ライフサイエンスコーパス: presynaptic terminal

1 ed depolarization of the giant calyx of Held presynaptic terminal.

2 regulating gap junction localization in the presynaptic terminal.

3 ing the behavior of neurotransmission at the presynaptic terminal.

4 omain in turn promotes the maturation of the presynaptic terminal.

5 ion by recycling the neurotransmitter to the presynaptic terminal.

6 dded in a complex filamentous network at the presynaptic terminal.

7 ic vesicle biogenesis and cycling within the presynaptic terminal.

8 ission requires graded Ca(2+) signals at the presynaptic terminal.

9 dritic spines that are not in contact with a presynaptic terminal.

10 CaV2.1 null background at the calyx of Held presynaptic terminal.

11 ate throughout the soma, dendrites, axon and presynaptic terminal.

12 ushroom spines, and had enlarged mossy fiber presynaptic terminals.

13 n and propagation and transmitter release at presynaptic terminals.

14 hanges at the axon initial segment (AIS) and presynaptic terminals.

15 ivity produces large and rapid acid loads in presynaptic terminals.

16 nglion (DRG) sensory neurons and spinal cord presynaptic terminals.

17 synaptic vesicles and dense core vesicles at presynaptic terminals.

18 on tuning is present also among bipolar cell presynaptic terminals.

19 ansport and activity-dependent remodeling of presynaptic terminals.

20 determinants of vesicle mobility in crowded presynaptic terminals.

21 outgrowth and neurotransmitter release from presynaptic terminals.

22 ia enhances vesicular glutamate release from presynaptic terminals.

23 increase in vesicular glutamate release from presynaptic terminals.

24 function of the BAD-BAX-caspase-3 pathway in presynaptic terminals.

25 on axonal membranes mostly outside of active presynaptic terminals.

26 er ligand-induced activation specifically at presynaptic terminals.

27 s (DCVs) for activity-dependent release from presynaptic terminals.

28 ynuclein aggregates are selectively found in presynaptic terminals.

29 neuronal cell bodies and displace axosomatic presynaptic terminals.

30 in response to the release of glutamate from presynaptic terminals.

31 the presence of functional alpha7 nAChRs at presynaptic terminals.

32 the subsynaptic reticulum (SSR) surrounding presynaptic terminals.

33 eases Ca(V) channel density in somata and in presynaptic terminals.

34 of neurotransmitter-containing vesicles from presynaptic terminals.

35 eceptor subtypes, respectively, localized to presynaptic terminals.

36 on of neurotransmitter release at individual presynaptic terminals.

37 regulating release of neurotransmitters from presynaptic terminals.

38 (alpha-syn), a cytosolic protein enriched in presynaptic terminals.

39 iceable accumulation at dendritic spines and presynaptic terminals.

40 ses plasma membrane expression of LTCCs near presynaptic terminals.

41 late the initiation of bouton formation from presynaptic terminals.

42 nic pathway that regulates SphK abundance at presynaptic terminals.

43 hanced neurotransmitter release from apposed presynaptic terminals.

44 hanges in nAChR clustering or alignment with presynaptic terminals.

45 ion relies on the structural organization of presynaptic terminals.

46 K cells develop significantly fewer inactive presynaptic terminals.

47 ently suppress neurotransmitter release from presynaptic terminals.

48 vesicle fusion and recycling at specialized presynaptic terminals.

49 e, calcium-dependent events within forebrain presynaptic terminals.

50 zebra finch depend on calcium influx within presynaptic terminals.

51 ansport of Nrxn1alpha at axonal processes to presynaptic terminals.

52 quired for proper localization of Imac in R8 presynaptic terminals.

53 1 trafficking in axons and APP processing at presynaptic terminals.

54 ivity produces large and rapid acid loads in presynaptic terminals.

55 he removal of BACE1 from distal AD axons and presynaptic terminals.

56 ne, while UNC5C may alter the composition of presynaptic terminals.

57 resulting in markedly reduced expression at presynaptic terminals.

58 utgrowth and enhances glutamate release from presynaptic terminals.

59 1's dendrites and the mitochondria in Tm5c's presynaptic terminals.

60 wth factor 2 (IGF2) for the stabilization of presynaptic terminals.

61 th a number of ion channels in the axons and presynaptic terminals.

62 ch may be concurrently present in individual presynaptic terminals.

63 tacts, and an increased proportion of orphan presynaptic terminals.

