ライフサイエンスコーパス: inhibitory

1 neural activity, and alpha oscillations are inhibitory.

2 y state, we found that dopamine is primarily inhibitory.

3 report that papaverine, a vasodilator, shows inhibitory action against various strains of influenza v

4 as the most promising candidate with potent inhibitory activities against both PARP-1/2 and PI3Kalph

5 The inhibitory activities of the LEKTI domain 4 (D4) and D6

6 in olfactory processing by orchestrating OB inhibitory activities.SIGNIFICANCE STATEMENT Neuronal mo

7 unds that we previously showed to have broad inhibitory activity across multiple Clostridioides diffi

8 owed to be endowed with potent and selective inhibitory activity against the cancer-related human car

9 Virulence inhibitory activity in the RND-negative background resul

10 Transient imbalances in excitatory and inhibitory activity may provide a general mechanism for

11 natural EEEV infection with potent (<20 pM) inhibitory activity of EEEV.

12 h atopic dermatitis (AD) affect the protease inhibitory activity of LEKTI or its susceptibility to me

13 cells with NAC completely abrogated the NKA inhibitory activity of plumbagin and atovaquone.

14 emicarbazones (1-5): one of them revealed an inhibitory activity stronger than kojic acid, used as re

15 The EtOAc and MeOH extracts presented higher inhibitory activity with respect to alpha-amylase and ty

16 Starting from quinoline 2 with weak ATR inhibitory activity, lead optimization efforts focusing

17 olerated substitutions without loss of RD3's inhibitory activity, substitutions in two distinct narro

18 alf of TIMP-1 is sufficient for TIMP-1's MMP-inhibitory activity, we propose that those C-terminal am

19 E (0.50-0.44mg/mL) and AChE (7.93-5.83mg/mL) inhibitory activity.

20 Furthermore, the beverages showed a good ACE inhibitory activity.

21 rest in developing complement regulatory and inhibitory agents to treat complement dysfunction.

22 e migration and adhesion of Schwann cells on inhibitory aggrecan and astrocytic substrates.

23 ed clustering phenotype when exposed to near-inhibitory amounts of cefotaxime.

24 IGLEC gene number rather than those encoding inhibitory and activating subsets, suggesting that lifet

25 In mice, the combination of anti-PD-1 inhibitory and anti-OX40 agonist antibodies reduces the

26 the presence of intestinal alpha-glucosidase inhibitory and augmenting cellular glucose uptake activi

27 transcriptional dynamics and disentangle its inhibitory and enhancing activities in transcription.

28 This circuit exhibits a balance of inhibitory and excitatory currents that persists on stim

29 ons between neurons, as well as map putative inhibitory and excitatory inputs.

30 , a biomarker reflecting the contribution of inhibitory and facilitatory circuits in M1.

31 ng surprise signalling as a shared driver of inhibitory and motivated control.

32 te, in which they are bound by proteins with inhibitory and protective functions.

33 as well as insights into evolution under sub-inhibitory antibiotic levels.

34 Injection of inhibitory antibodies to the alpha subunit of the Gs het

35 ion of T-cell polarizing cytokines or induce inhibitory antigen-presenting cells that suppress T-cell

36 An inhibitory aptamer against TAR RNA reduces KSHV infectio

37 tent analog was selected through an in vitro inhibitory assay to evaluate its pharmacokinetic paramet

38 ABAergic responses switch from excitatory to inhibitory at an early postnatal period in rodents.

39 Inhibitory autapses are self-innervating synaptic connec

40 ith a ~200 residue linker, is biased towards inhibitory autophosphorylation.

41 Inhibitory axons preferentially innervated either L2 or

42 s required for maintaining proper excitatory-inhibitory balance in the PFC and its control of behavio

43 owever, little is known about how excitatory-inhibitory balance is defined at most synapses or about

44 midal neurons, disrupt prefrontal excitatory-inhibitory balance, and alter processing of afferent inf

45 des three net negative charges appeared self-inhibitory because of ClC-5's voltage-gated properties,

46 entify side chains that are critical for the inhibitory binding of RD3 to RetGC.

