ライフサイエンスコーパス: postsynaptic

1 STDP rule in which pairs of single pre- and postsynaptic action potentials induce synaptic modificat

2 by mechanistically distinct presynaptic and postsynaptic actions.

3 al mitochondrial bioenergetics that the fuel postsynaptic activities of the respiratory motor drive.

4 Pairing pre- and postsynaptic activity induced plasticity at paired input

5 transient ACh signaling with more sustained postsynaptic activity patterns to support relatively per

6 , whereby similarity between presynaptic and postsynaptic activity selectively strengthens some synap

7 The postsynaptic adapter protein-coding gene, SHANK2, locate

8 teract trans-synaptically with multitudinous postsynaptic adhesion molecules, including SliTrks, SALM

9 n the AWC sensory neurons, which inhibit the postsynaptic AIA interneurons to override and disrupt AF

10 f synaptic plasticity involve the control of postsynaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolep

11 air cells from TMIE mutant mice show altered postsynaptic alpha9alpha10 function and retain alpha9alp

12 can interact with presynaptic neurexins and postsynaptic AMPA-type ionotropic glutamate receptors an

13 ergic currents by promoting the insertion of postsynaptic AMPARs that contain fast desensitizing flop

14 owever, the effects of mTORC1 on eEPSCs were postsynaptic and the effects of mTORC2 were presynaptic.

15 complex biochemical networks at presynaptic, postsynaptic, and astrocytic sites to the time window of

16 ental disorders, with the majority affecting postsynaptic apparatuses and much fewer in presynaptic p

17 s(2-4), and silences these neurons and their postsynaptic ascending neurons in the abdominal ganglion

18 ential interaction of presynaptic C1ql3 with postsynaptic Bai3.

19 While postsynaptic Bin1 shows colocalization with clathrin, a

20 of presynaptic partners and communicate with postsynaptic brain regions to convey features of the vis

21 s of Ca(2+) dynamics indicated that rises in postsynaptic Ca(2+) are necessary and sufficient for Z-L

22 electrical stimulation, and is sensitive to postsynaptic Ca(2+) chelation and blockers of nicotinic

23 induce LTP, which was prevented by chelating postsynaptic Ca(2+) or blocking nicotinic receptors.

24 Neuroligins (NLGNs) are a class of postsynaptic cell adhesion molecules that interact with

25 different behaviors at the level of a single postsynaptic cell.

26 However, the rules governing how postsynaptic cells differentiate between presynaptic inp

27 connections of dopaminergic cells and their postsynaptic cells, AII amacrine and melanopsin-containi

28 idelity was affected by both presynaptic and postsynaptic changes after ear occlusion and was only af

29 These postsynaptic changes parallel changes in visual response

30 echanisms, such as retrograde signaling from postsynaptic cholinergic and GABAergic systems, among ot

31 with NS9283 restores the rapid onset of the postsynaptic cholinergic response without triggering des

32 hrna5 is critical for the rapid onset of the postsynaptic cholinergic response.

33 This impairment correlates with disrupted postsynaptic clustering of Homer1b, Shank, and AMPAR sub

34 vity-dependent accumulation of Msp300 in the postsynaptic compartment of the Drosophila larval neurom

35 In the postsynaptic compartment, interactions with actin or its

36 1, and show that this protein is abundant in postsynaptic compartments, including spines.

37 , which determines the shape of the pre- and postsynaptic compartments, organizes the neurotransmitte

38 downstream mechanisms in the presynaptic and postsynaptic compartments.

39 ation of signaling molecules within pre- and postsynaptic compartments.

40 n in complex with PSD-95 or PSD-95-assembled postsynaptic complexes form highly concentrated and dyna

41 and confirm the involvement of ARC and NMDAR postsynaptic complexes.

