ライフサイエンスコーパス: GABAergic

1 ns between IP and MnR proved to be primarily GABAergic.

2 xcept for nNOS neurons of the ARH, which are GABAergic.

3 contralaterally projecting axons are largely GABAergic.

4 The largest terminals in the claustrum were GABAergic (0.51 +/- 0.02 mum(2) ), and these terminals c

5 unt for distinct effects and side-effects of GABAergic agents.

6 We find that inhibition of the LHb with GABAergic agonists did not alter cocaine SA under progre

7 nd inhibition mediated by wide-field spiking GABAergic amacrine cells.

8 During development, the relative amounts of GABAergic and cholinergic synaptic drive shift dendrites

9 for antipsychotic medication), and receives GABAergic and glutamatergic inputs.

10 ts in cerebellar hypoplasia and depletion of GABAergic and glutamatergic neurons.

11 th altered expression of proteins regulating GABAergic and glutamatergic signaling in the prefrontal

12 ferences in spontaneous neurotransmission at GABAergic and glutamatergic synapses.

13 findings are consistent with alterations in GABAergic and glutamatergic systems in patients with sch

14 ntrast to the auditory brainstem, coreleased GABAergic and glycinergic currents in the midbrain are s

15 ring excitatory lamina II interneurons while GABAergic and glycinergic inhibition were reduced.

16 presynaptic nicotinic receptors or biphasic GABAergic and nicotinic neurotransmission conveyed by GA

17 ecific layers and elicit robust monosynaptic GABAergic and nicotinic postsynaptic currents.

18 A confirmed that the transplanted cells were GABAergic and that some transplanted cells received an i

19 We mapped the distribution of glutamatergic, GABAergic, and cholinergic neurons in the brain of the A

20 in serotonergic, cholinergic, dopaminergic, GABAergic, and glutamergic synapse responses, as well as

21 The GABAergic anesthetics pentobarbital and propofol were al

22 ging the relative number of dopaminergic and GABAergic AOB interneurons or locally introducing DA or

23 c ARC projections synaptically converge with GABAergic ARC(AgRP) projections on melanocortin-4 recept

24 Teevra cells synaptically target GABAergic axo-axonic and some CCK interneurons in restri

25 owing increased expression of 5-HT2CR in non-GABAergic BLA cells in SNL rats.

26 as also dramatic loss of markers of afferent GABAergic cartridge synapses, resembling the cortical mi

27 also includes intermingled glutamatergic and GABAergic cell populations, and the precise roles of cho

28 (HILs), provide perisomatic inhibition onto GABAergic cells in the DG and project to the medial sept

29 er numbers of unidentified glutamatergic and GABAergic cells.

30 d and immature neurons were characterized as GABAergic, cells that might correspond to precursors of

31 Here we demonstrate that a subset of GABAergic chandelier cells (ChCs) in the prelimbic corte

32 y, as well as indirectly through feedforward GABAergic/cholinergic signals mediated by starburst amac

33 sults demonstrate that the maturation of the GABAergic circuit in the sensory cortex is altered durin

34 ain neurons that control reproduction, using GABAergic circuitry.

35 tion of convergent cortical inputs, gated by GABAergic circuits.

36 LTP) of synaptic strength selectively at the GABAergic component of dendrodendritic synapses of granu

37 vestigated aspects of the glycinergic versus GABAergic current components to probe functional consequ

38 rojection elicits monosynaptic nicotinic and GABAergic currents in glomerular layer-projecting intern

39 Medial DA neurons received predominantly GABAergic currents mediated by presynaptic nicotinic rec

40 nts; however, we found no evidence for tonic GABAergic currents.

41 for altered inhibitory function arising from GABAergic deficits across disorders and specifically in

42 Thus GABAergic deficits may causally contribute to depressive

43 interneurons may be the cause of supraspinal GABAergic disinhibition.

