(Q24337358)

rhodopsin mediated signaling pathway

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

S Fuchs

1

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M Nakazawa

2

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M Maw

3

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M Tamai

4

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Y Oguchi

5

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A Gal

The sequence of human retinal S-antigen reveals similarities with alpha-transducin

6

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language of work or name

English

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publication date

July 1995

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published in

Nature Genetics

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volume

10

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issue

3

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page(s)

360-2

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG0795-360

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-360

7 January 2021

Oguchi disease: suggestion of linkage to markers on chromosome 2q

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-360

7 January 2021

Fluorescence in situ hybridization mapping of 25 markers on distal human chromosome 2q surrounding the human Waardenburg syndrome, type I (WS1) locus (PAX3 gene)

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-360

7 January 2021

Genetic fine localization of the arrestin (S-antigen) gene 4 cM distal from D2S172

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-360

7 January 2021

Light-induced binding of 48-kDa protein to photoreceptor membranes is highly enhanced by phosphorylation of rhodopsin

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-360

7 January 2021

Phosphodiesterase activation by photoexcited rhodopsin is quenched when rhodopsin is phosphorylated and binds the intrinsic 48-kDa protein of rod outer segments

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-360

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-360

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%2FNG0795-360

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%2FNG0795-360

7 January 2021

A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-360

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-360

7 January 2021

Arrestin function in inactivation of G protein-coupled receptor rhodopsin in vivo

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-360

7 January 2021

Mizuo phenomenon in X-linked retinoschisis. Pathogenesis of the Mizuo phenomenon

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-360

7 January 2021

X-linked recessive cone dystrophy with tapetal-like sheen. A newly recognized entity with Mizuo-Nakamura phenomenon

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-360

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-360

7 January 2021