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

1 g the expression of one odorant receptor per olfactory sensory neuron.

2 astic activation of only one OR allele in an olfactory sensory neuron.

3 in antennal sensilla to receptors present in olfactory sensory neurons.

4 o transport in native mammalian tissue using olfactory sensory neurons.

5 resumed that the olfactory placode forms all olfactory sensory neurons.

6 properties of TAARs when expressed in native olfactory sensory neurons.

7 uces amyloid beta production, exclusively in olfactory sensory neurons.

8 hase of optogenetically driven activation of olfactory sensory neurons.

9 of nuclear organization that occurs in mouse olfactory sensory neurons.

10 code, where they are specified shortly after olfactory sensory neurons.

11 cess contributes to deficient replacement of olfactory sensory neurons.

12 ctivator of the unfolded protein response in olfactory sensory neurons.

13 hat express channelrhodopsin-2 in all of the olfactory sensory neurons.

14 GC-D is expressed in a special group of olfactory sensory neurons.

15 ural stem cells and down-regulated in mature olfactory sensory neurons.

16 mulation in the cytoplasm of differentiating olfactory sensory neurons.

17 , and are best studied in photoreceptors and olfactory sensory neurons.

18 ay be due, in part, to prolonged survival of olfactory sensory neurons.

19 cilia also occurs in auditory hair cells and olfactory sensory neurons.

20 e spatially circumscribed differentiation of olfactory sensory neurons.

21 the combinatorial activation of ensembles of olfactory sensory neurons.

22 eptors, inhibiting the basal spike firing in olfactory sensory neurons.

23 rant receptors expressed in the cilia of the olfactory sensory neurons.

24 ion required for the formation of functional olfactory sensory neurons.

25 Expression of human APPsw exclusively in olfactory sensory neurons also perturbs connectivity wit

26 heterologous expression, in both Drosophila olfactory sensory neurones and in human embryonic kidney

27 Thus, rodent olfactory sensory neurons and chemosensory receptors hav

28 , we examined the 3D nuclear organization of olfactory sensory neurons and determined the positions o

29 Here, we examined Drosophila olfactory sensory neurons and found that inhibitory odor

30 s in the OE extend beyond that of defects in olfactory sensory neurons and may include alterations in

31 as intermediaries in the excitation between olfactory sensory neurons and MCs.

32 does not determine the connectivity between olfactory sensory neurons and olfactory bulb projection

33 X, is the main Ca(2+)-extrusion mechanism in olfactory sensory neurons and photoreceptor cells.

34 fly brain, including three subpopulations of olfactory sensory neurons and projection neurons (PNs).

35 dy bridges the gap between the activation of olfactory sensory neurons and the odor percept.

36 We report marked loss of olfactory sensory neurons and their axonal projections a

37 ecifically expressed in newly differentiated olfactory sensory neurons and their axons during develop

38 u Hi-C on fluorescence-activated cell-sorted olfactory sensory neurons and their progenitors shows th

39 ection neurons receive odor information from olfactory sensory neurons and transmit it to higher brai

40 sly by capturing the population of activated olfactory sensory neurons and using expression profiling

41 We observed smaller olfactory bulbs, reduced olfactory sensory neurons, and disorganized epithelial u

42 (BBSome) as bona fide constituents of IFT in olfactory sensory neurons, and show that they exist in 1

43 f normal patterns of spontaneous activity in olfactory sensory neurons, and we uncover some of the me

44 asal cell (GBC) progenitor to differentiated olfactory sensory neuron are poorly characterized.

45 ew studies report how discrete identities of olfactory sensory neurons are converted into a spatial m

46 Here, we find olfactory sensory neurons are dramatically remodeled by

47 More than any other neuron, olfactory sensory neurons are exposed to environmental i

48 Olfactory sensory neurons are in direct contact with the

49 A subset of olfactory sensory neurons are labeled by expression of t

50 This model predicts that in mammals, where olfactory sensory neurons are replaced regularly, recept

51 Cilia of olfactory sensory neurons are the primary sensory organe

52 crucial to survival; however, the receptors, olfactory sensory neurons, are directly exposed to the e

53 The Netrin receptor DCC is expressed in olfactory sensory neurons around the time that they elab

54 elial cells, neuroepithelial taste cells, or olfactory sensory neurons at chemosensory mucosal surfac

55 We show that the major olfactory sensory neurons, AWB and AWC, play essential r

56 ely in the olfactory epithelium disrupts the olfactory sensory neuron axon targeting.

