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1 rmore, somatosensory and visual responses of ventrobasal and lateral geniculate neurones were enhance
2 -cyclic-GMP (8-Br-cGMP) onto neurones in the ventrobasal and lateral geniculate nuclei of the thalamu
3  The retinofugal axon terminal arbors in the ventrobasal and medial geniculate nuclei of mature, oper
4                              (2) In both the ventrobasal and medial geniculate nuclei of operated ham
5  labeling in the thalamus, especially in the ventrobasal complex (VB) and in the medial part of the p
6 ferent sensory thalamic nuclei including the ventrobasal complex (VB; somatosensory system) and the m
7 opographic maps of cortical afferents in the ventrobasal complex and medial part of the posterior com
8 l or corticothalamic projections between the ventrobasal complex and the microgyrus itself, although
9  cytochemical lesions placed in the thalamic ventrobasal complex at P0 (just as thalamocortical affer
10                               Stimulation of ventrobasal complex cells evoked inhibitory postsynaptic
11 dorsal lateral geniculate nucleus (dLGN) and ventrobasal complex exhibit tonic inhibition.
12 S-ir) immunoreactive neurons in the thalamic ventrobasal complex of the cat.
13         Arborizations and boutons within the ventrobasal complex of the thalamus were observed after
14 eurons project to third-order neurons in the ventrobasal complex of the thalamus.
15 f the opposite hemisphere, or in ipsilateral ventrobasal complex of the thalamus.
16 erve and recorded from single neurons in the ventrobasal complex of the thalamus.
17 rograde and anterograde) was observed in the ventrobasal complex of the thalamus.
18 us, cells engaged in sensory analyses in the ventrobasal complex or the medial division of the poster
19 fusion of etomidate (10 and 30 muM) into the ventrobasal complex produced effects on electrocortical
20 ]pyridin-3-ol (THIP; 10 and 50 muM) into the ventrobasal complex produced significant effects on elec
21 osensory thalamus, cells in one nucleus, the ventrobasal complex, can influence activity in another n
22 t of the posterior nucleus (POm), and in the ventrobasal complex.
23 fic variation also occurs in the somesthetic ventrobasal complex.
24 e current was significantly inhibited in the ventrobasal neurons that express Cav3.1, whereas in nucl
25 lly connected thalamocortical neurons in the ventrobasal nucleus (VB) and GABAergic neurons in the th
26 served: thalamocortical relay neurons in the ventrobasal nucleus (VB) exhibit a fast decaying IPSC, w
27 nock-out mice is increased cell death in the ventrobasal nucleus (VB) of the thalamus.
28 e BSTC, and in its main thalamic target, the ventrobasal nucleus (VB), coincides with the peak of nat
29  (1-15 sec duration) in nRt and the adjacent ventrobasal nucleus (VB).
30 unoreactivity [to identify boundaries of the ventrobasal nucleus (VB)].
31  relay neurons in acute slices of developing ventrobasal nucleus (VBN) of the thalamus from rats and
32 edial geniculate nucleus and from the caudal ventrobasal nucleus in particular.
33 atosensory cortex, but apparently not in the ventrobasal nucleus of the thalamus.
34  the earliest date studied (P0) and that the ventrobasal nucleus terminates upon the somatosensory co
35      When sniffer patches were placed in the ventrobasal nucleus, however, subsequent treatment with
36 e primary somatosensory cortex, the thalamic ventrobasal nucleus, the hippocampus, and the cerebellum
37  patches pulled from neurons in the adjacent ventrobasal nucleus, which does not contain endozepines,
38 etinal ganglion cell axons projecting to the ventrobasal or medial geniculate nuclei develop in three
39 ons to the principal thalamic somatosensory (ventrobasal) or auditory (medial geniculate) nuclei can
40 eurons, we injected Fluorogold (FG) into the ventrobasal thalamic complex (VB) and parabrachial regio
41 patterns in the trigeminal brainstem, in the ventrobasal thalamic complex or in the face-representati
42 aration to investigate their projection into ventrobasal thalamic nuclei (VB).
43 rtex, in basal ganglia, and in reticular and ventrobasal thalamic nuclei.
44  modulation of sensory processing in the rat ventrobasal thalamic nucleus (VB) has been extensively s
45                                Fifteen right ventrobasal thalamic units were antidromically activated
46 tory postsynaptic currents (IPSCs) evoked in ventrobasal thalamocortical (VB) neurons by stimulation
47                           Here we focused on ventrobasal thalamocortical neurones, which contribute t
48 ibition in postsynaptic relay neurons of the ventrobasal thalamus (VB).
