ライフサイエンスコーパス: inferior colliculus

1 in the torus semicircularis (homolog of the inferior colliculus).

2 ustic centers (e.g. dorsal cochlear nucleus, inferior colliculus).

3 etectal nuclei, and the dorsal cortex of the inferior colliculus.

4 of the external portion (EX) of the chicken inferior colliculus.

5 ogue of the central nucleus of the mammalian inferior colliculus.

6 ulation of neurons in central nucleus of the inferior colliculus.

7 tory cortices, medial geniculate nuclei, and inferior colliculus.

8 temporal processing within the brainstem and inferior colliculus.

9 maturation of their terminal endings in the inferior colliculus.

10 atus in the cochlea and auditory midbrain -- inferior colliculus.

11 show the tonotopic organization of the mouse inferior colliculus.

12 roles in shaping response properties in the inferior colliculus.

13 es in GABA have previously been shown in the inferior colliculus.

14 r diverse frequency selectivity in the mouse inferior colliculus.

15 ularis, the auditory midbrain homolog of the inferior colliculus.

16 ntal expansion and contribute throughout the inferior colliculus.

17 key role in directing plastic changes in the inferior colliculus.

18 receptors in the central nucleus of the rat inferior colliculus.

19 ipsilateral cochlear nucleus and ipsilateral inferior colliculus.

20 projected to the cochlear nucleus or to the inferior colliculus.

21 of the primary auditory cortex (AI) and the inferior colliculus.

22 e projections with corticofugal input to the inferior colliculus.

23 originate through neural interactions in the inferior colliculus.

24 they have divergent roles in modulating the inferior colliculus.

25 terminating in all three subdivisions of the inferior colliculus.

26 ian equivalent of the central nucleus of the inferior colliculus.

27 itatory and inhibitory circuits in the mouse inferior colliculus.

28 ent and produces the superior colliculus and inferior colliculus.

29 nsic mechanisms or the microcircuitry of the inferior colliculus.

30 of one such micro-organization in the rodent inferior colliculus.

31 ponses were similar to those reported in the inferior colliculus.

32 trophysiological studies have shown that the inferior colliculus, a critical auditory midbrain nucleu

33 Inhibition is also prominent in the inferior colliculus, a subcortical hub in auditory pathw

34 ave studied P-glycoprotein expression in the inferior colliculus after a temporary loss of blood-brai

35 In the inferior colliculus (an important subcortical auditory s

36 eport a novel neural plastic response in the inferior colliculus, an auditory center in the midbrain

37 e same as that in the central nucleus of the inferior colliculus and AI elicited by focal electric st

38 of the frequency (co-chleotopic) maps in the inferior colliculus and auditory cortex (AC).

39 e decoding of temporal sound features in the inferior colliculus and auditory cortex in adult mice wi

40 y are scattered in the frequency maps of the inferior colliculus and auditory cortex.

41 retectum, and nucleus of the brachium of the inferior colliculus and bilateral connections with the p

42 auditory thalamus is the major target of the inferior colliculus and connects in turn with the audito

43 nd D-stellate neurons, thought to project to inferior colliculus and contralateral cochlear nucleus,

44 a small fascicle at the anterior pole of the inferior colliculus and descending bilaterally through t

45 is a source of ascending projections to the inferior colliculus and descending projections to the co

46 tter characterize these modules in the mouse inferior colliculus and determine whether the connectivi

47 alian central auditory system, including the inferior colliculus and medial geniculate body (MGB).

48 trotemporal receptive field estimates in the inferior colliculus and primary auditory cortex.

49 sounds, recording neuronal responses in the inferior colliculus and primary fields of the auditory c

50 rther the understanding of inhibition in the inferior colliculus and suggest that these extracellular

51 d parvalbumin (PV)-positive cells within the inferior colliculus and superior olivary complex.

52 ly in terms of its inhibitory afferents from inferior colliculus and thalamic reticular nucleus and i

53 vidual superior olivary cells project to the inferior colliculus and the cochlear nucleus.

54 nclude that the ascending projections to the inferior colliculus and the descending projections to th

55 niscal nucleus, red nucleus, pontine nuclei, inferior colliculus and the parvocellular portion of the

56 of pyramidal-tract neuron projecting to the inferior colliculus, and corticocallosal neurons, a type

57 ne of the ascending auditory pathways to the inferior colliculus, and D stellate cells, which inhibit

58 ly expressed in primary auditory cortex than inferior colliculus, and directly impacted neural coding

59 lamus, nucleus isthmus, tectum mesencephali, inferior colliculus, and hindbrain.