64 concept of a tripartite synapse including a presynaptic terminal, a postsynaptic spine, and an astro

65 -type voltage-gated Ca(2+) channels that, at presynaptic terminals, abnormally contributes to evoked

66 fusion protein that is normally localized to presynaptic terminals along the dorsal axon of the DA9 m

67 e, we ask whether R-type calcium channels in presynaptic terminals also signal through calcium microd

68 lated by dynamic membrane trafficking at the presynaptic terminal and a PKC-sensitive negative endocy

69 olved in the release of neurotransmitters in presynaptic terminal and its aberrant aggregation is fou

70 three Ca(V) 2 subtype channel levels in the presynaptic terminal and not just Ca(V) 2.1.

71 ns in these nuclei to evaluate/compare their presynaptic terminal and postsynaptic target features in

72 prevented using VGLUT1-shRNA, the density of presynaptic terminals and accumulation of synapsin and s

73 e zone proteins cluster synaptic vesicles at presynaptic terminals and coordinate their release.

74 ormally high cytosolic calcium transients in presynaptic terminals and deficient working memory but d

75 release did not disrupt the morphogenesis of presynaptic terminals and dendritic spines, suggesting t

76 naptically but is ultimately communicated to presynaptic terminals and expressed as an accelerated tu

77 modulation of neurotransmitter release from presynaptic terminals and for hyperpolarization at posts

78 neurotransmission by recapturing DA into the presynaptic terminals and is a principal target of the p

79 tic arborization and densities of excitatory presynaptic terminals and postsynaptic dendritic spines

80 escribe how information transmission through presynaptic terminals and postsynaptic spines is related

81 entify an F-actin network present at nascent presynaptic terminals and required for presynaptic assem

82 vidence suggests that they may also exist at presynaptic terminals and reshape excitatory synaptic tr

83 brain, its expression is restricted to a few presynaptic terminals and scattered axonal growth cones.

84 IGF2, in turn, localizes to DGC presynaptic terminals and stabilizes them in an activity

85 on competence of immobile (tethered) DCVs in presynaptic terminals and that CAPS-1 localization to DC

86 amily, Cbln1 and Cbln2, bind to neurexins on presynaptic terminals and to GluRdeltas postsynaptically

87 incided with altered calcium kinetics in CA3 presynaptic terminals and upregulated sarco(endo)plasmic

88 mer acts as a SNARE complex chaperone at the presynaptic terminal, and may protect against neurodegen

89 and multivesicular bodies accumulate in the presynaptic terminal, and vesicles accumulate between me

90 te their proximal location, relatively large presynaptic terminals, and ability to excite target neur

91 en contained PSD fragments, contacted distal presynaptic terminals, and formed secondary synapses.

92 Aergic motor neurons, localizes to GABAergic presynaptic terminals, and functions cell-autonomously t

93 rn neurons had greater spine density, larger presynaptic terminals, and more putative efferent filopo

94 rtem samples exhibit loss of hippocampal CA3 presynaptic terminals, and murine studies revealed micro

95 d metabolic enzymes that are concentrated at presynaptic terminals, and mutants lacking one of these,

96 7 subunit-containing nAChRs at glutamatergic presynaptic terminals, and nicotine-induced presynaptic

97 ity can result in transient acidification of presynaptic terminals, and such shifts in cytosolic pH (

98 ity can result in transient acidification of presynaptic terminals, and such shifts in cytosolic pH (

99 zes to discrete, nonvesicular regions within presynaptic terminals, and this localization is critical

100 ll recordings, two-photon calcium imaging in presynaptic terminals, and two-photon glutamate uncaging

101 tein involved in neurotransmitter release in presynaptic terminals, and whose aberrant aggregation is

102 ron micrographs confirmed the lack of intact presynaptic terminals apposing spines on mature cells an

103 unctions in vivo to promote filopodia during presynaptic terminal arborization.

104 While individual molecular components of the presynaptic terminal are well known, exactly how the mol

105 innervation of their targets and because the presynaptic terminals are large and easily monitored.

106 Further, presynaptic terminals are less mature structurally and f

107 The postsynaptic and presynaptic terminals are molecular systems with highly

108 functions of alpha- and gamma-synucleins in presynaptic terminals are not fully redundant.

