(Q40257353)

English

Impacts of two point mutations of RPE65 from Leber's congenital amaurosis on the stability, subcellular localization and isomerohydrolase activity of RPE65.

scientific article published on 5 July 2006

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scholarly article

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Europe PubMed Central

18 September 2017

Impacts of two point mutations of RPE65 from Leber's congenital amaurosis on the stability, subcellular localization and isomerohydrolase activity of RPE65. (English)

1 reference

Europe PubMed Central

18 September 2017

congenital disorder

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author name string

Ying Chen

1

1 reference

Europe PubMed Central

18 September 2017

Gennadiy Moiseyev

2

1 reference

Europe PubMed Central

18 September 2017

Yusuke Takahashi

3

1 reference

Europe PubMed Central

18 September 2017

Jian-Xing Ma

4

1 reference

Europe PubMed Central

18 September 2017

language of work or name

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publication date

5 July 2006

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Europe PubMed Central

18 September 2017

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Europe PubMed Central

18 September 2017

580

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Europe PubMed Central

18 September 2017

17

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Europe PubMed Central

18 September 2017

4200-4204

1 reference

Europe PubMed Central

18 September 2017

How photons start vision

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

Confronting complexity: the interlink of phototransduction and retinoid metabolism in the vertebrate retina

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

The biochemistry of the visual cycle

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

Molecular mechanisms in visual pigment regeneration

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

Dark adaptation and the retinoid cycle of vision

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

Membrane phospholipids as an energy source in the operation of the visual cycle

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

Mutation of key residues of RPE65 abolishes its enzymatic role as isomerohydrolase in the visual cycle.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

RPE65 is the isomerohydrolase in the retinoid visual cycle

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

Rpe65 is the retinoid isomerase in bovine retinal pigment epithelium

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

Retinyl esters are the substrate for isomerohydrolase.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

Mutations in RPE65 cause Leber's congenital amaurosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

Retinal dystrophy of Swedish briard/briard-beagle dogs is due to a 4-bp deletion in RPE65.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

RPE65, the major retinal pigment epithelium microsomal membrane protein, associates with phospholipid liposomes

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.06.078

21 January 2018

Identifiers

10.1016/J.FEBSLET.2006.06.078

1 reference

Europe PubMed Central

18 September 2017

1 reference

Europe PubMed Central

18 September 2017

ResearchGate publication ID

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