ライフサイエンスコーパス: cochlear nucleus

1 of Held excitatory synapse arising from the cochlear nucleus.

2 typically within a single subdivision of the cochlear nucleus.

3 abeling them with injections into the dorsal cochlear nucleus.

4 lls with deafferented neurons in the ventral cochlear nucleus.

5 dantly labeled MOC collaterals which entered cochlear nucleus.

6 uditory nerve fibers onto bushy cells in the cochlear nucleus.

7 synapses on granule cells of the rat dorsal cochlear nucleus.

8 ir cells to refine the tonotopic maps in the cochlear nucleus.

9 , an initiator of apoptotic pathways, in the cochlear nucleus.

10 and form an inhibitory network in the dorsal cochlear nucleus.

11 tions with targets in the cochlea and in the cochlear nucleus.

12 26% showing decreased amounts of GFAP in the cochlear nucleus.

13 al destinations in the cerebellum and dorsal cochlear nucleus.

14 horn of upper cervical spinal segments, and cochlear nucleus.

15 y system from the inferior colliculus to the cochlear nucleus.

16 rneurons in the cerebellar cortex and dorsal cochlear nucleus.

17 dditional projection into the posteroventral cochlear nucleus.

18 ons in the GCD and deep layers of the dorsal cochlear nucleus.

19 ateral superior olive, and SNs in the dorsal cochlear nucleus.

20 tical cells that also project to the ventral cochlear nucleus.

21 to inferior colliculus or the contralateral cochlear nucleus.

22 and interpolaris and provided inputs to the cochlear nucleus.

23 quency excitatory input from the ipsilateral cochlear nucleus.

24 ive direct projections from the deafferented cochlear nucleus.

25 utamatergic synapses in neurons of the chick cochlear nucleus.

26 odies of the calyces, the bushy cells of the cochlear nucleus.

27 put from the contralateral IC and the dorsal cochlear nucleus.

28 ial for normal development of neurons in the cochlear nucleus.

29 colliculus and descending projections to the cochlear nucleus.

30 s project to the inferior colliculus and the cochlear nucleus.

31 There is no PN projection to the dorsal cochlear nucleus.

32 the GCD immediately surrounding the ventral cochlear nucleus.

33 cosities, were observed in many areas of the cochlear nucleus.

34 ultipolar cell regions of the posteroventral cochlear nucleus.

35 nd sensory epithelium and loss of the dorsal cochlear nucleus.

36 that GluA3 plays a role in plasticity in the cochlear nucleus.

37 lls in brain slices from mouse anteroventral cochlear nucleus.

38 ons, which carry the neuronal signals to the cochlear nucleus.

39 ger widespread inhibition in slices of mouse cochlear nucleus.

40 ction potential to convey information to the cochlear nucleus.

41 nto their postsynaptic target neurons in the cochlear nucleus.

42 OC; CNTF and neurturin most abundant in the cochlear nucleus.

43 ir cells and project from the cochlea to the cochlear nucleus.

44 rom the tuberculoventral cells of the dorsal cochlear nucleus.

45 tory nerve via an intermediate neuron in the cochlear nucleus.

46 eurons (cartwheel cells) of the mouse dorsal cochlear nucleus.

47 ibers and spherical bushy cells (BCs) in the cochlear nucleus.

48 ergic transmission in neurons of the chicken cochlear nucleus.

49 onto bushy cells (BCs) in the anteroventral cochlear nucleus.

50 ordings were made from the guinea pig dorsal cochlear nucleus, a cerebellar-like brainstem circuit.

51 in granule cell regions than in the ventral cochlear nucleus, a high density of fibers in some perio

52 Within the ventral cochlear nucleus, a large fraction of principal cells we

53 Although the ventral cochlear nucleus, a mainstream auditory structure, has b

54 ation of micro-magnetic fields to the dorsal cochlear nucleus activates inferior colliculus neurons.