60 rdings from electrodes placed in the cortex, inferior colliculus, and medulla of seizing GEPR-9s.

61 Cochlear nucleus, inferior colliculus, and primary auditory cortex did not

62 -, then up-regulation was discovered for the inferior colliculus Aqp4 expression.

63 receptive fields of neurons in the midbrain inferior colliculus are also modified during behavior.

64 map and the tiered tonotopy observed in the inferior colliculus are explored.

65 al (DCIC) and lateral cortices (LCIC) of the inferior colliculus are major targets of the auditory an

66 ular neurons projecting from layer 5B to the inferior colliculus are required for cholinergic-mediate

67 responses recorded in the cochlear nucleus, inferior colliculus, auditory thalamus, and primary and

68 t (LTG), a pathway medial to brachium of the inferior colliculus (BIC), significantly decreased freez

69 found in the nucleus of the brachium of the inferior colliculus (BIN), which provides a major audito

70 GABA and serotonin in the mammalian inferior colliculus both have a restrictive effect on fe

71 he lateral septum, ventral hypothalamus, and inferior colliculus, but did however include labeled cel

72 e we show the emergence of DS neurons in the inferior colliculus by mapping the three major subcortic

73 quency) maps in the auditory cortex (AC) and inferior colliculus can be changed by auditory condition

74 Interestingly, ILD processing in all inferior colliculus cell types (EE and EI) is largely co

75 The inferior colliculus central nucleus (ICC) has potential

76 The responses of neurons in the inferior colliculus changed in line with these perceptua

77 ese statistics in the central nucleus of the inferior colliculus (CNIC) of cats.

78 from the VNLL to the central nucleus of the inferior colliculus (CNIC) was investigated by using neu

79 eriodicity in the cat central nucleus of the inferior colliculus (CNIC) with modulated broadband nois

80 tonotopic axis of the central nucleus of the inferior colliculus (CNIC), whereas patterns are discont

81 from the ipsilateral central nucleus of the inferior colliculus (CNIC).

82 nsity of fibers in peripheral regions of the inferior colliculus compared with its core.

83 ams, here we show that local circuits in the inferior colliculus connect the module and matrix region

84 eurons projecting from layer 5B (L5B) to the inferior colliculus, corticocollicular neurons, are requ

85 Seizures induced by stimulation of the inferior colliculus could evoke SD that spread in a rost

86 lamus, hippocampus, superior colliculus, and inferior colliculus) elicited changes generally similar

87 suggest that the lateral cortex of the mouse inferior colliculus exhibits connectional as well as neu

88 jections of the medial superior olive to the inferior colliculus for evidence of a spatial topography

89 ich links FGF with the ERK pathway, prevents inferior colliculus formation by depleting a previously

90 e auditory cortex and central nucleus of the inferior colliculus formed patches that interdigitate wi

91 dings of neural activity from the guinea pig inferior colliculus have shown that individual auditory

92 Space-specific neurons in the barn owl's inferior colliculus have spatial receptive fields (RFs)

93 Space-specific neurons in the owl's inferior colliculus have spatial receptive fields (RFs)

94 SO) and medial (MSO) superior olive, and the inferior colliculus (IC) 145 days after UCA.

95 receives a large input from the ipsilateral inferior colliculus (IC) and a smaller but substantial i

96 ounds (deviant) in individual neurons in the inferior colliculus (IC) and at higher levels.

97 ate on central auditory system function, the inferior colliculus (IC) and auditory cortex (AC) respon

98 ipsi- and contralateral dorsal cortex of the inferior colliculus (IC) and central nucleus of the IC.

99 erties of single neurons in the awake gerbil inferior colliculus (IC) and compared them with primary

100 map of auditory space is synthesized in the inferior colliculus (IC) and conveyed to the optic tectu

101 tes in high-frequency representations of the inferior colliculus (IC) and depends on low and high fre

102 e complex neuroanatomical connections of the inferior colliculus (IC) and its major subdivisions offe

103 gh field fMRI (7 Tesla) to examine the human inferior colliculus (IC) and medial geniculate body (MGB

104 red the neural representation of ITDs in the inferior colliculus (IC) and primary auditory cortex (A1

105 ET to evaluate the glucose metabolism of the inferior colliculus (IC) and primary auditory cortex (PA

106 Given direct connections between the inferior colliculus (IC) and subcortical motor structure

107 1 hour) on the physiological response of the inferior colliculus (IC) and the AC, and the behavioral

108 tonotopic axis of the central nucleus of the inferior colliculus (IC) and the auditory cortex (Actx).

