(Q37213895)

19 August 2017

The severe autosomal dominant retinitis pigmentosa rhodopsin mutant Ter349Glu mislocalizes and induces rapid rod cell death (English)

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19 August 2017

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T J Hollingsworth

1

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19 August 2017

Alecia K Gross

series ordinal

2

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19 August 2017

language of work or name

English

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publication date

12 August 2013

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19 August 2017

9

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Journal of Biological Chemistry

inferred from page(s)

published in

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19 August 2017

288

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19 August 2017

40

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19 August 2017

29047-29055

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describes a project that uses

19 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3790004/fullTextXML

inferred from PubMed Central ID database lookup

cites work

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Mice with a D190N mutation in the gene encoding rhodopsin: a model for human autosomal-dominant retinitis pigmentosa

6 September 2017

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6 September 2017

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6 September 2017

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The conserved Bardet-Biedl syndrome proteins assemble a coat that traffics membrane proteins to cilia

6 September 2017

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

6 September 2017

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BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly

6 September 2017

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Trafficking of Crumbs3 during cytokinesis is crucial for lumen formation

6 September 2017

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

6 September 2017

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Bardet-Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia

6 September 2017

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A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity

6 September 2017

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Impaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet-Biedl syndrome

6 September 2017

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Gene expression analysis of photoreceptor cell loss in bbs4-knockout mice reveals an early stress gene response and photoreceptor cell damage

6 September 2017

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A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis

6 September 2017

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6 September 2017

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Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin

6 September 2017

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Rhodopsin signaling and organization in heterozygote rhodopsin knockout mice

6 September 2017

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Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)

6 September 2017

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6 September 2017

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

6 September 2017

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6 September 2017

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The cytoplasmic tail of rhodopsin acts as a novel apical sorting signal in polarized MDCK cells

6 September 2017

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

6 September 2017

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Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosa

6 September 2017

1 reference

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

6 September 2017

1 reference

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Efficient in vivo manipulation of mouse genomic sequences at the zygote stage

6 September 2017

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Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

6 September 2017

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Apoptotic photoreceptor cell death in mouse models of retinitis pigmentosa

6 September 2017

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Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsin.

6 September 2017

1 reference

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Fine structure of a periciliary ridge complex of frog retinal rod cells revealed by ultrahigh resolution scanning electron microscopy.

6 September 2017

1 reference

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The role of rhodopsin glycosylation in protein folding, trafficking, and light-sensitive retinal degeneration

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790004

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

3 September 2018

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Defective development of photoreceptor membranes in a mouse model of recessive retinal degeneration

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790004

Novel familial WT1 read-through mutation associated with Wilms tumor and slow progressive nephropathy.

3 September 2018

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Prenatal diagnosis of recessive congenital methaemoglobinaemia type II: novel mutation in the NADH-cytochrome b5 reductase gene leading to stop codon read-through.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790004

A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790004

A method for generating transgenic frog embryos

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790004

Instability of C₆₀ fullerene interacting with lipid bilayer.

3 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1074%2FJBC.M113.495184

Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1074%2FJBC.M113.495184

Assays for detection of constitutively active opsins

21 January 2018

1 reference

12 December 2020

Characterization of bovine rod outer segment G-protein

1 reference

12 December 2020

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

12 December 2020

Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. Online

1 reference

12 December 2020

Identifiers

DOI

10.1074/JBC.M113.495184

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

23940033

1 reference