(Q58782665)

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Application of the obligate aerobic yeast Yarrowia lipolytica as a eucaryotic model to analyse Leigh syndrome mutations in the complex I core subunits PSST and TYKY

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11004438%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Application of the obligate aerobic yeast Yarrowia lipolytica as a eucaryotic model to analyse Leigh syndrome mutations in the complex I core subunits PSST and TYKY (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11004438%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Yarrowia lipolytica

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based on heuristic

inferred from title

4

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31 October 2019

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P M Ahlers

1

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31 October 2019

A Garofano

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11004438%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

S J Kerscher

3

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31 October 2019

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1 August 2000

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31 October 2019

Biochimica et Biophysica Acta

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31 October 2019

1459

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31 October 2019

2-3

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31 October 2019

258-265

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31 October 2019

NADH:ubiquinone oxidoreductase from bovine heart mitochondria: sequence of a novel 17.2-kDa subunit.

1 reference

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7 January 2021

Human complex I deficiency: clinical spectrum and involvement of oxygen free radicals in the pathogenicity of the defect

1 reference

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7 January 2021

Mitochondrial DNA sequence variation in human evolution and disease.

1 reference

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7 January 2021

Mitochondrial diseases in man and mouse

1 reference

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7 January 2021

Biotinidase deficiency: a cause of subacute necrotizing encephalomyelopathy (Leigh syndrome). Report of a case with lethal outcome

1 reference

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7 January 2021

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

1 reference

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7 January 2021

Molecular genetic characterization of an X-linked form of Leigh's syndrome.

1 reference

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7 January 2021

Subacute necrotizing encephalopathy: oxidative phosphorylation defects and the ATPase 6 point mutation

1 reference

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7 January 2021

The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNA.

1 reference

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7 January 2021

Maternally inherited encephalopathy associated with a single-base insertion in the mitochondrial tRNATrp gene.

1 reference

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7 January 2021

A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

Recent developments in the molecular genetics of mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

Clinical spectrum of mitochondrial DNA mutation at base pair 8344

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

Leigh syndrome: clinical features and biochemical and DNA abnormalities.

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I.

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

The first nuclear-encoded complex I mutation in a patient with Leigh syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

Prediction of protein conformation

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

Na+ translocation by complex I (NADH:quinone oxidoreductase) of Escherichia coli.

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

Molecular basis of mitochondrial DNA disease

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

Catalytic activity of complex I in cell lines that possess replacement mutations in the ND genes in Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

Analysis of the pathogenic human mitochondrial mutation ND1/3460, and mutations of strictly conserved residues in its vicinity, using the bacterium Paracoccus denitrificans

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

The 49-kDa subunit of NADH-ubiquinone oxidoreductase (Complex I) is involved in the binding of piericidin and rotenone, two quinone-related inhibitors

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

NADH-quinone oxidoreductase: PSST subunit couples electron transfer from iron-sulfur cluster N2 to quinone

1 reference

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7 January 2021

An analysis of some thermodynamic properties of iron-sulphur centres in site I of mitochondria

1 reference

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7 January 2021

Proton-translocation by membrane-bound NADH:ubiquinone-oxidoreductase (complex I) through redox-gated ligand conduction

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

Proton translocation in the respiratory chain involving ubiquinone--a hypothetical semiquinone switch mechanism for complex I.

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

Redox components and structure of the respiratory NADH:ubiquinone oxidoreductase (complex I).

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2728%2800%2900160-2

7 January 2021

The NuoI subunit of the Rhodobacter capsulatus respiratory Complex I (equivalent to the bovine TYKY subunit) is required for proper assembly of the membraneous and peripheral domains of the enzyme

1 reference

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7 January 2021

An Escherichia coli hydrogenase-3-type hydrogenase in methanogenic archaea.

1 reference

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7 January 2021

Identifiers

10.1016/S0005-2728(00)00160-2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11004438%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11004438%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

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