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1 mon integrator site for both these reflexes (vestibular nuclei).
2 vermis) and the maintenance of equilibrium (vestibular nuclei).
3 ainstem nuclei (e.g., the inferior olive and vestibular nuclei).
4 were confined to the middle portions of the vestibular nuclei.
5 the anterior and the middle portions of the vestibular nuclei.
6 and other neurons located in the surrounding vestibular nuclei.
7 ns and terminals were also found in all four vestibular nuclei.
8 osits confined to the inferior and/or medial vestibular nuclei.
9 hin the medial pontine reticular and lateral vestibular nuclei.
10 he superior, lateral, medial, and descending vestibular nuclei.
11 whole continuum previously described in the vestibular nuclei.
12 the spinal, medial, and parvocellular medial vestibular nuclei.
13 ) receptor (R) agonist and antagonist in the vestibular nuclei.
14 nections of the vestibulocerebellum with the vestibular nuclei.
15 pses onto neurons in the deep cerebellar and vestibular nuclei.
16 GABAergic neurons projected to contralateral vestibular nuclei.
17 ement of the olfactory bulb, cerebellum, and vestibular nuclei.
18 and their postsynaptic targets in the medial vestibular nuclei.
19 plasticity in neurons of the cerebellar and vestibular nuclei.
20 it must be conveyed by neurons of the DCN or vestibular nuclei.
21 both projection and intrinsic neurons of the vestibular nuclei.
22 lateral, vestibulocerebellar, and descending vestibular nuclei.
23 vestibulocerebellar nucleus, and descending vestibular nuclei.
24 l nuclei, but did not label cells within the vestibular nuclei.
25 on is effected at least partly by the caudal vestibular nuclei.
26 ownstream of Purkinje cells, probably in the vestibular nuclei.
27 in histamine H(3) receptor expression in the vestibular nuclei.
28 es virus Bartha (PRV) into the contralateral vestibular nuclei.
29 s, were compared with those in the brainstem vestibular nuclei.
30 in the deep cerebellar nuclei and brainstem vestibular nuclei.
31 or olive nuclei, dorsal cochlear nuclei, and vestibular nuclei.
32 pinal cord including the red, reticular, and vestibular nuclei.
33 s primarily from the vestibular ganglion and vestibular nuclei.
34 all commissural connections between the two vestibular nuclei.
35 nuclei except the dorsal part of the lateral vestibular nuclei.
37 ng reactive cell proliferation occurs in the vestibular nuclei after unilateral vestibular neurectomy
40 the presence of a projection pattern in the vestibular nuclei and cerebellum similar to that of the
41 vity of cells in the autonomic region of the vestibular nuclei and suggest that these signals are pri
43 Kv3.3-immunoreactivity was widespread in the vestibular nuclei and was detected in somata, dendrites
44 afferent fibers from eight sites within the vestibular nuclei, and axon number and soma size was qua
45 ar formation, nucleus prepositus hypoglossi, vestibular nuclei, and raphe nuclei, were infected by tr
46 aminergic system on neurotransmission in the vestibular nuclei, and the changes that occur during ves
47 cts of histamine on neurotransmission in the vestibular nuclei, and the mechanisms by which histamine
48 d neurons in the inferior olivary subnuclei, vestibular nuclei, and their afferent cell groups in a p
53 ed by direct reciprocal connections with the vestibular nuclei, as well as direct vestibular afferent
54 ticular nucleus, lateral tegmental field and vestibular nuclei at a level in the brainstem 4.0-4.4 mm
55 nuclei, pontine nuclei, superior and lateral vestibular nuclei, brainstem reticular nuclei, and sever
56 ts that drive ipsiversive excitation of both vestibular nuclei but also suggest that both nerves comp
57 l levels of the superior, medial and lateral vestibular nuclei, but do show topographic organization.
