(Q34026125)

English

Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) gene

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) gene (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

photoreceptor protein

0 references

Stephen P. Daiger

8

object named as

Stephen P Daiger

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

author name string

Jiangang Gao

1

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Kyeongmi Cheon

2

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Steven Nusinowitz

3

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Qin Liu

4

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Di Bei

5

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Karen Atkins

6

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Asif Azimi

7

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Debora B Farber

9

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

John R Heckenlively

10

1 reference

Europe PubMed Central

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30 July 2017

Eric A Pierce

11

1 reference

Europe PubMed Central

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30 July 2017

Lori S Sullivan

12

1 reference

Europe PubMed Central

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30 July 2017

Jian Zuo

13

1 reference

Europe PubMed Central

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30 July 2017

language of work or name

0 references

publication date

1 April 2002

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

99

1 reference

Europe PubMed Central

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30 July 2017

8

1 reference

Europe PubMed Central

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30 July 2017

5698-5703

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Identification and subcellular localization of the RP1 protein in human and mouse photoreceptors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

A role for the Tubby-like protein 1 in rhodopsin transport

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Deficiency of rds/peripherin causes photoreceptor death in mouse models of digenic and dominant retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Genetic evidence for selective transport of opsin and arrestin by kinesin-II in mammalian photoreceptors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Microarray analysis of the transcriptional network controlled by the photoreceptor homeobox gene Crx.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model for X-linked retinitis pigmentosa (RP3)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Rhodopsin trafficking and its role in retinal dystrophies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Doublecortin, a stabilizer of microtubules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Myosin VIIa participates in opsin transport through the photoreceptor cilium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

The bZIP transcription factor Nrl stimulates rhodopsin promoter activity in primary retinal cell cultures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Specific binding of peanut lectin to a class of retinal photoreceptor cells. A species comparison.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

On the molecular genetics of retinitis pigmentosa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122834

5 July 2018

Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.042122399

21 January 2018

Retinopathy and attenuated circadian entrainment in Crx-deficient mice.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.042122399

21 January 2018

Development and degeneration of retina in rds mutant mice: light microscopy

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.042122399

21 January 2018

Rods and cones in the mouse retina. I. Structural analysis using light and electron microscopy

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.042122399

21 January 2018

Development and degeneration of retina in rds mutant mice: photoreceptor abnormalities in the heterozygotes

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.042122399

21 January 2018

Visual Pigment Renewal in the Mature Frog Retina

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.042122399

21 January 2018

Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/11960024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1)

1 reference

https://pubmed.ncbi.nlm.nih.gov/11960024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/11960024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.042122399

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

2002PNAS...99.5698G

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

ResearchGate publication ID

0 references

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