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OPN1LW gene

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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2020
Review
2020
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
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
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
  • 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
Mutations in the OPN1LW (L‐) and OPN1MW (M‐)cone opsin genes underlie a spectrum of cone photoreceptor defects from stationary… Expand
Highly Cited
2012
Highly Cited
2012
PURPOSE To evaluate retinal structure and photoreceptor mosaic integrity in subjects with OPN1LW and OPN1MW mutations. METHODS… Expand
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2011
2011
PURPOSE. To characterize anatomically and functionally the retinal degeneration observed in a transgenic mouse line (OPN1LW-EGFP… Expand
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2008
2008
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
Trichromatic color vision in humans results from the combination of red, green, and blue photopigment opsins. Although color… Expand
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