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. (Q47760273)

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English	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.	scientific article

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scholarly article

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9685604

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. (English)

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9685604

Rhodobacter capsulatus

object named as

Rhodobacter capsulatus

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inferred from title

author name string

J Lunardi

1

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Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9685604

E Darrouzet

2

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Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9685604

A Dupuis

3

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9685604

J P Issartel

4

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Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9685604

publication date

1 August 1998

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Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9685604

number of pages

11

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Biochimica et Biophysica Acta

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Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9685604

1407

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Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9685604

2

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Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9685604

114-124

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Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9685604

Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees

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Redox-linked proton translocation by NADH-ubiquinone reductase (complex I).

1 reference

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7 January 2021

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The proton-translocating NADH: ubiquinone oxidoreductase: a discussion of selected topics

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7 January 2021

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

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7 January 2021

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The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains

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A small isoform of NADH:ubiquinone oxidoreductase (complex I) without mitochondrially encoded subunits is made in chloramphenicol-treated Neurospora crassa

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Isolation and characterisation of subcomplexes of the mitochondrial NADH:ubiquinone oxidoreductase (complex I)

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Photolabelling of a mitochondrially encoded subunit of NADH dehydrogenase with [3H]dihydrorotenone.

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

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Defective brain and muscle energy metabolism shown by in vivo 31P magnetic resonance spectroscopy in nonaffected carriers of 11778 mtDNA mutation

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Abnormal lactate after effort in healthy carriers of Leber's hereditary optic neuropathy

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Leber's hereditary optic neuropathy and complex I deficiency in muscle.

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Electron transfer properties of NADH:ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON)

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Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy

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

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Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy.

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Purification and characterization of NADH dehydrogenase complex from Paracoccus denitrificans

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7 January 2021

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Characteristics of the energy-transducing NADH-quinone oxidoreductase of Paracoccus denitrificans as revealed by biochemical, biophysical, and molecular biological approaches

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Identifiers

10.1016/S0925-4439(98)00036-2

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9685604

1 reference

Europe PubMed Central

5 February 2018

http://europepmc.org/abstract/MED/9685604

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