ライフサイエンスコーパス: olfactory bulb

1 leus of the diagonal band of Broca, and main olfactory bulb.

2 PG) neurons in the granule cell layer of the olfactory bulb.

3 d cells, the projection neurons in the mouse olfactory bulb.

4 on, as well as in the frontal cortex and the olfactory bulb.

5 ide the initial sensory input to the brain's olfactory bulb.

6 d signal-to-noise ratio at the output of the olfactory bulb.

7 rate synchronized oscillations in the rodent olfactory bulb.

8 tion in the proportional size of the brain's olfactory bulb.

9 main olfactory bulb and one in the accessory olfactory bulb.

10 gene Fos in the SCN, dorsal hippocampus, and olfactory bulb.

11 during 28d Li-treatment, particularly in the olfactory bulb.

12 a basic feature of sensory processing in the olfactory bulb.

13 not seen in axons innervating the accessory olfactory bulb.

14 ior forebrain along a defined pathway to the olfactory bulb.

15 ture adult-born-granule-cells (abGCs) in the olfactory bulb.

16 synapses of granule and mitral cells in the olfactory bulb.

17 in the internal plexiform layer of the main olfactory bulb.

18 heir assembly into distinct glomeruli in the olfactory bulb.

19 s, and prefrontal cortex but not in liver or olfactory bulb.

20 s particularly remarkable upon injury to the olfactory bulb.

21 ve to odorants soon after they arrive in the olfactory bulb.

22 ne release from the locus coeruleus into the olfactory bulb.

23 of physiological properties exhibited by the olfactory bulb.

24 excitatory synapses within glomeruli of the olfactory bulb.

25 iven by bottom-up spontaneous input from the olfactory bulb.

26 blasts through the anterior forebrain to the olfactory bulb.

27 on the efficient reinsertion of OSNs to the olfactory bulb.

28 f connections to second-order neurons in the olfactory bulb.

29 iameter can enter the brain directly via the olfactory bulb.

30 olfactory neuropil similar to the vertebrate olfactory bulb.

31 resolved transcriptomics data from the mouse olfactory bulb.

32 ns into approximately 3,600 glomeruli in the olfactory bulb.

33 ortant developmental roles in the cortex and olfactory bulb.

34 r to transmission of odor information to the olfactory bulb.

35 Cs compared with analogous cells in the main olfactory bulb.

36 t of adult-born granule cells (abGCs) in the olfactory bulb.

37 ely 3,500 glomeruli are present in each main olfactory bulb.

38 neurons densely project in all layers of the olfactory bulb.

39 projections from both the main and accessory olfactory bulbs.

40 l cells is proportional to the size of their olfactory bulbs.

41 lls, which provide the primary output of the olfactory bulbs.

42 factory nerves and enter the CNS through the olfactory bulbs.

43 he human brain via the respiratory tract and olfactory bulbs.

44 ration on SWR occurrence was eliminated when olfactory bulb activity was inhibited.

45 that FMRP mediates structural plasticity of olfactory bulb adult-born neurons to support olfactory l

46 In the olfactory bulb, afferent olfactory receptor neurons resp

47 bers of nitrergic cells were observed in the olfactory bulb, all pallial divisions, lateral septum, s

48 RNA-Seq of olfactory bulbs also identified a novel ADNP hotspot mut

49 l processing of olfactory information by the olfactory bulb, an obligatory relay between sensory neur

50 l motor nucleus of the vagus, as well as the olfactory bulb and anterior olfactory nucleus, and then

51 ood and no detectable silver measured in the olfactory bulb and brain.

52 ate of breathing ( approximately 2-12 Hz) in olfactory bulb and cortex, and faster oscillatory bursts

53 itecture of cells and myelin, within coronal olfactory bulb and cortical sections, and from sagittal

54 n deep short axon cells (Cajal cells) of the olfactory bulb and its neuromodulatory effect on mitral

55 arallel olfactory circuits, four in the main olfactory bulb and one in the accessory olfactory bulb.

56 we obtained quantitative descriptions of the olfactory bulb and piriform cortex in six mammals using

57 nucleus (AON) receives direct input from the olfactory bulb and sends an associative projection to pi

58 ctions innervate multiple layers of the main olfactory bulb and strongly influence odor discriminatio

59 tations involve a dynamical loop between the olfactory bulb and the piriform cortex, with cortex expl

60 n the nasal cavity is first processed by the olfactory bulb and then sent via the lateral olfactory t

61 m ADNP mutation (c.2188C>T) in postmortem AD olfactory bulbs and hippocampi.

