ライフサイエンスコーパス: monosynaptic

1 majority of responses from area 3a were non-monosynaptic.

2 amage also shaped the relative prevalence of monosynaptic A- versus C-fiber-mediated input to mature

3 ents, bypass local circuitry and have direct monosynaptic access to neurons projecting to brainstem a

4 e via mutual projections that give each area monosynaptic access to the other area's CSPs.

5 ional transmission was chiefly restricted to monosynaptic actions.

6 ation induced unmasking and strengthening of monosynaptic Adelta drive to lamina I NK1R(+) neurons ma

7 ofold) and magnitude (by 75% in a subset) of monosynaptic Adelta-fiber but not monosynaptic C-fiber-e

8 ut (69%) with a smaller proportion receiving monosynaptic Adelta-fiber input (28%).

9 s revealed that a proportion received silent monosynaptic Adelta-fiber input, suggesting that these m

10 sults of the present study indicate that the monosynaptic afferent input to mitral cells depends on t

11 lomerulus revealed that mitral cells receive monosynaptic afferent inputs.

12 virus in a transgenic Gpr151-Cre mouse line, monosynaptic afferents of habenular and thalamic Gpr151-

13 l activity by timing the neuronal firing via monosynaptic afferents, thalamic nuclei act as a relay s

14 rograde labeling in the amgBST compared with monosynaptic and 48-hour cases, whereas MEAad-injected c

15 nism that depends on the activity balance of monosynaptic and disynaptic pathways to inhibitory neuro

16 d and new M1 generated putative long-latency monosynaptic and non-monosynaptic effects; the majority

17 The sensory to motor pathways are monosynaptic and oligosynaptic in this system, thus prov

18 ponses likely reflecting a mixture of slower monosynaptic and oligosynaptic pathways.

19 ns in three anesthetized monkeys revealed no monosynaptic and only one weak oligosynaptic EPSP after

20 ndicate that PPG neurons receive significant monosynaptic and polysynaptic input from brain regions i

21 cNTS PPG neurons in mice receive widespread monosynaptic and polysynaptic input from brain regions i

22 Monosynaptic and polysynaptic inputs specific to cNTS PP

23 (R)-CPP, GluN2A/B antagonists, blocked both monosynaptic and polysynaptic NMDA EPSCs initiated by pr

24 lamina III projection cells receive powerful monosynaptic and polysynaptic nociceptive input.

25 tion of synaptic NMDA receptors expressed in monosynaptic and polysynaptic pathways from peripheral s

26 Communication capacity via monosynaptic and polysynaptic pathways, in aggregate, la

27 and confirms their functional connection via monosynaptic and polysynaptic pathways.

28 mulation of excitatory afferents evoked both monosynaptic and polysynaptic responses distributed in t

29 Using monosynaptic and polysynaptic viral tracers, we found th

30 here were no significant differences between monosynaptic and PRV cases in the subnuclear distributio

31 in the central and medial extended amygdala, monosynaptic and transneuronal viral tracing experiments

32 n receptor, which allowed a demonstration of monosynaptic anterograde tracing from defined cells.

33 mined with network analysis tools applied to monosynaptic association (within one side) and commissur

34 ted that CFA inflammation reduced ADS in the monosynaptic C fiber input to lamina I neurokinin 1 rece

35 Control neurons predominantly received monosynaptic C-fiber input (69%) with a smaller proporti

36 subset) of monosynaptic Adelta-fiber but not monosynaptic C-fiber-evoked responses.

37 , possibly via the release of glutamate from monosynaptic C1 inputs.

38 I (ECII)-->dentate gyrus-->CA3-->CA1 and the monosynaptic circuit ECIII-->CA1 have been considered th

39 The monosynaptic circuit revealed here provides a neural sub

40 st, light inhibits pumping via the I2 neuron monosynaptic circuit.

