(Q33598499)

English

Q344ter mutation causes mislocalization of rhodopsin molecules that are catalytically active: a mouse model of Q344ter-induced retinal degeneration

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Q344ter mutation causes mislocalization of rhodopsin molecules that are catalytically active: a mouse model of Q344ter-induced retinal degeneration (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

retinal degeneration

1 reference

based on heuristic

inferred from title

author name string

Francis Concepcion

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Jeannie Chen

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

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publication date

2 June 2010

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

e10904

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

copyright license

Creative Commons Attribution 4.0 International

2 June 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

The molecular architecture of ribbon presynaptic terminals

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21 June 2018

Ciliary targeting motif VxPx directs assembly of a trafficking module through Arf4.

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21 June 2018

A novel form of transducin-dependent retinal degeneration: accelerated retinal degeneration in the absence of rod transducin

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21 June 2018

Transport of truncated rhodopsin and its effects on rod function and degeneration

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21 June 2018

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

1 reference

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21 June 2018

Stable rhodopsin/arrestin complex leads to retinal degeneration in a transgenic 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=2880002

21 June 2018

Retinitis pigmentosa

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21 June 2018

Characterization of peripherin/rds and rom-1 transport in rod photoreceptors of transgenic and knockout animals

1 reference

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21 June 2018

Mislocalized rhodopsin does not require activation to cause retinal degeneration and neurite outgrowth in Xenopus laevis.

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21 June 2018

Pathophysiological roles of G-protein-coupled receptor kinases

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21 June 2018

Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 2018

Rhodopsin C terminus, the site of mutations causing retinal disease, regulates trafficking by binding to ADP-ribosylation factor 4 (ARF4).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 2018

Molecular mechanisms of light-induced photoreceptor apoptosis and neuroprotection for retinal degeneration

1 reference

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21 June 2018

Gene mutations in retinitis pigmentosa and their clinical implications

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21 June 2018

The molecular acrobatics of arrestin activation

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 2018

Comparison of the clinical expression of retinitis pigmentosa associated with rhodopsin mutations at codon 347 and codon 23.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 2018

R9AP, a membrane anchor for the photoreceptor GTPase accelerating protein, RGS9-1

1 reference

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21 June 2018

Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns.

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21 June 2018

Activation of mislocalized opsin kills rod cells: a novel mechanism for rod cell death in retinal disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 2018

A role for the Tubby-like protein 1 in rhodopsin transport

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 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=2880002

21 June 2018

Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies

1 reference

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21 June 2018

A QTL on distal chromosome 3 that influences the severity of light-induced damage to mouse photoreceptors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 2018

Functional study of rhodopsin phosphorylation in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 2018

Increased susceptibility to light damage in an arrestin knockout mouse model of Oguchi disease (stationary night blindness)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 2018

Retinal degeneration in tulp1-/- mice: vesicular accumulation in the interphotoreceptor matrix

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 2018

Abnormal photoresponses and light-induced apoptosis in rods lacking rhodopsin kinase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 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=2880002

21 June 2018

Regulation of sorting and post-Golgi trafficking of rhodopsin by its C-terminal sequence QVS(A)PA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 2018

Genetic blindness: current concepts in the pathogenesis of human outer retinal dystrophies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 2018

Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments

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21 June 2018

Ontogeny of GTP-binding proteins, Gi and G(o), in rat retina

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21 June 2018

Visual arrestin interaction with rhodopsin. Sequential multisite binding ensures strict selectivity toward light-activated phosphorylated rhodopsin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 2018

Rhodopsin mutations responsible for autosomal dominant retinitis pigmentosa. Clustering of functional classes along the polypeptide chain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2880002

21 June 2018

Structure and function in rhodopsin. 7. Point mutations associated with autosomal dominant retinitis pigmentosa

1 reference

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Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.

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21 June 2018

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa

1 reference

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21 June 2018

Unusual topography of bovine rhodopsin promoter-lacZ fusion gene expression in transgenic mouse retinas.

1 reference

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21 June 2018

Retinal degeneration in the mutant mouse: Accumulation of spherules in the interphotoreceptor space

1 reference

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21 June 2018

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

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21 June 2018

Constitutively active mutants of rhodopsin

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21 June 2018

The carboxyl-terminal domain is essential for rhodopsin transport in rod photoreceptors

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010904

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010904

21 January 2018

Comparative analysis of transcriptional profiles between two apoptotic pathways of light-induced retinal degeneration

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010904

21 January 2018

Protection of Rpe65-deficient mice identifies rhodopsin as a mediator of light-induced retinal degeneration

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010904

21 January 2018

The formation of stable rhodopsin-arrestin complexes induces apoptosis and photoreceptor cell degeneration.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010904

21 January 2018

A molecular pathway for light-dependent photoreceptor apoptosis in Drosophila.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010904

21 January 2018

Evidence for two apoptotic pathways in light-induced retinal degeneration

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010904

21 January 2018

Rapid and reproducible deactivation of rhodopsin requires multiple phosphorylation sites

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010904

21 January 2018

Functional interaction between bovine rhodopsin and G protein transducin

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010904

21 January 2018

Susceptibility to retinal light damage in transgenic rats with rhodopsin mutations

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010904

21 January 2018

Neuroanatomical localization of receptor-activated G proteins in brain

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21 January 2018

GTPase regulators and photoresponses in cones of the eastern chipmunk.

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Disease progression in patients with dominant retinitis pigmentosa and rhodopsin mutations

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30 October 2018

Reversal of functional loss in the P23H-3 rat retina by management of ambient light

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Biochemical analysis of phototransduction and visual cycle in zebrafish larvae

1 reference

https://pubmed.ncbi.nlm.nih.gov/20532191

12 December 2020

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Retinal damage by light in rats

1 reference

https://pubmed.ncbi.nlm.nih.gov/20532191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Possible mechanisms of photoreceptor damage by light in mammalian eyes

1 reference

https://pubmed.ncbi.nlm.nih.gov/20532191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhodopsin-enhanced GTPase activity of the inhibitory GTP-binding protein of adenylate cyclase

1 reference

https://pubmed.ncbi.nlm.nih.gov/20532191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deactivation of photoactivated rhodopsin by rhodopsin-kinase and arrestin

1 reference

https://pubmed.ncbi.nlm.nih.gov/20532191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence against the role of rhodopsin in rod outer segment binding to RPE cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/20532191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antigen-antibody interaction. Synthetic peptides define linear antigenic determinants recognized by monoclonal antibodies directed to the cytoplasmic carboxyl terminus of rhodopsin

1 reference

https://pubmed.ncbi.nlm.nih.gov/20532191

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Anti-rhodopsin monoclonal antibodies of defined specificity: characterization and application

1 reference

https://pubmed.ncbi.nlm.nih.gov/20532191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of rhodopsin kinase activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20532191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20532191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytoplasmic domain of rhodopsin is essential for post-Golgi vesicle formation in a retinal cell-free system

1 reference

https://pubmed.ncbi.nlm.nih.gov/20532191

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/20532191

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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/20532191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0010904

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

2010PLoSO...510904C

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

0 references

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