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Last Updated: 10/31/2025

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Found 11665 publications

Non-Neoplastic Disorders Mimicking Posterior Segment Inflammation.

Non-Neoplastic Disorders Mimicking Posterior Segment Inflammation.

Journal: Ocular immunology and inflammation
Published: October 17, 2025

Choroidal neovascularization in a teenager with Kearns Sayre syndrome.

Choroidal neovascularization in a teenager with Kearns Sayre syndrome.

Journal: Ophthalmic genetics
Published: October 14, 2025

Preclinical Evaluation of Pitavastatin Nanoparticles for Preserving Cone Photoreceptors in Mouse Models of RP.

Preclinical Evaluation of Pitavastatin Nanoparticles for Preserving Cone Photoreceptors in Mouse Models of RP.

Journal: Investigative ophthalmology & visual science
Published: October 08, 2025

Long-Term Outcomes and Patient Experiences With the Argus II Retinal Prosthesis System.

Long-Term Outcomes and Patient Experiences With the Argus II Retinal Prosthesis System.

Journal: Journal of vitreoretinal diseases
Published: October 07, 2025

One down but many more to go: the state of gene therapy for inherited retinal disease.

One down but many more to go: the state of gene therapy for inherited retinal disease.

Journal: Regenerative medicine
Published: October 07, 2025

Super-resolution microscopy reveals a Rab6a-dependent trafficking hub for rhodopsin at the mammalian rod photoreceptor Golgi.

Super-resolution microscopy reveals a Rab6a-dependent trafficking hub for rhodopsin at the mammalian rod photoreceptor Golgi.

Journal: bioRxiv : the preprint server for biology
Published: October 03, 2025

RHO1-2 meganuclease gene editing targets human P23H rhodopsin-induced retinitis pigmentosa to rejuvenate rods and maintain cones.

RHO1-2 meganuclease gene editing targets human P23H rhodopsin-induced retinitis pigmentosa to rejuvenate rods and maintain cones.

Journal: bioRxiv : the preprint server for biology
Published: October 03, 2025

Membrane frizzled-related protein: a comprehensive analysis of genetic characteristics, phenotypic manifestations and impact on retinal microvasculature.

Membrane frizzled-related protein: a comprehensive analysis of genetic characteristics, phenotypic manifestations and impact on retinal microvasculature.

Journal: Ophthalmic genetics
Published: October 03, 2025

A new genotype of the IDH3A gene causes retinitis pigmentosa, generating functional dyschromatopsia from early childhood.

A new genotype of the IDH3A gene causes retinitis pigmentosa, generating functional dyschromatopsia from early childhood.

Journal: Ophthalmic genetics
Published: September 24, 2025

A sound vision: MYO7A gene therapy reaches the inner ear.

A sound vision: MYO7A gene therapy reaches the inner ear.

Journal: The Journal of physiology
Published: September 22, 2025

Exon Skipping Therapy Restores Ciliary Function in USH2A-Related Retinal Degeneration.

Exon Skipping Therapy Restores Ciliary Function in USH2A-Related Retinal Degeneration.

Journal: Investigative ophthalmology & visual science
Published: September 19, 2025

Update on Gene Therapy Clinical Trials for Eye Diseases.

Update on Gene Therapy Clinical Trials for Eye Diseases.

Journal: Human gene therapy
Published: September 18, 2025
Showing 1-12 of 11,665

Last Updated: 10/31/2025