ライフサイエンスコーパス: GABAergic neuron

1 ceptor properties of synapses on the partner GABAergic neuron.

2 a4 subunit (alpha4* nAChRs) is restricted to GABAergic neurons.

3 nucleus of basal ganglia mostly composed of GABAergic neurons.

4 mouse astrocytes generates glutamatergic or GABAergic neurons.

5 dentate granule (DG) neurons to both CA3 and GABAergic neurons.

6 in corticostriatal glutamatergic or striatal GABAergic neurons.

7 rgic neurons and inhibitory innervation from GABAergic neurons.

8 lls were reprogrammed into glutamatergic and GABAergic neurons.

9 g a differential effect on glutamatergic and GABAergic neurons.

10 tropine-sensitive inward current in putative GABAergic neurons.

11 bound to the cell surface of unpermeabilized GABAergic neurons.

12 nase in mice that express Cre recombinase in GABAergic neurons.

13 direct synaptic input from glutamatergic and GABAergic neurons.

14 rticularly important for the excitability of GABAergic neurons.

15 ce confirmed that GFP selectively labeled BF GABAergic neurons.

16 n of DNA methyltransferases in telencephalic GABAergic neurons.

17 so recapitulated by direct inhibition of VTA GABAergic neurons.

18 , is a chromosomal conformation specific for GABAergic neurons.

19 the parvalbumin basket cell (PVBC) class of GABAergic neurons.

20 n is low compared with the levels present in GABAergic neurons.

21 ion in the morphophysiological properties of GABAergic neurons.

22 tergic and GABAergic neurons and subtypes of GABAergic neurons.

23 or the development of both glutamatergic and GABAergic neurons.

24 eferentially increased on the cell bodies of GABAergic neurons.

25 s are detectable in hippocampal and striatal GABAergic neurons.

26 r conditional deletion of Scn1a in forebrain GABAergic neurons.

27 ebrain and contain cortical glutamatergic or GABAergic neurons.

28 ice simply by removing MeCP2 from inhibitory GABAergic neurons.

29 the K(+)Cl(-) co-transporter KCC2 within VTA GABAergic neurons.

30 g by inhibiting the activity of BST Type III GABAergic neurons.

31 this upregulation did not occur in midbrain GABAergic neurons.

32 accumbens (NAc) via inhibition of local VTA GABAergic neurons.

33 sequences of conditional deletion of Prlr in GABAergic neurons.

34 whereas ON DRN-projecting RGCs mainly target GABAergic neurons.

35 basolateral amygdala (BLA), was expressed in GABAergic neurons.

36 XG1 is responsible for the overproduction of GABAergic neurons.

37 cal inhibitory gamma-aminobutyric acidergic (GABAergic) neurons.

38 smission in wild-type glutamatergic, but not GABAergic, neurons.

39 zed the expression and chemical phenotype of GABAergic neurons across each subdivision of LS and in c

40 itory signaling by these hybrid dopaminergic-GABAergic neurons act to suppress LHb output under rewar

41 nnel ppk29 and was mediated by male-specific GABAergic neurons acting on the GABAA receptor RDL in ta

42 y and physiologically characterized cortical GABAergic neurons and conducted a computational genomic

43 were sufficient to selectively activate VTA GABAergic neurons and elicit acute hypolocomotion, with

44 and diminished levels of activation (Fos) of GABAergic neurons and glutamic acid decarboxylase (GAD)

45 hibited diminished loss of glutamatergic and GABAergic neurons and greatly reduced inflammation in th

46 onstrating its presence in mouse hippocampal GABAergic neurons and in their hippocamposeptal axons th

47 log of the PPN contains both cholinergic and GABAergic neurons and is connected with all the nuclei o

48 we identified a pool of parvalbumin-positive GABAergic neurons and neurons in the upper tier of imagi

49 noid receptor 1 (CB1) receptors on forebrain GABAergic neurons and pain reduction on activation of pe

50 This leads to sustained depolarizations in GABAergic neurons and reduced inhibitory activity in the

51 with distinct profiles in glutamatergic and GABAergic neurons and subtypes of GABAergic neurons.

