Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 103

1.

Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficiencies.

Metlapally R, Michaelides M, Bulusu A, Li YJ, Schwartz M, Rosenberg T, Hunt DM, Moore AT, Züchner S, Rickman CB, Young TL.

Invest Ophthalmol Vis Sci. 2009 Apr;50(4):1552-8. doi: 10.1167/iovs.08-2455. Epub 2008 Dec 20.

PMID:
19098318
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

X-linked high myopia associated with cone dysfunction.

Young TL, Deeb SS, Ronan SM, Dewan AT, Alvear AB, Scavello GS, Paluru PC, Brott MS, Hayashi T, Holleschau AM, Benegas N, Schwartz M, Atwood LD, Oetting WS, Rosenberg T, Motulsky AG, King RA.

Arch Ophthalmol. 2004 Jun;122(6):897-908.

PMID:
15197065
[PubMed - indexed for MEDLINE]
3.

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
[PubMed - indexed for MEDLINE]
4.

Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy.

McClements M, Davies WI, Michaelides M, Young T, Neitz M, MacLaren RE, Moore AT, Hunt DM.

Invest Ophthalmol Vis Sci. 2013 Feb 15;54(2):1361-9. doi: 10.1167/iovs.12-11156.

PMID:
23322568
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

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.

PMID:
20579627
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Blue cone monochromatism: clinical findings in patients with mutations in the red/green opsin gene cluster.

Kellner U, Wissinger B, Tippmann S, Kohl S, Kraus H, Foerster MH.

Graefes Arch Clin Exp Ophthalmol. 2004 Sep;242(9):729-35.

PMID:
15069569
[PubMed - indexed for MEDLINE]
7.

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
[PubMed - indexed for MEDLINE]
Free Article
8.

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.

PMID:
20854834
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

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.

PMID:
23337435
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing.

Ratnamala U, Lyle R, Rawal R, Singh R, Vishnupriya S, Himabindu P, Rao V, Aggarwal S, Paluru P, Bartoloni L, Young TL, Paoloni-Giacobino A, Morris MA, Nath SK, Antonarakis SE, Radhakrishna U.

Invest Ophthalmol Vis Sci. 2011 Aug 29;52(9):6814-9. doi: 10.1167/iovs.10-6815. Erratum in: Invest Ophthalmol Vis Sci. 2011 Oct;52(11):7909.

PMID:
21357393
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Identification of a gene within the tandem array of red and green color pigment genes.

Hanna MC, Platts JT, Kirkness EF.

Genomics. 1997 Aug 1;43(3):384-6.

PMID:
9268643
[PubMed - indexed for MEDLINE]
12.

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
[PubMed - indexed for MEDLINE]
13.

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
[PubMed - indexed for MEDLINE]
14.

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.

PMID:
20638402
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

An insertion/deletion TEX28 polymorphism and its application to analysis of red/green visual pigment gene arrays.

Ueyama H, Torii R, Tanabe S, Oda S, Yamade S.

J Hum Genet. 2004;49(10):548-57. Epub 2004 Sep 17.

PMID:
15378397
[PubMed - indexed for MEDLINE]
16.

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
[PubMed - indexed for MEDLINE]
17.

A new mechanism in blue cone monochromatism.

Ladekjaer-Mikkelsen AS, Rosenberg T, Jørgensen AL.

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

PMID:
8792812
[PubMed - indexed for MEDLINE]
18.

Genotype-phenotype relationships in human red/green color-vision defects: molecular and psychophysical studies.

Deeb SS, Lindsey DT, Hibiya Y, Sanocki E, Winderickx J, Teller DY, Motulsky AG.

Am J Hum Genet. 1992 Oct;51(4):687-700.

PMID:
1415215
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

[X-linked blue cone monochromatism. A familial case report].

Coco Martín RM.

Arch Soc Esp Oftalmol. 2005 Jan;80(1):35-40. Spanish.

PMID:
15692892
[PubMed - indexed for MEDLINE]
Free Article
20.

Red, green, and red-green hybrid pigments in the human retina: correlations between deduced protein sequences and psychophysically measured spectral sensitivities.

Sharpe LT, Stockman A, Jägle H, Knau H, Klausen G, Reitner A, Nathans J.

J Neurosci. 1998 Dec 1;18(23):10053-69.

PMID:
9822760
[PubMed - indexed for MEDLINE]
Free Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk