OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model ; volume:8 ; number:1 ; day:6 ; month:2 ; year:2018 ; pages:1-6 ; date:12.2018
Scientific reports ; 8, Heft 1 (6.2.2018), 1-6, 12.2018

Keyword: Augenheilkunde
Augenkrankheit

Creator: Sarzi, Emmanuelle

Contributor: Seveno, Marie
Piro-Mégy, Camille
Elzière, Lucie
Quilès, Mélanie
Péquignot, Marie
Müller, Agnès
Hamel, Christian P.
Lenaers, Guy
Delettre, Cécile
SpringerLink (Online service)

DOI: 10.1038/s41598-018-20838-8

URN: urn:nbn:de:1111-2018032711236

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:51 AM CEST

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Sarzi, Emmanuelle
Seveno, Marie
Piro-Mégy, Camille
Elzière, Lucie
Quilès, Mélanie
Péquignot, Marie
Müller, Agnès
Hamel, Christian P.
Lenaers, Guy
Delettre, Cécile
SpringerLink (Online service)

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OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model

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Other Objects (12)

Dominant optic atrophy

Mitochondrial oxidative phosphorylation in autosomal dominant optic atrophy

Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy

Dominant optic atrophy, OPA1, and mitochondrial quality control: understanding mitochondrial network dynamics

Genomic deletions in OPA1 in Danish patients with autosomal dominant optic atrophy

Dominant inheritance of retinal ganglion cell resistance to optic nerve crush in mice

OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background

First submicroscopic inversion of the OPA1 gene identified in dominant optic atrophy – a case report

Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

Mitochondrial pathophysiology beyond the retinal ganglion cell: occipital GABA is decreased in autosomal dominant optic neuropathy

Rgcs1, a dominant QTL that affects retinal ganglion cell death after optic nerve crush in mice

Autosomal dominant optic atrophy caused by six novel pathogenic OPA1 variants and genotype–phenotype correlation analysis

Dominant optic atrophy

Mitochondrial oxidative phosphorylation in autosomal dominant optic atrophy

Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy

Dominant optic atrophy, OPA1, and mitochondrial quality control: understanding mitochondrial network dynamics

Genomic deletions in OPA1 in Danish patients with autosomal dominant optic atrophy

Dominant inheritance of retinal ganglion cell resistance to optic nerve crush in mice

OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background

First submicroscopic inversion of the OPA1 gene identified in dominant optic atrophy – a case report

Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

Mitochondrial pathophysiology beyond the retinal ganglion cell: occipital GABA is decreased in autosomal dominant optic neuropathy

Rgcs1, a dominant QTL that affects retinal ganglion cell death after optic nerve crush in mice

Autosomal dominant optic atrophy caused by six novel pathogenic OPA1 variants and genotype–phenotype correlation analysis

Dominant optic atrophy

Mitochondrial oxidative phosphorylation in autosomal dominant optic atrophy

Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy

Dominant optic atrophy, OPA1, and mitochondrial quality control: understanding mitochondrial network dynamics

Genomic deletions in OPA1 in Danish patients with autosomal dominant optic atrophy

Dominant inheritance of retinal ganglion cell resistance to optic nerve crush in mice

OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background

First submicroscopic inversion of the OPA1 gene identified in dominant optic atrophy – a case report

Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

Mitochondrial pathophysiology beyond the retinal ganglion cell: occipital GABA is decreased in autosomal dominant optic neuropathy

Rgcs1, a dominant QTL that affects retinal ganglion cell death after optic nerve crush in mice

Autosomal dominant optic atrophy caused by six novel pathogenic OPA1 variants and genotype–phenotype correlation analysis

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