109 hlea along parallel pathways and reaches the inferior colliculus (IC) and the medial geniculate body

110 alysis revealed that auditory neurons in the inferior colliculus (IC) are avoiding spectrotemporal mo

111 Many cells in the inferior colliculus (IC) are excited by contralateral an

112 ration-tuned neurons (DTNs) in the mammalian inferior colliculus (IC) arise from a combination of exc

113 sking patterns of single neurons in the frog inferior colliculus (IC) before and during iontophoretic

114 ng low frequencies and is represented in the inferior colliculus (IC) by cells that respond maximally

115 Neurons in the inferior colliculus (IC) change their firing rates with

116 Severed axons of the inferior colliculus (IC) commissure can regenerate acros

117 Some neurons of the inferior colliculus (IC) exhibit "stimulus-specific adap

118 In this model, the inferior colliculus (IC) exhibits enhanced neuronal firi

119 cterized ITD tuning of single neurons in the inferior colliculus (IC) for pulse train stimuli in an u

120 d the spinal trigeminal nucleus (Sp5) to the inferior colliculus (IC) in the guinea pig, using both r

121 The inferior colliculus (IC) in the mammalian midbrain is th

122 Located in the midbrain, the inferior colliculus (IC) integrates information from num

123 itory sensitivity of neurons in the midbrain inferior colliculus (IC) ipsilateral and contralateral t

124 The central nucleus of the inferior colliculus (IC) is a laminated structure that r

125 The inferior colliculus (IC) is a processing center in both

126 The inferior colliculus (IC) is an obligatory relay for asce

127 The inferior colliculus (IC) is normally thought of as a pre

128 The inferior colliculus (IC) is the common target of separat

129 The inferior colliculus (IC) is the consensus site for seizu

130 The inferior colliculus (IC) is the first place in the centr

131 Located in the midbrain, the inferior colliculus (IC) is the hub of the central audit

132 The central nucleus of the inferior colliculus (IC) is the site of convergence for

133 Neural activity in the inferior colliculus (IC) likely plays an integral role i

134 s in the auditory cortex (ACx) targeting the inferior colliculus (IC) mediate an innate, sound-induce

135 rent density of calcium (Ca(2+)) channels in inferior colliculus (IC) neurons.

136 Responses of low-frequency neurons in the inferior colliculus (IC) of anesthetized guinea pigs wer

137 y deviant responses from single units in the inferior colliculus (IC) of anesthetized rats.

138 were recorded with patch electrodes from the inferior colliculus (IC) of awake bats to evaluate the t

139 g the average firing rates of neurons in the inferior colliculus (IC) of awake rabbits, that prevaili

140 eptors (AMPARs) to auditory responses in the inferior colliculus (IC) of awake, adult mustached bats.

141 We measured single-unit activity in the inferior colliculus (IC) of common marmosets of both sex

142 this form of task-related plasticity in the inferior colliculus (IC) of ferrets trained to detect a

143 ity of neurons in the central nucleus of the inferior colliculus (IC) of many animal species behave a

144 Here we investigated how neurons in the inferior colliculus (IC) of Mexican free-tailed bats res

145 sms that underlie processing this cue in the inferior colliculus (IC) of mouse.

146 at the recovery cycle of most neurons in the inferior colliculus (IC) of the big brown bat, Eptesicus

147 t, we recorded from 92 single neurons in the inferior colliculus (IC) of the little brown bat and inv

148 cal injections of retrograde tracer into the inferior colliculus (IC) of the mouse revealed that most

149 single-neuron responses at the level of the inferior colliculus (IC) of two awake and passively list

150 velope, we recorded from single units in the inferior colliculus (IC) of unanesthetized rabbit using

151 IHCT with varying F0 and sound level in the inferior colliculus (IC) of unanesthetized rabbits of bo

152 ctional sensitivity of single neurons in the inferior colliculus (IC) of unanesthetized rabbits.

