1990
DOI: 10.1016/0736-5748(90)90019-x
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Synapse formation on quail trochlear neurons transplanted in duck embryos before naturally occurring motor neuron death

Abstract: About half of the trochlear motor neurons in duck and quail embryos die during normal development. In a previous study the role of target muscle in controlling the number of surviving motor neurons was investigated by reducing the number of neurons innervating the muscle. This was accomplished by removing the midbrain of the duck embryo and grafting in its place the midbrain of the quail embryo before motor neuron death begins. It was observed that the number of surviving trochlear motor neurons in the quail-d… Show more

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Cited by 5 publications
(5 citation statements)
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References 21 publications
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“…This period of increase in afferent neuronal input to NA coincides with the occurrence of MCD. As MCD is responsive, in part, to signals from afferent neurons (Furber et al, 1987;Sohal et al, 1990;Clarke, 1992), the observed proliferation of afferent input to NA motoneurons at this time may play a modulatory role in the course of cell death.…”
Section: Discussionmentioning
confidence: 97%
“…This period of increase in afferent neuronal input to NA coincides with the occurrence of MCD. As MCD is responsive, in part, to signals from afferent neurons (Furber et al, 1987;Sohal et al, 1990;Clarke, 1992), the observed proliferation of afferent input to NA motoneurons at this time may play a modulatory role in the course of cell death.…”
Section: Discussionmentioning
confidence: 97%
“…One of the newly emerging avian models for analyzing the distinct functions of neural-crest-derived mesenchyme during craniofacial development is the quail-duck chimeric transplantation system (Schneider and Helms, 2003;Tucker and Lumsden, 2004;Eames and Schneider, 2005;Schneider, 2005). The domestic duck has a long history of being included in avian chimeras as a way to study those patterning mechanisms that make embryos morphologically distinct (Waddington, 1930(Waddington, , 1932Hampe, 1957;Zwilling, 1959;Dhouailly, 1967Dhouailly, , 1970Pautou, 1968;Sohal, 1976;Sohal et al, 1985Sohal et al, , 1990Sohal, 1986, 1987). But the combination of Japanese quail (Coturnix coturnix japonica) and White Pekin duck (Anas platyrhynchos) as donors and/or hosts adds value for at least four reasons (Lwigale and Schneider, 2008).…”
Section: Quail-duck Chimerasmentioning
confidence: 99%
“…The domestic duck has a long history of being included in avian chimeras as a way to study those patterning mechanisms that make embryos morphologically distinct (Waddington, 1930(Waddington, , 1932Hampe, 1957;Zwilling, 1959;Dhouailly, 1967Dhouailly, , 1970Pautou, 1968;Sohal, 1976;Sohal et al, 1985Sohal et al, , 1990Sohal, 1986, 1987). But the combination of Japanese quail (Coturnix coturnix japonica) and White Pekin duck (Anas platyrhynchos) as donors and/or hosts adds value for at least four reasons (Lwigale and Schneider, 2008).…”
Section: Quail-duck Chimerasmentioning
confidence: 99%
“…Moreover, determining mechanisms of species‐specific pattern was not really the primary goal of most studies that employed quail‐chick chimeras. In contrast, other experiments using avian chimeras have included domestic duck as a way to identify those patterning mechanisms that generate species‐specific differences (Dhouailly, ; Hampe, ; Lwigale & Schneider, ; Pautou, ; Schneider & Helms, ; Sohal, ; Sohal et al, ; Sohal et al, ; Tucker & Lumsden, ; Waddington, ; Waddington, ; Yamashita & Sohal, , Yamashita & Sohal, ; Zwilling, ). Additional studies on species‐specific size and control of scaling have also included chimeras between quail and emu (Hall et al, ), quail and zebra finch (Chen, Balaban, & Jarvis, ), and chick and zebra finch (Uygur et al, ).…”
Section: Origin Of Species‐specific Pattern As Revealed By Avian Chimmentioning
confidence: 99%