44 hemogenetic or optogenetic depolarization of GABAergic dorsal root ganglion neurons in vivo reduced a

45 l depolarizing gamma-aminobutyric acidergic (GABAergic) drive has been hypothesized to participate in

46 d transition model where the binding of each GABAergic drug additively and independently reduces the

47 ing independent energetic contributions from GABAergic drugs enables, at least for the drug combinati

48 gamma-Aminobutyric acidergic (GABAergic) drugs, the standard treatment for neonatal se

49 GABAergic dysfunction in the basal ganglia could disrupt

50 Therefore, the degree of GABAergic dysregulation in the PFC could be a clinically

51 de (AgRP) neurons in the arcuate nucleus are GABAergic, express leptin receptors (LepR), and are know

52 GABAergic expression dominates nuclei of the subpallial

53 es for glutamatergic AMPA, NMDA and kainate, GABAergic GABAA , muscarinic M1 , M2 and nicotinic acety

54 Cs) appears to result from interactions with GABAergic granule cells (GCs), yet the incidence of MC-G

55 s not known, but previous work suggests that GABAergic granule cells plays an important role, especia

56 sal that limbic seizures can be supported by GABAergic hyperactivity.

57 ion data showed nAChR subunit transcripts in GABAergic inferior colliculus neurons and glutamatergic

58 the visual cortex and that this decrease in GABAergic inhibition accompanies neuronal function degra

59 pends on opposing effects of glycinergic and GABAergic inhibition and can be explained by a circuit o

60 A dopamine neurons but caused an increase in GABAergic inhibition because of an increase in VTA GABAe

61 vivo prevented cocaine-induced reductions in GABAergic inhibition but did not further increase cocain

62 ancing activity by focally blocking cortical GABAergic inhibition had a similar relieving effect on t

63 functional decline is linked to compromised GABAergic inhibition has not been fully confirmed.

64 w of spiking can be delicately controlled by GABAergic inhibition in a cell-type-specific manner.

65 neuronal response properties and markers of GABAergic inhibition in the primary visual cortex (V1) o

66 onstrate that ageing may result in decreased GABAergic inhibition in the visual cortex and that this

67 and blocked the cocaine-induced reduction of GABAergic inhibition in VTA dopamine neurons.

68 Here we show that GABAergic inhibition of hippocampal retrieval activity f

69 icance, the contribution that alterations in GABAergic inhibition play in the pathophysiology of FXS

70 Deficits in GABAergic inhibition result in the abnormal neuronal act

71 We found decreases in either glycinergic or GABAergic inhibition to the medial nucleus of the trapez

72 es, leading to reductions in the efficacy of GABAergic inhibition via a postsynaptic mechanism.

73 C through NRG3/ErbB4-dependent regulation of GABAergic inhibition.

74 sium channels in prolonging pauses evoked by GABAergic inhibition.

75 hesised to be mediated, at least in part, by GABAergic inhibition: spatial suppression of motion and

76 strongly suppressed odor-evoked activity in GABAergic inhibitory interneuron populations in the OB.

77 propriate growth and synaptic integration of GABAergic inhibitory interneurons are essential for func

78 t, including loss of tangential migration of GABAergic inhibitory interneurons to the neocortex.

79 ition to the loss of tangential migration of GABAergic inhibitory interneurons to the neocortex.

80 Deficits in GABAergic inhibitory neurotransmission are a reliable fi

81 2 and c-Src in the inhibition by morphine of GABAergic inhibitory postsynaptic currents (IPSCs) recor

82 Thus enhancing GABAergic inhibitory synaptic inputs from SST(+) interne

83 Overall, glutamatergic and GABAergic innervation of newly born neurons in the adult

84 electron microscopic methods to examine the GABAergic innervation of the CG in Macaca fascicularis m

85 The source of this GABAergic input and whether GABA contributes to a specif

86 Rhythmic medial septal (MS) GABAergic input coordinates cortical theta oscillations.

87 ing actions, at least in part, by inhibiting GABAergic input onto substance P (SP) neurons in the ven

88 sensitizing rod bipolar cells by a sustained GABAergic input originating from a population of wide-fi

89 ice were more hyperpolarized, receiving more GABAergic input than their Fbxl3(+/+) counterparts.

