-
1
-
-
0000087516
-
The inheritance of a retinal abnormality in white mice
-
Keeler CE. The inheritance of a retinal abnormality in white mice. Proc Natl Acad Sci USA 1924;10:329-33.
-
(1924)
Proc Natl Acad Sci USA
, vol.10
, pp. 329-333
-
-
Keeler, C.E.1
-
2
-
-
0010059934
-
Spaltlampenmikroskopie und Ophthalmoskopie am Auge von Ratte und Maus
-
Bruckner R. Spaltlampenmikroskopie und Ophthalmoskopie am Auge von Ratte und Maus. DocOphthalmol 1951;5-6:452-4.
-
(1951)
DocOphthalmol
, vol.5-6
, pp. 452-454
-
-
Bruckner, R.1
-
3
-
-
0028890926
-
From mice to men: The cyclic GMP phosphodiesterase gene in vision and disease. the Proctor lecture
-
Farber DB. From mice to men: the cyclic GMP phosphodiesterase gene in vision and disease. The Proctor lecture. Invest Ophthalmol Vis Sci 1995;36:263-75.
-
(1995)
Invest Ophthalmol Vis Sci
, vol.36
, pp. 263-275
-
-
Farber, D.B.1
-
4
-
-
0024990758
-
Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase
-
Bowes C, Li T, Danciger M, et al. Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase. Nature 1990;347:677-80.
-
(1990)
Nature
, vol.347
, pp. 677-680
-
-
Bowes, C.1
Li, T.2
Danciger, M.3
-
5
-
-
0027363757
-
PCR analysis of DNA from 70-year-old sections of rodless retina demonstrates identity with the mouse rd defect
-
Pittler SJ, Keeler CE, Sidman RL, et al. PCR analysis of DNA from 70-year-old sections of rodless retina demonstrates identity with the mouse rd defect. Proc Natl Acad Sci USA 1993;90:9616-9.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 9616-9619
-
-
Pittler, S.J.1
Keeler, C.E.2
Sidman, R.L.3
-
6
-
-
0021960701
-
Autosomal dominant progressive retinal atrophy in Abyssinian cats
-
Barnett KC, Curtis R. Autosomal dominant progressive retinal atrophy in Abyssinian cats. J Hered 1985;76:168-70.
-
(1985)
J Hered
, vol.76
, pp. 168-170
-
-
Barnett, K.C.1
Curtis, R.2
-
7
-
-
0023064044
-
An early-onset retinal dystrophy with dominant inheritance in the Abyssinian cat. Clinical and pathological findings
-
Curtis R, Barnett KG, Leon A. An early-onset retinal dystrophy with dominant inheritance in the Abyssinian cat. Clinical and pathological findings. Invest Ophthalmol Vis Sci 1987;28:131-9.
-
(1987)
Invest Ophthalmol Vis Sci
, vol.28
, pp. 131-139
-
-
Curtis, R.1
Barnett, K.G.2
Leon, A.3
-
8
-
-
0025079681
-
Autosomal dominant rod-cone dysplasia in the Rdy cat. 1. Light and electron microscopic findings
-
Leon A, Curtis R. Autosomal dominant rod-cone dysplasia in the Rdy cat. 1. Light and electron microscopic findings. Exp Eye Res 1990;51:361-81.
-
(1990)
Exp Eye Res
, vol.51
, pp. 361-381
-
-
Leon, A.1
Curtis, R.2
-
9
-
-
0026076564
-
Autosomal dominant rod-cone dysplasia in the Rdy cat. 2. Electrophysiological findings
-
Leon A, Hussain AA, Curtis R. Autosomal dominant rod-cone dysplasia in the Rdy cat. 2. Electrophysiological findings. Exp Eye Res 1991;53:489-502.
-
(1991)
Exp Eye Res
, vol.53
, pp. 489-502
-
-
Leon, A.1
Hussain, A.A.2
Curtis, R.3
-
11
-
-
0018180182
-
Rod-cone dysplasia in Irish setters: A defect in cyclic GMP metabolism in visual cells
-
Aquirre G, Farber D, Lolley R, et al. Rod-cone dysplasia in Irish setters: a defect in cyclic GMP metabolism in visual cells. Science 1978;201:1133-4.
-
(1978)
Science
, vol.201
, pp. 1133-1134
-
-
Aquirre, G.1
Farber, D.2
Lolley, R.3
-
12
-
-
0026806221
-
The beta subunit of cyclic GMP phosphodiesterase mRNA is deficient in canine rod-cone dyspiasia 1
-
Farber DB, Danciger JS, Aguirre G. The beta subunit of cyclic GMP phosphodiesterase mRNA is deficient in canine rod-cone dyspiasia 1. Neuron 1992;9:349-56.
-
(1992)
Neuron
, vol.9
, pp. 349-356
-
-
Farber, D.B.1
Danciger, J.S.2
Aguirre, G.3
-
13
-
-
0028352516
-
Early morphometry of a retinal dystrophy in Labrador retrievers
-
Kommonen B, Penn JS, Kylma T, et al. Early morphometry of a retinal dystrophy in Labrador retrievers. Acta Ophthalmol Copenh 1994;72:203-10.
-
(1994)
Acta Ophthalmol Copenh
, vol.72
, pp. 203-210
-
-
Kommonen, B.1
Penn, J.S.2
Kylma, T.3
-
14
-
-
0027262347
-
Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit gene
-
Suber ML, Pittler SJ, Qin N, et al. Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit gene. Proc Natl Acad Sci USA 1993;90:3968-72.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 3968-3972
-
-
Suber, M.L.1
Pittler, S.J.2
Qin, N.3
-
15
-
-
0022374532
-
Ultrastructural changes in the retinal pigment epithelium of congenitally blind chickens
-
Ulshafer RJ, Allen CB. Ultrastructural changes in the retinal pigment epithelium of congenitally blind chickens. Curr Eye Res 1985;4:1009-21.
-
(1985)
Curr Eye Res
, vol.4
, pp. 1009-1021
-
-
Ulshafer, R.J.1
Allen, C.B.2
-
16
-
-
0032477872
-
A null mutation in the photoreceptor guanylate cyclase gene causes the retinal degeneration chicken phenotype
-
Semple Rowland SL, Lee NR, Van Hooser JP, et al. A null mutation in the photoreceptor guanylate cyclase gene causes the retinal degeneration chicken phenotype. Proc Natl Acad Sci USA 1998;95:1271-6.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 1271-1276
-
-
Semple Rowland, S.L.1
Lee, N.R.2
Van Hooser, J.P.3
-
17
-
-
0017892743
-
Age-related and light-associated retinal changes in Fischer rats
-
Lai YL, Jacoby RO, Jonas AM. Age-related and light-associated retinal changes in Fischer rats. Invest Ophthalmol Vis Sci 1978;17:634-8.
