Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
1996 1
1998 1
2008 3
2010 1
2014 1
2019 1
2020 1
2021 1
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

11 results

Results by year

Filters applied: . Clear all
Page 1
A study of unusual Rayleigh matches in deutan deficiency.
Barbur JL, Rodriguez-Carmona M, Harlow JA, Mancuso K, Neitz J, Neitz M. Barbur JL, et al. Vis Neurosci. 2008 May-Jun;25(3):507-16. doi: 10.1017/S0952523808080619. Vis Neurosci. 2008. PMID: 18598426 Free PMC article.
The Rayleigh match model predicted accurately the midpoint and the range for the spectral differences specified by the genes. The prediction also required plausible selection of effective optical density of the cone pigments and noise. ...
The Rayleigh match model predicted accurately the midpoint and the range for the spectral differences specified by the genes. The …
Color discrimination in anomalous trichromacy: Experiment and theory.
Boehm AE, Bosten J, MacLeod DIA. Boehm AE, et al. Vision Res. 2021 Nov;188:85-95. doi: 10.1016/j.visres.2021.05.011. Epub 2021 Jul 20. Vision Res. 2021. PMID: 34293614 Free article.
We examined cases where chromatic pedestals impair the color discrimination of normal trichromatic observers. As predicted, anomalous observers experienced less impairment than normal trichromats, though they remained less sensitive than normal trichromats. ...
We examined cases where chromatic pedestals impair the color discrimination of normal trichromatic observers. As predicted, anomalous …
Compensation for red-green contrast loss in anomalous trichromats.
Boehm AE, MacLeod DI, Bosten JM. Boehm AE, et al. J Vis. 2014 Nov 20;14(13):19. doi: 10.1167/14.13.19. J Vis. 2014. PMID: 25413625 Free PMC article.
Thus, the contraction along the L/(L + M) axis shown in the perceptual color spaces of anomalous trichromats is far smaller than predicted by their reduced sensitivity, suggesting that an adaptive adjustment of postreceptoral gain may magnify the cone signals of anomalous …
Thus, the contraction along the L/(L + M) axis shown in the perceptual color spaces of anomalous trichromats is far smaller than predicte
Empirical tests of the effectiveness of EnChroma multi-notch filters for enhancing color vision in deuteranomaly.
Somers LP, Franklin A, Bosten JM. Somers LP, et al. Vision Res. 2024 May;218:108390. doi: 10.1016/j.visres.2024.108390. Epub 2024 Mar 25. Vision Res. 2024. PMID: 38531192 Free article.
Informed by a model of anomalous trichromatic color vision, we selected stimuli predicted to reveal the effects of EnChroma filters. Using these stimuli, we tested the ability of EnChroma filters to enhance color vision for 10 deuteranomalous trichromats in three experimen …
Informed by a model of anomalous trichromatic color vision, we selected stimuli predicted to reveal the effects of EnChroma filters. …
Molecular basis of abnormal red-green color vision: a family with three types of color vision defects.
Drummond-Borg M, Deeb S, Motulsky AG. Drummond-Borg M, et al. Am J Hum Genet. 1988 Nov;43(5):675-83. Am J Hum Genet. 1988. PMID: 2847528 Free PMC article.
Currently used molecular methodology is not sufficiently sensitive to define these fusion points accurately, and the specific color-vision defect within the deutan or protan class cannot be predicted. The DNA patterns for color-vision genes of female heterozygotes have not …
Currently used molecular methodology is not sufficiently sensitive to define these fusion points accurately, and the specific color-vision d …
Severity of color vision defects: electroretinographic (ERG), molecular and behavioral studies.
Crognale MA, Teller DY, Motulsky AG, Deeb SS. Crognale MA, et al. Vision Res. 1998 Nov;38(21):3377-85. doi: 10.1016/s0042-6989(97)00425-2. Vision Res. 1998. PMID: 9893852 Free article.
Earlier research on phenotype/genotype relationships in color vision has shown imperfect predictability of color matching from the photopigment spectral sensitivities inferred from molecular genetic analysis. ...
Earlier research on phenotype/genotype relationships in color vision has shown imperfect predictability of color matching from the ph …
Protanomaly without darkened red is deuteranopia with rods.
Shevell SK, Sun Y, Neitz M. Shevell SK, et al. Vision Res. 2008 Nov;48(26):2599-603. doi: 10.1016/j.visres.2008.03.001. Epub 2008 Apr 18. Vision Res. 2008. PMID: 18423511 Free PMC article.
We recently had the opportunity to conduct genetic and psychophysical tests on such an observer. Genetic results predict he is a deuteranope. His Rayleigh match is consistent with L cones and a contribution from rods. ...
We recently had the opportunity to conduct genetic and psychophysical tests on such an observer. Genetic results predict he is a deut …
Visual pigment gene structure and the severity of color vision defects.
Neitz J, Neitz M, Kainz PM. Neitz J, et al. Science. 1996 Nov 1;274(5288):801-4. doi: 10.1126/science.274.5288.801. Science. 1996. PMID: 8864125
An examination of specific photopigment gene sites responsible for tuning photopigment absorption spectra revealed differences that predict these variations in the color defect. The results indicate that the severity of the defect in deuteranomalous color vision depends on …
An examination of specific photopigment gene sites responsible for tuning photopigment absorption spectra revealed differences that predi
Rayleigh matches in carriers of inherited color vision defects: the contribution from the third L/M photopigment.
Sun Y, Shevell SK. Sun Y, et al. Vis Neurosci. 2008 May-Jun;25(3):455-62. doi: 10.1017/S0952523808080346. Vis Neurosci. 2008. PMID: 18598418
The model showed that differences in Rayleigh matches among carriers can be due to individual differences in the number of the third type of L/M cone, and the spectral sensitivity peak and optical density of the third L/M pigment; surprisingly, however, individual differences in …
The model showed that differences in Rayleigh matches among carriers can be due to individual differences in the number of the third type of …
11 results