153 The inferior colliculus (IC) processes auditory information

154 The inferior colliculus (IC) receives its major ascending in

155 Neurons in the inferior colliculus (IC) show a remarkable diversity in

156 Auditory neurons in the inferior colliculus (IC) show remarkable selectively in

157 We measured the contribution of inferior colliculus (IC) sites to perception using combi

158 thway, which then splits at the level of the inferior colliculus (IC) such that the last computationa

159 eedback from the auditory cortex (AC) to the inferior colliculus (IC) supports critical aspects of au

160 Neurons in the inferior colliculus (IC) that are excited by one ear and

161 may be a specific marker for circuits in the inferior colliculus (IC) that code timing information.

162 trical stimulation of sites across the human inferior colliculus (IC) that was consistent with the IC

163 tion and progression of projections from the inferior colliculus (IC) to the medial geniculate body (

164 ecently, prosthetic stimulation in the human inferior colliculus (IC) was evaluated in a clinical tri

165 stimuli throughout the CNS, including in the inferior colliculus (IC), a major hub in both ascending

166 omodulatory regulation of latency within the inferior colliculus (IC), a midbrain auditory nexus, the

167 In the inferior colliculus (IC), an auditory midbrain nucleus,

168 le neuronal receptive fields reported in the Inferior Colliculus (IC), as well as auditory thalamus a

169 sal nucleus of the lateral lemniscus and the inferior colliculus (IC), both of which contain large po

170 eptors in the midbrain auditory nucleus, the inferior colliculus (IC), but have not examined the cell

171 In the mustached bat's inferior colliculus (IC), combination-sensitive neurons

172 al projections to the auditory midbrain, the inferior colliculus (IC), influence the way in which spe

173 xons throughout postnatal development in the inferior colliculus (IC), medial geniculate complex (MGC

174 Instead, in the inferior colliculus (IC), the diverse temporal firing pa

175 the population code for speech in the gerbil inferior colliculus (IC), the hub of the auditory system

176 In the inferior colliculus (IC), the hub of the central auditor

177 The inferior colliculus (IC), the midbrain component of the

178 enter mediating emotional expression, to the inferior colliculus (IC), the midbrain integration cente

179 ditory nerve fibres, but by the level of the inferior colliculus (IC), the midbrain nucleus of the au

180 ings were made in anesthetized rats from the inferior colliculus (IC), the nucleus of the brachium of

181 three stations of the auditory pathway, the inferior colliculus (IC), the ventral division of the me

182 In the mustached bat's inferior colliculus (IC), they are common in frequency r

183 e development of cochlear hair cells and the inferior colliculus (IC), which are important in tonotop

184 imaging, an increase in the T1 signal in the inferior colliculus (IC), which is localized in the audi

185 ed the data to recordings we obtained in the inferior colliculus (IC).

186 onse in the medial geniculate body (MGB) and inferior colliculus (IC).

187 viorally relevant vocalizations in the mouse inferior colliculus (IC).

188 ansformation is complete by the level of the inferior colliculus (IC).

189 chlear nucleus (DCN), a primary relay to the inferior colliculus (IC).

190 tex projects directly and bilaterally to the inferior colliculus (IC).

191 ently with postsynaptic action potentials in inferior colliculus (IC).

192 eus (DCN) target primarily the contralateral inferior colliculus (IC).

193 ganized neuron ensembles in the awake rabbit inferior colliculus (IC).

194 nd level at a lower level of processing: the inferior colliculus (IC).

195 without are part of the same networks in the inferior colliculus (IC).

196 nohistochemistry and confocal imaging in the inferior colliculus (IC, auditory midbrain) of the guine

197 inaural inputs to the central nucleus of the inferior colliculus (ICC) are from two groups of neurons

198 g to frequency in the central nucleus of the inferior colliculus (ICc) but according to response type

199 activity from the central nucleus of the cat inferior colliculus (ICC) in response to dynamic spectro

200 ly all neurons in the central nucleus of the inferior colliculus (ICc) in the auditory midbrain.

201 demonstrate that the central nucleus of the inferior colliculus (ICC) of cats encodes sound features

202 The central nucleus of the inferior colliculus (ICC) of the auditory midbrain, whic

203 naural integration in the central nucleus of inferior colliculus (ICC) plays a critical role in sound

204 ditory input from the central nucleus of the inferior colliculus (ICC) via topographic axonal project

205 unit responses in the central nucleus of the inferior colliculus (ICC) were recorded.