-
(1978)
Invest Ophthalmol Vis Sci
, vol.17
, pp. 634-638
-
-
Lai, Y.L.1
Jacoby, R.O.2
Jonas, A.M.3
-
18
-
-
0028291637
-
The influences of age, retinal topography, and gender on retinal degeneration in the Fischer 344 rat
-
DiLoreto D Jr, Cox C, Grover DA, et al. The influences of age, retinal topography, and gender on retinal degeneration in the Fischer 344 rat. Brain Res 1994;647:181-91.
-
(1994)
Brain Res
, vol.647
, pp. 181-191
-
-
DiLoreto Jr., D.1
Cox, C.2
Grover, D.A.3
-
19
-
-
0019134423
-
Development and degeneration of retina in rds mutant mice: Light microscopy
-
Sanyal S, De Ruiter A, Hawkins RK. Development and degeneration of retina in rds mutant mice: light microscopy. J Comp Neurol 1980;194:193-207.
-
(1980)
J Comp Neurol
, vol.194
, pp. 193-207
-
-
Sanyal, S.1
De Ruiter, A.2
Hawkins, R.K.3
-
20
-
-
0027521914
-
Apoptosis: Final common pathway of photoreceptor death in rd, rds, and rhodopsin mutant mice
-
Chang GQ, Hao Y, Wong F. Apoptosis: final common pathway of photoreceptor death in rd, rds, and rhodopsin mutant mice. Neuron 1993;11:595-605.
-
(1993)
Neuron
, vol.11
, pp. 595-605
-
-
Chang, G.Q.1
Hao, Y.2
Wong, F.3
-
21
-
-
0028972472
-
Mouse model for Usher syndrome: Linkage mapping suggests homology to Usher type I reported at human chromosome 11p15
-
Heckenlively JR, Chang B, Erway LC, et al. Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15. Proc Natl Acad Sci USA 1995;92:11100-4.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 11100-11104
-
-
Heckenlively, J.R.1
Chang, B.2
Erway, L.C.3
-
22
-
-
0024571803
-
Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)
-
Travis GH, Brennan MB, Danielson PE, et al. Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds). Nature 1989;338:70-3.
-
(1989)
Nature
, vol.338
, pp. 70-73
-
-
Travis, G.H.1
Brennan, M.B.2
Danielson, P.E.3
-
23
-
-
0021344697
-
Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28
-
Bhattacharya SS, Wright AF, Clayton JF, et al. Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28. Nature 1984;309:253-5.
-
(1984)
Nature
, vol.309
, pp. 253-255
-
-
Bhattacharya, S.S.1
Wright, A.F.2
Clayton, J.F.3
-
24
-
-
0024746978
-
Autosomal dominant retinitis pigmentosa: Exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21
-
Farrar GJ, McWilliam P, Sharp EM, et al. Autosomal dominant retinitis pigmentosa: exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21. Genomics 1989;5:612-8.
-
(1989)
Genomics
, vol.5
, pp. 612-618
-
-
Farrar, G.J.1
McWilliam, P.2
Sharp, E.M.3
-
25
-
-
0025043276
-
Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa
-
Dryja TP, McGee TL, Hahn LB, et al. Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa, N Engl J Med 1990;323:1302-7.
-
(1990)
N Engl J Med
, vol.323
, pp. 1302-1307
-
-
Dryja, T.P.1
McGee, T.L.2
Hahn, L.B.3
-
26
-
-
0025105161
-
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
-
Dryja TP, McGee TL, Reichel E, et al. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa. Nature 1990;343:364-6.
-
(1990)
Nature
, vol.343
, pp. 364-366
-
-
Dryja, T.P.1
McGee, T.L.2
Reichel, E.3
-
27
-
-
0031016243
-
Rhodopsin mutations in inherited retinal dystrophies and dysfunctions
-
Gal A, Apfelstedt-Sylla E, Janecke AR, et al. Rhodopsin mutations in inherited retinal dystrophies and dysfunctions. Prog Retin Eye Res 1997;16:51-79.
-
(1997)
Prog Retin Eye Res
, vol.16
, pp. 51-79
-
-
Gal, A.1
Apfelstedt-Sylla, E.2
Janecke, A.R.3
-
28
-
-
0028245437
-
Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci
-
Kajiwara K, Berson EL, Dryja TP. Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci. Science 1994;264:1604-8.
-
(1994)
Science
, vol.264
, pp. 1604-1608
-
-
Kajiwara, K.1
Berson, E.L.2
Dryja, T.P.3
-
29
-
-
0000051454
-
Microinjection of a rabbit beta-globin gene into zygotes and its subsequent expression in adult mice and their offspring
-
Wagner TE, Hoppe PC, Jollick JD, et al. Microinjection of a rabbit beta-globin gene into zygotes and its subsequent expression in adult mice and their offspring. Proc Natl Acad Sci USA 1981;78:6376-80.
-
(1981)
Proc Natl Acad Sci USA
, vol.78
, pp. 6376-6380
-
-
Wagner, T.E.1
Hoppe, P.C.2
Jollick, J.D.3
-
30
-
-
33750169845
-
Transgenic rat models of inherited retinal degeneration caused by mutant opsin genes
-
Abstract no 3190
-
Steinberg RH, Flannery JG, Naash M, et al. Transgenic rat models of inherited retinal degeneration caused by mutant opsin genes. Invest Ophthalmol Vis Sci 1996;37:S698 Abstract no 3190.
-
(1996)
Invest Ophthalmol Vis Sci
, vol.37
-
-
Steinberg, R.H.1
Flannery, J.G.2
Naash, M.3
-
31
-
-
0033564046
-
Activation of caspase-3 in the retina of transgenic rats with the rhodopsin mutation s334ter during photoreceptor degeneration
-
Liu C, Li Y, Peng M, et al. Activation of caspase-3 in the retina of transgenic rats with the rhodopsin mutation s334ter during photoreceptor degeneration. J Neurosci 1999;19:4778-85.
-
(1999)
J Neurosci
, vol.19
, pp. 4778-4785
-
-
Liu, C.1
Li, Y.2
Peng, M.3
-
32
-
-
0031880563
-
Ribozyme rescue of photoreceptor cells in a transgenic rat model of autosomal dominant retinitis pigmentosa
-
Lewin AS, Drenser KA, Hauswirth WW, et al. Ribozyme rescue of photoreceptor cells in a transgenic rat model of autosomal dominant retinitis pigmentosa. Nat Med 1998;4:967-71.
-
(1998)
Nat Med
, vol.4
, pp. 967-971
-
-
Lewin, A.S.1
Drenser, K.A.2
Hauswirth, W.W.3
-
33
-
-
0031980355
-
Rhodopsin transgenic pigs as a model for human retinitis pigmentosa
-
Li ZY, Wong F, Chang JH, et al. Rhodopsin transgenic pigs as a model for human retinitis pigmentosa. Invest Ophthalmol Vis Sci 1998;39:808-19.