57 ers largely characterize independent sets of olfactory sensory neuron axons and glomeruli.

58 lfactory bulb, where they envelop bundles of olfactory sensory neuron axons in a manner distinct from

59 organization of the cytoskeleton changed as olfactory sensory neuron axons moved from the ONLo to th

60 By contrast, olfactory sensory neuron axons project correctly in mice

61 n the terminals of hippocampal mossy fibers, olfactory sensory neuron axons, and growth cones of prim

62 (OECs) are specialized glia associated with olfactory sensory neuron axons.

63 Chemical destruction of the olfactory sensory neurons blocked both virus trafficking

64 ys originating from a discrete population of olfactory sensory neurons but fail to document any synap

65 posed to modulate the odorant sensitivity of olfactory sensory neurons by inhibiting activation of cy

66 amines, and concomitant activation of sparse olfactory sensory neurons by these diamines.

67 These data indicate that olfactory sensory neurons can adapt to reductions in the

68 Olfactory sensory neurons chemosensory cilia are elongat

69 Each olfactory sensory neuron chooses just one OR from the mo

70 ion, localization, and axonal projections of olfactory sensory neuron classes.

71 Olfactory sensory neurons converge onto glomeruli in the

72 We identified a subpopulation of olfactory sensory neurons, defined by receptor expressio

73 se disruptions are associated with increased olfactory sensory neuron degeneration.

74 The encoding of odorant mixtures by olfactory sensory neurons depends on molecular interacti

75 Remarkably, this odor-evoked inhibition of olfactory sensory neurons elicited by itself a full rang

76 attraction to avoidance, as did odor-evoked olfactory sensory neuron excitation.

77 In the fruit fly Drosophila, not all olfactory sensory neurons express a seven transmembrane

78 Drosophila olfactory sensory neurons express either odorant recepto

79 These olfactory sensory neurons express IR64a, a member of the

80 Olfactory sensory neurons express just one out of a poss

81 Individual olfactory sensory neurons express only a single odorant

82 Differentiated olfactory sensory neurons express specific presynaptic p

83 ng these is the popular notion that a single olfactory sensory neuron expresses a single odorant rece

84 Because each olfactory sensory neuron expresses a single OR gene, mul

85 Each olfactory sensory neuron expresses one single odorant re

86 genes ( approximately 1,400 in mouse), each olfactory sensory neuron expresses one, and only one, of

87 related neurons receive synaptic input from olfactory sensory neurons expressing different olfactory

88 Olfactory sensory neurons expressing Or67b are sensitive

89 Olfactory sensory neurons expressing particular olfactor

90 oid neuropil structures formed by axons from olfactory sensory neurons expressing the same olfactory

91 alcium imaging recordings of dissociated rat olfactory sensory neurons, expressing the recombinant OR

92 te Netrins as the only known attractants for olfactory sensory neurons, first drawing OR111-7-express

93 tic protein gene expression, suggesting that olfactory sensory neurons follow an intrinsic program of

94 lfactory system suggests that the peripheral olfactory sensory neurons form synaptic connections befo

95 ulator of neural stem cell proliferation and olfactory sensory neuron formation in the olfactory epit

96 Pressure sensitivity of olfactory sensory neurons has been shown recently in mic

97 orco mutant olfactory sensory neurons have greatly reduced spontaneo

98 hunger modulates the sensitivity of specific olfactory sensory neurons in Drosophila and facilitates

99 mouse olfactory epithelium, imaging ~10,000 olfactory sensory neurons in parallel.

100 ribe a functionally segregated population of olfactory sensory neurons in the fruitfly, Drosophila me

101 rant-induced, activity-dependent survival of olfactory sensory neurons in the main olfactory epitheli

102 ion of neural stem cells and regeneration of olfactory sensory neurons in the mature Chd7(Gt/+) olfac

103 CO2 is sensed by a population of olfactory sensory neurons in the maxillary palps of mosq

104 e virus gains access to the CNS by infecting olfactory sensory neurons in the nasal mucosa of mice.

105 rojections of spatially organized classes of olfactory sensory neurons in the nose.

106 actory epithelium revealed numerous axons of olfactory sensory neurons in the right hemisphere of 27

107 ponse profile and the axonal identity of the olfactory sensory neurons in which they are expressed.

