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Journal Abstract Search

685 related items for PubMed ID: 15811001

  • 1. The molecular basis of variation in human color vision.
    Deeb SS.
    Clin Genet; 2005 May; 67(5):369-77. PubMed ID: 15811001
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  • 6. Analysis of fusion gene and encoded photopigment of colour-blind humans.
    Neitz J, Neitz M, Jacobs GH.
    Nature; 1989 Dec 07; 342(6250):679-82. PubMed ID: 2574415
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  • 7. Polymorphism in the number of genes encoding long-wavelength-sensitive cone pigments among males with normal color vision.
    Neitz M, Neitz J, Grishok A.
    Vision Res; 1995 Sep 07; 35(17):2395-407. PubMed ID: 8594809
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  • 8. Polymorphism in red photopigment underlies variation in colour matching.
    Winderickx J, Lindsey DT, Sanocki E, Teller DY, Motulsky AG, Deeb SS.
    Nature; 1992 Apr 02; 356(6368):431-3. PubMed ID: 1557123
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  • 11. [Analysis of fusion points in hybrid genes and gene deletion for congenital red-green color vision defects].
    Shen H, Zhang Q, Xiao X, Li S, Guo L, Jiang F.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Oct 02; 16(5):290-2. PubMed ID: 10514533
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  • 12. The molecular basis of dichromatic color vision in males with multiple red and green visual pigment genes.
    Jagla WM, Jägle H, Hayashi T, Sharpe LT, Deeb SS.
    Hum Mol Genet; 2002 Jan 01; 11(1):23-32. PubMed ID: 11772996
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  • 13. [Genetics of congenital color vision defects. I. Common types of color blindness].
    Krawczyński MR.
    Klin Oczna; 1995 Jan 01; 97(1-2):34-8. PubMed ID: 7637311
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  • 16. Statistical and molecular analyses of evolutionary significance of red-green color vision and color blindness in vertebrates.
    Yokoyama S, Takenaka N.
    Mol Biol Evol; 2005 Apr 01; 22(4):968-75. PubMed ID: 15647522
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  • 17. Visual pigment gene changes in adrenoleukodystrophy.
    Sack GH, Morrell JC.
    Invest Ophthalmol Vis Sci; 1993 Aug 01; 34(9):2634-7. PubMed ID: 8344786
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  • 18. Analysis of L-cone/M-cone visual pigment gene arrays in Japanese males with protan color-vision deficiency.
    Ueyama H, Kuwayama S, Imai H, Oda S, Nishida Y, Tanabe S, Shichida Y, Yamade S.
    Vision Res; 2004 Aug 01; 44(19):2241-52. PubMed ID: 15208011
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  • 20. Rayleigh matches in carriers of inherited color vision defects: the contribution from the third L/M photopigment.
    Sun Y, Shevell SK.
    Vis Neurosci; 2008 Aug 01; 25(3):455-62. PubMed ID: 18598418
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