-
(1998)
Invest Ophthalmol Vis Sci
, vol.39
, pp. 808-819
-
-
Li, Z.Y.1
Wong, F.2
Chang, J.H.3
-
34
-
-
0026463972
-
Transgenic mice with a rhodopsin mutation (Pro23His): A mouse model of autosomal dominant retinitis pigmentosa
-
Olsson JE, Gordon JW, Pawlyk BS, et al. Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa. Neuron 1992;9:815-30.
-
(1992)
Neuron
, vol.9
, pp. 815-830
-
-
Olsson, J.E.1
Gordon, J.W.2
Pawlyk, B.S.3
-
35
-
-
0027260657
-
Cellular interactions implicated in the mechanism of photoreceptor degeneration in transgenic mice expressing a mutant rhodopsin gene
-
Huang PC, Gaitan AE, Hao Y, et al. Cellular interactions implicated in the mechanism of photoreceptor degeneration in transgenic mice expressing a mutant rhodopsin gene. Proc Natl Acad Sci USA 1993;90:8484-8.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 8484-8488
-
-
Huang, P.C.1
Gaitan, A.E.2
Hao, Y.3
-
36
-
-
0027251934
-
Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene
-
Naash MI, Hollyfield JG, al Ubaidi MR, et al. Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene. Proc Natl Acad Sci USA 1993;90:5499-503.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 5499-5503
-
-
Naash, M.I.1
Hollyfield, J.G.2
Al Ubaidi, M.R.3
-
37
-
-
0028110523
-
Rhodopsin accumulation at abnormal sites in retinas of mice with a human P23H rhodopsin transgene
-
Roof DJ, Adamian M, Hayes A. Rhodopsin accumulation at abnormal sites in retinas of mice with a human P23H rhodopsin transgene. Invest Ophthalmol Vis Sci 1994;35:4049-62.
-
(1994)
Invest Ophthalmol Vis Sci
, vol.35
, pp. 4049-4062
-
-
Roof, D.J.1
Adamian, M.2
Hayes, A.3
-
38
-
-
0030851707
-
Genetically engineered large animal model for studying cone photoreceptor survival and degeneration in retinitis pigmentosa
-
Petters RM, Alexander CA, Wells KD, et al. Genetically engineered large animal model for studying cone photoreceptor survival and degeneration in retinitis pigmentosa. Nat Biotechnol 1997;15:965-70.
-
(1997)
Nat Biotechnol
, vol.15
, pp. 965-970
-
-
Petters, R.M.1
Alexander, C.A.2
Wells, K.D.3
-
39
-
-
0030669676
-
A pathologic study of degeneration of the rod and cone populations of the rhodopsin Pro347Leu transgenic pigs
-
discussion 79-83
-
Tso MO, Li WW, Zhang C, et al. A pathologic study of degeneration of the rod and cone populations of the rhodopsin Pro347Leu transgenic pigs. Trans Am Ophthalmol Soc 1997;95:467-79; discussion 79-83.
-
(1997)
Trans am Ophthalmol Soc
, vol.95
, pp. 467-479
-
-
Tso, M.O.1
Li, W.W.2
Zhang, C.3
-
40
-
-
0028858741
-
Functional abnormalities in transgenic mice expressing a mutant rhodopsin gene
-
Goto Y, Peachey NS, Ripps H, et al. Functional abnormalities in transgenic mice expressing a mutant rhodopsin gene. Invest Ophthalmol Vis Sci 1995;36:62-71.
-
(1995)
Invest Ophthalmol Vis Sci
, vol.36
, pp. 62-71
-
-
Goto, Y.1
Peachey, N.S.2
Ripps, H.3
-
41
-
-
0027957662
-
Apoptotic photoreceptor cell death in mouse models of retinitis pigmentosa
-
Portera Cailliau C, Sung CH, Nathans J, et al. Apoptotic photoreceptor cell death in mouse models of retinitis pigmentosa. Proc Natl Acad Sci USA 1994;91:974-8.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 974-978
-
-
Portera Cailliau, C.1
Sung, C.H.2
Nathans, J.3
-
42
-
-
0031045823
-
Generation and analysis of transgenic mice expressing P216L-substituted rds/peripherin in rod photoreceptors
-
Kedzierski W, Lloyd M, Birch DG, et al. Generation and analysis of transgenic mice expressing P216L-substituted rds/peripherin in rod photoreceptors. Invest Ophthalmol Vis Sci 1997;38:498-509.
-
(1997)
Invest Ophthalmol Vis Sci
, vol.38
, pp. 498-509
-
-
Kedzierski, W.1
Lloyd, M.2
Birch, D.G.3
-
43
-
-
0032526453
-
Early onset photoreceptor abnormalities induced by targeted disruption of the interphotoreceptor retinoid-binding protein gene
-
Liou GI, Fei Y, Peachey NS, et al. Early onset photoreceptor abnormalities induced by targeted disruption of the interphotoreceptor retinoid-binding protein gene. J Neurosci 1998;18:4511-20.
-
(1998)
J Neurosci
, vol.18
, pp. 4511-4520
-
-
Liou, G.I.1
Fei, Y.2
Peachey, N.S.3
-
44
-
-
0029740113
-
Retinal degeneration in mice lacking the gamma subunit of the rod cGMP phosphodiesterase
-
Tsang SH, Gouras P, Yamashita CK, et al. Retinal degeneration in mice lacking the gamma subunit of the rod cGMP phosphodiesterase. Science 1996;272:1026-9.
-
(1996)
Science
, vol.272
, pp. 1026-1029
-
-
Tsang, S.H.1
Gouras, P.2
Yamashita, C.K.3
-
45
-
-
0031255068
-
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy
-
Gu SM, Thompson DA, Srikumari CR, et al. Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy. Nat Genet 1997;17:194-7.
-
(1997)
Nat Genet
, vol.17
, pp. 194-197
-
-
Gu, S.M.1
Thompson, D.A.2
Srikumari, C.R.3
-
46
-
-
0032539851
-
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis
-
Morimura H, Fishman GA, Grover SA, et al. Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. Proc Natl Acad Sci USA 1998;95:3088-93.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 3088-3093
-
-
Morimura, H.1
Fishman, G.A.2
Grover, S.A.3
-
47
-
-
0031252434
-
Mutations in RPE65 cause Leber's congenital amaurosis
-
Marlhens F, Bareil C, Griffoin JM, et al. Mutations in RPE65 cause Leber's congenital amaurosis, Nat Genet 1997;17:139-41.