109 pocampal neurons, for example, glutamatergic presynaptic terminals are selectively silenced, creating

110 Presynaptic terminals are specialized sites for informat

111 uced in the postsynaptic cell and act on the presynaptic terminal, are implicated in mechanisms of lo

112 n the mean distance between mitochondria and presynaptic terminals as well as a decrease in mean mito

113 acterized membranous organelle system of the presynaptic terminal, as well as with smaller vesicular

114 hese mutant animals also had fewer GABAergic presynaptic terminals at both ages.

115 ation of GAP-43 from the axonal shaft to the presynaptic terminal but also its activation in the axon

116 not simply the presence of Cortactin in the presynaptic terminal but its increase that is necessary

117 ogous proteins found at comparable levels in presynaptic terminals but beta-synuclein has a greatly r

118 promoting transmitter release, are mobile on presynaptic terminals but constrained in synaptic space

119 gly, Ca(2+) channels are not only located at presynaptic terminals, but also in the axon initial segm

120 pha-Synuclein is expressed at high levels at presynaptic terminals, but defining its role in the regu

121 s, GABA(B)Rs and 5-HT(1B)Rs both localize to presynaptic terminals, but target distinct effectors.

122 ase and regulates spontaneous release in the presynaptic terminal by cooperating with the neuronal so

123 tion were also observed when we bypassed the presynaptic terminal by iontophoretically applying GABA,

124 cle fusion, glycine is recovered back to the presynaptic terminal by the neuronal glycine transporter

125 P neurons reduces autophagic accumulation at presynaptic terminals by enhancing AV retrograde transpo

126 clustering factor neuronal pentraxin 1 from presynaptic terminals by signaling through presynaptic p

127 Presynaptic terminal cAMP elevation plays a central role

128 Stimulating presynaptic terminals can increase the proton concentrat

129 rexpression were accompanied by increases in presynaptic terminal circumference, total synapse number

130 of the dlPAG, whereas CB(1) was confined to presynaptic terminals, consistent with a role for 2-AG a

131 srupt synaptic organization, with inhibitory presynaptic terminals containing synaptotagmin 2 appeari

132 During earplugging, vGluT1 expression in the presynaptic terminal decreased and synaptic vesicles wer

133 Inhibition of AMPK activity in presynaptic terminals decreases GABA release at 10 mM gl

134 CVs, we propose that Gbb/Cmpy corelease from presynaptic terminals defines a neuronal protransmission

135 egment, and near/within nodes of Ranvier and presynaptic terminals, dendritic KChs found at sites ref

136 ircuit maturation impacted the calyx of Held presynaptic terminal development and function.

137 gitudinal and rapid time-lapse imaging of CC presynaptic terminal development.

138 ly the absence of any of DLG proteins at the presynaptic terminal disrupts the clustering and localiz

139 o sustain normal SNARE-complex assembly in a presynaptic terminal during aging.

140 ne studies revealed microglial engulfment of presynaptic terminals during acute infection and after r

141 hways regulating morphological properties of presynaptic terminals during an early stage of circuit m

142 Ca(2+) release from intracellular stores at presynaptic terminals during in vitro ischaemia.

143 s suggest that miR-8 limits the expansion of presynaptic terminals during larval synapse development

144 -GFP reversibly dispersed out of hippocampal presynaptic terminals during stimulation, and blockade o

145 pha, sequentially organize the glutamatergic presynaptic terminals during the initial synaptic differ

146 localized to microglia, infected neurons and presynaptic terminals during WNV neuroinvasive disease.

147 ich presynaptic glycine receptors depolarize presynaptic terminals, elevate resting calcium levels, a

148 nvade the CNS territory of the DREZ, forming presynaptic terminal endings on non-neuronal cells.

149 ice and conditional KO mice lacking Arrb2 in presynaptic terminals expressing Nav1.8.

150 urons and targeted to the plasma membrane of presynaptic terminals, facilitating neurotransmitter rel

151 ment of the priming protein UNC-13/Munc13 to presynaptic terminals following activation by muscarinic

152 pamine storage vesicles are available in the presynaptic terminals for release, a likely factor contr

153 lability of dopamine storage vesicles in the presynaptic terminals for release.