42 Cross talk between both pre- and postsynaptic components of glutamatergic neurotransmissi

43 d the relative importance of presynaptic and postsynaptic contributions to the faithful transfer of i

44 Specifically, spontaneous excitatory postsynaptic current amplitudes measured from individual

45 g Na(+)/H(+) exchange activity decreased the postsynaptic current and caused failures in postsynaptic

46 h ASD exhibited reduced miniature excitatory postsynaptic current frequency and N-methyl-D-aspartate

47 ecapitulated diminished miniature excitatory postsynaptic current frequency, supporting a role for th

48 t with an increase in spontaneous excitatory postsynaptic current frequency.

49 uction of synchronous spontaneous inhibitory-postsynaptic-current events in mutants, which was revers

50 /kainate receptor-mediated evoked excitatory postsynaptic currents (eEPSCs), by 94% and 72%, respecti

51 ls (BCs), we found that classical excitatory postsynaptic currents (EPSCs) are followed by GABA(A) re

52 In mature neurons, PVs evoke GABA(A) postsynaptic currents (GPSCs) with fast rise and decay p

53 led higher frequency of miniature excitatory postsynaptic currents (mEPSCs) immediately after 2-h imm

54 potentials (fEPSPs) and miniature excitatory postsynaptic currents (mEPSCs) in rat hippocampal slices

55 s and decreased frequency of mini inhibitory postsynaptic currents (mIPSC) in the NAc of susceptible

56 The observation of spontaneous excitatory postsynaptic currents (sEPSCs), spontaneous inhibitory p

57 ssion (versus N40) of spontaneous inhibitory postsynaptic currents (sIPSCs) across multiple subjects.

58 sant-induced burst of spontaneous inhibitory postsynaptic currents (sIPSCs) on CA1 pyramidal neurons

59 ic currents (sEPSCs), spontaneous inhibitory postsynaptic currents (sIPSCs), and bidirectional electr

60 the amplitude of the spontaneous excitatory postsynaptic currents and decreased the frequency of spo

61 nd modeled using intracellular recordings of postsynaptic currents and potentials, inferring synaptic

62 o evidence that NMDA receptors contribute to postsynaptic currents evoked in either amacrine.

63 ity of only one motoneuron and recordings of postsynaptic currents from inputs formed by the differen

64 ity by inferring the magnitude of excitatory postsynaptic currents from the N20 component of the soma

65 al examples of proton-evoked ASIC excitatory postsynaptic currents have emerged.

66 d dopamine release in the DMS and excitatory postsynaptic currents in DMS MSNs.

67 uced the frequency of spontaneous excitatory postsynaptic currents in the direct pathway MSNs, wherea

68 ased the frequency of spontaneous inhibitory postsynaptic currents in the indirect pathway MSNs.

69 viously shown that the physiological size of postsynaptic currents maximises energy efficiency rather

70 neurons in heterozygous mice evoked biphasic postsynaptic currents not significantly different from t

71 ferences that are associated with excitatory postsynaptic currents on mPFC principle neurons.

72 me of NMDAR-dependent spontaneous excitatory postsynaptic currents suggesting a prolonged open time o

73 Analysis of miniature postsynaptic currents support that M2 and M3 receptors m

74 ections to the PVT elicits direct excitatory postsynaptic currents.

75 t in part, by enhancing miniature inhibitory postsynaptic currents.

76 presses EPSCs in Chx10 neurons by activating postsynaptic D(2) receptors.

77 Activation of postsynaptic D1 dopamine receptors promoted the generati

78 igured as presynaptic axon terminations onto postsynaptic dendrites or somata, giving rise to axo-den

79 sed PSD95-eGFP mice, to visualise excitatory postsynaptic densities (PSDs) using high-resolution and

80 nt mono-ubiquitination, compartmentalized at postsynaptic densities, gates retrograde signaling and p

81 On individual postsynaptic densities, we observed GluA2-lacking nanodo

82 ation and experience-dependent regulation of postsynaptic densities.