-
(1997)
Nat Genet
, vol.17
, pp. 139-141
-
-
Marlhens, F.1
Bareil, C.2
Griffoin, J.M.3
-
48
-
-
0024417892
-
The Briard dog: A new animal model of congenital stationary night blindness
-
Narfstrom K, Wrigstad A, Nilsson, SE. The Briard dog: a new animal model of congenital stationary night blindness. Br J Ophthalmol 1989;73:750-6.
-
(1989)
Br J Ophthalmol
, vol.73
, pp. 750-756
-
-
Narfstrom, K.1
Wrigstad, A.2
Nilsson, S.E.3
-
49
-
-
0028075957
-
Slowly progressive changes of the retina and retinal pigment epithelium in briard dogs with hereditary retinal dystrophy. A morphological study
-
Wrigstad A, Narfstrom K, Nilsson SE. Slowly progressive changes of the retina and retinal pigment epithelium in briard dogs with hereditary retinal dystrophy. A morphological study Doc Ophthalmol 1994;87:337-54.
-
(1994)
Doc Ophthalmol
, vol.87
, pp. 337-354
-
-
Wrigstad, A.1
Narfstrom, K.2
Nilsson, S.E.3
-
50
-
-
0032582425
-
Congenital stationary night blindness in the dog: Common mutation in the RPE65 gene indicates founder effect
-
Aguirre GD, Baldwin V, Pearce-Kelling S, et al. Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect. Mol Vis 1998;4:23.
-
(1998)
Mol Vis
, vol.4
, pp. 23
-
-
Aguirre, G.D.1
Baldwin, V.2
Pearce-Kelling, S.3
-
51
-
-
0033118884
-
Retinal dystrophy of Swedish briard/briard-beagle dogs is due to a 4-bp deletion in RPE65
-
Veske A, Nilsson SE, Narfstrom K, et al. Retinal dystrophy of Swedish briard/briard-beagle dogs is due to a 4-bp deletion in RPE65. Genomics 1999;57:57-61.
-
(1999)
Genomics
, vol.57
, pp. 57-61
-
-
Veske, A.1
Nilsson, S.E.2
Narfstrom, K.3
-
52
-
-
17344366357
-
Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle
-
Redmond TM, Yu S, Lee E, et al. Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle. Nat Genet 1998;20:344-51.
-
(1998)
Nat Genet
, vol.20
, pp. 344-351
-
-
Redmond, T.M.1
Yu, S.2
Lee, E.3
-
53
-
-
0034105724
-
Protection of Rpe65-deficient mice identifies rhodopsin as mediator of light-induced retinal degeneration
-
in press
-
Grimm C, Wenzel A, Hafezi F, et al. Protection of Rpe65-deficient mice identifies rhodopsin as mediator of light-induced retinal degeneration. Nat Genet 2000 (in press).
-
(2000)
Nat Genet
-
-
Grimm, C.1
Wenzel, A.2
Hafezi, F.3
-
54
-
-
0030198411
-
Morphological and physiological consequences of the selective elimination of rod photoreceptors in transgenic mice
-
McCall MA, Gregg RG, Merriman K, et al. Morphological and physiological consequences of the selective elimination of rod photoreceptors in transgenic mice. Exp Eye Res 1996;63:35-50.
-
(1996)
Exp Eye Res
, vol.63
, pp. 35-50
-
-
McCall, M.A.1
Gregg, R.G.2
Merriman, K.3
-
55
-
-
0033595022
-
Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3
-
Biel M, Seeliger M, Pfeifer A, et al. Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3. Proc Natl Acad Sci 1999;96:7553-7.
-
(1999)
Proc Natl Acad Sci
, vol.96
, pp. 7553-7557
-
-
Biel, M.1
Seeliger, M.2
Pfeifer, A.3
-
56
-
-
0033538438
-
Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice
-
Weng J, Mata NL, Azarian SM, et al. Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice. Cell 1999;98:13-23.
-
(1999)
Cell
, vol.98
, pp. 13-23
-
-
Weng, J.1
Mata, N.L.2
Azarian, S.M.3
-
57
-
-
0031045876
-
Retinopathy induced in mice by targeted disruption of the rhodopsin gene
-
Humphries MM, Rancourt D, Farrar GJ, et al. Retinopathy induced in mice by targeted disruption of the rhodopsin gene. Nat Genet 1997;15:216-9.
-
(1997)
Nat Genet
, vol.15
, pp. 216-219
-
-
Humphries, M.M.1
Rancourt, D.2
Farrar, G.J.3
-
58
-
-
24844466604
-
Crossing the rhodopsin G90D transgenic mouse onto a rho-knockout background recreates autosomal dominant human congenital nightblindness
-
Abstract no 474
-
Sieving PA, Bush RA, Fowler M, et al. Crossing the rhodopsin G90D transgenic mouse onto a rho-knockout background recreates autosomal dominant human congenital nightblindness. Invest Ophthalmol Vis Sci 1998;39:S 101, Abstract no 474.
-
(1998)
Invest Ophthalmol Vis Sci
, vol.39
-
-
Sieving, P.A.1
Bush, R.A.2
Fowler, M.3
-
59
-
-
0033616582
-
Abnormal photoresponses and light-induced apoptosis in rods lacking rhodopsin kinase
-
Chen CK, Burns ME, Spencer M, et al. Abnormal photoresponses and light-induced apoptosis in rods lacking rhodopsin kinase. Proc Natl Acad Sci 1999;96:3718-22.
-
(1999)
Proc Natl Acad Sci
, vol.96
, pp. 3718-3722
-
-
Chen, C.K.1
Burns, M.E.2
Spencer, M.3
-
60
-
-
0032753090
-
Increased susceptibility to light damage in an arrestin knockout mouse model of Oguchi disease (stationary night blindness)
-
Chen J, Simon MI, Matthes MT, et al. Increased susceptibility to light damage in an arrestin knockout mouse model of Oguchi disease (stationary night blindness). Invest Ophthalmol Vis Sci 1999;40:2978-82.
-
(1999)
Invest Ophthalmol Vis Sci
, vol.40
, pp. 2978-2982
-
-
Chen, J.1
Simon, M.I.2
Matthes, M.T.3
-
61
-
-
0021679078
-
Cell death during differentiation of the retina in the mouse
-
Young RW. Cell death during differentiation of the retina in the mouse. J Comp Neurol 1984;229:362-73.
-
(1984)
J Comp Neurol
, vol.229
, pp. 362-373
-
-
Young, R.W.1
-
62
-
-
0031171328
-
Light-induced apoptosis: Differential timing in the retina and pigment epithelium
-
Hafezi F, Marti A, Munz K, et al. Light-induced apoptosis: differential timing in the retina and pigment epithelium. Exp Eye Res 1997;64:963-70.