47 blished, but the molecular mechanisms of its inhibitory binding to RetGC remain unclear.

48 stabilizes the interaction between the auto-inhibitory brace helix alpha6 and the four-helix bundle

49 ive effect by interfering with the branching-inhibitory BRC1 genes.

50 o task, both IL and PL inactivation impaired inhibitory but not active reward-seeking, the latter eff

51 esponse fluctuations of local excitatory and inhibitory cell populations.

52 Here we investigated how excitatory and VIP inhibitory cells in layer 2/3 of mouse visual cortex wer

53 Therapeutics that target the T cell inhibitory checkpoint proteins CTLA-4 and PD(L)1 are eff

54 Resting and activated TILC2s express the inhibitory checkpoint receptor PD-1.

55 to characterize the role of immune cells and inhibitory checkpoints, genome-wide frequencies of copy

56 are efficacious and more potent than single inhibitory chemotypes.

57 hese findings demonstrate how excitatory and inhibitory circuits interact to mediate an ethologically

58 co-receptor, but not that of FcgammaRIIB, an inhibitory co-receptor.

59 yeast translation system to demonstrate that inhibitory codon pairs slow elongation rates which are p

60 eved by a network with reciprocal excitatory-inhibitory competitive dynamics, similar to interactions

61 t substrate of 40 kDa (PRAS40), an intrinsic inhibitory component of mTORC1, and prevented activation

62 rea under the curve over 24 hours to minimum inhibitory concentration (AUC/MIC).

63 showed a 60-fold lower shifted-half-maximal inhibitory concentration (IC(50)) for CYP4Z1 compared to

64 chmark its performance with standard minimum inhibitory concentration (MIC) assays.

65 The minimum inhibitory concentration (MIC) of the peptide ranged fro

66 rains of Plasmodium falciparum (half maximal inhibitory concentration [IC50] = 1-2 uM), suggesting th

67 Minimum inhibitory concentration distributions of the resistance

68 ing recombinantly expressed enzymes, minimum inhibitory concentration measurements, steady-state enzy

69 vitro with remarkable potency (half-maximal inhibitory concentration of <2 ng/ml).

70 IRDye 800CW binds GLP-1R with a half-maximal inhibitory concentration of 3.96 nM.

71 affinity for the GLP-1R, with a half-maximal inhibitory concentration of 6.3 nM.

72 ity against HIV-1(HXB2), with a half maximal inhibitory concentration of 89 nM.

73 ounds inhibited M(pro), showing half-maximal inhibitory concentration values that ranged from 0.67 to

74 variants of the CXCR4 receptor (half-maximal inhibitory concentration, 8 nM [human]/2 nM [murine]) an

75 of two circular micropumps, and the minimum inhibitory concentrations (MIC) were then determined via

76 iotic mechanisms of action and resistance at inhibitory concentrations in the lab and in the clinic.

77 The AtMC4 structure exhibits an inhibitory conformation in which a large linker domain b

78 olateral amygdala (BLA) and their reciprocal inhibitory connectivity.

79 ened and L-theanine had a trend of worsening inhibitory control (i.e. increased Stop-signal reaction

80 nd their combination on sustained attention, inhibitory control and overall cognition in boys with at

81 eficial effects of acute aerobic exercise on inhibitory control are sustained for 60 min in children

82 nitive functions (e.g., executive functions, inhibitory control).

83 l models of dACC function primarily focus on inhibitory control, highlighting surprise, choice diffic

84 s known about the molecular basis underlying inhibitory control.