52 with antibodies that bind to the surface of GABAergic neurons and that could be pathogenic.

53 itory synaptic inputs onto glutamatergic and GABAergic neurons and that the nature of these reorganiz

54 nt of cell-cell contacts between presynaptic GABAergic neurons and their postsynaptic targets initiat

55 ccurring release events in glutamatergic and GABAergic neurons and their regulation is intensely deba

56 hannels is necessary for burst firing in SNr GABAergic neurons and their responsiveness to modulatory

57 esponses, maintained levels of activation of GABAergic neurons, and increased GAD expression in the a

58 Several drugs of abuse, act on VTA GABAergic neurons, and most studies have focused on loca

59 entral striatum, whereas those projecting to GABAergic neurons are distributed in the matrix compartm

60 As the network matures, GABAergic neurons are engaged more in GDPs and less in S

61 In the cerebellum, all GABAergic neurons are generated from the Ptf1a-expressin

62 VD class GABAergic neurons are generated in the late L1 and are p

63 During development, cortical GABAergic neurons are generated in ventral telencephalon

64 g REM sleep (REM-max), while the majority of GABAergic neurons are maximally active during wakefulnes

65 Substantia nigra pars reticulata (SNr) GABAergic neurons are projection neurons that convey out

66 ate that the activities of glutamatergic and GABAergic neurons are reduced in mice showing a depressi

67 In addition, the numbers of GABAergic neurons are reduced in the mutant and the dist

68 ate that soma-targeting parvalbumin-positive GABAergic neurons are the essential inhibitory neuron su

69 ng the delivery of timing information to the GABAergic neurons are unknown.

70 GABAergic neurons are vital for brain function.

71 g revealed that VTA DA neurons, but not tVTA GABAergic neurons, are tolerant to morphine after 2 week

72 aV1.1 FHM mutations and hyperexcitability of GABAergic neurons as the pathomechanism of FHM type 3.

73 fication and production of glutamatergic and GABAergic neurons as well as the subtypes for each of th

74 try and in permeabilized cultured cerebellar GABAergic neurons, as expected, but they also bound to t

75 s through a non cell-autonomous mechanism by GABAergic neurons, as selective deletion of GABAergic, b

76 AEX-2, the G-protein-coupled receptor on the GABAergic neurons, as the receptor for NLP-40.

77 Selectively silencing mouse ZI GABAergic neurons at birth decreased synaptic activity a

78 the limbic forebrain express ESR1, with ESR1-GABAergic neurons being more widespread and numerous tha

79 es-cre mice, while inhibition or deletion of GABAergic neurons blunted these behaviors.

80 esent study, CB1Rs are found not only on VTA GABAergic neurons, but also on VTA glutamatergic neurons

81 We conclude that leptin-responsive GABAergic neurons, but not glutamatergic neurons, act as

82 ediated knockdown of M1-AChR specifically in GABAergic neurons, but not glutamatergic neurons, in the

83 ted in a reduced number of glutamatergic and GABAergic neurons, but the latter additionally showed de

84 synaptic responses in both glutamatergic and GABAergic neurons by approximately 50%, due to an increa

85 r specifically in forebrain glutamatergic or GABAergic neurons by breeding GR(flox/flox) mice to Nex-

86 ieve unequivocal detection of cell bodies of GABAergic neurons by GAD mRNAs.

87 ium-dependent release and delivers it to the GABAergic neurons by instructing their activation.

88 suggesting that these long-range projecting GABAergic neurons can transmit aversive signals.

89 cate that under pathological conditions, SOM/GABAergic neurons can undergo substantial axonal reorgan

90 Recently, GABAergic neurons caudal to the VTA were discovered and

91 Conversely, knockout of mGluR5 or p11 in GABAergic neurons causes antidepressant-like behaviors.

92 ctive maternal deletion of Ube3a in cortical GABAergic neurons causes circuit hyperexcitability, incr

93 nic progenitors of forebrain cholinergic and GABAergic neurons causes dystonic-like twisting movement

94 ivity during learning: both dopaminergic and GABAergic neurons changed their activity in relation to

95 tional upregulation of alpha4* nAChRs in VTA GABAergic neurons confers increased sensitivity to nicot

96 Whereas GABAergic neurons containing endogenous morphine-like co

97 ibers apposed putative cortically projecting GABAergic neurons containing parvalbumin (PV).

98 cking nicotinic receptors, and many of these GABAergic neurons continue to fire after synaptic blocka

99 structure composed of mostly GABA-releasing (GABAergic) neurons, controls fear expression via project

100 This population of inspiratory-modulated GABAergic neurons could also play a role in inhibiting n

101 ng the excitatory/inhibitory balance through GABAergic neurons could prove a viable therapeutic optio

102 n excitatory (glutamatergic) and inhibitory (GABAergic) neurons (Dale's Law).

103 ully detected when sampling the cytoplasm of GABAergic neurons, demonstrating the exclusive nature of

104 ompatible with the increased excitability of GABAergic neurons determined by current-clamp recordings

105 he same genetic pathway as fmi-1 to regulate GABAergic neuron development.

106 pendent regulation of both glutamatergic and GABAergic neuron development.

107 sing calcium-binding proteins showed that LS GABAergic neurons displayed immunoreactivity for calbind

108 iatum driven by Rip2-Cre, or specifically in GABAergic neurons driven by Vgat-ires-Cre, both the hype

109 extrinsic factors, the changes we saw in the GABAergic neuron due to glutamatergic input may reflect

110 gers a single rapid calcium transient in the GABAergic neurons during each defecation cycle.

111 Dampening excitability of GABAergic neurons during nicotine withdrawal through IPN

112 te that therapeutic strategies to reduce IPN GABAergic neuron excitability during nicotine withdrawal

113 nal cord, glycinergic synapses on inhibitory GABAergic neurons exhibit LTP, occurring rapidly after e

114 The synaptic targeting of these GABAergic neurons exhibits an absolute dependence on pro

115 ces of guinea pig midbrain, we show that SNr GABAergic neurons express transient receptor potential m

116 Further, sSC GABAergic neurons expressing alpha6* nAChRs exhibit a to

117 GABAergic neurons expressing different isoforms of gluta

118 Unexpectedly, we found that RVM GABAergic neurons facilitate mechanical pain by inhibiti

119 Our data suggest that a shift toward GABAergic neuron fate caused by FOXG1 is a developmental

120 gic inhibition because of an increase in VTA GABAergic neuron firing.

121 e lineage that generates calretinin-positive GABAergic neurons for the OB.

122 2 (AD) induces the generation of exclusively GABAergic neurons from human PSCs with a high degree of

123 tify SAVAs as an effective tool to eliminate GABAergic neurons from neuronal circuits underpinning hi

124 erconnected, especially by glutamatergic and GABAergic neurons from the GT and GLv, respectively.

125 Transplanting embryonic precursors of GABAergic neurons from the medial ganglionic eminence (M

126 halic glutamatergic neurons (Glu-CB1 -RS) or GABAergic neurons (GABA-CB1 -RS) was studied by immunoel

127 R in forebrain gamma-aminobutyric acidergic (GABAergic) neurons (GABA-CB1R).

128 essing Leu9'Ser alpha4 nAChR subunits in VTA GABAergic neurons (Gad2(VTA):Leu9'Ser mice), subreward t

129 l deep mesencephalic nucleus (dDpMe) contain GABAergic neurons gating paradoxical sleep (PS) onset by

130 hed that a single inhibitory cell, the giant GABAergic neuron (GGN), is the main and perhaps sole sou

131 n contrast, manipulating Syngap1 function in GABAergic neurons had no effect on cognition, excitabili

132 utyric acid (GABA), and impaired function of GABAergic neurons has been implicated in the pathogenesi

133 earning and memory of fear, the diversity of GABAergic neurons has not been fully explored.

134 Remarkably, projections from ARN GABAergic neurons heavily contacted and even bundled wit

135 systems GAD65 and GAD67, and each subtype of GABAergic neurons identified by distinct calcium-binding

136 The spontaneously firing GABAergic neurons identified in this study that increase

137 Reducing the excitatory input on Type III GABAergic neurons, IL-18 can increase the firing of glut

138 The proportion of GABAergic neurons immunoreactive for CB or CR varied dep

139 it is shown that CB(1) receptors located on GABAergic neurons impede negative consequences of volunt

140 I describe analogies and differences between GABAergic neurons in BLA and cerebral cortex.

141 gs highlight the critical regulatory role of GABAergic neurons in certain behaviors and suggest that

142 Deletion of CB1 receptor in GABAergic neurons in GABA-CB1-KO mice leads to a signifi

143 , while monitoring the spontaneous firing of GABAergic neurons in mouse substantia nigra pars reticul

144 , we show that the individual involvement of GABAergic neurons in SPAs is correlated to their tempora

145 Furthermore, selective in vivo inhibition of GABAergic neurons in the basal forebrain by targeted exp

146 w that disrupting cholinergic innervation of GABAergic neurons in the C. elegans motor circuit alters

147 nd retrograde tracing in mice, we found that GABAergic neurons in the central nucleus of the amygdala

148 ntially increased by selective activation of GABAergic neurons in the central nucleus of the amygdala

149 in a subpopulation of both glutamatergic and GABAergic neurons in the central nucleus of the inferior

150 However, identifying the phenotype of GABAergic neurons in the CNS has been hampered by the lo

151 APP, highly expressed in the majority of GABAergic neurons in the dentate gyrus, enhances the inh

152 We hypothesized that GABAergic neurons in the dorsal raphe nucleus (DRN) may

153 se from a major subset of non-POMC, non-AgRP GABAergic neurons in the hypothalamus.

154 GABAergic neurons in the LH have been shown to mediate a

155 Although sleep-active GABAergic neurons in the medullary parafacial zone (PZ)

156 and support the widely held proposition that GABAergic neurons in the mesopontine tegmentum are an im

157 Here we show that a subset of GABAergic neurons in the mouse ventral zona incerta, whi

158 l intersectional targeting strategy to label GABAergic neurons in the mPFC that project to NAcc and f

159 ological properties of long-range projecting GABAergic neurons in the mPFC.

160 perties for a class of long-range projecting GABAergic neurons in the neocortex.

161 s, without changes in the number of cortical GABAergic neurons in the PFC ofTgDyrk1Amice, which sugge

162 eral noradrenergic neurons in the LC; medial GABAergic neurons in the pontine central gray; ventromed

163 Here I review the diversity of GABAergic neurons in the rodent basolateral amygdala (BL

164 Activation of GABAergic neurons in the rostromedial tegmental nucleus

165 umption, and that optogenetic stimulation of GABAergic neurons in the same region selectively reduces

166 ing projections to motor-related glycinergic/GABAergic neurons in the spinal cord and ventromedial me

167 tergic inputs, and preferentially innervated GABAergic neurons in the substantia nigra pars reticulat

168 GABAergic neurons in the tail of the ventral tegmental a

169 a novel dye-coupling technique to show that GABAergic neurons in the thalamic reticular nucleus (TRN

170 neurons in the ventrobasal nucleus (VB) and GABAergic neurons in the thalamic reticular nucleus (TRN

171 lay cells in dLGN, as well as GFP expressing GABAergic neurons in the thalamic reticular nucleus (TRN

172 GABAergic neurons in the thalamic reticular nucleus (TRN

173 GABAergic neurons in the ventral pallidum (VP) provide a

174 his study we have identified a population of GABAergic neurons in the ventrolateral medulla that rece

175 ted in part by inhibition of REM-suppressing GABAergic neurons in the ventrolateral periaqueductal gr

176 ess via projections to both dopaminergic and GABAergic neurons in the VTA, and that these projections

177 GABAergic neurons in TRN exhibited large initial excitat

178 articipation of parvalbumin-expressing (PV+) GABAergic neurons in two forms of experience-dependent m

179 hetic NLP-40-derived peptide depolarizes the GABAergic neurons in vivo.