41 opamine currents were separated into a fast, monosynaptic component and a slower-rising and decaying

42 that part of this locomotor drive involved a monosynaptic component coming directly from the lumbar l

43 ation (LTF) [6], which can be induced in the monosynaptic connection between Aplysia sensory and moto

44 gly, we uncovered a hitherto uncharacterized monosynaptic connection between cranial sensory neurons

45 onjugated cholera toxin subunit B, support a monosynaptic connection between these areas and poses th

46 ally assisted circuit mapping demonstrates a monosynaptic connection between these cholinergic neuron

47 e of a direct Cajal-Retzius cell-interneuron monosynaptic connection.

48 - to fourfold higher than the probability of monosynaptic connections among corticocortical or cortic

49 We first found that the frequency of monosynaptic connections among corticostriatal pyramidal

50 -induced intramembrane proteolysis to reveal monosynaptic connections arising from genetically labele

51 significantly increased numbers of putative monosynaptic connections between PhMNs and these sprouti

52 d with two-photon microscopy to characterize monosynaptic connections between the Purkinje cells of j

53 ss-correlations in these preparations showed monosynaptic connections from 16/19 (84%) of EBSNs, but

54 le-cell patch recording was used to test for monosynaptic connections from hilar GPHNs to granule cel

55 , but not the reverse, reflecting the direct monosynaptic connections from the PFC to STR.

56 ll types within the S1 cortex receive direct monosynaptic connections from these input sources.

57 found that corticoclaustral afferents formed monosynaptic connections onto both ClaC neurons and PV i

58 uron seen in nonprimates and the fast direct monosynaptic connections present in new M1.

59 even cortico-motoneuronal cells, which make monosynaptic connections to alpha-motoneurons, can becom

60 om vibrissa sensory afferent fibers and send monosynaptic connections to facial nucleus motoneurons t

61 re identified as likely premotor cells, with monosynaptic connections to motoneurons.

62 ticospinal tract in Old World primates makes monosynaptic connections to motoneurons; previous anatom

63 Monosynaptic connections were confirmed by measures of t

64 eshold mechanoreceptor (LTMR) input and form monosynaptic connections with GRPR neurons.

65 Stretch-sensitive Ia afferent monosynaptic connections with motoneurons form the stret

66 s in the primary motor cortex (M1) that make monosynaptic connections with motoneurons innervating sh

67 cells in the primary motor cortex (M1) have monosynaptic connections with motoneurons.

68 LGN afferents made monosynaptic connections with pyramidal (Pyr) and fast-s

69 axon, which forms anatomical and functional monosynaptic connections with the A08a lateral dendrite.

70 s (up to 90), helped us to identify apparent monosynaptic connections, confirming the excitatory and

71 e lOFC sends requisite input to the BLA, via monosynaptic connections, to promote CS-induced cocaine-

72 dition to putative excitatory and inhibitory monosynaptic connections, we uncovered prominent millise

73 ory afferents and motoneurons typically form monosynaptic connections, while neurons innervating anta

74 euron spike cross-correlations that indicate monosynaptic connections.

75 3 pyramidal cells at a latency indicative of monosynaptic connections.

76 uction in detected excitatory and inhibitory monosynaptic connections.

77 the subcortical targets with which they make monosynaptic connections.

78 s through two functionally distinct types of monosynaptic connections: (1) dendrodendritic synapses o

79 systematic biases in both their intralaminar monosynaptic connectivity and the post-synaptic partners

80 revealed short latency events indicative of monosynaptic connectivity between the inferior frontal g

81 in Sema3E and its receptor Plexin-D1 prevent monosynaptic connectivity in the cutaneous maximus muscl

82 the sensory response properties and upstream monosynaptic connectivity of cells mediating the CC or C

83 al rs-fMRI connectivity patterns that mirror monosynaptic connectivity with isocortex.

84 ncy (<20 ms) interneuron spiking, indicating monosynaptic connectivity, but firing probability progre

85 trains confirmed a fast and precisely timed monosynaptic connectivity, supporting the notion that SI

86 ary motor cortex ("new M1") and area 3a make monosynaptic cortico-motoneuronal connections with limb

87 ays afforded by the preceding elaboration of monosynaptic corticobulbar tracts, giving rise to enhanc

88 reveal any postspike effects consistent with monosynaptic corticomotoneuronal connections.

