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1 ied in the hypothalamus and one group in the pretectum.
2 the caudal thalamus, epithalamus and rostral pretectum.
3 thalamus, the zona incerta, and the anterior pretectum.
4 son with counterparts in the chick and mouse pretectum.
5 neurons were observed in the prethalamus and pretectum.
6 abnormally contribute to the epithalamus and pretectum.
7 f epithalamus are derived from the embryonic pretectum.
8 ucleus, the intergeniculate leaflet, and the pretectum.
9 vidual cells project to both the SCN and the pretectum.
10 IGL and their projections to hamster SCN and pretectum.
11 d in groups of cells in the diencephalon and pretectum.
12 ad, with 97% projecting to the contralateral pretectum.
13 eurons) across the mouse visual thalamus and pretectum.
14  in the prethalamus, posterior tubercle, and pretectum.
15 s intrathalamica (ZLI), the thalamus and the pretectum].
16 t optic projections to the SCN, thalamus and pretectum and a functional GHT.
17 ing from the optic tract at the level of the pretectum and anterior superior colliculus, the other em
18 lls in key non-image forming visual centres (pretectum and intergeniculate leaflet/ventral lateral ge
19                          In vertebrates, the pretectum and optic tectum (superior colliculus in mamma
20  of live prey show activity in visual areas (pretectum and optic tectum) and motor areas (cerebellum
21 microinjections of Fluoro-Gold into the OPN (pretectum and superior colliculus as controls) to retrog
22 opulations were located in the diencephalon (pretectum and thalamus), mesencephalon (reticular format
23 form these areas, and, instead, the adjacent pretectum and, to a lesser extent, the prethalamus expan
24 sory (medial olfactory bulb, parapineal, and pretectum) and not limbic areas, as they do in mammals;
25 ions from the thalamic reticular nucleus and pretectum, and a cholinergic projection from the parabig
26 orsal neural tube, and mesencephalic tectum, pretectum, and base, and at the midbrain-hindbrain bound
27 ates indicates that the vertebrate thalamus, pretectum, and midbrain domains jointly correspond to a
28 e ZLI (including the future dorsal thalamus, pretectum, and midbrain) was disrupted, supporting the i
29 ral lateral geniculate nuclei, nuclei of the pretectum, and nucleus of the brachium of the inferior c
30 m basal ganglia, zona incerta (ZI), anterior pretectum, and pontine reticular formation) provides tem
31  R-cadherin message in the hypothalamus, the pretectum, and the anterolateral optic tectum.
32 ged from the optic tract at the level of the pretectum/anterior mesencephalon.
33                              In the anterior pretectum (APT), a hub of connectivity of the somatosens
34 onventionally termed "ventral" thalamus) and pretectum but is downregulated in the body of the poster
35  all four types also send projections to the pretectum, but rarely do individual cells project to bot
36                                          The pretectum can be subdivided roughly into three areas bas
37  subnuclei in the geniculate complex and the pretectum contain labeled retinofugal axons in the Cdh3-
38 boundaries delineating the thalamus from the pretectum, epithalamus and prethalamus, revealing multip
39 pient areas-underlines the importance of the pretectum for sensory integration and visuomotor functio
40 m has been investigated in great detail, the pretectum has received far less attention.
41 lium and the subpallium, in the thalamus and pretectum, in the optic tectum and torus semicircularis,
42 s to the reticulospinal nuclei, and thus the pretectum indirectly affects the control of movement.
43                             In addition, the pretectum is reciprocally connected with the thalamus, t
44 s vulgaris-leucoagglutin, into nuclei of the pretectum (medial, commissural, posterior, olivary, ante
45 ganglion cells (RGC) that project to the rat pretectum, much of this evidence is circumstantial, and
46  the nucleus of the optic tract (NOT) in the pretectum of marmosets.
47 evious analysis of progenitor domains in the pretectum of Xenopus revealed three molecularly distinct
48 restricted to the roof plate of prosomere 2, pretectum, optic tectum, rhombencephalon, and spinal cor
49 to retinorecipient laminae of the tectum and pretectum or bilaterally to both tectal hemispheres.
50 and visual midbrain or neurotoxic lesions of pretectum or deep superior colliculus (but not of the su
51 s neuromodulator projections from the IGL to pretectum or SCN are discussed.
52 alistic motion cues, and the retinorecipient pretectum organizes these cues around the elements of be
53 enopus and show that the organization of the pretectum possesses many features shared with birds.
54                                     Both the pretectum (PT) and the superior colliculus (SC) play an
55 nnections formed by GABAergic neurons in the pretectum (PT) and visual sector of the thalamic reticul
56                                          The pretectum (PT) can supply the pulvinar nucleus (PUL), an
57 -sparing neurotoxic lesions were made to the pretectum (PT) or the SC.
58 acterize GABAergic cells that project to the pretectum (PT), ventral lateral geniculate nucleus (vLGN
59                           Most nuclei of the pretectum receive innervation largely, but not solely, f
60               In terms of afferentation, the pretectum receives electro- and mechanoreceptive inputs
61                                          The pretectum receives inhibitory input from the basal gangl
62                         At around E11.0, the pretectum replaces this structure.
63 l telencephalon, habenula, ventral thalamus, pretectum, rostral midbrain tegmentum, posterior tubercu
64 luded the amygdyla, auditory thalamus, pons, pretectum, superior and inferior colliculi, and central
65 ctory bulb, cerebral neocortex, hippocampus, pretectum, tectum, cranial nerve nuclei, and spinal cord
66        The primary retinal projection to the pretectum terminated in the ipsilateral and contralatera
67 cessed by a retinal-recipient nucleus in the pretectum, the nucleus lentiformis mesencephali (LM), wh
68 nd ipsilateral to the injection site, in the pretectum, the ventral tegmentum, the dorsal nucleus of
69 eedback facilitation to the optic tectum and pretectum to potentiate neural activity and increase the
70 amic and thalamic areas, posterior tubercle, pretectum, torus semicircularis, cerebellar nucleus, int
71 pathway), whereas abducens activation by the pretectum-vestibular pathway was not affected.
72 tion processing, most of them located in the pretectum, which had been functionally characterized in