83 ence point to glutamatergic signaling in the postsynaptic density (PSD) as a pathophysiologic mechani

84 SynGAP is a postsynaptic density (PSD) protein that binds to PDZ dom

85 ASD risk genes and genes encoding inhibitory postsynaptic density (PSD) proteins, but not for genes i

86 he dynamics of CaMKII phosphorylation in the postsynaptic density (PSD).

87 f neuronal nitric oxide synthase (nNOS) from postsynaptic density 95 (PSD95) and a reduced production

88 tal marker beta3-tubulin and synaptic marker postsynaptic density 95 protein (PSD-95).

89 SorCS2 specifically localizes to the postsynaptic density and endosomes within dendritic spin

90 compartments of excitable cells such as the postsynaptic density and juxtaparanodes of Ranvier.

91 tron microscope imaging demonstrated reduced postsynaptic density formation and fewer dendritic polyr

92 Correction of postsynaptic density protein 95 cerebellar misexpression

93 on through upregulation of synaptophysin and postsynaptic density protein 95.

94 The postsynaptic density protein PSD-95 contains a three-dom

95 m the smooth endoplasmic reticulum) near the postsynaptic density to promote the persistent firing ne

96 to cell bodies and dendrites, including the postsynaptic density, and within the last 5 years severa

97 guingly suggests that SR may be found at the postsynaptic density, yet the functional implications of

98 thyl-d-aspartate receptor subunit 2B (NR2B), postsynaptic density-95 (PSD-95) and microtubule-associa

99 ely 65%) of LDLR and LRP1 is associated with postsynaptic density-95 (PSD-95)-positive synaptosomes,

100 eceptors and scaffolding proteins within the postsynaptic density.

101 undergo constant cycling into and out of the postsynaptic density.

102 s implicated in learning and memory in which postsynaptic depolarization strengthens synapses, promot

103 ASP1 and LASP2 play an important role in the postsynaptic development of rat hippocampal neurons from

104 ecific exon are necessary and sufficient for postsynaptic differentiation and scaling growth, and the

105 by neuronal activity and requires increased postsynaptic differentiation induced by insulin receptor

106 ns of antipsychotic drugs on presynaptic and postsynaptic dopamine dysregulation, this study evaluate

107 ribbons are normally apposed to two distinct postsynaptic "dyad" partners, but in the absence of LRRT

108 Yet, their combined effect on postsynaptic dynamics has been largely unexplored.

109 e conditions allows the determination of the postsynaptic E/I ratio for at least 120 h after death, e

110 cross much of the striatum, via quantifiable postsynaptic effects that vary across subregions.

111 synaptic plasticity involves presynaptic and postsynaptic elements as well as adjacent astroglial pro

112 There was also a decrease in phagocytosis of postsynaptic elements by microglia expressing TREM2R47H

113 of postsynaptic spiking and slow changes in postsynaptic excitability.

114 The study of postsynaptic excitation to inhibition (E/I ratio) imbala

115 Electrophysiological measurements assessing postsynaptic expression mechanisms, and imaging studies

116 neuronal release of transmitter up-regulates postsynaptic expression of appropriate transmitter recep

117 postsynaptic current and caused failures in postsynaptic firing.

118 occurs through the local binding of TWEAK to postsynaptic Fn14.

119 ween an Aplysia sensory neuron (B21) and its postsynaptic follower, the motor neuron (B8).

120 Both presynaptic and postsynaptic forms of homeostasis are important, but the

121 scular function via effects on both pre- and postsynaptic function, in the face of disease.

122 HL1 regulates DRD2-dependent presynaptic and postsynaptic functions.

123 s, but the effect is mediated by the loss of postsynaptic GABA(A) receptors, gephyrin, and neuroligin

124 ic synapses strongly increases clustering of postsynaptic GABA(A)Rs.

125 ransmitter release in response to diminished postsynaptic GluR functionality, a process referred to a

126 necessary for the homeostatic modulation of postsynaptic GluRs in mammals, our data demonstrate that

127 about the auxiliary subunits associated with postsynaptic GluRs, far less is understood about presyna

128 factor BIN1, and that Amph itself modulated postsynaptic glutamate receptor (GluRII) localization.

