ライフサイエンスコーパス: chemosensory

1 labeled neurons of the body wall that may be chemosensory.

2 iny lobsters is growing, the effect on their chemosensory abilities has not yet been investigated.

3 of Kv may provide a mechanism to enhance the chemosensory activity of the CB and ventilation.

4 ne from males' antennae and maintained their chemosensory acuity and sexual discrimination among grou

5 nerves were used to study mechanosensory and chemosensory afferent function in 3-, 12- and 24-month-o

6 ons, via transmitters, between gustatory and chemosensory afferents inside taste buds will help expla

7 und pattern common to all investigated taxa: chemosensory afferents supplying thousands of intrinsic

8 e solitary tract (NTS), a site that receives chemosensory afferents, and the ventral surface of the m

9 a rational basis to initiate the design and chemosensory analysis of new low-calorie sweeteners.

10 itory electrical junction activity between a chemosensory and a mechanosensory circuit.

11 tem and basal forebrain, as well as with the chemosensory and basomedial amygdala.

12 ce that control sodium intake by integrating chemosensory and internal depletion signals.

13 earch is triggered by two parallel groups of chemosensory and mechanosensory glutamatergic neurons th

14 The chemosensory and mechanosensory modules are separate and

15 de-gated channel (CNGA), which suggests dual chemosensory and neurosecretory activities.

16 dence of functional interactions between the chemosensory and nutritional sciences.

17 Here, we identify chemosensory and oxygen-sensing circuits that affect the

18 turnal navigational abilities, which rely on chemosensory and tactile cues and, to a lesser degree, o

19 that is critical for maintaining an ordered chemosensory apparatus.

20 erior cortical amygdaloid nucleus (ACo) is a chemosensory area of the cortical amygdala that receives

21 However, the contribution of particular chemosensory areas (carotid vs. aortic bodies) to this r

22 potential oxygen-sensing cells in all three chemosensory areas innervated by branches of the Xth cra

23 However, the contribution of particular chemosensory areas, such as carotid (CB) vs. aortic bodi

24 olecular complexes: ribosome, virus capsids, chemosensory array, and photosynthetic chromatophore.

25 itical role of interface 2 in organizing the chemosensory array, in directing the clustered array to

26 clustered at the cell poles as in wild type chemosensory arrays.

27 cells possessing extended and highly ordered chemosensory arrays.

28 The chemosensory BAG neurons of C. elegans are striking exem

29 which is required for the differentiation of chemosensory BAG neurons, limits an ILP signal that repr

30 avoidance TOL-1 signaling is required in the chemosensory BAG neurons, where it regulates gene expres

31 Nevertheless, the neural mechanisms of chemosensory-based appetite regulation remain poorly und

32 e FOCE system approach and suggests that the chemosensory behavior of a deep-sea urchin may be impair

33 ecific aspects of the altered locomotory and chemosensory behavior of dauers.

34 nnective hub, and promote reestablishment of chemosensory behavior.

35 we increasingly know more about the role of chemosensory behaviors in mediating mosquito-host intera

36 f behavioural trials, lizards performed more chemosensory behaviour (tongue flicks, lip smacks and su

37 d provide a molecular basis for differential chemosensory behaviours driven by the brainstem raphe nu

38 sual gender perception draws on subconscious chemosensory biological cues, an effect that has been hi

39 ndicate that EGCs are selectively engaged by chemosensory blends, suggesting different roles for EGCs

40 We found the expression of the chemosensory cation channel dTRPA1 in these cells to be

41 e levels of neuromediators and expression of chemosensory cation channels, protein gene product 9.5 (

42 tems, the olfactory, gustatory, and solitary chemosensory cell (SCC) systems detect chemical stimuli

43 ns in the peripheral taste system: embryonic chemosensory cell fate determination and the specificati

44 olving a previously unidentified cholinergic chemosensory cell monitoring the chemical composition of

45 The tuft cell is a chemosensory cell that responds to signals in the extrac

46 Solitary chemosensory cells (SCCs) and their innervating fibers a

47 Solitary chemosensory cells (SCCs) are epithelial sentinels that

48 Solitary chemosensory cells (SCCs) of the nasal cavity are specia

49 t of airway T2Rs expressed in nasal solitary chemosensory cells activates a calcium wave that propaga

