ライフサイエンスコーパス: reticular nucleus

1 and in GLP-1 neurons in the dorsal medullary reticular nucleus.

2 es the nucleus tractus solitarius and dorsal reticular nucleus.

3 he vestibular nucleus arise from the lateral reticular nucleus.

4 nuclei, the facial nucleus, and the lateral reticular nucleus.

5 n the inhibitory neurons of the rat thalamic reticular nucleus.

6 beta1, and gamma2 were most abundant in the reticular nucleus.

7 rostral ventrolateral medulla, and medullary reticular nucleus.

8 y are colocalized in neurons of the thalamic reticular nucleus.

9 m two sources, substantia nigra and thalamic reticular nucleus.

10 acial mesenchyme, mesencephalon, and pontine reticular nucleus.

11 BAergic inhibition arising from the thalamic reticular nucleus.

12 uced the IPSPs originating from the thalamic reticular nucleus.

13 stained for NAAG and GAD(67) in the thalamic reticular nucleus.

14 e ipsilateral medulla, including the lateral reticular nucleus.

15 he retina, visual cortices, and the thalamic reticular nucleus.

16 ent thalamus, beta3 is largely restricted to reticular nucleus.

17 nvolving the GABAergic cells of the thalamic reticular nucleus.

18 lla, either dorsal or ventral to the lateral reticular nucleus.

19 s particularly abundant in the parvocellular reticular nucleus.

20 ling the human ventral thalamus and thalamic reticular nucleus.

21 mic interneurons and neurons in the thalamic reticular nucleus.

22 ypotheses about the function of the thalamic reticular nucleus.

23 uence thalamic relay nuclei via the thalamic reticular nucleus.

24 by driving inhibitory cells of the thalamic reticular nucleus.

25 the GABAergic neurons of the rodent thalamic reticular nucleus.

26 ons and precerebellar neurons of the lateral reticular nucleus.

27 c modulators of GABAARs) within the thalamic reticular nucleus.

28 us as well as activation of microglia in the reticular nucleus.

29 o include inhibitory neurons in the thalamic reticular nucleus.

30 tine reticular nucleus (68.9%), oral pontine reticular nucleus (64.5%), pedunculopontine tegmental nu

31 al tegmental nucleus (75.7%), caudal pontine reticular nucleus (68.9%), oral pontine reticular nucleu

32 hundreds of neurons labeled in the thalamic reticular nucleus, a structure that can only be labeled

33 rt a Brn3c(+) RGC projection to the thalamic reticular nucleus, a visual nucleus that was not previou

34 hus, recurrent inhibitory connections within reticular nucleus act as "desynchronizers."

35 The thalamic reticular nucleus also exhibited robust m2 immunostainin

36 The red nucleus, lateral reticular nucleus and cerebellum labeled intensely for N

37 on evoked responses from inhibitory thalamic reticular nucleus and excitatory tectothalamic terminals

38 apses (type S1), which likely arise from the reticular nucleus and GABAergic interneurons, and (c) GA

39 formed by GABAergic neurons in the thalamic reticular nucleus and glutamatergic relay neurons in the

40 The advance of knowledge of the thalamic reticular nucleus and its connections has been reviewed

41 erents from inferior colliculus and thalamic reticular nucleus and its GABA(A)R functional heterogene

42 r density in the dorsal thalamus than in the reticular nucleus and other parts of the ventral thalamu

43 nt for neuronal excitability in the thalamic reticular nucleus and other regions of the brain.

44 id (GABA)ergic projections from the thalamic reticular nucleus and pretectum, and a cholinergic proje

45 which was associated with decreased thalamic reticular nucleus and primary somatosensory cortex activ

46 sleep spindles are initiated by the thalamic reticular nucleus and regulated by thalamo-reticular and

47 tantia nigra, and the adjacent mesencephalic reticular nucleus and retrorubral area.

48 of the indirect pathways, the spino-lateral reticular nucleus and spino-olivary pathways, are in par

49 urons form mainly the indirect spino-lateral reticular nucleus and spino-olivary tracts and thoracolu

50 tions, and point to deficits in the thalamic reticular nucleus and thalamo-reticular circuits.

