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Basic & Translational Research

Subspecialties Retina

A DRAMatic Result

| Roisin McGuigan

A protein involved in autophagy, DRAM2, appears to be essential for photoreceptor survival

Subspecialties Imaging & Diagnostics

It’s Never as Simple as it Seems

| Mark Hillen

A simple, clean and elegant gene editing technique might not be that simple, clean or elegant.

Subspecialties Health Economics and Policy

The Economics of Gene Therapy

| Irv Arons

Gene and stem cell therapies hold the promise of restoring vision in patients with retinal diseases – but who should be paying for these treatments, and how?

Subspecialties Cornea / Ocular Surface

Success Second Time Round

Second corneal transplants are far more likely to be rejected than first-time grafts – but now that we know why, we might be able to prevent it

Subspecialties Cataract

Look How Far We’ve Come

We look at the last 50 years of Fight for Sight – the projects it has funded, and the discoveries its funding helped to achieve.

Subspecialties Imaging & Diagnostics

A Penny Pusher Model of Lens Growth

New research shows that lens epithelial cells proliferate along a narrow line, pushing older cells toward the equator and then the center of the lens

Subspecialties Retina

Plastic and Fantastic

| Roisin McGuigan

Damage to the primary visual cortex strengthens neuronal connectivity between the retina and pulvinar nucleus of the thalamus – and might explain a few phenomena.

Subspecialties Retina

Intrepid Ophthalmology: Replacing the RPE with Cells on a Scaffold

| Boris Stanzel

We talk with Boris Stanzel about growing retinal pigment epithelial (RPE) cells on carrier scaffolds, implanting them under the retina, and the potential it has to treat age-related macular degeneration (AMD).

Subspecialties Retina

Regenerating the Retina

| Irv Arons

Retinal progenitor cell transplantation offers a new approach to repairing damaged photoreceptors

Subspecialties Neuro-ophthalmology

Targeting Heritable Childhood Blindness

| Mark Hillen

Gene sequencing study identifies a gene mutation responsible for heritable cases of LCA and OMS for the first time

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