89 with weaker interneuron activity and reduced monosynaptic coupling between excitatory and inhibitory

90 count for this, we find that, in addition to monosynaptic coupling, PV-MSN interactions are mediated

91 Optogenetic activation of this monosynaptic craniofacial-to-PBL projection induced robu

92 significant glycinergic inputs for mediating monosynaptic crossover inhibition.

93 We compared monosynaptic CST amplitude input to segmental circuits w

94 e coronal slices containing V1, and recorded monosynaptic currents from excitatory and inhibitory neu

95 ation-specific interactions predicted by the monosynaptic distribution of horizontal connections.

96 spinal fibers from old M1 generate weak late monosynaptic effects in motoneurons.

97 d putative long-latency monosynaptic and non-monosynaptic effects; the majority of responses from are

98 he frequency of mEPSCs and the amplitudes of monosynaptic EPSCs evoked from the dorsal root and puff

99 ine significantly increased the amplitude of monosynaptic EPSCs evoked from the dorsal root and the f

100 nd long-lasting increase in the amplitude of monosynaptic EPSCs evoked from the dorsal root in approx

101 th oxotremorine-M decreased the amplitude of monosynaptic EPSCs in approximately 67% of neurons but i

102 /M4 double-KO mice, oxotremorine-M inhibited monosynaptic EPSCs in significantly fewer neurons ( appr

103 but increased the paired pulse ratio of the monosynaptic EPSCs in SNr GABA neurons, indicating a pre

104 rements exploiting the voltage dependence of monosynaptic EPSCs similarly indicated dominant expressi

105 inine on glycinergic IPSCs but not on evoked monosynaptic EPSCs.

106 t to prevent excessive depolarization by the monosynaptic EPSP and multiple action potential firings.

107 ve fields anywhere on the head evoked large, monosynaptic EPSPs ( approximately 5-20 mV) in tINs, at

108 ul inhibition by Purkinje cells or by direct monosynaptic excitation from the inferior olive.

109 ns from the pedunculopontine nucleus induced monosynaptic excitation in most recorded striatal cholin

110 nto CA3 pyramidal cells (PCs) provide strong monosynaptic excitation that exhibit prominent facilitat

111 al and electrosensory afferents elicit local monosynaptic excitation, quickly followed by inhibition

112 ifferentially influences the balance between monosynaptic excitatory and disynaptic inhibitory cortic

113 Monosynaptic excitatory connections from pyramidal cells

114 al retrosplenial cortex (RSC) and these form monosynaptic excitatory connections onto a wide spectrum

115 Axons from RSC formed monosynaptic excitatory connections onto M2 pyramidal ne

116 lls born before SE form functional recurrent monosynaptic excitatory connections with other granule c

117 nto BG output neurons sometimes precedes the monosynaptic excitatory drive from cortical afferents.

118 Hence, monosynaptic excitatory lemniscal TC connections onto la

119 SNAP significantly reduced the amplitude of monosynaptic excitatory postsynaptic currents (EPSCs) ev

120 ts in small DRG neurons and the amplitude of monosynaptic excitatory postsynaptic currents of dorsal

121 ased HVACC currents in small DRG neurons and monosynaptic excitatory postsynaptic currents of spinal

122 tion of corticoclaustral afferents generated monosynaptic excitatory responses as well as disynaptic

123 ls of double-projecting vCA1 neurons induced monosynaptic excitatory responses in both the mPFC and b

124 y coupled to all of the CPG neurons and made monosynaptic excitatory synapses with both Si3s.