51 g that the NSTc projects to the intermediate reticular nucleus and the compact division of the nucleu

52 Major differences distinguish the reticular nucleus and the dorsal thalamus and, within th

53 Two other precerebellar nuclei, the lateral reticular nucleus and the inferior olive, are present in

54 clicks was most pronounced in the brainstem reticular nucleus and the medial septal nucleus, while r

55 several large neurons of the gigantocellular reticular nucleus and the raphe magnus nucleus of mice,

56 unreported retinotopic maps in the thalamic reticular nucleus and the substantia nigra.

57 inhibitory network composed of the thalamic reticular nucleus and zona incerta, known to modulate th

58 and primary motor cortex and gigantocellular reticular nucleus) and high-level cortical regions (the

59 connectivity, especially within the thalamic reticular nucleus, and are linked to dysfunction in GABA

60 nals that arise from neurons of the thalamic reticular nucleus, and perhaps from VPL local circuit ne

61 us (SC), lateral hypothalamus (LH), midbrain reticular nucleus, and periaqueductal gray, whereas the

62 the cerebellar granule cell layer, thalamic reticular nucleus, and piriform cortex.

63 al nucleus, somatosensory thalamus, thalamic reticular nucleus, and primary somatosensory cortex.

64 ippocampus, medial septal nucleus, brainstem reticular nucleus, and the auditory cortex.

65 ers of the superior colliculus, the thalamic reticular nucleus, and the caudate nucleus.

66 he nucleus raphe magnus, the gigantocellular reticular nucleus, and the nucleus of the solitary tract

67 xonal collaterals to neurons in the thalamic reticular nucleus, and these thalamic reticular neurons

68 n the ventrolateral medulla near the lateral reticular nucleus, and were spread across the dorsal por

69 strema; dorsal nucleus of the vagus; lateral reticular nucleus; and spinal cord.

70 s between inhibitory neurons of the thalamic reticular nucleus are bidirectionally modulated by chang

71 s been proposed that neurons in the thalamic reticular nucleus are interconnected through GABAergic s

72 albumin interneurons in the sensory thalamic reticular nucleus are necessary and sufficient for regul

73 om the anteroventral portion of the thalamic reticular nucleus (avTRN) inhibit the firing rate of aPV

74 and cellular targets of individual thalamic reticular nucleus axons in the highly laminated lateral

75 Reconstructed thalamic reticular nucleus axons were narrowly aligned along a si

76 gene Cacna1h in iKOp/q mice reduces thalamic reticular nucleus burst firing and promotes rather than

77 g in the medial septal nucleus and brainstem reticular nucleus, but not the auditory cortex.

78 -mediated inhibition was nearly abolished in reticular nucleus, but was unaffected in relay cells.

79 The thalamic reticular nucleus can be divided into a number of sector

80 c binding of [(35)S]GTPgammaS in the pontine reticular nucleus, caudal part (79%); pontine reticular

81 efferents to the pons, superior colliculus, reticular nucleus, caudate, and putamen.

82 , and retrorubral area and adjacent midbrain reticular nucleus), central autonomic control system (ce

83 wed a functional perturbation of the lateral reticular nucleus-cerebellum internal feedback pathway i

84 cially in the hypothalamus, septum, thalamic reticular nucleus, certain cortices and other limbic str

85 se data implicate a corticothalamic-thalamic reticular nucleus circuit that modifies thalamic neurona

86 ral medulla, and lateral paragigantocellular reticular nucleus, contain a considerable amount of over

87 This model predicts that the isolated reticular nucleus could initiate sequences of spindle os

88 ions in the posterior level of the medullary reticular nucleus, dorsal part, whereas medial and later

89 is preferentially expressed in the thalamic reticular nucleus during development, pharmacological re

90 y enhanced in the barrel cortex and thalamic reticular nucleus during the second postnatal week, but

91 ulvinar projections that engage the thalamic reticular nucleus enable the pulvinar to estimate decisi