62 vulture brains, including the size of their olfactory bulbs and numbers of mitral cells, which provi

63 x6 results in devastated development of eye, olfactory bulb, and cortex.

64 eability was localized within the brainstem, olfactory bulb, and lateral ventricle.

65 the olfactory epithelium, translocate to the olfactory bulb, and migrate to the olfactory cortex.

66 tial recipient of odour information from the olfactory bulb, and the target of dense innervation conv

67 n is transmitted from olfactory receptors to olfactory bulb, and then to piriform cortex, where ensem

68 antennal lobe, the analog of the vertebrate olfactory bulb, and we dissect the network and intrinsic

69 correct glomeruli formation in the accessory olfactory bulb (AOB) and survival.

70 ivity in mitral cells of the mouse accessory olfactory bulb (AOB) emerges from interplay between intr

71 lient chemosensory encounters, the accessory olfactory bulb (AOB) experiences changes in the balance

72 increase in the amount of incoming accessory olfactory bulb (AOB) inputs, as confirmed by estimates o

73 eurotransmitter (NT) expression in accessory olfactory bulb (AOB) interneurons during development.

74 neurons.SIGNIFICANCE STATEMENT The accessory olfactory bulb (AOB) is a site of experience-dependent p

75 MENT Information processing in the accessory olfactory bulb (AOB) plays a central role in conspecific

76 mined local circuit changes in the accessory olfactory bulb (AOB) using targeted ex vivo recordings o

77 The accessory olfactory bulb (AOB), the first neural circuit in the mo

78 ons to both the main (MOB) and the accessory olfactory bulb (AOB).

79 demonstrated recently in the mouse accessory olfactory bulb (AOB).

80 major class of interneurons in the accessory olfactory bulb (AOB).

81 asal forebrain long-range projections to the olfactory bulb are important for olfactory sensitivity a

82 onal nose", glomerular input patterns in the olfactory bulb are massively perturbed and olfactory beh

83 is enhanced when noradrenergic inputs to the olfactory bulb are unaltered.

84 t subtypes of interneurons, destined for the olfactory bulb, are continuously generated by neural ste

85 le cells, the most common interneuron in the olfactory bulb, are known to broadly integrate sensory i

86 tral cells, the primary output neuron of the olfactory bulb, are solely activated by feedforward exci

87 results identify inhibitory circuits in the olfactory bulb as a mechanistic basis for many of the be

88 immunoreactive soma in cave Astyanax in the olfactory bulb, basal telencephalon, preoptic nuclei, ve

89 ocused on neurons and glial cells within the olfactory bulb because the virus enters the brain at thi

90 eripheral oscillators in the hippocampus and olfactory bulb become desynchronized, along with the beh

91 ippocampus (top) and glomerular layer of the olfactory bulb (bottom) of anaesthetized mice (represent

92 eurons innervate multiple layers in the main olfactory bulb but the precise circuitry of this input i

93 response is driven by direct input from the olfactory bulb, but is also shaped by a dense network of

94 Similarly, axons innervating the main olfactory bulb, but not the accessory olfactory bulb, co

95 efined intermediate targets in the zebrafish olfactory bulb called protoglomeruli well before they fo

96 ative traces from n = 7 CA1 cells and n = 13 olfactory bulb cells, n = 3 mice).

97 evident in the diencephalon, but also in the olfactory bulbs/cerebral hemispheres, optic tectum/tegme

98 the functional organization of the accessory olfactory bulb circuitry remain unclear.

99 biophysically explicit, multiscale model of olfactory bulb circuitry, we here demonstrate that an in

100 tributing to the functional integrity of the olfactory bulb circuitry.

101 Olfactory bulb circuits are dominated by multiple inhibi

102 Axons in all four main olfactory bulb circuits exhibited axonal localization of

103 idic protein-reactive astrocyte layer of the olfactory bulb constitutes the glia limitans of the olfa

104 e main olfactory bulb, but not the accessory olfactory bulb, contained the FXG-associated mRNA Omp (o

105 The olfactory bulb contains excitatory principal cells (mitr

106 -fixed mice, we found that odor responses in olfactory bulb degrade under ketamine/xylazine anesthesi

107 t of Pcdh-gammaC4 mRNA, being highest in the olfactory bulb, dentate gyrus, and cerebellum.