108 contribution of the cranial neural crest to olfactory sensory neurons in zebrafish and provide impor

109 r-evoked inhibition and excitation in single olfactory sensory neurons increases the odor-coding capa

110 or exposure to acetophenone, a ligand of M72 olfactory sensory neurons, increases the strength of M72

111 Olfactory sensory neurons innervate the olfactory bulb i

112 ory odorant response profiles to presynaptic olfactory sensory neuron inputs.

113 eceptor DAF-2, functionally switched the AWC olfactory sensory neuron into an interneuron in the salt

114 s the direct transduction of the activity of olfactory sensory neurons into motor response, whereas t

115 eparated by less than 1 mm [1], and a single olfactory sensory neuron is sufficient for near-normal g

116 receptor (OR) genes in the mouse genome, an olfactory sensory neuron is thought to express only one

117 ons of rationality arise when the circuit of olfactory sensory neurons is asymmetric.

118 MENT Spatially restricted differentiation of olfactory sensory neurons is both key to normal olfactor

119 R111-7:IRES:Gal4, in which a small subset of olfactory sensory neurons is labeled.

120 us, spatially constrained differentiation of olfactory sensory neurons is plastic, and any bias towar

121 e transport of ORs is regulated in mammalian olfactory sensory neurons is poorly understood.

122 y rectifying potassium channel Kir2.1 in the olfactory sensory neurons (Kir2.1 mice).

123 We also found that in these mice, the mature olfactory sensory neuron layer is reduced, and that olfa

124 nter of olfactory information, received from olfactory sensory neurons located on the antennae.

125 Odor/air stimulates CYP26B1 expression in olfactory sensory neurons mainly located in the dorsomed

126 The process by which an olfactory sensory neuron makes a decisive shift over tim

127 tional landscapes of Dnmt3a-deficient mature olfactory sensory neurons (mOSNs), the primary sensory n

128 cells through neuronal progenitors to mature olfactory sensory neurons (mOSNs).

129 r association with the continually generated olfactory sensory neurons, OEG have attracted interest f

130 Adaptation of the AWC olfactory sensory neurons of C. elegans requires the cGM

131 Here, we screened the olfactory sensory neurons of the maxillary palp (MP-OSNs

132 d by odorant receptors, which are located on olfactory sensory neurons of the nose.

133 e expressed in highly specialized cells, the olfactory sensory neurons of the nose.

134 its distribution was axonal-specific in both olfactory sensory neurons of the olfactory epithelium an

135 was unexpected because amino acid-sensitive olfactory sensory neurons of Xenopus commonly function i

136 The odor response properties of a mammalian olfactory sensory neuron (OSN) are determined by the tig

137 dy, we test the hypothesis that Tnc inhibits olfactory sensory neuron (OSN) axon growth in the develo

138 mechanisms contribute to the specificity of olfactory sensory neuron (OSN) axon innervation of the o

139 ) are thought to be critical determinants of olfactory sensory neuron (OSN) axon targeting and organi

140 or receptors (ORs) play an important role in olfactory sensory neuron (OSN) axon targeting/coalescenc

141 at allowed us to simultaneously label single olfactory sensory neuron (OSN) axonal arbors and their p

142 Olfactory sensory neuron (OSN) axonal extension and targ

143 the presence of a "glycocode" to help direct olfactory sensory neuron (OSN) axonal pathfinding.

144 R) are strongly implicated in coalescence of olfactory sensory neuron (OSN) axons and the formation o

145 The projection of olfactory sensory neuron (OSN) axons to the olfactory bu

146 s demonstrated considerable heterogeneity of olfactory sensory neuron (OSN) cell populations in wild-

147 precise role of the ion transporter NKCC1 in olfactory sensory neuron (OSN) chloride accumulation has

148 naling in starvation-dependent modulation of olfactory sensory neuron (OSN) function in the Drosophil

149 Much is known about the activation of olfactory sensory neuron (OSN) glomerular responses in t

150 Here, we examine olfactory sensory neuron (OSN) innervation of the Drosop

151 The mouse olfactory sensory neuron (OSN) repertoire is composed of

152 ttern likely results from both the intrinsic olfactory sensory neuron (OSN) sensitivity and the sorpt

153 We show that, whereas TCs respond to olfactory sensory neuron (OSN) stimulation with short la

154 etized mice, the physiological activation of olfactory sensory neuron (OSN) terminals reliably trigge

155 avoidance is mediated via a highly specific olfactory sensory neuron (OSN) type.

156 l receptors using Ca(2+) imaging in isolated olfactory sensory neurones (OSNs).

157 orting into a GFP+ sample enriched in mature olfactory sensory neurons (OSNs) and a GFP- sample enric

158 ion waveforms and examined spike patterns of olfactory sensory neurons (OSNs) and projection neurons

159 ribe a functionally segregated population of olfactory sensory neurons (OSNs) and projection neurons

160 hat can induce neurotransmitter release from olfactory sensory neurons (OSNs) and reduces the total t

161 It receives sensory input from the olfactory sensory neurons (OSNs) and sends, through its

162 h FAF1 is specifically expressed in immature olfactory sensory neurons (OSNs) and show that overexpre

163 y epithelium is mostly populated by ciliated olfactory sensory neurons (OSNs) and surrounding sustent

164 We determined that although olfactory sensory neurons (OSNs) are capable of supporti

165 Olfactory sensory neurons (OSNs) are chemoreceptors that

166 Vertebrate olfactory sensory neurons (OSNs) are located in direct c

167 ended beyond 48 h if EB- or CO(2)-responsive olfactory sensory neurons (OSNs) are silenced after eclo

168 Sustained OAZ expression arrests olfactory sensory neurons (OSNs) at an immature state an

169 Nonmotile cilia on olfactory sensory neurons (OSNs) compartmentalize signal

170 The cilia of olfactory sensory neurons (OSNs) compartmentalize the si

171 irst synapses of the olfactory system, where olfactory sensory neurons (OSNs) contact second-order pr

172 All olfactory sensory neurons (OSNs) derive from a NeuroD1-e

173 The mechanism by which olfactory sensory neurons (OSNs) detect ORs to signal to

174 Here we show that Or47b-and Or88a-expressing olfactory sensory neurons (OSNs) detect the fly-produced

175 In Drosophila melanogaster olfactory sensory neurons (OSNs) establish synapses with

176 odel of odor coding in which a population of olfactory sensory neurons (OSNs) expressing a single OR

177 Olfactory sensory neurons (OSNs) expressing a specific o

178 pecialized olfactory subsystem that includes olfactory sensory neurons (OSNs) expressing the receptor

179 n-promoting effect of synthetic cVA requires olfactory sensory neurons (OSNs) expressing the receptor

180 in mammals is the convergence of axons from olfactory sensory neurons (OSNs) expressing the same odo

181 In the olfactory bulb, axons of olfactory sensory neurons (OSNs) expressing the same olf

182 mmalian and insect olfactory systems is that olfactory sensory neurons (OSNs) expressing the same uni

183 tially but then are switched out, and/or the olfactory sensory neurons (OSNs) expressing them die.

184 Olfactory sensory neurons (OSNs) form synapses with loca

185 Mammalian olfactory sensory neurons (OSNs) form the primary elemen

186 retinoic acid-inactivating enzyme Cyp26B1 in olfactory sensory neurons (OSNs) forms a dorsomedial (DM

187 Oscillators in olfactory sensory neurons (OSNs) from Drosophila are bot

188 nd the axon hillock spiking mechanism of the olfactory sensory neurons (OSNs) have yet to be fully de

189 Primary olfactory sensory neurons (OSNs) impart both molecular a

190 tein (SNMP), is expressed in a population of olfactory sensory neurons (OSNs) implicated in pheromone

191 plete convergence when Mecp2 is deficient in olfactory sensory neurons (OSNs) in an otherwise wild-ty

192 so are much more sensitive to stimulation of olfactory sensory neurons (OSNs) in bulb slices.

193 Olfactory sensory neurons (OSNs) in chordates usually ha

194 We observed the synaptic output of olfactory sensory neurons (OSNs) in individual mice befo

195 icity also affects the input to the MOB from olfactory sensory neurons (OSNs) in the glomerular layer

196 We show that Atf5 is highly expressed in olfactory sensory neurons (OSNs) in the main olfactory e

197 Olfactory sensory neurons (OSNs) in the main olfactory e

198 In contrast to the widely held view that olfactory sensory neurons (OSNs) in the main olfactory e

199 orant receptor (OR) genes across millions of olfactory sensory neurons (OSNs) in the main olfactory e

200 Here we report that olfactory sensory neurons (OSNs) in the mammalian nose c

201 Curiously, olfactory sensory neurons (OSNs) in the mouse nose are d

202 ially detected by odorant receptors (ORs) on olfactory sensory neurons (OSNs) in the nose.

