(Q42428325)

English

Novel p.M96T variant of NRL and shRNA-based suppression and replacement of NRL mutants associated with autosomal dominant retinitis pigmentosa

scientific article published on 2 November 2011

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

Novel p.M96T variant of NRL and shRNA-based suppression and replacement of NRL mutants associated with autosomal dominant retinitis pigmentosa (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

Neural retina leucine zipper

1 reference

GOA release 2020-03-11

positive regulation of transcription by RNA polymerase II

1 reference

GOA release 2020-03-11

object named as

C Ayuso

7

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author name string

I Hernan

1

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

M J Gamundi

2

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Europe PubMed Central

PubMed publication ID

31 October 2017

E Borràs

3

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

M Maseras

4

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

B García-Sandoval

5

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

F Blanco-Kelly

6

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

M Carballo

8

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Europe PubMed Central

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31 October 2017

language of work or name

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publication date

2 November 2011

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Europe PubMed Central

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31 October 2017

Clinical Genetics

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Europe PubMed Central

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31 October 2017

82

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Europe PubMed Central

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31 October 2017

5

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Europe PubMed Central

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31 October 2017

446-452

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Europe PubMed Central

PubMed publication ID

31 October 2017

Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

Multiple phosphorylated isoforms of NRL are expressed in rod photoreceptors

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

The leucine zipper of NRL interacts with the CRX homeodomain. A possible mechanism of transcriptional synergy in rhodopsin regulation

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

Retinopathy mutations in the bZIP protein NRL alter phosphorylation and transcriptional activity

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

The basic motif-leucine zipper transcription factor Nrl can positively regulate rhodopsin gene expression

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

Ribozyme gene therapy for autosomal dominant retinal disease.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

Down-regulation of rhodopsin gene expression by AAV-vectored short interfering RNA.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

Suppression of mouse rhodopsin expression in vivo by AAV mediated siRNA delivery

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

Towards mutation-independent silencing of genes involved in retinal degeneration by RNA interference

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

Toward a gene therapy for dominant disease: validation of an RNA interference-based mutation-independent approach

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

RNA interference-mediated suppression and replacement of human rhodopsin in vivo

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

A transgenic mouse model for gene therapy of rhodopsin-linked Retinitis Pigmentosa

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

RNAi-based suppression and replacement of rds-peripherin in retinal organotypic culture

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

RNA based gene therapy for dominantly inherited diseases

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

Combinatorial RNAi: a winning strategy for the race against evolving targets?

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01796.X

21 January 2018

Identifiers

10.1111/J.1399-0004.2011.01796.X

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 October 2017

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