ライフサイエンスコーパス: thalamic reticular nucleus

1 ts from the retina, visual cortices, and the thalamic reticular nucleus.

2 ATPA reduced the IPSPs originating from the thalamic reticular nucleus.

3 e doubly stained for NAAG and GAD(67) in the thalamic reticular nucleus.

4 pathway involving the GABAergic cells of the thalamic reticular nucleus.

5 el resembling the human ventral thalamus and thalamic reticular nucleus.

6 ugh thalamic interneurons and neurons in the thalamic reticular nucleus.

7 mpeting hypotheses about the function of the thalamic reticular nucleus.

8 also influence thalamic relay nuclei via the thalamic reticular nucleus.

9 ibit them by driving inhibitory cells of the thalamic reticular nucleus.

10 nt among the GABAergic neurons of the rodent thalamic reticular nucleus.

11 allosteric modulators of GABAARs) within the thalamic reticular nucleus.

12 tions also include inhibitory neurons in the thalamic reticular nucleus.

13 least from two sources, substantia nigra and thalamic reticular nucleus.

14 th between the inhibitory neurons of the rat thalamic reticular nucleus.

15 , yet they are colocalized in neurons of the thalamic reticular nucleus.

16 ion on GABAergic inhibition arising from the thalamic reticular nucleus.

17 s we find hundreds of neurons labeled in the thalamic reticular nucleus, a structure that can only be

18 , we report a Brn3c(+) RGC projection to the thalamic reticular nucleus, a visual nucleus that was no

19 The thalamic reticular nucleus also exhibited robust m2 immu

20 e effect on evoked responses from inhibitory thalamic reticular nucleus and excitatory tectothalamic

21 circuits formed by GABAergic neurons in the thalamic reticular nucleus and glutamatergic relay neuro

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

23 itory afferents from inferior colliculus and thalamic reticular nucleus and its GABA(A)R functional h

24 s important for neuronal excitability in the thalamic reticular nucleus and other regions of the brai

25 utyric acid (GABA)ergic projections from the thalamic reticular nucleus and pretectum, and a choliner

26 hometry) which was associated with decreased thalamic reticular nucleus and primary somatosensory cor

27 cortex, sleep spindles are initiated by the thalamic reticular nucleus and regulated by thalamo-reti

28 ic medications, and point to deficits in the thalamic reticular nucleus and thalamo-reticular circuit

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

30 a larger inhibitory network composed of the thalamic reticular nucleus and zona incerta, known to mo

31 cortical connectivity, especially within the thalamic reticular nucleus, and are linked to dysfunctio

32 xon terminals that arise from neurons of the thalamic reticular nucleus, and perhaps from VPL local c

33 levels in the cerebellar granule cell layer, thalamic reticular nucleus, and piriform cortex.

34 trigeminal nucleus, somatosensory thalamus, thalamic reticular nucleus, and primary somatosensory co

35 diate layers of the superior colliculus, the thalamic reticular nucleus, and the caudate nucleus.

36 provide axonal collaterals to neurons in the thalamic reticular nucleus, and these thalamic reticular

37 l synapses between inhibitory neurons of the thalamic reticular nucleus are bidirectionally modulated

38 It has been proposed that neurons in the thalamic reticular nucleus are interconnected through GA

39 that parvalbumin interneurons in the sensory thalamic reticular nucleus are necessary and sufficient

40 inputs from the anteroventral portion of the thalamic reticular nucleus (avTRN) inhibit the firing ra

41 e laminar and cellular targets of individual thalamic reticular nucleus axons in the highly laminated

42 Reconstructed thalamic reticular nucleus axons were narrowly aligned a

43 y-linked gene Cacna1h in iKOp/q mice reduces thalamic reticular nucleus burst firing and promotes rat

44 The thalamic reticular nucleus can be divided into a number

45 ain, especially in the hypothalamus, septum, thalamic reticular nucleus, certain cortices and other l

46 These data implicate a corticothalamic-thalamic reticular nucleus circuit that modifies thalami

47 gh Ptchd1 is preferentially expressed in the thalamic reticular nucleus during development, pharmacol

48 nificantly enhanced in the barrel cortex and thalamic reticular nucleus during the second postnatal w

49 cortico-pulvinar projections that engage the thalamic reticular nucleus enable the pulvinar to estima

50 Interestingly, inborn deletion of thalamic reticular nucleus-enriched, human childhood abs

51 rom control subjects significantly decreased thalamic reticular nucleus excitability (P = 0.011).

