1989
DOI: 10.1016/0306-4522(89)90246-7
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Generation of retinal cells in the wallaby, Setonix brachyurus (quokka)

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Cited by 78 publications
(73 citation statements)
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References 37 publications
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“…The order of cell genesis in Xenopus retina apparent at the clonal level is very similar to that of other vertebrates [wallaby (Harman and Beazley, 1989); monkey (La Vail et al, 1991); rat (Rapaport et al, 2004)]. The only difference is that RPr are generated in close step with CPr in Xenopus, whereas in the wallaby, rat and non-foveal region of monkey retina, they are generated late, after Am.…”
Section: Research Articlesupporting
confidence: 52%
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“…The order of cell genesis in Xenopus retina apparent at the clonal level is very similar to that of other vertebrates [wallaby (Harman and Beazley, 1989); monkey (La Vail et al, 1991); rat (Rapaport et al, 2004)]. The only difference is that RPr are generated in close step with CPr in Xenopus, whereas in the wallaby, rat and non-foveal region of monkey retina, they are generated late, after Am.…”
Section: Research Articlesupporting
confidence: 52%
“…Were this model to operate one would expect consistent ordinal relationships between some cell types, but not between others. For example, if the phases of retinal cell birth reported in a number of vertebrates (Harman and Beazley, 1989;La Vail et al, 1991;Rapaport et al, 2004) represent competency periods for subsets of cell types, we would have expected to see variable ordinal relations within, but invariant relations between, phases. We always observe rigid ordinal relationships and this accords only with the stepwise model for shifting competence states of RPCs, a cell type at a time.…”
Section: Research Articlementioning
confidence: 99%
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“…Distinguishing ganglion cells from other neurons in the retinal ganglion cell layer is, to some extent, problematic without using a retrograde tracer such as horseradish peroxidase [Harman and Beazley, 1989]. This was not possible with the animals available to us and so, in the present study, we have identified ganglion cells in Nissl stained retinae using standard morphological criteria.…”
Section: Cell Identificationmentioning
confidence: 94%
“…During this phase, the retinae also undergo marked lateral expansion, particularly in the periphery, through the differential addition of second-phase cells to peripheral rather than central retina. 6 The retina is therefore potentially directly vulnerable to corticosteroid therapy, which has known antimitotic effects on DNA, RNA and protein synthesis in the nervous system. 7 , 8 Finally, although there is general agreement that low birthweight preterm infants are at risk for impaired motor development, recent evidence suggests they are also specifically vulnerable to impaired visual development.…”
mentioning
confidence: 99%