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)

1 reference

5 December 2017

3

1 reference

5 December 2017

Vincenzo Pignatelli

1

1 reference

5 December 2017

Constance Louise Cepko

series ordinal

2

1 reference

5 December 2017

language of work or name

English

0 references

publication date

1 February 2004

1 reference

The Journal of Comparative Neurology

5 December 2017

published in

1 reference

5 December 2017

volume

469

1 reference

5 December 2017

issue

3

1 reference

5 December 2017

page(s)

351-359

1 reference

Classification of congenital and early onset retinitis pigmentosa.

5 December 2017

cites work

1 reference

21 January 2018

1 reference

Mutations in the CRB1 gene cause Leber congenital amaurosis

21 January 2018

1 reference

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

1 reference

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

21 January 2018

1 reference

7 January 2021

Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Retinopathy and attenuated circadian entrainment in Crx-deficient mice.

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

The major cell populations of the mouse retina.

1 reference

7 January 2021

Retinal remodeling triggered by photoreceptor degenerations.

1 reference

7 January 2021

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

1 reference

7 January 2021

Cell transplantation as a treatment for retinal disease

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Novel frameshift mutations in CRX associated with Leber congenital amaurosis

1 reference

7 January 2021

Parvalbumin immunoreactivity in the rat retina

1 reference

7 January 2021

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

1 reference

7 January 2021

Modifications of retinal neurons in a mouse model of retinitis pigmentosa

1 reference

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

1 reference

7 January 2021

Differential localization of protein kinase C isozymes in retinal neurons

1 reference

7 January 2021

Meaningless minis? Mechanisms of neurotransmitter-receptor clustering

1 reference

7 January 2021

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

1 reference

7 January 2021

Identifiers

DOI

10.1002/CNE.11019

1 reference

5 December 2017

1 reference