(Q37783778)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20801145%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

title

Mouse models of dominant optic atrophy: what do they tell us about the pathophysiology of visual loss? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20801145%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

1 reference

1 reference

1

1 reference

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13 February 2020

Marcela Votruba

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20801145%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

author name string

J E Morgan

series ordinal

2

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13 February 2020

publication date

27 August 2010

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13 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20801145%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

volume

51

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20801145%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

issue

2

1 reference

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13 February 2020

page(s)

229-234

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20801145%20AND%20SRC:MED&resulttype=core&format=json

Developmental expression profile of the optic atrophy gene product: OPA1 is not localized exclusively in the mammalian retinal ganglion cell layer

13 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Subtle neurological and metabolic abnormalities in an Opa1 mouse model of autosomal dominant optic atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

OPA1-associated disorders: phenotypes and pathophysiology.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

OPA1 mutations associated with dominant optic atrophy influence optic nerve head size

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Experimental models of Parkinson's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Optic nerve degeneration and mitochondrial dysfunction: genetic and acquired optic neuropathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Critical dependence of neurons on mitochondrial dynamics

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Focus on molecules: the OPA1 protein.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Mitofusin-2 regulates mitochondrial and endoplasmic reticulum morphology and tethering: the role of Ras.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

OPA1 (Kjer type) dominant optic atrophy: a novel mitochondrial disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

eOPA1: an online database for OPA1 mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Disc excavation in dominant optic atrophy: differentiation from normal tension glaucoma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

The role of dynamin-related protein 1, a mediator of mitochondrial fission, in apoptosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Multicolor "DiOlistic" labeling of the nervous system using lipophilic dye combinations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Electrophysiological and histologic assessment of retinal ganglion cell fate in a mouse model for OPA1-associated autosomal dominant optic atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Dynamin self-assembles into rings suggesting a mechanism for coated vesicle budding

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Electrophysiological assessment of optic nerve disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Electrophysiological findings in dominant optic atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qter

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Mutation of OPA1 gene causes deafness by affecting function of auditory nerve terminals.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

A Clinicopathologic Study of Autosomal Dominant Optic Atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Dominant optic atrophy mapped to chromosome 3q region. II. Clinical and epidemiological aspects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

The molecular mechanism and cellular functions of mitochondrial division

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

OPA1 functions in mitochondria and dysfunctions in optic nerve.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

The importance of dendritic mitochondria in the morphogenesis and plasticity of spines and synapses

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Mitochondrial dynamics in mammalian health and disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Neural remodeling in retinal degeneration.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Axonal loss occurs early in dominant optic atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Mitochondrial disorder with OPA1 mutation lacking optic atrophy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Primary structure of a dynamin-related mouse mitochondrial GTPase and its distribution in brain, subcellular localization, and effect on mitochondrial morphology

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

The human dynamin-related protein OPA1 is anchored to the mitochondrial inner membrane facing the inter-membrane space

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Mitochondrial dynamics and disease, OPA1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Bipolar cells of the mouse retina: a gene gun, morphological study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Interpretation of the mouse electroretinogram.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Dominant optic atrophy: correlation between clinical and molecular genetic studies.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Mitofusins and OPA1 mediate sequential steps in mitochondrial membrane fusion

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

OPA1 deficiency associated with increased autophagy in retinal ganglion cells in a murine model of dominant optic atrophy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Opa1 deficiency in a mouse model of dominant optic atrophy leads to retinal ganglion cell dendropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Retinal ganglion cell dendrites undergo a visual activity-dependent redistribution after eye opening.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

The molecular mechanisms of OPA1-mediated optic atrophy in Drosophila model and prospects for antioxidant treatment

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Regulation of mitochondrial fission and apoptosis by the mitochondrial outer membrane protein hFis1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031

Multi-system neurological disease is common in patients with OPA1 mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.VISRES.2010.08.031