55 The dorsal cochlear nucleus also drove feedforward inhibition to VI

56 urons that extends throughout regions of the cochlear nucleus also extended well beyond the cochlear

57 tergic axons in slices containing the dorsal cochlear nucleus, an auditory brainstem nucleus hypothes

58 xtramural stream (CES) generates the ventral cochlear nucleus and cochlear granule neurons.

59 to a more stable form begins as early as the cochlear nucleus and continues up to auditory cortex.

60 density of serotonergic fibers in the dorsal cochlear nucleus and in granule cell regions than in the

61 ns also accumulated cGMP both in the ventral cochlear nucleus and in the granule cell domain.

62 nt collateral projections to the ipsilateral cochlear nucleus and ipsilateral inferior colliculus.

63 ives excitatory input from the contralateral cochlear nucleus and low-frequency excitatory input from

64 ar (MOC) neurons also project collaterals to cochlear nucleus and make synaptic contacts with dendrit

65 paration containing portions of the cochlea, cochlear nucleus and MNTB, we determined that synaptic i

66 odels, one of chopper neurons in the Ventral Cochlear Nucleus and one of a cortical microcircuit with

67 in stem, octopus cells in the posteroventral cochlear nucleus and principal cells of the medial super

68 topus cells and spherical bushy cells of the cochlear nucleus and principal neurons of the medial nuc

69 r persistent glial activation in the ventral cochlear nucleus and suggest that long-term interaction

70 the endbulbs of Held in the anterior ventral cochlear nucleus and the calyx of Held in the medial nuc

71 ephalic nucleus of the trigeminal nerve, the cochlear nucleus and the superior olivary complex.

72 g an in vitro brain slice preparation of the cochlear nucleus and the superior olivary complex.

73 VCN and PVCN compared with the contralateral cochlear nucleus and unoperated animals, but not compare

74 ne pattern was identified by inputs from the cochlear nucleus and ventral nucleus of the lateral lemn

75 ganglion neurons, reflex interneurons in the cochlear nucleus, and MOC neurons that project to the ou

76 hway was then revealed: it branched from the cochlear nucleus, and via caudal pontine reticular nucle

77 entral auditory system, including the dorsal cochlear nucleus, anteroventral cochlear nucleus, poster

78 Neurons in the avian cochlear nucleus are depolarized by GABAergic synaptic i

79 iculus and the descending projections to the cochlear nucleus arise almost exclusively from separate

80 to an increased central gain upstream of the cochlear nucleus at the level of the lateral lemniscus,

81 , neurturin, artemin, and CNTF-in the OC and cochlear nucleus at various ages from postnatal day 0 (P

82 ed patterns of input to the anterior ventral cochlear nucleus (AVCN) and medial nucleus of the trapez

83 s (age 12-14 months) in the anterior ventral cochlear nucleus (AVCN) depended on sex.

84 ical bushy cells (SBCs) of the anteroventral cochlear nucleus (AVCN) receive their primary excitatory

85 njections of biocytin into the anteroventral cochlear nucleus (AVCN) revealed that although the cochl

86 ojecting to cells in the mouse anteroventral cochlear nucleus (AVCN) using laser-scanning photostimul

87 In contrast, neurons in the anteroventral cochlear nucleus (AVCN) were found to be arranged in a d

88 rons, including neurons of the anteroventral cochlear nucleus (AVCN), depend on afferent input for su

89 y cells (BCs) of the mammalian anteroventral cochlear nucleus (AVCN).

90 w frequency-tuned sites in the anteroventral cochlear nucleus (AVCN).

91 e DCN and various cells in the anteroventral cochlear nucleus (AVCN).

92 FA imaging in dorsal cochlear nucleus brain slices from mice with behavioral

93 y paracrine ATP signalling, as shown for the cochlear nucleus bushy cells and principal neurons in th

94 Previous studies suggest that ventral cochlear nucleus bushy cells may be putative neural cont

95 er auditory nerve fiber terminals contacting cochlear nucleus bushy cells.