85 CD5 is characterized as an inhibitory coreceptor with an important regulatory role

86 Combining GDNF treatment with digestion of inhibitory CSPGs did not have a significant synergistic

87 neous and sensory-evoked swimming, the total inhibitory current was more than threefold larger than t

88 ly triggers prostaglandin E(2) release as an inhibitory DAMP to counterpoise the adjuvanticity of imm

89 -phase serum, with live-virus reciprocal 50% inhibitory dilution (ID(50)) geometric mean titers of 50

90 nteraction between its N-terminal diaphanous inhibitory domain (DID) and its C-terminal diaphanous au

91 memory discrimination and receives enhanced inhibitory drive from local cholecystokinin-expressing i

92 ated, can be highly successful as targets of inhibitory drugs.

93 mprove patient stratification for checkpoint inhibitory drugs.

94 oidogenic ability of TTR and its antiamyloid inhibitory effect are associated.

95 hanistic study shows a hitherto unrecognized inhibitory effect by the carboxylate anion on the cataly

96 calmodulin, whereas higher [Ca(2+) ] exerts inhibitory effect during depolarization.

97 The inhibitory effect of 4-OI and DMF extends to the replica

98 6 and Y226 that is critical to transduce the inhibitory effect of Ca(2+) and the stimulatory effect o

99 0 mimetics significantly increase the growth inhibitory effect of chemotherapeutic agents in vitro an

100 We further show using KLF2 shRNA that the inhibitory effect of NMP on endothelial inflammation and

101 lysine residues are mutated to arginine, the inhibitory effect of RGFP966 on expansions is largely by

102 In DM and AMPK-DN mice, the inhibitory effect of SF-PreCon upon p38 activation was s

103 to the improved interfacial performance, the inhibitory effect of the antioxidants was remarkably pro

104 slc13 transport function, thus mimicking the inhibitory effect of the slc13 inhibitor, slc26a6.

105 leaves them intact and thereby eliminates an inhibitory effect of TOMM34 on HSP70-mediated refolding

106 progesterone was determined to have a direct inhibitory effect on C. burnetii replication.

107 as the ethyl acetate extract had the highest inhibitory effect on heat-induced protein denaturation.

108 le, whereas 2-ethyl hexanoate minimizes this inhibitory effect.

109 The inhibitory effects of amino acids on Pro- and Ala-stimul

110 A pilot experiment confirmed the inhibitory effects of dosing a sample of wood materials

111 The latter findings suggested inhibitory effects of even resting cytosolic [Ca(2+)] on

112 and (3) ultrasound can reversibly alter the inhibitory effects of tetrodotoxin (TTX) in pharmacologi

113 Here, we examined the HIV-inhibitory effects of the MTOR-independent inducer of au

114 optotic activities but also presented strong inhibitory effects on cell mobility (migration and invas

115 In addition to IL-10's classic inhibitory effects on myeloid cells, we also describe th

116 Last, Neurog2 does not have cross-inhibitory effects on Neurog1, Neurog3, and Ascl1 These

117 a cell lines, and eight showed potent growth inhibitory effects with IC(50) values lower than 500 nM.

118 ellar GABAergic tone and cerebellar cortical inhibitory efficacy.

119 Leukemia inhibitory factor (LIF) injections were given intraperit

120 Macrophage migration inhibitory factor (MIF) has been recognized as a major p

121 the versatile cytokine macrophage migration inhibitory factor (MIF) in regulating a metabolic rhythm

122 We also tested the ability of neonatal NET-inhibitory factor (nNIF) to block NET formation induced

123 nd spheroid growth in vitro and elevated Wnt-inhibitory factor 1 (WIF1) activity.

124 newal of mESCs in combination with leukaemia inhibitory factor and regulates the formation of the mou

125 ative endogenous ligand macrophage migration inhibitory factor behaves opposite to CXCL12 in each ass

126 e neurons of the outer retina, which provide inhibitory feedback onto photoreceptors and contribute t

127 ggest that APs may play an important role in inhibitory feedback, and may have implications for under

128 Removing Syt1 or impairing its release inhibitory function (Syt1(9Pro)) increases spontaneous r

129 The inhibitory function of sulfonamides on CA was discovered

130 omain and the SNARE motif are needed for its inhibitory function.