129 , auditory neurons, presynaptic ribbons, and postsynaptic glutamate receptors.

130 n muscle size, presynaptic release sites and postsynaptic glutamate receptors.

131 tamate receptors and involved an increase in postsynaptic glycine receptor-mediated currents.

132 letion in granule cells of the OB of Bai3, a postsynaptic GPCR that binds C1ql3, similarly suppressed

133 scillations in a cell-intrinsic manner, with postsynaptic Group 1 metabotropic glutamate receptor act

134 thalamoreticular inputs but did not require postsynaptic Group 1 metabotropic glutamate receptor act

135 are presynaptic homomeric GlyRs, rather than postsynaptic heteromeric GlyRs (which mediate glycinergi

136 of presynaptic homomeric GlyRs (rather than postsynaptic heteromeric GlyRs), because homomeric GlyRs

137 show that selective block of Panx1 in single postsynaptic hippocampal CA1 neurons from male rat or mo

138 napses undergo bidirectional presynaptic and postsynaptic homeostatic changes with increased and decr

139 In parallel, LKB1 modulated postsynaptic horizontal cell refinement and presynaptic

140 Despite postsynaptic inhibition of evoked release, mTORC1 inacti

141 sion, with some contribution from changes in postsynaptic intrinsic properties.

142 neurotransmission.SIGNIFICANCE STATEMENT The postsynaptic ion and metabolite channel, pannexin-1, is

143 during synaptic transmission, modulating the postsynaptic ionotropic glutamate receptors.

144 n pre- and post-synaptic cells, we find that postsynaptic Kenyon cells set convergence ratio: Kenyon

145 c voltage-gated calcium channels (VGCCs) and postsynaptic ligand-gated ion channels such as AMPA rece

146 t likely involves binding to one or multiple postsynaptic ligands.

147 ere unitary release of glutamate can trigger postsynaptic local activation of voltage-gated Na(+)-cha

148 inotopic alignment, (2) the amplitude of the postsynaptic local field potential elicited near the int

149 Here, we show an age-dependent dendritic and postsynaptic localization of SR and d-serine by immunohi

150 Here, we show dendritic and postsynaptic localization of SR and d-serine in CA1 pyra

151 Certain transcriptional programs (e.g., postsynaptic machinery) are segregated to specialized do

152 by the increase of anatomic presynaptic and postsynaptic markers in the peri-infarct zone and corres

153 tic morphogenesis, increased accumulation of postsynaptic markers, early expression of synapse activi

154 reased frequency of sIPSCs without affecting postsynaptic measures, suggesting increased CeA GABA rel

155 cells in rodent hippocampus likely through a postsynaptic mechanism, and has a variable effect on the

156 hibitory input to VP(GABA) neurons through a postsynaptic mechanism.

157 s of electrically-evoked EPSCs, suggesting a postsynaptic mechanism.

158 ty is generated by a combination of pre- and postsynaptic mechanisms.

159 sion is mediated by multiple presynaptic and postsynaptic mechanisms.

160 smission from the presynaptic calyces to the postsynaptic medial nucleus of the trapezoid body (MNTB)

161 e that the focal insertion of AChRs into the postsynaptic membrane is regulated by stable MTs and hig

162 were dependent on Ca(2+) movement across the postsynaptic membrane, rather than neurotransmitter rele

163 bsequently, the insertion of AMPARs into the postsynaptic membrane.

164 of the plasma membrane Ca(2+)-ATPase at the postsynaptic membrane.

165 diated by the removal of AMPA receptors from postsynaptic membranes.

166 to influence active zone formation, whereas, postsynaptic miR-34 inhibits Hts to regulate the initiat

167 Here we report structural features of postsynaptic mitochondria in the pre-Botzinger complex (

168 Here, we analyze the response of a single postsynaptic model neuron receiving tuned excitatory con

169 provide functional evidence of Amh-mediated postsynaptic modulation of synaptic transmission and Amh

170 oforms in the presynaptic sensory neuron and postsynaptic motor neuron.