180 orphological comparison of glutamatergic and GABAergic neurons in which mTOR signaling was either inc

181 is expressed and translated by some POMC and GABAergic-neurons in the hypothalamic arcuate nucleus (A

182 itive (PV+) and somatostatin-positive (SOM+) GABAergic neurons - in the mouse brain.

183 linergic neurons strongly excite neighboring GABAergic neurons, including the subset of cortically pr

184 ion of a subset of lateral hypothalamus (LH) GABAergic neurons induced both appetitive (food-seeking)

185 on specifically in glutamatergic, but not in GABAergic, neurons induced hypothalamic-pituitary-adrena

186 of TrkB signalling in cholecystokinin (CCK)-GABAergic neurons induces glucocorticoid resistance, res

187 uring the integration of post-embryonic-born GABAergic neurons into the circuit, produces irreversibl

188 n for linking the relatively few inhibitory, GABAergic, neurons into large, effective networks within

189 ur data indicate the one-in-five fraction of GABAergic neurons is already established during their ne

190 ion of candidate gene promoters expressed in GABAergic neurons is associated with transcriptional dow

191 ntly, loss of Na(V)1.1 channels in forebrain GABAergic neurons is both necessary and sufficient to ca

192 moter, we determined that this population of GABAergic neurons is in close apposition to cardioinhibi

193 Furthermore, VMAT2 expression in GABAergic neurons lacking VGAT is sufficient to sustain

194 arinic receptors in two subpopulations of BF GABAergic neurons [large hyperpolarization-activated cat

195 a-PKA deficiency in a subset of hypothalamic GABAergic neurons leads to the lean phenotype.

196 The absence of CB1 receptors from GABAergic neurons led to a depression of VTA DA neuronal

197 Recent studies associated LHA GABAergic neurons (LHA (GABA) ), which densely innervate

198 of their inhibitory projection to the PS-off GABAergic neurons located in the VLPAG/dDpMe.

199 tions and TH-ir processes suggests that CAmy GABAergic neurons may directly inhibit noradrenergic pri

200 Reduced numbers or function of cortical GABAergic neurons may lead to hyperactivity states such

201 sed, the data reported suggest that these LH GABAergic neurons may modulate behaviors that function t

202 These data indicate that LH GABAergic neurons modulate consummatory behaviors regard

203 The current data indicate that DR GABAergic neurons not only may have the capacity to infl

204 esidue at the 9' position (Leu9'Ser)] in VTA GABAergic neurons of adult mice.

205 netically restoring Mecp2 expression only in GABAergic neurons of male Mecp2 null mice enhanced inhib

206 The channels are also expressed on GABAergic neurons of the basal ganglia, substantia nigra

207 These results demonstrate that GABAergic neurons of the CeA are sufficient and necessar

208 3 receptor or the inhibitory hM4 receptor in GABAergic neurons of the CeA.

209 Because GABAergic neurons of the central nucleus of the amygdala

210 are electrically different from 'classical' GABAergic neurons of the cortex, are neurochemically dis

211 utagenesis to elucidate receptor function in GABAergic neurons of the forebrain.

212 Gap junctions (GJs) electrically couple GABAergic neurons of the forebrain.

213 dopaminergic, cholinergic, and fast spiking GABAergic neurons of the mesostriatal circuit, imbalance

214 n alters sensory responses in two classes of GABAergic neurons of the mouse OB glomerular layer, peri

215 During sleep slow waves, both GABAergic neurons of the nucleus reticularis thalami (NR

216 The substantia nigra (SN) consists of GABAergic neurons of the pars reticulata that inhibit th

217 alic origin of dLGN-INs sets them apart from GABAergic neurons of the reticular thalamic nucleus.