-
(1997)
Exp Eye Res
, vol.64
, pp. 963-970
-
-
Hafezi, F.1
Marti, A.2
Munz, K.3
-
63
-
-
0031054783
-
The absence of c-fos prevents light-induced apoptotic cell death of photoreceptors in retinal degeneration in vivo
-
Hafezi F, Steinbach JP, Marti A, et al. The absence of c-fos prevents light-induced apoptotic cell death of photoreceptors in retinal degeneration in vivo. Nat Med 1997;3:346-9.
-
(1997)
Nat Med
, vol.3
, pp. 346-349
-
-
Hafezi, F.1
Steinbach, J.P.2
Marti, A.3
-
64
-
-
0003098244
-
Apoptosis in retinitis pigmentosa
-
Anderson RE, LaVail MM, Hollyfield JG, eds. New York: Plenum Press
-
Li Z-Y, Milam AH. Apoptosis in retinitis pigmentosa. In: Anderson RE, LaVail MM, Hollyfield JG, eds. Retinal degeneration. New York: Plenum Press, 1995:1-8
-
(1995)
Retinal Degeneration
, pp. 1-8
-
-
Li, Z.-Y.1
Milam, A.H.2
-
66
-
-
0030916669
-
The proto-oncogene Bcl-2 and its role in regulating apoptosis
-
Kroemer G. The proto-oncogene Bcl-2 and its role in regulating apoptosis. Nat Med 1997;3:614-260.
-
(1997)
Nat Med
, vol.3
, pp. 614-1260
-
-
Kroemer, G.1
-
67
-
-
0029801850
-
Overexpression of Bcl-2 or Bcl-XL transgenes and photoreceptor degeneration
-
Joseph RM, Li T. Overexpression of Bcl-2 or Bcl-XL transgenes and photoreceptor degeneration. Invest Ophthalmol Vis Sci 1996;37:2434-46.
-
(1996)
Invest Ophthalmol Vis Sci
, vol.37
, pp. 2434-2446
-
-
Joseph, R.M.1
Li, T.2
-
68
-
-
0029949082
-
Bcl-2 overexpression reduces apoptotic photoreceptor cell death in three different retinal degenerations
-
Chen J, Flannery JG, LaVail MM, et al. bcl-2 overexpression reduces apoptotic photoreceptor cell death in three different retinal degenerations. Proc Natl Acad Sci USA 1996;93:7042-7.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 7042-7047
-
-
Chen, J.1
Flannery, J.G.2
Lavail, M.M.3
-
69
-
-
0030948540
-
Retarding photoreceptor degeneration in Pdegtm1/Pdegtm1 mice by an apoptosis suppressor gene
-
Tsang SH, Chen J, Kjeldbye H, et al. Retarding photoreceptor degeneration in Pdegtm1/Pdegtm1 mice by an apoptosis suppressor gene. Invest Ophthalmol Vis Sci 1997;38:943-50.
-
(1997)
Invest Ophthalmol Vis Sci
, vol.38
, pp. 943-950
-
-
Tsang, S.H.1
Chen, J.2
Kjeldbye, H.3
-
70
-
-
0033630517
-
Early postnatal Muller cell death leads to retinal but not optic nerve degeneration in NSE-Hu-Bcl-2 transgenic mice
-
Dubois-Dauphin M, Poitry-Yamate C, de Bilbao F, et al. Early postnatal Muller cell death leads to retinal but not optic nerve degeneration in NSE-Hu-Bcl-2 transgenic mice. Neuroscience 2000;95:9-21.
-
(2000)
Neuroscience
, vol.95
, pp. 9-21
-
-
Dubois-Dauphin, M.1
Poitry-Yamate, C.2
De Bilbao, F.3
-
71
-
-
0031828871
-
Suppression of developmental retinal cell death but not of photoreceptor degeneration in Bax-deficient mice
-
Mosinger Ogilvie J, Deckwerth TL, Knudson CM, et al. Suppression of developmental retinal cell death but not of photoreceptor degeneration in Bax-deficient mice. Invest Ophthalmol Vis Sci 1998;39:1713-20.
-
(1998)
Invest Ophthalmol Vis Sci
, vol.39
, pp. 1713-1720
-
-
Mosinger Ogilvie, J.1
Deckwerth, T.L.2
Knudson, C.M.3
-
72
-
-
0031967933
-
Light-induced cell death of retinal photoreceptors in the absence of p53
-
Marti A, Hafezi F, Lansel N, et al. Light-induced cell death of retinal photoreceptors in the absence of p53. Invest Ophthalmol Vis Sci 1998;39:846-9.
-
(1998)
Invest Ophthalmol Vis Sci
, vol.39
, pp. 846-849
-
-
Marti, A.1
Hafezi, F.2
Lansel, N.3
-
73
-
-
0031679636
-
Absence of p53 delays apoptotic photoreceptor cell death in the rds mouse
-
Ali RR, Reichel MB, Kanuga N, et al. Absence of p53 delays apoptotic photoreceptor cell death in the rds mouse. Curr Eye Res 1998;17:917-23.
-
(1998)
Curr Eye Res
, vol.17
, pp. 917-923
-
-
Ali, R.R.1
Reichel, M.B.2
Kanuga, N.3
-
74
-
-
0034003412
-
C-fos controls the "private pathway" of light-induced apoptosis of retinal photoreceptors
-
Wenzel A, Grimm C, Marti A, et al. c-fos controls the "private pathway" of light-induced apoptosis of retinal photoreceptors. J Neurosci 2000;20:81-8.
-
(2000)
J Neurosci
, vol.20
, pp. 81-88
-
-
Wenzel, A.1
Grimm, C.2
Marti, A.3
-
75
-
-
0031733001
-
Retinal degeneration in the rd mouse in the absence of c-fos
-
Hafezi F, Abegg M, Grimm C, et al. Retinal degeneration in the rd mouse in the absence of c-fos. Invest Ophthalmol Vis Sci 1998;39:2239-44.
-
(1998)
Invest Ophthalmol Vis Sci
, vol.39
, pp. 2239-2244
-
-
Hafezi, F.1
Abegg, M.2
Grimm, C.3
-
76
-
-
0032917997
-
Differential DNA binding activities of the transcription factors AP-1 and Oct-1 during light-induced apoptosis of photoreceptors
-
Hafezi F, Marti A, Grimm C, et al. Differential DNA binding activities of the transcription factors AP-1 and Oct-1 during light-induced apoptosis of photoreceptors. Vis Res 1999;39:2511-8.
-
(1999)
Vis Res
, vol.39
, pp. 2511-2518
-
-
Hafezi, F.1
Marti, A.2
Grimm, C.3
-
77
-
-
0032710339
-
Retinal photoreceptors are apoptosis-competent in the absence of JunD/AP-1
-
Hafezi F, Grimm C, Wenzel A, et al. Retinal photoreceptors are apoptosis-competent in the absence of JunD/AP-1. Cell Death Differ 1999;6:934-6.
