Mitochondrial cytochrome c oxidase deficiency (Q26769015)

Europe PubMed Central

title

Mitochondrial cytochrome c oxidase deficiency (English)

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author

Malgorzata Rak

1

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Dominique Chrétien

3

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Paule Bénit

2

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Alexander Tzagoloff

7

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Pierre Rustin

8

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author name string

Juliette Bouchereau

4

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Manuel Schiff

5

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Riyad El-Khoury

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

6

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language of work or name

English

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publication date

March 2016

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published in

Clinical Science

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volume

130

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issue

6

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page(s)

393-407

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cites work

1 reference

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

7 April 2017

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

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

7 April 2017

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Functional and genetic studies demonstrate that mutation in the COX15 gene can cause Leigh syndrome

7 April 2017

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The role of the LRPPRC (leucine-rich pentatricopeptide repeat cassette) gene in cytochrome oxidase assembly: mutation causes lowered levels of COX (cytochrome c oxidase) I and COX III mRNA

7 April 2017

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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

7 April 2017

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

7 April 2017

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Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathy.

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Supercomplexes in the respiratory chains of yeast and mammalian mitochondria

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

7 April 2017

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

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Coa2 is an assembly factor for yeast cytochrome c oxidase biogenesis that facilitates the maturation of Cox1.

7 April 2017

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Mss51p and Cox14p jointly regulate mitochondrial Cox1p expression in Saccharomyces cerevisiae

7 April 2017

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MITRAC7 Acts as a COX1-Specific Chaperone and Reveals a Checkpoint during Cytochrome c Oxidase Assembly

7 April 2017

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Metabolic consequences of a novel missense mutation of the mtDNA CO I gene

7 April 2017

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A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy

7 April 2017

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From ventriculomegaly to severe muscular atrophy: expansion of the clinical spectrum related to mutations in AIFM1

7 April 2017

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A mutation of COX6A1 causes a recessive axonal or mixed form of Charcot-Marie-Tooth disease

7 April 2017

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Phosphorylation of mammalian cytochrome c and cytochrome c oxidase in the regulation of cell destiny: respiration, apoptosis, and human disease

7 April 2017

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The variability of the harlequin mouse phenotype resembles that of human mitochondrial-complex I-deficiency syndromes

7 April 2017

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Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy

7 April 2017

1 reference

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Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency

7 April 2017

1 reference

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Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2

7 April 2017

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Cytochrome c oxidase is required for the assembly/stability of respiratory complex I in mouse fibroblasts

7 April 2017

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Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

7 April 2017

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Respiration and substrate transport rates as well as reactive oxygen species production distinguish mitochondria from brain and liver

7 April 2017

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The oncoprotein HBXIP promotes glucose metabolism reprogramming via downregulating SCO2 and PDHA1 in breast cancer

28 September 2017

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The subunit composition and function of mammalian cytochrome c oxidase

28 September 2017

1 reference

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A novel AIFM1 mutation expands the phenotype to an infantile motor neuron disease

28 September 2017

1 reference

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Loss of apoptosis-inducing factor critically affects MIA40 function.

28 September 2017

1 reference

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Disruption of cytochrome c oxidase function induces the Warburg effect and metabolic reprogramming

28 September 2017

1 reference

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MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options

28 September 2017

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Nuclear expression of mitochondrial ND4 leads to the protein assembling in complex I and prevents optic atrophy and visual loss

28 September 2017

1 reference

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Interaction between AIF and CHCHD4 Regulates Respiratory Chain Biogenesis

28 September 2017

1 reference

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Nuclear-encoded cytochrome c oxidase subunit 4 regulates BMI1 expression and determines proliferative capacity of high-grade gliomas

28 September 2017

1 reference

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A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathy

28 September 2017

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Krüppel-like factor 6 regulates mitochondrial function in the kidney

28 September 2017

1 reference

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Genetic and biochemical intricacy shapes mitochondrial cytopathies.

28 September 2017

1 reference

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Metabolic reprogramming orchestrates cancer stem cell properties in nasopharyngeal carcinoma

28 September 2017

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A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency

28 September 2017

1 reference

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Tissue-specific responses to the LRPPRC founder mutation in French Canadian Leigh Syndrome

28 September 2017

1 reference

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Bound cardiolipin is essential for cytochrome c oxidase proton translocation

28 September 2017

1 reference

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Novel inhibitors of mitochondrial sn-glycerol 3-phosphate dehydrogenase.

