Vascular defects and sensorineural deafness in a mouse model of Norrie disease. (Q48591907)

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9 November 2019

title

Vascular defects and sensorineural deafness in a mouse model of Norrie disease (English)

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9 November 2019

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Heidi L Rehm

1

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9 November 2019

Duan-Sun Zhang

2

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9 November 2019

M Christian Brown

3

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9 November 2019

Barbara Burgess

4

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9 November 2019

Chris Halpin

5

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9 November 2019

Wolfgang Berger

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9 November 2019

Cynthia C Morton

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9 November 2019

David P Corey

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9 November 2019

Zheng-Yi Chen

9

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9 November 2019

language of work or name

English

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publication date

1 June 2002

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9 November 2019

published in

Journal of Neuroscience

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9 November 2019

volume

22

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9 November 2019

issue

11

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9 November 2019

page(s)

4286-4292

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Identification of novel missense mutations in the Norrie disease gene associated with one X-linked and four sporadic cases of familial exudative vitreoretinopathy

9 November 2019

cites work

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12 December 2020

Histopathology of the ears, eyes, and brain in Norrie's disease (oculoacousticocerebral degeneration).

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12 December 2020

Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structure

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12 December 2020

Norrie Disease Protein (Norrin) Forms Disulfide-linked Oligomers Associated with the Extracellular Matrix

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12 December 2020

Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins

1 reference

12 December 2020

Isolation of a candidate gene for Norrie disease by positional cloning

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12 December 2020

Audiological findings in Norrie's disease

1 reference

12 December 2020

A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy

1 reference

12 December 2020

Two new missense mutations (A105T and C110G) in the Norrin gene in two Italian families with Norrie disease and familial exudative vitreoretinopathy

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12 December 2020

Norie's disease (atrofia bulborum hereditaria).

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12 December 2020

Norrie's disease. A congenital progressive oculo-acoustico-cerebral degeneration

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12 December 2020

Three-dimensional and ultrastructural relationships between intermediate cells and capillaries in the gerbil stria vascularis

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12 December 2020

Electrophysiological study of norrie's disease: An X-Linked Recessive Trait with Hearing Loss

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12 December 2020

An animal model for Norrie disease (ND): gene targeting of the mouse ND gene

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12 December 2020

Development and regression of cochlear blood vessels in fetal and newborn mice

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12 December 2020

Retinal vasculature changes in Norrie disease mice

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12 December 2020

The effects of furosemide on the endocochlear potential and auditory-nerve fiber tuning curves in cats

1 reference

12 December 2020

Missense mutation (Arg121Trp) in the Norrie disease gene associated with x-linked exudative vitreoretinopathy

1 reference

12 December 2020

Norrie disease gene mutation in a large Costa Rican kindred with a novel phenotype including venous insufficiency

1 reference

12 December 2020

Missense mutations in the NDP gene in patients with a less severe course of Norrie disease

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12 December 2020

Identification of a recurrent missense mutation in the Norrie disease gene associated with a simplex case of exudative vitreoretinopathy

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12 December 2020

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12 December 2020

Isolation and characterization of a candidate gene for Norrie disease

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12 December 2020

Postnatal vascular development in the lateral wall of the cochlear duct of gerbils: quantitative analysis by electron microscopy and confocal laser microscopy

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12 December 2020

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

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12 December 2020

Targeted deletion of the mouse POU domain gene Brn-3a causes selective loss of neurons in the brainstem and trigeminal ganglion, uncoordinated limb movement, and impaired suckling

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12 December 2020

10.1523/JNEUROSCI.22-11-04286.2002

Identifiers

DOI

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9 November 2019

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9 November 2019

PubMed publication ID

12040033

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