52 iants that either had no effect or increased thalamic reticular nucleus excitability across disease s

53 cal properties of CaV3.3 channel variants on thalamic reticular nucleus excitability and found that c

54 nificant trend between variants that reduced thalamic reticular nucleus excitability and variants tha

55 neurons in the cerebral cortex, hippocampus, thalamic reticular nucleus, globus pallidus and the subs

56 The thalamic reticular nucleus has a critical role in modula

57 was evident in adjacent regions, such as the thalamic reticular nucleus, hypothalamus, and globus pal

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

59 neuron evoked disynaptic inhibition (via the thalamic reticular nucleus) in the same or a neighbourin

60 culate neuropil and in that of the overlying thalamic reticular nucleus, including the perigeniculate

61 ese results suggest that cells in the visual thalamic reticular nucleus influence the lateral genicul

62 ated that the visual sector of the GABAergic thalamic reticular nucleus is activated by attention in

63 The thalamic reticular nucleus is an important structure gov

64 By contrast, the acoustic sector of the thalamic reticular nucleus is not activated despite nois

65 ated that the visual sector of the GABAergic thalamic reticular nucleus is selectively c-fos activate

66 The visual sector of the thalamic reticular nucleus is the source of the primary

67 neurons in layer 6 (but not layer 5) or the thalamic reticular nucleus linearized the cortical respo

68 ections enabling dimensionality reduction, a thalamic reticular nucleus-mediated divisive normalizati

69 ons before we can understand exactly how the thalamic reticular nucleus might be influencing thalamoc

70 tically on inhibitory GABAergic terminals of thalamic reticular nucleus neurones, and that it is norm

71 lts identify a role for GABA(A) receptors on thalamic reticular nucleus neurons and suggest antagonis

72 tergic thalamocortical neurons and GABAergic thalamic reticular nucleus neurons and that these proper

73 We conclude that all thalamic reticular nucleus neurons have a similar dendri

74 oth cerebellar Purkinje cells and inhibitory thalamic reticular nucleus neurons have strongly reduced

75 Inhibition of NMDA receptors on GABAergic thalamic reticular nucleus neurons might activate thalam

76 receive major synaptic input from GABAergic thalamic reticular nucleus neurons, as well as neurons a

77 Moreover, in thalamic reticular nucleus neurons, burst firing is impa

78 In thalamocortical and thalamic reticular nucleus neurons, the site of AP gener

79 hich was accompanied by persistent firing in thalamic reticular nucleus neurons.

80 pend on phasic inhibition originating in the thalamic reticular nucleus (nRt) and are mediated by the

81 utyric acid (GABA)-containing neurons of the thalamic reticular nucleus (nRt) are a major source of i

82 Single electrical stimuli in the thalamic reticular nucleus (nRt) evoked rhythmic activit

83 For example, GABA-containing cells in the thalamic reticular nucleus (nRt) provide major inhibitor

84 GABAergic neurons of the thalamic reticular nucleus (nRt) provide thalamocortical

85 ission and responses to GABA uncaging in the thalamic reticular nucleus (nRT) that is absent in both

86 ediated by GABA released from neurons of the thalamic reticular nucleus (nRT), acting predominantly v

87 zepine) effect on synaptic inhibition in the thalamic reticular nucleus (nRT).

88 xcept for the first 2 weeks after birth, the thalamic reticular nucleus of the mouse lacks intrinsic

89 of plasticity at electrical synapses in the thalamic reticular nucleus - paired burst spiking in cou

90 The thalamic reticular nucleus (RE) provides inhibition to t

91 ions from restricted prefrontal areas to the thalamic reticular nucleus (RE), consistent with recent

92 The visual sector of the overlying thalamic reticular nucleus receives input from relay cel

93 The searchlight hypothesis proposes that the thalamic reticular nucleus regulates thalamic relay acti

94 ects of somatostatin (SST) on neurons in the thalamic reticular nucleus (RT) using whole-cell patch-c

95 ted a K+-selective current in neurons of the thalamic reticular nucleus (RT; 20/29 neurons) and ventr

96 roduced inhibitory effects on neurons of the thalamic reticular nucleus (RT; n = 18) and adjacent ven

97 nt types of synapses to the circuitry of the thalamic reticular nucleus (RTN) in the rat.

98 roposed that recurrent inhibition within the thalamic reticular nucleus serves to reduce synchrony an

99 (CL) resulted in the specific activation of thalamic reticular nucleus, striatum/putamen, and cortic

100 Specialized PFC pathways to the inhibitory thalamic reticular nucleus suggest a mechanism to allow

101 projections to cortical interneurons and the thalamic reticular nucleus, suggest a strong and synchro

102 ry projections from the visual sector of the thalamic reticular nucleus to the lateral geniculate nuc

103 argeted by two major inhibitory systems: the thalamic reticular nucleus (TRN) and extrathalamic inhib

104 l as GFP expressing GABAergic neurons in the thalamic reticular nucleus (TRN) and intrinsic interneur

105 l and multiple single-unit recordings in the thalamic reticular nucleus (TRN) and medial prefrontal c