218 synapses are strong and prevalent among the GABAergic neurons of the rodent thalamic reticular nucle

219 posed by axon terminals of glutamatergic and GABAergic neurons of the substantia innominata (SI) and

220 The spontaneously active GABAergic neurons of the substantia nigra pars reticulat

221 In contrast, expression of opto-MOR in GABAergic neurons of the ventral pallidum hedonic cold s

222 tivation of synaptic transmission from local GABAergic neurons of the VTA, demonstrating an important

223 tivation relieves the inhibitory tone of the GABAergic neurons on the IPCs, resulting in the secretio

224 Ablation or silencing of GABAergic neurons or disruption of metabotropic GABA rec

225 , the basal ganglia primodia from which many GABAergic neurons originate and migrate to other forebra

226 with selective removal of MeCP2 in forebrain GABAergic neurons, predominantly in the striatum, phenoc

227 Similar activation of BF GABAergic neurons produced sustained wakefulness and hig

228 e temporal identity transition of cerebellar GABAergic neuron progenitors from PCPs to PIPs is negati

229 Here we show temporal regulation of distinct GABAergic neuron progenitors in the cerebellum.

230 LH GABAergic neurons project extensively to the paraventric

231 de recording, we show that the preoptic area GABAergic neurons projecting to the tuberomammillary nuc

232 , activation of somatostatin-positive (SOM+) GABAergic neurons promoted NREM sleep, although only som

233 Optogenetic activation of ventral medulla GABAergic neurons rapidly and reliably initiated REM sle

234 ses, whereas expression of a long isoform in GABAergic neurons recruits acetylcholine receptors to GA

235 hat disruption of GABA release from adult LH GABAergic neurons reduced feeding.

236 the machinery to produce different types of GABAergic neurons remains elusive.

237 ned populations of functionally mature human GABAergic neurons represents an important step toward en

238 alic glutamatergic neurons but not forebrain GABAergic neurons rescued the deficits in corticospinal

239 evels of functional connectivity and loss of GABAergic neurons, respectively) and diffuse gliosis in

240 enerate different types of glutamatergic and GABAergic neurons, respectively.

241 eral posterior thalamus; another, comprising GABAergic neurons, responds to the sudden appearance or

242 inability to achieve selective access to the GABAergic neurons responsible for this unorthodox inhibi

243 DD GABAergic neurons reverse polarity during larval develop

244 ctory bulb and, with the exception of Type 2 GABAergic neurons, sent projections to both reproductive

245 echanism, feedback inhibition from the giant GABAergic neuron, serves this function.

246 rticostriatal circuits; (3) dopaminergic and GABAergic neurons show similar task-related activity, al

247 Although the somata of GABAergic neurons showed little orientation tuning, thei

248 om channelrhodopsin-2-tagged ventral medulla GABAergic neurons showed that they were most active duri

249 These results show that VTA GABAergic neurons signal expected reward, a key variable

250 in likely via modulation of deep dorsal horn GABAergic neurons.SIGNIFICANCE STATEMENT Pain is the mos

251 somatostatin-expressing (Sst) interneurons (GABAergic neurons specialized for dendritic inhibition),

252 e spinal cords, hESC-MGEs differentiate into GABAergic neuron subtypes and receive synaptic inputs, s

253 , an accompanying reduction in untransfected GABAergic neurons suggests hampered intercellular commun

254 urons in the C. elegans motor circuit alters GABAergic neuron synaptic connectivity.

255 ion of CEA (CEl) contains a subpopulation of GABAergic neurons that are marked by protein kinase C-de

256 Recent findings indicate that VTA GABAergic neurons that coexpress tyrosine hydroxylase (T

257 tion of cannabinoid CB1 receptors (CB1Rs) on GABAergic neurons that disinhibit dopaminergic neurons i

258 he pontine central gray; ventromedial, small GABAergic neurons that express FoxP2; and dorsolateral g

259 resent largely nonoverlapping populations of GABAergic neurons that express various subtype-specific

260 nsmitted by DRN-projecting RGCs activate DRN GABAergic neurons that in turn inhibit serotoninergic ne

261 teric muscle contractions through downstream GABAergic neurons that innervate enteric muscles.

