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Items: 1 to 20 of 106

1.

The chemistry of John Dalton's color blindness.

Hunt DM, Dulai KS, Bowmaker JK, Mollon JD.

Science. 1995 Feb 17;267(5200):984-8.

PMID:
7863342
2.

Colour vision. Dalton's eyes and monkey genes.

Tovée MJ.

Curr Biol. 1995 Jun 1;5(6):583-6. Review.

3.

John dalton: though in error, he still influenced our understanding of congenital color deficiency.

Fishman GA.

Ophthalmic Genet. 2008 Dec;29(4):162-5. doi: 10.1080/13816810802251446.

PMID:
19005986
4.

John Dalton (1766-1844).

Emery AE.

J Med Genet. 1988 Jun;25(6):422-6.

5.
6.

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
7.

[Inherited colour vision deficiencies--from Dalton to molecular genetics].

Cvetković D, Cvetković D.

Srp Arh Celok Lek. 2005 Nov-Dec;133(11-12):521-7. Review. Serbian.

8.

[Final clarification of Goethe's findings in the examination of color blind patients].

Jaeger W.

Klin Monbl Augenheilkd. 1989 Dec;195(6):382-7. German.

PMID:
2695690
9.

Abnormal distribution of red/green cone opsins in a patient with an autosomal dominant cone dystrophy.

Bonilha VL, Hollyfield JG, Grover S, Fishman GA.

Ophthalmic Genet. 2005 Jun;26(2):69-76.

PMID:
16020309
10.

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
11.

A novel middle-wavelength opsin (M-opsin) null-mutation in the retinal cone dysfunction rat.

Xie B, Nakanishi S, Guo Q, Xia F, Yan G, An J, Li L, Serikawa T, Kuramoto T, Zhang Z.

Exp Eye Res. 2010 Jul;91(1):26-33. doi: 10.1016/j.exer.2010.03.017.

PMID:
20371244
12.

Severity of color vision defects: electroretinographic (ERG), molecular and behavioral studies.

Crognale MA, Teller DY, Motulsky AG, Deeb SS.

Vision Res. 1998 Nov;38(21):3377-85.

13.

Color vision and Frithiof Holmgren's discordant retinal microstimulation findings.

Norrsell U.

J Hist Neurosci. 2010 Jul;19(3):228-38. doi: 10.1080/09647040902997721.

PMID:
20628952
14.

The opsins of the vertebrate retina: insights from structural, biochemical, and evolutionary studies.

Nickle B, Robinson PR.

Cell Mol Life Sci. 2007 Nov;64(22):2917-32. Review.

PMID:
17726575
15.
16.

Is adding a new class of cones to the retina sufficient to cure color-blindness?

Cornelissen FW, Brenner E.

J Vis. 2015;15(13):22. doi: 10.1167/15.13.22.

PMID:
26418498
17.

The zebrafish ultraviolet cone opsin reported previously is expressed in rods.

Raymond PA, Barthel LK, Stenkamp DL.

Invest Ophthalmol Vis Sci. 1996 Apr;37(5):948-50.

PMID:
8603882
18.

A novel missense mutation in both OPN1LW and OPN1MW cone opsin genes causes X-linked cone dystrophy (XLCOD5).

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.

Adv Exp Med Biol. 2012;723:595-601. doi: 10.1007/978-1-4614-0631-0_76. No abstract available.

PMID:
22183383
19.

Modeling color percepts of dichromats.

Wachtler T, Dohrmann U, Hertel R.

Vision Res. 2004 Nov;44(24):2843-55.

20.

Opsin expression: new mechanism for modulating colour vision.

Cheng CL, Novales Flamarique I.

Nature. 2004 Mar 18;428(6980):279.

PMID:
15029185
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