125 nes in the principal olivary nucleus receive monosynaptic extra-somatic glutamatergic input from the

126 ysis, an approach that enables assessment of monosynaptic extracellular currents generated in differe

127 that layer 2/3 Pyr cells receive excitatory monosynaptic FF and FB inputs, which are opposed by disy

128 descending glutamatergic signal, most likely monosynaptic, from the MLR to the reticular formation th

129 e obtained from layer V pyramidal cells, and monosynaptic GABA(A) receptor-mediated IPSCs were elicit

130 n cells in specific layers and elicit robust monosynaptic GABAergic and nicotinic postsynaptic curren

131 ing activation of MS axons, we observed fast monosynaptic GABAergic IPSPs in the majority (>60%) of f

132 Photostimulation of MCH projections evoked a monosynaptic glutamate release in the LS.

133 ulation of cholinergic interneurons triggers monosynaptic glutamate- and acetylcholine-mediated curre

134 parafascicular inputs evokes suprathreshold monosynaptic glutamatergic excitation in NGF interneuron

135 d that VTA-glutamate neurons receive a major monosynaptic glutamatergic input from the lateral hypoth

136 ation, to demonstrate that the activation of monosynaptic glutamatergic projections from anterior ins

137 Chemogenetic disconnection of monosynaptic glutamatergic vCA1 to mPFC projections usin

138 ntifies a novel neural pathway through which monosynaptic glutamatergic ventral hippocampal field CA1

139 re, we found that the mPFC provides a direct monosynaptic, glutamatergic drive to both DRN 5-HT and G

140 tINs produce small ( approximately 2-6 mV), monosynaptic, glutamatergic EPSPs in the hindbrain retic

141 vation of BLA terminals in the vHPC provided monosynaptic, glutamatergic inputs to vHPC pyramidal neu

142 and pyramidal tract (PT) dendrites, whereas monosynaptic hippocampal input primarily targeted IT, bu

143 the surround suppression through long-range monosynaptic horizontal spread.

144 types of fusimotor drive that transform the monosynaptic Ia afferent feedback into task-dependent co

145 types of spinal interneurons (propriospinal, monosynaptic Ia-excitatory, reciprocal Ia-inhibitory, Re

146 mitted across first-order synapses, probably monosynaptic, in the spinal cord.

147 f the substantia nigra that provide a robust monosynaptic inhibition of DA neurons.

148 entorhinal cortex (LEC) inputs, abGCs exert monosynaptic inhibition of mature granule cells (mGCs) t

149 OFF cone BCs mediate monosynaptic inhibition of rod BCs via motif C3 driven b

150 ncing widespread, GABA(B) receptor-mediated, monosynaptic inhibition.

151 om the auditory cortex and these form direct monosynaptic inhibitory connections onto lateral amygdal

152 collaterals; but reveal both excitatory and monosynaptic inhibitory currents in the ventral pallidum

153 thermore, continuous connections can undergo monosynaptic inhibitory LTP, independent of excitatory d

154 fference in the amplitude of stimulus-evoked monosynaptic inhibitory postsynaptic potentials (IPSPs)

155 ic SACs produced a GABA(A) receptor-mediated monosynaptic inhibitory response, followed by DA-D(1)-li

156 In contrast, tetanization elicited LTP of monosynaptic inhibitory responses in continuous, but not

157 m spiny projection neuron (MSN) activity via monosynaptic inhibitory signaling.

158 ell (NAcSh) MSNs was fine-tuned by GABAergic monosynaptic innervation from adjacent fast-spiking inte

159 e vast majority of NTS LepR neurons received monosynaptic innervation from vagal afferent fibers and

160 d disynaptic pathways to inhibitory neurons: Monosynaptic input causes more powerful oscillations whe

161 stablish that inhibitory SG neurones receive monosynaptic input from a subset of unmyelinated primary

162 rons, which included a greater prevalence of monosynaptic input from low-threshold A-fibers when prec

163 emonstrate that mitral cells receive direct, monosynaptic input from olfactory receptor neurons.

164 , a ventral striatum structure that receives monosynaptic input from the olfactory bulb, is uniquely

165 n though some of these cells received potent monosynaptic input from the same LGNd neurons whose rate

166 hibits feeding when excited by touch-induced monosynaptic input from the second type of interneuron,

167 The most prominent sources of PPG monosynaptic input include the lateral (LH) and paravent

168 hilus and stratum lucidum receive this dual monosynaptic input on MF stimulation.

