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Items: 1 to 20 of 261

1.

Severe retinal degeneration caused by a novel rhodopsin mutation.

Liu H, Wang M, Xia CH, Du X, Flannery JG, Ridge KD, Beutler B, Gong X.

Invest Ophthalmol Vis Sci. 2010 Feb;51(2):1059-65. doi: 10.1167/iovs.09-3585. Epub 2009 Sep 9.

2.

A monogenic dominant mutation in Rom1 generated by N-ethyl-N-nitrosourea mutagenesis causes retinal degeneration in mice.

Sato H, Suzuki T, Ikeda K, Masuya H, Sezutsu H, Kaneda H, Kobayashi K, Miura I, Kurihara Y, Yokokura S, Nishida K, Tamai M, Gondo Y, Noda T, Wakana S.

Mol Vis. 2010 Mar 10;16:378-91.

3.

An ENU-induced mutation in the Mertk gene (Mertknmf12) leads to a slow form of retinal degeneration.

Maddox DM, Hicks WL, Vollrath D, LaVail MM, Naggert JK, Nishina PM.

Invest Ophthalmol Vis Sci. 2011 Jul 1;52(7):4703-9. doi: 10.1167/iovs.10-7077.

4.

Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).

Pang JJ, Chang B, Hawes NL, Hurd RE, Davisson MT, Li J, Noorwez SM, Malhotra R, McDowell JH, Kaushal S, Hauswirth WW, Nusinowitz S, Thompson DA, Heckenlively JR.

Mol Vis. 2005 Feb 28;11:152-62.

5.

Photoreceptor degeneration, azoospermia, leukoencephalopathy, and abnormal RPE cell function in mice expressing an early stop mutation in CLCN2.

Edwards MM, Marín de Evsikova C, Collin GB, Gifford E, Wu J, Hicks WL, Whiting C, Varvel NH, Maphis N, Lamb BT, Naggert JK, Nishina PM, Peachey NS.

Invest Ophthalmol Vis Sci. 2010 Jun;51(6):3264-72. doi: 10.1167/iovs.09-4887. Epub 2010 Jan 13.

6.

Retinal degeneration in the rd mouse in the absence of c-fos.

Hafezi F, Abegg M, Grimm C, Wenzel A, Munz K, Stürmer J, Farber DB, Remé CE.

Invest Ophthalmol Vis Sci. 1998 Nov;39(12):2239-44.

PMID:
9804131
7.

Cone versus rod disease in a mutant Rpgr mouse caused by different genetic backgrounds.

Brunner S, Skosyrski S, Kirschner-Schwabe R, Knobeloch KP, Neidhardt J, Feil S, Glaus E, Luhmann UF, Rüther K, Berger W.

Invest Ophthalmol Vis Sci. 2010 Feb;51(2):1106-15. doi: 10.1167/iovs.08-2742. Epub 2009 Dec 10.

PMID:
20007830
9.

Severe retinal degeneration associated with disruption of semaphorin 4A.

Rice DS, Huang W, Jones HA, Hansen G, Ye GL, Xu N, Wilson EA, Troughton K, Vaddi K, Newton RC, Zambrowicz BP, Sands AT.

Invest Ophthalmol Vis Sci. 2004 Aug;45(8):2767-77.

PMID:
15277503
10.

Systemic administration of nilvadipine delays photoreceptor degeneration of heterozygous retinal degeneration slow (rds) mouse.

Takeuchi K, Nakazawa M, Mizukoshi S.

Exp Eye Res. 2008 Jan;86(1):60-9. Epub 2007 Sep 22.

PMID:
17976582
11.

Targeted inactivation of synaptic HRG4 (UNC119) causes dysfunction in the distal photoreceptor and slow retinal degeneration, revealing a new function.

Ishiba Y, Higashide T, Mori N, Kobayashi A, Kubota S, McLaren MJ, Satoh H, Wong F, Inana G.

Exp Eye Res. 2007 Mar;84(3):473-85. Epub 2006 Dec 18.

12.

Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens.

Hawes NL, Chang B, Hageman GS, Nusinowitz S, Nishina PM, Schneider BS, Smith RS, Roderick TH, Davisson MT, Heckenlively JR.

Invest Ophthalmol Vis Sci. 2000 Sep;41(10):3149-57.

PMID:
10967077
13.

BETA2/NeuroD1 null mice: a new model for transcription factor-dependent photoreceptor degeneration.

Pennesi ME, Cho JH, Yang Z, Wu SH, Zhang J, Wu SM, Tsai MJ.

J Neurosci. 2003 Jan 15;23(2):453-61.

15.

Dense nuclear cataract caused by the gammaB-crystallin S11R point mutation.

Li L, Chang B, Cheng C, Chang D, Hawes NL, Xia CH, Gong X.

Invest Ophthalmol Vis Sci. 2008 Jan;49(1):304-9. doi: 10.1167/iovs.07-0942.

PMID:
18172107
16.

Increased sensitivity to light-induced damage in a mouse model of autosomal dominant retinal disease.

White DA, Fritz JJ, Hauswirth WW, Kaushal S, Lewin AS.

Invest Ophthalmol Vis Sci. 2007 May;48(5):1942-51. Erratum in: Invest Ophthalmol Vis Sci. 2007 Aug;48(8):3436. Fritz, Jason J [added].

PMID:
17460245
17.

Electroretinographic study of the C57BL/6-mivit/mivit mouse model of retinal degeneration.

Smith SB, Hamasaki DI.

Invest Ophthalmol Vis Sci. 1994 Jun;35(7):3119-23.

PMID:
8206731
18.

Cone photoreceptor function loss-3, a novel mouse model of achromatopsia due to a mutation in Gnat2.

Chang B, Dacey MS, Hawes NL, Hitchcock PF, Milam AH, Atmaca-Sonmez P, Nusinowitz S, Heckenlively JR.

Invest Ophthalmol Vis Sci. 2006 Nov;47(11):5017-21.

PMID:
17065522
19.

Mutant rhodopsin transgene expression on a null background.

Frederick JM, Krasnoperova NV, Hoffmann K, Church-Kopish J, Rüther K, Howes K, Lem J, Baehr W.

Invest Ophthalmol Vis Sci. 2001 Mar;42(3):826-33.

PMID:
11222546
20.

Generation, characterization, and molecular cloning of the Noerg-1 mutation of rhodopsin in the mouse.

Pinto LH, Vitaterna MH, Shimomura K, Siepka SM, McDearmon EL, Fenner D, Lumayag SL, Omura C, Andrews AW, Baker M, Invergo BM, Olvera MA, Heffron E, Mullins RF, Sheffield VC, Stone EM, Takahashi JS.

Vis Neurosci. 2005 Sep-Oct;22(5):619-29.

PMID:
16332273

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