203 implicated in establishing the topography of olfactory sensory neurons (OSNs) in the olfactory bulb (

204 Olfactory sensory neurons (OSNs) in the periphery projec

205 Apoptosis of olfactory sensory neurons (OSNs) induced by olfactory bu

206 Afferent peripheral input from olfactory sensory neurons (OSNs) is modified via mostly

207 Input to the central nervous system from olfactory sensory neurons (OSNs) is modulated presynapti

208 Impaired ciliary protein transport in olfactory sensory neurons (OSNs) leads to anosmia, and i

209 Olfactory sensory neurons (OSNs) located in the dorsomed

210 dor molecules are transduced by thousands of olfactory sensory neurons (OSNs) located in the nasal ca

211 ctory behaviors are processed by first-order olfactory sensory neurons (OSNs) of the Drosophila larva

212 to bind odorant receptors (ORs) expressed in olfactory sensory neurons (OSNs) of the nose.

213 Olfactory sensory neurons (OSNs) project axons from the

214 Primary olfactory sensory neurons (OSNs) project their axons dir

215 Olfactory sensory neurons (OSNs) project their axons fro

216 As olfactory sensory neurons (OSNs) regenerate continuously

217 is a natural biosensor since its peripheral olfactory sensory neurons (OSNs) respond to the external

218 in olfactory epithelium contains a subset of olfactory sensory neurons (OSNs) responding to pheromone

219 is composed of multiple cell types including olfactory sensory neurons (OSNs) that are readily replac

220 2,000 glomeruli, each receiving inputs from olfactory sensory neurons (OSNs) that express a specific

221 Patch-clamp recordings reveal that olfactory sensory neurons (OSNs) that express SR1 respon

222 n olfactory bulb receives axonal inputs from olfactory sensory neurons (OSNs) that express the same o

223 In the mouse, axons of olfactory sensory neurons (OSNs) that express the same o

224 In addition, olfactory sensory neurons (OSNs) that express the transi

225 by the activation of a subset of ORs and the olfactory sensory neurons (OSNs) that express them.

226 screen for cilial membrane proteins of mouse olfactory sensory neurons (OSNs) that identified all the

227 detect odorous chemicals through specialized olfactory sensory neurons (OSNs) that transduce odorants

228 factory epithelium continues to generate new olfactory sensory neurons (OSNs) throughout life, we inv

229 he core determinant of identity for axons of olfactory sensory neurons (OSNs) to coalesce into glomer

230 is not known how M3-Rs affect the ability of olfactory sensory neurons (OSNs) to respond to odours.

231 G-protein-coupled olfactory receptors on the olfactory sensory neurons (OSNs) triggers a signaling ca

232 of the mammalian olfactory system, with new olfactory sensory neurons (OSNs) wiring into highly orga

233 Using patch-clamp technique on mouse olfactory sensory neurons (OSNs) with a defined odorant

234 In comparing purified mouse olfactory sensory neurons (OSNs) with neighboring cells,

235 adenylyl cyclase 3 (AC3), is coexpressed in olfactory sensory neurons (OSNs) with poly-N-acetyllacto

236 onally cooperate to provide individual mouse olfactory sensory neurons (OSNs) with the cell surface d

237 o flow-cytometrically sorted pools of mature olfactory sensory neurons (OSNs), and finally arriving a

238 was expressed in basal precursors, immature olfactory sensory neurons (OSNs), and olfactory ensheath

239 in and reporter are particularly abundant in olfactory sensory neurons (OSNs), and specific BBS8 anti

240 In vertebrate olfactory sensory neurons (OSNs), Ca(2+) plays key roles

241 ery mRNA detected in samples of mature mouse olfactory sensory neurons (OSNs), immature OSNs, and the

242 ually dimorphic neural coding of odorants by olfactory sensory neurons (OSNs), primary sensory neuron

243 In olfactory sensory neurons (OSNs), such regulation on the

244 These rhythms are dependent on clocks in olfactory sensory neurons (OSNs), suggesting that odoran

245 The olfactory epithelium (OE) is composed of olfactory sensory neurons (OSNs), sustentacular supporti

246 Since activity also affects olfactory sensory neurons (OSNs), we further examined th

247 nose, odorants are detected on the cilia of olfactory sensory neurons (OSNs), where a cAMP-mediated

248 C]GV1-57, that appears to specifically label olfactory sensory neurons (OSNs), which are essential fo

249 Quantification of the olfactory sensory neurons (OSNs), which detect odors wit

250 the dorsal OB is determined by two types of olfactory sensory neurons (OSNs), which reside in the do

251 osophila olfactory system, odorants activate olfactory sensory neurons (OSNs), which stimulate projec

252 activate unique, overlapping populations of olfactory sensory neurons (OSNs).

