Literature DB >> 7863325

Numbers and ratios of visual pigment genes for normal red-green color vision.

M Neitz1, J Neitz.   

Abstract

Red-green color vision is based on middle-wavelength- and long-wavelength-sensitive visual pigments encoded by an array of genes on the X chromosome. The numbers and ratios of genes in this cluster were reexamined in men with normal color vision by means of newly refined methods. These methods revealed that many men had more pigment genes on the X chromosome than had previously been suggested and that many had more than one long-wave pigment gene. These discoveries challenge accepted ideas that are the foundation for theories of normal and anomalous color vision.

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Year:  1995        PMID: 7863325     DOI: 10.1126/science.7863325

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  19 in total

Review 1.  New aspects of an old theme: the genetic basis of human color vision.

Authors:  B Wissinger; L T Sharpe
Journal:  Am J Hum Genet       Date:  1998-11       Impact factor: 11.025

2.  Evolution of multigene families by gene duplication. A haploid model.

Authors:  H Tachida; T Kuboyama
Journal:  Genetics       Date:  1998-08       Impact factor: 4.562

3.  Red, green, and red-green hybrid pigments in the human retina: correlations between deduced protein sequences and psychophysically measured spectral sensitivities.

Authors:  L T Sharpe; A Stockman; H Jägle; H Knau; G Klausen; A Reitner; J Nathans
Journal:  J Neurosci       Date:  1998-12-01       Impact factor: 6.167

Review 4.  Advances in understanding the molecular basis of the first steps in color vision.

Authors:  Lukas Hofmann; Krzysztof Palczewski
Journal:  Prog Retin Eye Res       Date:  2015-07-15       Impact factor: 21.198

Review 5.  The genetics of normal and defective color vision.

Authors:  Jay Neitz; Maureen Neitz
Journal:  Vision Res       Date:  2010-12-15       Impact factor: 1.886

6.  Global variation in copy number in the human genome.

Authors:  Richard Redon; Shumpei Ishikawa; Karen R Fitch; Lars Feuk; George H Perry; T Daniel Andrews; Heike Fiegler; Michael H Shapero; Andrew R Carson; Wenwei Chen; Eun Kyung Cho; Stephanie Dallaire; Jennifer L Freeman; Juan R González; Mònica Gratacòs; Jing Huang; Dimitrios Kalaitzopoulos; Daisuke Komura; Jeffrey R MacDonald; Christian R Marshall; Rui Mei; Lyndal Montgomery; Kunihiro Nishimura; Kohji Okamura; Fan Shen; Martin J Somerville; Joelle Tchinda; Armand Valsesia; Cara Woodwark; Fengtang Yang; Junjun Zhang; Tatiana Zerjal; Jane Zhang; Lluis Armengol; Donald F Conrad; Xavier Estivill; Chris Tyler-Smith; Nigel P Carter; Hiroyuki Aburatani; Charles Lee; Keith W Jones; Stephen W Scherer; Matthew E Hurles
Journal:  Nature       Date:  2006-11-23       Impact factor: 49.962

7.  Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy.

Authors:  Michelle McClements; Wayne I L Davies; Michel Michaelides; Terri Young; Maureen Neitz; Robert E MacLaren; Anthony T Moore; David M Hunt
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-02-15       Impact factor: 4.799

8.  X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene.

Authors:  Michelle McClements; Wayne I L Davies; Michel Michaelides; Joseph Carroll; Jungtae Rha; John D Mollon; Maureen Neitz; Robert E MacLaren; Anthony T Moore; David M Hunt
Journal:  Vision Res       Date:  2013-01-18       Impact factor: 1.886

Review 9.  Primate photopigments and primate color vision.

Authors:  G H Jacobs
Journal:  Proc Natl Acad Sci U S A       Date:  1996-01-23       Impact factor: 11.205

Review 10.  Genetic Variation, Comparative Genomics, and the Diagnosis of Disease.

Authors:  Evan E Eichler
Journal:  N Engl J Med       Date:  2019-07-04       Impact factor: 91.245

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