(Q28512560)

English

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

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scholarly article

1 reference

Europe PubMed Central

21 June 2017

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

1 reference

Europe PubMed Central

21 June 2017

Heme A:farnesyltransferase cytochrome c oxidase assembly factor 10

1 reference

GOA release 2020-03-11

cytochrome c, somatic

1 reference

GOA release 2020-03-11

Cytochrome c oxidase subunit 5B, mitochondrial

1 reference

GOA release 2020-03-11

Superoxide dismutase 2, mitochondrial

1 reference

GOA release 2020-03-11

cytochrome c oxidase subunit 4I1

1 reference

GOA release 2020-03-11

Ubiquinol cytochrome c reductase core protein 2

1 reference

GOA release 2020-03-11

Cytochrome c oxidase subunit I

1 reference

GOA release 2020-03-11

Succinate dehydrogenase complex, subunit B, iron sulfur (Ip)

1 reference

GOA release 2020-03-11

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Francisca Diaz

1

1 reference

Europe PubMed Central

21 June 2017

Sofia Garcia

3

1 reference

Europe PubMed Central

21 June 2017

Dayami Hernandez

4

1 reference

Europe PubMed Central

21 June 2017

Christine K Thomas

2

1 reference

Europe PubMed Central

21 June 2017

Carlos T Moraes

5

1 reference

Europe PubMed Central

21 June 2017

publication date

15 August 2005

1 reference

Europe PubMed Central

21 June 2017

Human Molecular Genetics

1 reference

Europe PubMed Central

21 June 2017

14

1 reference

Europe PubMed Central

21 June 2017

18

1 reference

Europe PubMed Central

21 June 2017

2737-2748

1 reference

Europe PubMed Central

21 June 2017

Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

19 March 2017

Role of phosphate and calcium stores in muscle fatigue

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

19 March 2017

Cytochrome c oxidase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

19 March 2017

The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 A

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

19 March 2017

Isolation of a human cDNA for heme A:farnesyltransferase by functional complementation of a yeast cox10 mutant

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

19 March 2017

Sequence and organization of the human mitochondrial genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

19 March 2017

Physiological types and histochemical profiles in motor units of the cat gastrocnemius

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

19 March 2017

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

19 March 2017

Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

7 April 2017

Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

The molecular basis of skeletal muscle atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Molecular mechanisms modulating muscle mass

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Cytochrome c oxidase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Increased mitochondrial mass in mitochondrial myopathy mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Intensity-controlled treadmill running in mice: cardiac and skeletal muscle hypertrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Blue Native electrophoresis to study mitochondrial and other protein complexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

In vivo and in organello assessment of OXPHOS activities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Cytochrome oxidase in health and disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Leber hereditary optic neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Ultrastructure of the spermatozoa from a Florida manatee (Trichechus manatus latirostris).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Human cytochrome oxidase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Proton pumping by cytochrome oxidase: progress, problems and postulates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Alpha-mannosidase-II deficiency results in dyserythropoiesis and unveils an alternate pathway in oligosaccharide biosynthesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Genomic structure and expression of the human heme A:farnesyltransferase (COX10) gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Mechanisms underlying changes of tetanic [Ca2+]i and force in skeletal muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Biosynthesis and functional role of haem O and haem A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Cre-stimulated recombination at loxP-containing DNA sequences placed into the mammalian genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

COX10 codes for a protein homologous to the ORF1 product of Paracoccus denitrificans and is required for the synthesis of yeast cytochrome oxidase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

29 September 2017

Beef heart cytochrome c oxidase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

2 June 2018

Isolation, characterization and inactivation of the mouse Mgat3 gene: the bisecting N-acetylglucosamine in asparagine-linked oligosaccharides appears dispensable for viability and reproduction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

2 June 2018

Measuring the quantity and activity of mitochondrial electron transport chain complexes in tissues of central nervous system using blue native polyacrylamide gel electrophoresis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

27 November 2018

Selective expression of Cre recombinase in skeletal muscle fibers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

27 November 2018

Quantification of muscle mitochondrial oxidative phosphorylation enzymes via histochemical staining of blue native polyacrylamide gels.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2778476

27 November 2018

Cytochemistry and immunocytochemistry of mitochondria in tissue sections

1 reference

https://pubmed.ncbi.nlm.nih.gov/16103131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

1 reference

https://pubmed.ncbi.nlm.nih.gov/16103131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heme deficiency selectively interrupts assembly of mitochondrial complex IV in human fibroblasts: revelance to aging

1 reference

https://pubmed.ncbi.nlm.nih.gov/16103131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac dysfunction in mice lacking cytochrome-c oxidase subunit VIaH

1 reference

https://pubmed.ncbi.nlm.nih.gov/16103131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of the functional domains in heme O synthase. Site-directed mutagenesis studies on the cyoE gene of the cytochrome bo operon in Escherichia coli

1 reference

https://pubmed.ncbi.nlm.nih.gov/16103131

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/HMG/DDI307

1 reference

Europe PubMed Central

21 June 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Europe PubMed Central

21 June 2017

ResearchGate publication ID

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