206 AVCN and DCN) and the central nucleus of the inferior colliculus (ICc) were studied in cortically int

207 noic acid (AP7), into the central nucleus of inferior colliculus (ICc), deep layers of superior colli

208 ity of neurons in the central nucleus of the inferior colliculus (ICC).

209 tory brainstem to the central nucleus of the inferior colliculus (ICC).

210 on information in the central nucleus of the inferior colliculus (ICC).

211 l interactions in the central nucleus of the inferior colliculus (ICC).

212 l pathway that terminates at the core of the inferior colliculus (ICcc).

213 lateral shell of the central nucleus of the inferior colliculus (ICCls).

214 lar tegmentum (ICt), the rostral pole of the inferior colliculus (ICrp), and the nucleus of the brach

215 The owl's external nucleus of the inferior colliculus (ICx) contains a map of auditory spa

216 owl (Tyto alba), the external nucleus of the inferior colliculus (ICX) contains a map of auditory spa

217 ory space map in the external nucleus of the inferior colliculus (ICX) of barn owls is highly plastic

218 auditory inputs, the external cortex of the inferior colliculus (ICX) receives prominent somatosenso

219 ory space map in the external nucleus of the inferior colliculus (ICX) shifts according to the optica

220 is relayed from the external nucleus of the inferior colliculus (ICX) to the deep and intermediate l

221 ll nuclei within the external nucleus of the inferior colliculus (ICX) were unimodal.

222 s takes place in the external nucleus of the inferior colliculus (ICX).

223 projection from the external nucleus of the inferior colliculus (ICX).

224 al Delta ITD thresholds from 53 cells in the inferior colliculus in guinea pigs.

225 e neural activity in auditory neurons of the inferior colliculus in guinea pigs.

226 me of reference of auditory responses in the inferior colliculus in monkeys fixating visual stimuli a

227 cording local field potentials (LFPs) in the inferior colliculus in response to suprathreshold optica

228 fails to rescue the tectal stem zone and the inferior colliculus in the absence of Fgf8 and the isthm

229 from cortical layer V pyramidal cells to the inferior colliculus in the midbrain.

230 protein immunoreactivity returned across the inferior colliculus, in parallel with astrocytic repopul

231 n of the AC and acetylcholine applied to the inferior colliculus increase the short-term collicular B

232 e projection from the auditory cortex to the inferior colliculus is a massive, yet poorly understood,

233 tion of Fmr1 in glutamatergic neurons of the inferior colliculus is necessary for AGSs.

234 The inferior colliculus is one such modular structure, conta

235 The lateral cortex of the inferior colliculus (LCIC) forms a nexus between diverse

236 the diagonal band, nucleus accumbens shell, inferior colliculus, locus coeruleus, and flocculus comp

237 olivary nuclear complex, lateral lemniscus, inferior colliculus, medial geniculate body, and auditor

238 e divisions of the superior olivary complex, inferior colliculus, medial geniculate body, and primary

239 uch as the ectorhinal and temporal cortices, inferior colliculus, medial geniculate body, and some of

240 n of sound location along the azimuth in the inferior colliculus most likely relies on a complex, non

241 t SC from the nucleus of the brachium of the inferior colliculus (nBIC), its main source of auditory

242 howed nAChR subunit transcripts in GABAergic inferior colliculus neurons and glutamatergic auditory c

243 ith increasing modulation depth, some rabbit inferior colliculus neurons increased firing rates where

244 lds to the dorsal cochlear nucleus activates inferior colliculus neurons.

245 s for neurons in the midbrain nucleus of the inferior colliculus; neurons with relatively low best fr

246 eucoagglutinin (PHA-L) was injected into one inferior colliculus of 10 animals and the pontine nuclei

247 found that a majority of single units in the inferior colliculus of acutely deafened, anesthetized ca

248 on activity from the external nucleus of the inferior colliculus of adult male and female barn owls.

249 with in vivo whole-cell recordings from the inferior colliculus of awake bats.

250 of the umbo and neural activation within the inferior colliculus of guinea pigs, corresponding to the

251 of adrenergic receptor-encoding mRNA in the inferior colliculus of male and female mice.