90 me transplanted cells received an inhibitory GABAergic input.

91 depends on the location and kinetics of the GABAergic inputs and is achieved by the balance between

92 Functionally, these long-range GABAergic inputs are necessary and sufficient to maintai

93 these results indicate that the relevance of GABAergic inputs from AgRP to POMC neurons is state depe

94 GABAergic inputs from the NAc and local VTA GABA neurons

95 undescribed sites at which glutamatergic and GABAergic inputs may stimulate and inhibit dopamine rele

96 uron firing, evoked by either stimulation of GABAergic inputs or hyperpolarizing current injections,

97 ferentially modulating striatal and pallidal GABAergic inputs.

98 he cortical microcircuit, where SST-positive GABAergic interneuron deficits may disrupt functioning i

99 ngs provide a new perspective on the role of GABAergic interneuron diversity in cortical development.

100 sensory processing in the olfactory system, GABAergic interneuron signaling shapes principal neuron

101 contains a single type of horizontal cell, a GABAergic interneuron that samples from all cone photore

102 Cortical circuits include diverse types of GABAergic interneurons (INs) that shape activity of exci

103 tion mediated through the 5-HT2 receptors on GABAergic interneurons and direct inhibition via the 5-H

104 t gamma-aminobutyric acid (GABA) to identify GABAergic interneurons and non-GABAergic projection cell

105 s mice showed a decreased number of cortical GABAergic interneurons and reduced proliferation of inte

106 ated neurotransmission and fast-spiking (FS) GABAergic interneurons are central to cortical circuit d

107 GABAergic interneurons are central to the correct format

108 GABAergic interneurons are essential for neural circuit

109 erneuron migration to the differentiation of GABAergic interneurons arising from the basal telencepha

110 We focused on somatostatin-positive (SST(+)) GABAergic interneurons because of evidence that their fu

111 annels are expressed on parvalbumin-positive GABAergic interneurons in corticolimbic brain regions an

112 cy significantly correlated with the loss of GABAergic interneurons in or adjacent to the granule cel

113 To date, most ErbB4 studies have focused on GABAergic interneurons in the hippocampus and neocortex,

114 intraspinal transplantation of precursors of GABAergic interneurons in the IL-31Tg mice.

115 the extent of astrogliosis, or the number of GABAergic interneurons in the molecular layer or hilus.

116 Appropriate integration of GABAergic interneurons into nascent cortical circuits is

117 Here, we show tangential migration of young GABAergic interneurons into the developing hippocampus i

118 vulnerability and plasticity of hippocampal GABAergic interneurons is a topic of broad interest and

119 The function of cortical GABAergic interneurons is largely determined by their in

120 support the hypothesis that degeneration of GABAergic interneurons may be the cause of supraspinal G

121 requirement for parvalbumin (PV) expressing GABAergic interneurons of the nucleus accumbens (NAc) in

122 GABAergic interneurons play critical roles in seizures,

123 GABAergic interneurons play important roles in cortical

124 These results indicate that GABAergic interneurons regulate cortical activity indire

125 How GABAergic interneurons regulate the segregation and comm

126 tudies suggests a selective vulnerability of GABAergic interneurons that coexpress the neuropeptide s

127 MCs also synapse with GABAergic interneurons that mediate feed-forward inhibit

128 ly, we address functional differences within GABAergic interneurons to highlight the importance of di

129 nstead proliferating neuronal precursors and GABAergic interneurons were present.

130 lx function disrupted the differentiation of GABAergic interneurons with global reduction in GABA lev

131 ale C57Bl/6 mice receive input not only from GABAergic interneurons, but also from multiple glutamate

132 ylase-positive (TH+) neurons, but not in PV+ GABAergic interneurons, exhibit different regional imbal

133 We show here that many GABAergic interneurons, from their generation in the med

134 ibuted to 5-HT2 receptor activation exciting GABAergic interneurons.

