ライフサイエンスコーパス: sensory receptor

1 tro, identifying it as a probable ionotropic sensory receptor.

2 ed the electrical responses of the olfactory sensory receptors.

3 mbrane (BM) ultimately stimulate the mechano-sensory receptors.

4 ction of genes encoding immune functions and sensory receptors.

5 ntrol through deamidation and methylation of sensory receptors.

6 whether rescued hair cells could function as sensory receptors.

7 at function as light-responsive ion pumps or sensory receptors.

8 orking memory, suggesting even activation of sensory receptors.

9 a stimulus that can be readily transduced by sensory receptors.

10 t be involved in touch sensation by ciliated sensory receptors.

11 ress has been made towards restoring damaged sensory receptors.

12 he inner ear to proliferate and replace lost sensory receptors.

13 engaged neural circuits and, when possible, sensory receptors.

14 and bitter denatonium, reliant on different sensory receptors.

15 , which arrive in the reference frame of the sensory receptors.

16 ntry or retrograde IFT transport, of various sensory receptors.

17 veform into spike-timing differences between sensory receptors.

18 rns of expression and modes of regulation of sensory receptors.

19 some-targeted degradative sorting of ciliary sensory receptors.

20 haped by the movements of the animal and its sensory receptors.

21 ting the proper ciliary targeting of various sensory receptors.

22 lear inner hair cells (IHCs) are specialized sensory receptors able to provide dynamic coding of soun

23 posal of acid (H+) generated by neuronal and sensory receptor activity.

24 The inner hair cells (IHCs) are the primary sensory receptors adapted for rapid auditory signaling,

25 rotein expression of inflammatory cytokines, sensory receptors, adherens and tight junction (E cadher

26 ient-Receptor-Potential-Vanilloid-1 (TRPV-1) sensory receptor agonists, which alter sensory perceptio

27 t two decades, research has shown that these sensory receptors also regulate physiological processes

28 the specificity of oleocanthal for a single sensory receptor and the anatomical restriction of this

29 promote the cell-type-specific expression of sensory receptors and cell-surface proteins regulating s

30 late the proper ciliary targeting of various sensory receptors and consequently compromise the corres

31 e senses depend on high-fidelity encoding by sensory receptors and error-free processing in the brain

32 mice were the reduction of incisor ligament sensory receptors and increased molar CGRP.

33 subtypes, and start to express a variety of sensory receptors and ion channels.

34 ed that sneezing and coughing involve common sensory receptors and molecular neurotransmission mechan

35 e rise to high density arrays of specialised sensory receptors and neurons, evolved from these domain

36 chemical signals into electrical signals in sensory receptors and neurons.

37 ing and unbinding into electrical signals in sensory receptors and neurons.

38 ogether, our study reveals the difference in sensory receptors and neurotransmission/modulation mecha

39 EPSCs at the synapses of sensory receptors and of some CNS neurons include large

40 sharks, much remains uncertain regarding the sensory receptors and pathways involved, or the exact na

41 by nonvisual sensory systems as early as the sensory receptors and that these signals inform the emot

42 ward pathways bypass cranial taste and aroma sensory receptors and the cortical networks that give ri

43 bud cells that use distinct combinations of sensory receptors and transduction molecules.

44 er proprioceptors innervate their respective sensory receptors, and expression of three of these mark

45 Cilia function as sensory receptors, and mutants with defective sensory ci

46 O neurons expressing the V2R-A4 subfamily of sensory receptors, and the number of VNO neurons activat

47 the visual cortex, heterogeneous kinetics of sensory receptors, and the presence of giant cells in th

48 Each of our movements activates our own sensory receptors, and therefore keeping track of self-m

49 due to expression of different cell surface sensory receptors, and therefore the receptive field of

50 ferences to murine EECs, including hormones, sensory receptors, and transcription factors.

51 In addition, most sensory receptors are G protein-coupled receptors, which

52 involve the body for the trivial reason that sensory receptors are located in the body.

53 However, how the sensory receptors are properly targeted to the ciliary s

54 Sensory receptors are the functional link between the en

55 oprioceptive circuit elements, including the sensory receptors, are beginning to offer new and unprec

56 tionships of cuticular sensilla and internal sensory receptors, are the first computerized reconstruc

57 ons that extract meaningful information from sensory receptor arrays at the organism's periphery and

58 also be achieved through alterations in the sensory receptor arrays, or changes in sensory driven ac

59 ology and epidermal associations of internal sensory receptors BAG and URX.

60 he potential to enhance our understanding of sensory receptor biology and pave the way for innovative

61 de- and parasite-specific facets of nematode sensory receptor biology.

62 ys a mechanical role in stimulating cochlear sensory receptors, but the presence of fixed charge in T

63 s and are covered with specialized epidermal sensory receptors called Eimer's organs.

64 elective pressure to modify and even reverse sensory receptor capabilities.(5-7) Neither the extent t

65 een E12.5 and E14.5 before the initiation of sensory receptor cell differentiation, making it a uniqu

66 provide approaches to successfully stimulate sensory receptor cell regeneration.

67 nternal excitation is generated by a type of sensory receptor cells (the outer hair cells) in respons

68 Epidermal Merkel cells display features of sensory receptor cells and make 'synapse-like' contacts

69 ty of cell types ranging from lens fibres to sensory receptor cells and neurons.

