(Q33510152)

27 July 2017

title

Mutations in the DNA-binding domain of NR2E3 affect in vivo dimerization and interaction with CRX. (English)

1 reference

27 July 2017

1

Raphael Roduit

1 reference

27 July 2017

Daniel F Schorderet

3

0 references

author name string

Pascal Escher

series ordinal

2

1 reference

27 July 2017

language of work or name

English

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publication date

12 October 2009

1 reference

27 July 2017

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27 July 2017

volume

4

1 reference

27 July 2017

issue

10

1 reference

27 July 2017

page(s)

e7379

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Creative Commons Attribution 4.0 International

27 July 2017

copyright license

start time

12 October 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP).

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Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family

21 June 2018

1 reference

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Monitoring protein-protein interactions in living cells by bioluminescence resonance energy transfer (BRET).

21 June 2018

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Regulation of photoreceptor gene expression by Crx-associated transcription factor network

21 June 2018

1 reference

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Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa

21 June 2018

1 reference

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In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development

21 June 2018

1 reference

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Illuminating insights into protein-protein interactions using bioluminescence resonance energy transfer (BRET).

21 June 2018

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21 June 2018

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Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced S-cone syndrome demonstrate compound heterozygosity

21 June 2018

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The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes

21 June 2018

1 reference

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The rod photoreceptor-specific nuclear receptor Nr2e3 represses transcription of multiple cone-specific genes.

21 June 2018

1 reference

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Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome

21 June 2018

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Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors

21 June 2018

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Heterodimerization of V1a and V2 vasopressin receptors determines the interaction with beta-arrestin and their trafficking patterns

21 June 2018

1 reference

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Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration

21 June 2018

1 reference

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SWISS-MODEL: An automated protein homology-modeling server

21 June 2018

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The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration

21 June 2018

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Origins and evolutionary diversification of the nuclear receptor superfamily

21 June 2018

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Detection of beta 2-adrenergic receptor dimerization in living cells using bioluminescence resonance energy transfer (BRET)

21 June 2018

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The orphan nuclear receptor Tlx regulates Pax2 and is essential for vision

21 June 2018

1 reference

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Structure of the RXR-RAR DNA-binding complex on the retinoic acid response element DR1

21 June 2018

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Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757917

Identification of a photoreceptor cell-specific nuclear receptor

21 June 2018

1 reference

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Structural elements of an orphan nuclear receptor-DNA complex

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757917

SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling

21 June 2018

1 reference

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The nuclear receptor superfamily: the second decade

21 June 2018

1 reference

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Relationship between Drosophila gap gene tailless and a vertebrate nuclear receptor Tlx.

21 June 2018

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Retinoid X receptor alpha forms tetramers in solution

21 June 2018

1 reference

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SWS (blue) cone hypersensitivity in a newly identified retinal degeneration.

21 June 2018

1 reference

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Spatial control of the gap gene knirps in the Drosophila embryo by posterior morphogen system

21 June 2018

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The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation.

21 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007379

Homo- and hetero-oligomerization of beta-arrestins in living cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007379

Adenosine A2A-dopamine D2 receptor-receptor heteromerization: qualitative and quantitative assessment by fluorescence and bioluminescence energy transfer

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007379

Pias3-dependent SUMOylation directs rod photoreceptor development

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007379

The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2757917

A rigorous experimental framework for detecting protein oligomerization using bioluminescence resonance energy transfer

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19823680

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0007379

1 reference

27 July 2017

0 references

1 reference

27 July 2017

1 reference