-
(1999)
Cell Death Differ
, vol.6
, pp. 934-936
-
-
Hafezi, F.1
Grimm, C.2
Wenzel, A.3
-
78
-
-
0002164692
-
Aspects of experimental and hereditary retinal degeneration
-
Graymore CN, ed. London: Academic Press
-
Noëll WK. Aspects of experimental and hereditary retinal degeneration. In: Graymore CN, ed. Biochemistry of the retina. London: Academic Press, 1965:51-72.
-
(1965)
Biochemistry of the Retina
, pp. 51-72
-
-
Noëll, W.K.1
-
79
-
-
0022530727
-
Development and degeneration of retina in rds mutant mice: Effects of light on the rate of degeneration in albino and pigmented homozygous and heterozygous mutant and normal mice
-
Sanyal S, Hawkins RK. Development and degeneration of retina in rds mutant mice: effects of light on the rate of degeneration in albino and pigmented homozygous and heterozygous mutant and normal mice. Vis Res 1986;26:1177-85.
-
(1986)
Vis Res
, vol.26
, pp. 1177-1185
-
-
Sanyal, S.1
Hawkins, R.K.2
-
80
-
-
0030808480
-
Expression of a mutant opsin gene increases the susceptibility of the retina to light damage
-
Wang M, Lam TT, Tso MO, et al. Expression of a mutant opsin gene increases the susceptibility of the retina to light damage. Vis Neurosci 1997;14:55-62.
-
(1997)
Vis Neurosci
, vol.14
, pp. 55-62
-
-
Wang, M.1
Lam, T.T.2
Tso, M.O.3
-
81
-
-
0033037955
-
Increased susceptibility to constant light in nr and pcd mice with inherited retinal degenerations
-
LaVail MM, Gorrin GM, Yasumura D, et al. Increased susceptibility to constant light in nr and pcd mice with inherited retinal degenerations. Invest Ophthalmol Vis Sci 1999;40:1020-4.
-
(1999)
Invest Ophthalmol Vis Sci
, vol.40
, pp. 1020-1024
-
-
LaVail, M.M.1
Gorrin, G.M.2
Yasumura, D.3
-
82
-
-
0028298405
-
Autosomal dominant retinitis pigmentosa caused by the threonine-17-methionine rhodopsin mutation: Retinal histopathology and immunocytochemistry
-
Li ZY, Jacobson SG, Milam AH. Autosomal dominant retinitis pigmentosa caused by the threonine-17-methionine rhodopsin mutation: retinal histopathology and immunocytochemistry. Exp Eye Res 1994;58:397-408.
-
(1994)
Exp Eye Res
, vol.58
, pp. 397-408
-
-
Li, Z.Y.1
Jacobson, S.G.2
Milam, A.H.3
-
83
-
-
0025967305
-
Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin
-
Heckenlively JR, Rodriguez JA, Daiger SP. Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin. Arch Ophthalmol 1991;109:84-91.
-
(1991)
Arch Ophthalmol
, vol.109
, pp. 84-91
-
-
Heckenlively, J.R.1
Rodriguez, J.A.2
Daiger, S.P.3
-
86
-
-
0031664966
-
Apoptotic cell death in retinal degenerations
-
Reme CE, Grimm C, Hafezi F, et al. Apoptotic cell death in retinal degenerations. Prog Retin Eye Res 1998;17:443-64.
-
(1998)
Prog Retin Eye Res
, vol.17
, pp. 443-464
-
-
Reme, C.E.1
Grimm, C.2
Hafezi, F.3
-
87
-
-
0002917338
-
Light-induced apoptosis in the rat retina in vivo: Morphological features, threshold and time course
-
Anderson RE, LaVail MM, Hollyfield JG, eds. New York: Plenum Press
-
Remé CE, Weller M, Szczesny P, et al. Light-induced apoptosis in the rat retina in vivo: Morphological features, threshold and time course. In: Anderson RE, LaVail MM, Hollyfield JG, eds. Retinal degeneration. New York: Plenum Press, 1995.
-
(1995)
Retinal Degeneration
-
-
Remé, C.E.1
Weller, M.2
Szczesny, P.3
-
88
-
-
0026462896
-
Multiple growth factors, cytokines, and neurotrophins rescue photoreceptors from the damaging effects of constant light
-
LaVail MM, Unoki K, Yasumura D, et al. Multiple growth factors, cytokines, and neurotrophins rescue photoreceptors from the damaging effects of constant light. Proc Natl Acad Sci USA 1992;89:11249-53.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 11249-11253
-
-
LaVail, M.M.1
Unoki, K.2
Yasumura, D.3
-
89
-
-
0020584543
-
Action spectrum of retinal light-damage in albino rats
-
Williams TP, Howell WL. Action spectrum of retinal light-damage in albino rats. Invest Ophthalmol Vis Sci 1983;24:285-7.
-
(1983)
Invest Ophthalmol Vis Sci
, vol.24
, pp. 285-287
-
-
Williams, T.P.1
Howell, W.L.2
-
90
-
-
0022181210
-
Amelioration of photic injury in rat retina by ascorbic acid: A histopathologic study
-
Li ZY, Tso MO, Wang HM, et al. Amelioration of photic injury in rat retina by ascorbic acid: a histopathologic study. Invest Ophthalmol Vis Sci 1985;26:1589-98.
-
(1985)
Invest Ophthalmol Vis Sci
, vol.26
, pp. 1589-1598
-
-
Li, Z.Y.1
Tso, M.O.2
Wang, H.M.3
-
91
-
-
0017755882
-
Rhodopsin content and electroretinographic sensitivity in light-damaged rat retina
-
Rapp LM, Williams TP. Rhodopsin content and electroretinographic sensitivity in light-damaged rat retina. Nature 1977;267:835-6.
-
(1977)
Nature
, vol.267
, pp. 835-836
-
-
Rapp, L.M.1
Williams, T.P.2
-
92
-
-
0024375326
-
Retinal light damage in rats exposed to intermittent light. Comparison with continuous light exposure
-
Organisciak DT, Jiang YL, Wang HM, et al. Retinal light damage in rats exposed to intermittent light. Comparison with continuous light exposure. Invest Ophthalmol Vis Sci 1989;30:795-805.
-
(1989)
Invest Ophthalmol Vis Sci
, vol.30
, pp. 795-805
-
-
Organisciak, D.T.1
Jiang, Y.L.2
Wang, H.M.3
-
93
-
-
0028329957
-
Retinal light damage: Practical and theoretical considerations
-
Osborne NN, Chader GJ, eds. Oxford, New York, Tokyo: Pergamon
-
Organisciak DT, Winkler BS. Retinal light damage: practical and theoretical considerations. In: Osborne NN, Chader GJ, eds. Progress in retinal and eye research. Oxford, New York, Tokyo: Pergamon, 1994:1-29.
