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Cone Phosphodiesterase-6γ’ Subunit Augments Cone PDE6 Holoenzyme Assembly and Stability in a Mouse Model Lacking Both Rod and Cone PDE6 Catalytic Subunits.
- Published in:
- Frontiers in Molecular Neuroscience, 2018, p. N.PAG, doi. 10.3389/fnmol.2018.00233
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- Article
Inhibitor of Apoptosis-Stimulating Protein of p53 (iASPP) Is Required for Neuronal Survival after Axonal Injury.
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0094175
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- Article
AAV-Mediated Cone Rescue in a Naturally Occurring Mouse Model of CNGA3-Achromatopsia.
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- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0035250
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- Article
DICER1 deficit induces Alu RNA toxicity in age-related macular degeneration.
- Published in:
- Nature, 2011, v. 471, n. 7338, p. 325, doi. 10.1038/nature09830
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- Publication type:
- Article
NADH-dehydrogenase Type-2 Suppresses Irreversible Visual Loss and Neurodegeneration in the EAE Animal Model of MS.
- Published in:
- Molecular Therapy, 2013, v. 21, n. 10, p. 1876, doi. 10.1038/mt.2013.104
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- Publication type:
- Article
Safety and Effects of the Vector for the Leber Hereditary Optic Neuropathy Gene Therapy Clinical Trial.
- Published in:
- JAMA Ophthalmology, 2014, v. 132, n. 4, p. 409, doi. 10.1001/jamaophthalmol.2013.7630
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- Article
Identification, genetic analysis and DNA sequence of a 7.8-kb virulence region of the Salmonella typhimurium virulence plasmid.
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- Molecular Microbiology, 1992, v. 6, n. 10, p. 1395, doi. 10.1111/j.1365-2958.1992.tb00860.x
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- Article
In vivo knockdown of Piccolino disrupts presynaptic ribbon morphology in mouse photoreceptor synapses.
- Published in:
- Frontiers in Cellular Neuroscience, 2014, v. 8, p. 1, doi. 10.3389/fncel.2014.00259
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- Publication type:
- Article
Human L- and M-opsins restore M-cone function in a mouse model for human blue cone monochromacy.
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- Molecular Vision, 2018, v. 24, p. 17
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- Article
Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach.
- Published in:
- 2018
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- Publication type:
- journal article
Organizational motifs for ground squirrel cone bipolar cells.
- Published in:
- Journal of Comparative Neurology, 2012, v. 520, n. 13, p. 2864, doi. 10.1002/cne.23068
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- Publication type:
- Article
Vitreal delivery of AAV vectored Cnga3 restores cone function in CNGA3<sup>-/-</sup>/Nrl<sup>-/-</sup> mice, an all-cone model of CNGA3 achromatopsia.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 13, p. 3699, doi. 10.1093/hmg/ddv114
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- Publication type:
- Article
Viral-mediated vision rescue of a novel AIPL1 cone-rod dystrophy model.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 3, p. 670, doi. 10.1093/hmg/ddu487
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- Publication type:
- Article
RD3 gene delivery restores guanylate cyclase localization and rescues photoreceptors in the Rd3 mouse model of Leber congenital amaurosis 12.
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- Human Molecular Genetics, 2013, v. 22, n. 19, p. 3894, doi. 10.1093/hmg/ddt244
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- Publication type:
- Article
Gene therapy rescues cone function in congenital achromatopsia.
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- Human Molecular Genetics, 2011, v. 20, n. 24, p. 5024, doi. 10.1093/hmg/ddr429
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- Publication type:
- Article
Gene therapy using self-complementary Y733F capsid mutant AAV2/8 restores vision in a model of early onset Leber congenital amaurosis.
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- Human Molecular Genetics, 2011, v. 20, n. 23, p. 4569, doi. 10.1093/hmg/ddr391
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- Publication type:
- Article
AAV-Mediated Clarin-1 Expression in the Mouse Retina: Implications for USH3A Gene Therapy.
- Published in:
- PLoS ONE, 2016, v. 11, n. 2, p. 1, doi. 10.1371/journal.pone.0148874
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- Publication type:
- Article
Novel Properties of Tyrosine-mutant AAV2 Vectors in the Mouse Retina.
- Published in:
- Molecular Therapy, 2011, v. 19, n. 2, p. 293, doi. 10.1038/mt.2010.234
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- Publication type:
- Article
High-efficiency Transduction of the Mouse Retina by Tyrosine-mutant AAV Serotype Vectors.
- Published in:
- Molecular Therapy, 2009, v. 17, n. 3, p. 463, doi. 10.1038/mt.2008.269
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- Publication type:
- Article
Gene Therapy Restores Vision-Dependent Behavior as Well as Retinal Structure and Function in a Mouse Model of RPE65 Leber Congenital Amaurosis.
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- Molecular Therapy, 2006, v. 13, n. 3, p. 565, doi. 10.1016/j.ymthe.2005.09.001
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- Publication type:
- Article
Localized Gene Expression Following Administration of Adeno-associated Viral Vectors via Pancreatic Ducts
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- Molecular Therapy, 2005, v. 12, n. 3, p. 519, doi. 10.1016/j.ymthe.2005.04.017
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- Publication type:
- Article
Transgene expression of Stanniocalcin-1 provides sustained intraocular pressure reduction by increasing outflow facility.
- Published in:
- PLoS ONE, 2022, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0269261
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- Publication type:
- Article
Gene therapy rescues cone function in congenital achromatopsia.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 13, p. 2581
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- Publication type:
- Article
Cone Phosphodiesterase-6α' Restores Rod Function and Confers Distinct Physiological Properties in the Rod Phosphodiesterase-6β-Deficient rd1O Mouse.
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- Journal of Neuroscience, 2013, v. 33, n. 29, p. 11745, doi. 10.1523/JNEUROSCI.1536-13.2013
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- Publication type:
- Article
ELOVL4-Mediated Production of Very Long-Chain Ceramides Stabilizes Tight Junctions and Prevents Diabetes-Induced Retinal Vascular Permeability.
- Published in:
- Diabetes, 2018, v. 67, n. 4, p. 769, doi. 10.2337/db17-1034
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- Publication type:
- Article