(Q41791773)

10 October 2017

title

OPA1, the disease gene for optic atrophy type Kjer, is expressed in the inner ear. (English)

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10 October 2017

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Stefanie Bette

1

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10 October 2017

Ulrike Zimmermann

series ordinal

2

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10 October 2017

Bernd Wissinger

series ordinal

3

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10 October 2017

Marlies Knipper

series ordinal

4

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10 October 2017

publication date

8 September 2007

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Histochemistry and Cell Biology

10 October 2017

published in

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10 October 2017

volume

128

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10 October 2017

issue

5

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10 October 2017

page(s)

421-430

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The varieties of auditory neuropathy.

10 October 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00418-007-0321-7

A Clinicopathologic Study of Autosomal Dominant Optic Atrophy

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00418-007-0321-7

Regulation of mitochondrial morphology through proteolytic cleavage of OPA1

21 January 2018

1 reference

12 December 2020

KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

1 reference

12 December 2020

Dominant optic atrophy, deafness, ptosis, ophthalmoplegia, dystaxia, and myopathy. A new syndrome.

1 reference

12 December 2020

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

1 reference

12 December 2020

Thyroid hormone affects Schwann cell and oligodendrocyte gene expression at the glial transition zone of the VIIIth nerve prior to cochlea function.

1 reference

12 December 2020

Two classes of outer hair cells along the tonotopic axis of the cochlea

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12 December 2020

Intracellular calcium regulation in inner hair cells from neonatal mice

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12 December 2020

Transmission between the type I hair cell and its calyx ending

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12 December 2020

Serca isoform expression in the mammalian retina

1 reference

12 December 2020

Identification of a fission yeast dynamin-related protein involved in mitochondrial DNA maintenance.

1 reference

12 December 2020

Roles of the mammalian mitochondrial fission and fusion mediators Fis1, Drp1, and Opa1 in apoptosis

1 reference

12 December 2020

Hair Cells in Mammalian Utricles

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutation spectrum and splicing variants in the OPA1 gene

1 reference

12 December 2020

Regeneration of broken tip links and restoration of mechanical transduction in hair cells

1 reference

12 December 2020

Functional structure of the organ of Corti: a review

1 reference

12 December 2020

Rapid renewal of auditory hair bundles

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12 December 2020

The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 gene

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12 December 2020

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

1 reference

12 December 2020

Loss of OPA1 perturbates the mitochondrial inner membrane structure and integrity, leading to cytochrome c release and apoptosis

1 reference

12 December 2020

Thyroid hormone deficiency before the onset of hearing causes irreversible damage to peripheral and central auditory systems

1 reference

12 December 2020

OPA1 requires mitofusin 1 to promote mitochondrial fusion

1 reference

12 December 2020

Plasma membrane Ca2+-ATPase isoform 2a is the PMCA of hair bundles.

1 reference

12 December 2020

Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene.

1 reference

12 December 2020

Identification of neonatal hearing impairment: infants with hearing loss

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12 December 2020

Release of OPA1 during apoptosis participates in the rapid and complete release of cytochrome c and subsequent mitochondrial fragmentation.

1 reference

12 December 2020

[Hereditary optic atrophy]

1 reference

12 December 2020

[Hereditary optic atrophy with dominant transmission; with special reference to the associated color-sense disorder]

1 reference

12 December 2020

Autosomal dominant optic atrophy. A spectrum of disability.

1 reference

12 December 2020

M-like K+ currents in type I hair cells and calyx afferent endings of the developing rat utricle

1 reference

12 December 2020

Clinical features in affected individuals from 21 pedigrees with dominant optic atrophy

1 reference

12 December 2020

Differential sublocalization of the dynamin-related protein OPA1 isoforms in mitochondria

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1.

1 reference

12 December 2020

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

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12 December 2020

A novel mutation in the OPA1 gene in a Japanese patient with optic atrophy

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12 December 2020

Defining and determining sensitive periods.

1 reference

12 December 2020

OPA1, associated with autosomal dominant optic atrophy, is widely expressed in the human brain

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12 December 2020

A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy.

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12 December 2020

Disruption of fusion results in mitochondrial heterogeneity and dysfunction

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12 December 2020

OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion

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12 December 2020

Novel membranous structures in apical and basal compartments of inner hair cells

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12 December 2020

OPA1, the disease gene for autosomal dominant optic atrophy, is specifically expressed in ganglion cells and intrinsic neurons of the retina

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12 December 2020

OPA1 R445H mutation in optic atrophy associated with sensorineural deafness.

1 reference

12 December 2020

Normal mitochondrial structure and genome maintenance in yeast requires the dynamin-like product of the MGM1 gene.

1 reference

12 December 2020

Optic atrophy and sensorineural hearing loss in a family caused by an R445H OPA1 mutation

1 reference

12 December 2020

Loss of the intermembrane space protein Mgm1/OPA1 induces swelling and localized constrictions along the lengths of mitochondria

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12 December 2020

10.1007/S00418-007-0321-7

Identifiers

DOI

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10 October 2017

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