-
(1994)
Progress in Retinal and Eye Research
, pp. 1-29
-
-
Organisciak, D.T.1
Winkler, B.S.2
-
94
-
-
0026026358
-
A pathologic study of photoreceptor cell death in retinal photic injury
-
Shahinfar S, Edward DP, Tso MO. A pathologic study of photoreceptor cell death in retinal photic injury. Curr Eye Res 1991;10:47-59.
-
(1991)
Curr Eye Res
, vol.10
, pp. 47-59
-
-
Shahinfar, S.1
Edward, D.P.2
Tso, M.O.3
-
95
-
-
0017797958
-
Retinal damage produced by intraocular fiber optic light
-
Fuller D, Machemer R, Knighton RW, Retinal damage produced by intraocular fiber optic light. Am J Ophthalmol 1978;85:519-37.
-
(1978)
Am J Ophthalmol
, vol.85
, pp. 519-537
-
-
Fuller, D.1
Machemer, R.2
Knighton, R.W.3
-
96
-
-
0023678388
-
Retinal degeneration in the mouse induced transplacentally by N-methyl-N-nitrosourea: Effects of constant illumination or total darkness
-
Smith SB, Hashimi W, Yielding KL. Retinal degeneration in the mouse induced transplacentally by N-methyl-N-nitrosourea: effects of constant illumination or total darkness. Exp Eye Res 1988;47:347-59.
-
(1988)
Exp Eye Res
, vol.47
, pp. 347-359
-
-
Smith, S.B.1
Hashimi, W.2
Yielding, K.L.3
-
97
-
-
0029908025
-
Pigmentary degeneration induced by N-methyl-N-nitrosourea and the fate of pigment epithelial cells in the rat retina
-
Nakajima M, Nambu H, Shikata N, et al. Pigmentary degeneration induced by N-methyl-N-nitrosourea and the fate of pigment epithelial cells in the rat retina. Pathol Int 1996;46:874-82.
-
(1996)
Pathol int
, vol.46
, pp. 874-882
-
-
Nakajima, M.1
Nambu, H.2
Shikata, N.3
-
98
-
-
0027178816
-
Retinal degeneration induced by N-methyl-N-nitrosourea and detection of 7-methyldeoxyguanosine in the rat retina
-
Ogino H, Ito M, Matsumoto K, et al. Retinal degeneration induced by N-methyl-N-nitrosourea and detection of 7-methyldeoxyguanosine in the rat retina. Toxicol Pathol 1993;21:21-5.
-
(1993)
Toxicol Pathol
, vol.21
, pp. 21-25
-
-
Ogino, H.1
Ito, M.2
Matsumoto, K.3
-
99
-
-
0014145833
-
Pigmentary degeneration of the retina induced by N-methyl-N-nitrosourea. An experimental study in Syrian hamsters
-
Herrold KM. Pigmentary degeneration of the retina induced by N-methyl-N-nitrosourea. An experimental study in Syrian hamsters. Arch Ophthalmol 1967;78:650-3.
-
(1967)
Arch Ophthalmol
, vol.78
, pp. 650-653
-
-
Herrold, K.M.1
-
100
-
-
0030614285
-
Morphologic characteristics of N-methyl-N-nitrosourea-induced retinal degeneration in C57BL mice
-
Nambu H, Yuge K, Nakajima M, et al. Morphologic characteristics of N-methyl-N-nitrosourea-induced retinal degeneration in C57BL mice. Pathol Int 1997;47:377-83.
-
(1997)
Pathol int
, vol.47
, pp. 377-383
-
-
Nambu, H.1
Yuge, K.2
Nakajima, M.3
-
101
-
-
0015949574
-
Experimental retinal degeneration in the rabbit produced by intraocular iron
-
Burger PC, Klintworth GK. Experimental retinal degeneration in the rabbit produced by intraocular iron. Lab Invest 1974;30:9-19.
-
(1974)
Lab Invest
, vol.30
, pp. 9-19
-
-
Burger, P.C.1
Klintworth, G.K.2
-
102
-
-
0031935652
-
Iron-induced apoptosis in the photoreceptor cells of rats
-
Wang ZJ, Lam KW, Lam TT, et al. Iron-induced apoptosis in the photoreceptor cells of rats. Invest Ophthalmol Vis Sci 1998;39:631-3.
-
(1998)
Invest Ophthalmol Vis Sci
, vol.39
, pp. 631-633
-
-
Wang, Z.J.1
Lam, K.W.2
Lam, T.T.3
-
103
-
-
0031917626
-
Apoptosis of photoreceptor cells in ornithine-induced retinopathy
-
Maeda H, Ogata N, Yi X, et al. Apoptosis of photoreceptor cells in ornithine-induced retinopathy. Graefes Arch Clin Exp Ophthalmol 1998;236:207-12.
-
(1998)
Graefes Arch Clin Exp Ophthalmol
, vol.236
, pp. 207-212
-
-
Maeda, H.1
Ogata, N.2
Yi, X.3
-
104
-
-
0345161473
-
Management of hereditary retinal degenerations: Present status and future directions
-
Sharma RK, Ehinger B. Management of hereditary retinal degenerations: present status and future directions. Surv Ophthalmol 1999;43:427-44.
-
(1999)
Surv Ophthalmol
, vol.43
, pp. 427-444
-
-
Sharma, R.K.1
Ehinger, B.2
-
105
-
-
0030707839
-
Gene therapy for inherited retinal degeneration
-
Ali RR, Reichel MB, Hunt DM, et al. Gene therapy for inherited retinal degeneration. Br J Ophthalmol 1997;81:795-801.
-
(1997)
Br J Ophthalmol
, vol.81
, pp. 795-801
-
-
Ali, R.R.1
Reichel, M.B.2
Hunt, D.M.3
-
106
-
-
0032971670
-
Management of inherited outer retinal dystrophies: Present and future
-
Chong NH, Bird AC. Management of inherited outer retinal dystrophies: present and future. Br J Ophthalmol 1999;83:120-2.
-
(1999)
Br J Ophthalmol
, vol.83
, pp. 120-122
-
-
Chong, N.H.1
Bird, A.C.2
-
107
-
-
0030797322
-
Progression of cochlear and retinal degeneration in the tubby (rd5) mouse
-
Ohlemiller KK, Hughes RM, Lett JM, et al. Progression of cochlear and retinal degeneration in the tubby (rd5) mouse. Audiol Neurootol 1997;2:175-85.
-
(1997)
Audiol Neurootol
, vol.2
, pp. 175-185
-
-
Ohlemiller, K.K.1
Hughes, R.M.2
Lett, J.M.3
-
109
-
-
0027076760
-
C57BL/6J-vit/vit mouse model of retinal degeneration: Light microscopic analysis and evaluation of rhodopsin levels
-
Smith SB. C57BL/6J-vit/vit mouse model of retinal degeneration: light microscopic analysis and evaluation of rhodopsin levels. Exp Eye Res 1992;55:903-10.