96 ut not to innocuous noise, in neurons of the cochlear nucleus, but not in the vestibular or trigemina

97 e identity of MOC reflex interneurons in the cochlear nucleus by assaying their regional distribution

98 o MNTB neurons at E17 and stimulation of the cochlear nucleus can evoke action potentials (APs) and C

99 reflex pathway; however, in this pathway the cochlear nucleus cell type that provides input to MOC ne

100 nt of excitatory somatosensory inputs to the cochlear nucleus, changing their effects on DCN neurons.

101 o delete Atoh1 from different regions of the cochlear nucleus (CN) and accessory auditory nuclei (AAN

102 is represented by increased activity in the cochlear nucleus (CN) and IC and reduced inhibition in t

103 C, we explored the dual projections from the cochlear nucleus (CN) and the spinal trigeminal nucleus

104 Neurons in the ventral cochlear nucleus (CN) are dependent on excitatory affere

105 gic somatosensory and auditory fibers to the cochlear nucleus (CN) are mostly nonoverlapping: project

106 In cochlear nucleus (CN) bushy cells, ATP increases spontan

107 y explored whether optical activation of the cochlear nucleus (CN) elicited responses in neurons in h

108 The mammalian cochlear nucleus (CN) has been a model structure to stud

109 glion-like neurons (ScNs) and mouse auditory cochlear nucleus (CN) neurons to understand whether ScNs

110 topographic connection to the hair cells or cochlear nucleus (CN) neurons.

111 ccurs after removal of afferent input to the cochlear nucleus (CN) of young mammals and birds.

112 The cochlear nucleus (CN) receives innervation from auditory

113 In the cochlear nucleus (CN), the first central relay of the au

114 steroventral (PVCN) and anteroventral (AVCN) cochlear nucleus (CN), the lateral (LSO) and medial (MSO

115 multisensory integration first occurs in the cochlear nucleus (CN), where auditory nerve and somatose

116 The cochlear nucleus (CN), which initiates all ascending aud

117 The cochlear nucleus (CN), which is the first central audito

118 n dramatic neuron death in the anteroventral cochlear nucleus (CN), while the same manipulation perfo

119 ore hearing by electrical stimulation of the cochlear nucleus (CN).

120 neurons (SGNs) and their projections to the cochlear nucleus (CN).

121 magnocellular part of the LRN project to the cochlear nucleus (CN).

122 the cat cochlear spiral ganglion (SG) to the cochlear nucleus (CN).

123 so correlates with tonotopic position in the cochlear nucleus (CN).

124 erences is composed of monaural cells in the cochlear nucleus (CN; nucleus magnocellularis in birds)

125 ates diverse types of neurons, including the cochlear nucleus complex of the auditory system.

126 er ear structures, are also found in the bat cochlear nucleus complex, associated with major fiber tr

127 cell bodies in the guinea-pig anteroventral cochlear nucleus contain GABA, glycine or both (colocali

128 tory nerve (endbulb of Held) synapses in the cochlear nucleus could explain these long-lasting change

129 f cartwheel interneurons in the mouse dorsal cochlear nucleus (DCN) alter the effective convergence r

130 nhibits synaptic AMPA currents in the dorsal cochlear nucleus (DCN) and hippocampus.