171 (MuSK) or other AChR-related proteins in the postsynaptic muscle membrane.

172 s glutamatergic motoneurons that coinnervate postsynaptic muscles of male or female Drosophila melano

173 creasing release of ACh onto presynaptic and postsynaptic nAChRs in primary auditory cortex (A1).

174 These pre- and postsynaptic nanodomains are characterized by a high den

175 napses with highly organized presynaptic and postsynaptic nanomachines that are aligned by synaptic a

176 inding to presynaptic neurexin-1alpha and to postsynaptic neuroligin-1B, thereby catalyzing formation

177 napses by bridging presynaptic neurexins and postsynaptic neuroligins.

178 in layer 2/3 and favoured locations near the postsynaptic neuron and ahead of its preferred direction

179 he postsynaptic neuron, and how recently the postsynaptic neuron has spiked.

180 retina via coordinate regulation of pre and postsynaptic neuron structure and the localization of sy

181 The direction selectivity of a postsynaptic neuron was unrelated to the selectivity of

182 d, synapses, the overall excitability of the postsynaptic neuron, and how recently the postsynaptic n

183 coaxial to the preferred orientation of the postsynaptic neuron, favouring the region opposite to it

184 sensory cortex, we show that a signal from a postsynaptic neuron, orchestrated by endocannabinoids, a

185 findings support a cell-autonomous role for postsynaptic neuronal SR in regulating synaptic NMDAR fu

186 e transfer anterogradely from presynaptic to postsynaptic neurons in the adult Drosophila olfactory s

187 second Cre-driver line (Pdzk1ip1-Cre) labels postsynaptic neurons in the MTN.

188 nergic amacrine cells and some of their main postsynaptic neurons in the retina of PD.

189 y starting at receptor neurons and following postsynaptic neurons into the brain.

190 Structural changes in pre and postsynaptic neurons that accompany synapse formation of

191 A fraction (10-20%) of postsynaptic neurons that received cholinergic input fro

192 tical structures to bi-directionally control postsynaptic neurons, thus helping to orchestrate severa

193 e optogenetic manipulations of input-defined postsynaptic neurons, we show that dCA1 PYRs drive NAc m

194 entary molecular programs in presynaptic and postsynaptic neurons.

195 NARE fusion machinery play critical roles in postsynaptic neurotransmitter receptor trafficking, whic

196 ll understood, the basis of specification of postsynaptic neurotransmitter receptors matching the new

197 but control synapse properties by regulating postsynaptic NMDA-receptors via a trans-synaptic mechani

198 -induced tonic activation of presynaptic and postsynaptic NMDARs at the spinal cord level and that pr

199 duced aberrant activation of presynaptic and postsynaptic NMDARs in the spinal cord.

200 ory synapses whereby Ca(2+)-entering through postsynaptic NMDARs promotes the recruitment and strengt

201 the ectodomain of neuroligin NLG-1, itself a postsynaptic organizer of inhibitory synapses.

202 unexpected role for metabotropic NMDARs and postsynaptic Panx1 in suppression of facilitated glutama

203 Neurons often contact more than one postsynaptic partner type and display stereotypic patter

204 ses of the primary auditory receptors, their postsynaptic partners and their supporting cells.

205 We found that postsynaptic partners are able to find and connect to th

206 cting to the protocerebral bridge (DA-PB) as postsynaptic partners of P1 neurons.

207 signaling between potential presynaptic and postsynaptic partners, the extracellular factors and the

208 ntials propagate through long axons to their postsynaptic partners, which requires axons not only to

209 re needed for the appropriate recruitment of postsynaptic partners.

210 Long-lasting forms of postsynaptic plasticity commonly involve protein synthes

211 ndidates for the syntaxin isoform underlying postsynaptic plasticity.

