The Effect of Peripherin/rds Haploinsufficiency on Rod and Cone Photoreceptors (Q50526833)

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scientific article published on November 1, 1997

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English	The Effect of Peripherin/rds Haploinsufficiency on Rod and Cone Photoreceptors	scientific article published on November 1, 1997

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scholarly article

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Europe PubMed Central

PMC publication ID

6573736

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9334387%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 November 2019

title

The effect of peripherin/rds haploinsufficiency on rod and cone photoreceptors (English)

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stated in

Europe PubMed Central

PMC publication ID

6573736

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9334387%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 November 2019

The Effect of Peripherin/rds Haploinsufficiency on Rod and Cone Photoreceptors (English)

1 reference

stated in

Crossref

DOI

10.1523/JNEUROSCI.17-21-08118.1997

reference URL

https://api.crossref.org/works/10.1523/JNEUROSCI.17-21-08118.1997

retrieved

19 November 2024

main subject

haploinsufficiency

0 references

photoreceptor protein

0 references

membrane glycoprotein

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9334387

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9334387

retrieved

19 November 2024

author

Neal S Peachey

series ordinal

2

object named as

N. S. Peachey

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Europe PubMed Central

PubMed publication ID

9334387

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9334387

retrieved

19 November 2024

author name string

T. Cheng

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1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9334387

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9334387

retrieved

19 November 2024

S. Li

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9334387

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9334387

retrieved

19 November 2024

Y. Goto

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4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9334387

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9334387

retrieved

19 November 2024

Y. Cao

series ordinal

5

1 reference

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Europe PubMed Central

PubMed publication ID

9334387

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9334387

retrieved

19 November 2024

M. I. Naash

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9334387

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9334387

retrieved

19 November 2024

language of work or name

English

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publication date

1 November 1997

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stated in

Europe PubMed Central

PMC publication ID

6573736

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9334387%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 November 2019

full work available at URL

https://www.jneurosci.org/content/jneuro/17/21/8118.full.pdf

file format

PDF

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9334387

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9334387

retrieved

19 November 2024

http://www.jneurosci.org/cgi/content/abstract/17/21/8118

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9334387

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9334387

retrieved

19 November 2024

https://europepmc.org/articles/PMC6573736

file format

HTML

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9334387

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9334387

retrieved

19 November 2024

https://europepmc.org/articles/PMC6573736?pdf=render

file format

PDF

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9334387

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9334387

retrieved

19 November 2024

https://doi.org/10.1523/jneurosci.17-21-08118.1997

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9334387

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9334387

retrieved

19 November 2024

https://syndication.highwire.org/content/doi/10.1523/JNEUROSCI.17-21-08118.1997

1 reference

stated in

Crossref

DOI

10.1523/JNEUROSCI.17-21-08118.1997

reference URL

https://api.crossref.org/works/10.1523/JNEUROSCI.17-21-08118.1997

retrieved

19 November 2024

published in

Journal of Neuroscience

1 reference

stated in

Europe PubMed Central

PMC publication ID

6573736

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9334387%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 November 2019

volume

17

1 reference

stated in

Europe PubMed Central

PMC publication ID

6573736

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9334387%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 November 2019

issue

21

1 reference

stated in

Europe PubMed Central

PMC publication ID

6573736

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9334387%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 November 2019

page(s)

8118-8128

1 reference

stated in

Europe PubMed Central

PMC publication ID

6573736

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9334387%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 November 2019

cites work

Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rod phototransduction in transgenic mice expressing a mutant opsin gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ocular findings associated with a 3 base pair deletion in the peripherin-RDS gene in autosomal dominant retinitis pigmentosa

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Postnatal development of photoreceptor-specific proteins in mice with hereditary retinal degeneration. An immunocytochemical study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new H-2-linked mutation, rds, causing retinal degeneration in the mouse

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development and degeneration of retina in rds mutant mice: observations in chimaeras of heterozygous mutant and normal genotype

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two different visual pigments in one retinal cone cell

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Properties of the mouse cone-mediated electroretinogram during light adaptation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ocular findings in patients with autosomal dominant retinitis pigmentosa and transversion mutation in codon 244 (Asn244Lys) of the peripherin/RDS gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Opsin gene expression during early and late phases of retinal degeneration in rds mice

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinal degeneration slow (rds) in mouse results from simple insertion of a t haplotype-specific element into protein-coding exon II.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase beta-subunit gene of the rd mouse

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional abnormalities in transgenic mice expressing a mutant rhodopsin gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A quantitative account of the activation steps involved in phototransduction in amphibian photoreceptors

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis of genetic dominance

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse opsin. Gene structure and molecular basis of multiple transcripts

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polygenic disease and retinitis pigmentosa: albinism exacerbates photoreceptor degeneration induced by the expression of a mutant opsin in transgenic mice

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rod photoreceptor transduction is affected in central retinal vein occlusion associated with iris neovascularization

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antigen-antibody interaction. Synthetic peptides define linear antigenic determinants recognized by monoclonal antibodies directed to the cytoplasmic carboxyl terminus of rhodopsin

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Photoreceptor function in heterozygotes with insertion or deletion mutations in the RDS gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The components of the retinal action potential in mammals and their relation to the discharge in the optic nerve

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of peripherin/rds in the disk membranes of cone and rod photoreceptors: relationship to disk membrane morphogenesis and retinal degeneration

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural and developmental analysis of the mouse peripherin/rds gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recovery phase of the murine rod photoresponse reconstructed from electroretinographic recordings

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A sequence upstream of the mouse blue visual pigment gene directs blue cone-specific transgene expression in mouse retinas

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amplification and kinetics of the activation steps in phototransduction

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of ERG a-wave amplification and kinetics in terms of the G-protein cascade of phototransduction.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential effect of the rd mutation on rods and cones in the mouse retina

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinal receptors in rodents maximally sensitive to ultraviolet light

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional consequences of oncogene-induced photoreceptor degeneration in transgenic mice

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical Features of a Previously Undescribed Codon 216 (proline to serine) Mutation in the Peripherin/Retinal Degeneration Slow Gene in Autosomal Dominant Retinitis Pigmentosa

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unique topographic separation of two spectral classes of cones in the mouse retina

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rod phototransduction in retinitis pigmentosa. Distinguishing alternative mechanisms of degeneration.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete rescue of photoreceptor dysplasia and degeneration in transgenic retinal degeneration slow (rds) mice

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morphological and Physiological Consequences of the Selective Elimination of Rod Photoreceptors in Transgenic Mice

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rod phototransduction in retinitis pigmentosa: estimation and interpretation of parameters derived from the rod a-wave.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Circadian photoreception in the retinally degenerate mouse (rd/rd)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9334387

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1523/JNEUROSCI.17-21-08118.1997

1 reference

stated in

Europe PubMed Central

PMC publication ID

6573736

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9334387%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 November 2019

PMC publication ID

6573736

1 reference

stated in

Europe PubMed Central

PMC publication ID

6573736

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9334387%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 November 2019

PubMed publication ID

9334387

1 reference

stated in

Europe PubMed Central

PMC publication ID

6573736

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9334387%20AND%20SRC:MED&resulttype=core&format=json

retrieved

6 November 2019

 

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