ライフサイエンスコーパス: olfactory receptor neuron

1 ll relies on hundreds of distinct classes of olfactory receptor neuron.

2 the simple fruitfly has around 50 classes of olfactory receptor neuron.

3 l number are selected for expression by each olfactory receptor neuron.

4 ct with axons of their presynaptic partners, olfactory receptor neurons.

5 sitive transporters in Cl(-) accumulation in olfactory receptor neurons.

6 ble for generating current responses in frog olfactory receptor neurons.

7 s in intracellular calcium in cultured mouse olfactory receptor neurons.

8 of multiple purinergic receptor subtypes in olfactory receptor neurons.

9 ells receive direct, monosynaptic input from olfactory receptor neurons.

10 cellular abnormalities affecting peripheral olfactory receptor neurons.

11 e aqueous lymph surrounding the dendrites of olfactory receptor neurons.

12 oteins were detected in the processes of the olfactory receptor neurons.

13 T-10, an alpha tubulin, were specific to the olfactory receptor neurons.

14 lation of which are immediate progenitors of olfactory receptor neurons.

15 scussed in terms of natural turnover time of olfactory receptor neurons.

16 duction and concomitant decreased numbers of olfactory receptor neurons.

17 tory transduction, the outer dendrite of the olfactory receptor neurons.

18 tions to modulate the odorant sensitivity of olfactory receptor neurons.

19 ative of G(s)alpha that is also expressed in olfactory receptor neurons.

20 rather promoted survival of newly generated olfactory receptor neurons.

21 ate olfactory systems, in particular lobster olfactory receptor neurons.

22 ir through the nasal cavity to stimulate the olfactory receptor neurons.

23 ns present in the aqueous medium surrounding olfactory receptor neurons.

24 tribution of odorant receptors on individual olfactory receptor neurons.

25 r and CO biosynthesis in primary cultures of olfactory receptor neurons.

26 ce expressing the Ca(2+) indicator GCaMP3 in olfactory receptor neurons.

27 ular rind, overlapping with the terminals of olfactory receptor neurons.

28 y of citronellal-evoked action potentials in olfactory receptor neurons.

29 ll-autonomously for the production of mature olfactory receptor neurons.

30 hosphoinositide signaling pathway in lobster olfactory receptor neurons, a G protein alpha subunit of

31 to an inhibitory chemical synapse between an olfactory receptor neuron and an interneuron changed the

32 t possess a sense of smell, synapses between olfactory receptor neurons and central neurons occur in

33 mbly, including axon-axon interactions among olfactory receptor neurons and dendro-dendritic interact

34 early spatial and temporal interactions with olfactory receptor neurons and glia during the construct

35 ways regulating the expression of peripheral olfactory receptor neurons and in the glomerular process

36 mine modulates synaptic transmission between olfactory receptor neurons and OB neurons via a presynap

37 This finding suggests that olfactory receptor neurons and olfactory epithelium supp

38 The functional synaptic connectivity between olfactory receptor neurons and principal cells within th

39 ay a role in mediating communication between olfactory receptor neurons and projection neurons in the

40 nervous system occurs at the synapse between olfactory receptor neurons and second-order neurons in o

41 ic receptors are differentially expressed in olfactory receptor neurons and sustentacular support cel

42 gest that GnRH increases the excitability of olfactory receptor neurons and that the terminal nerve f

43 a we have confirmed the connectivity between olfactory receptor neurons and their postsynaptic target

44 st two layers of this system: the peripheral olfactory receptor neurons and their postsynaptic target

45 d to the kinetics of odor tracking in insect olfactory receptor neurons and to the latency of initial

46 actory bulb ablation results in apoptosis of olfactory receptor neurons and up-regulation of prolifer

47 expression of specific Phr1 splice forms in olfactory receptor neurons and vestibular and cochlear h

48 early, severe loss of neural precursors and olfactory receptor neurons, and the subsequent collapse

49 Olfactory receptor neurons are continuously replaced pos

50 ion times and pulse tracking capabilities of olfactory receptor neurons are faster than previously re

51 erties of presynaptic glutamate release from olfactory receptor neurons are similar between mitral an

52 projections and odor responses of mammalian olfactory receptor neurons, as well as the physiology of

53 Odorant treatment of olfactory receptor neurons augments HO2 phosphorylation

54 in other systems, is transiently present on olfactory receptor neuron axons and on glia during the c