135 t coexpress PAX2, a transcription factor for GABAergic interneurons.

136 ls, mossy fiber sprouting, astrogliosis, and GABAergic interneurons.

137 different functional classes of hippocampal GABAergic interneurons.

138 uxtacrine interactions with ErbB4 present on GABAergic interneurons.

139 orphology of different functional classes of GABAergic interneurons.

140 essant-like behavior, using disinhibition of GABAergic interneurons.

141 in by inhibiting dorsal horn enkephalinergic/GABAergic interneurons.

142 al hyperactivity, arising from dysfunctional GABAergic interneurons.

143 nAChRs are highly expressed, particularly in GABAergic interneurons.

144 and inhibitory gamma-aminobutyric acidergic (GABAergic) interneurons.

145 Moreover, they support a cardinal role of GABAergic IP/MnR interconnections in the behavioral resp

146 HA) regulates motivated feeding behavior via GABAergic LHA neurons.

147 In mice trained to self-administer cocaine, GABAergic LTD was abolished in D2-, but not in D1-MSN sy

148 to acute olfactory bulb slices elicited the GABAergic LTP in mitral cells by enhancing postsynaptic

149 The GABAergic LTP is mimicked with PKA or PKC activation.

150 the same pathway with a presynaptic form of GABAergic LTP, while interneurons of stratum radiatum, d

151 pes producing glutamatergic, dopaminergic or GABAergic markers for synaptic neurotransmission and har

152 ronounced day/night variation and involves a GABAergic mechanism.

153 y complete Freund's adjuvant (CFA) increased GABAergic miniature IPSCs (mIPSCs).

154 CB1/CB2 receptor agonist WIN55212 inhibited GABAergic mIPSCs in both naive and CFA-treated rats.

155 of NAc shell (NAcSh) MSNs was fine-tuned by GABAergic monosynaptic innervation from adjacent fast-sp

156 left/right axon guidance choices within the GABAergic motor neuron circuit.

157 Caenorhabditis elegans possesses 19 GABAergic motor neurons (MNs) called D MNs, which are di

158 ltogether, the present results show that the GABAergic nature of POMC neurons can be dynamically regu

159 aluate the correlation between interneuronal GABAergic network activity and seizure-like events.

160 pharmacological manipulations targeting the GABAergic network restored gathering behaviour.

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

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

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

164 nergic neuronal loss in the basal forebrain, GABAergic neuronal loss in the cortex, hippocampus and b

165 ominant-negative form of Trp53 revealed that GABAergic neuronal progenitors as well as cerebellar gra

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

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

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

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

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

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

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

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

174 2 (AD) induces the generation of exclusively GABAergic neurons from human PSCs with a high degree of

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

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

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

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

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

180 Activation of GABAergic neurons in the rostromedial tegmental nucleus

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

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

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

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

185 3 receptor or the inhibitory hM4 receptor in GABAergic neurons of the CeA.

186 Because GABAergic neurons of the central nucleus of the amygdala

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

203 ebrain and contain cortical glutamatergic or GABAergic neurons.

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

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

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

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

208 er several emerging mechanisms that modulate GABAergic neurotransmission dynamically from either the

209 GABAergic neurotransmission in the amygdala contributes

210 nd supports growing evidence that defects in GABAergic neurotransmission participate in the pathogene

211 types has not been sufficient to explain how GABAergic neurotransmission sculpts principal cell activ

212 electrophysiological data indicated enhanced GABAergic neurotransmission within the medial CeA in LgA

213 that the projection co-expresses markers for GABAergic neurotransmission.