131 We evaluated two nuclei, the dorsal cochlear nucleus (DCN) and the medial nucleus of the tra

132 Unipolar brush cells (UBCs) of the dorsal cochlear nucleus (DCN) and vestibular cerebellar cortex

133 Principal neurons (PNs) of the dorsal cochlear nucleus (DCN) are known to be spatially selecti

134 e of neuron birth was observed in the dorsal cochlear nucleus (DCN) beginning on E14.5 and lasts unti

135 The dorsal cochlear nucleus (DCN) consists of many cell types with

136 mulation, it is not yet clear how the dorsal cochlear nucleus (DCN) contributes to patients' hearing

137 ) is induced in fusiform cells of the dorsal cochlear nucleus (DCN) following intense sound exposure

138 Synaptic plasticity in the dorsal cochlear nucleus (DCN) follows Hebbian and anti-Hebbian

139 Circuits in the adult dorsal cochlear nucleus (DCN) have been shown to preserve signa

140 m cartwheel cells (CWCs) of the mouse dorsal cochlear nucleus (DCN) in the auditory brainstem that pr

141 major lines of evidence implicate the dorsal cochlear nucleus (DCN) in tinnitus.

142 The dorsal cochlear nucleus (DCN) integrates auditory nerve input w

143 The dorsal cochlear nucleus (DCN) integrates the synaptic informati

144 The dorsal cochlear nucleus (DCN) is a second-order auditory struct

145 The dorsal cochlear nucleus (DCN) is an auditory brainstem nucleus

146 One possible function of the dorsal cochlear nucleus (DCN) is discrimination of head-related

147 The dorsal cochlear nucleus (DCN) is one of the first stations with

148 The dorsal cochlear nucleus (DCN) is the first neural site of bimod

149 inylated dextran amine (BDA) into the dorsal cochlear nucleus (DCN) of the rat label axons and swelli

150 served at the zinc-rich glutamatergic dorsal cochlear nucleus (DCN) parallel fiber synapses onto cart

151 The dorsal cochlear nucleus (DCN) receives direct tonotopic project

152 Neurons in the dorsal cochlear nucleus (DCN) respond specifically to spectral

153 buting to excitability changes in the dorsal cochlear nucleus (DCN) shortly after exposure to loud so

154 Ascending projections of the dorsal cochlear nucleus (DCN) target primarily the contralatera

155 We investigated this problem in mouse dorsal cochlear nucleus (DCN) where principal cells integrate p

156 te sound-induced hyperactivity in the dorsal cochlear nucleus (DCN), a neural correlate of certain fo

157 T-IR cell bodies were observed in the dorsal cochlear nucleus (DCN), a primary relay to the inferior

158 ions but not in fusiform cells of the dorsal cochlear nucleus (DCN), key brainstem neurons in tinnitu

159 it is unknown whether neurons in the dorsal cochlear nucleus (DCN), the putative tinnitus-induction

160 y (bimodal) integration occurs in the dorsal cochlear nucleus (DCN), where electrical activation of s

161 ngs from pyramidal neurons in the rat dorsal cochlear nucleus (DCN), where intensity selectivity firs

162 bbian LTD in principal neurons of the dorsal cochlear nucleus (DCN).

163 d from principal neurons of the mouse dorsal cochlear nucleus (DCN).

164 al (AVCN), posteroventral (PVCN), and dorsal cochlear nucleus (DCN).

165 a collateral axon to the ipsilateral dorsal cochlear nucleus (DCN).

166 ory integration and plasticity in the dorsal cochlear nucleus (DCN).

167 Additional evidence for cochlear nucleus defects was obtained by electrophysiolo

168 Cochlear nucleus defects were also apparent in mice with

169 lready modulates second order neurons in the cochlear nucleus, e.g. spherical bushy cells (SBCs).

170 Fiber segments were most dense in the dorsal cochlear nucleus (especially in the molecular layer) and

171 In fusiform cells of the dorsal cochlear nucleus, excitatory synapses activate a TTX-sen

172 B neurons and their afferent inputs from the cochlear nucleus express three other members of the Kv1

173 ces of Held, the globular bushy cells of the cochlear nucleus, expressed somatodendritic receptors (a

174 ion was the result of an increased number of cochlear nucleus fibers converging onto one LSO neuron,

175 s of the overall cellular environment of the cochlear nucleus following bilateral cochlear ablation.

176 onto bushy cells in the mouse anteroventral cochlear nucleus following occlusion of the ear canal.

