(Q40775533)

English

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

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scholarly article

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Europe PubMed Central

PubMed publication ID

23 September 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

phosphorylation

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mitochondrial DNA

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author name string

D'Aurelio M

1

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Europe PubMed Central

PubMed publication ID

23 September 2017

Pallotti F

2

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Europe PubMed Central

PubMed publication ID

23 September 2017

Barrientos A

3

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Gajewski CD

4

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Kwong JQ

5

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Bruno C

6

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Beal MF

7

1 reference

Europe PubMed Central

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23 September 2017

Manfredi G

8

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Europe PubMed Central

PubMed publication ID

23 September 2017

language of work or name

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publication date

10 October 2001

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Europe PubMed Central

PubMed publication ID

23 September 2017

number of pages

8

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inferred from page(s)

Journal of Biological Chemistry

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Europe PubMed Central

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23 September 2017

276

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Europe PubMed Central

PubMed publication ID

23 September 2017

50

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Europe PubMed Central

PubMed publication ID

23 September 2017

46925-46932

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Europe PubMed Central

PubMed publication ID

23 September 2017

Separation of mammalian cytochrome c oxidase into 13 polypeptides by a sodium dodecyl sulfate-gel electrophoretic procedure

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Structure at 2.8 A resolution of cytochrome c oxidase from Paracoccus denitrificans

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Isoforms of mammalian cytochrome c oxidase: correlation with human cytochrome c oxidase deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndrome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Mitochondrial DNA mutations and pathogenesis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Low reserve of cytochrome c oxidase capacity in vivo in the respiratory chain of a variety of human cell types.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

RNA molecular weight determinations by gel electrophoresis under denaturing conditions, a critical reexamination

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Isolation and subfractionation of mitochondria from animal cells and tissue culture lines

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Assay of mitochondrial ATP synthesis in animal cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Assembly of cytochrome-c oxidase in cultured human cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Blue native electrophoresis for isolation of membrane protein complexes in enzymatically active form

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Relationship of genotype to phenotype in fibroblast-derived transmitochondrial cell lines carrying the 3243 mutation associated with the MELAS encephalomyopathy: shift towards mutant genotype and role of mtDNA copy number

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

The cytochrome bc1 and cytochrome c oxidase complexes associate to form a single supracomplex in yeast mitochondria.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Tight control of respiration by NADH dehydrogenase ND5 subunit gene expression in mouse mitochondria

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Bioenergetic consequences of accumulating the common 4977-bp mitochondrial DNA deletion

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Use of ethidium bromide to manipulate ratio of mutated and wild-type mitochondrial DNA in cultured cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Expression of mtDNA and nDNA encoded respiratory chain proteins in chemically and genetically-derived Rho0 human fibroblasts: a comparison of subunit proteins in normal fibroblasts treated with ethidium bromide and fibroblasts from a patient with mt

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Use of fibroblast and lymphoblast cultures for detection of respiratory chain defects

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

A pathogenic 15-base pair deletion in mitochondrial DNA-encoded cytochrome c oxidase subunit III results in the absence of functional cytochrome c oxidase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Submitochondrial distributions and stabilities of subunits 4, 5, and 6 of yeast cytochrome oxidase in assembly defective mutants

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Flux control of cytochrome c oxidase in human skeletal muscle

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106429200

21 January 2018

Identifiers

10.1074/JBC.M106429200

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

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