214 e investigated gamma-aminobutyric acidergic (GABAergic) neurotransmission in the medial CeA and the s

215 ing network reveals a predominance of either GABAergic or glutamatergic cells within individual nucle

216 equires CB1R in astroglial cells (but not in GABAergic or glutamatergic neurons) and postsynaptic glu

217 pathway important for licking behavior, the GABAergic output projections from the substantia nigra p

218 While many studies examined the GABAergic output side of these reciprocal connections, l

219 tors, which also suppresses proliferation of GABAergic pallido-STN inputs in PD mice, reduced loss of

220 rons, glutamatergic parvalbumin neurons, and GABAergic parvalbumin neurons.

221 The numbers and distribution of GABAergic parvalbumin or nitric oxide-expressing and cho

222 double transgenics expressing hVOS probe in GABAergic, parvalbumin, and calretinin interneurons, as

223 antiviral innate immunity by activating the GABAergic pathway.

224 antimalarial drug artemether, which acts on GABAergic pathways, can drive pancreatic cells with an a

225 e that transplanted MGE neurons retain their GABAergic phenotype and integrate dynamically into host-

226 The present results show that the GABAergic phenotype of POMC neurons is decreased selecti

227 The fact the GABAergic phenotype of POMC neurons is sensitive to ener

228 and Bcl11b to regulate the dopaminergic and GABAergic phenotypes.

229 tamatergic and gamma-aminobutyric acidergic (GABAergic) plasticity in many neuronal populations.

230 investigated the role of PI3P at developing GABAergic postsynapses by using a membrane-permeant PI3P

231 Receptor recruitment to inhibitory GABAergic postsynapses requires the scaffold protein gep

232 ise roles of cholinergic, glutamatergic, and GABAergic PPT cell groups in regulating cortical activit

233 reveal that glutamatergic, cholinergic, and GABAergic PPT neurons differentially influence cortical

234 reveal that cholinergic, glutamatergic, and GABAergic PPT neurons each have distinct effects on slee

235 Last, activation of GABAergic PPT neurons slightly reduced REM sleep.

236 PL) and from dopaminergic amacrine cells and GABAergic processes in the outermost OFF layer of the IP

237 ) to identify GABAergic interneurons and non-GABAergic projection cells.

238 Here, we identify GABAergic projection neurons from the medial septum (MS)

239 usly, we found prolonged development of some GABAergic proteins in human V1.

240 ., GluA1, PRRT2) with no changes in synaptic GABAergic proteins.

241 We found that the asynchronous GABAergic release component is diminished in SynII-delet

242 rate that SynII regulates the time course of GABAergic release, and that this SynII function is depen

243 responses underwent LTD, the simultaneous MF GABAergic responses of stratum lucidum interneurons, but

244 whereas in stratum lucidum interneurons only GABAergic responses were potentiated.

245 This is accompanied by increased GABAergic signaling and by enhanced responsiveness to a

246 GABAergic signaling is involved in modulating the reinfo

247 GABAergic signaling is vital to the maintenance of corti

248 ress reduced levels of KCC2, indicating that GABAergic signaling may produce excitation in RT neurons

249 transplant-mediated long-term enhancement of GABAergic signaling not only reduced spontaneous scratch

250 plasticity of MF simultaneous glutamatergic-GABAergic signaling onto interneurons of the different s

251 ]i) preserves appropriate, often inhibitory, GABAergic signaling within the brain.

252 ity threshold required to produce excitatory GABAergic signaling, weaker stimuli are able to propagat

253 m, that this SCN reorganization depends upon GABAergic signaling.

254 extrude Cl(-) following periods of elevated GABAergic signaling.

255 Here we use virally mediated GABAergic-specific GCaMP6f expression to demonstrate tha

256 iology was used to measure glutamatergic and GABAergic strength in DMS D1- and D2-MSNs of alcohol-dri

257 matergic strength exclusively in D1-MSNs and GABAergic strength specifically in D2-MSNs of the DMS, w

258 These studies identify a GABAergic subpopulation of neurons in the ventral zona i

259 bset of neurons in the brachium of the IC is GABAergic, suggesting that part of this descending pathw

260 ner that correlates highly with the level of GABAergic suppression by KYNA.