50 Tuft cells-rare solitary chemosensory cells in mucosal epithelia-are undergoing i

51 Chemosensory cells in the mucosal surface of the respira

52 ebrafish in both i) apical microvilli of the chemosensory cells of taste buds including the epitheliu

53 Tuft (or brush) cells are solitary chemosensory cells scattered throughout the epithelia of

54 Tuft cells are specialized taste-chemosensory cells that detect the presence of intestina

55 gain stronger insight for the role of these chemosensory cells, we examined immunocytochemical and i

56 hey are consumed, particularly the impact of chemosensory characteristics on their use.

57 Olfactory sensory neurons chemosensory cilia are elongated, mucus embedded, fully

58 o perturb the dendritic input of proteins to chemosensory cilia in living Caenorhabditis elegans.

59 he surface forming a knob projecting several chemosensory cilia of approximately 50 x 0.2 mum, devoid

60 B microcircuits thus adds a new dimension to chemosensory coding along the accessory olfactory pathwa

61 Chemosensory communication is essential to insect biolog

62 role for OXT signaling in the modulation of chemosensory communication of stress in humans.

63 peptide hormone oxytocin (OXT) influence the chemosensory communication of stress.

64 ogy categories related to muscle adaptation, chemosensory communication, detoxification of food plant

65 est control strategies based on manipulating chemosensory communication.

66 lb (AOB) plays a central role in conspecific chemosensory communication.

67 ic basis for stimulus pH detection in rodent chemosensory communication.

68 e results demonstrate the convergence of the chemosensory components of flavor onto single GC neurons

69 d glial cells which together are involved in chemosensory control of breathing and sleep homeostasis.

70 n the RTN region, which is necessary for the chemosensory control of breathing.

71 or interaction in quiet wakefulness when the chemosensory control system is intact, response gains ph

72 the presence of an evolutionarily conserved chemosensory cue within the blood odor mixture.

73 novel study suggests that species reliant on chemosensory cues to locate their prey may be at an incr

74 vity in response to attractive and repulsive chemosensory cues, characterizing multimodal coding for

75 males as well as responses of MeA neurons to chemosensory cues.

76 guided by photosensory, mechanosensory, and chemosensory cues.

77 ns, which was preceded by severe progressive chemosensory defects.

78 signaling pathways involved in these insect chemosensory-dependent behaviors requires the activity o

79 Here, we show that chemosensory detection of two secondary metabolites prod

80 most extensively studied for their roles in chemosensory detection, recent work has implicated two f

81 Artificial chemosensory devices have a wide range of applications i

82 l transduction systems to develop artificial chemosensory devices.

83 Altogether, our results provide evidence for chemosensory divergence between H. melpomene and H. cydn

84 drive inspiratory motor output or increased chemosensory drive.

85 future climate change conditions, alter the chemosensory-driven behavior of P. argus and may result

86 plasticity is induced after male-male social chemosensory encounters, resulting in enhanced MC suppre

87 After salient chemosensory encounters, the accessory olfactory bulb (A

88 uronal plasticity following male-male social chemosensory encounters.

89 ere we show that tuft cells, which are taste-chemosensory epithelial cells, accumulate during parasit

90 central nervous system (CNS) evolved from a chemosensory epithelium, but a simple epithelium has lim

91 e is a marker for perception of a variety of chemosensory experiences.

92 However, chemosensory families often display the strongest genome

93 kinase Ret, regulates the expression of the chemosensory fate determinant Phox2b early in GG develop

94 tions in regulating expression of a specific chemosensory fate.

95 the oral cavity are carried to the brain in chemosensory fibers that contribute to chemesthesis, the

96 haracterizing interindividual differences in chemosensory function and how they affect ingestive beha

97 We propose that this chemosensory function enables a mouse to rapidly assess

98 rimary cilia, it is possible to emulate this chemosensory function in CCA cells; these data warrant f

99 Here, we tested the hypothesis that the chemosensory function of cholangiocyte primary cilia act

100 ese findings highlight the importance of the chemosensory function of primary cilia for the control o

101 Chemosensory function was attenuated in the 24-month col

102 ting genes with potential implications in CB chemosensory function.