28 September 2017

1 reference

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A founder mutation in PET100 causes isolated complex IV deficiency in Lebanese individuals with Leigh syndrome

28 September 2017

1 reference

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Safety and effects of the vector for the Leber hereditary optic neuropathy gene therapy clinical trial.

28 September 2017

1 reference

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Loss of LRPPRC causes ATP synthase deficiency

28 September 2017

1 reference

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Expression of alternative oxidase in Drosophila ameliorates diverse phenotypes due to cytochrome oxidase deficiency

28 September 2017

1 reference

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28 September 2017

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Mutations in CYC1, encoding cytochrome c1 subunit of respiratory chain complex III, cause insulin-responsive hyperglycemia.

28 September 2017

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NDUFA4 mutations underlie dysfunction of a cytochrome c oxidase subunit linked to human neurological disease.

28 September 2017

1 reference

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Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men.

28 September 2017

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Functional recurrent mutations in the human mitochondrial phylogeny: dual roles in evolution and disease

28 September 2017

1 reference

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A defect in the mitochondrial complex III, but not complex IV, triggers early ROS-dependent damage in defined brain regions.

28 September 2017

1 reference

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Cytochrome c oxidase subunit 4 isoform 2-knockout mice show reduced enzyme activity, airway hyporeactivity, and lung pathology

28 September 2017

1 reference

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The Many Clinical Faces of Cytochrome c Oxidase Deficiency

28 September 2017

1 reference

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Copper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with SCO2 mutations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Structural studies on bovine heart cytochrome c oxidase

28 September 2017

1 reference

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Mice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathy.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Cytochrome c oxidase: evolution of control via nuclear subunit addition

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

A mutation in C2orf64 causes impaired cytochrome c oxidase assembly and mitochondrial cardiomyopathy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Comparing phylogeny and the predicted pathogenicity of protein variations reveals equal purifying selection across the global human mtDNA diversity

28 September 2017

1 reference

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Inventory control: cytochrome c oxidase assembly regulates mitochondrial translation

28 September 2017

1 reference

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Severe X-linked mitochondrial encephalomyopathy associated with a mutation in apoptosis-inducing factor

28 September 2017

1 reference

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Modulation of mitochondrial protein phosphorylation by soluble adenylyl cyclase ameliorates cytochrome oxidase defects

28 September 2017

1 reference

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Expression of the alternative oxidase complements cytochrome c oxidase deficiency in human cells

28 September 2017

1 reference

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Respiratory chain alternative enzymes as tools to better understand and counteract respiratory chain deficiencies in human cells and animals

28 September 2017

1 reference

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Exocrine pancreatic insufficiency, dyserythropoeitic anemia, and calvarial hyperostosis are caused by a mutation in the COX4I2 gene

28 September 2017

1 reference

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A critical approach to the therapy of mitochondrial respiratory chain and oxidative phosphorylation diseases

28 September 2017

1 reference

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Optimized allotopic expression of the human mitochondrial ND4 prevents blindness in a rat model of mitochondrial dysfunction

28 September 2017

1 reference

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FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency

28 September 2017

1 reference

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Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase

28 September 2017

1 reference

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A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations

28 September 2017

1 reference

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Analysis of nuclear and mitochondrial genes in patients with pseudoexfoliation glaucoma.

28 September 2017

1 reference

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Mutations in cytochrome c oxidase subunit VIa cause neurodegeneration and motor dysfunction in Drosophila

28 September 2017

1 reference

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Mitochondrial abnormalities in patients with LHON-like optic neuropathies

28 September 2017

1 reference

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Post-transcriptional silencing and functional characterization of the Drosophila melanogaster homolog of human Surf1.

28 September 2017

1 reference

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mtDNA mutations increase tumorigenicity in prostate cancer

28 September 2017

1 reference

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AIF deficiency compromises oxidative phosphorylation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Bioenergetics of mitochondrial diseases associated with mtDNA mutations

28 September 2017

1 reference

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Mitochondrial import and the twin-pore translocase

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

The harlequin mouse mutation downregulates apoptosis-inducing factor

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Cytochrome oxidase in health and disease.

28 September 2017

1 reference

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In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

What do mitochondrial diseases teach us about normal mitochondrial functions...that we already knew: threshold expression of mitochondrial defects.

28 September 2017

1 reference

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Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA.

