Inner retinal abnormalities in a mouse model of Leber's congenital amaurosis (Q44733603)

5 December 2017

title

Inner retinal abnormalities in a mouse model of Leber's congenital amaurosis (English)

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5 December 2017

3

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5 December 2017

Vincenzo Pignatelli

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5 December 2017

Constance Louise Cepko

series ordinal

2

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5 December 2017

language of work or name

English

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publication date

1 February 2004

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The Journal of Comparative Neurology

5 December 2017

published in

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5 December 2017

volume

469

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issue

3

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5 December 2017

page(s)

351-359

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Classification of congenital and early onset retinitis pigmentosa.

5 December 2017

cites work

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21 January 2018

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Mutations in the CRB1 gene cause Leber congenital amaurosis

21 January 2018

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Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p.

21 January 2018

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Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes

21 January 2018

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7 January 2021

Crx, a Novel Otx-like Paired-Homeodomain Protein, Binds to and Transactivates Photoreceptor Cell-Specific Genes

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7 January 2021

Shared and unique roles of CAP23 and GAP43 in actin regulation, neurite outgrowth, and anatomical plasticity

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7 January 2021

Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation.

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7 January 2021

Retinopathy and attenuated circadian entrainment in Crx-deficient mice.

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7 January 2021

Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy

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7 January 2021

Control of dopamine release in the retina: a transgenic approach to neural networks

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7 January 2021

The major cell populations of the mouse retina.

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7 January 2021

Retinal remodeling triggered by photoreceptor degenerations.

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7 January 2021

Microarray analysis of the transcriptional network controlled by the photoreceptor homeobox gene Crx.

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7 January 2021

Cell transplantation as a treatment for retinal disease

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7 January 2021

Developmentally regulated postsynaptic localization of a metabotropic glutamate receptor in rat rod bipolar cells

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7 January 2021

Morphological types of horizontal cell in rodent retinae: a comparison of rat, mouse, gerbil, and guinea pig

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7 January 2021

Retinal-specific guanylate cyclase gene mutations in Leber's congenital amaurosis

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7 January 2021

Novel frameshift mutations in CRX associated with Leber congenital amaurosis

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7 January 2021

Parvalbumin immunoreactivity in the rat retina

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7 January 2021

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

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7 January 2021

Modifications of retinal neurons in a mouse model of retinitis pigmentosa

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7 January 2021

Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function

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7 January 2021

Differential localization of protein kinase C isozymes in retinal neurons

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7 January 2021

Meaningless minis? Mechanisms of neurotransmitter-receptor clustering

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7 January 2021

Screening for CRX gene mutations in Chinese patients with Leber congenital amaurosis and mutational phenotype

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7 January 2021

Identifiers

DOI

10.1002/CNE.11019

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5 December 2017

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