ライフサイエンスコーパス: olfactory system

1 mble observations from neurons in the insect olfactory system.

2 ts exhibit FXGs in mature axons in the adult olfactory system.

3 al cavity likely reflects a highly sensitive olfactory system.

4 a code can be read by neural circuits of the olfactory system.

5 imary afferent connections in the Drosophila olfactory system.

6 Here, we examined the role of UPF3B in the olfactory system.

7 he initial signal transformation site of the olfactory system.

8 is ability is particularly important for the olfactory system.

9 ons we directly test this idea in the locust olfactory system.

10 re plasticity in the gross morphology of the olfactory system.

11 sensing has been attributed to any mammalian olfactory system.

12 ns in the first brain relay of the fruit fly olfactory system.

13 bout how experience changes circuitry in the olfactory system.

14 is necessary for correct development of the olfactory system.

15 have acted as axonal guidepost cells in the olfactory system.

16 lar cues for natural behavior in a mammalian olfactory system.

17 ding of information processing in the insect olfactory system.

18 th both speed and accuracy in the Drosophila olfactory system.

19 relevant physiological input to the Xenopus olfactory system.

20 initial stages of signal transduction in the olfactory system.

21 ork with this architecture in the Drosophila olfactory system.

22 three neuronal connections in the Drosophila olfactory system.

23 differentiation of CSPs in the A. lineolatus olfactory system.

24 re, we investigated this issue in the insect olfactory system.

25 t dynamics we here use a model of the locust olfactory system.

26 ning of this sensory-motor transition in the olfactory system.

27 initial site of synaptic integration in the olfactory system.

28 rons (OSNs) form the primary elements of the olfactory system.

29 rst stage of sensory processing in the mouse olfactory system.

30 s translated into perceived intensity by the olfactory system.

31 ing already at the first synapse of the main olfactory system.

32 maintain circadian rhythms in the mammalian olfactory system.

33 th of which are key components of the insect olfactory system.

34 issue in the locust (Schistocerca americana) olfactory system.

35 nt insights into the assembly of the nascent olfactory system.

36 Glomeruli are functional units in the olfactory system.

37 key molecular and anatomical features of the olfactory system.

38 an important site of integration in the fly olfactory system.

39 s underlying ORN diversity in the Drosophila olfactory system.

40 ature neurons of both the main and accessory olfactory system.

41 uron (PN) target selection in the Drosophila olfactory system.

42 l organization of glomeruli in the zebrafish olfactory system.

43 m for future studies of the adult Drosophila olfactory system.

44 to modulate early sensory information in the olfactory system.

45 oregulatory capacity at the expense of their olfactory system.

46 gue" platforms are inspired by the mammalian olfactory system.

47 nal and anatomical organization of the human olfactory system.

48 asal sensory neurons (VSNs) in the accessory olfactory system.

49 large-scale processing pathways of the human olfactory system.

50 epresentations in the detection layer of the olfactory system.

51 l areas in multisensory integration with the olfactory system.

52 of the profound structural plasticity of the olfactory system.

53 postsynaptic neurons in the adult Drosophila olfactory system.

54 anges in this initial cortical region of the olfactory system.

55 the nervous system, including the peripheral olfactory system.

56 in olfactory system but not in the accessory olfactory system.

57 nriched for genes associated with immune and olfactory systems.

58 chanosensitivity may be a general feature in olfactory systems.

59 lecular relationship between single and dual olfactory systems.

60 ed in most mammals by the main and accessory olfactory systems.

61 he neural crest and placodes to the otic and olfactory systems.

62 in the mouse retina and in the mouse and fly olfactory systems.

63 t and early functioning of the gustatory and olfactory systems.

64 ts of the digestive, respiratory, visual and olfactory systems.

65 to be functionally expressed in several non-olfactory systems.

66 ed four critical developmental stages of the olfactory system: 3rd instar larval (prepatterning), 8 h

67 Albeit located in parallel partitions of the olfactory system, 5-HT largely elicited MC excitation in

68 In the Drosophila olfactory system, 50 classes of olfactory receptor neuro

69 here we demonstrate that, in the adult mouse olfactory system, a 1-week-long exposure to an artificia

70 Insects modulate their olfactory system according to their physiological state

71 aling mechanism by which interneurons of the olfactory system act as directors for the activity-depen

72 roplasticity, we investigated the effects of olfactory system activation on neurotransmitter (NT) exp

73 is also evidence for asymmetry in the human olfactory system, although evidence in non-human animal

74 ophila antennal lobe, the first relay in the olfactory system and a model circuit for understanding o

75 ur, a response pathway through the accessory olfactory system and a new role for vomeronasal organ si

76 10-14 molar, spermine stimulated the lamprey olfactory system and attracted ovulatory females but did

77 t the ACo is reciprocally connected with the olfactory system and basal forebrain, as well as with th

78 howed abnormal development of the peripheral olfactory system and defective embryonic migration of th

79 s of metal-induced neurotoxicity of the fish olfactory system and identify novel miRNA biomarkers of

80 ctin depolymerization protein cofilin in the olfactory system and in the hippocampus.

81 onounced sexual dimorphism of the peripheral olfactory system and its representation in higher brain

82 elopment of the central nervous system, eye, olfactory system and pancreas, and is implicated in huma

83 have been studied extensively in the insect olfactory system and proposed to serve pattern separatio

84 HCDs were undetectable in the primary olfactory system and skeletal muscle of Carns1-deficient

85 is required for amino acid detection by the olfactory system and suggest that it plays a role in the

86 irst validated trans-Tango in the Drosophila olfactory system and then implemented it in the gustator

87 reby labeling immature OSNs in both the main olfactory system and vomeronasal organ.

88 ion but also for the development of the CNS, olfactory system, and pancreas.

89 targeted for serotonergic modulation in the olfactory system, and reveals novel extrinsic neurons th

90 he main olfactory system (MOS) and accessory olfactory system (AOS) detect and process pheromonal sti

91 The accessory olfactory system (AOS) guides behaviours that are import

92 B.SIGNIFICANCE STATEMENT The mouse accessory olfactory system (AOS) interprets social chemosignals, b

93 se cues is the primary role of the accessory olfactory system (AOS).

94 The olfactory system appears to be generally enlarged and is

95 onclusion, axonal regeneration in the locust olfactory system appears to be possible, precise, and fa

96 primary sensory receptive field maps of the olfactory system are exquisitely organized and respond d

97 The central processing pathways of the human olfactory system are not fully understood.

98 the different ORN classes in the developing olfactory system are unknown.

99 y of the interhemispheric connections in the olfactory system arise from AONpP, the third set examine

100 d serotonergic neurons within the Drosophila olfactory system as a model to establish a framework for

101 s use various biological components from the olfactory system as sensing elements, possessing great c

102 e calcium imaging techniques to identify the olfactory system as the primary sense used for salt dete

103 An extreme example is the olfactory system, as individual olfactory receptor neuro

104 on for M71 or MOR23 odorant receptors in the olfactory system, as is observed in F1-Trained-Ace or F1

105 ent of the visual, auditory, vestibular, and olfactory systems, attributable to profound defects in s

106 During development of the primary olfactory system, axon targeting is inaccurate and axons

107 rally assumed wiring principle in vertebrate olfactory systems, axons of single receptor neurons of X

108 The olfactory system becomes more sensitive when odor inputs

109 Olfactory system beta (15-35 Hz) and gamma (40-110 Hz) o

110 arbor in mature sensory neurons in the main olfactory system but not in the accessory olfactory syst

111 on classes is essential for functions of the olfactory system, but the underlying mechanisms that gen

112 e addressed this question in the adult mouse olfactory system by combining odor discrimination studie

113 OBPs contribute to the sensitivity of the olfactory system by transporting odorants through the se

114 phagocytosis by OECs in the developing mouse olfactory system by utilizing two transgenic reporter li

115 lastic, suggesting a means through which the olfactory system can assign related odour cues to common

116 The olfactory system can discriminate a vast number of odora

117 Olfactory systems can adopt different strategies to cont

118 ir body, no teeth, poor vision, and an acute olfactory system, comprise the only placental order (Pho

119 at Ts65Dn mice demonstrate an abnormality in olfactory system connectivity, a defect in the refinemen

120 The insect olfactory system consists of thousands of sensory neuron

121 s), some of which are perceived by the human olfactory system, contributing to a myriad flavors.

122 The accessory olfactory system controls social and sexual behavior.

123 udy demonstrated that the in vivo biomimetic olfactory system could provide novel approaches to enhan

124 t that hormonal modulation of the peripheral olfactory system could underlie differences in how males

125 The anatomically relatively simple olfactory system demonstrates lateralization in both hum

126 Coding of information in the peripheral olfactory system depends on two fundamental : interactio

127 The mammalian olfactory system detects a plethora of environmental che

128 onasal organ, a sensory structure within the olfactory system, detects chemical signals that affect s

129 A detailed description of olfactory system development in ants reveals that - unli

130 files suggesting they have a key role during olfactory system development.

131 The chemical specificity of the olfactory system does not come from specific receptors f

132 Through this transformation, the fish olfactory system dramatically expanded its capacity to d

133 and spread of other toxins and pathogens in olfactory system-driven animals.

134 In the mammalian olfactory system, each sensory neuron stochastically exp

135 The olfactory system encodes information about molecules by

136 The main olfactory system encodes information about molecules in

137 The olfactory system encodes odor stimuli as combinatorial a

138 in olfaction and suggest that the peripheral olfactory system, especially the central zone, may be st

139 The first synapse in the Drosophila olfactory system exhibits short-term depression, but can

140 The mammalian accessory olfactory system extracts information about species, sex

141 The olfactory system faces a hard problem: on the basis of n

142 The olfactory system faces the difficult task of identifying

143 approaches for the development of artificial olfactory systems for flavor and smell evaluation.

144 ry oscillations are a ubiquitous hallmark of olfactory system function in animals, direct evidence fo

145 w conceptual understanding on how changes in olfactory system function may have implications for neur

146 e first station of sensory processing in the olfactory system, GABAergic interneuron signaling shapes

147 Olfactory system gamma (40-110 Hz) and beta (15-35 Hz) o

148 nformation processing in the mouse accessory olfactory system guides the expression of social behavio

149 lopmental programs underlying the Drosophila olfactory system harbor a disproportionate amount of int

150 Interestingly, the honey bee olfactory system harbors two central parallel pathways,

151 The fly olfactory system has a three-layer architecture: The fly

152 Thus, the mammalian olfactory system has evolved multiple, parallel mechanis

153 Our study indicates that the olfactory system has powerful analytic abilities that ar

154 The mammalian olfactory system has the natural capacity to regenerate

155 However, the maximum temporal resolution of olfactory systems has not been accurately determined.

156 h the numerical simplicity of the Drosophila olfactory system, has produced rapid gains in our unders

157 odorants will interact with receptors in the olfactory system have achieved a success rate of 70%.

158 Odor receptors of the mammalian olfactory system have long been known to be activated in

159 molecular and cellular components of natural olfactory systems have been incorporated into artificial

160 This work demonstrated that artificial olfactory systems have potential for use as an innovativ

161 xamples from the mouse retina and Drosophila olfactory system, I present worked examples illustrating

162 d, sensitivity, and selectivity by which the olfactory system in animals can probe the chemical natur

163 We create a new method to stimulate the olfactory system in Drosophila or fruit flies.

164 f so, how such resolution is achieved by the olfactory system in flies.

165 at the antennal lobe, the first relay of the olfactory system in insects and analog to the olfactory

166 Aggression is controlled by the olfactory system in many animal species.

167 ays formed by mitral and tufted cells of the olfactory system in mice and characterized the emergence

168 anization of sensory cells in the peripheral olfactory system in mice for better odor detection.

169 Here, we examine the responses of the olfactory system in Plasmodium falciparum infected Anoph

170 The olfactory system in rodents serves a critical function i

171 al cortex and perirhinal cortex, septum, and olfactory system in the initial phase status epilepticus

172 e role of sensory systems, in particular the olfactory system, in the detection and perception of cue

173 This arrangement is much like the fly's olfactory system, in which afferents target uniquely ide

174 that DEET targets multiple components of the olfactory system, including OBPs and odorant receptors.

175 undantly expressed genes related to the moth olfactory system, including those encoding the olfactory

176 The need to breathe links the mammalian olfactory system inextricably to the respiratory rhythms

177 In the mammalian olfactory system, inhibitory interneurons called short a

178 erception of these odors within the mosquito olfactory system involves the interplay of odorant-bindi

179 The olfactory system is a natural biosensor since its periph

180 m and demonstrate that the Drosophila larval olfactory system is a powerful model in which to underst

181 The honeybee olfactory system is a well-established model for underst

182 ides novel insight into the way in which the olfactory system is affected in CNS demyelinating diseas

183 ling, these results imply that the mammalian olfactory system is capable of very high transient infor

184 The olfactory system is divided into processing channels (gl

185 The olfactory system is intricately linked with the endocrin

186 Axon targeting during the development of the olfactory system is not always accurate, and numerous ax

187 these results suggest that carnosine in the olfactory system is not essential for information proces

188 The olfactory system is particularly vulnerable to sensory d

189 attern of underlying pathology affecting the olfactory system is shown to be complex, involving multi

190 The mammalian accessory olfactory system is specialized for the detection of che

191 paucity of information available on the aged olfactory system is startling.

192 How odor information is encoded in the olfactory system is still poorly understood.

193 Together, these results suggest that the rat olfactory system is symmetric, with highly lateralized o

194 tor neurons, so the central challenge of the olfactory system is to demix its input.

195 first neural circuit in the mouse accessory olfactory system, is critical for interpreting social ch

196 ith specific focus on chemosensation and the olfactory system, is of appeal.

197 rneurons, partially instructed by the larval olfactory system laid down during embryogenesis, pattern

198 The olfactory system, like other sensory systems, can detect

199 The olfactory system maintains well-defined neural connectio

200 c OR expression, but also elucidates how the olfactory system maximizes and maintains the diversity o

201 In the mouse olfactory system, mitral cells (MCs) and tufted cells (T

202 ts show a similar level of complexity of the olfactory system morphology of small and large wasps.

203 Recent studies indicate that both the main olfactory system (MOS) and accessory olfactory system (A

204 If this is the case, the olfactory system must have neural mechanisms capable of

205 In the olfactory system, odorants evoke specific patterns of se

206 In the first brain relay of the olfactory system, odors are encoded by combinations of g

207 In the insect olfactory system, odors are initially represented in the

208 v2r expression pattern in main and accessory olfactory system of amphibians presents an excellent opp

209 Here, we use the olfactory system of awake locusts to test whether the ti

210 we analyzed microRNA (miRNA) profiles in the olfactory system of Cu-exposed zebrafish.

211 roadly projecting serotonergic neuron in the olfactory system of Drosophila Collectively, our study d

212 The larval olfactory system of Drosophila melanogaster contains 21

213 In the olfactory system of Drosophila melanogaster, it is relat

214 and odorant response properties of the early olfactory system of Drosophila melanogaster.

215 e deutocerebral neurons" (CSDns), within the olfactory system of Drosophila Specifically, we determin

216 Taking advantage of the well-characterized olfactory system of Drosophila, we derive a simple quant

217 correlates of novelty and familiarity in the olfactory system of Drosophila.

218 lectrophysiological analysis reveal that the olfactory system of female An. coluzzii undergoes concer

219 tive set-point that has been observed in the olfactory system of flies.SIGNIFICANCE STATEMENT The fir

220 Taking inspiration from the olfactory system of insects, we constructed a spiking ne

221 ction neurons and local neurons in the early olfactory system of insects.

222 In the main olfactory system of mammals, odours are detected by sens

223 ng with temperature sensitivity found in the olfactory system of mice and Xenopus laevis tadpoles, a

224 The olfactory system of Periplaneta americana is particularl

225 mperature perception also takes place in the olfactory system of rodents.

226 The distribution of HA in the olfactory system of S. officinalis is similar to the pre

227 s to the complexity of the morphology of the olfactory system of small and large T. evanescens.

228 r organization to that of other mammals, the olfactory system of the African wild dog has certain fea

229 ntly described the localization of HA in the olfactory system of the cuttlefish Sepia officinalis.

230 how these strategies are implemented in the olfactory system of the fruit fly.

231 Chemosensory specificity in the main olfactory system of the mouse relies on the expression o

232 We investigated the olfactory system of the primary wingless bristletail Lep

233 ptional profiles in the adult and developing olfactory system of the six species suggest the possibil

234 ene expression during the development of the olfactory system of two specialist Drosophila species to

235 associated with such transformations in the olfactory system of zebrafish, a small vertebrate that o

236 atus, has one of the most acute and eclectic olfactory systems of all mosquito species hitherto studi

237 Neural oscillations are ubiquitous in olfactory systems of mammals, insects and molluscs.

238 Whereas the olfactory systems of several bee and ant species have be

239 l the organization of the main and accessory olfactory systems of the African wild dog.

240 The insect olfactory system operates as a well-choreographed ensemb

241 n inhibitory circuit motif in the Drosophila olfactory system, parallel inhibition, which differs fro

242 t genes or sets of genes underlie visual and olfactory system phenotypes.