92 Interestingly, inborn deletion of thalamic reticular nucleus-enriched, human childhood absence epil

93 ral nucleus and the GABAergic neurons of the reticular nucleus express significant 8B3 immunoreactivi

94 Thalamic nuclei, including the reticular nucleus, express low to moderate levels.

95 r cingulate cortex (dACC) neurons to pontine reticular nucleus GABAergic inhibitory neurons (PnC(GABA

96 tine oral reticular nucleus, gigantocellular reticular nucleus (Gi) and dorsal paragigantocellular nu

97 localized exclusively to the gigantocellular reticular nucleus (Gi) of the rostral medulla.

98 The pontine oral reticular nucleus, gigantocellular reticular nucleus (Gi

99 n the cerebral cortex, hippocampus, thalamic reticular nucleus, globus pallidus and the substantia ni

100 In the reticular nucleus, GluR4 is by far the most prominent, a

101 The thalamic reticular nucleus has a critical role in modulating info

102 address the question of whether cells in the reticular nucleus have receptive fields small enough to

103 gracilis nuclei whilst rarer in the lateral reticular nucleus, hypoglossal nucleus and raphe nucleus

104 nt in adjacent regions, such as the thalamic reticular nucleus, hypothalamus, and globus pallidus.

105 eticular nucleus while low expression in the reticular nucleus implies weak, GABA(B)-mediated intrare

106 Sleep spindles are generated by the thalamic reticular nucleus in conjunction with specific thalamic

107 In addition, given the central role of the reticular nucleus in generating spike-wave discharge, th

108 ection from the ipsilesional gigantocellular reticular nucleus in response to the injury.

109 oked disynaptic inhibition (via the thalamic reticular nucleus) in the same or a neighbouring relay n

110 gmental area, retrorubral area, and midbrain reticular nucleus) in the tegmentum that are implicated

111 uropil and in that of the overlying thalamic reticular nucleus, including the perigeniculate nucleus.

112 ts suggest that cells in the visual thalamic reticular nucleus influence the lateral geniculate nucle

113 of nerve terminals were found in the lateral reticular nucleus ipsilateral to the stimulation site.

114 us (mRN, rostral hindbrain) and the inferior reticular nucleus (iRN, caudal hindbrain).

115 hether neurons in the medullary intermediate reticular nucleus (IRt) are components of a central patt

116 estigate whether neurons in the intermediate reticular nucleus (IRt) form the central pattern generat

117 f the solitary tract (cNTS) and intermediate reticular nucleus (IRt) that express the glucagon gene (

118 lular reticular nucleus (PCRt), intermediate reticular nucleus (IRt), and dorsal medullary reticular

119 the visual sector of the GABAergic thalamic reticular nucleus is activated by attention in rats.

120 The thalamic reticular nucleus is an important structure governing th

121 ontrast, the acoustic sector of the thalamic reticular nucleus is not activated despite noise generat

122 the visual sector of the GABAergic thalamic reticular nucleus is selectively c-fos activated in rats

123 The visual sector of the thalamic reticular nucleus is the source of the primary inhibitor

124 s of the thalamus are linked directly to the reticular nucleus, it now becomes important to define ho

125 NPYs were released from sites in the lateral reticular nucleus, lateral tegmental field and vestibula

126 y in the nucleus tractus solitarius, lateral reticular nucleus, lateral tegmental field, vestibular n

127 show that regulation of excitability in the reticular nucleus leads to dynamical modulation of the s

128 in layer 6 (but not layer 5) or the thalamic reticular nucleus linearized the cortical responses, sug

129 re input system originating from the lateral reticular nucleus (LRN) can represent sensory event timi

130 The lateral reticular nucleus (LRN) resides in the rostral medulla a

131 l eyeblink conditioning with tone or lateral reticular nucleus (LRN) stimulation as conditioned stimu

132 of the projection from the principal lateral reticular nucleus (LRN) to the electrophysiologically de

133 es to stimulation of the ipsilateral lateral reticular nucleus (LRN) were also tested.