108 Neuronal identity in the olfactory bulb depends on the existence of defined micro

109 support the argument that odor coding in the olfactory bulb depends on the recent history of the sens

110 (V-SVZ), in which neural stem cells generate olfactory bulb-destined interneurons.

111 ron (OSN) glomerular responses in the dorsal olfactory bulb (dOB) during odor presentation.

112 ive ranges (MRRs) of glomeruli in the dorsal olfactory bulb (dOB) innervated by the MOR18-2 olfactory

113 gic projections from the raphe nuclei to the olfactory bulb dramatically enhance the responses of two

114 ow that the presence of noradrenaline in the olfactory bulb during acquisition renders olfactory memo

115 e, simple network effect of noradrenaline on olfactory bulb dynamics can underlie these seemingly dif

116 netically identified glomerulus in the mouse olfactory bulb, early odorant exposure increases the num

117 ed that FXG expression in frontal cortex and olfactory bulb followed consistent patterns in all speci

118 n infected cell populations connected to the olfactory bulbs following intranasal instillation of H1N

119 l olfactory organ extend long axons into the olfactory bulb forming synapses with projection neurons

120 m-210 ((210)Po) in the olfactory epithelium, olfactory bulb, frontal lobe, and lung tissues in cadave

121 Additionally, fast (85 Hz) and slow (70 Hz) olfactory bulb gamma oscillation sub-bands have been hyp

122 Interstitial Po2 has similar values in the olfactory bulb glomerular layer and the somatosensory co

123 This larger main olfactory bulb glomerular size and number of glomeruli i

124 Olfactory bulb glomeruli are regions of neuropil that co

125 By imaging OSN axon terminals in olfactory bulb glomeruli as well as OSN cell bodies with

126 ctionally discrete cortical modules known as olfactory bulb glomeruli.

127 aricosities, and neuronal cell bodies of the olfactory bulb, granular zones of cortical regions, hipp

128 ricular zone neural stem cells that generate olfactory bulb granule cell neurons were electroporated

129 tem of interest, the reciprocal spine of the olfactory bulb granule cell, is known to feature a speci

130 cement occurred in inflammatory CM hotspots (olfactory bulb > rostral migratory stream > brainstem >

131 The olfactory bulb had higher (210)Po levels than either olf

132 f large numbers of local interneurons in the olfactory bulb has demonstrated an extensive local signa

133 he arrangement of computational units in the olfactory bulb has still not been resolved.

134 tained in the main (MOB) and accessory (AOB) olfactory bulb have distinct intrinsic membrane properti

135 tatory mitral projection neurons of the main olfactory bulb; here, these two classes of neurons form

136 The combination of large olfactory bulbs, high mitral cell counts and a greatly e

137 accumulation in discrete areas of the brain (olfactory bulb, hippocampus, and midbrain) and reduction

138 D2(-/-) mice also have a reduced size of the olfactory bulb, hippocampus, cerebellum and cortex besid

139 i pallidi, dysgenesis of the caudate nuclei, olfactory bulbs hypoplasia, and anomaly of the diencepha

140 r with a potential therapeutic target in the olfactory bulb (i.e. via intranasal delivery) for contro

141 The turkey vulture has the largest olfactory bulbs in absolute terms and adjusted for brain

142 In the mouse olfactory bulb, inhalation of different odors leads to c

143 serve odor-evoked activity in populations of olfactory bulb inhibitory interneurons and of synaptic t

144 cal descriptors of odors and the activity of olfactory bulb inputs and outputs in awake mice.

145 pending on their location, generate distinct olfactory bulb interneuron subtypes.

146 slices, we test how the two major classes of olfactory bulb interneurons differentially contribute to

147 move GABAergic transmission from a subset of olfactory bulb interneurons, EPL interneurons (EPL-INs),

148 Our data suggest that olfactory bulb interneurons, through exerting distinct i

149 the anterior olfactory cortex projecting to olfactory bulb interneurons.

150 are key elements in organizing the accessory olfactory bulb into functional microcircuits, each chara

151 d microcircuits that subdivide the accessory olfactory bulb into segregated functional clusters.

152 We found that the astrocytic layer of the olfactory bulb is a distinct barrier to bacterial infect

153 The human olfactory bulb is actually quite large in absolute terms

154 eptor neurons and principal cells within the olfactory bulb is not well understood.