131 found that Tyr-251 is critical for LAIR-1's inhibitory function.

132 ovide detailed mechanistic insights into its inhibitory function.

133 The inhibitory G protein alpha-subunit (Galpha(z)) is an imp

134 dentify a novel role for NO in strengthening inhibitory GABA(A) receptor-mediated transmission in mol

135 glutamatergic synapses, MOC neurons receive inhibitory GABAergic and glycinergic synaptic inputs.

136 terplay between excitatory glutamatergic and inhibitory GABAergic receptor effects.

137 junctions between inferior olive neurons by inhibitory GABAergic synapses.

138 ns in CCI-Pain animals showed a reduction in inhibitory, GABAergic inputs.

139 is the stromal ecology, which can be either inhibitory, highly reactive (supportive) or non-reactive

140 JH was described in 1934 as a "metamorphosis inhibitory hormone" in Rhodnius prolixus by Sir Vincent

141 tter GABA, from excitatory depolarization to inhibitory hyperpolarization.

142 voked, temporally dynamic excitatory (E) and inhibitory (I) activity.

143 acid (GABA) are the major excitatory (E) and inhibitory (I) neurotransmitters in the brain, respectiv

144 eatures enabling them to impart a widespread inhibitory influence on neural activity.

145 concentration correlated negatively with the inhibitory influence on the excitatory neuronal populati

146 ter environmental enrichment, differences in inhibitory innervation and ocular dominance plasticity b

147 of PNNs enwrapping PV+ cells regulates their inhibitory input and has a potent influence on their act

148 tability of mPFC->pPVT neurons and increased inhibitory input drive from low-threshold-spiking somato

149 onse is mediated by the S-ON pathway through inhibitory input from an undiscovered S-cone amacrine ce

150 xcitable, had stronger responses and reduced inhibitory input to CC stimulation.

151 s the perineuronal net to potentially reduce inhibitory input to these neurons.

152 nectivity, we built models of excitatory and inhibitory inputs onto a single neuron, to study how rec

153 ERCA) in cardiac myocytes is modulated by an inhibitory interaction with a transmembrane peptide, pho

154 gs provide a molecular basis for controlling inhibitory interneuron population size during circuit fo

155 Inhibitory-interneuron networks, consisting of multiple

156 Spikes from inhibitory interneurons (cartwheel cell) and principal o

157 Cortical inhibitory interneurons (cINs) are born in the ventral f

158 Inhibitory interneurons are essential for proper brain d

159 rived from the dorsal telencephalon, whereas inhibitory interneurons are generated in its ventral por

160 Inhibitory interneurons comprise a fraction of the total

161 orms of circuit motifs including reciprocal (inhibitory interneurons inhibiting other interneurons) a

162 ibiting other interneurons) and feedforward (inhibitory interneurons inhibiting principal neurons) co

163 Preferential deletion of Shank3 in vS1 inhibitory interneurons led to pyramidal neuron hyperact

164 ns (mEC LVa and LVb) as well as fast-spiking inhibitory interneurons receive direct excitatory input

165 Recent studies found that two most common inhibitory interneurons, parvalbumin- (PV) and somatosta

166 neurocircuits that encompass excitatory and inhibitory interneurons, similarly to those driven by se

167 Cortical areas comprise multiple types of inhibitory interneurons, with stereotypical connectivity

168 nectivity in intrinsic connections involving inhibitory interneurons.

169 me, suggesting a pathophysiological role for inhibitory interneurons.

170 al regions, and connections between cortical inhibitory interneurons.

171 Here we show that the excitatory and inhibitory intracortical connections to a layer 2/3 neur

172 The GABA response switch from excitatory to inhibitory is a key event in neuronal maturation that de

173 PE) signals to trigger extinction, a type of inhibitory learning that is responsible for suppressing

174 require cAMP signaling in the antennal lobe inhibitory local interneurons.