134 = 82) were in the area dorsal to the lateral reticular nucleus (LRN).

135 eticular nucleus (IRt), and dorsal medullary reticular nucleus (MdD).

136 Medullary gigantocellular reticular nucleus (mGi) neurons have been ascribed a var

137 region and caudal to it, the gigantocellular reticular nucleus, midline neurons and the caudal ventro

138 e we can understand exactly how the thalamic reticular nucleus might be influencing thalamocortical p

139 In the reticular nucleus, most subunit transcripts were not exp

140 LR sends bilateral projections to the middle reticular nucleus (mRN, rostral hindbrain) and the infer

141 tified neurons in the middle rhombencephalic reticular nucleus (MRRN), displayed delayed excitation (

142 gial cerebellar nucleus and/or ventrolateral reticular nucleus (n.Rvl).

143 n inhibitory GABAergic terminals of thalamic reticular nucleus neurones, and that it is normally acti

144 sterior nucleus neurons (VP) from P7, and in reticular nucleus neurons (RTN) from P8.

145 ify a role for GABA(A) receptors on thalamic reticular nucleus neurons and suggest antagonism of alph

146 alamocortical neurons and GABAergic thalamic reticular nucleus neurons and that these properties are

147 We conclude that all thalamic reticular nucleus neurons have a similar dendritic morph

148 ellar Purkinje cells and inhibitory thalamic reticular nucleus neurons have strongly reduced synaptic

149 tion of NMDA receptors on GABAergic thalamic reticular nucleus neurons might activate thalamocortical

150 Overall, brainstem reticular nucleus neurons showed the greatest gating of

151 major synaptic input from GABAergic thalamic reticular nucleus neurons, as well as neurons and astroc

152 Moreover, in thalamic reticular nucleus neurons, burst firing is impaired acco

153 In thalamocortical and thalamic reticular nucleus neurons, the site of AP generation and

154 rebellar nuclei neurons onto gigantocellular reticular nucleus neurons, which might produce an action

155 accompanied by persistent firing in thalamic reticular nucleus neurons.

156 of them originating from the gigantocellular reticular nucleus (NRG), have been observed.

157 hasic inhibition originating in the thalamic reticular nucleus (nRt) and are mediated by the neurotra

158 id (GABA)-containing neurons of the thalamic reticular nucleus (nRt) are a major source of inhibitory

159 Single electrical stimuli in the thalamic reticular nucleus (nRt) evoked rhythmic activity (1-15 s

160 al (POm) nucleus, the zona incerta (ZI), the reticular nucleus (nRT) of the thalamus, and the princip

161 ample, GABA-containing cells in the thalamic reticular nucleus (nRt) provide major inhibitory innerva

162 GABAergic neurons of the thalamic reticular nucleus (nRt) provide thalamocortical relay ne

163 d responses to GABA uncaging in the thalamic reticular nucleus (nRT) that is absent in both nm1054 mi

164 y GABA released from neurons of the thalamic reticular nucleus (nRT), acting predominantly via synapt

165 quely expressed by inhibitory neurons of the reticular nucleus (nRT).

166 ffect on synaptic inhibition in the thalamic reticular nucleus (nRT).

167 situs hypoglossi, dorsal paragigantocellular reticular nucleus, nucleus of the tractus solitarius and

168 to terminate uncrossed in the caudal lateral reticular nucleus of the medulla.

169 the first 2 weeks after birth, the thalamic reticular nucleus of the mouse lacks intrinsic GABAergic

170 atosensory cortex, the somatic region of the reticular nucleus of the thalamus (reticular thalamus).

171 Because the reticular nucleus of the thalamus (RtN) provides tonic f

172 verlap in their distribution, except for the reticular nucleus of the thalamus in which alpha7 mRNA w

173 caudate-putamen, 0.26 ug . g(-1) +/- 0.05 in reticular nucleus of the thalamus, 0.24 ug . g(-1) +/- 0

174 ion in olfactory bulb, pontine gray, lateral reticular nucleus of the thalamus, and piriform cortex.