262 reactive glial cells into glutamatergic and GABAergic neurons that integrate into the host's neural

263 PPT nucleus also contains glutamatergic and GABAergic neurons that likely contribute to the regulati

264 pontaneous firing in these cardiorespiratory GABAergic neurons that possess a pacemaker phenotype.

265 ndreds of cells, we identified individual LH GABAergic neurons that preferentially encode aspects of

266 Suppression of GABAergic neurons that project from SNpr results in the

267 b-Cre mice, we found anatomical evidence for GABAergic neurons that project from the mouse medial pre

268 ivates JAK/STAT signaling in a population of GABAergic neurons that project onto the IPCs.

269 thalamic reticular nucleus (TRN), a group of GABAergic neurons that regulate thalamocortical transmis

270 Several populations of GABAergic neurons that were not previously known to be p

271 e determined the fraction of all neocortical GABAergic neurons that will become inhibitory (GAD67(+))

272 Compared with the GABAergic neurons, the activity of dopaminergic neurons

273 Among GABAergic neurons, the so-called intercalated cells (ITC

274 We report a specialized population of septal GABAergic neurons, the Teevra cells, selectively innerva

275 In addition to these mesohabenular TH-GABAergic neurons, the VTA has many neurons expressing v

276 trategies and tools will facilitate studying GABAergic neurons throughout the mouse brain.

277 we found that glutamatergic input caused the GABAergic neuron to modify its output by way of an incre

278 tions of mouse hippocampal glutamatergic and GABAergic neurons to investigate how synaptic input and

279 r findings reveal a major contribution of BF GABAergic neurons to wakefulness and the fast cortical r

280 eurogliaform cell (NGFC), a widely expressed GABAergic neuron type, detected in vivo during theta rhy

281 We discovered that cardinal GABAergic neuron types are delineated by a transcription

282 Various GABAergic neuron types of the amygdala cooperate to cont

283 urochemical and anatomical classification of GABAergic neuron types.

284 control of Gq signals in 5-HT2c-R domains in GABAergic neurons upstream of 5-HT neurons provides nega

285 inergic neurons and cortically projecting BF GABAergic neurons using immunohistochemistry and whole-c

286 he contribution of predominantly inhibitory (GABAergic) neurons versus excitatory (glutamatergic) neu

287 Optical activation of IPN GABAergic neurons via light stimulation of channelrhodop

288 The spontaneous firing in these GABAergic neurons was not altered by the voltage-gated c

289 n retinal afferents and DRN serotonergic and GABAergic neurons were observed.

290 t, surprisingly, functional synapses from SI GABAergic neurons were rare.

291 glutamatergic and parvalbumin-positive (PV+) GABAergic neurons, were more active during wakefulness a

292 henotypes, such as microglia, astrocytes, or GABAergic neurons, whereas animals eventually recover co

293 n that was present in both glutamatergic and GABAergic neurons, whereas mice without GDDs showed stab

294 its are composed of mainly glutamatergic and GABAergic neurons, which communicate through synaptic co

295 d a Cre-dependent viral opto-MOR in RMTg/VTA GABAergic neurons, which led to a real-time place prefer

296 synthesize our findings of specification of GABAergic neurons with previous reports on the specifica

297 We 'tagged' dopaminergic and GABAergic neurons with the light-sensitive protein chann

298 Recent evidence highlights a subdivision of GABAergic neurons within anterior bed nuclei of the stri

299 sical nicotine withdrawal symptoms activates GABAergic neurons within the interpeduncular nucleus (IP

300 e findings suggest that the vast majority of GABAergic neurons within the LS have the potential for s