Results 261 to 270 of about 125,005 (308)
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Modeling of retinal degeneration
Bulletin of Experimental Biology and Medicine, 2021We developed a model of retinal degeneration in rabbits based on exposure to light with a wavelength of 405 nm. This model allows reproducing structural and functional disorders in the central parts of the retina, including primarily degeneration of the outer layers of the retina (retinal pigment epithelium and layer of photoreceptor cells), and is ...
A A, Suetov +4 more
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Retinal Degeneration in Kittens
Journal of the American Veterinary Medical Association, 1973SUMMARY Diffuse outer segment retinal degeneration was found in 2 Persian kittens in each of 2 successive litters by 15 weeks of age. Clinical signs were mydriasis, tapetal hyperreflectivity, retinal vascular attenuation, and abnormalities in visual behavior. The disease seemed to be inherited as a simple autosomal recessive trait.
L F, Rubin, D E, Lipton
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RETINAL DEGENERATION IN GREYHOUNDS
Australian Veterinary Journal, 1980Retinal degeneration in 10 Greyhounds with clinical and ophthalmoscopic features is described, including results of electroretinography and fluorescein angiography for one affected dog. Clinical and histologic features differed from other kinds of retinal degeneration in dogs.
D H, Slatter, J R, Blogg, I J, Constable
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Retinal remodeling during retinal degeneration
Experimental Eye Research, 2005Retinal degenerations, regardless of the initiating event or gene defect, often result in a loss of photoreceptors. This formal deafferentation of the neural retina eliminates the intrinsic glutamatergic drive of the sensory retina and, perhaps more importantly, removes coordinated Ca++-coupled signaling to the neural retina.
Bryan W, Jones, Robert E, Marc
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Nutrition and Retinal Degenerations
International Ophthalmology Clinics, 2000Considerable progress has been made in the understanding and management of degenerative diseases of the retina involving photoreceptors. Nutritional approaches to treatment have proved successful in the case of the common forms of retinitis pigmentosa (supplementation with vitamin A), Bassen-Kornzweig disease (supplementation with vitamins A, E, and K),
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Calpain activity in retinal degeneration
Journal of Neuroscience Research, 2006AbstractRetinal degenerations such as retinitis pigmentosa (RP) or glaucoma are a major cause of blindness in humans. Understanding the mechanisms underlying the various types of retinal degeneration is a pre‐requisite for the development of rational therapies for these diseases. Activation of the calcium dependent protease, calpain, has been suggested
François, Paquet-Durand +2 more
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Lipid peroxidation and retinal degeneration
Current Eye Research, 1984Retinal degenerations were produced in albino rats by exposure to constant illumination or in frogs and albino rats by intravitreal injections of ferrous sulfate. Both treatments resulted in the loss of long-chain polyunsaturated fatty acids and the accumulation of lipid hydroperoxides in isolated rod outer segments.
R E, Anderson, L M, Rapp, R D, Wiegand
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Retinitis pigmentosa and retinal degeneration in animals: a review
Canadian Journal of Biochemistry and Cell Biology, 1984Recent biochemical findings in the human disease, retinitis pigmentosa, and related retinal degenerative diseases in animals were reviewed and discussed. While the biochemical etiology of the human disease is not known, there are indications that retinal degeneration in the rd mouse and the Irish Setter dog are related to a deficiency in cGMP ...
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Peripheral retinal degenerations and the risk of retinal detachment
American Journal of Ophthalmology, 2003To review the degenerative diseases of the peripheral retina in relationship with the risk to develop a rhegmatogenous retinal detachment and to present recommendations for use in eyes at increased risk of developing a retinal detachment.Focused literature review and author's clinical experience.Retinal degenerations are common lesions involving the ...
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