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OPN1LW gene

Known as: OPN1LW, RED CONE PIGMENT, OPSIN 1, LONG-WAVE-SENSITIVE 
 
National Institutes of Health

Related topics

Related topics

2 relations
Color Blindness, RedOPN1MW gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2020
Review
2020
A two-step method for identifying photopigment opsin and rhodopsin gene sequences underlying human color vision phenotypes
Purpose To present a detailed, reliable long range-PCR and sequencing (LR-PCR-Seq) procedure to identify human opsin gene… Expand
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2016
2016
De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy
X-linked cone dysfunction disorders such as Blue Cone Monochromacy and X-linked Cone Dystrophy are characterized by complete loss… Expand
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2016
2016
Cone Photoreceptor Structure in Patients With X-Linked Cone Dysfunction and Red-Green Color Vision Deficiency
Purpose Mutations in the coding sequence of the L and M opsin genes are often associated with X-linked cone dysfunction (such as… Expand
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2015
2015
Unique Variants in OPN1LW Cause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1.
  • J. Li, Bei Gao, +10 authors Q. Zhang
  • Investigative ophthalmology & visual science
  • 2015
    • Corpus ID: 25454749
PURPOSE MYP1 is a locus for X-linked syndromic and nonsyndromic high myopia. Recently, unique haplotypes in OPN1LW were found to… Expand
2014
2014
Three Different Cone Opsin Gene Array Mutational Mechanisms with Genotype–Phenotype Correlation and Functional Investigation of Cone Opsin Variants
Mutations in the OPN1LW (L‐) and OPN1MW (M‐)cone opsin genes underlie a spectrum of cone photoreceptor defects from stationary… Expand
2013
2013
Exon 3 genotypes of OPN1LW/OPN1MW associated with X-linked congenital cone dysfunction
 
Highly Cited
2012
Highly Cited
2012
The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic.
PURPOSE To evaluate retinal structure and photoreceptor mosaic integrity in subjects with OPN1LW and OPN1MW mutations. METHODS… Expand
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2011
2011
Characterization of a dominant cone degeneration in a green fluorescent protein-reporter mouse with disruption of Loci associated with human dominant retinal dystrophy.
PURPOSE. To characterize anatomically and functionally the retinal degeneration observed in a transgenic mouse line (OPN1LW-EGFP… Expand
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2008
2008
Different selective pressures shape the molecular evolution of color vision in chimpanzee and human populations.
A population genetic analysis of the long-wavelength opsin (OPN1LW, "red") color vision gene in a global sample of 236 human… Expand
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Highly Cited
2004
Highly Cited
2004
Signatures of selection and gene conversion associated with human color vision variation.
Trichromatic color vision in humans results from the combination of red, green, and blue photopigment opsins. Although color… Expand
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