49 al area (VTA), somatosensory cortex (S1) and ventrobasal thalamus (VBT) from perinatal fentanyl expos
50 KA antagonist GYKI 52466, and lesions of the ventrobasal thalamus attenuated DOI-elicited Fos express
51              Cobalt injection into the right ventrobasal thalamus blocked the right insular response
52 cleus and glutamatergic relay neurons in the ventrobasal thalamus generated slow oscillatory activity
53 ity between the rat posterior insula and the ventrobasal thalamus has been demonstrated anatomically.
54 thalamocortical neurones (n = 57) of the cat ventrobasal thalamus in order to investigate the mechani
55                           The projections of ventrobasal thalamus into somatosensory cortex were stud
56 ation in thalamocortical neurones of the cat ventrobasal thalamus is mediated by the concerted action
57 THIP did not affect the synaptic currents in ventrobasal thalamus neurons or striatal MSNs, it reduce
58 P evoked differential degrees of currents in ventrobasal thalamus neurons, a diversity that could ari
59 al and E38 MAM-treated animals, in which the ventrobasal thalamus projects primarily to central layer
60  modulation of synaptic responses in the rat ventrobasal thalamus using the novel antagonist LY382884
61 hether similar convergent cells exist in the ventrobasal thalamus was investigated in 30 urethane ane
62 d axonal varicosities in the neostriatum and ventrobasal thalamus were analyzed quantitatively to com
63 repinephrine and serotonin levels within the ventrobasal thalamus, as determined by in vivo microdial
64  of local neuron excitation by GT release in ventrobasal thalamus, CA1 hippocampus, and somatosensory
65 NS, including thalamocortical neurons of the ventrobasal thalamus, dentate gyrus granule cells, and c
66 known projection in mammals from nTTD to the ventrobasal thalamus, suggesting that the ascending trig
67 er with anterogradely labeled axons from the ventrobasal thalamus, which have previously been shown t
68 s present in TC neurons of the somatosensory ventrobasal thalamus, which lacks GABAergic interneurons
69 ic synapses onto TC neurons in somatosensory ventrobasal thalamus.
70 e contralateral somatosensory cortex via the ventrobasal thalamus.
71 rs of simultaneously recorded neurons in the ventrobasal thalamus.
72 the posterior insula through the ipsilateral ventrobasal thalamus.
73 r than the amount of overlap observed in the ventrobasal thalamus.
74  also labeled thalamocortical neurons in the ventrobasal thalamus.
75 overlap was approximately the same as in the ventrobasal thalamus.
76 the Pa5 is predominately directed toward the ventrobasal thalamus.
77 eocortex, piriform cortex, caudoputamen, and ventrobasal thalamus.
78 al animals also received injections into the ventrobasal thalamus.
79 lasses of cells were identified in the right ventrobasal thalamus: (a) 83/159 (52%) baroreceptive and
80 ry nociceptive convergent units exist in the ventrobasal thalamus; (b) thalamic convergent neurons pr
81  secondary (SII) somatosensory cortices, the ventrobasal (VB) and posterior group (POm) nuclei of the
82 cision of corticothalamic projections to the ventrobasal (VB) complex and the medial part of the post
83 naptically coupled nRT and TC neurons of the ventrobasal (VB) complex in brain slices derived from wi
84 s in a matching gradient across the thalamic ventrobasal (VB) complex, which provides S1 input.
85 ion of somatosensory thalamic axons from the ventrobasal (VB) nuclei, causing them to shift caudally
86                Thalamic projections from the ventrobasal (VB) nucleus to rodent somatosensory cortex
87                                     Thalamic ventrobasal (VB) relay neurones express multiple GABA(A)
88 c reticular nucleus (TRN) powerfully inhibit ventrobasal (VB) thalamic relay neurons via GABAergic sy
89                                 By contrast, ventrobasal (VB) thalamic stimulation, while activating
90 eviously showed that N-cadherin localizes to ventrobasal (VB) thalamocortical synapses in rat somatos
91  followed by selective neuronal death in the ventrobasal (VB) thalamus 3 days later.
92 nes and those of one interneurone in the cat ventrobasal (VB) thalamus were examined using an in vitr
93 er, in thalamocortical neurones of the mouse ventrobasal (VB) thalamus, the major alteration to mIPSC
94 er, in thalamocortical neurones of the mouse ventrobasal (VB) thalamus, the major alteration to mIPSC
95 ABA(A)-Rs and Gly-Rs in neurons in the mouse ventrobasal (VB) thalamus.