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pmid: 7207866
In mice homozygous for the newly reported rds (retinal degeneration slow) gene, a progressive loss of visual cells occurs throughout life. Histogenesis of the retina proceeds normally with the exception of the receptor layer which remains rudimentary. Electron microscopic observations of the retina at different stages of development have revealed that the outer segments of the visual cells in this mutant fail to develop and that the receptor layer consists of inner segments only. In the absorption spectra of the retinal extract from the mutant the characteristic rhodopsin peak is lacking.
Mice, Inbred BALB C, Rhodopsin, Retinal Degeneration, Genes:, Organs:, Rodent Diseases, Mice, Mice, Neurologic Mutants, Microscopy, Electron, Strains:, Morphology:, Animals, Pathology:, Photoreceptor Cells
Mice, Inbred BALB C, Rhodopsin, Retinal Degeneration, Genes:, Organs:, Rodent Diseases, Mice, Mice, Neurologic Mutants, Microscopy, Electron, Strains:, Morphology:, Animals, Pathology:, Photoreceptor Cells
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 188 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 1% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |