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 receive from an inhibitory neuron, the Giant GABAergic neuron.

3 ebrain and contain cortical glutamatergic or GABAergic neurons.

4 ng P2Y2 purinoceptor activation matured into GABAergic neurons.

5 ice simply by removing MeCP2 from inhibitory GABAergic neurons.

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

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

8 this upregulation did not occur in midbrain GABAergic neurons.

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

10 sequences of conditional deletion of Prlr in GABAergic neurons.

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

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

13 XG1 is responsible for the overproduction of GABAergic neurons.

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

15 f cortical and hippocampal glutamatergic and GABAergic neurons.

16 nucleus of basal ganglia mostly composed of GABAergic neurons.

17 mouse astrocytes generates glutamatergic or GABAergic neurons.

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

19 in corticostriatal glutamatergic or striatal GABAergic neurons.

20 rgic neurons and inhibitory innervation from GABAergic neurons.

21 x5/6 enhancer, which restricts expression to GABAergic neurons.

22 lls were reprogrammed into glutamatergic and GABAergic neurons.

23 g a differential effect on glutamatergic and GABAergic neurons.

24 hanced yellow fluorescent protein to GAD1(+) GABAergic neurons.

25 tropine-sensitive inward current in putative GABAergic neurons.

26 ictal increase in firing of substantia nigra GABAergic neurons.

27 nists such as ketamine act preferentially on GABAergic neurons.

28 s in the MeA are specifically represented in GABAergic neurons.

29 n of the hippocampus, and midbrain embryonic GABAergic neurons.

30 m sensor GCaMP6 into genetically defined CeA GABAergic neurons.

31 udal ventromedial medulla, where they excite GABAergic neurons.

32 t also in the presynaptic nerve terminals of GABAergic neurons.

33 th the upstream glutamatergic and downstream GABAergic neurons.

34 anges in GABA release, suggesting effects on GABAergic neurons.

35 eneration occurred in both glutamatergic and GABAergic neurons.

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

37 ion of beta-klotho in glutamatergic, but not GABAergic, neurons abrogated the effects of dietary prot

38 Likewise, deletion of Orai1 in GABAergic neurons abrogates the chemoconvulsant-induced

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

40 We discovered a distinct population of GABAergic neurons activated by GA in the mouse central a

41 Mice with selective deletion of Orai1 in GABAergic neurons alone also showed stronger seizures to

42 etic manipulations showed that the medullary GABAergic neurons also promote NREM sleep, and they inne

43 tinct class of long-range dendrite-targeting GABAergic neuron and delineate an unusual cortical circu

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

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

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

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

48 e mutation resulting in the loss of striatal GABAergic neurons and motor functional deficits.

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

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

51 gulate chemoconvulsant-induced excitation in GABAergic neurons and that destabilization of the excita

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

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

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

55 K signaling in gamma-aminobutyric acidergic (GABAergic) neurons and decreased Ras/MAPK signaling in c

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

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

58 hat, in both rats and mice, LPB contains few GABAergic neurons, and that most of its GABAergic inputs

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

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

61 lateral clusters of serotonergic cells while GABAergic neurons are localized under the adhesive pit.

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

63 ion cells at their firing frequency, whereas GABAergic neurons are only inhibited.

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

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

66 e early postnatal period in developing mice, GABAergic neurons are transient preferential recipients

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

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

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

70 itself is only very sparsely populated with GABAergic neurons at postnatal day (P)8.

71 Furthermore, we found that CeA GABAergic neurons became highly synchronized during pred

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

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

74 sses the inhibitory drive on the "rewarding" GABAergic neurons but ceases to modulate the inhibitory

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

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

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

78 Surprisingly, PAG GABAergic neurons, but not glutamatergic neurons, may en

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

80 hAT is transcribed in many glutamatergic and GABAergic neurons, but these transcripts typically do no

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

82 y enhancing endogenous NMDAR activity on the GABAergic neurons can effectively enhance inhibitory act

83 Optogenetic manipulations of NI GABAergic neurons can shift hippocampal network state an

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

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

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

87 In contrast, Ndufs4 deletion in GABAergic neurons causes basal ganglia inflammation with

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

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

90 er of reports provide evidence that cortical GABAergic neurons comprise a smaller population of 'proj

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

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

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

94 t its localization in both glutamatergic and GABAergic neurons could be compatible with a role in inf

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

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

97 tions emanating from diverse basal forebrain GABAergic neurons densely project in all layers of the o

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

99 pendent regulation of both glutamatergic and GABAergic neuron development.