169 g corticospinal projections providing direct monosynaptic input to alpha-motoneurons.

170 titative brain-wide map of neurons providing monosynaptic input to KNDy cells, as well as identify th

171 Over 90% of monosynaptic input to KNDy neurons originated from hypot

172 monstrated that NI GABAergic neurons receive monosynaptic inputs from brain areas processing importan

173 ubpopulation of BA neurons receives stronger monosynaptic inputs from context-responding vCA1 neurons

174 e contralateral somatosensory cortex receive monosynaptic inputs from grafted neurons.

175 rd, we show that connections compatible with monosynaptic inputs from mechanosensory Rohon-Beard neur

176 rons in all layers of MEC receive convergent monosynaptic inputs from PrS and PaS and second, that el

177 (TC) recipient areas receive weak but direct monosynaptic inputs from the thalamus.

178 ) to selectively identify and quantify their monosynaptic inputs in vivo.

179 To understand how monosynaptic inputs onto adult-born dentate granule cell

180 s were explained by changes in the weight of monosynaptic inputs received by interneurons from new py

181 d a strategy to genetically target and trace monosynaptic inputs to a single neuron in vitro and in v

182 Here we describe the monosynaptic inputs to a subpopulation of mouse S1 inhib

183 Rabies tracing of monosynaptic inputs to A1 L6 CT neurons revealed a narro

184 ieved to not project to CA2, send functional monosynaptic inputs to CA2 pyramidal cells through abund

185 tion, to characterize the firing patterns of monosynaptic inputs to dopamine neurons while mice perfo

186 Furthermore, we obtain brain-wide maps of monosynaptic inputs to MCH and OH cells, and demonstrate

187 ole-brain light-sheet imaging, we mapped the monosynaptic inputs to midbrain dopamine neurons project

188 e a powerful system for revealing the direct monosynaptic inputs to specific cell types in Cre-expres

189 cally targeted viral tracing to identify the monosynaptic inputs to the projection neurons of layer I

190 e, we comprehensively identified each area's monosynaptic inputs using the rabies virus.

191 c insult that generates prominent excitatory monosynaptic inputs, both local recurrent and widespread

192 eurons, profoundly affected their pattern of monosynaptic inputs.

193 ies virus results in unambiguous labeling of monosynaptic inputs.

194 ead transsynaptically and label their direct monosynaptic inputs.

195 defined neuronal cell types and their direct monosynaptic inputs.

196 mined laminar distribution does not preclude monosynaptic interaction with neurons located in deeper

197 9% of sites), minimal focal shocks activated monosynaptic IPSCs at fixed latency (low jitter) that of

198 However, LSP4-2022 also reduced evoked monosynaptic IPSCs in CA1 pyramidal cells and, in contra

199 ation of GABAergic LH --> PVH fibers induced monosynaptic IPSCs in PVH neurons, and potently increase

200 No monosynaptic IPSPs could be recorded in the presence of

201 nsmission, we evoked GABAA receptor-mediated monosynaptic IPSPs in deep cerebellar nuclei neurons by

202 rons in the LGN in a pattern consistent with monosynaptic labeling of koniocells, rather than disynap

203 ippocampal long-term potentiation, through a monosynaptic LH(GABA) to CA3(GABA) projection.

204 57) occurred at latencies compatible with a monosynaptic linkage, including in motoneurons projectin

205 r long-latency monosynaptic (n = 108) or non-monosynaptic linkages (n = 108).

206 Monosynaptic mossy fiber inputs to fast-spiking basket c

207 of oculomotor activation, comparable to the monosynaptic motor-evoked potential evoked by TMS of pri

208 es as likely mediated by either long-latency monosynaptic (n = 108) or non-monosynaptic linkages (n =

209 Antidromic (n=35), monosynaptic (n=2), di-or tri-synaptic (n=18) and long-l

210 enetic activation of this projection elicits monosynaptic nicotinic and GABAergic currents in glomeru

211 N2B antagonist, caused modest suppression of monosynaptic NMDA EPSC amplitudes, but had a widely vari

212 In contrast, there is no evidence of monosynaptic nonvisual inputs to the superficial layers.

213 Excitatory postsynaptic currents (EPSCs) in monosynaptic nTS neurons were recorded in the horizontal

214 ST shocks activated EPSCs along monosynaptic or polysynaptic pathways.

215 ssed by application of serotonin leaving the monosynaptic output of GABAergic cells unaffected.

