339 related articles for article (PubMed ID: 15044842)
1. 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. PubMed ID: 15044842
[TBL] [Abstract][Full Text] [Related]
2. ENU-induced late-onset night blindness associated with rod photoreceptor cell degeneration in zebrafish.
Maaswinkel H; Mason B; Li L
Mech Ageing Dev; 2003 Dec; 124(10-12):1065-71. PubMed ID: 14659595
[TBL] [Abstract][Full Text] [Related]
3. Behavioral screening for nightblindness mutants in zebrafish reveals three new loci that cause dominant photoreceptor cell degeneration.
Maaswinkel H; Riesbeck LE; Riley ME; Carr AL; Mullin JP; Nakamoto AT; Li L
Mech Ageing Dev; 2005 Oct; 126(10):1079-89. PubMed ID: 15922406
[TBL] [Abstract][Full Text] [Related]
4. Lazy eyes zebrafish mutation affects Müller glial cells, compromising photoreceptor function and causing partial blindness.
Kainz PM; Adolph AR; Wong KY; Dowling JE
J Comp Neurol; 2003 Aug; 463(3):265-80. PubMed ID: 12820161
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 23328348
[TBL] [Abstract][Full Text] [Related]
6. Functional and structural modifications during retinal degeneration in the rd10 mouse.
Barhoum R; Martínez-Navarrete G; Corrochano S; Germain F; Fernandez-Sanchez L; de la Rosa EJ; de la Villa P; Cuenca N
Neuroscience; 2008 Aug; 155(3):698-713. PubMed ID: 18639614
[TBL] [Abstract][Full Text] [Related]
7. Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene.
Orosz O; Czeglédi M; Kántor I; Balogh I; Vajas A; Takács L; Berta A; Losonczy G
Mol Vis; 2015; 21():124-30. PubMed ID: 25684977
[TBL] [Abstract][Full Text] [Related]
8. Regressive and reactive changes in the connectivity patterns of rod and cone pathways of P23H transgenic rat retina.
Cuenca N; Pinilla I; Sauvé Y; Lu B; Wang S; Lund RD
Neuroscience; 2004; 127(2):301-17. PubMed ID: 15262321
[TBL] [Abstract][Full Text] [Related]
9. Cone loss is delayed relative to rod loss during induced retinal degeneration in the diurnal cone-rich rodent Arvicanthis ansorgei.
Boudard DL; Tanimoto N; Huber G; Beck SC; Seeliger MW; Hicks D
Neuroscience; 2010 Sep; 169(4):1815-30. PubMed ID: 20600653
[TBL] [Abstract][Full Text] [Related]
10. 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; 11():542-53. PubMed ID: 16052170
[TBL] [Abstract][Full Text] [Related]
11. Development and degeneration of retina in rds mutant mice: light microscopy.
Sanyal S; De Ruiter A; Hawkins RK
J Comp Neurol; 1980 Nov; 194(1):193-207. PubMed ID: 7440795
[TBL] [Abstract][Full Text] [Related]
12. Detailed histopathologic characterization of the retinopathy, globe enlarged (rge) chick phenotype.
Montiani-Ferreira F; Fischer A; Cernuda-Cernuda R; Kiupel M; DeGrip WJ; Sherry D; Cho SS; Shaw GC; Evans MG; Hocking PM; Petersen-Jones SM
Mol Vis; 2005 Jan; 11():11-27. PubMed ID: 15660021
[TBL] [Abstract][Full Text] [Related]
13. 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; 11():152-62. PubMed ID: 15765048
[TBL] [Abstract][Full Text] [Related]
14. A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder.
Littink KW; van Genderen MM; Collin RW; Roosing S; de Brouwer AP; Riemslag FC; Venselaar H; Thiadens AA; Hoyng CB; Rohrschneider K; den Hollander AI; Cremers FP; van den Born LI
Invest Ophthalmol Vis Sci; 2009 May; 50(5):2344-50. PubMed ID: 19074807
[TBL] [Abstract][Full Text] [Related]
15. A dominant form of inherited retinal degeneration caused by a non-photoreceptor cell-specific mutation.
Li L; Dowling JE
Proc Natl Acad Sci U S A; 1997 Oct; 94(21):11645-50. PubMed ID: 9326664
[TBL] [Abstract][Full Text] [Related]
16. Structural and functional remodeling in the retina of a mouse with a photoreceptor synaptopathy: plasticity in the rod and degeneration in the cone system.
Specht D; Tom Dieck S; Ammermüller J; Regus-Leidig H; Gundelfinger ED; Brandstätter JH
Eur J Neurosci; 2007 Nov; 26(9):2506-15. PubMed ID: 17970721
[TBL] [Abstract][Full Text] [Related]
17. Disruption of the olfactoretinal centrifugal pathway may relate to the visual system defect in night blindness b mutant zebrafish.
Li L; Dowling JE
J Neurosci; 2000 Mar; 20(5):1883-92. PubMed ID: 10684889
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 12601061
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 10967077
[TBL] [Abstract][Full Text] [Related]
20. Functional and structural changes in the retina of wire-haired dachshunds with early-onset cone-rod dystrophy.
Ropstad EO; Narfström K; Lingaas F; Wiik C; Bruun A; Bjerkås E
Invest Ophthalmol Vis Sci; 2008 Mar; 49(3):1106-15. PubMed ID: 18326738
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