155 Strikingly, Per1 and Fos expression in the olfactory bulb is reversed, mirroring the inverted olfac

156 naturalistic stimuli, afferent input to the olfactory bulb is subject to strong synaptic depression,

157 he amygdala does not directly project to the olfactory bulb, joint pharmacological inactivation of th

158 Slack channel expression was detected in the olfactory bulb, lateral septal nuclei, basal ganglia, an

159 s provide direct evidence that the mammalian olfactory bulb likely participates in generating the per

160 ke but had variable effects on uptake by the olfactory bulb, liver, spleen and kidney.

161 r activity from both the dOB and the lateral olfactory bulb (lOB), thus describing odor-specific spat

162 r-mediated inhibition.SIGNIFICANCE STATEMENT Olfactory bulb mitral and tufted cells display different

163 verrepresented in piriform cortex but not in olfactory bulb mitral and tufted cells.

164 or the first time that some rodent accessory olfactory bulb mitral cells-the direct link between vome

165 In the main olfactory bulb (MOB), inhibitory circuits regulate the a

166 In the main olfactory bulb (MOB), the first station of sensory proce

167 ctions (two to three synapses) onto the main olfactory bulb (MOB).

168 is poorly understood compared with the main olfactory bulb (MOB).

169 present study uncover a new function for an olfactory bulb neuron (deep short axon cells, Cajal cell

170 olfactory learning task requiring adult-born olfactory bulb neurons and cell-specific ablation of FMR

171 ectrophysiological recordings from accessory olfactory bulb neurons in ex vivo preparations show that

172 xygen causes Gucy1b2-dependent activation of olfactory bulb neurons in the vicinity of the glomeruli

173 raphic two-photon optogenetic stimulation of olfactory bulb neurons with cellular and single-action-p

174 n potentials evoked synchronously across <20 olfactory bulb neurons.

175 s a medial pathway originating in the medial olfactory bulb (OB) and a lateral pathway originating fr

176 ptor subtypes are distributed throughout the olfactory bulb (OB) and antennal lobe (AL), the first la

177 n vivo recordings from two distinct regions: olfactory bulb (OB) and anterior piriform cortex (PC).

178 alized niches in which young neurons for the olfactory bulb (OB) and hippocampus, respectively, are g

179 ng respiration and field potentials from the olfactory bulb (OB) and hippocampus.

180 neurons (OSNs) wiring into highly organized olfactory bulb (OB) circuits throughout life.

181 s (OSNs) project their axons directly to the olfactory bulb (OB) glomeruli, where their synaptic rele

182 Neuronal morphology and organization in the olfactory bulb (OB) have been extensively studied, howev

183 udy is the first to look at NE modulation of olfactory bulb (OB) in regards to S/N in vivo We show, i

184 em cells along the ventricular walls produce olfactory bulb (OB) interneurons with varying neurotrans

185 he separation of the glomerular layer of the olfactory bulb (OB) into dorsomedial and ventrolateral r

186 Here we tested the hypothesis that the olfactory bulb (OB) is a locus for the generation of HFO

187 Adult neurogenesis in the olfactory bulb (OB) is considered as a competition in wh

188 The highly specific organization of the olfactory bulb (OB) is well known, but the impact of ear

189 ion along with hippocampal, neocortical, and olfactory bulb (OB) LFPs in rats anesthetized with ureth

190 ated by short axon cells (SACs) in the mouse olfactory bulb (OB) might shape odor representations as

191 During postnatal olfactory bulb (OB) neurogenesis, predetermined stem cel

192 subventricular zone (SVZ) proliferation and olfactory bulb (OB) neurogenesis.

193 -subventricular zone (V-SVZ) produce diverse olfactory bulb (OB) neurons.

194 ors are encoded by mitral cells (MCs) in the olfactory bulb (OB) of male mice.

195 In this study, we examined how the olfactory bulb (OB) performs 'whitening', a fundamental

196 FICANCE STATEMENT Inhibitory circuits in the olfactory bulb (OB) play a major role in odor processing

197 The mammalian olfactory bulb (OB) plays an essential role in odor proc

198 The olfactory bulb (OB) receives top-down inputs from the ol

199 The olfactory bulb (OB) serves as a relay region for sensory

200 al cells are major projection neurons of the olfactory bulb (OB) that form an axonal bundle known as

201 tion of glutamatergic AON projections to the olfactory bulb (OB) transiently inhibited the excitabili

202 are synaptically processed initially in the olfactory bulb (OB) where neural circuits are formed amo

203 rnal stimuli and transmit the signals to the olfactory bulb (OB) where they are integrated and proces

204 In the olfactory bulb (OB), diverse interneuron subtypes vastly

205 naptic projections onto granule cells in the olfactory bulb (OB), express the synaptogenic molecule C

206 In the olfactory bulb (OB), glomeruli are the functional units

207 P cells receive differential inputs from the olfactory bulb (OB), little is known about their project

208 the two main output channels from the mouse olfactory bulb (OB), mitral and tufted cells (MTCs).