252 n or torus semicircularis, homologous to the inferior colliculus of mammals.

253 ic connections in the central nucleus of the inferior colliculus of newborn mice until after hearing

254 Aergic neurons in the central nucleus of the inferior colliculus of normal hearing mice.

255 the first time in the central nucleus of the inferior colliculus of the auditory midbrain.

256 collected electrophysiological data from the inferior colliculus of the awake big brown bat, Eptesicu

257 entral shell and the external portion of the inferior colliculus of the chicken.

258 tral integration performed by neurons in the inferior colliculus of the mustached bat (Pteronotus par

259 hypothesis, we recorded from single units in inferior colliculus of two groups of bilaterally implant

260 ec tones was measured in single units in the inferior colliculus of urethane-anesthetized guinea pigs

261 AD67 in the superior olivary complex and the inferior colliculus of young and aged rhesus macaques.

262 dbrain neurons in the central nucleus of the inferior colliculus (of chinchilla) effectively encode I

263 trograde tracer Fluorogold was injected into inferior colliculus or cochlear nucleus to label T-stell

264 make contacts with neurons not projecting to inferior colliculus or the contralateral cochlear nucleu

265 areas, suggesting that the thalamus and the inferior colliculus receive differential degrees of cort

266 The inferior colliculus receives convergent input from multi

267 The lateral cortex of the inferior colliculus receives information from both audit

268 her, our data show that the formation of the inferior colliculus relies on the provision of new cells

269 Space-specific neurons in the owl's inferior colliculus respond only to a sound coming from

270 the SC, although neurons in the neighboring inferior colliculus responded to auditory stimuli.

271 es chosen among the following areas: cortex, inferior colliculus, reticular formation and caudal medu

272 Moreover, in vivo imaging within the inferior colliculus revealed that auditory neurons withi

273 projection from the rostral pole of the cat inferior colliculus (rpIC) to the superior colliculus (S

274 Auditory space-specific neurons in the owl's inferior colliculus selectively respond to the direction

275 Recordings from the cat inferior colliculus show that neurons with the lowest sp

276 ond, we find 7% of all Purkinje cells in the inferior colliculus, similar to what is seen in the Unc5

277 nucleus of the lateral lemniscus and in the inferior colliculus, suggesting that these structures co

278 nges were restricted to the subregion of the inferior colliculus that received optically displaced in

279 e rats (Rattus norvegicus) revealed that the inferior colliculus, the auditory midbrain, receives den

280 dorsal nucleus of the lateral lemniscus, the inferior colliculus, the auditory thalamus, and the audi

281 s, as recorded in rabbit at the level of the inferior colliculus, the first level of the ascending au

282 ter ITD tuning in the central nucleus of the inferior colliculus, the primary source of input to the

283 mporal dimensions in a single structure, the inferior colliculus, the principal auditory nucleus in t

284 As in the inferior colliculus, the shape of the firing-rate versus

285 neural connections in rat, we show that the inferior colliculus, the subcortical, midbrain center fo

286 o detected in other hypothamamic nuclei, the inferior colliculus, the ventral central gray matter, th

287 t of the descending auditory system from the inferior colliculus to the cochlear nucleus.

288 ne tegmentum extending from the level of the inferior colliculus to the motor nucleus of the trigemin

289 do not support a robust projection from the inferior colliculus to the pontine nuclei in guinea pig.

290 tudy examined the neural projection from the inferior colliculus to the pontine nuclei in guinea pig.

291 This newly described connection from the inferior colliculus to the TeO provides a solid basis fo

292 f the pure-tone frequency in the cochlea and inferior colliculus) to detect the minute changes in ech

293 leotopic map alters tuning properties of the inferior colliculus units, which display abnormal freque

294 ponses across the cochleotopically organized inferior colliculus using multichannel recording techniq

295 tory space map of the barn owl's (Tyto alba) inferior colliculus using two spatially separated source

296 neurons of the owl's external nucleus of the inferior colliculus, where auditory space is represented

297 cells observed in males, and in the PAG and inferior colliculus, where significantly more FG+ cells

298 CM targeted the dorsomedial quadrant of the inferior colliculus, whereas the CM projection also incl

299 elated mRNA gene expression in the CBA mouse inferior colliculus with age and hearing loss were exami

300 vator, restores the tectal stem zone and the inferior colliculus without Ptpn11.