175 Whereas the CSDn targets inhibitory local neurons in the antennal lobe, the CSDn

176 ith a noncompetitive, potentially allosteric inhibitory mechanism at the nAChRs.

177 Our results provide insights into the inhibitory mechanism of SOST on Wnt signaling.

178 To elucidate their catalytic cycle and inhibitory mechanism, we report 11 x-ray crystal structu

179 insights into setron-binding poses and their inhibitory mechanisms are just beginning to emerge.

180 ir cognate transcription regulators, but the inhibitory mechanisms employed have thus far remained a

181 f sustaining repetitive activity, overcoming inhibitory mechanisms that restrict excitatory bursts, a

182 surface PVR, which interacts with TIGIT, an inhibitory molecule on CD8(+) effector memory T cells.

183 T cell exhaustion is marked by inhibitory molecule upregulation and the development of

184 marizes recent data regarding the role of co-inhibitory molecules in the control of T(reg) cell funct

185 activase (Rca) regulates rubisco by removing inhibitory molecules such as ribulose-1,5-bisphosphate (

186 sought to characterize ARGX-117, a humanized inhibitory monoclonal antibody against complement C2.

187 the production by the developing cell of an inhibitory morphogen, but how this cell becomes immune t

188 Feedback inhibitory motifs are thought to be important for patter

189 ns to disentangle reciprocal and feedforward-inhibitory motifs.

190 In the neocortex, inhibitory network formation occurs concurrently with th

191 may have the potential to reestablish tonic inhibitory networks and thus suppress tinnitus.

192 of L1 interneurons participate in different inhibitory networks in superficial layers by targeting e

193 stic sensory input patterns, but that global inhibitory networks were unable to produce input-output

194 stinct sets of genes in human excitatory and inhibitory neural progenitors and neurons.

195 ies revealed diverse types of excitatory and inhibitory neuron in each circumventricular organ struct

196 e the RF selectively enhances excitatory and inhibitory neuron responses to task-irrelevant stimuli a

197 GFP-expressing inhibitory neurons (GIN), representing a fraction of mai

198 Deletion of 4E-BP2 specifically in inhibitory neurons also prevented the ketamine-induced i

199 ether and how their expression changes in PV inhibitory neurons and excitatory neurons track with sen

200 y observations in the primary visual cortex: inhibitory neurons are broadly tuned in vivo and show no

201 Whereas somatostatin-expressing inhibitory neurons are driven by these large stimuli, in

202 te subpopulations of cortical excitatory and inhibitory neurons are significantly enriched for schizo

203 ory areas have elucidated that pyramidal and inhibitory neurons belonging to distinct layers show dis

204 ine firing rates (FRs) in GC with deep-layer inhibitory neurons displaying highest FRs at baseline an

205 A1 axons preferentially innervating specific inhibitory neurons in layer 1 and superficial layers.

206 1) expression in parvalbumin-expressing (PV) inhibitory neurons in mouse visual cortex.

207 is impairment appeared to critically involve inhibitory neurons in the auditory cortex called parvalb

208 novo translation in somatostatin-expressing inhibitory neurons in the centrolateral amygdala is nece

209 nslation in protein kinase Cdelta-expressing inhibitory neurons in the centrolateral amygdala is nece

210 ar terminals innervated excitatory relay and inhibitory neurons in the MDmc that facilitate faithful

211 nitor the activity of putative pyramidal and inhibitory neurons located in deep and superficial layer

212 expressing and somatostatin (SOM)-expressing inhibitory neurons modulate responses in mouse visual co

213 reveal that Lm128C cells are CaMKIIalpha(+) inhibitory neurons of parvalbumin or somatostatin subtyp

214 tracing to identify inputs to excitatory and inhibitory neurons of the intermediate and deep SC.

