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1 dance or synaptogenesis, particularly in the retinotectal and motor systems.
2 undamental differences in the development of retinotectal and retinocollicular maps.
3                                        Avian retinotectal and rodent retinocollicular systems are gen
4  the expression of ephrin-As on axons of the retinotectal and vomeronasal projections suggests that t
5                               Here we imaged retinotectal axon arbor location and structural plastici
6 ion also increased the growth of presynaptic retinotectal axon arbors.
7                                     Accurate retinotectal axon pathfinding depends upon the correct e
8 l(ty54)) mutant was identified by defects in retinotectal axon projections.
9 ic HS sequences are essential for regulating retinotectal axon targeting and suggest that regionalise
10  an increase in the synaptic excitability of retinotectal axon terminals.
11 tectal neurons can modify the development of retinotectal axons in Xenopus.
12 tinotectal axons was investigated by imaging retinotectal axons labeled with the fluorescent indicato
13                                   As growing retinotectal axons navigate from the eye to the tectum,
14 n 5-HT it induces, on the terminal arbors of retinotectal axons rather than on their parent cells.
15  of melatonin on calcium dynamics in Xenopus retinotectal axons was investigated by imaging retinotec
16 since depolarization-evoked calcium rises in retinotectal axons were inhibited by GABA(C) receptor bl
17 ta therefore support the hypothesis that, in retinotectal axons, melatonin reduces cAMP levels, there
18 ls, GABA(C) receptors mediate inhibition, in retinotectal axons, the opposite appears to occur since
19 involvement in the unilateral containment of retinotectal axons.
20 ury to optic tectal neurons without damaging retinotectal axons.
21 dynamics of presynaptic sites within labeled retinotectal axons.
22 uRs) counteracted the effect of melatonin on retinotectal axons.
23                  We find that in the Xenopus retinotectal circuit, during a period in development whe
24 or permissive for shaping development of the retinotectal circuit.
25  excitation and inhibition in the developing retinotectal circuit.
26 induce persistent modification of developing retinotectal circuits via spike timing-dependent plastic
27  development of the temporonasal axis of the retinotectal/collicular map, but the role of these molec
28      We show that the laminar specificity of retinotectal connections does not depend on self-sorting
29 nor OMR were found to be dependent on intact retinotectal connections.
30 ation was examined in the developing Xenopus retinotectal connections.
31 which is required for Eph receptor-dependent retinotectal development in chick and for development of
32 te missorted axons in the optic tract during retinotectal development in zebrafish.
33 e test the role of axon-axon interactions in retinotectal development, by devising a technique to sel
34  increased SC concentrations of 5-HT altered retinotectal development.
35 t a novel role for netrin in later phases of retinotectal development.
36 cing intracellular calcium concentrations in retinotectal fibers in the frog optic tectum in vitro.
37 ectum, using confocal imaging of DiI-labeled retinotectal fibers in whole-mount tecta of embryos pret
38       This result provides evidence that the retinotectal fibers serving the pupil light reflex are l
39 inase II (CaMKII) promotes the maturation of retinotectal glutamatergic synapses in Xenopus.
40    Despite several studies, knowledge of the retinotectal guidance molecules is far from being comple
41 iling and identified several novel candidate retinotectal guidance molecules.
42 al layers, as demonstrated by destruction of retinotectal input by intraocular application of the dru
43                                Glutamatergic retinotectal inputs mediated principally by NMDA recepto
44  from a selective elimination of feedforward retinotectal inputs.
45 euromodulator that binds to receptors in the retinotectal laminae of the amphibian optic tectum.
46 ularia), species capable of regenerating the retinotectal map as adults.
47                                     Although retinotectal map formation is a prominent manifestation
48 for their function as putative regulators of retinotectal map formation.
49                                          The retinotectal map is the best characterized model system
50 me period when significant refinement of the retinotectal map occurs.
51 uit, during a period in development when the retinotectal map undergoes activity-dependent refinement
52 priate to contribute to the formation of the retinotectal map, and we suggest that these methods be u
53 e influence the fine-scale topography of the retinotectal map, indicating that lineage relationships
54 nt sets of guidance cues to give rise to the retinotectal map.
55  of the tectum, where they form a compressed retinotectal map.
56 the retina and controls the formation of the retinotectal map.
57 is is important for establishing the correct retinotectal map.
58 both before and after the development of the retinotectal map.
59 ion of molecules that are needed to form the retinotectal map.
60 s an axon guidance molecule, plays a role in retinotectal mapping along the medial-lateral axis, coun
61  ephrin-B cytoplasmic domain is critical for retinotectal mapping in this axis.