154 In postnatal mice, the time-course of CC presynaptic terminal formation and elimination was highl

155 Presynaptic terminal formation is a complex process that

156 that activated microglia displace inhibitory presynaptic terminals from cortical neurons in adult mic

157 sing visually and pharmacologically isolated presynaptic terminals from dissociated rat hippocampal n

158 Whole-cell patch-clamp recordings of presynaptic terminals from S218L KI mice showed a strong

159 cell of interest and that structures such as presynaptic terminals from surrounding, nontargeted neur

160 Moreover, presynaptic terminals from Wnt signalling-deficient mice

161 rvical ganglion neurons in culture show that presynaptic terminal function is compromised if clathrin

162 is of a single neurotransmitter vesicle in a presynaptic terminal has been a question of significant

163 eter-scale monitoring of vesicle dynamics in presynaptic terminals has remained elusive.

164 details of synaptic vesicle exocytosis from presynaptic terminals have been intensely studied for de

165 At the NMJ, it functions at the presynaptic terminal in a cell-autonomous fashion, but m

166 The calyx of Held, a large glutamatergic presynaptic terminal in the auditory brainstem undergoes

167 Held terminal, an experimentally accessible presynaptic terminal in the CNS.

168 s induces complement-mediated elimination of presynaptic terminals in a murine WNV neuroinvasive dise

169 mine transporter (DaT) protein, a marker for presynaptic terminals in dopaminergic nigrostriatal neur

170 Presynaptic terminals in female right MePD had a higher

171 investigate whether similar rules exist for presynaptic terminals in mixed networks of pyramidal and

172 tal ultrastructure-function relationships of presynaptic terminals in native circuits are revealed.

173 ively and noninvasively stimulate individual presynaptic terminals in rat brain slices.

174 er suggest that this complex is important in presynaptic terminals in regulating protein phosphorylat

175 in the number of GABAergic and glutamatergic presynaptic terminals in S1.

176 al electron tomographic analysis of enlarged presynaptic terminals in several brain areas revealed th

177 Most presynaptic terminals in the central nervous system are

178 and GABAB receptors are co-expressed at many presynaptic terminals in the central nervous system.

179 on of VGLUT1 is important for development of presynaptic terminals in the cortex.

180 N and increased the size and density of 5-HT presynaptic terminals in the dentate gyrus and vmPFC.

181 increase in vesicular glutamate release from presynaptic terminals in the early phase of brain ischae

182 increase in vesicular glutamate release from presynaptic terminals in the early phase of brain ischae

183 tic organizers and help to organize specific presynaptic terminals in the mammalian brain.

184 for the activity-dependent stabilization of presynaptic terminals in the mammalian hippocampus.

185 pproximately 0.5 mum in diameter) inhibitory presynaptic terminals in the same area where identified

186 mum in diameter) VGLUT1-positive excitatory presynaptic terminals in the stratum lucidum of area CA3

187 PSD95 remained tethered to presynaptic terminals in Vezatin-deficient hippocampal n

188 portions of longer motor axons and in their presynaptic terminals, including disruption of the smoot

189 ger PSDs, increased PSD perforations, larger presynaptic terminal) indicative of increased synaptic a

190 We propose that presynaptic terminals induce postsynaptic receptor clust

191 These results indicate that the size of the presynaptic terminal is an independent control for the d

192 However, the presynaptic terminal is filled with filamentous material

193 We found that the amount of clathrin in a presynaptic terminal is not fixed.

194 e report that when activity of an individual presynaptic terminal is selectively elevated by light-co

195 nover of neurotransmitter-filled vesicles at presynaptic terminals is a crucial step in information t

196 Microglia-mediated stripping of presynaptic terminals is considered neuroprotective, but

197 evelopmental processes of auditory brainstem presynaptic terminals is critical to understanding audit

198 Surprisingly, the density of presynaptic terminals is not affected by betaIII spectri

199 ha-synuclein (alphaS), a protein abundant at presynaptic terminals, is associated with a range of hig

200 nnabinoid type 1 receptor, mainly present at presynaptic terminals, is coupled to the Gi/o protein an

201 bilities: simultaneously labelling axons and presynaptic terminals, labelling both dendrites and post

202 generation of Nrxn-CTF, which accumulate at presynaptic terminals lacking PS function.

203 lated alpha-synuclein deposits were found in presynaptic terminals mainly in the form of small aggreg

204 ve snapin mutants induced SV accumulation at presynaptic terminals, mimicking the snapin(-/-) phenoty

205 clude that postsynaptic cell type determines presynaptic terminal molecular identity and that preNMDA

206 ransmitter release.SIGNIFICANCE STATEMENT In presynaptic terminals, neurotransmitter release is dynam

207 eceptors are inhibitory GPCRs located on the presynaptic terminal of both serotonin and non-serotonin

208 dye, we have imaged the AP waveform from the presynaptic terminal of male and female frog NMJs and sh

209 ocytotic FM1-43 (SynaptoGreen) uptake in the presynaptic terminal of neuromuscular junctions was rest

210 Here, we demonstrate that the presynaptic terminal of the frog NMJ has a very brief AP

211 ere significantly decreased or absent in the presynaptic terminal of the mutant GF.

212 we found that topographic separation of the presynaptic terminals of adjacent nociceptive neurons re

213 orescent quantification showed that efferent presynaptic terminals of BKalpha(-/-) OHCs were smaller

214 to the dendrites of the MBn, surrounding the presynaptic terminals of cholinergic afferent fibers fro

215 chloride (ACC) channel family, localizes to presynaptic terminals of cholinergic motor neurons and r

216 osphorylated alpha-synuclein is found at the presynaptic terminals of dementia with Lewy bodies cases

217 opamine receptor subtype 1 (D1) signaling in presynaptic terminals of direct pathway striatal spiny p

218 -mu treatment supported hDAT delivery to the presynaptic terminals of dopaminergic neurons and restor

219 te from and are subsequently detected by the presynaptic terminals of GABAergic neurons in the molecu

220 ptic vesicle release events, the ribbon-type presynaptic terminals of goldfish retinal bipolar cells

221 Presynaptic terminals of incipient synaptic contacts gen

222 ntracortical axon collaterals and en passant presynaptic terminals of layer 5 pyramidal cells exhibit

223 rough serial inhibitory connections onto the presynaptic terminals of ON bipolar cells.

224 essed in the cerebellum, particularly in the presynaptic terminals of parallel fibers-Purkinje neuron

225 to track single vesicles at voltage-clamped presynaptic terminals of retinal bipolar neurons, whose

226 ions, particularly as these diverge from the presynaptic terminals of sensory neurons.

227 h contrasts with the stereotypy reported for presynaptic terminals of sensory neurons.

228 minals requires reliable localization of the presynaptic terminals of single neurons as well as genet

229 ference in distance between mitochondria and presynaptic terminals of SNpc neurons in PD brains vs. D

230 ogenously generated H2S acted selectively on presynaptic terminals of splanchnic nerves to modulate f

231 ined large dense core vesicles in excitatory presynaptic terminals of the adult mouse hippocampus.

232 lpha1 homomers either in HEK-293 cells or at presynaptic terminals of the calyceal synapses in the au

233 Although alphaS is abundant in the presynaptic terminals of the central nervous system, its

234 ic K(v) channels in synaptic facilitation at presynaptic terminals of the hippocampus upstream of the

235 We demonstrate that the presynaptic terminals of the identified T1 and PPM3 dopa

236 nd PKA-dependent synapsin phosphorylation in presynaptic terminals of the nucleus accumbens is increa

237 , but these neurons form significantly fewer presynaptic terminals on motor neurons.

238 the attraction of an additional excitatory, presynaptic terminal onto an existing synapse.

239 through an increase in VGLUT1 at individual presynaptic terminals or through addition of VGLUT1-posi

240 cells regulate the structure and function of presynaptic terminals, ostensibly through changes in gen

241 tage-clamp recordings from rat calyx of Held presynaptic terminals, our data show, for the first time

242 chondria as well as their vicinity to the DA presynaptic terminals postmortem caudate and putamen of

243 decreased intracellular glutamate density in presynaptic terminals, presynaptic mitochondria, and in

244 Targeted to presynaptic terminals, preSynTagMA allows discrimination

245 with hypertrophy of membrane systems of the presynaptic terminal previously shown to have a role in

246 ndent recruitment to membrane regions within presynaptic terminals promotes neurotransmitter release.

247 These findings indicate that, within presynaptic terminals, R-type calcium channels produce c

248 Mature presynaptic terminals release neurotransmitter both in r

249 Presynaptic terminals release neurotransmitters spontane

250 Efficient neurotransmitter release at the presynaptic terminal requires docking of synaptic vesicl

251 Conversely, inactivity of the presynaptic terminal results in removal of transporters

252 Quantitative fluorescence imaging of live presynaptic terminals reveals that blocking presynaptic

253 ges to be caused primarily by an increase in presynaptic terminal size and enhanced vesicle release p

254 Ultrastructurally, presynaptic terminal size was similar in amygdala, stria

255 hat synucleins are important determinants of presynaptic terminal size.