177 hibitory stellate interneurons of the dorsal cochlear nucleus form an electrically coupled network th

178 not so well known is the neural input to the cochlear nucleus from cells containing serotonin that re

179 ough parallel pathways that originate in the cochlear nucleus from different classes of cells.

180 ermore, the axons of SGNs ascending into the cochlear nucleus had disrupted bifurcation patterns.

181 puts to the granule cell domain (GCD) of the cochlear nucleus have been shown to arise from somatosen

182 ated whether multipolar cells of the ventral cochlear nucleus have projections to MOC neurons by labe

183 EN immunostaining was observed in the dorsal cochlear nucleus, hypothalamus, and cortex.

184 haracteristic frequency (LCF) neurons in the cochlear nucleus improve phase-locking precision relativ

185 ithin neurons and glial cells of the ventral cochlear nucleus in adult rats at 1, 7, 15, and 30 days

186 were made into the dorsal subdivision of the cochlear nucleus in order to restrict labeling only to t

187 transmitted along the auditory nerve to the cochlear nucleus in the brainstem (the first relay stati

188 e found in the molecular layer of the dorsal cochlear nucleus, in the small cell cap region, and in t

189 n of brainstem acoustic centers (e.g. dorsal cochlear nucleus, inferior colliculus).

190 Cochlear nucleus, inferior colliculus, and primary audit

191 ise from multiunit responses recorded in the cochlear nucleus, inferior colliculus, auditory thalamus

192 Cochlear nucleus injections retrogradely labeled small g

193 The dorsal cochlear nucleus integrates acoustic with multimodal sen

194 zed with Na(+) channels in the AIS of dorsal cochlear nucleus interneurons and that activation of the

195 AVCN, and contralateral ICc suggest that the cochlear nucleus is a major contributor to SA in the ICc

196 the serotoninergic projection pattern to the cochlear nucleus is divergent and non-specific.

197 ditory brainstem as early as E15.5, when the cochlear nucleus is still immature.

198 The cochlear nucleus is the site of the first synapse in the

199 The cochlear nucleus is well known as an obligatory relay ce

200 In the dorsal cochlear nucleus, long-term synaptic plasticity can be i

201 nd chickens, Kv3.1 mRNA was expressed in the cochlear nucleus magnocellularis (NM) and the nucleus la

202 The avian cochlear nucleus magnocellularis (NM) integrates excitat

203 In birds, cochlear nucleus magnocellularis (NM) neurons encode the

204 gether, these factors improve the ability of cochlear nucleus magnocellularis neurons to faithfully t

205 e synapses in the rostromedial region of the cochlear nucleus magnocellularis of the chick.

206 f bushy cells of the mammalian anteroventral cochlear nucleus, maintain high [Cl-]i and depolarize in

207 Neural output from the cochlear nucleus measured at 10 dB above threshold is re

208 Fluorogold injections resulted in labeled cochlear nucleus multipolar neurons.

209 les, and identified transynaptically labeled cochlear nucleus neurons at multiple survival times.

210 role in deafferentation-induced apoptosis of cochlear nucleus neurons during a developmental critical

211 rs between microglial cells and deafferented cochlear nucleus neurons following bilateral cochlear ab

212 in vivo multichannel spike trains of dorsal cochlear nucleus neurons to disentangle reciprocal and f

213 provided observation of spiral ganglion and cochlear nucleus neurons to facilitate targeted electrop

214 synaptic inputs from ipsi- and contralateral cochlear nucleus neurons.

215 magnocellularis (NM; a division of the avian cochlear nucleus) neurons as detected by immunocytochemi

216 on, Kuo and Trussell show that in the dorsal cochlear nucleus, noradrenaline functions to simultaneou

217 Approximately 20-30% of neurons in the avian cochlear nucleus, nucleus magnocellularis (NM) die follo

218 The chick cochlear nucleus, nucleus magnocellularis (NM), exhibits

219 the death of 30% of the neurons in the chick cochlear nucleus, nucleus magnocellularis (NM).

