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Your search keyword '"Color blindness -- Genetic aspects -- Research"' showing total 8 results
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8 results on '"Color blindness -- Genetic aspects -- Research"'

1. Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the α subunit of cone transducin (GNAT2). (Short Report)

Author

Aligianis, I.A., Forshew, T., Johnson, S., Michaelides, M., Johnson, C.A., Trembath, R.C., Hunt, D.M., Moore, A.T., and Maher, E.R.

Subjects
Consanguinity -- Research -- Health aspects -- Genetic aspects, Familial diseases -- Research -- Genetic aspects, Dysplasia -- Genetic aspects -- Research, Color blindness -- Genetic aspects -- Research, Pakistanis -- Health aspects -- Research, Medical genetics -- Research -- Health aspects, Chromosome mapping -- Research -- Health aspects -- Genetic aspects, Health
Abstract

Objective: To determine the molecular basis for achromatopsia using autozygosity mapping and positional candidate gene analysis. Design and methods: A large consanguineous Pakistani family containing six subjects with autosomal recessive [...]

Published
2002

2. Gene mutation for color blindness found

Subjects
Johns Hopkins University -- Research, Color blindness -- Genetic aspects -- Research, Heredity -- Observations -- Genetic aspects -- Research, Science and technology, Observations, Genetic aspects, Research
Abstract

In about 1775, a devastating typhoon swept over the island of Pingelap, a Pacific atoll that's now part of Micronesia. Twenty people survived the storm and subsequent famine to repopulate [...]

Published
2000

3. Tandem array of human visual pigment genes at Xq28

Author

Vollrath, Douglas, Nathans, Jeremy, and Davis, Ronald W.

Subjects
Color blindness -- Genetic aspects -- Research, Human genetics -- Research -- Genetic aspects, Chromosome mapping -- Research -- Genetic aspects, Science and technology, Genetic aspects, Research
Abstract

Tandem Array of Human Visual Pigment Genes at Xq28 COLOR BLINDNESS IS A COMMON trait in humans. Approximately 1 in 12 Caucasian males and 1 in 200 females are color-blind [...]

Published
1988

4. Molecular genetics of inherited variation in human color vision

Author

Nathans, Jeremy, Piantanida, Thomas P., Eddy, Roger L., Shows, Thomas B., and Hogness, David S.

Subjects
Color blindness -- Genetic aspects -- Research, Molecular biology -- Research -- Genetic aspects, Color vision -- Genetic aspects -- Research, Chromosome mapping -- Research -- Genetic aspects, Science and technology, Research, Genetic aspects
Abstract

Molecular Genetics of Inherited Variation in Human Color Vision MOST HUMANS CAN MATCH ANY COLOR EITHER BY COMbining three suitably chosen primary colors or by combining two primaries and adding [...]

Published
1986

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

Author

Nathans, Jeremy, Thomas, Darcy, and Hogness, David S.

Subjects
DNA -- Research -- Genetic aspects, Genetic research -- Research -- Genetic aspects, Color blindness -- Genetic aspects -- Research, Molecular biology -- Research -- Genetic aspects, Color vision -- Genetic aspects -- Research, Science and technology, Genetic aspects, Research
Abstract

Molecular Genetics of Human Color Vision: The Genes Encoding Blue, Green, and Red Pigments VISUAL PIGMENTS ARE THE LIGHT-ABSORBING MOLECULES that mediate vision. They consist of an apoprotein, opsin, that [...]

Published
1986

6. Molecular genetics of human blue cone monochromacy

Author

Nathans, Jeremy, Davenport, Carol M., Maumenee, Irene H., Lewis, Richard Alan, Hejtmancik, J. Fielding, Litt, Michael, Lovrien, Everett, Weleber, Richard, Bachynski, Brian, Zwas, Fred, Klingaman, Roger, and Fishman, Gerald

Subjects
Molecular genetics -- Research -- Genetic aspects, Genetic disorders -- Research -- Genetic aspects, Color blindness -- Genetic aspects -- Research, Chromosome deletion -- Research -- Genetic aspects, Science and technology, Research, Genetic aspects
Abstract

Molecular Genetics of Human Blue Cone Monochromacy NORMAL HUMAN COLOR VISION IS MEDIATED BY THREE types of photoreceptors called cones. One type is maximally sensitive at 565 nanometers (nm) (the [...]

Published
1989

7. New Eye Disorders Study Findings Recently Were Reported by Researchers at University of California (Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia)

Subjects
Color blindness -- Genetic aspects -- Research, Biochemistry, Medical research, Biological sciences, Health, University of California
Abstract

2015 JUL 28 (NewsRx) -- By a News Reporter-Staff News Editor at Life Science Weekly -- New research on Eye Disorders is the subject of a report. According to news [...]

Published
2015

8. The molecular biology of color vision

Author

Botstein, David

Subjects
Color blindness -- Genetic aspects -- Research, Molecular biology -- Research -- Genetic aspects, Color vision -- Genetic aspects -- Research, Science and technology, Genetic aspects, Research
Abstract

The Molecular Biology of Color Vision THERE ARE PROBABLY AS MANY REASONS TO DO SCIENCE AS there are scientists. Too often, the esthetic excitement of science is sacrificed to its [...]

Published
1986

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