Found: 16
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Excess cones in the retinal degeneration rd7 mouse, caused by the loss of function of orphan nuclear receptor Nr2e3, originate from early-born photoreceptor precursors.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4102, doi. 10.1093/hmg/ddr334
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- Article
A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration.
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- Human Molecular Genetics, 2011, v. 20, n. 10, p. 2000, doi. 10.1093/hmg/ddr080
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- Article
Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene.
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- Human Molecular Genetics, 2008, v. 17, n. 24, p. 3929, doi. 10.1093/hmg/ddn295
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- Article
Inherited Retinal Degeneration: Genetics, Disease Characterization, and Outcome Measures.
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- Journal of Ophthalmology, 2017, p. 1, doi. 10.1155/2017/2109014
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- Article
A Mouse Model with Ablated Asparaginase and Isoaspartyl Peptidase 1 (Asrgl1) Develops Early Onset Retinal Degeneration (RD) Recapitulating the Human Phenotype.
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- Genes, 2022, v. 13, n. 8, p. 1461, doi. 10.3390/genes13081461
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- Article
Expansion of Severely Constricted Visual Field Using Google Glass.
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- 2016
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- journal article
Prolonged Inner Retinal Photoreception Depends on the Visual Retinoid Cycle.
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- Journal of Neuroscience, 2016, v. 36, n. 15, p. 4209, doi. 10.1523/JNEUROSCI.2629-14.2016
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- Article
Contrast sensitivity deficits in patients with mutation-proven inherited retinal degenerations.
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- 2018
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- journal article
Rd9 Is a Naturally Occurring Mouse Model of a Common Form of Retinitis Pigmentosa Caused by Mutations in RPGR-ORF15.
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- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0035865
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- Article
Distinct Signature of Altered Homeostasis in Aging Rod Photoreceptors: Implications for Retinal Diseases.
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- PLoS ONE, 2010, v. 5, n. 11, p. 1, doi. 10.1371/journal.pone.0013885
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- Article
IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis.
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- Human Genetics, 2018, v. 137, n. 6/7, p. 447, doi. 10.1007/s00439-018-1897-9
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- Article
Autoimmune retinopathy associated with monoclonal gammopathy of undetermined significance: a case report.
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- 2020
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- Publication type:
- journal article
Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis.
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- PLoS Genetics, 2021, v. 17, n. 10, p. 1, doi. 10.1371/journal.pgen.1009848
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- Article
ISCEV extended protocol for the photopic On-Off ERG.
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- Documenta Ophthalmologica, 2018, v. 136, n. 3, p. 199, doi. 10.1007/s10633-018-9645-y
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- Article
Macular hyperpigmentary changes in ABCA4-Stargardt disease.
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- International Journal of Retina & Vitreous, 2019, v. 5, n. 1, p. N.PAG, doi. 10.1186/s40942-019-0160-4
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- Article
Acute Panretinal Structural and Functional Abnormalities After Intravitreous Ocriplasmin Injection.
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- JAMA Ophthalmology, 2014, v. 132, n. 4, p. 484, doi. 10.1001/jamaophthalmol.2013.8142
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- Article