Found: 6
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Spontaneous allelic variant in deafness–blindness gene Ush1g resulting in an expanded phenotype.
- Published in:
- Genes, Brain & Behavior, 2023, v. 22, n. 4, p. 1, doi. 10.1111/gbb.12849
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- Article
Natural History of Cone Disease in the Murine Model of Leber Congenital Amaurosis Due to <i>CEP290</i> Mutation: Determining the Timing and Expectation of Therapy.
- Published in:
- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0092928
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- Article
Targeting Photoreceptors via Intravitreal Delivery Using Novel, Capsid-Mutated AAV Vectors.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0062097
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- Article
Preformed Vesicle Approach to LNP Manufacturing Enhances Retinal mRNA Delivery.
- Published in:
- Small, 2024, v. 20, n. 37, p. 1, doi. 10.1002/smll.202400815
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- Article
The effects of PEGylation on LNP based mRNA delivery to the eye.
- Published in:
- PLoS ONE, 2020, v. 15, n. 10, p. 1, doi. 10.1371/journal.pone.0241006
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- Publication type:
- Article
Retinal Neuroprotective Effects of Flibanserin, an FDA-Approved Dual Serotonin Receptor Agonist-Antagonist.
- Published in:
- PLoS ONE, 2016, v. 11, n. 7, p. 1, doi. 10.1371/journal.pone.0159776
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- Article