55 lfactory bulb we (1) labeled radial glia and olfactory receptor neuron axons at 24-hour intervals by

56 2 is unable to protect transected Drosophila olfactory receptor neuron axons in vivo, mutant Nmnat2s

57 We show that a bursting subset of primary olfactory receptor neurons (bORNs) in lobster has the un

58 lations of rhythmically active or 'bursting' olfactory receptor neurons (bORNs) to extract and encode

59 eurons were distinct from those reported for olfactory receptor neurons but similar to embryonic LHRH

60 amily ligand GDF11, regulates the genesis of olfactory receptor neurons by inhibiting proliferation o

61 Removal of the synaptic targets of olfactory receptor neurons by olfactory bulb ablation re

62 Thus, insect olfactory receptor neurons can track stimuli of very sho

63 to HZ males and the normal HV antenna lacks olfactory receptor neurons capable of responding to the

64 This organ contains only 120 olfactory receptor neurons, compartmentalized in sensory

65 nor antenna develops a normal donor antennal olfactory receptor neuron complement.

66 ly, is expressed by the axons of a subset of olfactory receptor neurons during development and that,

67 ly, LN innervation required interaction with olfactory receptor neurons during development, and some

68 etronasal odorants can effectively reach the olfactory receptor neurons, eliciting glomerular respons

69 In Drosophila, about 50 classes of olfactory receptor neurons enter the brain where their a

70 ccurred in almost 60% of the total number of olfactory receptor neurons examined and appeared to be s

71 In the mouse, each class of olfactory receptor neurons expressing a given odorant re

72 ells receive exclusive excitatory input from olfactory receptor neurons expressing identical receptor

73 ansgenic lines of Anopheles gambiae in which olfactory receptor neurons expressing the odorant recept

74 Olfactory receptor neurons expressing the same receptor

75 olfactory system of the moth Manduca sexta, olfactory receptor neurons extend axons from the olfacto

76 Olfactory receptor neurons extend axons into the olfacto

77 irus-specific antigens in the cell bodies of olfactory receptor neuron for both the viruses, but only

78 Since olfactory receptor neurons form synaptic contacts with t

79 ometer GnRH on voltage-activated currents in olfactory receptor neurons from epithelial slices.

80 We tested this hypothesis by exposing olfactory receptor neurons from mudpuppies (Necturus mac

81 On-cell current-clamp recordings of olfactory receptor neurons from neonatal mouse slices re

82 naptic release in the vast majority of other olfactory receptor neurons has no effect on this behavio

83 The odor responses of olfactory receptor neurons have been characterized, and

84 Among neurons, olfactory receptor neurons have the highest level of HO

85 In this insect, two olfactory receptor neurons housed in antennal sensilla p

86 odors are encoded by the activity of primary olfactory receptor neurons, how odor codes may be transf

87 Highly sensitive, pheromone-specific olfactory receptor neurons in male antennae were complet

88 cortex explaining incoming activity from the olfactory receptor neurons in terms of a mixture of odor

89 comes restricted to the pheromone-responsive olfactory receptor neurons in the adult male.

90 stem depends on complex interactions between olfactory receptor neurons in the antenna, antennal-lobe

91 eurons (PNs) receive input by synapsing with olfactory receptor neurons in the antennal lobe and rela

92 Olfactory receptor neurons in the lobster express a nons

93 In addition to the expected lack of olfactory receptor neurons in the main olfactory epithel

94 Although olfactory receptor neurons in the nose face similar stim

95 histochemistry revealed segregation of CR-ir olfactory receptor neurons in the olfactory mucosa and t

96 The functional identity of an olfactory receptor neuron is determined in part by its r

97 Signal transduction in olfactory receptor neurons is believed to proceed via G-

98 sensory adaptation in rod photoreceptors and olfactory receptor neurons is thought to be the regulati

99 e activation of an odor-specific ensemble of olfactory receptor neurons leads to the activation of a

100 o the plasma membrane in mature cells of the olfactory receptor neuron lineage.

101 ends on the maturation state of cells in the olfactory receptor neuron lineage.

102 gnaling events at the dendrites and axons of olfactory receptor neurons mediate distinct functions.