103 s gene expression and is necessary for their chemosensory function.

104 respiratory A. flavus may impair motile and chemosensory functions of airway cilia, contributing to

105 s cydno We provide a detailed description of chemosensory gene-expression profiles as they relate to

106 ative genomic and transcriptomic analyses of chemosensory genes in the citrus fruit fly B. minax prov

107 Large expansions of chemosensory genes involved in the reception of pheromon

108 The increase in expression of chemosensory genes suggests an enhanced role in adult bu

109 determinants of vectorial capacity, such as chemosensory genes, do not show elevated turnover but in

110 Of the 252 chemosensory genes, HmOBP20 (involved in volatile detect

111 These chemosensory GPCRs are expressed in highly specialized c

112 he expression of pth2 was neither visual nor chemosensory in origin but instead was mechanical, induc

113 Chemosensory information processing in the mouse accesso

114 It integrates chemosensory information that are both peripheral from t

115 w these rare and unique cell types transduce chemosensory information to the nervous system has been

116 regulates two parallel circuits that process chemosensory information, the accessory and main olfacto

117 nd loss of Phox2b expression with subsequent chemosensory innervation deficits, indicating that Ret i

118 x/fx) mice, although there was not a loss of chemosensory innervation of the remaining fungiform tast

119 ility of the animal to discriminate distinct chemosensory inputs.

120 gr2-Pet1 neurons, which project primarily to chemosensory integration centers and are themselves chem

121 pitations and dyspnea via stimulation of non-chemosensory interoceptive channels would be sufficient

122 TRPA1 is a chemosensory ion channel that functions as a sentinel fo

123 nic altricial birds are capable of acquiring chemosensory knowledge of their parents during early dev

124 re we reveal the evolutionary origins of the chemosensory machinery that controls flagellar motility

125 rdinate cell division and segregation of the chemosensory machinery.

126 gths and limitations of different biological chemosensory material at the heart of these devices, as

127 changes mediated by remodeling of canonical chemosensory modules.

128 evoked by repeatedly touching the food with chemosensory mouthparts.

129 onas aeruginosa PAO1 has a much more complex chemosensory network, which consists of 26 chemoreceptor

130 ate a G-protein-signaling pathway in the ASJ chemosensory neuron pair that induces expression of the

131 We identified a single larval chemosensory neuron that detects these molecules.

132 a bacterial-produced signal and the nematode chemosensory neuron that permit cross-kingdom interactio

133 ted variant of channelrhodopsin, in specific chemosensory neurons and expose large numbers of freely

134 Second, peripheral sensory neurons-olfactory chemosensory neurons and nociceptor sensory neurons-dete

135 Here, using Caenorhabditis elegans chemosensory neurons as a model system, we provide proof

136 larvae, suggesting a role of the intestine, chemosensory neurons ASI and ASJ, and the interneuron PV

137 ous expression of unc-7 in touch-insensitive chemosensory neurons confers ectopic touch sensitivity,

138 ing the sensory endings of C. elegans' major chemosensory neurons exhibit strong and sustained decrea

139 Chemosensory neurons extract information about chemical

140 hown to be expressed in different Drosophila chemosensory neurons for sensing a variety of chemicals.

141 Aedae-KR was immunolocalized in contact chemosensory neurons in prothoracic tarsi and in sensory

142 The mouse geniculate ganglion contains chemosensory neurons innervating lingual and palatal tas

143 ion of the proton-activated receptor GPR4 in chemosensory neurons of the mouse retrotrapezoid nucleus

144 or-type guanylate cyclase GCY-9, to cilia in chemosensory neurons of the nematode Caenorhabditis eleg

145 In chordates, mechanosensory and chemosensory neurons of the peripheral nervous system (P

146 s involved in the regulation of breathing by chemosensory neurons of the retrotrapezoid nucleus in th

147 l map reveals that despite the dense wiring, chemosensory neurons represent the environment using spa

148 ractive odors, and inhibition of one or more chemosensory neurons that are inhibited by attractive od

149 AIA interneurons receive input from multiple chemosensory neurons that detect attractive odors.

150 ansmembrane proteins, which are expressed in chemosensory neurons that detect environmental stimuli.

