Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindness (Q24328892)

GOA release 2020-03-11

visual perception

1 reference

GOA release 2020-03-11

author name string

T P Dryja

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L B Hahn

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T Reboul

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B Arnaud

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

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language of work or name

English

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publication date

July 1996

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358-60

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cites work

1 reference

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

21 April 2017

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Structural determinants for activation of the alpha-subunit of a heterotrimeric G protein

21 April 2017

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Coupling of bitter receptor to phosphodiesterase through transducin in taste receptor cells

21 April 2017

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Activation of Ha-ras p21 by substitution, deletion, and insertion mutations

21 April 2017

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Structural differences between a ras oncogene protein and the normal protein

21 January 2018

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The Drosophila dgq gene encodes a G alpha protein that mediates phototransduction.

21 January 2018

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[Visual function in essential hemeralopia in the Nougaret family]

21 January 2018

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0796-358

7 January 2021

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

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7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

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7 January 2021

Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa

1 reference

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7 January 2021

Characterization and chromosomal localization of the gene for human rhodopsin kinase

1 reference

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7 January 2021

Characterization of the human rod transducin alpha-subunit gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0796-358

7 January 2021

Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0796-358

7 January 2021

Isolation of human retinal genes: recoverin cDNA and gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0796-358

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0796-358

7 January 2021

Cloning of the human and murine ROM1 genes: genomic organization and sequence conservation

1 reference

https://api.crossref.org/works/10.1038%2FNG0796-358

7 January 2021

[Analysis of the human electroretinogram]

1 reference

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7 January 2021

Electroretinogram in nyctalopia

1 reference

https://api.crossref.org/works/10.1038%2FNG0796-358

7 January 2021

Comparative electroretinographic studies in congenital night blindness and total color blindness

1 reference

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7 January 2021

Mechanism of activation of a human oncogene

1 reference

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7 January 2021

A point mutation is responsible for the acquisition of transforming properties by the T24 human bladder carcinoma oncogene

1 reference

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7 January 2021

Spontaneous activation of a human proto-oncogene

1 reference

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7 January 2021

Biological properties of human c-Ha-ras1 genes mutated at codon 12.

1 reference

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7 January 2021

Yeast and mammalian ras proteins have conserved biochemical properties

1 reference

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7 January 2021

A cyclic−nucleotide−suppressible conductance activated by transducin in taste cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0796-358

7 January 2021