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During this process, we elaborate on responses of AMD vulnerable cells, including photoreceptors, retinal pigment epithelial cells, microglia, and choroidal endothelial cells, based on in vitro and in vivo studies, to select stressful agents, and discuss current therapeutic developments in the field, targeting different aspects of AMD pathobiology

Loss of the oxidative stress sensor NPGPx compromises GRP78 chaperone activity and induces systemic disease

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Tailoring to RB: tumour suppressor status and therapeutic response

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