(Q60205139)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16284789%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

title

Introducing a novel human mtDNA mutation into the Paracoccus denitrificans COX I gene explains functional deficits in a patient (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16284789%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

main subject

Paracoccus denitrificans

object named as

Paracoccus denitrificans

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16284789%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Rosalba Carrozzo

3

1 reference

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9 January 2020

Filippo Maria Santorelli

6

object named as

Filippo M Santorelli

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16284789%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

author name string

Klaus Hoffmeier

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16284789%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Alessandra Tessa

4

1 reference

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9 January 2020

Bernd Ludwig

5

1 reference

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9 January 2020

publication date

12 November 2005

1 reference

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9 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16284789%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

volume

7

1 reference

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9 January 2020

issue

1

1 reference

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9 January 2020

page(s)

51-57

1 reference

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https://scigraph.springernature.com/pub.10.1007/s10048-005-0015-z

9 January 2020

exact match

0 references

cites work

A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samples

1 reference

12 December 2020

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

12 December 2020

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

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A two-subunit cytochrome c oxidase (cytochrome aa3) from Paracoccus dentrificans

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

The nuoM arg368his mutation in NADH:ubiquinone oxidoreductase from Rhodobacter capsulatus: a model for the human nd4-11778 mtDNA mutation associated with Leber's hereditary optic neuropathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Application of the yeast Yarrowia lipolytica as a model to analyse human pathogenic mutations in mitochondrial complex I (NADH:ubiquinone oxidoreductase).

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Cytochrome aa3 of Rhodobacter sphaeroides as a model for mitochondrial cytochrome c oxidase. Purification, kinetics, proton pumping, and spectral analysis

1 reference

12 December 2020

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

1 reference

12 December 2020

Overexpression and purification of cytochrome c oxidase from Rhodobacter sphaeroides

1 reference

12 December 2020

Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II gene

1 reference

12 December 2020

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

12 December 2020

Cytochrome c oxidase (heme aa3) from Paracoccus denitrificans: analysis of mutations in putative proton channels of subunit I.

1 reference

12 December 2020

Tracing the D-pathway in reconstituted site-directed mutants of cytochrome c oxidase from Paracoccus denitrificans

1 reference

12 December 2020

A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene

1 reference

12 December 2020

Redox-driven proton pumping by heme-copper oxidases

1 reference

12 December 2020

Cytochrome c oxidase from Paracoccus denitrificans

1 reference

12 December 2020

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

1 reference

12 December 2020

The T9176G mutation of human mtDNA gives a fully assembled but inactive ATP synthase when modeled in Escherichia coli

1 reference

12 December 2020

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

1 reference

12 December 2020

Cytochrome c oxidase--structure, function, and physiology of a redox-driven molecular machine

1 reference

12 December 2020

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

1 reference

12 December 2020

SWISS-MODEL: An automated protein homology-modeling server

1 reference

12 December 2020

Structures and Proton-Pumping Strategies of Mitochondrial Respiratory Enzymes

1 reference

12 December 2020

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

1 reference

12 December 2020

1 reference

12 December 2020

Simultaneous determination of hemes a, b, and c from pyridine hemochrome spectra

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S10048-005-0015-Z

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16284789%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference