ライフサイエンスコーパス: axon terminal

1 ey induce cytoskeletal reorganization at the axon terminal.

2 evin-labeled presynaptic specializations per axon terminal.

3 on disease, characterized by degeneration of axon terminals.

4 tive and closely juxtaposed to prefrontal D1 axon terminals.

5 bits synaptic transmission at CB1-expressing axon terminals.

6 occurred throughout dendrites, axons, and in axon terminals.

7 rimary role of the 5-HT1B receptors in these axon terminals.

8 B)Rs was also present at lower levels on PVI axon terminals.

9 in inhibiting the growth of R7 photoreceptor axon terminals.

10 which preserve in vivo-like connectivity of axon terminals.

11 elease of synaptic vesicles from presynaptic axon terminals.

12 e also expressed both in PC dendrites and BC axon terminals.

13 -level tonic calcium influx into presynaptic axon terminals.

14 support fast, highly processive runs toward axon terminals.

15 None was found in axon terminals.

16 % of the postsynaptic targets of cholinergic axon terminals.

17 tic tips and somas and was weak or absent in axon terminals.

18 ic (inhibitory-type) synapses from unlabeled axon terminals.

19 on firing patterns, are poorly understood at axon terminals.

20 ate neuropeptides from secretory granules in axon terminals.

21 rather than direct activation of interneuron axon terminals.

22 o areas where alpha-MSH1-13 is released from axon terminals.

23 by GABAC receptors, probably on bipolar cell axon terminals.

24 ease throughout individual presynaptic motor axon terminals.

25 ules, and in neuronal perikarya but never in axon terminals.

26 xtrasynaptic regions in dendritic spines and axon terminals.

27 mitter of single vesicles release by retinal axon terminals.

28 of SP-ir profiles were presynaptic axons and axon terminals.

29 ion of myelin and VGLUT1-positive excitatory axon terminals.

30 by axonal swellings) and degeneration of the axon terminals.

31 evidence that GABAARs are localized at MNTB axon terminals.

32 ealed eukaryotic ribosomes in CB1-expressing axon terminals.

33 ise control of neurotransmitter release from axon terminals.

34 ive vesicles were also observed in axons and axon terminals.

35 ric acid, and acetylcholine from presynaptic axon terminals.

36 nal transport, must be actively localized to axon terminals.

37 tic nicotinic receptors (nAChRs) on dopamine axon terminals.

38 to the hippocampus in order to illuminate RE axon terminals.

39 present on both GABAergic and glutamatergic axon terminals.

40 fferent transmitter released from peripheral axon terminals.

41 endritic spines, and clusters of vesicles in axon terminals.

42 ximately 10% of EAAT2 molecules are found in axon terminals.

43 uctural alterations in these cells and their axon terminals.

44 pharmacology at the level of individual cone axon terminals.

45 optical excitation or inhibition of amygdala axon terminals.

46 nfection of projection neurons through their axon terminals, (3) targeted infection of genetically sp

47 ) profiles) and presynaptically in axons and axon terminals (45%).

48 as GluR5,6,7-ir dendrites contacted by SP-ir axon terminals; 54% of the dendritic targets of SP-ir ax

49 tration of d-aspartate (an EAAT2 substrate), axon terminals accumulate d-aspartate as quickly as astr

50 ity in hundreds of cell bodies or long-range axon terminals, across all six layers in visual cortex o

51 Imaging studies identified the BC axon terminal and PC dendrites as loci of AC-dependent K

52 ; approximately 30% of labeled profiles were axon terminals and 30% were dendrites and dendritic spin

53 al activity directs fine-scale topography of axon terminals and a new system to study this process at

54 in Nav subtype expression between CH and SR axon terminals and between CH and SR dendrites and spine

55 designated here as type 5b, exhibit diffuse axon terminals and can be distinguished from the narrowl

56 elease coincided with the degeneration of DA axon terminals and decreased expression of DA neuron-enr

57 1 cannabinoid receptors (CB1) are located at axon terminals and effectively control synaptic communic

58 in neurons, highlighted by concentrations in axon terminals and euchromatin-rich nuclear domains.

59 light stimulus-evoked Ca(2+) signals in cone axon terminals and horizontal cell dendrites as well as

60 to area 9), m2 receptors predominated in ACC axon terminals and in more than half of the targeted den

61 d at the somatodendritic compartment, or the axon terminals and it can be transported anterogradely,

62 es delta opioid receptors that reside on FSI axon terminals and negatively couple to adenylyl cyclase

63 synaptic inhibitory synapses on bipolar cell axon terminals and possibly amacrine cell dendrites.

64 taneously recorded from presynaptic pallidal axon terminals and postsynaptic thalamocortical neurons

65 for the maintenance of local homeostasis of axon terminals and protection against axonal degeneratio

66 e-strand RNA viruses, infect neurons through axon terminals and spread trans-synaptically in a retrog

67 hat most synapses between CRF-immunoreactive axon terminals and TH neurons are asymmetric (in the maj

68 r maintaining stable contacts between basket axon terminals and the Purkinje AIS during pinceau organ

69 uences the branching pattern of regenerating axon terminals and the redistribution of acetylcholine r

70 e they formed appositions with glutamatergic axon terminals and unidentified cells and therefore are

71 ked whether RhoA is present in photoreceptor axon terminals and whether activity in the RhoA-ROCK pat

72 by multiple neurotransmitters from the same axon terminal (and even from the same vesicle) now is we

73 l features of chemically distinct classes of axon terminals, and a major autonomic source of axons la

74 s localized in dendrites, but also in axons, axon terminals, and glial processes in all hippocampal s

75 motor neurons, lack of mitochondria in motor axon terminals, and immature neuromuscular junctions.

76 NDCBE is in most glutamatergic axon terminals, and is also present in the terminals of

77 66% were somatodendritic profiles, 22% were axon terminals, and the remaining 12% were associated wi

78 neuropil, including being present in spines, axons, terminals, and glial processes.

79 1 [labeling all ON and OFF bipolar cell (BC) axon terminals] and G-protein gamma13 (labeling all ON B

80 nt axon growth in vitro as well as cutaneous axon terminal arborization in vivo.

81 In primary auditory cortex the bulk of MGV axon terminals are in layer IV/lower layer III with mino

82 dendritic or spine atrophy, indicating that axon terminals are much more vulnerable to autophagy imp

83 Comparable experiments in central axon terminals are prohibitively difficult but the bioph

84 These findings show that axon terminals are unstable without M(2) and that muscle

85 nstrate that responses in dendrites, but not axon terminals, are end inhibited by flanking gratings b

86 Finally, ordered geometric axon terminal arrangements that are not required for neu

87 he presynaptic plasma membrane of a neuron's axon terminals as a precondition for fusing with the mem

88 evidence that S1P can be produced at mature axon terminals as well as at immature growth cones in re

89 anogaster, for GABAergic synaptic markers on axon terminals as well as dendrites.

90 matergic corticostriatal and thalamostriatal axon terminals at dendritic spines of medium spiny neuro

91 d with fusion probability at active zones of axon terminals at frog neuromuscular junctions.

92 ules composing active zone material (AZM) in axon terminals at mouse neuromuscular junctions.

93 d network coupled by gap junctions while the axon terminals (ATs) form a third independent network in

94 Both of these nuclei send columnar axon terminals back to the same tectal position receivin

95 Within 12 h, axon terminals begin to atrophy and withdraw from normal

96 while HCN1 channels were concentrated in the axon terminal boutons.

97 odistributing with anterogradely labeled Ipc axon-terminal boutons, further supporting a glutamatergi

98 naling molecules have been identified in the axon terminal, but their specific role in axon guidance

99 in forming synaptic specializations at their axon terminals, but in excess of the usual number.

100 subtypes on dendrites, dendritic spines, and axon terminals, but the proportion of pre- and post-syna

101 of intrabouton Ca(2+) influx into GABAergic axon terminals by CB1, leading to the effective suppress

102 otal gray matter (by 10%) and in parvalbumin axon terminals (by 49%).

103 eactivity was preferentially localized to CH axon terminals compared to SR, and in SR dendrites and s

104 eptide release from the somato/dendritic and axon terminal compartment.

105 d with dendrites, M5R was less often seen in axon terminals, comprising only 10.8% (n = 102) of the t

106 ry cortex and found that practically all ChC axon terminals contact axon initial segments, with an av

107 g: [1] lateral efferent olivocochlear (LEOC) axon terminals contain endogenous dynorphin neuromodulat

108 In contrast, few axon terminals contained both DYN and ENK.

109 s contained SP; while 11% of SP-ir axons and axon terminals contained GluR5,6,7).

110 ynaptic sites (18% of GluR5,6,7-ir axons and axon terminals contained SP; while 11% of SP-ir axons an

111 py showed coexistence of DYN and CRF; 35% of axon terminals containing DYN were also immunoreactive f

112 s associated with the formation of retracted axon terminals containing multivesicular bodies and seco

113 The mesoaccumbens axon terminals containing VGluT2 vesicles make asymmetri

114 Long-distance organelle transport toward axon terminals, critical for neuron development and func

115 tial to travel from the neuronal soma to the axon terminal, defining the temporal manner in which inf

116 An acute and highly reproducible motor axon terminal degeneration followed by complete regenera

117 pTrkB-ir was in axons, axon terminals, dendrites, and dendritic spines of neuro

118 roBDNF) stabilizes or eliminates presynaptic axon terminals, depending on its proteolytic conversion

119 le fibers, postsynaptic differentiation, and axon terminal development.

120 These findings suggest that serotonergic axon terminals differentially innervate several neuronal

121 trastructurally defined synapses per GPe-STN axon terminal doubled with no alteration in terminal/syn

122 adder and developed varicosities along their axon terminal endings.

123 ial-like processes to a circuit in which RGC axon terminals establish synapses with dendritic shafts

124 found CRF immunoreactivity present mostly in axon terminals establishing either symmetric or asymmetr

125 imulation of ChR2-expressing thalamocortical axons/terminals evoked robust synaptic responses in cort

126 ed for kappaOR and ppDYN showed that, of the axon terminals exhibiting kappaOR, 47% (223/477) also ex

127 In the IPL, DB1 bipolar cell axon terminals expressed the glycine receptor, GlyRalpha

128 icroscopy, we resolved the ultrastructure of axon terminals fated for laminar stabilization versus th

129 ae were implanted above the indirect pathway axon terminal field in the dlVP, or the direct pathway t

130 g of dendrites, dendritic spines, axons, and axon terminal fields within a few hours to a few days af

131 y, our results indicate that horizontal cell axon terminals form two independent sets of homotypic ga

132 target nucleus (LA or BL), ~90% of cortical axon terminals formed asymmetric synapses with dendritic

133 ximately 49% (98/200) of the kappaOR-labeled axon terminals formed asymmetric synapses with TH-labele

134 In both cases, most (76-86%) PHAL(+) axon terminals formed asymmetric synapses, typically wit

135 und that double-labeled PHA-L (+)/VGluT2 (+) axon terminals formed synaptic contacts on dendrites of

136 mate transporter 1-positive terminals and of axon terminals forming asymmetric synapses in the dorsol

137 s with CB1r-ir typically received input from axon terminals forming asymmetric-type synapses.

138 s in the LC, and also revealed CB1r-positive axon terminals forming synaptic contact with MOR-contain

139 at mCherry-VGluT2 varicosities correspond to axon terminals, forming asymmetric synapses on neighbori

140 ervations of anterogradely labeled (PHAL(+)) axon terminals found at perirhinal sites adjacent to or

141 ortin-alpha3 as being required to prevent R7 axon terminals from overlapping with the terminals of R7

142 neurons establish local synapses, we tagged axon terminals from resident VTA neurons by intra-VTA in

143 C1 level, there was extensive withdrawal of axon terminals from thalamus and cortex, detectable a de

144 ncode object motion retinotopically, but the axon terminals fuse into a glomerular structure in the c

145 n pathway was shown previously to inhibit R7 axon terminal growth.

146 tely 29% (200/688) of the kappaOR-containing axon terminals identified targeted TH-containing profile

147 ation of the cholinergic neurons or their V1 axon terminals improved performance of a visual discrimi

148 s/cm(2)/s) light-evoked calcium spikes in Mb axon terminals in an NEM-sensitive manner, but light res

149 elrhodopsin (ChR2) in CST cell bodies and in axon terminals in cervical spinal cord.

150 sing long-range posteromedial (POm) thalamic axon terminals in cortex and induced CaMPARI conversion

151 neurons in dorsal root ganglia (DRG) and on axon terminals in lamina II (the substantia gelatinosa)

152 maged the regeneration of trigeminal sensory axon terminals in live zebrafish larvae following laser

153 loss of motor neurons and atrophy of distal axon terminals in muscle, resulting in loss of motor fun

154 es to the actin cytoskeleton, is enriched at axon terminals in neurons, and activates the axon growth

155 so evident in the innervation pattern of OSN axon terminals in olfactory bulbs.

156 been implicated in compensatory sprouting of axon terminals in paralyzed or denervated muscles.

157 tion of SC-projecting neurons in V1 or their axon terminals in SC sufficiently elicits the behavior,

158 urons are known to enlarge their presynaptic axon terminals in size and strength, thereby compensatin

159 ffect was strongest when puffed to STN-->SNr axon terminals in SNr, indicating a primary role of the

160 dition, illumination of Mrgprd-ChR2-Venus(+) axon terminals in spinal cord slices evoked EPSCs in hal

161 ceive excitatory inputs from ON bipolar cell axon terminals in sublamina-b of the inner plexiform lay

162 mus, we next recorded directly from pallidal axon terminals in thalamic nucleus DLM, and found that a

163 k, we also found that directly activating M2 axon terminals in the auditory cortex suppresses spontan

164 ing this period, the density of mPFC-derived axon terminals in the BA also decrease significantly, an

165 d vGlut1 was localized primarily to separate axon terminals in the DRN, with a subset co-localizing C

166 ruit both GABA and GABA-A receptors to their axon terminals in the EB, and optogenetic stimulation co

167 tes, cells of the dermis, and on nociceptive axon terminals in the epidermis.

168 B1Rs are located on Schaffer collateral (Sc) axon terminals in the hippocampus, where they inhibit gl

169 mical analysis revealed the absence of GLP-1 axon terminals in the HPFv, suggesting volume transmissi

170 r (VGLUT1) was used to identify bipolar cell axon terminals in the inner retina.

171 ealed abundant rod bipolar cells (RBCs) with axon terminals in the innermost sublamina of the inner p

172 e release from more than 13,000 bipolar cell axon terminals in the intact retina, we show that bipola

173 led a prominent localization of kappa-ORs in axon terminals in the LC that also contained either the

174 found mainly extra-synaptically in axons and axon terminals in the NAc and are enriched in glutamater

175 extracellular GABA concentration around RHT axon terminals in the SCN.

176 ulder responsive sites in CN densely labeled axon terminals in the shoulder representation in VPL, bu

177 Conversely, inhibition of PVN OXT axon terminals in the VTA decreased social interactions.

178 GABAergic, insofar as the CRF-immunolabeled axon terminals in these synapses coexpressed glutamic ac

179 tamatergic, insofar as the CRF-immunolabeled axon terminals in these synapses coexpressed the vesicul

180 over, optogenetic activation of serotonergic axon terminals increased excitability of fusiform cells.

181 tative synapses were formed by GABA-positive axon terminals, indicating synaptogenesis by interneuron

182 tyramine, which displaces noradrenaline from axon terminals) induced vasoconstriction.

183 to the periphery and relocate photoreceptor axon terminals into the center.

184 asion occurs prenatally, organization of PrV axon terminals into whisker-specific rows and patches ta

185 the outward transport of dynein from soma to axon terminal is driven by direct interactions with the

186 tials, and the rate of depolarization of the axon terminal is instead governed by the rate of rise of

187 ed from the infected neuron cell body to the axon terminal is poorly understood.

188 tification of co-transmitters within DRN CRF axon terminals is important for elucidating the complex

189 Cabp5 immunolabeling of type 3 bipolar cell axon terminals is reduced in Vsx1-null mice.

190 that in rhesus monkeys (Macaca mulatta) most axon terminals labeled from tracers injected into ACC ar

191 ing for HCN4 was seen in two sets of bipolar axon terminals located in s2 and s3 and positioned betwe

192 Competitive interactions between axon terminals may determine the number of synapses each

193 GABA spillover excitation between MNTB axon terminals may entrain neighboring MNTB neurons, whi

194 Excitatory GABA spillover between inhibitory axon terminals may have important implications for the d

195 at CRF and vGlut2 were found within the same axon terminal more frequently than CRF and vGlut1.

196 hese data indicate that DYN- and CRF-labeled axon terminals, most likely arising from amygdalar sourc

197 R immunoreactivity (M1R-ir) was also seen in axon terminals, most of which formed asymmetrical synaps

198 M2R-ir was also seen in axon terminals, most of which formed asymmetrical synaps

199 Traditional fluorescent dyes label axon terminals near an injection site, but unfortunately

200 The autoreceptor population located on the axon terminals of 5-HT neurons is a difficult population

201 Two-photon imaging of the axon terminals of a single PN innervating the CO2 glomer

202 teral prefrontal cortex, is contained in the axon terminals of a subpopulation of perisomatic-targeti

203 hy on tissue sections from fixed and stained axon terminals of active and resting frog neuromuscular

204 tative OFF-type cone bipolar cell and in the axon terminals of an ON-type bipolar that ramifies in st

205 The axon terminals of cb5b bipolar cells costratify with the

206 Nav 1.6 immunoreactivity were found between axon terminals of CH and SR or between dendrites and spi

207 g melanopsin cells also received inputs from axon terminals of dopaminergic amacrine cells.

208 at the orexin neurons are heavily apposed by axon terminals of glutamatergic and GABAergic neurons of

209 Axon terminals of glutamatergic retinal rod bipolar cell

210 Direct recordings from the large axon terminals of goldfish retinal bipolar cells (BCs) h

211 puncta were predominantly localized on large axon terminals of horizontal cells.

212 ransmitter GABA by directly depolarizing the axon terminals of inhibitory interneurons, thus bypassin

213 modulates autophagy of synaptic vesicles in axon terminals of motoneurons via its function as a guan

214 The presynaptic axon terminals of one neuron release neurotransmitters t

215 used to quantify GAD67 protein levels in the axon terminals of parvalbumin-containing GABA neurons, w

216 ranslation of the protein, especially in the axon terminals of parvalbumin-containing neurons, suppor

217 We found that axon terminals of perisomatically projecting GABAergic i

218 , a synaptic lamina that is comprised of the axon terminals of photoreceptors and the dendrites of ho

219 s to defects in inner and outer segments and axon terminals of photoreceptors.

220 overlap of their distribution in spines and axon terminals of prefrontal cortical area 9 in the Maca

221 PTEN protein is enriched in cell bodies and axon terminals of purified motor neurons.

222 to NL was mapped, and the morphology of the axon terminals of SON neurons in NL was examined in chic

223 motoneurons, axons in the sciatic nerve, and axon terminals of the neuromuscular junctions.

224 ompartments: HCN1 channels were localized to axon terminals of the perforant path (the major hippocam

225 s of neurons; the enzyme was not detected in axon terminals or in the cells of 24-hydroxylase knockou

226 in a few somata, large dendrites, axons, and axon terminals or more rarely in glial processes.

227 e lipase, which is located in the inhibitory axon terminal, or by alpha-beta-hydrolase domain 6, whic

228 ts with C1 cell lesions, the mCherry-labeled axon terminals originating from the transfected noncatec

229 ynapses from inhibitory- and excitatory-type axon terminals, over 88% of which were unlabeled and oth

230 ns have reached the medulla; ttk69 mutant R7 axon terminal overgrowth begins shortly after this time

231 DYN- and CRF-containing axon terminals overlapped noradrenergic dendrites in thi

232 Early loss of synaptic vesicles in axon terminals preceding motor deficits, accumulation of

233 The distance between cell bodies and axon terminals predicts that glutamine-glutamate cycle i

234 coupling involves an elaborate dance between axon terminals, presynaptic and postsynaptic dendrites,

235 nologies, is highly specific for determining axon terminal projections within particular neuronal pop

236 The HBC(R/MC)s with axon terminals ramifying between 0% and 30% of the inner

237 uts from rods and M-cones, the HBC(MC)s with axon terminals ramifying between 10% and 50% of the IPL

238 marily from M-cones, and the HBC(M/SC)s with axon terminals ramifying between 25% and 50% of IPL rece

239 ity preceded by the occurrence of dystrophic axon terminals, reduced axonal transport, organelle-fill

240 EM) reconstruction of rat CA3 pyramidal cell axon terminals revealed approximately 1.7-1.9 times high

241 Ca(2+) responses in the ePN axon terminals show no detectable suppression by iPNs, a

242 Kv3.3 proteins were observed in axons, terminals, somas, and, unlike other Kv3 proteins,

243 Based on their axon terminal stratification, these bipolar cells could

244 2 contained mainly Lewy neurites in presumed axon terminals, suggesting the involvement of the EC -->

245 The sagittal array of Golgi cell axon terminals suggests that they contribute to the orga

246 Basket cells, whose axon terminals surround principal cell somata and proxim

247 Here, we show that the morphology of the axon terminal system and the dendritic field are selecti

248 o the pedicles of cone photoreceptors and an axon terminal system contacting the spherules of rod pho

249 morphology and stratification level of their axon terminal system in the inner plexiform layer and in

250 dendritic field is hypertrophic, whereas the axon terminal system is underdeveloped.

251 s an atrophic dendritic field yet leaves the axon terminal system largely intact.

252 rtical slices revealed the morphology of the axon terminal system of individual bipolar cells.

253 isoforms are co-localized in thalamocortical axon terminals targeting layer IV, but not in those targ

254 types of immunoreactivities: basally located axon terminals that are colocalized with myoinhibitory p

255 2) travels retrogradely to nearby inhibitory axon terminals that express the primary type 1 cannabino

256 New AChR clustering is also induced by axon terminals that follow SC processes extended during

257 ith immunogold labeling demonstrated labeled axon terminals that formed symmetric synapses on dendrit

258 2) in axon segments that are continuous with axon terminals that lack VMAT2, but contain vesicular gl

259 d reproducible fluorescence changes in motor axon terminals that vary with stimulus frequency and, wh

260 anscript into protein, and protein levels in axon terminals, the key site of GABA production and func

261 which the NGF signal is propagated from the axon terminal to the cell body are yet to be fully eluci

262 nner, leading to tiled arrangements of their axon terminals to allow optimal allocation of serotonin

263 neurotransmitter GABA can spill over between axon terminals to cause excitation of nearby synapses to

264 osis signal is retrogradely transported from axon terminals to cell bodies to induce cell death.

265 ced ambiguities in the correct assignment of axon terminals to identified motor units imaged at lower

266 id signaling stimulates protein synthesis in axon terminals to induce long-term depression of hippoca

267 n-dependent transport of organelles from the axon terminals to the cell bodies is essential to the su

268 sites of input from DB6 diffuse bipolar cell axon terminals to the inner stratifying type of melanops

269 ry, neuroinvasive herpesviruses traffic from axon terminals to the nuclei of neurons resident in peri

270 of GABAAR-mediated depolarizations from MNTB axon terminals to the soma, some hundreds of microns awa

271 e number of synaptic connections per GPe-STN axon terminal, to substantial strengthening of the GPe-S

272 ns and damaged mitochondria, particularly at axon terminals, ultimately might overwhelm the capacity

273 lycan secreted by the motor neuron's growing axon terminal upon contact with the muscle during embryo

274 t localize ionotropic GABA receptors on cone axon terminals using electron microscopy, we suggest tha

275 by inhibiting Ca(2+) entry into presynaptic axon terminals via N-type (Cav2.2) Ca(2+) channels.

276 onal innervation by CCK-positive basket cell axon terminals was confirmed by reduced frequency of inh

277 with this, membrane localization of NHE1 at axon terminals was greatly reduced in Chp1-deficient Pur

278 to the cytoplasm, whereas CB1r-ir located in axon terminals was more commonly localized on the plasma

279 endritic peptide release, while release from axon terminals was not altered, suggesting that high-K(+

280 ABA transporter and bassoon coimmunoreactive axon terminals was unchanged; and (5) the number of ultr

281 Using viral vectors taken up at axon terminals, we expressed chemogenetic actuators sele

282 inals; 54% of the dendritic targets of SP-ir axon terminals were GluR5,6,7-ir.

283 e FG injection, and (2) GLP-1-immunoreactive axon terminals were observed adjacent to the ventricular

284 EAATs reside on rod bipolar cell axon terminals where GABA and glycine receptors also med

285 lso expressed in cerebellar basket cell (BC) axon terminals, where its blockade increases BC inhibiti

286 ein synthesis by cytoplasmic RNP granules in axon terminals, where RNP granules regulate local RNA me

287 that accumbens DBS antidromically stimulates axon terminals, which ultimately activates GABAergic int

288 l bodies and dendrites, as well as unlabeled axon terminals, which, in turn, form inhibitory-like syn

289 ains of axons (e.g. the nodes of Ranvier and axon terminals) whose development depends on the interac

290 Our approach was to label RGC axon terminals with an indicator of activity and quantit

291 e inhibitory or excitatory by reacting their axon terminals with antibodies to reveal glutamate decrb

292 ive vesicles also were present in somata and axon terminals with or without CRFr labeling.

293 ynaptic efficacy are concurrently somata and axon terminals, with the direction of cortical current f

294 , and branching of the retinal ganglion cell axon terminals, with the N-terminal region of Olfm1 bein

295 Perforant path (PP) axon terminals within the dentate gyrus (DG) contained a

296 This study investigated whether CRF-labeled axon terminals within the DRN contain immunoreactivity f

297 Retinal ganglion cell axon terminals within the P and K layers were reconstruc

298 Optogenetic activation of CCK(NTS) axon terminals within the PVH reveal the satiating funct

299 ressed in dendrites, unmyelinated axons, and axon terminals within the STN.

300 Surprisingly, however, the dark-reared axons' terminal zones are normal in mediolateral and ros