103 pil that contain input and output processes: olfactory receptor neuron nerve terminals (input) and mi

104 , fucose-containing glycoprotein on axons of olfactory receptor neurons, O-linked glycoproteins on an

105 e the olfactory marker protein (OMP) gene in olfactory receptor neurons of adult OMP-null mice and de

106 quitous, cytoplasmic protein found in mature olfactory receptor neurons of all vertebrates.

107 ly differentiating photoreceptor cells), and olfactory receptor neurons of stage embryonic day 14 emb

108 A subset of olfactory receptor neurons of the Caribbean spiny lobste

109 ations; among these is a generalized loss of olfactory receptor neurons of the olfactory epithelium.

110 h-associated protein 43 [GAP43]), and mature olfactory receptor neurons (olfactory marker protein).

111 -treated animals had a decrease in OMP-IR in olfactory receptor neurons on the non-occluded side and

112 n-occluded side and an increase in OMP-IR in olfactory receptor neurons on the occluded side of the n

113 cytochemical method was devised to study the olfactory receptor neurons on the surface of the human o

114 uch may prolong odorant association with the olfactory receptor neurons, or the OP may contain specia

115 orant receptor gene defines a unique type of olfactory receptor neuron (ORN) and a corresponding type

116 ction does not compromise several aspects of olfactory receptor neuron (ORN) and olfactory ensheathin

117 Olfactory receptor neuron (ORN) axon diameters and the c

118 thesis, we studied morphological features of olfactory receptor neuron (ORN) axonal arbors on postnat

119 d interactions of radial glia with ingrowing olfactory receptor neuron (ORN) axons in late embryonic

120 To address the question of whether olfactory receptor neuron (ORN) axons preserve their top

121 n electron microscopy to reconstruct all the olfactory receptor neuron (ORN) axons that target a left

122 mbly of the Drosophila olfactory circuit, 50 olfactory receptor neuron (ORN) classes and 50 projectio

123 Odors typically activate multiple olfactory receptor neuron (ORN) classes and are therefor

124 hila olfactory circuit assembly, axons of 50 olfactory receptor neuron (ORN) classes and dendrites of

125 Drosophila uses 50 different olfactory receptor neuron (ORN) classes that are cluster

126 secreted semaphorin, Sema-2b, in Drosophila olfactory receptor neuron (ORN) development, we identifi

127 enets in the field of olfaction is that each olfactory receptor neuron (ORN) expresses a single odora

128 transcription factor combinations specifying olfactory receptor neuron (ORN) fates.

129 l that varied probabilistically depending on olfactory receptor neuron (ORN) input levels.

130 ugh it has been known for over 50 years that olfactory receptor neuron (ORN) neurogenesis and subsequ

131 pulses, oscillations suddenly slowed as net olfactory receptor neuron (ORN) output decreased; thus,

132 zation scales with the total activity of the olfactory receptor neuron (ORN) population.

133 We previously described a rat olfactory receptor neuron (ORN) subpopulation [the 2A4(+

134 odor representations in vivo by imaging from olfactory receptor neuron (ORN) terminals during control

135 Each receptor was expressed in a mutant olfactory receptor neuron (ORN) used as a "decoder," and

136 ontaining a morphologically distinct type of olfactory receptor neuron (ORN).

137 ach receiving input from a different type of olfactory receptor neuron (ORN).

138 e report here the signaling threshold of the olfactory receptor neuron (ORN).

139 urons (PNs) postsynaptic to the same type of olfactory receptor neuron (ORN).

140 as observed in the interstial spaces between olfactory receptor neurons (ORN).

141 i using mice that express synaptopHluorin in olfactory receptor neurons (ORN).

142 ordings were obtained from SCs and also from olfactory receptor neurones (ORNs) in situ.

