(Q33825000)

English

Mutations of the opsin gene (Y102H and I307N) lead to light-induced degeneration of photoreceptors and constitutive activation of phototransduction in mice

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Mutations of the opsin gene (Y102H and I307N) lead to light-induced degeneration of photoreceptors and constitutive activation of phototransduction in mice (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

photoreceptor protein

0 references

author name string

Ewa Budzynski

1

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Alecia K Gross

2

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Suzanne D McAlear

3

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Neal S Peachey

4

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Meera Shukla

5

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Feng He

6

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Malia Edwards

7

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Jungyeon Won

8

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Wanda L Hicks

9

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Theodore G Wensel

10

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Jurgen K Naggert

11

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Patsy M Nishina

12

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

language of work or name

0 references

publication date

5 March 2010

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Journal of Biological Chemistry

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

285

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

19

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

14521-14533

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Clinical light exposure, photoreceptor degeneration, and AP-1 activation: a cell death or cell survival signal in the rhodopsin mutant retina?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Increased sensitivity to light-induced damage in a mouse model of autosomal dominant retinal disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Crystal structure of a photoactivated deprotonated intermediate of rhodopsin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Generation, characterization, and molecular cloning of the Noerg-1 mutation of rhodopsin in the mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Delayed dark adaptation in 11-cis-retinol dehydrogenase-deficient mice: a role of RDH11 in visual processes in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Characterization of rhodopsin congenital night blindness mutant T94I.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

The relationship between opsin overexpression and photoreceptor degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Sensitivity and kinetics of mouse rod flash responses determined in vivo from paired-flash electroretinograms.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Morphological, physiological, and biochemical changes in rhodopsin knockout mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Effect of vitamin A supplementation on rhodopsin mutants threonine-17 --> methionine and proline-347 --> serine in transgenic mice and in cell cultures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Using targeted large deletions and high-efficiency N-ethyl-N-nitrosourea mutagenesis for functional analyses of the mammalian genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

A comparison of the efficiency of G protein activation by ligand-free and light-activated forms of rhodopsin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Retinitis pigmentosa. The Friedenwald Lecture

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Constitutive activation of phototransduction by K296E opsin is not a cause of photoreceptor degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Constitutive activation of opsin: interaction of mutants with rhodopsin kinase and arrestin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Total synthesis of a gene for bovine rhodopsin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

4 July 2018

Genetically engineered large animal model for studying cone photoreceptor survival and degeneration in retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.112409

21 January 2018

Generation of a transgenic rabbit model of retinal degeneration

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.112409

21 January 2018

Mouse models of ocular diseases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.112409

21 January 2018

Ocular abnormalities in Large(myd) and Large(vls) mice, spontaneous models for muscle, eye, and brain diseases.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.112409

21 January 2018

Fundamental computations in neural systems.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.112409

21 January 2018

Slow binding of retinal to rhodopsin mutants G90D and T94D.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.112409

21 January 2018

An opsin mutant with increased thermal stability

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.112409

21 January 2018

Ida Mann Lecture. Transduction in human photoreceptors.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.112409

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.112409

21 January 2018

A morphometric study of light-induced damage in transgenic rat models of retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.112409

21 January 2018

Identification and functional characterization of a novel rhodopsin mutation associated with autosomal dominant CSNB.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110.112409

21 January 2018

Phototransduction, dark adaptation, and rhodopsin regeneration the proctor lecture.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

29 October 2018

Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

29 October 2018

Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2863193

29 October 2018

The electroretinogram of the rhodopsin knockout mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/20207741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20207741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness

1 reference

https://pubmed.ncbi.nlm.nih.gov/20207741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rod phototransduction in transgenic mice expressing a mutant opsin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/20207741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recovery kinetics of human rod phototransduction inferred from the two-branched alpha-wave saturation function

1 reference

https://pubmed.ncbi.nlm.nih.gov/20207741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polygenic disease and retinitis pigmentosa: albinism exacerbates photoreceptor degeneration induced by the expression of a mutant opsin in transgenic mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/20207741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinopathy induced in mice by targeted disruption of the rhodopsin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/20207741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of a mutant opsin gene increases the susceptibility of the retina to light damage

1 reference

https://pubmed.ncbi.nlm.nih.gov/20207741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-performance liquid chromatography analysis of visual cycle retinoids

1 reference

https://pubmed.ncbi.nlm.nih.gov/20207741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of geometrically isomeric vitamin A compounds

1 reference

https://pubmed.ncbi.nlm.nih.gov/20207741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative determination of retinals with complete retention of their geometric configuration

1 reference

https://pubmed.ncbi.nlm.nih.gov/20207741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A single amino acid substitution in rhodopsin (lysine 248----leucine) prevents activation of transducin

1 reference

https://pubmed.ncbi.nlm.nih.gov/20207741

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1074/JBC.M110.112409

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q33825000&oldid=1976352457"