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Titlebook: Retinal Pigment Epithelium and Macular Diseases; Gabriel Coscas,Felice Cardillo Piccolino Book 1998 Springer Science+Business Media Dordre

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Subretinal protein and serous detachmentrole of protein in serous detachment in man.. These experiments also examine the effects of vitreous within the subretinal space, as may occur in rhegmatogenous detachment, and the source of protein when serous detachments form after focal ischaemia or toxic damage to the RPE and choroid.
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Ageing of the human retinal pigment epitheliumthe age pigment lipofuscin, have reduced antioxidant capacity and progressively accumulate deposits on, and within, the underlying Bruch’s membrane. These age-related changes in both the RPE and Bruch’s membrane appear to be strongly associated with the pathogenesis of age-related macular degeneration (ARMD).
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Local administration of interferon-beta promotes proliferation of retinal pigment epithelial cells itemic administration of IFN, however, remains a problem with respect to side effects and a high cost. We therefore performed animal experiments to clarify the effect of local administration of human IFN-. on repair of the RPE after laser photocoagulation (PC).
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A short history of the retinal pigment epitheliumtempt to clarify the more fundamental role of the retinal tissues. The notion of a net-like structure was adopted by Celsus and then Galen, and it was finally the mediaeval scholar Gerard of Cremona who coined the Latin translation ‘retina’ in the 12th century. The term has remained in use for more then 800 years.
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Blood—retinal barrier and new perspectives of management of retinal diseasefile of the drug, the volume of its distribution, the rate of metabolism of the drug, its plasma protein binding and the relative permeability of the BRB for that drug. All parameters affect the therapeutic efficacy of the drug and are also relevant for potential side effects.
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Sub-RPE deposits might be related to defective ubiquitin-dependent proteolysislved in the non-lysosomal degradation process of abnormal proteins, especially in neurodegenerative diseases. Using immunohistochemical methods, we investigate the human retina and RPE and in particular sub-RPE deposits for the presence and distribution of Ub and related enzymes.
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