215 y neurons are driven by these large stimuli, inhibitory neurons that express parvalbumin and vasoacti

216 Thus, NPY neurons are a novel class of inhibitory neurons that use GABA and NPY signaling to re

217 The selectivity of excitatory and inhibitory neurons within decision circuits and, hence,

218 cortical circuitry and alterations in these inhibitory neurons, especially in the medial prefrontal

219 controlled by somatostatin-expressing (SOM) inhibitory neurons, which are excited by head movements

220 e putative efferent filopodial contacts onto inhibitory neurons.

221 excitatory neurons, and 4E-BP1 and 4E-BP2 in inhibitory neurons.

222 s phenomenon is most prevalent in deep-layer inhibitory neurons.

223 ow O-GlcNAcylation modulates the efficacy of inhibitory neurotransmission.

224 etamine to induce a long-lasting decrease in inhibitory neurotransmission.

225 of excitatory neurotransmitter glutamate and inhibitory neurotransmitter GABA in regulating delay act

226 Efficient reuptake of the inhibitory neurotransmitter GABA is essential, and reupt

227 itive RGCs (ipRGCs) in mice that release the inhibitory neurotransmitter gamma-aminobutyric acid (GAB

228 These mediate inhibitory olivocochlear feedback through the activation

229 ine whether a neurosteroid has potentiating, inhibitory, or competitive antagonist activity on GABA(A

230 rm synaptic plasticity (STP) profiles of the inhibitory parvalbumin (PV) and somatostatin (SST) inter

231 a lesser degree layer 4 neurons, as well as inhibitory parvalbumin-expressing interneurons (INs).

232 two distinct regulatory sites: Na(+) and the inhibitory peptide.

233 aMKII inhibition (AIP [autocamtide-2 related inhibitory peptide]).

234 Among the identified peptides were ACE-inhibitory peptides (LDAQSAPLR, LKGYGGVSLPEW, and LKALPM

235 AEKTKIPAVF, IDALNENK, and VLVLDTDYK), DPP-IV-inhibitory peptides (LKALPMH, LKPTPEGDLEIL, LKGYGGVSLPE,

236 To explore the role of this inhibitory phosphorylation in vivo, new phosphorylation-

237 We show that inhibitory phosphorylation of eIF2alpha (P-eIF2alpha), a

238 Also projecting to the antRNs are inhibitory photoreceptor relay interneurons.

239 d responsiveness to arginine-vasopressin (an inhibitory PKC-dependent response).

240 Synapses from each inhibitory population change according to distinct plast

241 s and decreased the frequency of spontaneous inhibitory postsynaptic currents in the indirect pathway

242 cently demonstrated how these drugs modulate inhibitory postsynaptic signaling by direct binding to t

243 ed drugs for OATP2B1 inhibition and quantify inhibitory potencies necessary for extrapolation of clin

244 ich were found to possess human PNMT (hPNMT) inhibitory potency <5 nM versus AdoMet.

245 entification of compound 4 with desired FXIa inhibitory potency and good oral bioavailability but hig

246 This study shows that high CD73 inhibitory potency can be achieved by simply introducing

247 atest chemical compounds that show promising inhibitory potential as INSTI candidates.

248 CB1r activation mainly decreased the inhibitory, potentially direct pathway component while s

249 In this study, the inhibitory potentials of food originated 34 phenolic aci

250 renic MN output by connecting phrenic MNs to inhibitory premotor neurons.

251 m memories (LTM) but also the suppression of inhibitory processes that prevent them.

252 ision (vLGN) connects subcortically, sending inhibitory projections to sensorimotor structures, inclu

253 ted network of long-range excitatory but not inhibitory projections with subtype-specific patterning.

254 hat PIAS1 interacted with the liver-enriched inhibitory protein (LIP) region of C/EBPbeta.

255 expression and overexpression of complement inhibitory proteins on MM target cells as well as DARA-i

256 terns and significantly lower frequencies of inhibitory receptor expression, i.e., PD-1 and coexpress

257 control, CD4+ T cells quickly downregulated inhibitory receptors and differentiated into long-lived

258 e that balancing of immune responses through inhibitory receptors is an important quality control che

259 he tumor microenvironment (TME), blockade of inhibitory receptors that limit NK cell functions, and t

260 enome encodes more than 300 potential immune inhibitory receptors.