151 have identified different classes of contact chemosensory neurons that detect female or male pheromon

152 by promoting the development and function of chemosensory neurons that surveil the metabolic activity

153 porally restricted stimulation of Drosophila chemosensory neurons with an array of different chemical

154 protein Cx36 between Caenorhabditis elegans chemosensory neurons with opposite intrinsic responses t

155 evelopment and subsequent diversification of chemosensory neurons within the geniculate ganglion (GG)

156 eneberg ganglion, the vomeronasal organ, and chemosensory neurons within the main olfactory epitheliu

157 on of the insulin peptide INS-6 from the ASI chemosensory neurons, resulting in diminished neuroendoc

158 and pheromone signals both originate in ASI chemosensory neurons, we hypothesized that they might ac

159 a high-throughput pipeline to quantify brain chemosensory neurons, we identify the conserved tyrosine

160 y short isoform of VAB-3 is expressed in BAG chemosensory neurons, where it promotes gene expression

161 The olfactory epithelium houses chemosensory neurons, which transmit odor information fr

162 xpressed in five types of amphid and phasmid chemosensory neurons.

163 P, expressed in distinct types of Drosophila chemosensory neurons.

164 urons, the bilaterally symmetric pair of ASJ chemosensory neurons.

165 requiring coordinated activity from multiple chemosensory neurons.

166 ls, that interact with PHOX2B-expressing RTN chemosensory neurons.

167 This chemosensory odorant receptor response was not mediated

168 n the rhodopsin family, known to contain the chemosensory olfactory receptor subfamily.

169 ensitive glomus cells of the carotid body, a chemosensory organ at the carotid artery bifurcation tha

170 ula, but not at later stages when a putative chemosensory organ forms.

171 alis is similar to the presence of HA in the chemosensory organs of gastropods but is different than

172 Previous studies identified the Dif chemosensory pathway as crucial for the regulation of EP

173 Sensory adaptation in the Escherichia coli chemosensory pathway has been the subject of interest fo

174 The Frz chemosensory pathway regulates the cell polarity axis th

175 taxis that has 5 chemoreceptors and a single chemosensory pathway, Pseudomonas aeruginosa PAO1 has a

176 ental data allowed us to conclude that three chemosensory pathways in P. aeruginosa utilize one chemo

177 cholerae, this organism has three different chemosensory pathways that together contain over 50 prot

178 nsure their survival, these bacteria rely on chemosensory pathways to sense and respond to changing e

179 sists of 26 chemoreceptors feeding into four chemosensory pathways.

180 An investigation into proteins involved in chemosensory perception in the melon fly, Bactrocera cuc

181 plications for models of social identity and chemosensory perception.

182 ator attraction by exploiting the visual and chemosensory perceptual biases of drosophilid flies.

183 sulfide-reactive functionalities on the same chemosensory platform in probe SNAN-3, a much broader ra

184 ght alter the cells and circuits involved in chemosensory processing and thereby change perception.

185 Electrophysiological recordings revealed chemosensory processing during the sampling period and t

186 te-dependent changes in the ECS may modulate chemosensory processing to regulate food choices.

187 rents to understand its inherent thermo- and chemosensory properties as well as the role of the ankyr

188 -degrading phosphodiesterases (PDEs) and the chemosensory protein BdlA, with BdlA playing a pivotal r

189 By couching population genomic analyses of chemosensory protein families within parallel analyses o

190 rant-binding receptors (OBPs), 4 single-copy chemosensory proteins (CSPs) and 53 candidate odorant re

191 Insect chemosensory proteins (CSPs) are a family of small solub

192 of other large families, we demonstrate that chemosensory proteins are not outliers for adaptive dive

193 Finally, we provide evidence that chemosensory proteins have experienced relaxed constrain

194 foundation for future functional studies of chemosensory proteins in the melon fly and for making mo

195 to control bees, while they do not differ in chemosensory proteomic profiles.

