Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy. (Q52541439)

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28 October 2019

title

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

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28 October 2019

10

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28 October 2019

Valerio Carelli

2

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28 October 2019

author name string

M Degli Esposti

1

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28 October 2019

A Ghelli

3

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28 October 2019

M Ratta

4

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28 October 2019

M Crimi

5

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28 October 2019

S Sangiorgi

6

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28 October 2019

P Montagna

7

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28 October 2019

G Lenaz

8

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28 October 2019

E Lugaresi

9

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language of work or name

English

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publication date

1 October 1994

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28 October 2019

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28 October 2019

volume

352

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issue

3

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28 October 2019

page(s)

375-379

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Leber's hereditary optic neuropathy. New genetic considerations

28 October 2019

cites work

1 reference

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

21 January 2018

1 reference

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Leber's hereditary optic neuropathy: Genetic, biochemical, and phosphorus magnetic resonance spectroscopy study in an Italian family

21 January 2018

1 reference

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

21 January 2018

1 reference

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Electron flux through the mitochondrial ubiquinone

21 January 2018

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Rapid diagnosis of pyruvate and ketoglutarate dehydrogenase deficiencies in platelet-enriched preparations from blood

21 January 2018

1 reference

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Mitochondrial DNA analysis in Leber's hereditary optic neuropathy

21 January 2018

1 reference

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Prediction and comparison of the haem-binding sites in membrane haemoproteins

21 January 2018

1 reference

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Mitochondrial cytochrome b: evolution and structure of the protein

21 January 2018

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

21 January 2018

1 reference

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Conservation of sequences of subunits of mitochondrial complex I and their relationships with other proteins

21 January 2018

1 reference

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Characterization of mutations in the cytochrome b subunit of the bc1 complex of Rhodobacter sphaeroides that affect the quinone reductase site (Qc).

21 January 2018

1 reference

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Coupling site I and the rotenone-sensitive ubisemiquinone in tightly coupled submitochondrial particles

21 January 2018

1 reference

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Cytochrome c oxidase mutations in Leber hereditary optic neuropathy

21 January 2018

1 reference

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The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathy

21 January 2018

1 reference

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A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy

21 January 2018

1 reference

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Platelet mitochondrial function in Leber's hereditary optic neuropathy

21 January 2018

1 reference

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Organic structural specificity and sites of coenzyme Q in succinoxidase and DPNH-oxidase systems

21 January 2018

1 reference

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Assay conditions for the mitochondrial NADH:coenzyme Q oxidoreductase

21 January 2018

1 reference

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Complex I and complex III of mitochondria have common inhibitors acting as ubiquinone antagonists

21 January 2018

1 reference

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Requirement of histidine 217 for ubiquinone reductase activity (Qi site) in the cytochrome bc1 complex

21 January 2018

1 reference

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10.1016/0014-5793(94)00971-6

21 January 2018

Identifiers

DOI

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28 October 2019

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