220 and distribution of IL-1beta in the ventral cochlear nucleus of ablated animals was temporally and s

221 reported to modify neuronal activity in the cochlear nucleus of adult rats.

222 s were made from single-units in the ventral cochlear nucleus of anesthetized guinea pigs in response

223 Recording from single neurons in the cochlear nucleus of anesthetized guinea pigs, we show th

224 h is highly conserved in vertebrates, in the cochlear nucleus of chicken embryos.

225 s a precise tonotopic pattern in the ventral cochlear nucleus of developing gerbils.

226 itory nerve synapses onto bushy cells in the cochlear nucleus of mice of both sexes.

227 Cx36 expression is absent in the cochlear nucleus of normal mice, which have high-frequen

228 '-cyclic monophosphate (cGMP) pathway in the cochlear nucleus of Sprague-Dawley rats.

229 re recorded from single units in the ventral cochlear nucleus of the anaesthetised guinea-pig in resp

230 (IHCs) and transmit that information to the cochlear nucleus of the brainstem.

231 ce of pontine noradrenergic afferents to the cochlear nucleus of the cat.

232 In the cochlear nucleus of this knockout, 5-HT-IR cell bodies w

233 suggested that synaptic transmission in the cochlear nucleus of young chicks may undergo further dev

234 injected biotinylated dextran amine into the cochlear nucleus or dorsal root ganglion (DRG) at the se

235 r than 2% of the cells that projected to the cochlear nucleus or to the inferior colliculus.

236 abeled fiber segments in subdivisions of the cochlear nucleus other than the dorsal cochlear nucleus,

237 Compared to other ventral cochlear nucleus output neurons, bushy cells show high f

238 ggest that NO is a signaling molecule in the cochlear nucleus, perhaps functioning in both a paracrin

239 These data suggest that cochlear nucleus planar multipolar neurons drive the MOC

240 g the dorsal cochlear nucleus, anteroventral cochlear nucleus, posteroventral cochlear nucleus, some

241 increased spontaneous firing rate in dorsal cochlear nucleus principal neurons, fusiform cells.

242 ultipolar neurons of the ipsilateral ventral cochlear nucleus, principal neurons of the ipsilateral m

243 Unknown interneurons in the ventral cochlear nucleus project either directly or indirectly t

244 Lesions involving the posteroventral cochlear nucleus (PVCN), but not the other subdivisions,

245 that develop tinnitus and only in the dorsal cochlear nucleus regions that are sensitive to high freq

246 f fibers in the fusiform layer of the dorsal cochlear nucleus relative to surrounding layers and a re

247 ect to inferior colliculus and contralateral cochlear nucleus, respectively.

248 t specialized auditory nerve synapses in the cochlear nucleus results from many release sites (N), hi

249 teroventral cochlear nucleus, posteroventral cochlear nucleus, some divisions of the superior olivary

250 gests that it originates from posteroventral cochlear nucleus stellate/multipolar neurons.

251 sole, sources of serotonin within the dorsal cochlear nucleus subdivision are known to be the dorsal

252 i, sources of serotonin located within other cochlear nucleus subdivisions are not currently known.

253 mporal fidelity seen across the eighth nerve/cochlear nucleus synapse.

254 two major projection neurons of the ventral cochlear nucleus, the bushy and T-stellate cells, receiv

255 In the ventral cochlear nucleus, the first central station along the au

256 twheel inhibitory interneurons of the dorsal cochlear nucleus, the likelihood of bursts and the inter

257 These results show that at the level of the cochlear nucleus there exists sufficient information in

258 In the cochlear nucleus, there is a magnocellular core of neuro

259 rge spherical cell area of the anteroventral cochlear nucleus; they were moderately dense in the smal

260 ry inputs and projects in turn to the dorsal cochlear nucleus, thus appearing to serve as a central l

261 of sound in the human auditory pathway from cochlear nucleus to cortex.