196 aster females are highly selective about the chemosensory quality of their egg-laying sites, an impor

197 of protein sequences putatively involved in chemosensory reception were identified and characterized

198 ll-specific markers and all but one of their chemosensory receptor classes expressed in the single ze

199 l an early evolutionary origin of the insect chemosensory receptor family and raise the possibility t

200 ur analyses have expanded annotations of the chemosensory receptor gene families, and provide first-t

201 the CO(2)-sensitive neurons and abundance of chemosensory receptor gene transcripts in the maxillary

202 Zebrafish chemosensory receptor genes are expressed across a large

203 e projections of 34 GAL4-lines of individual chemosensory receptor genes.

204 and chemical approaches to identify putative chemosensory receptor proteins and perturb chemotaxis ph

205 Chemosensory receptor proteins, including odorant recept

206 nd quantitative analysis of the codling moth chemosensory receptor repertoire.

207 The GRoSS alignment places the chemosensory receptor subfamilies for bitter taste (TAS2

208 systems; and 4) discovering new ligands for chemosensory receptors (e.g., those produced by the micr

209 omone transduction in mammals, including (a) chemosensory receptors and signaling components of the m

210 dinated reception of signals by mechano- and chemosensory receptors in fish.

211 Multiple Serpentine Receptor B (SRB) chemosensory receptors regulate Galpha pathways in gusta

212 We show that EC cells express specific chemosensory receptors, are electrically excitable, and

213 mouse nose has an additional small family of chemosensory receptors, called trace amine-associated re

214 enzymes producing pheromones, perception by chemosensory receptors, through to the neural circuits p

215 s of neuronal sub-types expressing different chemosensory receptors.

216 CB chemosensory reflex activation also results in unstable

217 the expression of AOE genes, ROS levels, CB chemosensory reflex and BP, and also stabilized breathin

218 s and ROS levels, reversed the heightened CB chemosensory reflex and hypertension, and also stabilize

219 wn to exhibit a heightened carotid body (CB) chemosensory reflex and hypertension.

220 wn to exhibit a heightened carotid body (CB) chemosensory reflex and hypertension.

221 ular breathing with apnoeas, an augmented CB chemosensory reflex as indicated by elevated CB neural a

222 necessary for maintaining a functional O(2) chemosensory reflex in the adult, modulate sleep homeost

223 gen (O2) sensing by the carotid body and its chemosensory reflex is critical for homeostatic regulati

224 re-programming of the redox state in the CB chemosensory reflex pathway.

225 ubstantial interindividual variation in this chemosensory reflex response, with profound effects on c

226 essure (BP), breathing and carotid body (CB) chemosensory reflex were examined in adult rats.

227 essure (BP), breathing and carotid body (CB) chemosensory reflex were examined in adult rats.

228 r breathing with apnoea and augmented the CB chemosensory reflex, with all these responses becoming n

229 Upon contact, several chemosensory related genes are repressed, especially odo

230 lixus showed increased expression of several chemosensory-related genes in imaginal bugs, while both

231 linked to traumatic insemination, a reduced chemosensory repertoire of genes related to obligate hem

232 The insect chemosensory repertoires of Odorant Receptors (ORs) and

233 Perturbation of chemosensory responses in specific subsystems through di

234 ely involved in transmission of skin-induced chemosensory responses to odorant stimulation, which mig

235 tudy provides a molecular description of the chemosensory sensilla of a greatly understudied taste or

236 Tuft cells are ideally positioned as chemosensory sentinels that can detect and relay informa

237 r injured or not, and decreased mechano- and chemosensory signal transduction in uninjured bystander

238 Bacterial chemosensory signal transduction systems that regulate m

239 In order to better understand the role of chemosensory signaling in filarial worm taxis, we employ

240 in the perception, storage and transport of chemosensory signaling molecules including air-borne odo

241 Specific diets or agonists that target these chemosensory signaling pathways may be considered as new

242 f phosphate flow and novel output signals in chemosensory signaling pathways that are involved in cys

243 al genetic and functional diversification of chemosensory signaling proteins in filarial worms and en

244 ass spectrometry the copy number of nineteen chemosensory signaling proteins in sperm flagella from t

245 Disruption of chemosensory signaling through the loss of TRMP5 abrogat

246 eveals a neural architecture that integrates chemosensory signals and the internal need to maintain s

247 Prey-derived chemosensory signals are synaptically transmitted to acu

248 Processing of chemosensory signals in the brain is dynamically regulat

249 Early processing of chemosensory signals occurs in two functionally and anat

250 hemosensory systems, and C) the interplay of chemosensory signals, cognitive signals, dietary intake,

251 A chemosensory signature of "self" that modulates behavior

252 etence (bacterial clearance tests) and their chemosensory specialization (proteomics of olfactory org

253 Chemosensory specificity in the main olfactory system of

254 behavioral choices of all animals, and many chemosensory stimuli can be either attractive or repulsi

255 Many chemosensory stimuli evoke innate behavioral responses t

256 enables integration and binding of multiple chemosensory stimuli over a prolonged time scale.

