ArticleMolecular therapy. Advances2026
Interrogating the dependency of AAV capsids on AAVR for retinal transduction.
Article in Molecular therapy. Advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- AAV8-Mediated Retinal PD-L1 Gene Transfer Attenuates Experimental Autoimmune Uveitis by Restoring Local Immune Tolerance.Investigative ophthalmology & visual science · 2026Article
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Authors and funding
10 authors.
Funding
Abstract
Adeno-associated virus (AAV) is an established vector for gene therapy, yet there remains much that we do not know regarding mechanisms of transduction in target tissues. The retina is an attractive organ for gene therapy with many programs in development. Thus, further research into the mechanisms of retinal transduction could lead to more effective therapies. Since the AAV receptor (AAVR) (KIAA0319L) has been shown to play a critical role in AAV transduction, we intravitreally injected (IVtI) or subretinally injected (SRI) recombinant AAV vectors packaged in a diverse group of AAV capsids into AAVR
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Registered trials
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