(Q44579156)

4 December 2017

title

Prolonged survival of the phosphorylated form of rhodopsin during dark adaptation of Royal College Surgeons rat. (English)

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4 December 2017

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5

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4 December 2017

Hiroshi Ohguro

1

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4 December 2017

Ikuyo Ohguro

series ordinal

2

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4 December 2017

Kazuhisa Mamiya

series ordinal

3

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4 December 2017

Tadao Maeda

series ordinal

4

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4 December 2017

language of work or name

English

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publication date

1 September 2003

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4 December 2017

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4 December 2017

volume

551

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4 December 2017

issue

1-3

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4 December 2017

page(s)

128-132

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Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat

4 December 2017

cites work

1 reference

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Human pancreatic islets in culture: effects of supplementing the medium with homologous and heterologous serum

21 January 2018

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Mertk triggers uptake of photoreceptor outer segments during phagocytosis by cultured retinal pigment epithelial cells

21 January 2018

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Correction of the retinal dystrophy phenotype of the RCS rat by viral gene transfer of Mertk

21 January 2018

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Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa

21 January 2018

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GTP-binding-protein-coupled receptor kinases--two mechanistic models

21 January 2018

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https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900908-6

Multiple phosphorylation of rhodopsin and the in vivo chemistry underlying rod photoreceptor dark adaptation

21 January 2018

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https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900908-6

Structural and enzymatic aspects of rhodopsin phosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900908-6

The catalytic subunit of phosphatase 2A dephosphorylates phosphoopsin

21 January 2018

1 reference

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Doyne Lecture. Rhodopsin and autosomal dominant retinitis pigmentosa

21 January 2018

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Retinitis pigmentosa: defined from a molecular point of view

21 January 2018

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Mechanisms of rhodopsin inactivation in vivo as revealed by a COOH-terminal truncation mutant.

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.1016%2FS0014-5793%2803%2900908-6

Null mutation in the rhodopsin kinase gene slows recovery kinetics of rod and cone phototransduction in man

21 January 2018

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Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture

21 January 2018

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Molecular forms of human rhodopsin kinase (GRK1)

21 January 2018

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Sequential phosphorylation of rhodopsin at multiple sites

21 January 2018

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Rhodopsin phosphorylation and dephosphorylation in vivo

21 January 2018

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High levels of rhodopsin phosphorylation in missense mutations of C-terminal region of rhodopsin

21 January 2018

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Rhodopsin trafficking and its role in retinal dystrophies.

21 January 2018

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A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment

21 January 2018

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Mice lacking G-protein receptor kinase 1 have profoundly slowed recovery of cone-driven retinal responses

7 January 2021

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10.1016/S0014-5793(03)00908-6

7 January 2021

Identifiers

DOI

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4 December 2017

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