62 requirement for endogenous EphA receptors in retinotectal mapping, show that the receptor intracellul
63 ation along RGC axons are critical events in retinotectal mapping.
64 ong the D-V axis of the retina and influence retinotectal mapping.
65 onal EphAs and has a key role in controlling retinotectal mapping.
66 ss-of-function analysis of EphA receptors in retinotectal mapping.
67 f their expression gradients with developing retinotectal maps and gradients of cellular development
68                                The zebrafish retinotectal mutants represent a new resource for the st
69                               Lesions of the retinotectal neuropil primarily abolished orienting move
70 est that nucleus isthmi input can facilitate retinotectal neurotransmission, and the mechanism could
71        To address how the highly stereotyped retinotectal pathway develops in zebrafish, we used fixe
72 ssed distractors and implicate a role of the retinotectal pathway in many blindsight phenomena.
73    These fibers may represent either a novel retinotectal pathway or collateral branches from centrif
74 e that NO has some signaling function in the retinotectal pathway, but this function is not critical
75 P, to determine its capacity to activate the retinotectal pathway.
76                         At later stages, the retinotectal projection also degenerates in ako mutants.
77 -thymidine neuronography, we have mapped the retinotectal projection and the spatiotemporal progressi
78 olved in refinement of the topography of the retinotectal projection as well as in other aspects of r
79 visual system, topographic refinement of the retinotectal projection depends on electrical activity.
80                                          The retinotectal projection has long been studied experiment
81                                          The retinotectal projection has served as an important model
82 resent a detailed phenotypic analysis of the retinotectal projection in nev and show that dorsonasal
83 glion cell axons of the developing and adult retinotectal projection in vivo.
84                                          The retinotectal projection is a premier model system for th
85 ptor-mediated elimination of the ipsilateral retinotectal projection is completely mediated via nitri
86                      A transient ipsilateral retinotectal projection is normally eliminated during em
87 ing of retinal axons after the time that the retinotectal projection is normally topographically orga
88                                          The retinotectal projection is the predominant model for stu
89 have been implicated in the formation of the retinotectal projection map.
90 conclusion that the effect of 5,7-DHT on the retinotectal projection may primarily be a function of t
91 dertaken to determine whether changes in the retinotectal projection of 5,7-DHT-treated animals were
92 r introduction of radiolabeled NT-3 into the retinotectal projection of chick embryos.
93                                  We used the retinotectal projection of goldfish to test this idea in
94         Here, we show that in the developing retinotectal projection of young Xenopus tadpoles, visua
95 , resulted in abnormalities in the uncrossed retinotectal projection similar to those observed in the
96 o the embryonic chick eye in vivo caused the retinotectal projection to develop without normal topogr
97 st that Tctp supports the development of the retinotectal projection via its regulation of pro-surviv
98      The degree of rescue of the ipsilateral retinotectal projection was compared in embryos treated
99                 Thus, the paradigmatic chick retinotectal projection, due to its neighborhood preserv
100                                In the visual retinotectal projection, ELF-1, a ligand in the tectum,
101 d in oligodendrocytes along the regenerating retinotectal projection, mirroring up-regulation of endo
102 ions during the formation of the topographic retinotectal projection, we coexpressed cytosolic fluore
103 of neuronal processes in the Xenopus tadpole retinotectal projection.
104 tectum influences topographic mapping of the retinotectal projection.
105 lso prevented elimination of the ipsilateral retinotectal projection.
106 axons and in retaining the laterality of the retinotectal projection.
107 ormal terminal distribution of the uncrossed retinotectal projection.
108 N-cadherin in the development of the Xenopus retinotectal projection.
109 ific abnormalities in the development of the retinotectal projection.
110 ng CNS development, including patterning the retinotectal projection.
111 f proximal branches during refinement of the retinotectal projection.
112  necessary for the normal development of the retinotectal projection.
113 inal innervation in spinal motoaxons and the retinotectal projection.
114 f optic axons, or during regeneration of the retinotectal projection.
115 inal OFF pathway controls turn movements via retinotectal projections and establishes correct orienta
116                             Developing chick retinotectal projections extend rostrally in the superfi
117 elimination of topographically inappropriate retinotectal projections in a dose-dependent manner.
118 they have different roles in the guidance of retinotectal projections in vivo.