212 glutamate transporter inhibition reduced the postsynaptic population response to TBS, calcium respons

213 Amh exposure also increased the excitatory postsynaptic potential at CA1 synapses.

214 ration time window of concomitant excitatory postsynaptic potentials (EPSPs) and dampens their tempor

215 were examined by recording field excitatory postsynaptic potentials (fEPSPs) and miniature excitator

216 Unitary excitatory postsynaptic potentials (uEPSPs) revealed a high degree

217 itic propagation attenuates the amplitude of postsynaptic potentials and widens their temporal spread

218 e and sharpens the time course of excitatory postsynaptic potentials by reducing current sinks and mo

219 tracellularly recorded action potentials and postsynaptic potentials from thousands of neurons.

220 ion and even decrease the temporal spread of postsynaptic potentials, if active subthreshold potassiu

221 and the frequency of spontaneous excitatory postsynaptic potentials.

222 eading to responses that resemble excitatory postsynaptic potentials.

223 eta accumulation in microglia as well as the postsynaptic protein PSD95.

224 ns were regulated, including pre- as well as postsynaptic proteins with diverse molecular functions.

225 disease caused by autoantibodies that target postsynaptic proteins, primarily the acetylcholine recep

226 us fluorescent labeled presynaptic VAMP2 and postsynaptic PSD95 in long-term cultured live primary ne

227 INs) and decreased intrinsic excitability of postsynaptic Purkinje neurons (PNs) resulted in low PN f

228 Furthermore, the postsynaptic Rac1-GEF kalirin-7 regulated spinule format

229 btypes, including in presynaptic plasticity, postsynaptic receptor function, and synaptic connectivit

230 presynaptic ligand cerebellin-1 (Cbln1) and postsynaptic receptor GluD2 mediate synaptogenesis betwe

231 d, and these switches require changes in the postsynaptic receptor population.

232 ransmission, synaptic plasticity and impairs postsynaptic receptor trafficking.

233 naptic function through its interaction with postsynaptic receptors and adhesion molecules.

234 concentrations of GABA can both activate the postsynaptic receptors generating sustained low-amplitud

235 cation requires the expression of functional postsynaptic receptors that match the presynaptically re

236 n-3 (Lphn3) are adhesion GPCRs that serve as postsynaptic recognition molecules in CA1 pyramidal neur

237 ressed in larval muscles and enriched in the postsynaptic regions of the glutamatergic neuromuscular

238 resulted in sustained synaptic inhibition in postsynaptic relay neurons of the ventrobasal thalamus (

239 underlying estradiol-induced alterations in postsynaptic response to GABA, and also AMPA, receptor a

240 mic interaction creates a mechanism by which postsynaptic responses can quickly change.

241 mulation of the claustrum induced excitatory postsynaptic responses in most neocortical neurons, but

242 lances excitation, resulting in uncorrelated postsynaptic responses regardless of the inhibitory tuni

243 elated nAChR subunit-selective reductions in postsynaptic responses to ACh.

244 at may contribute to the observed changes in postsynaptic responses.

245 at mTORC1 and mTORC2 differentially modulate postsynaptic responsiveness and presynaptic release to o

246 Although previous studies have delineated postsynaptic roles for mTOR, whether it regulates presyn

247 The SHANK3 gene encodes a postsynaptic scaffold protein in excitatory synapses, an

248 tsynaptic signaling by direct binding to the postsynaptic scaffolding protein gephyrin.

249 at complexes containing CaMKII and Shank3, a postsynaptic scaffolding protein known to interact with

250 ssemblies likely form via interactions among postsynaptic scaffolding proteins and receptors and alig

251 n brain circuits, uniform downscaling on the postsynaptic side is implicated in sleep- and memory-rel

252 inputs formed on neurons, as well as on the postsynaptic side.

253 ved only within central circuits, and on the postsynaptic side.

254 erefore operates on both the presynaptic and postsynaptic sides to maintain target cell activity.