253 ted basal body apical migration in postnatal olfactory sensory neurons (OSNs).

254 mutated amyloid precursor protein (hAPP) in olfactory sensory neurons (OSNs).

255 of LSD1 and promotes the differentiation of olfactory sensory neurons (OSNs).

256 te to response termination and adaptation of olfactory sensory neurons (OSNs).

257 in vivo model system of axon guidance, mouse olfactory sensory neurons (OSNs).

258 o be mediated by direct synaptic inputs from olfactory sensory neurons (OSNs).

259 ic as a result of the loss of cilia on their olfactory sensory neurons (OSNs).

260 mination and proper adaptation of vertebrate olfactory sensory neurons (OSNs).

261 both concentrated in the axons of developing olfactory sensory neurons (OSNs).

262 m the placode, and extension of axons by the olfactory sensory neurons (OSNs).

263 uch genome-wide inversion is not observed in olfactory sensory neurons (OSNs).

264 neurosecretory activity in random subsets of olfactory sensory neurons (OSNs).

265 CD11b- and Iba-1-positive cells, and loss of olfactory sensory neurons (OSNs).

266 d that VEEV and WEEV enter the brain through olfactory sensory neurons (OSNs).

267 , CCKergic TCs receive direct input from the olfactory sensory neurons (OSNs).

268 nd TAAR expression in appropriate subsets of olfactory sensory neurons (OSNs).

269 by the odorant receptors on the membrane of olfactory sensory neurons, plays a vital role in their h

270 he adult olfactory system, except in a small olfactory sensory neuron population.

271 We report that deletion of Ric-8b in olfactory sensory neurons prevents stable expression of

272 n 2 (Nrp2), is known to mediate targeting of olfactory sensory neurons (primary neurons), to the post

273 Despite constant neurogenesis, olfactory sensory neurons project to precise, stereotypi

274 effect on cell proliferation in the OE or on olfactory sensory neurons projecting to the OB, but indu

275 ACE1 null mice have axon guidance defects in olfactory sensory neuron projections to glomeruli in the

276 targeting, fasciculation, and segregation of olfactory sensory neuron projections.

277 ry sensory neuron layer is reduced, and that olfactory sensory neurons show increased rate of cell de

278 Our results suggest that damage to olfactory sensory neurons (such as from air pollution) c

279 Our findings in mouse olfactory sensory neurons suggest that mechanisms that a

280 in the probability of glutamate release from olfactory sensory neuron synapses.

281 eir own expression and the patterning of the olfactory sensory neurons' synaptic connections in the b

282 Visualization of synaptic output from olfactory sensory neuron terminals into the olfactory bu

283 potentially mediated by local inhibition of olfactory sensory neuron terminals.

284 e) tested, suggesting that TFM inhibits both olfactory sensory neurons tested.

285 We observe that immature olfactory sensory neurons that express a given odorant r

286 We show that olfactory sensory neurons that express a subset of the T

287 Olfactory sensory neurons that express transient recepto

288 ich a fluorescent reporter selectively marks olfactory sensory neurons that have been activated recen

289 ry interneurons and of synaptic terminals of olfactory sensory neurons (the primary sensory neurons o

290 In a small subset of the olfactory sensory neurons, the odorant receptor ONE-GC g

291 ues are recognized by receptors expressed on olfactory sensory neurons, the primary sensory neurons o

292 EET blocks electrophysiological responses of olfactory sensory neurons to attractive odors in Anophel

293 tly of the number of odor components, to any olfactory sensory neuron type with a response curve that

294 th great precision by the axons of different olfactory sensory neuron types and act as functional uni

295 This subpopulation of olfactory sensory neurons was over-represented in sex-se

296 is phenotype is caused by ciliary defects of olfactory sensory neurons, we examined mice with deletio

297 ry epithelium (OE) generates only a very few olfactory sensory neurons when the basic helix-loop-heli

298 duction of tph-1 by functional regulation of olfactory sensory neurons, which underscores the importa

299 ry inputs to individual glomeruli, we loaded olfactory sensory neurons with a Ca(2+) indicator and me

300 utilized the genetically labeled murine M72 olfactory sensory neurons with the green fluorescent pro