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Results: 1 to 20 of 303

1.

Transgenic zebrafish expressing mutant human RETGC-1 exhibit aberrant cone and rod morphology.

Collery RF, Cederlund ML, Kennedy BN.

Exp Eye Res. 2013 Mar;108:120-8. doi: 10.1016/j.exer.2013.01.003. Epub 2013 Jan 15.

PMID:
23328348
[PubMed - indexed for MEDLINE]
2.

Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophy.

Kelsell RE, Gregory-Evans K, Payne AM, Perrault I, Kaplan J, Yang RB, Garbers DL, Bird AC, Moore AT, Hunt DM.

Hum Mol Genet. 1998 Jul;7(7):1179-84.

PMID:
9618177
[PubMed - indexed for MEDLINE]
Free Article
3.

Biochemical analysis of a dimerization domain mutation in RetGC-1 associated with dominant cone-rod dystrophy.

Tucker CL, Woodcock SC, Kelsell RE, Ramamurthy V, Hunt DM, Hurley JB.

Proc Natl Acad Sci U S A. 1999 Aug 3;96(16):9039-44.

PMID:
10430891
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Cone survival despite rod degeneration in XOPS-mCFP transgenic zebrafish.

Morris AC, Schroeter EH, Bilotta J, Wong RO, Fadool JM.

Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4762-71.

PMID:
16303977
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Identification of a zebrafish cone photoreceptor-specific promoter and genetic rescue of achromatopsia in the nof mutant.

Kennedy BN, Alvarez Y, Brockerhoff SE, Stearns GW, Sapetto-Rebow B, Taylor MR, Hurley JB.

Invest Ophthalmol Vis Sci. 2007 Feb;48(2):522-9.

PMID:
17251445
[PubMed - indexed for MEDLINE]
Free Article
6.

A mutation in ZNF513, a putative regulator of photoreceptor development, causes autosomal-recessive retinitis pigmentosa.

Li L, Nakaya N, Chavali VR, Ma Z, Jiao X, Sieving PA, Riazuddin S, Tomarev SI, Ayyagari R, Riazuddin SA, Hejtmancik JF.

Am J Hum Genet. 2010 Sep 10;87(3):400-9. doi: 10.1016/j.ajhg.2010.08.003.

PMID:
20797688
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Predominant rod photoreceptor degeneration in Leber congenital amaurosis.

van der Spuy J, Munro PM, Luthert PJ, Preising MN, Bek T, Heegaard S, Cheetham ME.

Mol Vis. 2005 Jul 22;11:542-53.

PMID:
16052170
[PubMed - indexed for MEDLINE]
Free Article
8.

A Pro23His mutation alters prenatal rod photoreceptor morphology in a transgenic swine model of retinitis pigmentosa.

Scott PA, Fernandez de Castro JP, Kaplan HJ, McCall MA.

Invest Ophthalmol Vis Sci. 2014 Apr 28;55(4):2452-9. doi: 10.1167/iovs.13-13723.

PMID:
24618321
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

A 221-bp fragment of the mouse opsin promoter directs expression specifically to the rod photoreceptors of transgenic mice.

Quiambao AB, Peachey NS, Mangini NJ, Röhlich P, Hollyfield JG, al-Ubaidi MR.

Vis Neurosci. 1997 Jul-Aug;14(4):617-25.

PMID:
9278991
[PubMed - indexed for MEDLINE]
10.

Loss of cone molecular markers in rhodopsin-mutant human retinas with retinitis pigmentosa.

John SK, Smith JE, Aguirre GD, Milam AH.

Mol Vis. 2000 Nov 3;6:204-15.

PMID:
11063754
[PubMed - indexed for MEDLINE]
Free Article
11.

PRE-1, a cis element sufficient to enhance cone- and rod- specific expression in differentiating zebrafish photoreceptors.

Morrissey ME, Shelton S, Brockerhoff SE, Hurley JB, Kennedy BN.

BMC Dev Biol. 2011 Jan 24;11:3. doi: 10.1186/1471-213X-11-3.

PMID:
21261954
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Constitutive activation of photoreceptor guanylate cyclase by Y99C mutant of GCAP-1. Possible role in causing human autosomal dominant cone degeneration.

Dizhoor AM, Boikov SG, Olshevskaya EV.

J Biol Chem. 1998 Jul 10;273(28):17311-4.

PMID:
9651312
[PubMed - indexed for MEDLINE]
Free Article
13.

Double cone dystrophy and RPE degeneration in the retina of the zebrafish gnn mutant.

Biehlmaier O, Neuhauss SC, Kohler K.

Invest Ophthalmol Vis Sci. 2003 Mar;44(3):1287-98.

PMID:
12601061
[PubMed - indexed for MEDLINE]
Free Article
14.

Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy.

Roosing S, Lamers IJ, de Vrieze E, van den Born LI, Lambertus S, Arts HH; POC1B Study Group, Peters TA, Hoyng CB, Kremer H, Hetterschijt L, Letteboer SJ, van Wijk E, Roepman R, den Hollander AI, Cremers FP.

Am J Hum Genet. 2014 Aug 7;95(2):131-42. doi: 10.1016/j.ajhg.2014.06.012. Epub 2014 Jul 10.

PMID:
25018096
[PubMed - indexed for MEDLINE]
Free Article
15.

Controlled rod cell ablation in transgenic Xenopus laevis.

Hamm LM, Tam BM, Moritz OL.

Invest Ophthalmol Vis Sci. 2009 Feb;50(2):885-92. doi: 10.1167/iovs.08-2337. Epub 2008 Oct 3.

PMID:
18836175
[PubMed - indexed for MEDLINE]
Free Article
16.

Slow-progressing photoreceptor cell degeneration in night blindness c mutant zebrafish.

Maaswinkel H, Ren JQ, Li L.

J Neurocytol. 2003 Nov;32(9):1107-16.

PMID:
15044842
[PubMed - indexed for MEDLINE]
17.

Age-related cone abnormalities in zebrafish with genetic lesions in sonic hedgehog.

Stenkamp DL, Satterfield R, Muhunthan K, Sherpa T, Vihtelic TS, Cameron DA.

Invest Ophthalmol Vis Sci. 2008 Oct;49(10):4631-40. doi: 10.1167/iovs.07-1224. Epub 2008 May 23.

PMID:
18502998
[PubMed - indexed for MEDLINE]
Free PMC Article
18.
19.

Retinal degeneration in cone photoreceptor cell-ablated transgenic mice.

Ying S, Jansen HT, Lehman MN, Fong SL, Kao WW.

Mol Vis. 2000 Jun 24;6:101-8.

PMID:
10869099
[PubMed - indexed for MEDLINE]
Free Article
20.

myosin 7aa(-/-) mutant zebrafish show mild photoreceptor degeneration and reduced electroretinographic responses.

Wasfy MM, Matsui JI, Miller J, Dowling JE, Perkins BD.

Exp Eye Res. 2014 May;122:65-76. doi: 10.1016/j.exer.2014.03.007. Epub 2014 Apr 1.

PMID:
24698764
[PubMed - indexed for MEDLINE]

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