(Q43723701)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11528395%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

title

New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis (English)

1 reference

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10 November 2019

0 references

6

1 reference

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10 November 2019

Robert N. Fariss

12

1 reference

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10 November 2019

T. Michael Redmond

13

1 reference

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10 November 2019

author name string

Seeliger MW

1

1 reference

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10 November 2019

Grimm C

2

1 reference

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10 November 2019

Ståhlberg F

3

1 reference

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10 November 2019

Friedburg C

4

1 reference

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10 November 2019

Jaissle G

5

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10 November 2019

Guo H

7

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10 November 2019

Remé CE

8

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10 November 2019

Humphries P

9

1 reference

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10 November 2019

Hofmann F

10

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10 November 2019

Biel M

11

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10 November 2019

Wenzel A

14

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10 November 2019

language of work or name

English

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publication date

1 September 2001

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10 November 2019

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10 November 2019

volume

29

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10 November 2019

issue

1

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10 November 2019

page(s)

70-74

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https://scigraph.springernature.com/pub.10.1038/ng712

10 November 2019

exact match

0 references

cites work

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Mutations in RPE65 cause Leber's congenital amaurosis

1 reference

7 January 2021

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

1 reference

7 January 2021

Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3.

1 reference

7 January 2021

Retinopathy induced in mice by targeted disruption of the rhodopsin gene

1 reference

7 January 2021

Cloning and immunocytochemical localization of a cyclic nucleotide-gated channel alpha-subunit to all cone photoreceptors in the mouse retina

1 reference

7 January 2021

Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel

1 reference

7 January 2021

Standard for clinical electroretinography (1994 update)

1 reference

7 January 2021

Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindness

1 reference

7 January 2021

Night blindness, dark adaptation, and the electroretinogram

1 reference

7 January 2021

Light adaptation and dark adaptation of human rod photoreceptors measured from the a-wave of the electroretinogram.

1 reference

7 January 2021

Human cone photoreceptor responses measured by the electroretinogram [correction of electoretinogram] a-wave during and after exposure to intense illumination

1 reference

7 January 2021

Rod photoreceptors detect rapid flicker

1 reference

7 January 2021

Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in man.

1 reference

7 January 2021

c-fos controls the "private pathway" of light-induced apoptosis of retinal photoreceptors

1 reference

7 January 2021

Genetic analysis of RPE65: from human disease to mouse model

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG712

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11528395%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

10 November 2019

1031063377

0 references

1 reference