(Q27324143)

2

0 references

Biju B Thomas

3

0 references

Akemi Matsuno-Yagi

4

0 references

Takao Yagi

Creative Commons Attribution 4.0 International

5

0 references

language of work or name

English

0 references

publication date

2010

0 references

published in

PLOS One

0 references

volume

5

0 references

issue

7

0 references

page(s)

e11472

0 references

copyright license

start time

8 July 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ImageJ

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2900204/fullTextXML

inferred from PubMed Central ID database lookup

cites work

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Safety and efficacy of gene transfer for Leber's congenital amaurosis

21 March 2017

1 reference

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Protection by the NDI1 gene against neurodegeneration in a rotenone rat model of Parkinson's disease

21 March 2017

1 reference

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21 March 2017

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Effect of gene therapy on visual function in Leber's congenital amaurosis

21 March 2017

1 reference

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Mitochondrial dysfunction as a cause of optic neuropathies

21 March 2017

1 reference

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

21 March 2017

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Expression of the yeast NADH dehydrogenase Ndi1 in Drosophila confers increased lifespan independently of dietary restriction.

21 March 2017

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Neuronal expression of a single-subunit yeast NADH-ubiquinone oxidoreductase (Ndi1) extends Drosophila lifespan

28 September 2017

1 reference

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Parkinson's disease and mitochondrial complex I: a perspective on the Ndi1 therapy

28 September 2017

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Neuroprotective effect of long-term NDI1 gene expression in a chronic mouse model of Parkinson disorder

28 September 2017

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A critical approach to the therapy of mitochondrial respiratory chain and oxidative phosphorylation diseases

28 September 2017

1 reference

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Optimized allotopic expression of the human mitochondrial ND4 prevents blindness in a rat model of mitochondrial dysfunction

28 September 2017

1 reference

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The optimized allotopic expression of ND1 or ND4 genes restores respiratory chain complex I activity in fibroblasts harboring mutations in these genes

28 September 2017

1 reference

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Mechanism of cell death caused by complex I defects in a rat dopaminergic cell line

28 September 2017

1 reference

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Axonal loss and neuroprotection in optic neuropathies

28 September 2017

1 reference

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Yeast NDI1 improves oxidative phosphorylation capacity and increases protection against oxidative stress and cell death in cells carrying a Leber's hereditary optic neuropathy mutation

28 September 2017

1 reference

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The single subunit NADH dehydrogenase reduces generation of reactive oxygen species from complex I.

28 September 2017

1 reference

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Possibility of transkingdom gene therapy for complex I diseases

28 September 2017

1 reference

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Complex I deficiency primes Bax-dependent neuronal apoptosis through mitochondrial oxidative damage

28 September 2017

1 reference

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Gene therapy for optic nerve disease

28 September 2017

1 reference

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Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegeneration

28 September 2017

1 reference

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Mechanism of toxicity in rotenone models of Parkinson's disease

28 September 2017

1 reference

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Leber hereditary optic neuropathy

28 September 2017

1 reference

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Lack of complex I activity in human cells carrying a mutation in MtDNA-encoded ND4 subunit is corrected by the Saccharomyces cerevisiae NADH-quinone oxidoreductase (NDI1) gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900204

Characterization of a transformed rat retinal ganglion cell line

28 September 2017

1 reference

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Selective targeting of a redox-active ubiquinone to mitochondria within cells: antioxidant and antiapoptotic properties

28 September 2017

1 reference

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Modulation of oxidative phosphorylation of human kidney 293 cells by transfection with the internal rotenone-insensitive NADH-quinone oxidoreductase (NDI1) gene of Saccharomyces cerevisiae

28 September 2017

1 reference

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Molecular remedy of complex I defects: rotenone-insensitive internal NADH-quinone oxidoreductase of Saccharomyces cerevisiae mitochondria restores the NADH oxidase activity of complex I-deficient mammalian cells

28 September 2017

1 reference

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Evidence for preserved direct pupillary light response in Leber's hereditary optic neuropathy

28 September 2017

1 reference

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A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology

28 September 2017

1 reference

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Suppression of complex I gene expression induces optic neuropathy

28 September 2017

1 reference

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Mouse model of optic neuropathy caused by mitochondrial complex I dysfunction

2 June 2018

1 reference

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Leber hereditary optic neuropathy: mitochondrial mutations and degeneration of the optic nerve

2 June 2018

1 reference

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Complex I inhibitors induce dose-dependent apoptosis in PC12 cells: relevance to Parkinson's disease

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900204

Can a single subunit yeast NADH dehydrogenase (Ndi1) remedy diseases caused by respiratory complex I defects?

2 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011472

Use of the NADH-quinone oxidoreductase (NDI1) gene of Saccharomyces cerevisiae as a possible cure for complex I defects in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011472

A single-subunit NADH-quinone oxidoreductase renders resistance to mammalian nerve cells against complex I inhibition

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011472

Functional expression of the single subunit NADH dehydrogenase in mitochondria in vivo: a potential therapy for complex I deficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011472

Molecular gene therapy: overexpression of the alternative NADH dehydrogenase NDI1 restores overall physiology in a fungal model of respiratory complex I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011472

In vivo complementation of complex I by the yeast Ndi1 enzyme. Possible application for treatment of Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011472

Expression of Ndi1p, an alternative NADH:ubiquinone oxidoreductase, increases mitochondrial membrane potential in a C. elegans model of mitochondrial disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011472

Optokinetic test to evaluate visual acuity of each eye independently

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011472

Childhood Leber's hereditary optic neuropathy (ND1/3460) with visual recovery.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011472

Annonacin, a natural mitochondrial complex I inhibitor, causes tau pathology in cultured neurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011472

Caspase-independent death of Leber's hereditary optic neuropathy cybrids is driven by energetic failure and mediated by AIF and Endonuclease G.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0011472

Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20628600

12 December 2020

inferred from PubMed ID database lookup

Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20628600

12 December 2020

inferred from PubMed ID database lookup

Pupillary light reflexes in patients with Leber's hereditary optic neuropathy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20628600

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1371/JOURNAL.PONE.0011472

1 reference

1892046

ADS bibcode

2010PLoSO...511472M

0 references

1892046

1 reference

1 reference

1 reference