143 ample is the olfactory system, as individual olfactory receptor neurons (ORNs) adopt unique sensory i

144 REB activity in rat olfactory epithelium and olfactory receptor neurons (ORNs) after stimulation with

145 fly olfactory system, axons of 50 classes of olfactory receptor neurons (ORNs) and dendrites of 50 cl

146 system of Drosophila melanogaster, axons of olfactory receptor neurons (ORNs) and dendrites of secon

147 In Drosophila, axons of first-order olfactory receptor neurons (ORNs) and dendrites of secon

148 hat Bex-ir is colocalized with OMP in mature olfactory receptor neurons (ORNs) and in the OMP-positiv

149 synaptic-depression at the synapses between olfactory receptor neurons (ORNs) and neurons within the

150 on depends on the differential activation of olfactory receptor neurons (ORNs) and on the proper tran

151 SDns received glomerulus-specific input from olfactory receptor neurons (ORNs) and projection neurons

152 The synapse between olfactory receptor neurons (ORNs) and projection neurons

153 nt only in these layers are the axons of the olfactory receptor neurons (ORNs) and the juxtaglomerula

154 ion to a limited set of neurons that include olfactory receptor neurons (ORNs) and the mushroom body

155 alteration of connection specificity between olfactory receptor neurons (ORNs) and their postsynaptic

156 ponse properties of different populations of olfactory receptor neurons (ORNs) and their spatial dist

157 Olfactory receptor neurons (ORNs) are a useful model, be

158 d channels (CNGCs) on the dendritic cilia of olfactory receptor neurons (ORNs) are critical for senso

159 ties in neuronal development in RTT, because olfactory receptor neurons (ORNs) are replaced throughou

160 Vertebrate olfactory receptor neurons (ORNs) are stimulated in a rh

161 In this study, we used olfactory receptor neurons (ORNs) as a model, because th

162 the Ca2+ transients that occur in salamander olfactory receptor neurons (ORNs) as a result of cyclic

163 expressed in the olfactory nerve and on the olfactory receptor neurons (ORNs) commencing with the ea

164 re we show that compartmentalized Drosophila olfactory receptor neurons (ORNs) communicate with each

165 Olfactory receptor neurons (ORNs) convey sensory informa

166 pulses and steps, but it remains unclear how olfactory receptor neurons (ORNs) detect the intensity a

167 Previous studies suggest that olfactory receptor neurons (ORNs) distributed in the nas

168 Drosophila olfactory receptor neurons (ORNs) elaborate a precise in

169 Olfactory receptor neurons (ORNs) express the GABA(B) re

170 From insects to mammals, olfactory receptor neurons (ORNs) expressing a common ol

171 In both insects and mammals, olfactory receptor neurons (ORNs) expressing specific ol

172 Olfactory receptor neurons (ORNs) expressing the same od

173 Recently, it has been shown that axons from olfactory receptor neurons (ORNs) expressing the same od

174 In Drosophila and mice, olfactory receptor neurons (ORNs) expressing the same re

175 that expression is restricted to subsets of olfactory receptor neurons (ORNs) for a number of these

176 hat Psidin is required in several classes of olfactory receptor neurons (ORNs) for survival and subse

177 ophila, axons of approximately 50 classes of olfactory receptor neurons (ORNs) form one-to-one connec

178 phila antennal lobe, early-arriving axons of olfactory receptor neurons (ORNs) from the antenna are r

179 This study shows that olfactory receptor neurons (ORNs) function upstream of a

180 a, we show that Notch is activated in select olfactory receptor neurons (ORNs) in an odorant-specific

181 f olfactory epithelia (OE) and physiology of olfactory receptor neurons (ORNs) in cat models of MPS I

182 Different classes of olfactory receptor neurons (ORNs) in Drosophila innervat

183 tegration of olfactory information begins in olfactory receptor neurons (ORNs) in Drosophila.

184 asked whether retinoic acid (RA) influences olfactory receptor neurons (ORNs) in the developing and

185 ypes of olfactory sensilla, which harbor the olfactory receptor neurons (ORNs) in the Drosophila ante

186 Olfactory receptor neurons (ORNs) in the nasal cavity de

187 hamsters and that induction of apoptosis in olfactory receptor neurons (ORNs) in the OSE resulted in

188 to bombykol and is expressed in specialized olfactory receptor neurons (ORNs) in the pheromone sensi

189 mined by a functional analysis of individual olfactory receptor neurons (ORNs) in vivo.