209 Principal cells in the olfactory bulb (OB), mitral and tufted cells, play key r

210 studied the two output neuron layers in the olfactory bulb (OB), mitral and tufted cells, using chro

211 input activity is initially processed in the olfactory bulb (OB), serving as the first central relay

212 The OE, the olfactory bulb (OB), the cerebral cortex, and the cerebe

213 the nose, which then send information to the olfactory bulb (OB), the first brain region for processi

214 ental toxin-initiated OM inflammation on the olfactory bulb (OB), we induced persistent rhinitis in m

215 A possible exception is the olfactory bulb (OB), where activity guides interneuron t

216 We investigated this question in the mouse olfactory bulb (OB), where mitral and tufted cells (MTCs

217 ides a constant supply of new neurons to the olfactory bulb (OB).

218 vity in all areas of the human brain but the olfactory bulb (OB).

219 , and loss of excitatory synapses within the olfactory bulb (OB).

220 zations of SAC morphologies taken from mouse olfactory bulb (OB).

221 organ (OO), but dampened inflammation in the olfactory bulb (OB).

222 heir ultimate site of differentiation in the olfactory bulbs (OBs).

223 , protein carbonylation was increased in the olfactory bulb of aged Carns1-deficient mice.

224 Indeed, we detected mistargeted axons in the olfactory bulb of conditional ADAM10-/- mice, which corr

225 nced high gamma and beta power (PRP), in the olfactory bulb of mice learning to discriminate odorants

226 ution-in the cortex, subventricular zone and olfactory bulb of mouse brain, using a standard confocal

227 d range of odorants is occurring in the main olfactory bulb of the African wild dog.

228 olfactory sensory neuron terminals into the olfactory bulb of the brain revealed that amygdalar inac

229 aging is associated with an expansion of the olfactory bulbs of the brain in vertebrates, but no such

230 an extracranial site supplying input to the olfactory bulbs of the brain.

231 d alpha-synuclein preformed fibrils into the olfactory bulbs of wild type male and female mice.

232 indeed, reflect the idle state of accessory olfactory bulb output in awake male and female mice.

233 his study shows that AON activation inhibits olfactory bulb output neurons in both anesthetized as we

234 afferent activation alters the responses of olfactory bulb output neurons in vivo These results eluc

235 ular circuitry produces potent inhibition of olfactory bulb output neurons via direct chemical and el

236 ed cells (TCs) comprise parallel pathways of olfactory bulb output that are thought to play distinct

237 Cortical inhibition transforms olfactory bulb output to sharpen these dynamics.

238 and are thought to form parallel channels of olfactory bulb output.

239 input can be transformed to yield meaningful olfactory bulb output.

240 By measuring and comparing olfactory bulb outputs to inputs, the authors show that

241 catecholaminergic cells were observed in the olfactory bulb, pallium, and preoptic area of the telenc

242 outputs to inputs, the authors show that the olfactory bulb participates in generating the perception

243 ngs suggest that feedforward inhibition from olfactory bulb periglomerular cells can mediate this sig

244 ry discrimination.SIGNIFICANCE STATEMENT The olfactory bulb plays a central role in converting broad,

245 ion is functional.SIGNIFICANCE STATEMENT The olfactory bulb plays a central role in processing sensor

246 activity patterns.SIGNIFICANCE STATEMENT The olfactory bulb plays a critical role in transforming bro

247 l cells, or deletion of IGF1 receptor in the olfactory bulb prevented the socially relevant GABAergic

248 dynamically enhanced the inhibitory input to olfactory bulb projection neurons and increased the sign

249 tivity between olfactory sensory neurons and olfactory bulb projection neurons.

250 The olfactory bulb projects directly to a number of cortical

251 primary neurons), to the posteroventral main olfactory bulb (PV MOB) in mice.

252 al bridge represent responses from the human olfactory bulb - recordings we term Electrobulbogram (EB

253 cuitry of this cholinergic input to the main olfactory bulb remains unclear, however.