256 anin B, which are normally found in neuronal presynaptic terminals storing catecholamines such as dop

257 are consistent with the idea that defects in presynaptic terminal structure and function precede, and

258 lted in reduced turnover of RIM1 and CASK at presynaptic terminals, suggesting that liprin-alpha2 pro

259 The finding of a tonotopic gradient in presynaptic terminals suggests that Kv1.3 may regulate n

260 estrogen synthesis enzyme (aromatase) within presynaptic terminals suggests that neuroestrogens can b

261 43) plays a central role in the formation of presynaptic terminals, synaptic plasticity, and axonal g

262 fuse at morphological specializations in the presynaptic terminal termed active zones (AZs).

263 of Ca(2+) fluxes and Ca(2+) buffering in the presynaptic terminal that is not fully understood.

264 ine generating large rises of Na+ inside the presynaptic terminal that must be efficiently reduced by

265 Depolarization of presynaptic terminals that arises from activation of pre

266 at clathrin levels are a dynamic property of presynaptic terminals that can influence short-term plas

267 5 and 12 days in culture, the percentage of presynaptic terminals that expressed VGLUT1 increased du

268 croautophagy that follows mTOR inhibition in presynaptic terminals, therefore, rapidly alters presyna

269 Here we address what occurs within the presynaptic terminal to achieve homeostatic potentiation

270 mine reuptake, and altering the state of the presynaptic terminal to enhance evoked over basal transm

271 ry brainstem, synaptic zinc is released from presynaptic terminals to modulate neurotransmission.

272 s required coincident activation of multiple presynaptic terminals to reach firing threshold.

273 ransporter (VGAT) as a marker for inhibitory presynaptic terminals to study the development of inhibi

274 These features allow presynaptic terminals to translate complex firing freque

275 plays a critical role in removing BACE1 from presynaptic terminals toward the soma, thus reducing syn

276 own to decrease the ATP concentration within presynaptic terminals transiently, an observation that w

277 uring an action potential, Ca(2+) entering a presynaptic terminal triggers synaptic vesicle exocytosi

278 arly ischaemia, increased Ca(2+) influx into presynaptic terminals was due to reverse operation of th

279 In contrast, alpha-synuclein in presynaptic terminals was in at least three different po

280 The number of opposed excitatory presynaptic terminals was sharply reduced upon postsynap

281 xpression of plasma membrane transporters at presynaptic terminals, we aim to elucidate some of the m

282 inals or through addition of VGLUT1-positive presynaptic terminals, we examined the spatio-temporal d

283 As neuronal activity drives acid loading in presynaptic terminals, we hypothesized that the same act

284 In old mice, ultrastructural alterations in presynaptic terminals were observed at PP-to-granule cel

285 central nucleus (CeL), where PACAP-positive presynaptic terminals were predominantly found within th

286 Young presynaptic terminals were remarkably dynamic - moving,

287 been thought to be transported to axons and presynaptic terminals where they signal via ErbB3/4 rece

288 ched in the periactive zone of photoreceptor presynaptic terminals where Tulp1 colocalizes with major

289 t rat brain, and selectively concentrates in presynaptic terminals, where it is closely associated wi

290 cally translated beta-catenin accumulates at presynaptic terminals, where it regulates synaptic vesic

291 ed excitability and Ca(2+) transients in the presynaptic terminals, where Kv1.2 potassium channels ar

292 function, structure, and development of the presynaptic terminal which leads to altered short term-d

293 mutation affected Nrxn1alpha localization at presynaptic terminals which correlated with a decrease i

294 The shape of action potentials invading presynaptic terminals, which can vary significantly from

295 e was dependent on a rise in basal Ca(2+) at presynaptic terminals, which resulted from extracellular

296 ion: [Ca(2+)]ER controls STIM1 activation in presynaptic terminals, which results in the local modula

297 o the normal function and development of the presynaptic terminal, whose properties shape short-term

298 ures encompassing branch points and numerous presynaptic terminals with undefined molecular partners

299 d reduced surface areas and lower volumes of presynaptic terminals, with depressed nerve control, inc

300 Munc18-1 was strongly expressed at presynaptic terminals, with individual synapses showing