Autosomal recessive retinitis pigmentosa E150K opsin mice exhibit photoreceptor disorganization. (Q42438771)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23221340 AND SRC:MED&resulttype=core&format=json

19 February 2020

title

Autosomal recessive retinitis pigmentosa E150K opsin mice exhibit photoreceptor disorganization (English)

1 reference

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19 February 2020

main subject

photoreceptor protein

0 references

1 reference

4

1 reference

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19 February 2020

Vladimir J. Kefalov

9

1 reference

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19 February 2020

3

Beata Jastrzebska

1 reference

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19 February 2020

10

Krzysztof Palczewski

1 reference

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19 February 2020

7

Christel Genoud

1 reference

19 February 2020

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6

Tadao Maeda

1 reference

19 February 2020

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23221340 AND SRC:MED&resulttype=core&format=json

Ning Zhang

1

1 reference

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19 February 2020

Alexander V Kolesnikov

2

1 reference

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19 February 2020

Osamu Sawada

5

1 reference

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19 February 2020

Andreas Engel

8

1 reference

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19 February 2020

language of work or name

English

0 references

publication date

10 December 2012

1 reference

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Journal of Clinical Investigation

19 February 2020

published in

1 reference

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19 February 2020

volume

123

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19 February 2020

issue

1

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19 February 2020

page(s)

121-137

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describes a project that uses

19 February 2020

ImageJ

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3533307/fullTextXML

inferred from PubMed Central ID database lookup

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28 May 2018

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28 May 2018

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28 May 2018

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28 May 2018

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Light-dependent delay in the falling phase of the retinal rod photoresponse

28 May 2018

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Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase beta-subunit gene of the rd mouse

28 May 2018

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28 May 2018

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28 May 2018

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RGS expression rate-limits recovery of rod photoresponses

28 May 2018

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Light responses and light adaptation in rat retinal rods at different temperatures

16 August 2018

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16 August 2018

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Photoreceptor preservation in the S334ter model of retinitis pigmentosa by a novel estradiol analog

16 August 2018

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Spontaneous activity of opsin apoprotein is a cause of Leber congenital amaurosis

16 August 2018

1 reference

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Evidence for two apoptotic pathways in light-induced retinal degeneration

16 August 2018

1 reference

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

16 August 2018

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16 August 2018

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

16 August 2018

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12 December 2020

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Identifiers

DOI

10.1172/JCI66176

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23221340 AND SRC:MED&resulttype=core&format=json

19 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23221340 AND SRC:MED&resulttype=core&format=json

19 February 2020

PubMed publication ID

23221340

1 reference