(Q45045560)

8 December 2017

title

Retinal abnormalities associated with the G90D mutation in opsin (English)

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8 December 2017

11

Harris Ripps

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8 December 2017

Muna I Naash

1

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8 December 2017

Ting-Huai Wu

2

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8 December 2017

Dibyendu Chakraborty

3

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8 December 2017

Steven J Fliesler

4

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8 December 2017

Xi-Qin Ding

5

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8 December 2017

May Nour

6

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8 December 2017

Neal S Peachey

7

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8 December 2017

Janis Lem

8

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8 December 2017

Nasser Qtaishat

9

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8 December 2017

Muayyad R Al-Ubaidi

10

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8 December 2017

language of work or name

English

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publication date

1 October 2004

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The Journal of Comparative Neurology

8 December 2017

published in

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8 December 2017

volume

478

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8 December 2017

issue

2

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8 December 2017

page(s)

149-163

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Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His).

8 December 2017

cites work

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A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness

21 January 2018

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7 January 2021

Rhodopsin bleaching signals in essential night blindness

1 reference

7 January 2021

Bilateral retinal and brain tumors in transgenic mice expressing simian virus 40 large T antigen under control of the human interphotoreceptor retinoid-binding protein promoter

1 reference

7 January 2021

Phototransduction in transgenic mice after targeted deletion of the rod transducin alpha -subunit

1 reference

7 January 2021

Mechanism of activation and inactivation of opsin: role of Glu113 and Lys296

1 reference

7 January 2021

Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosa

1 reference

7 January 2021

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

1 reference

7 January 2021

Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness

1 reference

7 January 2021

Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa

1 reference

7 January 2021

Postembedding immunocytochemical techniques for light and electron microscopy.

1 reference

7 January 2021

Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness

1 reference

7 January 2021

The eye photoreceptor protein rhodopsin. Structural implications for retinal disease

1 reference

7 January 2021

Slow binding of retinal to rhodopsin mutants G90D and T94D.

1 reference

7 January 2021

Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase

1 reference

7 January 2021

On the molecular genetics of retinitis pigmentosa

1 reference

7 January 2021

Retinopathy induced in mice by targeted disruption of the rhodopsin gene

1 reference

7 January 2021

Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site

1 reference

7 January 2021

Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation

1 reference

7 January 2021

Morphological, physiological, and biochemical changes in rhodopsin knockout mice

1 reference

7 January 2021

Constitutive activation of phototransduction by K296E opsin is not a cause of photoreceptor degeneration

1 reference

7 January 2021

Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa

1 reference

7 January 2021

Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene

1 reference

7 January 2021

Polygenic disease and retinitis pigmentosa: albinism exacerbates photoreceptor degeneration induced by the expression of a mutant opsin in transgenic mice

1 reference

7 January 2021

Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa

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7 January 2021

Germ-line transformation of mice

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7 January 2021

Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase beta-subunit gene of the rd mouse

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7 January 2021

Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness

1 reference

7 January 2021

Computer analysis of photochemical changes in the human retina

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7 January 2021

Constitutively active mutants of rhodopsin

1 reference

7 January 2021

Opsins with mutations at the site of chromophore attachment constitutively activate transducin but are not phosphorylated by rhodopsin kinase

1 reference

7 January 2021

The first step in vision: femtosecond isomerization of rhodopsin

1 reference

7 January 2021

Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation

1 reference

7 January 2021

Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell loss.

1 reference

7 January 2021

Mechanisms of cell death in the inherited retinal degenerations

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7 January 2021

Further screening of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

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7 January 2021

Photochemical reactions in the living cat's retina

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7 January 2021

Opsin localization and rhodopsin photochemistry in a transgenic mouse model of retinitis pigmentosa

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7 January 2021

Characterization of the mutant visual pigment responsible for congenital night blindness: a biochemical and Fourier-transform infrared spectroscopy study

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7 January 2021

Identifiers

DOI

10.1002/CNE.20283

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8 December 2017

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