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1 ypotheses about the function of the thalamic reticular nucleus.
2 he vestibular nucleus arise from the lateral reticular nucleus.
3 nuclei, the facial nucleus, and the lateral reticular nucleus.
4 n the inhibitory neurons of the rat thalamic reticular nucleus.
5 rostral ventrolateral medulla, and medullary reticular nucleus.
6 y are colocalized in neurons of the thalamic reticular nucleus.
7 acial mesenchyme, mesencephalon, and pontine reticular nucleus.
8 BAergic inhibition arising from the thalamic reticular nucleus.
9 uced the IPSPs originating from the thalamic reticular nucleus.
10 stained for NAAG and GAD(67) in the thalamic reticular nucleus.
11 e ipsilateral medulla, including the lateral reticular nucleus.
12 ent thalamus, beta3 is largely restricted to reticular nucleus.
13 nvolving the GABAergic cells of the thalamic reticular nucleus.
14 lla, either dorsal or ventral to the lateral reticular nucleus.
15 uence thalamic relay nuclei via the thalamic reticular nucleus.
16 s particularly abundant in the parvocellular reticular nucleus.
17 by driving inhibitory cells of the thalamic reticular nucleus.
18 the GABAergic neurons of the rodent thalamic reticular nucleus.
19 ons and precerebellar neurons of the lateral reticular nucleus.
20 c modulators of GABAARs) within the thalamic reticular nucleus.
21 us as well as activation of microglia in the reticular nucleus.
22 o include inhibitory neurons in the thalamic reticular nucleus.
23 and in GLP-1 neurons in the dorsal medullary reticular nucleus.
24 es the nucleus tractus solitarius and dorsal reticular nucleus.
25 tine reticular nucleus (68.9%), oral pontine reticular nucleus (64.5%), pedunculopontine tegmental nu
26 al tegmental nucleus (75.7%), caudal pontine reticular nucleus (68.9%), oral pontine reticular nucleu
27 hundreds of neurons labeled in the thalamic reticular nucleus, a structure that can only be labeled
31 on evoked responses from inhibitory thalamic reticular nucleus and excitatory tectothalamic terminals
33 erents from inferior colliculus and thalamic reticular nucleus and its GABA(A)R functional heterogene
34 r density in the dorsal thalamus than in the reticular nucleus and other parts of the ventral thalamu
35 id (GABA)ergic projections from the thalamic reticular nucleus and pretectum, and a cholinergic proje
36 which was associated with decreased thalamic reticular nucleus and primary somatosensory cortex activ
37 sleep spindles are initiated by the thalamic reticular nucleus and regulated by thalamo-reticular and
40 g that the NSTc projects to the intermediate reticular nucleus and the compact division of the nucleu
42 Two other precerebellar nuclei, the lateral reticular nucleus and the inferior olive, are present in
43 clicks was most pronounced in the brainstem reticular nucleus and the medial septal nucleus, while r
44 several large neurons of the gigantocellular reticular nucleus and the raphe magnus nucleus of mice,
46 nals that arise from neurons of the thalamic reticular nucleus, and perhaps from VPL local circuit ne
48 al nucleus, somatosensory thalamus, thalamic reticular nucleus, and primary somatosensory cortex.
51 he nucleus raphe magnus, the gigantocellular reticular nucleus, and the nucleus of the solitary tract
52 xonal collaterals to neurons in the thalamic reticular nucleus, and these thalamic reticular neurons
53 n the ventrolateral medulla near the lateral reticular nucleus, and were spread across the dorsal por
55 s between inhibitory neurons of the thalamic reticular nucleus are bidirectionally modulated by chang
56 s been proposed that neurons in the thalamic reticular nucleus are interconnected through GABAergic s
57 and cellular targets of individual thalamic reticular nucleus axons in the highly laminated lateral
60 -mediated inhibition was nearly abolished in reticular nucleus, but was unaffected in relay cells.
62 c binding of [(35)S]GTPgammaS in the pontine reticular nucleus, caudal part (79%); pontine reticular
64 , and retrorubral area and adjacent midbrain reticular nucleus), central autonomic control system (ce
65 ral medulla, and lateral paragigantocellular reticular nucleus, contain a considerable amount of over
67 y enhanced in the barrel cortex and thalamic reticular nucleus during the second postnatal week, but
68 ral nucleus and the GABAergic neurons of the reticular nucleus express significant 8B3 immunoreactivi
70 tine oral reticular nucleus, gigantocellular reticular nucleus (Gi) and dorsal paragigantocellular nu
73 n the cerebral cortex, hippocampus, thalamic reticular nucleus, globus pallidus and the substantia ni
76 address the question of whether cells in the reticular nucleus have receptive fields small enough to
77 gracilis nuclei whilst rarer in the lateral reticular nucleus, hypoglossal nucleus and raphe nucleus
78 nt in adjacent regions, such as the thalamic reticular nucleus, hypothalamus, and globus pallidus.