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

107 Clues for a specific involvement of the thalamic reticular nucleus (TRN) come from its unique ne

108 The inhibitory neurons of the thalamic reticular nucleus (TRN) contribute to the gener

109 The thalamic reticular nucleus (TRN) displays high expressio

110 It is generally thought that neurons in the thalamic reticular nucleus (TRN) form GABAergic synapses

111 GABAergic neurons in the thalamic reticular nucleus (TRN) form powerful inhibitor

112 It is known that the thalamic reticular nucleus (TRN) gates sensory informati

113 The thalamic reticular nucleus (TRN) has been implicated in

114 The thalamic reticular nucleus (TRN) has unique integrative

115 The inhibitory thalamic reticular nucleus (TRN) intercepts and modulate

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

117 The thalamic reticular nucleus (TRN) is a critical inhibitor

118 The inhibitory thalamic reticular nucleus (TRN) is a hub of the attenti

119 The thalamic reticular nucleus (TRN) is a unique brain struc

120 The thalamic reticular nucleus (TRN) is essential for sleep

121 The thalamic reticular nucleus (TRN) is hypothesized to regu

122 The thalamic reticular nucleus (TRN) is hypothesized to regu

123 The thalamic reticular nucleus (TRN) is implicated in schizo

124 as well as intrinsic thalamic neurons (e.g. thalamic reticular nucleus (TRN) neurons and dLGN intern

125 Thalamic interneurons and thalamic reticular nucleus (TRN) neurons provide inhibit

126 backpropagation in thalamocortical (TC) and thalamic reticular nucleus (TRN) neurons remains unknown

127 or more eliminates rebound bursting in model thalamic reticular nucleus (TRN) neurons.

128 hnique to show that GABAergic neurons in the thalamic reticular nucleus (TRN) of mice and rats form t

129 During sleep, neurons in the thalamic reticular nucleus (TRN) participate in distinct

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

131 Neurons within the mature thalamic reticular nucleus (TRN) powerfully inhibit vent

132 Neurons of the thalamic reticular nucleus (TRN) provide inhibitory inpu

133 The thalamic reticular nucleus (TRN) provides inhibitory inn

134 logy, we show that local tonic activation of thalamic reticular nucleus (TRN) rapidly induces slow wa

135 iously unachieved thalamic patterning with a thalamic reticular nucleus (TRN) signature, a GABAergic

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

137 y describes the organization of cells in the thalamic reticular nucleus (TRN) that project to the aud

138 to the cortex and inhibitory neurons of the thalamic reticular nucleus (TRN) that regulate the flow

139 ed inhibitory synaptic transmission from the thalamic reticular nucleus (TRN) to the primary auditory

140 The thalamic reticular nucleus (TRN), a brain area rich in g

141 The thalamic reticular nucleus (TRN), a brain area rich in g

142 liable cholinergic transmission in the mouse thalamic reticular nucleus (TRN), a brain structure esse

143 on cholinergic synaptic transmission in the thalamic reticular nucleus (TRN), a brain structure inti

144 mouse Ptchd1 is selectively expressed in the thalamic reticular nucleus (TRN), a group of GABAergic n

145 n's emotional center, targets the inhibitory thalamic reticular nucleus (TRN), a key node in the brai

146 d cortex in both directions pass through the thalamic reticular nucleus (TRN), a thin layer of GABAer

147 e preferentially influenced microglia in the thalamic reticular nucleus (TRN), and local depletion of

148 mGluR subtypes are localized within the rat thalamic reticular nucleus (TRN), and we have examined t

149 terconnected inhibitory neurons, such as the thalamic reticular nucleus (TRN), often regulate neural

150 The thalamic reticular nucleus (TRN), the major source of th

151 However, neurons in the thalamic reticular nucleus (TRN), which exert powerful i

152 d Kv3.3 subunits are highly expressed in the thalamic reticular nucleus (TRN), which is thought to ac

153 e dorsal thalamus arises from neurons in the thalamic reticular nucleus (TRN), which use gamma-aminob

154 ngly inhibited by the GABAergic cells of the thalamic reticular nucleus (TRN).

155 omata and proximal dendrites of cells in the thalamic reticular nucleus (TRN).

156 isruptions to the parvalbumin neurons in the thalamic reticular nucleus (TRN).

157 cal feedback inhibition mediated through the thalamic reticular nucleus (TRN).

158 athway relies on indirect modulation via the thalamic reticular nucleus (TRN).

159 al nucleus (VB) and GABAergic neurons in the thalamic reticular nucleus (TRN).

160 n sensory-evoked inhibition arising from the thalamic reticular nucleus (TRN).

161 ic relay cells and inhibitory neurons of the thalamic reticular nucleus (TRN).

162 in the neurons of the strategically located thalamic reticular nucleus (TRN).

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

164 vital relay is another thalamic nucleus, the thalamic reticular nucleus (TRN).

165 ptor subunit from parvalbumin neurons in the thalamic reticular nucleus using CRISPR-Cas9 gene editin

166 this notion, we found neurons of the visual thalamic reticular nucleus (visTRN) to exhibit PFC-depen

167 the pretectum (PT) and visual sector of the thalamic reticular nucleus (vTRN), as well as the intrin

168 hat layer 6 corticothalamic feedback via the thalamic reticular nucleus was responsible for gating st

169 Neurons in different regions of the rat thalamic reticular nucleus were labeled with biotin dext