Format
Sort by
Items per page

Send to

Choose Destination

Links from Gene

Items: 1 to 20 of 35

1.

X-linked cone dystrophy caused by mutation of the red and green cone opsins.

Gardner JC, Webb TR, Kanuga N, Robson AG, Holder GE, Stockman A, Ripamonti C, Ebenezer ND, Ogun O, Devery S, Wright GA, Maher ER, Cheetham ME, Moore AT, Michaelides M, Hardcastle AJ.

Am J Hum Genet. 2010 Jul 9;87(1):26-39. doi: 10.1016/j.ajhg.2010.05.019. Epub 2010 Jun 24.

2.

Blue cone monochromacy: causative mutations and associated phenotypes.

Gardner JC, Michaelides M, Holder GE, Kanuga N, Webb TR, Mollon JD, Moore AT, Hardcastle AJ.

Mol Vis. 2009;15:876-84. Epub 2009 May 1.

3.

The molecular basis of variation in human color vision.

Deeb SS.

Clin Genet. 2005 May;67(5):369-77. Review.

PMID:
15811001
4.

Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals.

Michaelides M, Johnson S, Simunovic MP, Bradshaw K, Holder G, Mollon JD, Moore AT, Hunt DM.

Eye (Lond). 2005 Jan;19(1):2-10.

PMID:
15094734
5.

[A genetic study of color blindness].

NEMOTO H, MURAO M.

Jinrui Idengaku Zasshi. 1961 Dec;6:165-73. Japanese. No abstract available.

PMID:
14479006
6.

THE X-LINKED RECESSIVE INHERITANCE OF ATYPICAL MONOCHROMATISM.

SPIVEY BE.

Arch Ophthalmol. 1965 Sep;74:327-33. No abstract available.

PMID:
14338644
7.

RECOMBINATION BETWEEN PROTAN AND DEUTAN GENES; DATA ON THEIR RELATIVE POSITONS IN RESPECT OF THE G6PD LOCUS.

SINISCALCO M, FILIPPI G, LATTE B.

Nature. 1964 Dec 12;204:1062-4. No abstract available.

PMID:
14243382
8.

Evaluation of the Tokyo Medical College Color Vision Test.

SLOAN LL.

Am J Ophthalmol. 1961 Nov;52:650-9. No abstract available.

PMID:
13913884
9.

The enigma of typical total monochromacy.

ALPERN M, FALLS HF, LEE GB.

Am J Ophthalmol. 1960 Nov;50:996-1012. No abstract available.

PMID:
13682677
10.

Spectral sensitivity in color-defective subjects and heterozygous carriers.

CRONE RA.

Am J Ophthalmol. 1959 Aug;48(2):231-8. No abstract available.

PMID:
13670291
11.

Two families with parents of different types of red-green blindness.

FRANCESCHETTI A, KLEIN D.

Acta Genet Stat Med. 1957;7(2):255-9. No abstract available.

PMID:
13469157
12.

A sign of manifest heterozygosity in carriers of color deficiency.

SCHMIDT I.

Am J Optom Arch Am Acad Optom. 1955 Aug;32(8):404-8. No abstract available.

PMID:
13238560
13.

Congenital achromatopsia; a report of 19 cases.

SLOAN LL.

J Opt Soc Am. 1954 Feb;44(2):117-28. No abstract available.

PMID:
13131176
14.

Novel missense mutations in red/green opsin genes in congenital color-vision deficiencies.

Ueyama H, Kuwayama S, Imai H, Tanabe S, Oda S, Nishida Y, Wada A, Shichida Y, Yamade S.

Biochem Biophys Res Commun. 2002 Jun 7;294(2):205-9.

PMID:
12051694
15.

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 1;11(1):23-32.

PMID:
11772996
16.

Is color vision deficiency an advantage under scotopic conditions?

Simunovic MP, Regan BC, Mollon JD.

Invest Ophthalmol Vis Sci. 2001 Dec;42(13):3357-64.

PMID:
11726645
17.

Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy.

Ayyagari R, Kakuk LE, Bingham EL, Szczesny JJ, Kemp J, Toda Y, Felius J, Sieving PA.

Hum Genet. 2000 Jul;107(1):75-82.

18.

A new mechanism in blue cone monochromatism.

Ladekjaer-Mikkelsen AS, Rosenberg T, Jørgensen AL.

Hum Genet. 1996 Oct;98(4):403-8.

PMID:
8792812
19.

Melatonin regulation in humans with color vision deficiencies.

Ruberg FL, Skene DJ, Hanifin JP, Rollag MD, English J, Arendt J, Brainard GC.

J Clin Endocrinol Metab. 1996 Aug;81(8):2980-5.

PMID:
8768862
20.

Gene conversion between red and defective green opsin gene in blue cone monochromacy.

Reyniers E, Van Thienen MN, Meire F, De Boulle K, Devries K, Kestelijn P, Willems PJ.

Genomics. 1995 Sep 20;29(2):323-8.

PMID:
8666378

Supplemental Content

Support Center