262 it the dorsal acoustic stria of the injected cochlear nucleus to cross the brainstem in the dorsal ha

263 merged with a normalized 3D template of the cochlear nucleus to demonstrate quantitatively that the

264 chlear nucleus also extended well beyond the cochlear nucleus to include at least the superior olivar

265 old was injected into inferior colliculus or cochlear nucleus to label T-stellate and D-stellate neur

266 ls, are a source of ascending input from the cochlear nucleus to the LSO.

267 of commissural neurons that project from one cochlear nucleus to the other were studied after labelin

268 changes in calretinin immunostaining in the cochlear nucleus, unilateral cochlear ablations were per

269 spinal trigeminal neurons projecting to the cochlear nucleus using the retrograde tracer, Fast Blue,

270 comparable states for neurons of the ventral cochlear nucleus (VCN) and medial nucleus of the trapezo

271 a (VAS) are primarily located in the ventral cochlear nucleus (VCN) and project bilaterally to the su

272 1 gene, is expressed strongly in the ventral cochlear nucleus (VCN) and the medial nucleus of the tra

273 Ventral cochlear nucleus (VCN) axons normally project to the med

274 T-stellate cells in the ventral cochlear nucleus (VCN) form an ascending pathway that co

275 n the projections from the mammalian ventral cochlear nucleus (VCN) is essential for sound localizati

276 The main source of excitation to the ventral cochlear nucleus (VCN) is from glutamatergic auditory ne

277 ge patterns of single units from the ventral cochlear nucleus (VCN) of anaesthetized guinea-pigs in r

278 In the auditory brainstem, the ventral cochlear nucleus (VCN) projects to the contralateral but

279 ar cells are multipolar cells in the ventral cochlear nucleus (VCN) that project a collateral axon to

280 Neurons in the ventral cochlear nucleus (VCN) that respond primarily at the ons

281 organization of projections from the ventral cochlear nucleus (VCN) to the ventral nucleus of the lat

282 , even at its earliest stages in the ventral cochlear nucleus (VCN).

283 he ear, the bushy cells (BCs) of the ventral cochlear nucleus (VCN).

284 ents bushy cell projections from the ventral cochlear nucleus (VCN).

285 recording spikes from neurons in the ventral cochlear nucleus (VCN).

286 They enter the opposite cochlear nucleus via the dorsal and ventral acoustic str

287 The terminal field in the cochlear nucleus was concentrated in the subpeduncular c

288 in the pontine tegmentum that project to the cochlear nucleus was determined with retrograde tract tr

289 perior olivary complex, and divisions of the cochlear nucleus was generally sparse; thus a clear topo

290 -1 immunostaining of microglial cells in the cochlear nucleus was observed at all survival times afte

291 CNTF and neurturin expression in the cochlear nucleus was unaffected by deafening or age.

292 f the cochlear nucleus other than the dorsal cochlear nucleus, we concluded that the serotoninergic p

293 n of extracellular zinc levels in the dorsal cochlear nucleus, we determined the tonic zinc levels to

294 In brain slices containing the dorsal cochlear nucleus, we reveal a tinnitus-specific increase

295 iched auditory brainstem nucleus--the dorsal cochlear nucleus--we discovered that synaptic Zn(2+) and

296 and the mean gray levels within cells of the cochlear nucleus were observed at 1, 7, and 15 days comp

297 We have investigated this in the mouse cochlear nucleus, where auditory nerve (AN) fibers conta

298 additional projection into the anteroventral cochlear nucleus, whereas dorsally placed injections had

299 by comparing bushy cells (BCs) in the mouse cochlear nucleus with T-stellate cells (SCs), which do h

300 pses (endbulb synapses) in the anteroventral cochlear nucleus, yet the specific roles of GluA3 in the