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1 pathway involving the GABAergic cells of the thalamic reticular nucleus.
2 also influence thalamic relay nuclei via the thalamic reticular nucleus.
3 ibit them by driving inhibitory cells of the thalamic reticular nucleus.
4 nt among the GABAergic neurons of the rodent thalamic reticular nucleus.
5 allosteric modulators of GABAARs) within the thalamic reticular nucleus.
6 tions also include inhibitory neurons in the thalamic reticular nucleus.
7 th between the inhibitory neurons of the rat thalamic reticular nucleus.
8 , yet they are colocalized in neurons of the thalamic reticular nucleus.
9 mpeting hypotheses about the function of the thalamic reticular nucleus.
10 ion on GABAergic inhibition arising from the thalamic reticular nucleus.
11 ATPA reduced the IPSPs originating from the thalamic reticular nucleus.
12 e doubly stained for NAAG and GAD(67) in the thalamic reticular nucleus.
13 s we find hundreds of neurons labeled in the thalamic reticular nucleus, a structure that can only be
15 e effect on evoked responses from inhibitory thalamic reticular nucleus and excitatory tectothalamic
17 itory afferents from inferior colliculus and thalamic reticular nucleus and its GABA(A)R functional h
18 utyric acid (GABA)ergic projections from the thalamic reticular nucleus and pretectum, and a choliner
19 hometry) which was associated with decreased thalamic reticular nucleus and primary somatosensory cor
20 cortex, sleep spindles are initiated by the thalamic reticular nucleus and regulated by thalamo-reti
21 ic medications, and point to deficits in the thalamic reticular nucleus and thalamo-reticular circuit
22 reviously unreported retinotopic maps in the thalamic reticular nucleus and the substantia nigra.
23 xon terminals that arise from neurons of the thalamic reticular nucleus, and perhaps from VPL local c
25 trigeminal nucleus, somatosensory thalamus, thalamic reticular nucleus, and primary somatosensory co
26 diate layers of the superior colliculus, the thalamic reticular nucleus, and the caudate nucleus.
27 provide axonal collaterals to neurons in the thalamic reticular nucleus, and these thalamic reticular
28 l synapses between inhibitory neurons of the thalamic reticular nucleus are bidirectionally modulated
29 It has been proposed that neurons in the thalamic reticular nucleus are interconnected through GA
30 e laminar and cellular targets of individual thalamic reticular nucleus axons in the highly laminated
33 nificantly enhanced in the barrel cortex and thalamic reticular nucleus during the second postnatal w
34 neurons in the cerebral cortex, hippocampus, thalamic reticular nucleus, globus pallidus and the subs
36 was evident in adjacent regions, such as the thalamic reticular nucleus, hypothalamus, and globus pal
38 neuron evoked disynaptic inhibition (via the thalamic reticular nucleus) in the same or a neighbourin
39 culate neuropil and in that of the overlying thalamic reticular nucleus, including the perigeniculate
40 ese results suggest that cells in the visual thalamic reticular nucleus influence the lateral genicul
41 ated that the visual sector of the GABAergic thalamic reticular nucleus is activated by attention in
44 ated that the visual sector of the GABAergic thalamic reticular nucleus is selectively c-fos activate
46 ons before we can understand exactly how the thalamic reticular nucleus might be influencing thalamoc
47 tically on inhibitory GABAergic terminals of thalamic reticular nucleus neurones, and that it is norm
48 tergic thalamocortical neurons and GABAergic thalamic reticular nucleus neurons and that these proper
50 oth cerebellar Purkinje cells and inhibitory thalamic reticular nucleus neurons have strongly reduced
51 Inhibition of NMDA receptors on GABAergic thalamic reticular nucleus neurons might activate thalam
52 receive major synaptic input from GABAergic thalamic reticular nucleus neurons, as well as neurons a
54 pend on phasic inhibition originating in the thalamic reticular nucleus (nRt) and are mediated by the
55 utyric acid (GABA)-containing neurons of the thalamic reticular nucleus (nRt) are a major source of i
57 For example, GABA-containing cells in the thalamic reticular nucleus (nRt) provide major inhibitor
59 ission and responses to GABA uncaging in the thalamic reticular nucleus (nRT) that is absent in both
60 ediated by GABA released from neurons of the thalamic reticular nucleus (nRT), acting predominantly v
62 xcept for the first 2 weeks after birth, the thalamic reticular nucleus of the mouse lacks intrinsic
63 of plasticity at electrical synapses in the thalamic reticular nucleus - paired burst spiking in cou
65 ions from restricted prefrontal areas to the thalamic reticular nucleus (RE), consistent with recent
67 The searchlight hypothesis proposes that the thalamic reticular nucleus regulates thalamic relay acti
68 ects of somatostatin (SST) on neurons in the thalamic reticular nucleus (RT) using whole-cell patch-c
69 ted a K+-selective current in neurons of the thalamic reticular nucleus (RT; 20/29 neurons) and ventr
70 roduced inhibitory effects on neurons of the thalamic reticular nucleus (RT; n = 18) and adjacent ven
72 roposed that recurrent inhibition within the thalamic reticular nucleus serves to reduce synchrony an
73 (CL) resulted in the specific activation of thalamic reticular nucleus, striatum/putamen, and cortic
74 projections to cortical interneurons and the thalamic reticular nucleus, suggest a strong and synchro
75 ry projections from the visual sector of the thalamic reticular nucleus to the lateral geniculate nuc
76 argeted by two major inhibitory systems: the thalamic reticular nucleus (TRN) and extrathalamic inhib
77 l as GFP expressing GABAergic neurons in the thalamic reticular nucleus (TRN) and intrinsic interneur
78 l and multiple single-unit recordings in the thalamic reticular nucleus (TRN) and medial prefrontal c
81 It is generally thought that neurons in the thalamic reticular nucleus (TRN) form GABAergic synapses
90 as well as intrinsic thalamic neurons (e.g. thalamic reticular nucleus (TRN) neurons and dLGN intern
92 backpropagation in thalamocortical (TC) and thalamic reticular nucleus (TRN) neurons remains unknown
94 hnique to show that GABAergic neurons in the thalamic reticular nucleus (TRN) of mice and rats form t
99 logy, we show that local tonic activation of thalamic reticular nucleus (TRN) rapidly induces slow wa
100 y describes the organization of cells in the thalamic reticular nucleus (TRN) that project to the aud
103 liable cholinergic transmission in the mouse thalamic reticular nucleus (TRN), a brain structure esse
104 on cholinergic synaptic transmission in the thalamic reticular nucleus (TRN), a brain structure inti
105 mouse Ptchd1 is selectively expressed in the thalamic reticular nucleus (TRN), a group of GABAergic n
106 n's emotional center, targets the inhibitory thalamic reticular nucleus (TRN), a key node in the brai
107 d cortex in both directions pass through the thalamic reticular nucleus (TRN), a thin layer of GABAer
108 mGluR subtypes are localized within the rat thalamic reticular nucleus (TRN), and we have examined t
109 terconnected inhibitory neurons, such as the thalamic reticular nucleus (TRN), often regulate neural
111 d Kv3.3 subunits are highly expressed in the thalamic reticular nucleus (TRN), which is thought to ac
112 e dorsal thalamus arises from neurons in the thalamic reticular nucleus (TRN), which use gamma-aminob
121 this notion, we found neurons of the visual thalamic reticular nucleus (visTRN) to exhibit PFC-depen
122 Neurons in different regions of the rat thalamic reticular nucleus were labeled with biotin dext
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