175 ajority of Cck cells, excluding those in the reticular nucleus of the thalamus, are non-GABAergic.

176 -selective mGlu2/3 agonist, LY379268, in the reticular nucleus of the thalamus, significantly reduced

177 teral geniculate nuclei of the thalamus, the reticular nucleus of the thalamus, the lateral posterior

178 nctively expressed in cells in the GABAergic reticular nucleus of the thalamus.

179 r colliculus, the pretectal area, and/or the reticular nucleus of the thalamus.

180 as very prominent in the striatum and in the reticular nucleus of the thalamus; it was also observed

181 caused a release of irNPYs from the lateral reticular nucleus on the contralateral side of the brain

182 eticular nucleus, caudal part (79%); pontine reticular nucleus, oral part (131%); laterodorsal tegmen

183 thesis that GABA(A) receptors in the pontine reticular nucleus, oral part (PnO) of mouse modulate fiv

184 icity at electrical synapses in the thalamic reticular nucleus - paired burst spiking in coupled neur

185 within the raphe magnus and gigantocellular reticular nucleus, pars alpha.

186 l nucleus (Vme) project to the parvocellular reticular nucleus (PCRt) and dorsomedial spinal trigemin

187 hree specific RF subdivisions: parvocellular reticular nucleus (PCRt), intermediate reticular nucleus

188 e tegmental nucleus (PPTg), and oral pontine reticular nucleus (PnO) also severely disrupted approach

189 the cochlear nucleus, and via caudal pontine reticular nucleus, pontine central gray, and MS, reached

190 larly those in the posterior rhombencephalic reticular nucleus (PRRN), either adapted very quickly, a

191 a population of cells in the peri-tegmental reticular nucleus (pTRN(ADRB1)) that regulate sleep-wake

192 The thalamic reticular nucleus (RE) provides inhibition to the dorsal

193 restricted prefrontal areas to the thalamic reticular nucleus (RE), consistent with recent anatomica

194 The visual sector of the overlying thalamic reticular nucleus receives input from relay cells and su

195 hlight hypothesis proposes that the thalamic reticular nucleus regulates thalamic relay activity thro

196 retrorubral area, and lateral mesencephalic reticular nucleus), respiratory control (lateral nucleus

197 f the dorsal nucleus ambiguus, parvicellular reticular nucleus, retrorubral area, and lateral mesence

198 omatostatin (SST) on neurons in the thalamic reticular nucleus (RT) using whole-cell patch-clamp tech

199 s (VPI), posterior group of nuclei (Po), and reticular nucleus (Rt).

200 selective current in neurons of the thalamic reticular nucleus (RT; 20/29 neurons) and ventral basal

201 nhibitory effects on neurons of the thalamic reticular nucleus (RT; n = 18) and adjacent ventral basa

202 ing from synaptically coupled neurons of the reticular nucleus (RTN) and ventral posterior nucleus (V

203 caying IPSC, whereas neurons in the adjacent reticular nucleus (RTN) display a long-lasting, slowly d

204 of synapses to the circuitry of the thalamic reticular nucleus (RTN) in the rat.

205 In the thalamus, virtually all reticular nucleus (RTN) neurons were immunopositive for

206 bunits in ventral posterior nucleus (VP) and reticular nucleus (RTN) of control rats and WAG/Rij rats

207 inhibition of relay cells by neurons in the reticular nucleus (RTN) under the influence of corticoth

208 intranuclear synaptic inhibition within the reticular nucleus (RTN).

209 us (VPL) and in the associated sector of the reticular nucleus (RTN).

210 down-regulation of GABA inhibition from the reticular nucleus (RTN).

211 vasomotor neurons in the rostroventrolateral reticular nucleus (RVL) of the medulla oblongata and sym

212 piratory neurones in the rostroventrolateral reticular nucleus (RVL) of the medulla oblongata.