261 older mice (P40-P46), when ChC synapses are inhibitory, resulted instead in an increase in axo-axoni

262 ncoding RNA (lncRNA) that we named Stem Cell Inhibitory RNA Transcript (SCIRT), which was markedly up

263 e-catalyst mediated by the CB7 portal and an inhibitory role attributed to the lower interaction of t

264 pathogenic protein in SD weakened the normal inhibitory self-coupling of network hubs in both antero-

265 apping and distinct mechanisms to potentiate inhibitory signalling in the brain.

266 leep, with excited reward processing sending inhibitory signals to suppress noise in visual processin

267 dentified molecules that operate on both the inhibitory 'slender retainer' and activatory 'stumpy ind

268 BMP-2 induction leads to the expression of inhibitory Smad 6/7-dependent negative transcriptional r

269 ility of regenerating axons to penetrate the inhibitory spinal cord glial scar.

270 Recently, first therapeutic miRNA-based inhibitory strategies have been tested in heart failure

271 Zona incerta (ZI) is a largely inhibitory subthalamic region connecting with many brain

272 tochondrial calcium uniporter complex (MCUC) inhibitory subunit MCUb overexpression.

273 Abnormal excitatory and inhibitory synapse assembly and elevated expression of t

274 tion of neuroligin-2, a key component of the inhibitory synapse, in the NAc that modifies behavioral

275 nduction of long-term plasticity at distinct inhibitory synapses and its regulation of hippocampal ne

276 c ephrin-B1 to influence both excitatory and inhibitory synapses during development can potentially c

277 ncaging confirms MNTB neurons as a source of inhibitory synapses onto MOC neurons.

278 We show that the strength of inhibitory synapses relative to excitatory synapses can

279 ay involves crosstalk between excitatory and inhibitory synapses whereby Ca(2+)-entering through post

280 namic regulation of GABA(A)R accumulation at inhibitory synapses, thereby regulating the strength of

281 e and triggers an increase in the density of inhibitory synapses, which is accompanied by enhanced ax

282 ermit rapid crosstalk between excitatory and inhibitory synapses.

283 y nerve and T-stellate cells, and made local inhibitory synaptic contacts on principal cells of the V

284 lthough little is known about stress-induced inhibitory synaptic plasticity and its relevance for neu

285 Hence, inhibitory synaptic plasticity occurs in parallel with e

286 Here, we reveal a hidden form of inhibitory synaptic plasticity that prevents accumulatio

287 Although it is known that inhibitory synaptic strength is malleable, induction of

288 opioids induce a long-lasting suppression of inhibitory synaptic transmission onto OFC pyramidal neur

289 tissue damage induces long-term deficits in inhibitory synaptic transmission within the spinal super

290 In addition to Tn-actin interactions, inhibitory Tm positioning requires associations between

291 ss, but they further indicate that sequences inhibitory to as well as supportive of Nef activity resi

292 tion would play a role in setting the spinal inhibitory tone and influencing sensory signaling, as sp

293 e findings suggest a common state of reduced inhibitory tone in the NAc in depression and stress susc

294 e and potentiate the synaptic excitatory and inhibitory tone onto mutant SF1 neurons, respectively.

295 n is independent of glycosylation and is not inhibitory toward endoRNase activity.

296 r 1 (CB(1))-mediated long-term depression of inhibitory transmission (iLTD), a form of presynaptic pl

297 ex than expected interplay of excitatory and inhibitory transmitter systems in modulating working mem

298 s, an immature or impaired immune system and inhibitory tumor microenvironment can further complicate

299 Phosphorylation of the inhibitory tyrosine of SFKs was almost completely abolis

300 gibbon and human) the highest proportion of inhibitory WMICs contain calretinin.