Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness (Q28116973)

4 January 2017

title

Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness (English)

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4 January 2017

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S. Yamamoto

1

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4 January 2017

K. C. Sippel

series ordinal

2

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4 January 2017

E. L. Berson

series ordinal

3

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4 January 2017

T. P. Dryja

series ordinal

4

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4 January 2017

language of work or name

English

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publication date

1 February 1997

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4 January 2017

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4 January 2017

volume

15

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4 January 2017

issue

2

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4 January 2017

page(s)

175–178

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The photocurrent, noise and spectral sensitivity of rods of the monkey Macaca fascicularis

4 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

7 January 2021

https://api.crossref.org/works/10.1038%2FNG0297-175

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7 January 2021

Characterization and chromosomal localization of the gene for human rhodopsin kinase

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

7 January 2021

Isoprenylation in regulation of signal transduction by G-protein-coupled receptor kinases

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

7 January 2021

The influence of arrestin (48K protein) and rhodopsin kinase on visual transduction

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

7 January 2021

Rhodopsin phosphorylation and dephosphorylation in vivo

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

7 January 2021

Dark-adaptation and the regeneration of rhodopsin

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

7 January 2021

Kinetics of the Photocurrent of Retinal Rods

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

7 January 2021

The quantity of rhodopsin in human eyes

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

7 January 2021

Human photoreceptor topography

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

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%2FNG0297-175

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

7 January 2021

Variable number of tandem repeat (VNTR) markers for human gene mapping

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-175

7 January 2021