100 ockout mice with DORs deleted from forebrain GABAergic neurons (Dlx-DOR), and investigated the outcom

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

102 ortical networks, the collective dynamics of GABAergic neurons during that neonatal period remain unk

103 arvalbumin interneurons are a major class of GABAergic neurons, essential for DG function, and are in

104 t regions, GLP-1R primarily colocalized with GABAergic neurons, except within some regions such as th

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

106 lipopolysaccharides, glutamatergic, but not GABAergic, neurons exhibit an enhanced synaptic strength

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

108 GABAergic neurons expressing different isoforms of gluta

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

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

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

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

113 2 (AD) induces the generation of exclusively GABAergic neurons from human PSCs with a high degree of

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

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

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

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

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

119 PD, we find associations between SN DaNs and GABAergic neuron gene expression and multiple neuropsych

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

121 1-KO) or in both glutamatergic and forebrain GABAergic neurons (Glu/GABA-CB1-KO) resulted in an incre

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

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

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

125 s of neurons coincide with glutamatergic and GABAergic neurons identified by optotagging after Chrims

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

127 ults indicate a possible pathogenic role for GABAergic neuron in the cerebral cortex of patients with

128 t was never found to colocalize with labeled GABAergic neurons in any of the three transgenic strains

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

130 nology to reprogram striatal astrocytes into GABAergic neurons in both R6/2 and YAC128 HD mouse model

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

132 etically defined type of cortical long-range GABAergic neurons in CLA communication.SIGNIFICANCE STAT

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

134 amma-Protocadherins (Pcdhgs) from developing GABAergic neurons in mice of either sex causes a severe

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

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

137 sables chemoconvulsant-induced excitation of GABAergic neurons in the CA1 hippocampus.

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

139 Recent studies showed activation of the GABAergic neurons in the central nucleus of the amygdala

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

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

142 nic eminence represent the largest cohort of GABAergic neurons in the hippocampus.

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

144 mice expressing GCaMP6s in GABAergic or non-GABAergic neurons in the IC to investigate their spatial

145 s, accounting for approximately one-third of GABAergic neurons in the IC.

146 ime, that GLP-1Rs are expressed primarily on GABAergic neurons in the LDTg and that the efficacy of E

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

148 Contrary to traditional views, activation of GABAergic neurons in the MeA promotes parental behavior

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

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

151 mouse hippocampus, and functional imaging of GABAergic neurons in the mouse lateral hypothalamus in v

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

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

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

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

156 wever, we report here on GFP labeling of non-GABAergic neurons in the nucleus endopiriformis of this

157 We tested the hypothesis that premotor, GABAergic neurons in the nucleus tractus solitarius (NTS

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

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

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

161 Activation of GABAergic neurons in the rostromedial tegmental nucleus

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

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

164 atal asphyxia on different subpopulations of GABAergic neurons in the striatum and to assess the outc

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

166 GABAergic neurons in the tail of the ventral tegmental a

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

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

169 We found that circuits formed by GABAergic neurons in the thalamic reticular nucleus and

170 Here, we identify a novel population of GABAergic neurons in the ventral brainstem, distinguishe

171 ointed to glutamatergic/nitrergic (NOS1) and GABAergic neurons in the ventral tegmental area (VTA).

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

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

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

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

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

177 pulations of glutamatergic neurons and 15 of GABAergic neurons, including known and novel cell types.

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

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

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

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

182 These GABAergic neurons integrate wide-ranging inputs and inne

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

184 The phenotypic diversity of cortical GABAergic neurons is probably necessary for their functi

185 leus reticularis of the thalamus composed of GABAergic neurons is termed as guardian of the gateway a

186 The first type is an inhibitory GABAergic neuron: its activation leads to a decrease in

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

188 Here, we reveal a local population of GABAergic neurons (LC-GABA) capable of modulating LC-NA

189 ere, we find that selective loss of CDKL5 in GABAergic neurons leads to autistic-like phenotypes in m

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

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

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

193 normal activation and synchronization of CeA GABAergic neurons may trigger emotion-induced cataplexy.

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

195 th NCOR1 and NORC2 depletion specifically in GABAergic neurons (NS-V mice) recapitulated the memory d

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

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

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

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

200 3 receptor or the inhibitory hM4 receptor in GABAergic neurons of the CeA.

201 expressed in somatostatin-positive (SOM(+)) GABAergic neurons of the central lateral amygdala (CeL),

202 Because GABAergic neurons of the central nucleus of the amygdala

203 thway operates in both endothelial cells and GABAergic neurons of the embryonic telencephalon; howeve

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

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

206 Mice lacking ALK4 in GABAergic neurons of the medial ganglionic eminence (MGE

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

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

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

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

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

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

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

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

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

216 populations of cells (glutamatergic neurons, GABAergic neurons, oligodendrocytes, and microglia/astro

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

218 Furthermore, activation of PAG GABAergic neurons or inhibition of glutamatergic neurons

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

220 tical and thalamic innervation onto striatal GABAergic neurons output was revealed.

221 d the synaptic output of individual striatal GABAergic neurons paired with a glutamatergic partner an

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

223 ic and glutamatergic neurons, suggesting the GABAergic neuron-preferential activity of the minimal e1

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

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

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

227 LH GABAergic neurons project extensively to the paraventric

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

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

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

231 er, there is still no direct evidence on CeA GABAergic neurons' real-time dynamic during cataplexy.

232 We demonstrated that NI GABAergic neurons receive monosynaptic inputs from brain

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

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

235 t glutamatergic or parvalbumin (PV)-positive GABAergic, neurons reduced prepulse inhibition of the st

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

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

242 DD GABAergic neurons reverse polarity during larval develop

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

244 Both GABAergic and non-GABAergic neurons showed spatial microheterogeneity in t

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

246 lretinin+ cells, a specific subpopulation of GABAergic neurons, showed an increase caused by PA.

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

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

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

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

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

252 perties and functions of GGN, a unique giant GABAergic neuron that plays a central role in structurin

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

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

255 second largest subpopulation of neocortical GABAergic neurons that contain diverse subtypes, which p

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

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

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

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

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

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

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

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

264 We found that GABAergic neurons that project to the PBG are primarily

265 and horizontal dendritic morphologies, while GABAergic neurons that project to the PT and vLGN are pr

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

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

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

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

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

271 f forebrain interneurons and globus pallidus GABAergic neurons, thereby leading to the development of

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

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

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

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

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

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

278 Various GABAergic neuron types of the amygdala cooperate to cont

279 An enrichment of neuroligin-1 A1 in GABAergic neuron types suggests a role in synchrony of c

280 urochemical and anatomical classification of GABAergic neuron types.

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

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

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

284 Nr gamma-aminobutyric acid (GABA)-releasing (GABAergic) neurons was preferentially active in states o

285 Of these GABAergic neurons, we identified three categories of pot

286 dely-labeled, glutamatergic, glycinergic and GABAergic neurons were found in the ventral respiratory

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

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

289 Surprisingly, these VTA GABAergic neurons were wake- and REM sleep-active.

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

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

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

293 thermore, EGFP is predominantly expressed in GABAergic neurons, whereas the total GPR56 protein is ev

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

295 e activity of the major subpopulation of TRN GABAergic neurons, which express the calcium-binding pro

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

297 We find that CA1->RSCg projections stem from GABAergic neurons with a distinct morphology, electrophy

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

299 c A- versus C-fiber-mediated input to mature GABAergic neurons, with an increased prevalence of Abeta

300 ns, such as lateral habenula neurons and VTA GABAergic neurons, with minor input to reward-related ne