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OPN1LW gene
Known as:
OPN1LW
, RED CONE PIGMENT
, OPSIN 1, LONG-WAVE-SENSITIVE
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National Institutes of Health
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Related topics
Related topics
2 relations
Color Blindness, Red
OPN1MW 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
Shari R. Atilano
,
M. C. Kenney
,
A. D. Briscoe
,
K. Jameson
Molecular vision
2020
Corpus ID: 212739364
Purpose To present a detailed, reliable long range-PCR and sequencing (LR-PCR-Seq) procedure to identify human opsin gene…
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2016
2016
De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy
Elena Buena-Atienza
,
K. Rüther
,
+20 authors
B. Wissinger
Scientific reports
2016
Corpus ID: 4915920
X-linked cone dysfunction disorders such as Blue Cone Monochromacy and X-linked Cone Dystrophy are characterized by complete loss…
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2016
2016
Cone Photoreceptor Structure in Patients With X-Linked Cone Dysfunction and Red-Green Color Vision Deficiency
Emily J. Patterson
,
M. Wilk
,
+18 authors
J. Carroll
Investigative ophthalmology & visual science
2016
Corpus ID: 6811548
Purpose Mutations in the coding sequence of the L and M opsin genes are often associated with X-linked cone dysfunction (such as…
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2015
2015
Unique Variants in OPN1LW Cause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1.
Jiali Li
,
Bei Gao
,
+10 authors
Qingjiong 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…
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2014
2014
Three Different Cone Opsin Gene Array Mutational Mechanisms with Genotype–Phenotype Correlation and Functional Investigation of Cone Opsin Variants
J. C. Gardner
,
G. Liew
,
+16 authors
A. Hardcastle
Human mutation
2014
Corpus ID: 9021978
Mutations in the OPN1LW (L‐) and OPN1MW (M‐)cone opsin genes underlie a spectrum of cone photoreceptor defects from stationary…
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2013
2013
Exon 3 genotypes of OPN1LW/OPN1MW associated with X-linked congenital cone dysfunction
S. Kohl
,
B. Baumann
,
+6 authors
B. Wissinger
2013
Corpus ID: 82548841
Highly Cited
2012
Highly Cited
2012
The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic.
J. Carroll
,
A. Dubra
,
+17 authors
M. Michaelides
Investigative ophthalmology & visual science
2012
Corpus ID: 15367264
PURPOSE To evaluate retinal structure and photoreceptor mosaic integrity in subjects with OPN1LW and OPN1MW mutations. METHODS…
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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.
D. Lipiński
,
Mohammed Yusuf
,
+7 authors
R. MacLaren
Investigative ophthalmology & visual science
2011
Corpus ID: 9520511
PURPOSE. To characterize anatomically and functionally the retinal degeneration observed in a transgenic mouse line (OPN1LW-EGFP…
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2008
2008
Different selective pressures shape the molecular evolution of color vision in chimpanzee and human populations.
B. Verrelli
,
Cecil M. Lewis
,
A. Stone
,
G. Perry
Molecular biology and evolution
2008
Corpus ID: 11949364
A population genetic analysis of the long-wavelength opsin (OPN1LW, "red") color vision gene in a global sample of 236 human…
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Highly Cited
2004
Highly Cited
2004
Signatures of selection and gene conversion associated with human color vision variation.
B. Verrelli
,
S. Tishkoff
American journal of human genetics
2004
Corpus ID: 35760796
Trichromatic color vision in humans results from the combination of red, green, and blue photopigment opsins. Although color…
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