Literature DB >> 8864125

Visual pigment gene structure and the severity of color vision defects.

J Neitz1, M Neitz, P M Kainz.   

Abstract

Rearrangements of the visual pigment genes are associated with defective color vision and with differences between types of red-green color blindness. Among individuals within the most common category of defective color vision, deuteranomaly, there is a large variation in the severity of color vision loss. 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 the degree of similarity among the residual photopigments that serve vision in the color-anomalous eye.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8864125     DOI: 10.1126/science.274.5288.801

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


  17 in total

1.  The L:M cone ratio in males of African descent with normal color vision.

Authors:  Carrie McMahon; Joseph Carroll; Stella Awua; Jay Neitz; Maureen Neitz
Journal:  J Vis       Date:  2008-02-20       Impact factor: 2.240

2.  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

3.  Compensation for red-green contrast loss in anomalous trichromats.

Authors:  A E Boehm; D I A MacLeod; J M Bosten
Journal:  J Vis       Date:  2014-11-20       Impact factor: 2.240

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.  Color-deficient cone mosaics associated with Xq28 opsin mutations: a stop codon versus gene deletions.

Authors:  Melissa Wagner-Schuman; Jay Neitz; Jungtae Rha; David R Williams; Maureen Neitz; Joseph Carroll
Journal:  Vision Res       Date:  2010-09-17       Impact factor: 1.886

7.  Variety of genotypes in males diagnosed as dichromatic on a conventional clinical anomaloscope.

Authors:  Maureen Neitz; Joseph Carroll; Agnes Renner; Holger Knau; John S Werner; Jay Neitz
Journal:  Vis Neurosci       Date:  2004 May-Jun       Impact factor: 3.241

8.  Cone photoreceptor mosaic disruption associated with Cys203Arg mutation in the M-cone opsin.

Authors:  Joseph Carroll; Rigmor C Baraas; Melissa Wagner-Schuman; Jungtae Rha; Cory A Siebe; Christina Sloan; Diane M Tait; Summer Thompson; Jessica I W Morgan; Jay Neitz; David R Williams; David H Foster; Maureen Neitz
Journal:  Proc Natl Acad Sci U S A       Date:  2009-11-23       Impact factor: 11.205

9.  A study of unusual Rayleigh matches in deutan deficiency.

Authors:  J L Barbur; M Rodriguez-Carmona; J A Harlow; K Mancuso; J Neitz; M Neitz
Journal:  Vis Neurosci       Date:  2008 May-Jun       Impact factor: 3.241

10.  Adaptive optics retinal imaging reveals S-cone dystrophy in tritan color-vision deficiency.

Authors:  Rigmor C Baraas; Joseph Carroll; Karen L Gunther; Mina Chung; David R Williams; David H Foster; Maureen Neitz
Journal:  J Opt Soc Am A Opt Image Sci Vis       Date:  2007-05       Impact factor: 2.129

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.