216 ortex and sensory pathways and, in turn, has monosynaptic outputs to spinal motorneurons.

217 e identified and characterized a nigro-vagal monosynaptic pathway in rats that controls gastric tone

218 n the trigeminal motor nucleus, suggesting a monosynaptic, possibly proprioceptive, pathway.

219 Here we report the discovery of a monosynaptic prefrontal cortex (predominantly anterior c

220 Our results confirm the concept that the monosynaptic projection between HC and mPFC contributes

221 Here, we optogenetically silenced the direct monosynaptic projection from ventral/intermediate hippoc

222 Hence, we hypothesized that monosynaptic projections between these brain regions med

223 Our results demonstrate that monosynaptic projections from hippocampus to mPFC contri

224 we show that glutamatergic and, most likely, monosynaptic projections from the MLR activate stop cell

225 Here we investigate the role of monosynaptic projections from ventral/intermediate hippo

226 the whether any contribution is via direct, monosynaptic projections, or the direction of informatio

227 Monosynaptic rabies tracing of the presynaptic organizat

228 Monosynaptic rabies tracing reveals that CC neurons pref

229 dent single-cell transcriptomic analyses and monosynaptic rabies tracing to compare mouse primary vis

230 veloped a complementary targeting system for monosynaptic rabies virus (RV) tracing that identifies d

231 Surprisingly, experiments using monosynaptic rabies virus showed that proopiomelanocorti

232 ion segregation in these circuits, we used a monosynaptic rabies virus system to generate brain-wide

233 We used the monosynaptic rabies virus system, in conjunction with mi

234 We used a monosynaptic rabies virus to define the circuit's functi

235 We employed cell-type-specific monosynaptic rabies virus tracings to characterize affer

236 Using a monosynaptic rabies virus-based tracing technique, we st

237 Using a modified monosynaptic rabies virus-based transsynaptic tracing st

238 Using a monosynaptic rabies viruses-based transneuronal tracing

239 ults are therefore critical for interpreting monosynaptic rabies-based tracing in the sensory system.

240 crucial prerequisite of spoken language: (i) monosynaptic refinement of the projections of motor cort

241 g systems, inducing hyperexcitability of the monosynaptic reflex.

242 l circuits leads to hyperexcitability of the monosynaptic reflex.

243 IC and the lateral hypothalamus (LH) with a monosynaptic relay in the CeA and shed new light on the

244 macological sensitivity, our results suggest monosynaptic release of both GABA and ACh.

245 lation of SuM(vgat/vglut2) terminals elicits monosynaptic release of both glutamate and GABA onto den

246 We found that commissural inputs evoked monosynaptic responses in both intratelencephalic (IT) a

247 ated a rapid and substantial decrease in the monosynaptic responses recorded at the first central sta

248 t connectivity of newborn Tau(VLW) DGCs, and monosynaptic retrograde rabies virus tracing showed that

249 ectroporation of DNA to target infection and monosynaptic retrograde spread of a genetically modifiab

250 nitial rabies virus infection and subsequent monosynaptic retrograde spread.

251 he B-subunit of the cholera toxin which is a monosynaptic retrograde tracer was used as a control to

252 Rabies-mediated monosynaptic retrograde tracing identified the central n

253 e developed a modified rabies virus-mediated monosynaptic retrograde tracing method to interrogate pr

254 Using rabies virus -mediated monosynaptic retrograde tracing to label the inputs and

255 ghput single-cell transcriptional profiling, monosynaptic retrograde tracing, and multiplexed FISH to

256 n to demonstrate cell-specific infection and monosynaptic retrograde transport of virus, which strong

257 analyses show diminished EPSP amplitudes in monosynaptic sensory-motor circuits in these mutants.