213 tion of neurons of the rostral ventrolateral reticular nucleus (RVL) would elevate regional cerebral

214 e not the same for each sector; (2) that the reticular nucleus serves as a nexus, where several funct

215 hat recurrent inhibition within the thalamic reticular nucleus serves to reduce synchrony and thus pr

216 e Kv3.3-IR neurones in the ventral medullary reticular nucleus, spinal trigeminal nucleus, dorsal hor

217 ulted in the specific activation of thalamic reticular nucleus, striatum/putamen, and cortical layers

218 ized PFC pathways to the inhibitory thalamic reticular nucleus suggest a mechanism to allow passage o

219 ns to cortical interneurons and the thalamic reticular nucleus, suggest a strong and synchronous cont

220 al nucleus, and dorsal paragigantocellularis reticular nucleus) that project to the head direction ci

221 atory control, including the gigantocellular reticular nucleus, the lateral paragigantocellular nucle

222 s, the cochlear nucleus, the gigantocellular reticular nucleus, the motor trigeminal nucleus, and the

223 a large-scale, two-dimensional model of the reticular nucleus, the network showed transient or self-

224 tal cortex, limbic thalamus, gigantocellular reticular nucleus, the somatosensory system, and cerebel

225 the pons, the ventral part of the medullary reticular nucleus, the ventral horn in the spinal cord o

226 tions from the visual sector of the thalamic reticular nucleus to the lateral geniculate nucleus comp

227 e input from the anterior pole of the monkey reticular nucleus to the motor-related thalamic nuclei i

228 y two major inhibitory systems: the thalamic reticular nucleus (TRN) and extrathalamic inhibitory (ET

229 expressing GABAergic neurons in the thalamic reticular nucleus (TRN) and intrinsic interneurons of dL

230 tiple single-unit recordings in the thalamic reticular nucleus (TRN) and medial prefrontal cortex (mP

231 Neurons in the thalamic reticular nucleus (TRN) are a primary source of inhibiti

232 s for a specific involvement of the thalamic reticular nucleus (TRN) come from its unique neuronal ch

233 The inhibitory neurons of the thalamic reticular nucleus (TRN) contribute to the generation of

234 The thalamic reticular nucleus (TRN) displays high expression of the

235 nerally thought that neurons in the thalamic reticular nucleus (TRN) form GABAergic synapses with oth

236 GABAergic neurons in the thalamic reticular nucleus (TRN) form powerful inhibitory connect

237 It is known that the thalamic reticular nucleus (TRN) gates sensory information en rou

238 The thalamic reticular nucleus (TRN) has been implicated in attention

239 The thalamic reticular nucleus (TRN) has unique integrative functions

240 The inhibitory thalamic reticular nucleus (TRN) intercepts and modulates all cor

241 The thalamic reticular nucleus (TRN) is a brain region that influence

242 The thalamic reticular nucleus (TRN) is a critical inhibitory modulat

243 The inhibitory thalamic reticular nucleus (TRN) is a hub of the attentional syst

244 The thalamic reticular nucleus (TRN) is a unique brain structure at t

245 The thalamic reticular nucleus (TRN) is essential for sleep maintenan

246 The thalamic reticular nucleus (TRN) is hypothesized to regulate neoc

247 The thalamic reticular nucleus (TRN) is hypothesized to regulate thal

248 The thalamic reticular nucleus (TRN) is implicated in schizophrenia p

249 as intrinsic thalamic neurons (e.g. thalamic reticular nucleus (TRN) neurons and dLGN interneurons).

250 Thalamic interneurons and thalamic reticular nucleus (TRN) neurons provide inhibitory inner

251 agation in thalamocortical (TC) and thalamic reticular nucleus (TRN) neurons remains unknown.

252 liminates rebound bursting in model thalamic reticular nucleus (TRN) neurons.

253 show that GABAergic neurons in the thalamic reticular nucleus (TRN) of mice and rats form two types

254 During sleep, neurons in the thalamic reticular nucleus (TRN) participate in distinct types of

255 Inhibitory neurons in the thalamic reticular nucleus (TRN) play a critical role in controll

256 Neurons within the mature thalamic reticular nucleus (TRN) powerfully inhibit ventrobasal (

257 Neurons of the thalamic reticular nucleus (TRN) provide inhibitory input to thal

258 The thalamic reticular nucleus (TRN) provides inhibitory innervation

259 show that local tonic activation of thalamic reticular nucleus (TRN) rapidly induces slow wave activi

260 achieved thalamic patterning with a thalamic reticular nucleus (TRN) signature, a GABAergic nucleus l

261 activity through modality-specific thalamic reticular nucleus (TRN) subnetworks.