79 eticular nucleus while low expression in the reticular nucleus implies weak, GABA(B)-mediated intrare
80 Sleep spindles are generated by the thalamic reticular nucleus in conjunction with specific thalamic
81 In addition, given the central role of the reticular nucleus in generating spike-wave discharge, th
83 oked disynaptic inhibition (via the thalamic reticular nucleus) in the same or a neighbouring relay n
84 uropil and in that of the overlying thalamic reticular nucleus, including the perigeniculate nucleus.
85 ts suggest that cells in the visual thalamic reticular nucleus influence the lateral geniculate nucle
86 of nerve terminals were found in the lateral reticular nucleus ipsilateral to the stimulation site.
88 lular reticular nucleus (PCRt), intermediate reticular nucleus (IRt), and dorsal medullary reticular
91 ontrast, the acoustic sector of the thalamic reticular nucleus is not activated despite noise generat
92 the visual sector of the GABAergic thalamic reticular nucleus is selectively c-fos activated in rats
94 s of the thalamus are linked directly to the reticular nucleus, it now becomes important to define ho
95 NPYs were released from sites in the lateral reticular nucleus, lateral tegmental field and vestibula
96 y in the nucleus tractus solitarius, lateral reticular nucleus, lateral tegmental field, vestibular n
97 show that regulation of excitability in the reticular nucleus leads to dynamical modulation of the s
98 re input system originating from the lateral reticular nucleus (LRN) can represent sensory event timi
100 l eyeblink conditioning with tone or lateral reticular nucleus (LRN) stimulation as conditioned stimu
101 of the projection from the principal lateral reticular nucleus (LRN) to the electrophysiologically de
106 region and caudal to it, the gigantocellular reticular nucleus, midline neurons and the caudal ventro
107 e we can understand exactly how the thalamic reticular nucleus might be influencing thalamocortical p
109 LR sends bilateral projections to the middle reticular nucleus (mRN, rostral hindbrain) and the infer
110 tified neurons in the middle rhombencephalic reticular nucleus (MRRN), displayed delayed excitation (
112 n inhibitory GABAergic terminals of thalamic reticular nucleus neurones, and that it is normally acti
114 alamocortical neurons and GABAergic thalamic reticular nucleus neurons and that these properties are
116 ellar Purkinje cells and inhibitory thalamic reticular nucleus neurons have strongly reduced synaptic
117 tion of NMDA receptors on GABAergic thalamic reticular nucleus neurons might activate thalamocortical
119 major synaptic input from GABAergic thalamic reticular nucleus neurons, as well as neurons and astroc
121 hasic inhibition originating in the thalamic reticular nucleus (nRt) and are mediated by the neurotra
122 id (GABA)-containing neurons of the thalamic reticular nucleus (nRt) are a major source of inhibitory
123 Single electrical stimuli in the thalamic reticular nucleus (nRt) evoked rhythmic activity (1-15 s
124 al (POm) nucleus, the zona incerta (ZI), the reticular nucleus (nRT) of the thalamus, and the princip
125 ample, GABA-containing cells in the thalamic reticular nucleus (nRt) provide major inhibitory innerva
127 d responses to GABA uncaging in the thalamic reticular nucleus (nRT) that is absent in both nm1054 mi
128 y GABA released from neurons of the thalamic reticular nucleus (nRT), acting predominantly via synapt
131 situs hypoglossi, dorsal paragigantocellular reticular nucleus, nucleus of the tractus solitarius and
133 the first 2 weeks after birth, the thalamic reticular nucleus of the mouse lacks intrinsic GABAergic
134 atosensory cortex, the somatic region of the reticular nucleus of the thalamus (reticular thalamus).
136 verlap in their distribution, except for the reticular nucleus of the thalamus in which alpha7 mRNA w
137 ion in olfactory bulb, pontine gray, lateral reticular nucleus of the thalamus, and piriform cortex.
138 ajority of Cck cells, excluding those in the reticular nucleus of the thalamus, are non-GABAergic.