257 m multiple glomeruli, enables integration of chemosensory stimuli over extended time scales by interg

258 play a role in emotional learning involving chemosensory stimuli, such as olfactory fear conditionin

259 tatory cortex has been proposed to integrate chemosensory stimuli; however, no study has examined the

260 ely assign positive or negative valence to a chemosensory stimulus requires a gene-regulatory program

261 es behavioral and neural responses to social chemosensory stress cues utilizing a randomized, double-

262 duals exhibit heightened sensitivity towards chemosensory stress signals in sweat; however, it is sti

263 red this in the main olfactory epithelium, a chemosensory structure with over a thousand distinct cel

264 We demonstrate that FimL, a Chp chemosensory system accessory protein of unknown functio

265 stulated as an interface between the Frz(Mx) chemosensory system and gliding or pilus-motility appara

266 Oxygen activates the Che2 chemosensory system by binding to the PAS-heme domain of

267 The Escherichia coli chemosensory system consists of large arrays of transmem

268 dog genomes, with an expansion of the feline chemosensory system for detecting pheromones at the expe

269 er, the molecular components of the B. minax chemosensory system have not been well characterized.

270 A chemosensory system is reported that operates without th

271 thus support a mechanochemical model where a chemosensory system measures the mechanically induced co

272 selection has shaped the well-characterized chemosensory system of Drosophila melanogaster, we have

273 interspecific variation indicating that the chemosensory system of lacertids has undergone substanti

274 ailed examination of the neuroanatomy of the chemosensory system of P. pacificus.

275 ce contact, TFP retraction activates the Chp chemosensory system phosphorelay to upregulate 3', 5'-cy

276 thelium are therefore equipped with a subtle chemosensory system that communicates the sensory inform

277 tion and signal transduction through the Chp chemosensory system, a chemotaxis-like sensory system th

278 defective in both EPS production and the Frz chemosensory system, indicating that EPS regulates cellu

279 pili-based "twitching" motility and the Chp chemosensory system.

280 interacts with plant hosts via the efficient chemosensory system.

281 the rapid evolution and expansion of the ant chemosensory system.

282 Chemosensory systems are complex, highly modified two-co

283 Here, we provide an overview of the chemosensory systems in V. cholerae and the advances tow

284 Chemosensory systems provide attractive models to addres

285 scriminative capacity of the human olfactory chemosensory systems relies on the generation of a combi

286 ation of unique profile HMMs to link complex chemosensory systems with corresponding chemoreceptors i

287 Our results suggest that two ancient chemosensory systems with different inputs and outputs (

288 testing and assessment, B) the plasticity of chemosensory systems, and C) the interplay of chemosenso

289 ses and responds to its environment via four chemosensory systems.

290 into the developmental evolution of complex chemosensory systems.

291 is an opportunity to study the evolution of chemosensory systems.

292 ere addressed: A) the need to optimize human chemosensory testing and assessment, B) the plasticity o

293 The mouse olfactory mucosa is a complex chemosensory tissue composed of multiple cell types, neu

294 show that subtypes of hugin neurons connect chemosensory to endocrine system by combinations of syna

295 ) imaging in an ex vivo preparation to study chemosensory tuning in AOB external granule cells (EGCs)

296 itatory mitral cells (MCs), would show broad chemosensory tuning, suggesting a role in divisive norma

297 ural circuit function to generate changes in chemosensory valence are poorly understood.

298 e for biogenic amine signaling in regulating chemosensory valence as a function of hunger state.

299 Chemosensory valence-encoding interneurons exist across

300 anism for generating rapid changes in innate chemosensory valence.