(Q37589555)

English

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

scientific article

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

1 reference

Europe PubMed Central

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

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

retinal degeneration

1 reference

based on heuristic

inferred from title

retinitis pigmentosa

1 reference

based on heuristic

inferred from title

author name string

Daniel F Schorderet

1

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

Pascal Escher

2

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 November 2009

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

30

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

1475-1485

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Phenotypic variation in enhanced S-cone syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of the involvement of the NR2E3 gene in autosomal recessive retinal dystrophies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Anatomical profiling of nuclear receptor expression reveals a hierarchical transcriptional network

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of photoreceptor-specific nuclear receptor NR2E3 in rod photoreceptors of fetal human retina

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

An Arg311Gln NR2E3 mutation in a family with classic Goldmann-Favre syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Crx, a Novel Otx-like Paired-Homeodomain Protein, Binds to and Transactivates Photoreceptor Cell-Specific Genes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Retina-specific nuclear receptor: A potential regulator of cellular retinaldehyde-binding protein expressed in retinal pigment epithelium and Müller glial cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Effects of L1 retrotransposon insertion on transcript processing, localization and accumulation: lessons from the retinal degeneration 7 mouse and implications for the genomic ecology of L1 elements

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic ablation of cone photoreceptors eliminates retinal folds in the retinal degeneration 7 (rd7) mouse

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

A hybrid photoreceptor expressing both rod and cone genes in a mouse model of enhanced S-cone syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

[Two cases of hyaloid-retinal degeneration]

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

The Enhanced S Cone Syndrome: An Analysis of Receptoral and Post-receptoral Changes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Mapping of genetic modifiers of Nr2e3 rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Optical coherence tomography in enhanced S-cone syndrome: large macular retinoschisis with disorganized retinal lamination

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Enhanced S cone syndrome: evidence for an abnormally large number of S cones

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Treatment of adult-onset acute macular retinoschisis in enhanced s-cone syndrome with oral acetazolamide

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Relatively enhanced S cone function in the Goldmann-Favre syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical findings in autosomal recessive syndrome of blue cone hypersensitivity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

The enhanced S-cone syndrome in children.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a photoreceptor cell-specific nuclear receptor

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression and functional analysis of Nr2e3, a photoreceptor-specific nuclear receptor, suggest common mechanisms in retinal development between avians and mammals.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Atypical Mild Enhanced S-Cone Syndrome with Novel Compound Heterozygosity of the NR2E3 Gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

The nuclear receptor superfamily: the second decade

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Diagnostic clinical findings of a new syndrome with night blindness, maculopathy, and enhanced S cone sensitivity.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

A teenager with nightblindness and cystic maculopathy: enhanced S cone syndrome (Goldmann-Favre syndrome)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Nrl is required for rod photoreceptor development

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Enhanced S-cone syndrome with subfoveal neovascularization.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Enhanced S-cone syndrome in a Japanese family with a nonsense NR2E3 mutation (Q350X).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

A thyroid hormone receptor that is required for the development of green cone photoreceptors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Pias3-dependent SUMOylation directs rod photoreceptor development

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Phenotypic features of patients with NR2E3 mutations.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Activation of the blue opsin gene in cone photoreceptor development by retinoid-related orphan receptor beta

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

A cell cycle-dependent co-repressor mediates photoreceptor cell-specific nuclear receptor function

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical and histopathologic findings in clumped pigmentary retinal degeneration

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Physiological function of S-cone system is not enhanced in rd7 mice

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Bilateral giant macular schisis in a patient with enhanced S-cone syndrome from a family showing pseudo-dominant inheritance.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Dual role of Nr2e3 in photoreceptor development and maintenance

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Improving sequence variant descriptions in mutation databases and literature using the Mutalyzer sequence variation nomenclature checker.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of potent agonists of photoreceptor-specific nuclear receptor (NR2E3) and preparation of a radioligand

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Electroretinograms and visual evoked potentials elicited by spectral stimuli in a patient with enhanced S-cone syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21096

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.21096

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 August 2017

ResearchGate publication ID

0 references

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=Q37589555&oldid=1640458561"