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Items: 1 to 20 of 685

1.

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.

3.

Rhodopsin transgenic pigs as a model for human retinitis pigmentosa.

Li ZY, Wong F, Chang JH, Possin DE, Hao Y, Petters RM, Milam AH.

Invest Ophthalmol Vis Sci. 1998 Apr;39(5):808-19.

PMID:
9538889
4.

Rod photoreceptor neurite sprouting in retinitis pigmentosa.

Li ZY, Kljavin IJ, Milam AH.

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

5.

Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.

Jacobson SG, Buraczynska M, Milam AH, Chen C, Järvaläinen M, Fujita R, Wu W, Huang Y, Cideciyan AV, Swaroop A.

Invest Ophthalmol Vis Sci. 1997 Sep;38(10):1983-97.

PMID:
9331262
6.

Early loss of synaptic protein PSD-95 from rod terminals of rhodopsin P347L transgenic porcine retina.

Blackmon SM, Peng YW, Hao Y, Moon SJ, Oliveira LB, Tatebayashi M, Petters RM, Wong F.

Brain Res. 2000 Dec 1;885(1):53-61.

PMID:
11121529
7.

Clinicopathologic effects of the Q64ter rhodopsin mutation in retinitis pigmentosa.

Milam AH, Li ZY, Cideciyan AV, Jacobson SG.

Invest Ophthalmol Vis Sci. 1996 Apr;37(5):753-65.

PMID:
8603860
8.

Life history of cones in the rhodopsin-mutant P23H-3 rat: evidence of long-term survival.

Chrysostomou V, Stone J, Valter K.

Invest Ophthalmol Vis Sci. 2009 May;50(5):2407-16. doi: 10.1167/iovs.08-3003.

PMID:
19117918
9.

Connexin 36 in photoreceptor cells: studies on transgenic rod-less and cone-less mouse retinas.

Dang L, Pulukuri S, Mears AJ, Swaroop A, Reese BE, Sitaramayya A.

Mol Vis. 2004 May 11;10:323-7.

10.
11.

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
12.

Characterization of rhodopsin mis-sorting and constitutive activation in a transgenic rat model of retinitis pigmentosa.

Green ES, Menz MD, LaVail MM, Flannery JG.

Invest Ophthalmol Vis Sci. 2000 May;41(6):1546-53.

PMID:
10798675
13.

A frameshift mutation in RPGR exon ORF15 causes photoreceptor degeneration and inner retina remodeling in a model of X-linked retinitis pigmentosa.

Beltran WA, Hammond P, Acland GM, Aguirre GD.

Invest Ophthalmol Vis Sci. 2006 Apr;47(4):1669-81.

PMID:
16565408
15.
16.

Localization of tubby-like protein 1 in developing and adult human retinas.

Milam AH, Hendrickson AE, Xiao M, Smith JE, Possin DE, John SK, Nishina PM.

Invest Ophthalmol Vis Sci. 2000 Jul;41(8):2352-6.

PMID:
10892883
17.

Growth of the postnatal rat retina in vitro: quantitative RT-PCR analyses of mRNA expression for photoreceptor proteins.

Liljekvist-Larsson I, Törngren M, Abrahamson M, Johansson K.

Mol Vis. 2003 Dec 9;9:657-64.

18.

Retinal histopathology in eyes from patients with autosomal dominant retinitis pigmentosa caused by rhodopsin mutations.

Bonilha VL, Rayborn ME, Bell BA, Marino MJ, Beight CD, Pauer GJ, Traboulsi EI, Hollyfield JG, Hagstrom SA.

Graefes Arch Clin Exp Ophthalmol. 2015 Dec;253(12):2161-9. doi: 10.1007/s00417-015-3099-7.

PMID:
26202387
19.

High-resolution imaging with adaptive optics in patients with inherited retinal degeneration.

Duncan JL, Zhang Y, Gandhi J, Nakanishi C, Othman M, Branham KE, Swaroop A, Roorda A.

Invest Ophthalmol Vis Sci. 2007 Jul;48(7):3283-91.

PMID:
17591900
20.

The status of cones in the rhodopsin mutant P23H-3 retina: light-regulated damage and repair in parallel with rods.

Chrysostomou V, Stone J, Stowe S, Barnett NL, Valter K.

Invest Ophthalmol Vis Sci. 2008 Mar;49(3):1116-25. doi: 10.1167/iovs.07-1158.

PMID:
18326739

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