxidase deficiency

@ast

Mitochondrial cytochrome c oxidase deficiency

@en

Mitochondrial cytochrome c oxidase deficiency

@nl

type

label

Mitochondrial cytochrome c oxidase deficiency

@ast

Mitochondrial cytochrome c oxidase deficiency

@en

Mitochondrial cytochrome c oxidase deficiency

@nl

prefLabel

Mitochondrial cytochrome c oxidase deficiency

@ast

Mitochondrial cytochrome c oxidase deficiency

@en

Mitochondrial cytochrome c oxidase deficiency

@nl

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Clinical Science

P1476

Mitochondrial cytochrome c oxidase deficiency

@en

P2093

Juliette Bouchereau

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

Manuel Schiff

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

Riyad El-Khoury

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

P2860

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency

LRPPRC is necessary for polyadenylation and coordination of translation of mitochondrial mRNAs

NDUFA4 is a subunit of complex IV of the mammalian electron transport chain

Unexpected vascular enrichment of SCO1 over SCO2 in mammalian tissues: implications for human mitochondrial disease

Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease

MITRAC links mitochondrial protein translocation to respiratory-chain assembly and translational regulation

Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency

Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy

Mutations in SCO2 are associated with autosomal-dominant high-grade myopia

P304

393-407

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scholarly article

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10.1042/CS20150707

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6

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130

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Dominique Chrétien

Alexander Tzagoloff

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2016-03-01T00:00:00Z

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26846578

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4948581

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