262 es the organization of cells in the thalamic reticular nucleus (TRN) that project to the auditory par

263 ortex and inhibitory neurons of the thalamic reticular nucleus (TRN) that regulate the flow of those

264 tory synaptic transmission from the thalamic reticular nucleus (TRN) to the primary auditory thalamus

265 The thalamic reticular nucleus (TRN), a brain area rich in gap juncti

266 The thalamic reticular nucleus (TRN), a brain area rich in gap-juncti

267 olinergic transmission in the mouse thalamic reticular nucleus (TRN), a brain structure essential for

268 nergic synaptic transmission in the thalamic reticular nucleus (TRN), a brain structure intimately in

269 hd1 is selectively expressed in the thalamic reticular nucleus (TRN), a group of GABAergic neurons th

270 onal center, targets the inhibitory thalamic reticular nucleus (TRN), a key node in the brain's atten

271 in both directions pass through the thalamic reticular nucleus (TRN), a thin layer of GABAergic cells

272 ntially influenced microglia in the thalamic reticular nucleus (TRN), and local depletion of TRN micr

273 btypes are localized within the rat thalamic reticular nucleus (TRN), and we have examined the effect

274 ted inhibitory neurons, such as the thalamic reticular nucleus (TRN), often regulate neural oscillati

275 The thalamic reticular nucleus (TRN), the major source of thalamic in

276 However, neurons in the thalamic reticular nucleus (TRN), which exert powerful inhibitory

277 ubunits are highly expressed in the thalamic reticular nucleus (TRN), which is thought to act as a pa

278 thalamus arises from neurons in the thalamic reticular nucleus (TRN), which use gamma-aminobutyric ac

279 cells and inhibitory neurons of the thalamic reticular nucleus (TRN).

280 eurons of the strategically located thalamic reticular nucleus (TRN).

281 neuronal responses in the adjacent thalamic reticular nucleus (TRN).

282 ay is another thalamic nucleus, the thalamic reticular nucleus (TRN).

283 bited by the GABAergic cells of the thalamic reticular nucleus (TRN).

284 proximal dendrites of cells in the thalamic reticular nucleus (TRN).

285 s to the parvalbumin neurons in the thalamic reticular nucleus (TRN).

286 ack inhibition mediated through the thalamic reticular nucleus (TRN).

287 lies on indirect modulation via the thalamic reticular nucleus (TRN).

288 s (VB) and GABAergic neurons in the thalamic reticular nucleus (TRN).

289 -evoked inhibition arising from the thalamic reticular nucleus (TRN).

290 nit from parvalbumin neurons in the thalamic reticular nucleus using CRISPR-Cas9 gene editing increas

291 GABA neurons of ventral thalamus (reticular nucleus, ventral lateral geniculate nucleus, z

292 riaqueductal gray matter and gigantocellular reticular nucleus, ventral part also showed a similar ov

293 neurons located in the vibrissa intermediate reticular nucleus (vIRt(PV)) in the brainstem.

294 ion, we found neurons of the visual thalamic reticular nucleus (visTRN) to exhibit PFC-dependent chan

295 ectum (PT) and visual sector of the thalamic reticular nucleus (vTRN), as well as the intrinsic conne

296 6 corticothalamic feedback via the thalamic reticular nucleus was responsible for gating stochastic

297 antagonist within the middle rhombencephalic reticular nucleus was sufficient to decrease reticulospi

298 ons in different regions of the rat thalamic reticular nucleus were labeled with biotin dextran amine

299 the high density of synaptic inputs from the reticular nucleus while low expression in the reticular

300 her FEF connections were with the claustrum, reticular nucleus, zona incerta, lateral posterior and m