190 of the olfactory bulb, translate input from olfactory receptor neurons (ORNs) into projection-neuron

191 ensory identities of Drosophila melanogaster olfactory receptor neurons (ORNs) involved in sex-specif

192 Olfactory transduction in vertebrate olfactory receptor neurons (ORNs) involves primarily a c

193 2+ elevations within the cilia of vertebrate olfactory receptor neurons (ORNs) is a widely proposed c

194 Odor adaptation in vertebrate olfactory receptor neurons (ORNs) is commonly attributed

195 Olfactory receptor neurons (ORNs) of crustaceans are hou

196 day 14 (E14) to E19 expressed Sema3A in the olfactory receptor neurons (ORNs) of the olfactory epith

197 uron (PN) receives two sources of input: the olfactory receptor neurons (ORNs) of the same glomerulus

198 ich are detected with extreme sensitivity by olfactory receptor neurons (ORNs) on the antennae of Cul

199 the three major types of sensilla that house olfactory receptor neurons (ORNs) on the Drosophila ante

200 Olfactory receptor neurons (ORNs) produce a constant syn

201 In Drosophila, most individual olfactory receptor neurons (ORNs) project bilaterally to

202 Olfactory receptor neurons (ORNs) project to the rodent

203 xons and cell bodies of a specific subset of olfactory receptor neurons (ORNs) projecting to a limite

204 originates almost entirely from the primary olfactory receptor neurons (ORNs) rather than from spont

205 This process includes continuous addition of olfactory receptor neurons (ORNs) related to indetermina

206 vertebrate nose and the insect antenna, most olfactory receptor neurons (ORNs) respond to multiple od

207 a supported, in part, by the assumption that olfactory receptor neurons (ORNs) respond to odorants wi

208 A remarkable problem in neurobiology is how olfactory receptor neurons (ORNs) select, from among a l

209 Little is known about how individual olfactory receptor neurons (ORNs) select, from among man

210 Individual olfactory receptor neurons (ORNs) selectively express on

211 In Drosophila, approximately 50 classes of olfactory receptor neurons (ORNs) send axons to 50 corre

212 oscillations of synchronized populations of olfactory receptor neurons (ORNs) that appear after the

213 In doing so, we identify three olfactory receptor neurons (ORNs) that are organized in

214 The V glomerulus receives projections from olfactory receptor neurons (ORNs) that coexpress two GPC

215 Olfactory receptor neurons (ORNs) that express a common

216 The basis for host odor responses resides in olfactory receptor neurons (ORNs) that express chemorece

217 nique that depends on entry of agmatine into olfactory receptor neurons (ORNs) through cation channel

218 The responses of olfactory receptor neurons (ORNs) to odors have complex

219 he FEZF1 product is known to enable axons of olfactory receptor neurons (ORNs) to penetrate the CNS b

220 information about odors is transferred from olfactory receptor neurons (ORNs) to projection neurons

221 issues, continuous cell cultures containing olfactory receptor neurons (ORNs) were obtained from olf

222 and odorant receptors expressed in different olfactory receptor neurons (ORNs), but the origin of tem

223 In Drosophila olfactory receptor neurons (ORNs), DEET is detected thro

224 layers containing nuclei belonging to mature olfactory receptor neurons (ORNs), immature ORNs, and ba

225 In squid olfactory receptor neurons (ORNs), physiological studies

226 ological damage in both supporting cells and olfactory receptor neurons (ORNs), suggesting that non-n

227 In vertebrate olfactory receptor neurons (ORNs), the odorant-triggered

228 inding to membrane receptors on the cilia of olfactory receptor neurons (ORNs), thereby activating a

229 eactive processes relative to each other, to olfactory receptor neurons (ORNs), to projection neurons

230 pond to odors depends on the function of its olfactory receptor neurons (ORNs), which in turn depends

231 almost exclusively, expressed in vertebrate olfactory receptor neurons (ORNs).

232 tion neurons (PNs) than in their presynaptic olfactory receptor neurons (ORNs).

233 Or genes is found to be expressed in larval olfactory receptor neurons (ORNs).

234 rse sensitivities and response properties of olfactory receptor neurons (ORNs).

235 ulb (OB) requires innervation of the bulb by olfactory receptor neurons (ORNs).

236 g progenitor cells and blocked production of olfactory receptor neurons (ORNs).

237 ole in intracellular signaling in vertebrate olfactory receptor neurons (ORNs).

238 rmation and sensory adaptation in vertebrate olfactory receptor neurons (ORNs).

239 iating inhibitory odorant input to mammalian olfactory receptor neurons (ORNs).

240 s from their presynaptic partners, the adult olfactory receptor neurons (ORNs).

241 g in patterning axon targeting of Drosophila olfactory receptor neurons (ORNs).