-
(1992)
Exp Eye Res
, vol.55
, pp. 903-910
-
-
Smith, S.B.1
-
110
-
-
0028293242
-
Effects of dark-rearing on the retinal degeneration of the C57BL/6-mivit/mivit mouse
-
Smith SB, Cope BK, McCoy JR. Effects of dark-rearing on the retinal degeneration of the C57BL/6-mivit/mivit mouse. Exp Eye Res 1994;58:77-84.
-
(1994)
Exp Eye Res
, vol.58
, pp. 77-84
-
-
Smith, S.B.1
Cope, B.K.2
McCoy, J.R.3
-
111
-
-
0027167542
-
New mouse primary retinal degeneration (rd-3)
-
Chang B, Heckenlively JR, Hawes NL, et al. New mouse primary retinal degeneration (rd-3). Genomics 1993;16:45-9.
-
(1993)
Genomics
, vol.16
, pp. 45-49
-
-
Chang, B.1
Heckenlively, J.R.2
Hawes, N.L.3
-
112
-
-
0020440792
-
Retinal degeneration in the pcd cerebellar mutant mouse. I. Light microscopic and autoradiographic analysis
-
La Vail MM, Blanks JC, Mullen RJ. Retinal degeneration in the pcd cerebellar mutant mouse. I. Light microscopic and autoradiographic analysis. J Comp Neurol 1982;212:217-30.
-
(1982)
J Comp Neurol
, vol.212
, pp. 217-230
-
-
La Vail, M.M.1
Blanks, J.C.2
Mullen, R.J.3
-
113
-
-
0031570686
-
A new dominant retinal degeneration (Rd4) associated with a chromosomal inversion in the mouse
-
Roderick TH, Chang B, Hawes NL, et al. A new dominant retinal degeneration (Rd4) associated with a chromosomal inversion in the mouse. Genomics 1997;42:393-6.
-
(1997)
Genomics
, vol.42
, pp. 393-396
-
-
Roderick, T.H.1
Chang, B.2
Hawes, N.L.3
-
114
-
-
0032518299
-
Pax2 expression and retinal morphogenesis in the normal and Krd mouse
-
Otteson DC, Shelden E, Jones JM, et al. Pax2 expression and retinal morphogenesis in the normal and Krd mouse. Dev Biol 1998;193:209-24.
-
(1998)
Dev Biol
, vol.193
, pp. 209-224
-
-
Otteson, D.C.1
Shelden, E.2
Jones, J.M.3
-
116
-
-
0026128416
-
Pathogenesis of retinal dystrophy in the Royal College of Surgeons rat
-
Davidorf FH, Mendlovic DB, Bowyer DW, et al. Pathogenesis of retinal dystrophy in the Royal College of Surgeons rat. Ann Ophthalmol 1991;23:87-94.
-
(1991)
Ann Ophthalmol
, vol.23
, pp. 87-94
-
-
Davidorf, F.H.1
Mendlovic, D.B.2
Bowyer, D.W.3
-
117
-
-
0017119173
-
Inherited retinal dystrophy: Primary defect in pigment epithelium determined with experimental rat chimeras
-
Mullen RJ, La Vail MM. Inherited retinal dystrophy: primary defect in pigment epithelium determined with experimental rat chimeras. Science 1976;192:799-801.
-
(1976)
Science
, vol.192
, pp. 799-801
-
-
Mullen, R.J.1
La Vail, M.M.2
-
118
-
-
0030447981
-
The mouse Pax2 (1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney
-
Favor J, Sandulache R, Neuhauser Klaus A, et al. The mouse Pax2 (1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney. Proc Natl Acad Sci USA 1996;93:13870-5.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 13870-13875
-
-
Favor, J.1
Sandulache, R.2
Neuhauser Klaus, A.3
-
119
-
-
0033565767
-
Disruption of a retinal guanylyl cyclase gene leads to cone-specific dystrophy and paradoxical rod behavior
-
Yang RB, Robinson SW, Xiong WH, et al. Disruption of a retinal guanylyl cyclase gene leads to cone-specific dystrophy and paradoxical rod behavior. J Neurosci 1999;19:5889-97.
-
(1999)
J Neurosci
, vol.19
, pp. 5889-5897
-
-
Yang, R.B.1
Robinson, S.W.2
Xiong, W.H.3
-
120
-
-
0026557171
-
Photoreceptor degeneration induced by the expression of simian virus 40 large tumor antigen in the retina of transgenic mice
-
al Ubaidi MR, Hollyfield JG, Overbeek PA, et al. Photoreceptor degeneration induced by the expression of simian virus 40 large tumor antigen in the retina of transgenic mice. Proc Natl Acad Sci USA 1992;89:1194-8.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 1194-1198
-
-
Al Ubaidi, M.R.1
Hollyfield, J.G.2
Overbeek, P.A.3
-
122
-
-
0030043018
-
Genetic predisposition to coronavirus-induced retinal disease
-
Wang Y, Burnier M, Derrick B, et al. Genetic predisposition to coronavirus-induced retinal disease. Invest Ophthalmol Vis Sci 1996;37:250-1.
-
(1996)
Invest Ophthalmol Vis Sci
, vol.37
, pp. 250-251
-
-
Wang, Y.1
Burnier, M.2
Derrick, B.3
-
123
-
-
0029617590
-
Nutritionally induced retinal degeneration in rats
-
el Hifnawi S, Lincoln DT, Dashti H. Nutritionally induced retinal degeneration in rats. Nutrition 1995;11(5 Suppl);705-7.
-
(1995)
Nutrition
, vol.11
, Issue.5 SUPPL.
, pp. 705-707
-
-
El Hifnawi, S.1
Lincoln, D.T.2
Dashti, H.3
-
124
-
-
0025350044
-
Studies of experimentally induced retinal degeneration: 2. Early morphological changes produced by lipid peroxides in the albino rabbit
-
Armstrong D, Hiramitsu T. Studies of experimentally induced retinal degeneration: 2. Early morphological changes produced by lipid peroxides in the albino rabbit. Jpn J Ophthalmol 1990;34:158-73.
-
(1990)
Jpn J Ophthalmol
, vol.34
, pp. 158-173
-
-
Armstrong, D.1
Hiramitsu, T.2
-
125
-
-
0030826430
-
Tissue oxygen during a critical developmental period controls the death and survival of photoreceptors
-
Maslim J, Valter K, Egensperger R, et al. Tissue oxygen during a critical developmental period controls the death and survival of photoreceptors. Invest Ophthalmol Vis Sci 1997;38:1667-77.
-
(1997)
Invest Ophthalmol Vis Sci
, vol.38
, pp. 1667-1677
-
-
Maslim, J.1
Valter, K.2
Egensperger, R.3
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