Progressive optic atrophy in a retinal ganglion cell-specific mouse model of complex I deficiency (Q100416006)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:33004958 AND SRC:MED&resulttype=core&format=json

16 October 2020

title

Progressive optic atrophy in a retinal ganglion cell-specific mouse model of complex I deficiency (English)

1 reference

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16 October 2020

1 reference

retinal ganglion cell

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Luyu Wang

1

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16 October 2020

Mikael Klingeborn

2

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16 October 2020

Amanda M Travis

3

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16 October 2020

Ying Hao

4

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16 October 2020

Vadim Y Arshavsky

5

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16 October 2020

Sidney M Gospe

6

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16 October 2020

publication date

1 October 2020

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16 October 2020

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16 October 2020

volume

10

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16 October 2020

issue

1

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16 October 2020

page(s)

16326

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Perspective on AMD Pathobiology: A Bioenergetic Crisis in the RPE.

16 October 2020

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Prevalence and Genetics of Leber Hereditary Optic Neuropathy in the Danish Population

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LHON: Mitochondrial Mutations and More

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7 January 2021

Bipolar cell reduction precedes retinal ganglion neuron loss in a complex 1 knockout mouse model

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7 January 2021

Complex I deficiency due to loss of Ndufs4 in the brain results in progressive encephalopathy resembling Leigh syndrome

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Mice with mitochondrial complex I deficiency develop a fatal encephalomyopathy

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Mitochondrial complex I deficiency leads to inflammation and retinal ganglion cell death in the Ndufs4 mouse

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Mathematically modeling the involvement of axons in Leber's hereditary optic neuropathy.

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7 January 2021

Defined neuronal populations drive fatal phenotype in a mouse model of Leigh syndrome

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7 January 2021

The major cell populations of the mouse retina.

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7 January 2021

Electron Microscopy of the Mouse Optic Nerve: A Quantitative Study of the Total Optic Nerve Fibers

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7 January 2021

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7 January 2021

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7 January 2021

The mutant human ND4 subunit of complex I induces optic neuropathy in the mouse

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7 January 2021

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