139 -selective mGlu2/3 agonist, LY379268, in the reticular nucleus of the thalamus, significantly reduced
140 teral geniculate nuclei of the thalamus, the reticular nucleus of the thalamus, the lateral posterior
143 as very prominent in the striatum and in the reticular nucleus of the thalamus; it was also observed
144 caused a release of irNPYs from the lateral reticular nucleus on the contralateral side of the brain
145 eticular nucleus, caudal part (79%); pontine reticular nucleus, oral part (131%); laterodorsal tegmen
146 thesis that GABA(A) receptors in the pontine reticular nucleus, oral part (PnO) of mouse modulate fiv
147 icity at electrical synapses in the thalamic reticular nucleus - paired burst spiking in coupled neur
149 l nucleus (Vme) project to the parvocellular reticular nucleus (PCRt) and dorsomedial spinal trigemin
150 hree specific RF subdivisions: parvocellular reticular nucleus (PCRt), intermediate reticular nucleus
151 e tegmental nucleus (PPTg), and oral pontine reticular nucleus (PnO) also severely disrupted approach
152 the cochlear nucleus, and via caudal pontine reticular nucleus, pontine central gray, and MS, reached
153 larly those in the posterior rhombencephalic reticular nucleus (PRRN), either adapted very quickly, a
155 restricted prefrontal areas to the thalamic reticular nucleus (RE), consistent with recent anatomica
156 The visual sector of the overlying thalamic reticular nucleus receives input from relay cells and su
157 hlight hypothesis proposes that the thalamic reticular nucleus regulates thalamic relay activity thro
158 retrorubral area, and lateral mesencephalic reticular nucleus), respiratory control (lateral nucleus
159 f the dorsal nucleus ambiguus, parvicellular reticular nucleus, retrorubral area, and lateral mesence
160 omatostatin (SST) on neurons in the thalamic reticular nucleus (RT) using whole-cell patch-clamp tech
162 selective current in neurons of the thalamic reticular nucleus (RT; 20/29 neurons) and ventral basal
163 nhibitory effects on neurons of the thalamic reticular nucleus (RT; n = 18) and adjacent ventral basa
164 ing from synaptically coupled neurons of the reticular nucleus (RTN) and ventral posterior nucleus (V
165 caying IPSC, whereas neurons in the adjacent reticular nucleus (RTN) display a long-lasting, slowly d
168 bunits in ventral posterior nucleus (VP) and reticular nucleus (RTN) of control rats and WAG/Rij rats
169 inhibition of relay cells by neurons in the reticular nucleus (RTN) under the influence of corticoth
173 vasomotor neurons in the rostroventrolateral reticular nucleus (RVL) of the medulla oblongata and sym
175 tion of neurons of the rostral ventrolateral reticular nucleus (RVL) would elevate regional cerebral
176 e not the same for each sector; (2) that the reticular nucleus serves as a nexus, where several funct
177 hat recurrent inhibition within the thalamic reticular nucleus serves to reduce synchrony and thus pr
178 e Kv3.3-IR neurones in the ventral medullary reticular nucleus, spinal trigeminal nucleus, dorsal hor
179 ulted in the specific activation of thalamic reticular nucleus, striatum/putamen, and cortical layers
180 ns to cortical interneurons and the thalamic reticular nucleus, suggest a strong and synchronous cont
181 atory control, including the gigantocellular reticular nucleus, the lateral paragigantocellular nucle
182 s, the cochlear nucleus, the gigantocellular reticular nucleus, the motor trigeminal nucleus, and the
183 a large-scale, two-dimensional model of the reticular nucleus, the network showed transient or self-
184 tal cortex, limbic thalamus, gigantocellular reticular nucleus, the somatosensory system, and cerebel
185 the pons, the ventral part of the medullary reticular nucleus, the ventral horn in the spinal cord o
186 tions from the visual sector of the thalamic reticular nucleus to the lateral geniculate nucleus comp
187 e input from the anterior pole of the monkey reticular nucleus to the motor-related thalamic nuclei i
188 y two major inhibitory systems: the thalamic reticular nucleus (TRN) and extrathalamic inhibitory (ET
189 expressing GABAergic neurons in the thalamic reticular nucleus (TRN) and intrinsic interneurons of dL
190 tiple single-unit recordings in the thalamic reticular nucleus (TRN) and medial prefrontal cortex (mP
191 s for a specific involvement of the thalamic reticular nucleus (TRN) come from its unique neuronal ch
193 nerally thought that neurons in the thalamic reticular nucleus (TRN) form GABAergic synapses with oth
202 as intrinsic thalamic neurons (e.g. thalamic reticular nucleus (TRN) neurons and dLGN interneurons).
206 show that GABAergic neurons in the thalamic reticular nucleus (TRN) of mice and rats form two types
211 show that local tonic activation of thalamic reticular nucleus (TRN) rapidly induces slow wave activi
212 es the organization of cells in the thalamic reticular nucleus (TRN) that project to the auditory par
215 olinergic transmission in the mouse thalamic reticular nucleus (TRN), a brain structure essential for
216 nergic synaptic transmission in the thalamic reticular nucleus (TRN), a brain structure intimately in
217 hd1 is selectively expressed in the thalamic reticular nucleus (TRN), a group of GABAergic neurons th
218 onal center, targets the inhibitory thalamic reticular nucleus (TRN), a key node in the brain's atten
219 in both directions pass through the thalamic reticular nucleus (TRN), a thin layer of GABAergic cells
220 btypes are localized within the rat thalamic reticular nucleus (TRN), and we have examined the effect
221 ted inhibitory neurons, such as the thalamic reticular nucleus (TRN), often regulate neural oscillati
223 ubunits are highly expressed in the thalamic reticular nucleus (TRN), which is thought to act as a pa
224 thalamus arises from neurons in the thalamic reticular nucleus (TRN), which use gamma-aminobutyric ac
234 riaqueductal gray matter and gigantocellular reticular nucleus, ventral part also showed a similar ov
235 ion, we found neurons of the visual thalamic reticular nucleus (visTRN) to exhibit PFC-dependent chan
236 ons in different regions of the rat thalamic reticular nucleus were labeled with biotin dextran amine
237 the high density of synaptic inputs from the reticular nucleus while low expression in the reticular
238 her FEF connections were with the claustrum, reticular nucleus, zona incerta, lateral posterior and m
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