242 elated with changes in the firing pattern of olfactory receptor neurons (ORNs).

243 ng wiring and receptor characteristics of MP olfactory receptor neurons (ORNs).

244 of fish contains three intermingled types of olfactory receptor neurons (ORNs): ciliated, microvillou

245 ansiently expressed in newly differentiating olfactory-receptor neurons (ORNs) and has a key role in

246 Olfactory receptor neurons project from the sensory epit

247 actory system include the demonstration that olfactory receptor neurons project to specific glomeruli

248 Drosophila olfactory receptor neurons project to the antennal lobe,

249 During development, the axons of olfactory receptor neurons project to the CNS and conver

250 irmed that NOS was expressed in the axons of olfactory receptor neurons projecting to all glomeruli.

251 lar organization of a small subset of murine olfactory receptor neuron projection patterns-bilateral

252 ounterpart of the vertebrate olfactory bulb: olfactory receptor neurons, projection neurons, and inhi

253 depending on the amount of odor stimulation olfactory receptor neurons receive.

254 idual subunits to native channel function in olfactory receptor neurons remain unclear.

255 hese receptors in initiating transduction in olfactory receptor neurons remains to be established.

256 In the olfactory bulb, afferent olfactory receptor neurons respond to increasing concent

257 When olfactory receptor neurons respond to odours, a depolari

258 Little is known about how an olfactory receptor neuron selects a receptor, or how the

259 em has a three-layer architecture: The fly's olfactory receptor neurons send odor information to the

260 ysiological recordings from L-glutamate-best olfactory receptor neurons showed that NMDA and L-cystei

261 rent odors excite overlapping populations of olfactory receptor neurons, so the central challenge of

262 tarsus, and wing anterior margin, but not in olfactory receptor neurons, suggesting a gustatory role.

263 rganized into glomerular compartments, where olfactory receptor neurons synapse onto projection neuro

264 Primary olfactory receptor neurons terminate in anatomically and

265 times more pore plates and three times more olfactory receptor neurons than females.

266 blem: on the basis of noisy information from olfactory receptor neurons (the neurons that transduce c

267 A previously described subpopulation of rat olfactory receptor neurons, the 2A4(+)ORNs, is 1) distin

268 In isolated olfactory receptor neurons, the Na(+)-K(+)-2Cl(-) cotran

269 ivity in the outer dendritic segments of the olfactory receptor neurons, the site of olfactory transd

270 ected in the outer dendritic segments of the olfactory receptor neurons, the site of olfactory transd

271 In the olfactory mucosa containing the olfactory receptor neurons, the Us9 deletion mutant viru

272 Since cAMP mediates signal transduction in olfactory receptor neurons, this could contribute to the

273 Although odorants are known to activate olfactory receptor neurons through cAMP, the long-term e

274 We follow the progress from olfactory receptor neurons, through the first processing

275 reveal that NOS is expressed in the axons of olfactory receptor neurons throughout development and in

276 G(o) is expressed ubiquitously on axons of olfactory receptor neurons throughout the olfactory neur

277 t, maturation, targeting, and/or turnover of olfactory receptor neurons throughout the olfactory orga

278 rin repulsion regulates interactions between olfactory receptor neurons to help axons find their corr

279 y, in view of the symmetrical projections of olfactory receptor neurons to medial and lateral glomeru

280 The response of olfactory receptor neurons to odor mixtures is not well

281 ine herpesvirus 5 (BHV-5) infection from the olfactory receptor neurons to the brain.

282 ort of the gE epitope-deleted virus from the olfactory receptor neurons to the olfactory bulb is defe

283 s, the metyrapone treatment had no effect on olfactory receptor neurons tuned to the plant volatile (

284 Each olfactory receptor neuron typically expresses only one o

285 We have previously demonstrated that olfactory receptor neurons use glutamate to excite OB ne

286 The basal conductance of unstimulated frog olfactory receptor neurons was investigated using whole-

287 brane-rich preparation from the dendrites of olfactory receptor neurons, we have identified two types

288 In double-labeling experiments, olfactory receptor neurons were stained with 3,3' dihexa

289 Odours generate activity in olfactory receptor neurons, whose axons contact the dend

290 We labeled PC and VNO olfactory receptor neurons with injections of retrograde

291 Stimulation of olfactory receptor neurons with odors culminates in open