Literature DB >> 1386496

Human tritanopia associated with a third amino acid substitution in the blue-sensitive visual pigment.

C J Weitz, L N Went, J Nathans.   

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Year:  1992        PMID： 1386496      PMCID： PMC1682686     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  4 in total

1.  Lutropin-choriogonadotropin receptor: an unusual member of the G protein-coupled receptor family.

Authors:  K C McFarland; R Sprengel; H S Phillips; M Köhler; N Rosemblit; K Nikolics; D L Segaloff; P H Seeburg
Journal:  Science       Date:  1989-08-04       Impact factor: 47.728

2.  Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin.

Authors:  C J Weitz; Y Miyake; K Shinzato; E Montag; E Zrenner; L N Went; J Nathans
Journal:  Am J Hum Genet       Date:  1992-03       Impact factor: 11.025

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

Authors:  J Nathans; D Thomas; D S Hogness
Journal:  Science       Date:  1986-04-11       Impact factor: 47.728

4.  Color-vision mechanisms in the peripheral retinas of normal and dichromatic observers.

Authors:  B R Wooten; G Wald
Journal:  J Gen Physiol       Date:  1973-02       Impact factor: 4.086
  4 in total
  13 in total

Review 1.  Molecular genetics of human color vision.

Authors:  S S Deeb; A G Motulsky
Journal:  Behav Genet       Date:  1996-05       Impact factor: 2.805

Review 2.  Photoreceptor Cilia and Retinal Ciliopathies.

Authors:  Kinga M Bujakowska; Qin Liu; Eric A Pierce
Journal:  Cold Spring Harb Perspect Biol       Date:  2017-10-03       Impact factor: 10.005

Review 3.  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

4.  Adaptive optics retinal imaging: emerging clinical applications.

Authors:  Pooja Godara; Adam M Dubis; Austin Roorda; Jacque L Duncan; Joseph Carroll
Journal:  Optom Vis Sci       Date:  2010-12       Impact factor: 1.973

5.  Substitution of isoleucine for threonine at position 190 of S-opsin causes S-cone-function abnormalities.

Authors:  Rigmor C Baraas; Lene A Hagen; Elise W Dees; Maureen Neitz
Journal:  Vision Res       Date:  2012-09-26       Impact factor: 1.886

6.  Tritan color vision deficiency may be associated with an OPN1SW splicing defect and haploinsufficiency.

Authors:  Maureen Neitz; Elise D Krekling; Lene A Hagen; Hilde R Pedersen; Jessica Rowlan; Rachel Barborek; Jay Neitz; Adam Crain; Rigmor C Baraas
Journal:  J Opt Soc Am A Opt Image Sci Vis       Date:  2020-04-01       Impact factor: 2.129

Review 7.  Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.

Authors:  P J Rosenfeld; V A McKusick; J S Amberger; T P Dryja
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

Review 8.  The genetics of normal and defective color vision.

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

9.  A new form of inherited red-blindness identified in zebrafish.

Authors:  S E Brockerhoff; J B Hurley; G A Niemi; J E Dowling
Journal:  J Neurosci       Date:  1997-06-01       Impact factor: 6.167

10.  Discrimination thresholds of normal and anomalous trichromats: Model of senescent changes in ocular media density on the Cambridge Colour Test.

Authors:  Keizo Shinomori; Athanasios Panorgias; John S Werner
Journal:  J Opt Soc Am A Opt Image Sci Vis       Date:  2016-03       Impact factor: 2.129
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