28 September 2017

1 reference

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An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy

28 September 2017

1 reference

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Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Heteroplasmic point mutations of mitochondrial DNA affecting subunit I of cytochrome c oxidase in two patients with acquired idiopathic sideroblastic anemia

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Expression of human cytochrome c oxidase subunits during fetal development

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Electron flux through the mitochondrial ubiquinone

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

MicroRNA-21 regulates non-small cell lung cancer cell proliferation by affecting cell apoptosis via COX-19

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Analysis of reported SCO2 gene mutations affecting cytochrome c oxidase activity in various diseases

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

RETRACTED: Bezafibrate improves mitochondrial function in the CNS of a mouse model of mitochondrial encephalopathy

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Complex I function is defective in complex IV-deficient Caenorhabditis elegans

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Pathophysiology and fate of hepatocytes in a mouse model of mitochondrial hepatopathies

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Mutations in SURF1 are not specifically associated with Leigh syndrome

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Fate and expression of the deleted mitochondrial DNA differ between human heteroplasmic skin fibroblast and Epstein-Barr virus-transformed lymphocyte cultures.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Valproate-induced hepatic failure in a case of cytochrome c oxidase deficiency

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Assessment of the mitochondrial respiratory chain

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

The mitochondria-targeted antioxidant MitoQ extends lifespan and improves healthspan of a transgenic Caenorhabditis elegans model of Alzheimer disease

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Deletion of heart-type cytochrome c oxidase subunit 7a1 impairs skeletal muscle angiogenesis and oxidative phosphorylation

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

MELAS-like encephalomyopathy caused by a new pathogenic mutation in the mitochondrial DNA encoded cytochrome c oxidase subunit I.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

High-resolution melting analysis of 15 genes in 60 patients with cytochrome-c oxidase deficiency.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Early prenatal ventriculomegaly due to an AIFM1 mutation identified by linkage analysis and whole exome sequencing

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Combined OXPHOS complex I and IV defect, due to mutated complex I assembly factor C20ORF7

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Infantile cardioencephalopathy due to a COX15 gene defect: report and review.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Novel single base pair COX III subunit deletion of mitochondrial DNA associated with rhabdomyolysis

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

What limits the allotopic expression of nucleus-encoded mitochondrial genes? The case of the chimeric Cox3 and Atp6 genes.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

The effect of antiepileptic drugs on mitochondrial activity: a pilot study

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Novel insights into the assembly and function of human nuclear-encoded cytochromecoxidase subunits 4, 5a, 6a, 7a and 7b

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Novel mitochondrial DNA mutations associated with Chinese familial hypertrophic cardiomyopathy

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Identification of novel mutations in five patients with mitochondrial encephalomyopathy.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Sporadic bilateral optic neuropathy in children: the role of mitochondrial abnormalities

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Activation of peroxisome proliferator-activated receptor pathway stimulates the mitochondrial respiratory chain and can correct deficiencies in patients' cells lacking its components

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Early developmental pathology due to cytochrome c oxidase deficiency is revealed by a new zebrafish model

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Mutations in mitochondrial-encoded cytochrome c oxidase subunits I, II, and III genes detected in Alzheimer's disease using single-strand conformation polymorphism

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Mitochondrial myopathy and rhabdomyolysis associated with a novel nonsense mutation in the gene encoding cytochrome c oxidase subunit I.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Significance of respirasomes for the assembly/stability of human respiratory chain complex I.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Remarkable improvement in adult Leigh syndrome with partial cytochrome c oxidase deficiency

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

A mutation in mitochondrial DNA-encoded cytochrome c oxidase II gene in a child with Alpers-Huttenlocher-like disease

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNA.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

OXA1, a Saccharomyces cerevisiae nuclear gene whose sequence is conserved from prokaryotes to eukaryotes controls cytochrome oxidase biogenesis

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4948581

Malate Oxidation in Plant Mitochondria via Malic Enzyme and the Cyanide-insensitive Electron Transport Pathway

28 November 2018

1 reference

12 December 2020

Molecular-clinical correlation in a family with a novel heteroplasmic Leigh syndrome missense mutation in the mitochondrial cytochrome c oxidase III gene

1 reference

12 December 2020

Biochemical and molecular investigations in respiratory chain deficiencies

1 reference

12 December 2020

Genetic background influences mitochondrial function: modeling mitochondrial disease for therapeutic development

1 reference

12 December 2020

Cardiac dysfunction in mice lacking cytochrome-c oxidase subunit VIaH

1 reference

12 December 2020

Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing

1 reference

12 December 2020

Two novel mutations in COII and tRNA(His) mitochondrial genes in asthenozoospermic infertiles men

1 reference

12 December 2020

Impact of the mitochondrial genetic background in complex III deficiency

1 reference

Crossref

https://api.crossref.org/works/10.1042%2FCS20150707

7 January 2021