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 classically respond to hypoxia by increasing chemosensory activity in the carotid sinus nerve (CSN),

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

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

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

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

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

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

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

10 ctivity also controlled immunity through ADF chemosensory and AFD thermosensory neurons that regulate

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

12 st L. tripustulatus relies mainly on contact chemosensory and gustatory cues.

13 imulate ventral axon branching in C. elegans chemosensory and mechanosensory neurons.

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

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

16 ecause AIY neurons are post-synaptic to most chemosensory and thermosensory neurons, it is probable t

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

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

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

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

21 Furthermore, the findings indicate that the chemosensory array is a promising platform for the devel

22 Bacteria utilize a large multiprotein chemosensory array to sense attractants and repellents i

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

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

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

26 and GLP-1 regulate two C. elegans behaviors: chemosensory avoidance of octanol and quiescence during

27 termined the chemical tuning of isolated CO2 chemosensory BAG neurons of the nematode Caenorhabditis

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

29 er concentrations as predicted by the gbBLM, chemosensory-based BLMs, the USEPA BLM, and hardness-adj

30 We took advantage of the disrupted chemosensory behavior characteristic of Caenorhabditis e

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

32 nnective hub, and promote reestablishment of chemosensory behavior.

33 ve greatly advanced our understanding of the chemosensory behaviors of host-seeking parasites.

34 To quantitatively understand chemosensory behaviors, it is desirable to present many

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

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

37 M) generated wings with ectopic sensilla and chemosensory bristle duplications.

38 receptors and are among the core proteins of chemosensory cascades.

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

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

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

42 eviously unidentified cholinergic, polymodal chemosensory cell in the mammalian urethra, the potentia

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

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

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

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

47 Chemosensory cells in the mucosal surface of the respira

48 that transduction by the intranasal solitary chemosensory cells is necessary to evoke trigeminally me

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

50 Isolated nasal chemosensory cells respond to the classic bitter ligand

51 Each barbel carries taste buds, solitary chemosensory cells, and epithelial nerve endings, all of

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

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

54 copy revealed that CheS is part of the polar chemosensory cluster and that its cellular localization

55 ulators that they phosphorylate and (ii) the chemosensory cluster to which they localize.

56 fficient to localize the CheAs to a specific chemosensory cluster.

57 est control strategies based on manipulating chemosensory communication.

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

59 In Escherichia coli the membrane-spanning chemosensory complexes are polar and new static complexe

60 e followed the relative positions of the two chemosensory complexes, FtsZ and MreB in aerobic and in

61 iated and cytoplasmic, chromosome-associated chemosensory complexes.

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

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

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

65 sex (dsx)-expressing neurons that respond to chemosensory cues (P1 neurons) were artificially activat

66 show that mammals can make use of bilateral chemosensory cues combined with serial sampling to local

67 guided by photosensory, mechanosensory, and chemosensory cues.

68 formation of interaction networks depends on chemosensory cues.

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

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

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

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

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

74 drive inspiratory motor output or increased chemosensory drive.

75 However, assessing these chemosensory effects is difficult because gastric infusi

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

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

78 uronal plasticity following male-male social chemosensory encounters.

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

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

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

82 However, chemosensory families often display the strongest genome

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

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

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

86 Chemosensory function was attenuated in the 24-month col

87 n with Galpha(q/11), did not affect Ce-GRK-2 chemosensory function, disruption of the predicted PH do

88 erentiate between nuclei that have a primary chemosensory function, versus those that are relays in t

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

90 bound conformation, also eliminated Ce-GRK-2 chemosensory function.

91 ting genes with potential implications in CB chemosensory function.

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

93 Olfactory and gustatory ligands bind to chemosensory G protein-coupled receptors (GPCRs) in spec

94 Taste is a major chemosensory gate used to decide whether or not an anima

95 Within the chemosensory gene families, we observed a general reduct

96 observed a general reduction in the level of chemosensory gene transcripts, although a subset of odor

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

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

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

100 These chemosensory GPCRs are expressed in highly specialized c

101 Neurons in mPFC can encode the chemosensory identity of gustatory stimuli.

102 Chemosensory information processing in the mouse accesso

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

104 fundamentally different strategies to encode chemosensory information, and that distinct receptor sub

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

106 litarius caudal region, which receives vagal chemosensory information.