119 es between the organization of the uncrossed retinotectal projections of 5-HT-treated animals vs. eit
120 tp deficiency results in stunted and splayed retinotectal projections that fail to innervate the opti
121 placed over the SC on either P-1 or P-3, and retinotectal projections were assessed via anterograde t
122 ormalities in both the crossed and uncrossed retinotectal projections when these animals reach adulth
123 tain the refined topographic organization of retinotectal projections.
124 roposed role in specification of topographic retinotectal projections.
125 f cytoarchitecture as well as the pattern of retinotectal projections.
126             The role of GABA(C) receptors in retinotectal responses was also evaluated.
127 to be anteroposterior mapping labels for the retinotectal/retinocollicular projection.
128 d occur with S-cone stimuli invisible to the retinotectal route.
129  ELF-1 could determine nasal versus temporal retinotectal specificity, and providing a direct demonst
130 rons indicate that CPG15 expression promotes retinotectal synapse maturation by recruiting functional
131 f ephrin-B signaling increased the number of retinotectal synapses and stabilized the axon arbors of
132             These fine structural changes at retinotectal synapses are consistent with the role that
133 elatively immature synaptic circuit in which retinotectal synapses are formed on developing filopodia
134                                              Retinotectal synapses comprise the majority of synapses
135                                       LTP of retinotectal synapses in developing Xenopus was also rev
136 ely occluded long-term potentiation (LTP) of retinotectal synapses induced by direct electrical stimu
137 in the number of docked synaptic vesicles at retinotectal synapses made by RGC axons expressing GFP-T
138 e report that LTP and LTD induced in vivo at retinotectal synapses of Xenopus tadpoles undergo rapid
139                                       Mutant retinotectal synapses release less glutamate, per vesicl
140 Xenopus tectal neurons shows that convergent retinotectal synapses undergo activity-dependent coopera
141 um, which induced persistent potentiation of retinotectal synapses, led to a rapid modification of sy
142  short period after the initial formation of retinotectal synapses, spike visual RFs of tectal neuron
143 ncement can be attributed to potentiation of retinotectal synapses.
144 vity-induced long-term potentiation (LTP) of retinotectal synapses.
145 s morphological and functional maturation of retinotectal synapses.
146 ownstream of NMDA receptor activation during retinotectal synaptic competition because NMDA receptor
147 It is possible, however, that BDNF modulates retinotectal synaptic connectivity by differentially inf
148          As tectal cell dendrites elaborate, retinotectal synaptic responses acquire an AMPA receptor
149 ing the formation of topographic maps in the retinotectal system have long been debated.
150 ects of sensory stimuli in refinement of the retinotectal system in Xenopus.
151 of the optic nerve in the developing Xenopus retinotectal system induces long-term potentiation (LTP)
152 lead on several parameters of the developing retinotectal system of frog tadpoles was tested.
153 recise axon pathfinding and targeting in the retinotectal system of the zebrafish (Danio rerio).
154 xpression of Homer in the developing Xenopus retinotectal system results in axonal pathfinding errors
155  ultrastructural organization of the Xenopus retinotectal system to understand better the maturation
156 , ligands for EphB2, in the developing chick retinotectal system using riboprobes, immunocytochemistr
157 alization of guidance cues in the developing retinotectal system, a three-compartment chamber was cre
158           However, in the developing Xenopus retinotectal system, activity-induced synaptic modificat
159                            In the developing retinotectal system, APP, contactin 4 and NgCAM are expr
160                             In the zebrafish retinotectal system, retinal ganglion cells (RGCs) proje
161 In addition, as has been demonstrated in the retinotectal system, some of these genes are likely to c
162  report here that, in the developing Xenopus retinotectal system, the receptive field of tectal neuro
163 and physiological development of the Xenopus retinotectal system.
164 R2Ct) in optic tectal neurons of the Xenopus retinotectal system.
165 fication also exists in an intact developing retinotectal system.
166 f optimal shape, as might be relevant in the retinotectal system.Two distinct spatial limits on guida
167 5 protein is exported along RGC axons to the retinotectal terminals and may act as a neurotrophin car
168 sential for vertebrate eye morphogenesis and retinotectal topographic mapping.
169 ial interactions suggest that development of retinotectal topography critically depends on cell-speci
170 eviously proposed role in the development of retinotectal topography.
171 re did not interfere with the development of retinotectal topography.
172 lopmental increase in AMPA receptor-mediated retinotectal transmission and increased GABAergic synapt
173 epolarizing Cl- conductances that facilitate retinotectal transmission by NMDA receptors.
174 etinorecipient layers of the frog tectum, on retinotectal transmission.
175 aling within these structures or anterograde retinotectal trophic support.

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