(Q28116973)

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

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scholarly article

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PubMed publication ID

4 January 2017

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

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PubMed publication ID

4 January 2017

night blindness

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author name string

S. Yamamoto

1

1 reference

PubMed publication ID

4 January 2017

K. C. Sippel

2

1 reference

PubMed publication ID

4 January 2017

E. L. Berson

3

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4 January 2017

T. P. Dryja

4

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PubMed publication ID

4 January 2017

language of work or name

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publication date

1 February 1997

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PubMed publication ID

4 January 2017

Nature Genetics

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PubMed publication ID

4 January 2017

15

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PubMed publication ID

4 January 2017

2

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PubMed publication ID

4 January 2017

175–178

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PubMed publication ID

4 January 2017

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

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

OGUCHI'S DISEASE

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterization and chromosomal localization of the gene for human rhodopsin kinase

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

Rhodopsin phosphorylation and dephosphorylation in vivo

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

Dark-adaptation and the regeneration of rhodopsin

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

Kinetics of the Photocurrent of Retinal Rods

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

The quantity of rhodopsin in human eyes

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

Human photoreceptor topography

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

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/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

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/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038/NG0297-175

7 January 2021

based on heuristic

inferred from DOI database lookup

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