(Q35014281)

5 August 2017

title

Cone photoreceptor mosaic disruption associated with Cys203Arg mutation in the M-cone opsin (English)

1 reference

5 August 2017

main subject

photoreceptor protein

0 references

David R Williams

11

0 references

Summer Thompson

Summer Thompson

8

0 references

Rigmor C. Baraas

Rigmor C Baraas

2

0 references

David H. Foster

David H Foster

12

0 references

Maureen Neitz

13

Maureen Neitz

1 reference

5 August 2017

10

Jay Neitz

1 reference

5 August 2017

7

Diane M Tait

1 reference

5 August 2017

Joseph Carroll

1

1 reference

5 August 2017

Melissa Wagner-Schuman

3

1 reference

5 August 2017

Jungtae Rha

4

1 reference

5 August 2017

Cory A Siebe

5

1 reference

5 August 2017

Christina Sloan

6

1 reference

5 August 2017

Jessica I W Morgan

9

1 reference

5 August 2017

language of work or name

English

0 references

publication date

23 November 2009

1 reference

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

5 August 2017

published in

1 reference

5 August 2017

volume

106

1 reference

5 August 2017

issue

49

1 reference

5 August 2017

page(s)

20948-20953

1 reference

describes a project that uses

5 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2791574/fullTextXML

inferred from PubMed Central ID database lookup

cites work

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Gene therapy for red-green colour blindness in adult primates

8 July 2018

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Nucleotide polymorphisms upstream of the X-chromosome opsin gene array tune L:M cone ratio

8 July 2018

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A pyramid approach to subpixel registration based on intensity

8 July 2018

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Enhancing the signal-to-noise ratio in ophthalmic optical coherence tomography by image registration--method and clinical examples

8 July 2018

1 reference

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Human cone photoreceptor dependence on RPE65 isomerase

8 July 2018

1 reference

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Adaptive optics retinal imaging reveals S-cone dystrophy in tritan color-vision deficiency

8 July 2018

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

8 July 2018

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Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa

8 July 2018

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Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success

8 July 2018

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Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy

8 July 2018

1 reference

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Variety of genotypes in males diagnosed as dichromatic on a conventional clinical anomaloscope

8 July 2018

1 reference

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Characterization of a novel form of X-linked incomplete achromatopsia

8 July 2018

1 reference

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Functional photoreceptor loss revealed with adaptive optics: an alternate cause of color blindness

8 July 2018

1 reference

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Finding and interpreting genetic variations that are important to ophthalmologists

8 July 2018

1 reference

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An A-71C substitution in a green gene at the second position in the red/green visual-pigment gene array is associated with deutan color-vision deficiency

8 July 2018

1 reference

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GPCRDB information system for G protein-coupled receptors

8 July 2018

1 reference

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Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

Structure and function in rhodopsin: further elucidation of the role of the intradiscal cysteines, Cys-110, -185, and -187, in rhodopsin folding and function

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

Mutation of a conserved cysteine in the X-linked cone opsins causes color vision deficiencies by disrupting protein folding and stability

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsin

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

Molecular genetics of inherited variation in human color vision

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

Cysteine residues 110 and 187 are essential for the formation of correct structure in bovine rhodopsin

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

Molecular genetics of human color vision: the genes encoding blue, green, and red pigments

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

Molecular genetics of human blue cone monochromacy

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

Iso-orientation areas in the foveal cone mosaic.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

Genotype-phenotype relationships in human red/green color-vision defects: molecular and psychophysical studies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

Selective expression of human X chromosome-linked green opsin genes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

Defective colour vision associated with a missense mutation in the human green visual pigment gene

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

The molecular basis of dichromatic color vision in males with multiple red and green visual pigment genes

8 July 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0910128106

Analysis of L-cone/M-cone visual pigment gene arrays in Japanese males with protan color-vision deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0910128106

Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0910128106

Automated identification of cone photoreceptors in adaptive optics retinal images

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0910128106

Progressive cone dystrophy with deutan genotype and phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0910128106

Macular dystrophy with protan genotype and phenotype studied with cone type specific ERGs

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0910128106

X-linked cone dysfunction syndrome with myopia and protanopia

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0910128106

Estimates of L:M cone ratio from ERG flicker photometry and genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0910128106

Organization of the human trichromatic cone mosaic.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0910128106

Improvements on Littmann's method of determining the size of retinal features by fundus photography

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0910128106

[Analysis of rhodopsin and peripherin/RDS genes in Chinese patients with retinitis pigmentosa].

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

Selective cone dystrophy with protan genotype.

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791574

L-cone pigment genes expressed in normal colour vision

25 October 2018

1 reference

12 December 2020

Red, green, and red-green hybrid pigments in the human retina: correlations between deduced protein sequences and psychophysically measured spectral sensitivities

1 reference

12 December 2020

Visual pigment gene structure and the severity of color vision defects

1 reference

12 December 2020

Disruption of conserved rhodopsin disulfide bond by Cys187Tyr mutation causes early and severe autosomal dominant retinitis pigmentosa

1 reference

12 December 2020

Cone pigment gene expression in individual photoreceptors and the chromatic topography of the retina

1 reference

12 December 2020

An electroretinographic and molecular genetic study of X-linked cone degeneration

1 reference

12 December 2020

Trichromatic color vision with only two spectrally distinct photopigments

1 reference

12 December 2020

Visual pigment gene structure and expression in human retinae

1 reference

12 December 2020

Retinal microscotomas revealed with adaptive-optics microflashes

1 reference

12 December 2020

Variations in cone populations for red-green color vision examined by analysis of mRNA

1 reference

12 December 2020

Luminance noise and the rapid determination of discrimination ellipses in colour deficiency

1 reference

12 December 2020

Assessment of foveal cone photoreceptors in Stargardt's macular dystrophy using a small dot detection task

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.0910128106

1 reference

5 August 2017

0 references

1 reference

5 August 2017

1 reference