258 neurons is required for synapse formation in monosynaptic sensory-motor circuits.

259 oper synapse formation in the development of monosynaptic sensory-motor circuits.

260 anisms underlying synapse formation in these monosynaptic sensory-motor connections are unknown.

261 o GTPase Cdc42 controls synapse formation in monosynaptic sensory-motor connections in presynaptic, b

262 ctive role in the establishment of patterned monosynaptic sensory-motor connections.

263 d that firing of individual CHIs resulted in monosynaptic spontaneous inhibitory post-synaptic curren

264 rgent ST afferent inputs (22% two; 14% three monosynaptic ST-EPSCs).

265 -CTB neuronal transport was target specific, monosynaptic, stable for several weeks, and reproducible

266 and weak oscillations; in contrast, stronger monosynaptic stimulation (e.g., suppressive contextual s

267 el predicted characteristic contributions to monosynaptic stLFP signatures both for the regular-spiki

268 s finding suggests that twitches trigger the monosynaptic stretch reflex and, by doing so, contribute

269 ico-striatal pathways, emerges primarily via monosynaptic structural connections.

270 m rs-fMRI in female mice with the underlying monosynaptic structural connectome as provided by the Al

271 bellum identified brainstem neurons that are monosynaptic targets of inhibition from the cerebellar f

272 rt and non-alert EEG states, we examined the monosynaptic TC responses and short-term synaptic dynami

273 no state-related changes in the amplitude of monosynaptic TC responses when TC spikes with similar pr

274 However, monosynaptic TC synaptic transmission has not been direc

275 To probe monosynaptic thalamic activation of cortical postsynapti

276 f the focal LFP signature of the single-axon monosynaptic thalamocortical connection as measured by s

277 than 1.2 ms were classified as definitively monosynaptic; these were seen only after stimulation wit

278 eling of contralateral LVST neurons within a monosynaptic time window all indicate an overwhelmingly

279 Recently anterograde polysynaptic and monosynaptic tracers were developed from H129 and have b

280 Retrograde monosynaptic tracing and electrophysiological whole-cell

281 Glycoprotein-deleted rabies virus-mediated monosynaptic tracing has become a standard method for ne

282 Rabies virus-based monosynaptic tracing has been used to identify neuronal

283 vering DNA plasmids that allowed retrograde, monosynaptic tracing of each neuron's presynaptic inputs

284 ion of genetically specified neurons and (4) monosynaptic tracing of neuronal inputs.

285 Here, we use G-deleted rabies virus-mediated monosynaptic tracing to identify inputs to excitatory an

286 The development of retrograde monosynaptic tracing vectors has enabled visualization o

287 Retrograde monosynaptic tracing with rabies virus reveals that this

288 rus (RABV) has been the reagent of choice in monosynaptic tracing, since it permits the mapping of sy

289 Using rabies virus monosynaptic tracing, we mapped cocaine-induced global c

290 Using in vivo electroporation and monosynaptic tracing, we show that postnatal-born granul

291 Finally, using rabies-virus-assisted monosynaptic tracing, we show that the GPh is embedded i

292 ersectional labeling method and rabies viral monosynaptic tracing, which enables subtype-specific vis

293 efficient and prolonged photostimulation of monosynaptic transmission at the neuromuscular junction

294 This monosynaptic transmission exhibits high fidelity in resp

295 ad short latency excitation, compatible with monosynaptic transmission over fast-conducting pathways,

296 o demonstrate a progressive delay of C fiber monosynaptic transmission to the spinal cord that is sim

297 , including both muscle stretch encoding and monosynaptic transmission, could be separated from other

298 Monosynaptic transsynaptic rabies tracing indicated the

299 Additionally, PPG neurons receive monosynaptic vagal sensory input from the nodose ganglia

300 reflexes (SRs) in ventral roots, presumably monosynaptic, were evoked by electrical stimulation of a