ライフサイエンスコーパス: cochlear nucleus

1 lls with deafferented neurons in the ventral cochlear nucleus.

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

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

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

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

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

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

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

9 26% showing decreased amounts of GFAP in the cochlear nucleus.

10 al destinations in the cerebellum and dorsal cochlear nucleus.

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

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

13 rneurons in the cerebellar cortex and dorsal cochlear nucleus.

14 dditional projection into the posteroventral cochlear nucleus.

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

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

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

18 and interpolaris and provided inputs to the cochlear nucleus.

19 quency excitatory input from the ipsilateral cochlear nucleus.

20 ive direct projections from the deafferented cochlear nucleus.

21 utamatergic synapses in neurons of the chick cochlear nucleus.

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

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

24 colliculus and descending projections to the cochlear nucleus.

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

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

27 the GCD immediately surrounding the ventral cochlear nucleus.

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

29 lls in brain slices from mouse anteroventral cochlear nucleus.

30 ultipolar cell regions of the posteroventral cochlear nucleus.

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

32 dal and dorsal part of the mammalian ventral cochlear nucleus.

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

34 of nuclei that receive information from the cochlear nucleus.

35 amine into a restricted region of the dorsal cochlear nucleus.

36 ger widespread inhibition in slices of mouse cochlear nucleus.

37 ction potential to convey information to the cochlear nucleus.

38 nto their postsynaptic target neurons in the cochlear nucleus.

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

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

41 rom the tuberculoventral cells of the dorsal cochlear nucleus.

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

43 ergic transmission in neurons of the chicken cochlear nucleus.

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

45 typically within a single subdivision of the cochlear nucleus.

46 abeling them with injections into the dorsal cochlear nucleus.

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

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

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

50 ous release to GABAergic transmission in the cochlear nucleus across a 40-fold range of electrical st

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

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

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

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

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

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

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

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

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

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

61 rapid, potentiated transmission through the cochlear nucleus and motor cortex for its generation.

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

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

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

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

66 and anterograde labeling was examined in the cochlear nucleus and superior olivary complex.

67 that the trigeminal ganglion innervates the cochlear nucleus and superior olivary complex.

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

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

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

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

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

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

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

75 The cochlear nucleus angularis (NA) of the barn owl (Tyto al

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

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

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

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

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

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

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

83 the survival of neurons of the anteroventral cochlear nucleus (AVCN) of mice were examined with the h

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

110 The cochlear nucleus (CN) receives innervation from auditory

111 Neurons in the cochlear nucleus (CN) require afferent activity for main

112 At the level of the cochlear nucleus (CN), the auditory pathway divides into

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

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

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

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

127 ts also indicated that neurons in the dorsal cochlear nucleus could be activated by contralateral sti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

152 Pyramidal cells in the dorsal cochlear nucleus (DCN) show three distinct temporal disc

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

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

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

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

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

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

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

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

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

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

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

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

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

166 Additional evidence for cochlear nucleus defects was obtained by electrophysiolo

167 Cochlear nucleus defects were also apparent in mice with

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

169 ibers leave the ventral and enter the dorsal cochlear nucleus, each octopus cell spanning about one-t

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 jections from the inferior colliculus to the cochlear nucleus in guinea pigs.

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

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

189 3 was expressed in the cerebellum and dorsal cochlear nucleus in which it was detected in granule neu

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

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

192 Cochlear nucleus, inferior colliculus, and primary audit

193 Cochlear nucleus injections retrogradely labeled small g

194 The dorsal cochlear nucleus integrates acoustic with multimodal sen

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

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

197 The marginal shell of the anteroventral cochlear nucleus is anatomically and physiologically dif

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

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

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

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

202 ng injection of a retrograde tracer into one cochlear nucleus, labeled cells were found bilaterally i

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

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

205 The avian cochlear nucleus magnocellularis (NM) integrates excitat

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

207 aps with, and is rostral and lateral to, the cochlear nucleus magnocellularis (NM).

208 observed in the rostromedial regions of the cochlear nucleus magnocellularis and the nucleus laminar

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

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

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

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

213 em comprising the cochlea, cochlear neurons, cochlear nucleus, medial olivocochlear neurons, and coch

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

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

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

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

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

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

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

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

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

223 Neurons of the chick cochlear nucleus, nucleus magnocellularis (NM), require

224 binding protein calretinin (CR) in the chick cochlear nucleus, nucleus magnocellularis (NM), was exam

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

246 upport the conclusion that the anteroventral cochlear nucleus projects to medial olivocochlear neuron

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

273 1 gene, is expressed strongly in the ventral cochlear nucleus (VCN) and the medial nucleus of the tra

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

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

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

284 ily in the magnocellular area of the ventral cochlear nucleus (VCN).

285 NTB and LNTB, respectively), and the ventral cochlear nucleus (VCN).

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

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

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

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

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

291 -1 immunostaining of microglial cells in the cochlear nucleus was observed at all survival times afte

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

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

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

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

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

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

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

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

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