107 ting the notion of integrative processing of chemosensory information.

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

109 These findings strengthen the link between chemosensory inputs and conserved mechanisms of lifespan

110 ility of the animal to discriminate distinct chemosensory inputs.

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

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

113 The OSNs express IR92a, a member of the chemosensory ionotropic receptor (IR) family and project

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

115 endent on uncharacterized maternally derived chemosensory ligands.

116 rdinate cell division and segregation of the chemosensory machinery.

117 By comparing chemosensory mechanisms to those in the visual system we

118 changes mediated by remodeling of canonical chemosensory modules.

119 or in Drosophila melanogaster males, but the chemosensory molecules, cells, and mechanisms involved r

120 evoked by repeatedly touching the food with chemosensory mouthparts.

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

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

123 to perform a systematic characterization of chemosensory neuron responses to multiple odors, odor co

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

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

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

127 thermal receptor 1 (gtr-1), is expressed in chemosensory neurons and has no role in heat sensing but

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

129 d RIH interneurons uptake 5-HT released from chemosensory neurons and secretory neurons.

130 og, distal-less, is required both to specify chemosensory neurons and to regulate the morphologies of

131 fic rescue experiments, we show that the ASI chemosensory neurons are newly identified components of

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

133 the conclusion that most, if not all, nasal chemosensory neurons derive from NeuroD1-expressing glob

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

135 Chemosensory neurons extract information about chemical

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

137 ed in part by environmental cues received by chemosensory neurons in the amphidial sensillae.

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

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

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

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

142 es several novel insights: (1) it shows that chemosensory neurons play important roles in the nematod

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

144 cuous warming, we find that TRPA1-expressing chemosensory neurons respond to chemicals but not warmth

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

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

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

148 depth; AGS-3 activates Galpha(o) in the ASH chemosensory neurons to allow food-deprived animals to d

149 e C. elegans connectome for pathways linking chemosensory neurons to neck motor neurons, and prune th

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

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

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

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

154 mouse retina, and in vivo in Caenorhabditis chemosensory neurons, Drosophila larval neuromuscular ju

155 n of familiar food activates the pair of ADF chemosensory neurons, which subsequently increase seroto

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

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

158 mic reticulum (ER) stress in the ASI pair of chemosensory neurons.

159 protein-coupled receptor DAF-37 in specific chemosensory neurons.

160 which is expressed exclusively by olfactory chemosensory neurons.

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

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

163 MIP is expressed in chemosensory-neurosecretory cells in the annelid larval

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

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

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

167 idence that two CheW proteins coexist in one chemosensory pathway and that both are essential for che

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

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

170 The chemosensory pathway of Rhodobacter sphaeroides comprise

171 The Frz chemosensory pathway regulates the cell polarity axis th

172 The Frz chemosensory pathway regulates the frequency of cell rev

173 heW(1) and CheW(3) are incorporated into one chemosensory pathway that is essential for B. burgdorfer

174 Trafficking is stimulated by a chemosensory pathway that is not dependent on the calori

175 domain of FrzCD, the receptor for the frizzy chemosensory pathway, interacts with two A-motility prot

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

177 ricter definitions for the components of the chemosensory pathway.

178 ulate lifespan and stress resistance through chemosensory pathways and the sirtuin SIR-2.1.

179 Chemosensory pathways are a major signal transduction me

180 switch is used to toggle between orthogonal chemosensory pathways by controlling the expression of C

181 However, we know that respiratory chemosensory pathways converge on the parabrachial nucle

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

183 sists of 26 chemoreceptors feeding into four chemosensory pathways.

184 cules not normally recognized by the natural chemosensory pathways.

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

186 plications for models of social identity and chemosensory perception.

