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Items: 1 to 20 of 128

1.

Rod photoreceptor temporal properties in retinitis pigmentosa.

Wen Y, Locke KG, Hood DC, Birch DG.

Exp Eye Res. 2011 Mar;92(3):202-8. doi: 10.1016/j.exer.2010.12.014. Epub 2011 Jan 8.

2.
3.

Photoresponses of human rods in vivo derived from paired-flash electroretinograms.

Pepperberg DR, Birch DG, Hood DC.

Vis Neurosci. 1997 Jan-Feb;14(1):73-82.

PMID:
9057270
4.

Recovery of the rod photoresponse in infants.

Hansen RM, Fulton AB.

Invest Ophthalmol Vis Sci. 2005 Feb;46(2):764-8.

PMID:
15671311
5.

Cone and rod ERG phototransduction parameters in retinitis pigmentosa.

Tzekov RT, Locke KG, Hood DC, Birch DG.

Invest Ophthalmol Vis Sci. 2003 Sep;44(9):3993-4000.

PMID:
12939320
6.

Molecular screening of rhodopsin and peripherin/RDS genes in Mexican families with autosomal dominant retinitis pigmentosa.

Matias-Florentino M, Ayala-Ramirez R, Graue-Wiechers F, Zenteno JC.

Curr Eye Res. 2009 Dec;34(12):1050-6. doi: 10.3109/02713680903283169.

PMID:
19958124
7.

RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function.

Kemp CM, Jacobson SG, Cideciyan AV, Kimura AE, Sheffield VC, Stone EM.

Invest Ophthalmol Vis Sci. 1994 Jul;35(8):3154-62.

PMID:
8045710
8.

Genetic supplementation of RDS alleviates a loss-of-function phenotype in C214S model of retinitis pigmentosa.

Nour M, Fliesler SJ, Naash MI.

Adv Exp Med Biol. 2008;613:129-38. doi: 10.1007/978-0-387-74904-4_14. No abstract available.

9.

Rod phototransduction in retinitis pigmentosa. Distinguishing alternative mechanisms of degeneration.

Shady S, Hood DC, Birch DG.

Invest Ophthalmol Vis Sci. 1995 May;36(6):1027-37.

PMID:
7730012
10.

Autosomal dominant retinitis pigmentosa in Norway: a 20-year clinical follow-up study with molecular genetic analysis. Two novel rhodopsin mutations: 1003delG and I179F.

Grøndahl J, Riise R, Heiberg A, Leren T, Christoffersen T, Bragadottir R.

Acta Ophthalmol Scand. 2007 May;85(3):287-97.

11.

Rod photoreceptor neurite sprouting in retinitis pigmentosa.

Li ZY, Kljavin IJ, Milam AH.

J Neurosci. 1995 Aug;15(8):5429-38.

12.

Dark adaptation of rod photoreceptors in normal subjects, and in patients with Stargardt disease and an ABCA4 mutation.

Kang Derwent JJ, Derlacki DJ, Hetling JR, Fishman GA, Birch DG, Grover S, Stone EM, Pepperberg DR.

Invest Ophthalmol Vis Sci. 2004 Jul;45(7):2447-56.

PMID:
15223829
13.

A common microRNA signature in mouse models of retinal degeneration.

Loscher CJ, Hokamp K, Wilson JH, Li T, Humphries P, Farrar GJ, Palfi A.

Exp Eye Res. 2008 Dec;87(6):529-34. doi: 10.1016/j.exer.2008.08.016. Epub 2008 Sep 13.

14.
15.

Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS.

Ekström U, Ponjavic V, Abrahamson M, Nilsson-Ehle P, Andrëasson S, Stenström I, Ehinger B.

Ophthalmic Genet. 1998 Mar;19(1):27-37.

PMID:
9587927
16.

[A molecular biological study on retinitis pigmentosa].

Nakazawa M.

Nippon Ganka Gakkai Zasshi. 1993 Dec;97(12):1394-405. Review. Japanese.

PMID:
7904791
17.

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.

18.

Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies.

Sohocki MM, Daiger SP, Bowne SJ, Rodriquez JA, Northrup H, Heckenlively JR, Birch DG, Mintz-Hittner H, Ruiz RS, Lewis RA, Saperstein DA, Sullivan LS.

Hum Mutat. 2001;17(1):42-51.

19.

Toward a unified model of vertebrate rod phototransduction.

Hamer RD, Nicholas SC, Tranchina D, Lamb TD, Jarvinen JL.

Vis Neurosci. 2005 Jul-Aug;22(4):417-36.

20.

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.

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