243 OSNs are the first cells in the olfactory system, physically contacting the odor molecul

244 e are congenitally anosmic and have abnormal olfactory system physiology, additionally Karstensen et

245 the largely feedforward organization of the olfactory system precludes reconstruction using standard

246 red piriform cortex, an integral part of the olfactory system, processes odor information relayed by

247 In the insect olfactory system, projection neurons of the antennal lob

248 on and glycation end products in the primary olfactory system, protein carbonylation was increased in

249 nstrate that during early development of the olfactory system, radial glia play an important role in

250 ensory processing circuits in the visual and olfactory systems receive input from complex, rapidly ch

251 The olfactory system receives intermittent and fluctuating i

252 elementary stimulus features encoded by the olfactory system remain poorly understood.

253 The olfactory system remains plastic throughout life because

254 he difficulty in monitoring how the mosquito olfactory system responds to repellent odors.

255 er of vital behaviors, the components of the olfactory system responsible for assigning meaning to od

256 How the olfactory system routes predator signals detected in the

257 ional explanation to account for patterns of olfactory system scaling in vertebrates, the primacy of

258 In the insect olfactory system, second order projection neurons target

259 Therefore, the role of CFAP69 in the olfactory system seems to be to allow the olfactory tran

260 The olfactory system senses odors, but not exclusively, as s

261 In the olfactory system, sensory inputs are arranged in differe

262 HR1 neurons, which were found throughout the olfactory system, striatum, and hypothalamus.

263 e exhibited no neurotoxicity, as measured by olfactory system testing and H&E staining of nasal tissu

264 Here we describe a feedforward model of the olfactory system that achieves both strong compression a

265 However, the cells and signals in the olfactory system that generate and coordinate these circ

266 s (OBPs) are small soluble proteins found in olfactory systems that are capable of binding several ty

267 tructural correlates of developing and adult olfactory systems, the paucity of information available

268 The coevolution of the OR repertoire and the olfactory system therefore reveals general principles of

269 ow known circuit mechanisms in the fruit fly olfactory system to derive a simple algorithm for habitu

270 n of responses increases the capacity of the olfactory system to distinguish complex odor mixtures.

271 s of information transmission may enable the olfactory system to efficiently identify and localize od

272 r, and highlight the dynamic capacity of the olfactory system to engage both object-level and compone

273 Here, we use the mammalian olfactory system to investigate such mechanisms.

274 athway that regulates the sensitivity of the olfactory system to odor concentrations, demonstrating t

275 How these cues signal through the olfactory system to promote behavior is largely unknown.

276 tudy used encoding characteristics of insect olfactory systems to develop a new paradigm for quantify

277 Insects use their olfactory systems to obtain chemical information on mati

278 The olfactory system translates a vast array of volatile che

279 The amphibian olfactory system undergoes massive remodeling during met

280 The mammalian olfactory system uses a large family of odorant receptor

281 We propose that the early olfactory system uses approximate Bayesian inference to

282 It is unclear whether the olfactory system utilizes a similar organizational schem

283 ptically suppressed the first synapse of the olfactory system via GABAB receptors on sensory terminal

284 ala's anatomical proximity to the peripheral olfactory system, we combined high-resolution fMRI with

285 processed, transformed, and stored within an olfactory system, we examined the anatomy of the input r

286 Using the locust olfactory system, we isolated two main causes of odor in

287 To Investigate the mouse olfactory system, we selectively remove GABAergic transm

288 lobe (AL) contains the first synapses of the olfactory system, where olfactory sensory neurons (OSNs)

289 del system for studying sparse coding in the olfactory system, where this format is important for acc

290 We are specifically interested in the olfactory system, wherein recent experimental studies ha

291 ation is particularly important in the human olfactory system, which is highly dependent on non-olfac

292 neurons (the primary sensory neurons of the olfactory system, which provide the initial olfactory in

293 fixed neural architecture of the vertebrate olfactory system, which requires that new olfactory rece

294 ty can occur in the periphery of adult mouse olfactory system, which should improve odor detection an

295 issues in the context of the mouse accessory olfactory system, which specializes in detection of chem

296 ated neural pathways, the main and accessory olfactory systems, which are specialized to detect odors

297 entities is particularly timely in the human olfactory system, whose structural differences from nonp

298 Honeybees possess an elaborate olfactory system with unique neuronal architecture: a du

299 It demonstrates that the human olfactory system, with its hundreds of different olfacto

300 urogenesis is a key feature of the mammalian olfactory system, with new olfactory sensory neurons (OS