(Q40163894)

18 September 2017

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

1 reference

Neural retina leucine zipper

18 September 2017

0 references

1 reference

positive regulation of transcription by RNA polymerase II

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Anand Swaroop

series ordinal

4

1 reference

18 September 2017

Atsuhiro Kanda

1

1 reference

PubMed ID

17335001

18 September 2017

James S Friedman

series ordinal

2

1 reference

PubMed ID

17335001

18 September 2017

Koji M Nishiguchi

series ordinal

3

1 reference

18 September 2017

1 June 2007

1 reference

18 September 2017

1 reference

18 September 2017

28

1 reference

18 September 2017

6

1 reference

18 September 2017

589-598

1 reference

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

18 September 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

A mutation in NRL is associated with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Molecular genetics and prospects for therapy of the inherited retinal dystrophies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Implication of tubby proteins as transcription factors by structure-based functional analysis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

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.20488

7 January 2021

Functional analysis of cone-rod homeobox (CRX) mutations associated with retinal dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Phylogenomic analysis and expression patterns of large Maf genes in Xenopus tropicalis provide new insights into the functional evolution of the gene family in osteichthyans

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

The PROSITE database, its status in 2002

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Regulating the regulators: lysine modifications make their mark

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

The minimal transactivation domain of the basic motif-leucine zipper transcription factor NRL interacts with TATA-binding protein

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

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.20488

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

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.20488

7 January 2021

Retinopathy induced in mice by targeted disruption of the rhodopsin gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Light in retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Nrl and Sp nuclear proteins mediate transcription of rod-specific cGMP-phosphodiesterase beta-subunit gene: involvement of multiple response elements

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Molecular genetics of Axenfeld-Rieger malformations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Nrl is required for rod photoreceptor development

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

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/10.1002%2FHUMU.20488

7 January 2021

Interaction of retinal bZIP transcription factor NRL with Flt3-interacting zinc-finger protein Fiz1: possible role of Fiz1 as a transcriptional repressor

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

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.20488

7 January 2021

The stability of the lens-specific Maf protein is regulated by fibroblast growth factor (FGF)/ERK signaling in lens fiber differentiation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Functional analysis of the rod photoreceptor cGMP phosphodiesterase alpha-subunit gene promoter: Nrl and Crx are required for full transcriptional activity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

ELM server: A new resource for investigating short functional sites in modular eukaryotic proteins

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Molecular genetics of human retinal disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Multiple phosphorylated isoforms of NRL are expressed in rod photoreceptors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Conserved transcriptional activators of the Xenopus rhodopsin gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Multisite protein modification and intramolecular signaling

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Characterization of the chicken L-Maf, MafB and c-Maf in crystallin gene regulation and lens differentiation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Expression profiling of the developing and mature Nrl-/- mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of Nrl

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Altered expression of genes of the Bmp/Smad and Wnt/calcium signaling pathways in the cone-only Nrl-/- mouse retina, revealed by gene profiling using custom cDNA microarrays

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20488

7 January 2021

Identifiers

DOI

10.1002/HUMU.20488

1 reference

18 September 2017

1 reference

PubMed ID

17335001