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Items: 1 to 20 of 96

1.

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

Carroll J, Baraas RC, Wagner-Schuman M, Rha J, Siebe CA, Sloan C, Tait DM, Thompson S, Morgan JI, Neitz J, Williams DR, Foster DH, Neitz M.

Proc Natl Acad Sci U S A. 2009 Dec 8;106(49):20948-53. doi: 10.1073/pnas.0910128106. Epub 2009 Nov 23.

2.

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

Wagner-Schuman M, Neitz J, Rha J, Williams DR, Neitz M, Carroll J.

Vision Res. 2010 Nov 23;50(23):2396-402. doi: 10.1016/j.visres.2010.09.015. Epub 2010 Sep 17.

3.

Cone Photoreceptor Structure in Patients With X-Linked Cone Dysfunction and Red-Green Color Vision Deficiency.

Patterson EJ, Wilk M, Langlo CS, Kasilian M, Ring M, Hufnagel RB, Dubis AM, Tee JJ, Kalitzeos A, Gardner JC, Ahmed ZM, Sisk RA, Larsen M, Sjoberg S, Connor TB, Dubra A, Neitz J, Hardcastle AJ, Neitz M, Michaelides M, Carroll J.

Invest Ophthalmol Vis Sci. 2016 Jul 1;57(8):3853-63. doi: 10.1167/iovs.16-19608.

4.

The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic.

Carroll J, Dubra A, Gardner JC, Mizrahi-Meissonnier L, Cooper RF, Dubis AM, Nordgren R, Genead M, Connor TB Jr, Stepien KE, Sharon D, Hunt DM, Banin E, Hardcastle AJ, Moore AT, Williams DR, Fishman G, Neitz J, Neitz M, Michaelides M.

Invest Ophthalmol Vis Sci. 2012 Dec 5;53(13):8006-15. doi: 10.1167/iovs.12-11087.

5.

Three different cone opsin gene array mutational mechanisms with genotype-phenotype correlation and functional investigation of cone opsin variants.

Gardner JC, Liew G, Quan YH, Ermetal B, Ueyama H, Davidson AE, Schwarz N, Kanuga N, Chana R, Maher ER, Webster AR, Holder GE, Robson AG, Cheetham ME, Liebelt J, Ruddle JB, Moore AT, Michaelides M, Hardcastle AJ.

Hum Mutat. 2014 Nov;35(11):1354-62. doi: 10.1002/humu.22679.

6.

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.

7.

Deletion of the X-linked opsin gene array locus control region (LCR) results in disruption of the cone mosaic.

Carroll J, Rossi EA, Porter J, Neitz J, Roorda A, Williams DR, Neitz M.

Vision Res. 2010 Sep 15;50(19):1989-99. doi: 10.1016/j.visres.2010.07.009. Epub 2010 Jul 16.

8.

X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene.

McClements M, Davies WI, Michaelides M, Carroll J, Rha J, Mollon JD, Neitz M, MacLaren RE, Moore AT, Hunt DM.

Vision Res. 2013 Mar 22;80:41-50. doi: 10.1016/j.visres.2012.12.012. Epub 2013 Jan 18.

9.

Variable retinal phenotypes caused by mutations in the X-linked photopigment gene array.

Mizrahi-Meissonnier L, Merin S, Banin E, Sharon D.

Invest Ophthalmol Vis Sci. 2010 Aug;51(8):3884-92. doi: 10.1167/iovs.09-4592. Epub 2010 Mar 10.

PMID:
20220053
10.
11.

Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis.

Zhang T, Zhang N, Baehr W, Fu Y.

Proc Natl Acad Sci U S A. 2011 May 24;108(21):8879-84. doi: 10.1073/pnas.1017127108. Epub 2011 May 9.

12.

Cone opsins, colour blindness and cone dystrophy: Genotype-phenotype correlations.

Gardner JC, Michaelides M, Hardcastle AJ.

S Afr Med J. 2016 May 25;106(6 Suppl 1):S75-8. doi: 10.7196/SAMJ.2016.v106i6.11001.

PMID:
27245533
13.

Peripherin-2 differentially interacts with cone opsins in outer segments of cone photoreceptors.

Nguyen ON, Böhm S, Gießl A, Butz ES, Wolfrum U, Brandstätter JH, Wahl-Schott C, Biel M, Becirovic E.

Hum Mol Genet. 2016 Jun 15;25(12):2367-2377. Epub 2016 Mar 30.

PMID:
27033727
14.

Integrity of the cone photoreceptor mosaic in oligocone trichromacy.

Michaelides M, Rha J, Dees EW, Baraas RC, Wagner-Schuman ML, Mollon JD, Dubis AM, Andersen MK, Rosenberg T, Larsen M, Moore AT, Carroll J.

Invest Ophthalmol Vis Sci. 2011 Jul 1;52(7):4757-64. doi: 10.1167/iovs.10-6659.

15.

Retarded developmental expression and patterning of retinal cone opsins in hypothyroid mice.

Lu A, Ng L, Ma M, Kefas B, Davies TF, Hernandez A, Chan CC, Forrest D.

Endocrinology. 2009 Mar;150(3):1536-44. doi: 10.1210/en.2008-1092. Epub 2008 Oct 30.

16.

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. Epub 2010 Apr 3.

PMID:
20371244
17.

South American Weakly Electric Fish (Gymnotiformes) Are Long-Wavelength-Sensitive Cone Monochromats.

Liu DW, Lu Y, Yan HY, Zakon HH.

Brain Behav Evol. 2016;88(3-4):204-212. doi: 10.1159/000450746. Epub 2016 Nov 8.

PMID:
27820927
18.

The role of opsin expression and apoptosis in determination of cone types in human retina.

Cornish EE, Xiao M, Yang Z, Provis JM, Hendrickson AE.

Exp Eye Res. 2004 Jun;78(6):1143-54.

PMID:
15109921
19.

Protection of cone photoreceptor M-opsin degradation with 9-cis-β-carotene-rich alga Dunaliella bardawil in Rpe65(-/-) mouse retinal explant culture.

Ozaki T, Nakazawa M, Kudo T, Hirano S, Suzuki K, Ishiguro S.

Curr Eye Res. 2014 Dec;39(12):1221-31. doi: 10.3109/02713683.2014.907430. Epub 2014 Jul 9.

PMID:
25006880
20.

X-linked cone dysfunction syndrome with myopia and protanopia.

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

Ophthalmology. 2005 Aug;112(8):1448-54.

PMID:
15953640

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