254 iform cortex and its sensory inputs from the olfactory bulb represent chemical odour relationships th

255 ABSTRACT: A dominant feature of the olfactory bulb response to odour is fast synchronized os

256 Other findings included olfactory bulb signal abnormalities (seven of 37; 19%),

257 all regions compared with control mice; mean olfactory bulb signal intensity ratio: 1.40 +/- 0.07 vs

258 merary neurons matured and integrated in the olfactory bulb similarly to physiologically generated ne

259 Conversely, the addition of IGF1 to acute olfactory bulb slices elicited the GABAergic LTP in mitr

260 g patch-clamp recordings and optogenetics in olfactory bulb slices from transgenic mice.

261 used single glomerular stimulation in mouse olfactory bulb slices to measure the synaptic dynamics o

262 Here, in acute mouse olfactory bulb slices, we test how the two major classes

263 the neuromodulator norepinephrine modulates olfactory bulb spontaneous activity and odor responses s

264 oreactive (DA-ir) cells were observed in the olfactory bulb, subpallium, and preoptic area of the tel

265 in which glomeruli (or mitral cells) in the olfactory bulb synapse with neurons distributed througho

266 howed TRH-immunoreactive cells/fibers in the olfactory bulb, telencephalon, preoptic area (POA), hypo

267 bLPXRFa-immunoreactive (ir) perikarya in the olfactory bulbs-terminal nerve, ventral telencephalon, c

268 It also had a much more developed olfactory bulb than congeners, indicating an unexpectedl

269 ve analyses show that the turkey vulture has olfactory bulbs that are 4x larger and contain twice as

270 In the rodent olfactory bulb the smooth dendrites of the principal glu

271 It remains unclear whether the olfactory bulb, the brain structure that mediates the fi

272 In the mouse accessory olfactory bulb, the first central stage of information p

273 We show here that noradrenaline in the olfactory bulb, the first cortical relay of the olfactor

274 basal forebrain project heavily to the main olfactory bulb, the first processing station in the olfa

275 Within the accessory olfactory bulb, the glomeruli did not appear distinct, r

276 In the mammalian olfactory bulb, the inhibitory axonless granule cells (G

277 two excitatory cell classes of the mammalian olfactory bulb, the mitral cells (MCs) and tufted cells

278 of the sub-ependymal zone NSC niche and the olfactory bulb, the region to which newly generated neur

279 Within the main olfactory bulb, the size of the glomeruli, at approximat

280 ermined circuit-extending from the accessory olfactory bulb to the posterior medial amygdala-that is

281 is widely expressed in many nuclei from the olfactory bulbs to the hindbrain, while vglut3 is restri

282 nal lobe, the insect analog of the mammalian olfactory bulb, to higher-order brain regions in an adul

283 The olfactory bulb transforms not only the information conte

284 ultrastructural analyses of glomeruli in rat olfactory bulb under conditions in which specific cells

285 y of adult-born granule cells (abGCs) in the olfactory bulb using multiphoton imaging in awake and an

286 immunoreactive perikarya were present in the olfactory bulbs, ventral telencephalon, caudal preoptic

287 but conspicuous projections also reached the olfactory bulbs, ventral/dorsal telencephalon, habenula,

288 the number of differentiated neurons in the olfactory bulb was dramatically reduced, whereas the rel

289 zation of the deeper layers of the accessory olfactory bulb was indistinct, perhaps as a consequence

290 the eutopic neuroblast migration towards the olfactory bulb was observed.

291 I-S1 uptake in the hippocampus and olfactory bulb was reduced by lipopolysaccharide-induced

292 de array recordings of odor responses in the olfactory bulb, we find that concentration-invariant uni

293 Our results show that interneurons of the olfactory bulb were the primary cell type able to surviv

294 Investigating the mouse olfactory bulb, where ongoing neurogenesis continually s

295 ia the rostral migratory stream (RMS) to the olfactory bulb, where they differentiate into local inte

296 Most notably, interneurons in the olfactory bulb, which are known to be inhibitory, repres

297 this plasticity are the granule cells of the olfactory bulb, which integrate bottom-up sensory inputs

298 by inactivation of LC or pretreatment of the olfactory bulb with a broad-spectrum noradrenergic recep

299 uts regulate inhibition in all layers of the olfactory bulb with a previously overlooked synaptic com

300 o controls, most women with uRPL had smaller olfactory bulbs, yet increased hypothalamic response in