261 enesis and establish a general framework for GABAergic synapse development.

262 napse, and the basket/stellate cell-Purkinje GABAergic synapse in the cerebellum.

263 ommunication, we are studying the effects on GABAergic synapses after chronic in vivo transgenic expr

264 r (CB1R)-dependent suppression of inhibitory GABAergic synapses and an in vivo LTD of excitatory glut

265 in synaptic plasticity in D1- versus D2-MSN GABAergic synapses in the ventral pallidum could explain

266 We have previously reported the effects on GABAergic synapses of the acute overexpression of CBSH3-

267 Here we show that at GABAergic synapses on rat VTA dopamine neurons, a single

268 KYNA in the PFC occurred primarily at local GABAergic synapses through an alpha7nAChR-dependent pres

269 ion in the medial CeA and the sensitivity of GABAergic synapses to modulation of the HCRT system in S

270 control the strength of glycinergic but not GABAergic synapses via modulation of the diffusion dynam

271 unctions and possibly via chemical dendritic GABAergic synapses, as well as classical axonal GABA rel

272 mediated excitotoxicity and promoted loss of GABAergic synapses.

273 he circuit, produces irreversible effects on GABAergic synaptic connectivity that mimic those produce

274 ronic corticosterone-exposed animals through GABAergic synaptic disinhibition, represent a new class

275 reduced frequency and increased amplitude of GABAergic synaptic events.

276 is classically attributed to an increase in GABAergic synaptic input triggered by non-preferred stim

277 Previously, we showed that some GABAergic synaptic proteins change across the lifespan,

278 , while antidepressant therapies may enhance GABAergic synaptic transmission.

279 rized states of vSCN cells through increased GABAergic synaptic transmission.SIGNIFICANCE STATEMENT T

280 eptual changes following perturbation of the GABAergic system, it is conceivable that the resting lev

281 tion in mosquitoes through activation of the GABAergic system.

282 uisition by mosquitoes via activation of the GABAergic system.

283 ealthy nonrelatives, suggesting that altered GABAergic systems in schizophrenia are associated with e

284 m(2) ) than those contacted by cortex or non-GABAergic terminals (0.28 +/- 0.02 mum(2) and 0.25 +/- 0

285 In the claustrum, non-GABAergic terminals (0.34 +/- 0.01 mum(2) ) and striate

286 RS, 3.19% (glutamatergic terminals); 85.07% (GABAergic terminals).

287 RS, 1.92% (glutamatergic terminals); 77.92% (GABAergic terminals).

288 RS, 21.89% (glutamatergic terminals); 2.38% (GABAergic terminals); GABA-CB1 -RS, 1.92% (glutamatergic

289 RS, 53.19% (glutamatergic terminals); 2.30% (GABAergic terminals); GABA-CB1 -RS, 3.19% (glutamatergic

290 , TRPV1 recruits more glutamatergic, but not GABAergic, terminals to OLM neurons in vitro.

291 nceivable that the resting level of cortical GABAergic tone directly relates to the spatial specifici

292 the hypothesis that sustained enhancement of GABAergic transmission alone is sufficient to elicit ant

293 In developing neurons, the establishment of GABAergic transmission depends on Neuroligin 2 (NL2), a

294 ed glutamatergic transmission in D1-MSNs and GABAergic transmission in D2-MSNs.

295 emonstrate that AIE exposure disrupts DA and GABAergic transmission in the adult medial prefrontal co

296 he parvalbumin interneurons, and facilitated GABAergic transmission in wild type mice but not in tran

297 Importantly, suppression of GABAergic transmission via D2 receptor-glycogen synthase

298 e results provide the morphological basis of GABAergic transmission within the normal human subthalam

299 turation culminates in a period of exuberant GABAergic transmission.

300 tamatergic and gamma-aminobutyric acidergic (GABAergic) transmission.