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

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

189 n, but does not decrease channel function in chemosensory primary signal transduction, also restores

190 Circadian regulation of chemosensory processes is common in animals, but little

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

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

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

194 For example, CSP (chemosensory protein) and takeout genes, the dopamine pa

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

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

197 Membrane-associated chemosensory proteins form a number of dynamic unit-clus

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

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

200 tro phosphorylation studies with all the Dif chemosensory proteins that were expressed and purified f

201 Similar patterns were observed with chemosensory proteins, "plus-C" odorant-binding proteins

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

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

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

205 Insects sense odours via several chemosensory receptor families, including the odorant re

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

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

208 Zebrafish chemosensory receptor genes are expressed across a large

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

210 Chemosensory receptor proteins, including odorant recept

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

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

213 Further, a subset of GPCRs, chemosensory receptors (including olfactory and taste re

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

215 Thus, rodent olfactory sensory neurons and chemosensory receptors have the capacity for recognizing

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

217 n of olfactory signaling, although odors and chemosensory receptors involved are unknown.

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

219 d to uncover the relevant signaling ligands, chemosensory receptors, and responsive sensory neurons t

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

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

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

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

224 CB chemosensory reflex activation also results in unstable

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

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

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

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

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

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

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

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

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

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

235 initions for the different components of the chemosensory reflex, going from the salient molecules an

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

237 Chemosensory reflexes initiated by the carotid body and

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

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

240 ally tested this hypothesis by measuring the chemosensory response of newborn snakes to prey odors at

241 Snakes fed dragonfly larvae increased their chemosensory response to both dragonfly larvae and crayf

242 Perturbation of chemosensory responses in specific subsystems through di

243 We used OCPI microscopy to record chemosensory responses in the mouse vomeronasal epitheli

244 Our study demonstrates that innate chemosensory responses to prey can be modified by prey a

245 hemotaxis pathway, and CheR1 forms part of a chemosensory route that controls biofilm formation.

246 ar hydrocarbons (CHCs) at mating and utilise chemosensory self-referencing to recognise recent mates.

247 Chemosensory self-referencing, therefore, could be a wid

248 nique chemical cues are available to support chemosensory self-referencing.

249 s, including mammalian taste buds and insect chemosensory sensilla, show a marked compartmentalizatio

250 Bacterial chemosensory signal transduction systems that regulate m

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

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

253 Disruption of chemosensory signaling through the loss of TRMP5 abrogat

254 liminated the ability of Ce-GRK-2 to restore chemosensory signaling.

255 Processing of chemosensory signals in the brain is dynamically regulat

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

257 e identities and behavioral role(s) of these chemosensory signals, and how they interact, are incompl

258 A chemosensory signature of "self" that modulates behavior

259 but not warmth, a specificity conferred by a chemosensory-specific TRPA1 isoform with reduced thermos

260 Chemosensory specificity in the main olfactory system of

261 I (glomus) cells exhibit hypersensitivity to chemosensory stimuli and elevated sympathoexcitatory res

262 Many chemosensory stimuli evoke innate behavioral responses t

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

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

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

266 ing GRK-2 function are not hypersensitive to chemosensory stimuli.

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

268 e molecules are involved in the detection of chemosensory stimuli?

269 that just happen to display sensitivity to a chemosensory stimulus?

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

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

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

273 ry systems or the consequences of rhythms in chemosensory system function.

274 The Dif chemosensory system is essential for the regulation of E

275 A chemosensory system is reported that operates without th

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

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

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

279 e have identified and characterized the Che7 chemosensory system of Myxococcus xanthus, a common soil

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

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

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

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

284 y relation is tested in the Escherichia coli chemosensory system, which exhibits near-perfect chemore

285 approach to better understand the bacterial chemosensory system.

286 cluster encoding a putative chemotaxis-like chemosensory system.

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

288 Chemosensory systems and TCS both modulate phosphorelays

289 Chemosensory systems are complex, highly modified two-co

290 is known about how circadian clocks control chemosensory systems or the consequences of rhythms in c

291 Chemosensory systems provide attractive models to addres

292 the functional difference between these two chemosensory systems remains unclear.

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 minate rigorously between molecules that are chemosensory transducers at the head of a physiological

296 ng with an ever increasing list of potential chemosensory transducing molecules.

297 rylation of the histidine kinase CheA in the chemosensory transduction chain is a widespread mechanis

298 efinitions, re-evaluate current knowledge of chemosensory transduction, and propose the 'multiple sal

299 Chemosensory valence-encoding interneurons exist across

300 anism for generating rapid changes in innate chemosensory valence.