255 nstrated how these drugs modulate inhibitory postsynaptic signaling by direct binding to the postsyna

256 istinct vHC-PrL projection neurons modulates postsynaptic signaling in both inhibitory and excitatory

257 structure and morphology, neurotransmission, postsynaptic signaling pathways, and neural circuitry to

258 Postsynaptic signaling through alpha1A ARs in PDGFRalpha

259 functions, such as nonlinear integration of postsynaptic signals.

260 Failure of the postsynaptic site, rather than hyperexcitation, drives d

261 aling mediated long-term depression (LTD) at postsynaptic sites in ovBNST neurons.

262 f synaptic activity in ovBNST, which acts at postsynaptic sites to dampen excitability at short and l

263 onstrate that SULT4A1 is highly expressed at postsynaptic sites where it sequesters Pin1, preventing

264 NAcylation are found at both presynaptic and postsynaptic sites, and O-GlcNAcylated proteins localize

265 er of efferent synapses per OHCs, defined as postsynaptic SK2 puncta, was reduced in aged OHCs of all

266 between neuronal arbors with mixed pre- and postsynaptic specializations.

267 t-mediated changes in the number of pre- and postsynaptic spike pairing events and by firing rate cha

268 sticity can only be recovered when bursts of postsynaptic spikes are used, or when neurons fire at su

269 well as effects due to the recent history of postsynaptic spiking and slow changes in postsynaptic ex

270 eters estimated from ongoing presynaptic and postsynaptic spiking are highly uncertain, our results a

271 her or not a synaptic current contributes to postsynaptic spiking depends not only on the amplitude o

272 reases the peak amplitude of EPSPs, and thus postsynaptic spiking probability.

273 , using only observations of presynaptic and postsynaptic spiking, aims to describe the dynamics of i

274 fects based only on observed presynaptic and postsynaptic spiking.

275 ly confined mitochondrial alterations within postsynaptic spines in the pre-BotC neurons.

276 netic deletion of SR, we establish a role of postsynaptic SR in regulating NMDAR function.

277 density, yet the functional implications of postsynaptic SR on synaptic transmission are not yet kno

278 We identified two presynaptic and two postsynaptic steps of synaptic transmission which are mo

279 A1 and its products regulate the activity of postsynaptic striatal neurons is unclear.

280 educed active zone (AZ) number and decreased postsynaptic subsynaptic reticulum volume, with the emer

281 ndothelium-derived neurotoxins disrupted the postsynaptic synaptic response.

282 ecific neuronal classes innervating the same postsynaptic target display distinct types of plasticity

283 c inputs that depends on the identity of the postsynaptic target MSN.

284 al transmission of ACh and GABA based on the postsynaptic target neuron is reflected in VIP(+)/ChAT(+

285 V) 1.2 supports its surface localization and postsynaptic targeting in neurons.

286 le of GluA3 may be important to allowing the postsynaptic targets of spherical bushy cells in mice us

287 ctivity that occur at the synapse in vivo to postsynaptic targets that use rate information for sound

288 initial over-innervation by multiple pre- or postsynaptic targets, followed by a process of refinemen

289 perties of inhibitory interneurons and their postsynaptic targets.

290 NPY neurons may drive tonic inhibition onto postsynaptic targets.

291 ividual vestibular afferent inputs and their postsynaptic targets.

292 Exposure to loud sound damages the postsynaptic terminals of spiral ganglion neurons (SGNs)

293 transmission at both presynaptic termini and postsynaptic termini.

294 ed extensive neuronal apoptosis with loss of postsynaptic termini.

295 Postsynaptic to the antenna cells are a group of inhibit

296 insights into the mesoscale architecture of postsynaptic trafficking compartments and their regulati

297 Postsynaptic trafficking plays a key role in regulating

298 how interplay between adhesion molecules and postsynaptic transmitter receptors orchestrates function

299 The assembly of the postsynaptic transmitter sensing machinery at inhibitory

300 erences were observed in any of the pre- and postsynaptic variables measured.