58 Ultrastructural observations in the caudal vestibular nuclei confirm the IAA-RP immunolocalization
59 rgets a large diversity of cell types in the vestibular nuclei, consistent with a broad functional si
61 own that a region of the medial and inferior vestibular nuclei contributes to cardiovascular and resp
62 rtical structures such as the cerebellum and vestibular nuclei, cortical lesions have suggested that
63 ly in the magnocellular reticular formation, vestibular nuclei, cranial nerve motor nuclei, sensory t
64 sms of neural and synaptic plasticity in the vestibular nuclei during 'vestibular compensation', the
65 o calretinin staining was seen in any of the vestibular nuclei except for a population of intrinsic n
67 ated generally in the lateral regions of all vestibular nuclei in areas that were separate from the p
70 er tracer injections into the cerebellar and vestibular nuclei indicated that most vestibular respons
71 voke optic field flow signals that enter the vestibular nuclei, indicating head velocity, and hence a
72 inergic neurons project to the contralateral vestibular nuclei, indicating that commissural inhibitio
73 ojection of afferent fibers into the central vestibular nuclei, indicating that functional connection
74 thalamic nuclei, medullary reticular nuclei, vestibular nuclei, inferior olivary complex, and deep ce
75 e made in alert macaques from neurons in the vestibular nuclei involved in postural control and self-
76 that MRF neurons that receive input from the vestibular nuclei make inhibitory connections with diaph
77 ated within the caudal medial and descending vestibular nuclei (MVN and DVN, respectively), the paras
78 in ipsi-lesional and contra-lesional medial vestibular nuclei (MVN) of rats, 1 week after either sha
79 ame millisecond time scale within inhibitory vestibular nuclei networks contributes to ensuring a rel
81 rent fibers and terminals was studied in the vestibular nuclei of 4-5-day hatchling chicks by using s
84 due to the imbalance in excitability of the vestibular nuclei of the lesioned and intact sides, and
89 Other regions of the brainstem including the vestibular nuclei, prepositus hypoglossi, dorsal paragig
90 Injections of retrograde tracers into the vestibular nuclei produced retrogradely labeled neurons
92 he majority of neurons in this region of the vestibular nuclei receive signals from the skin, muscle,
93 l, comprising both the cerebellar cortex and vestibular nuclei, reproduces behavioral data and accoun
94 d neurons were those of the red nucleus, the vestibular nuclei, reticular formation, locus coeruleus,
97 disinhibition of cholinergic neurons in the vestibular nuclei--suppresses presynaptic LTP to prevent
98 explored the types of neurons in the macaque vestibular nuclei targeted by nodulus/ventral uvula inhi
99 utricular fibers projected to regions in the vestibular nuclei that overlapped with the horizontal se
100 resulted in labeling of neurons in all four vestibular nuclei, the prepositus hypoglossi, the reticu
101 y sparse labeling was noticed in the lateral vestibular nuclei, the red nucleus and the motor cortex
103 itary nucleus, the parasolitary nucleus, the vestibular nuclei, the ventral medial medulla, the raphe
104 lateral, medial, descending, and tangential vestibular nuclei; the A and B groups; the intermediate,
105 n to demonstrate direct projections from the vestibular nuclei to the Edinger-Westphal and anteromedi
106 via axons descending ipsilaterally from the vestibular nuclei via the lateral vestibulospinal tract.
107 urones within the medial, lateral and spinal vestibular nuclei (VN(M), VN(L) and VN(S), respectively)
108 cell proliferation occurs rapidly in the cat vestibular nuclei (VN) after unilateral vestibular neure
110 tors, undergo remarkable fluctuations within vestibular nuclei (VN), strongly suggesting that GABA ac
111 tantial projection to the medial and lateral vestibular nuclei was seen with horizontal canal afferen
112 ye movement-sensitive neurons in the rostral vestibular nuclei were examined during pure translation
113 neurons of the spinal, lateral, and superior vestibular nuclei were heavily decorated with synapses,
114 l projections to the superior and descending vestibular nuclei were much more centrally located than
115 canal projections to the medial and lateral vestibular nuclei were observed but were less prominent.
117 rate numbers of labeled axons, and the other vestibular nuclei were well innervated by protein kinase
118 dings identify discrete regions of the chick vestibular nuclei where second-order vestibular neurons
119 stigial nucleus, in contrast to cells in the vestibular nuclei, which primarily encoded motion in a h
120 projection patterns and destinations in the vestibular nuclei, with intranuclear parcellation in the
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