70 lobe of insects, precise connections between sensory receptor cells and olfactory glomeruli form the

71 st olfactory behavior.SIGNIFICANCE STATEMENT Sensory receptor cells are generally thought to evolve t

72 sible for setting the resting sensitivity of sensory receptor cells are not well understood, it has g

73 lly, we found that vomeronasal and olfactory sensory receptor cells do express TRPML3 mRNA and protei

74 Although sensory receptor cells in the mammalian retina and inner

75 SIGNIFICANCE STATEMENT: Sensory receptor cells maintain high sensitivity at rest

76 Sensory receptor cells of the mammalian cochlea are morp

77 The endings of sensory receptor cells often lie within specialized comp

78 various sensory systems, where mutations of sensory receptor cells often resulted in reduced respons

79 In vision, balance and hearing, sensory receptor cells translate sensory stimuli into el

80 mination and proper adaptation of peripheral sensory receptor cells tune the sensory system for optim

81 systems is the exquisite sensitivity of the sensory receptor cells.

82 is thought to be essential for adaptation of sensory receptor cells.

83 and also, in some instances, the associated sensory receptor cells.

84 ing the terminal differentiation of multiple sensory receptor cells.

85 constantly released into the Corti fluid by sensory receptor cells.

86 accurate encoding of stimulus information by sensory receptor cells.

87 vertebrate nociceptors, including conserved sensory receptor channels.(9)(,)(10) We found that velve

88 main that is found in two types of microbial sensory receptors: chemotaxis transducers and histidine

89 hypoxia is reflex in nature and carotid body sensory receptor constitutes the afferent limb of this r

90 In mechanotransduction, sensory receptors convert force into electrical signals

91 es necessary for establishing competence for sensory receptor differentiation in the inner ear.

92 No sensory receptors directly specify the weight of body pa

93 sensory processing, including how peripheral sensory receptors encode external stimuli and how these

94 Maps of sensory receptor epithelia and computed features of the

95 Topographically organized maps of the sensory receptor epithelia are regarded as cornerstones

96 ing cells in chicken auditory and vestibular sensory receptor epithelia.

97 I stimulated DNA synthesis in the vestibular sensory receptor epithelium in a dose-dependent manner.

98 formation is not directly represented at the sensory receptor epithelium in the auditory system.

99 s stimulated DNA synthesis in the vestibular sensory receptor epithelium.

100 octopus CRs to probe the structural basis of sensory receptor evolution.

101 into structure-function relationships during sensory receptor evolution.

102 Sensory receptors evolve, and changes to their response

103 eal stochastic resonance in the responses of sensory receptors except for one study on human psychoph

104 d compare it with the mechanisms controlling sensory receptor expression patterns in the mouse retina

105 to the mechanisms that generate and maintain sensory receptor expression patterns.

106 robust, but imperfect, in defining selective sensory receptor expression.

107 t ganglion (DRG) neurons, where it acts as a sensory receptor for environmental irritants and oxidant

108 een individuals in eusocial insects, but the sensory receptors for CHCs are unclear.

109 nments and that NHR proteins may function as sensory receptors for external or internal sensory cues

110 The sensory receptors for hearing and balance are the hair c

111 gnaling by regulating the ciliary removal of sensory receptors for lysosomal degradation.

112 Hair cells are sensory receptors for the auditory and vestibular system

113 Cilia harbor sensory receptors for various signaling cascades critica

114 ous sources of neurotrophins by showing that sensory receptors from different cochlear regions were c

115 eurons requires restricted expression of one sensory receptor gene and the exclusion of all others wi

116 nsory systems where expression of a specific sensory receptor gene is selected randomly from a set of

117 We also describe the identification of a sensory receptor gene, srh-2, whose expression is induce

118 We therefore investigated CNVs in sensory receptor genes among 270 healthy humans by using

119 Moreover, sensory receptor genes are preferentially found in heter

120 sensory neurons, and match the expression of sensory receptor genes to specific neuron classes.

121 The number of sensory receptor genes varies extensively among differen

122 neuron typically expresses one, or very few, sensory receptor genes, excluding all others.

123 L/R asymmetric expression of three putative sensory receptor genes, gcy-5, expressed only in ASER, a

124 generating intra- and interspecific CNVs of sensory receptor genes.

125 viously unappreciated transcription factors, sensory receptors, growth factors, and kinases.

126 Sensory receptor hair cells (HCs) are necessary for tran

127 vestibular maculae of the inner ear contain sensory receptor hair cells that detect linear accelerat

128 signals, comprises a highly ordered array of sensory receptor (hair) cells and nonsensory supporting

129 We monitored the synaptic output of saccular sensory receptors (hair cells) by measuring the increase

130 For example, the signal-to-noise ratio of sensory receptors has been suggested to limit absolute t

131 hysiological and pathophysiological roles of sensory receptors has the potential to substantially imp

132 rk highlights a functional conservation of a sensory receptor in flies and mammals and shows that the

133 role for Otd in preventing co-expression of sensory receptors in blue vs. green-sensitive R8 photore

134 ing into account the concomitant movement of sensory receptors in freely moving animals.

135 Sensory receptors in human skin transmit a wealth of tac

136 ough the vagus nerve and function as primary sensory receptors in most of the gastrointestinal tract,

137 r pain-sensitive receptors, are unique among sensory receptors in that their sensitivity is increased

138 ese experiences begin with the excitation of sensory receptors in the body, which send somatosensory

139 neurons convey auditory information from the sensory receptors in the cochlea to the CNS.

140 Inner hair cells (IHCs) are the true sensory receptors in the cochlea; they transmit auditory

141 ditory impairment because of degeneration of sensory receptors in the eye and inner ear as in Usher s

142 ch a change in inner hair cells, the primary sensory receptors in the mammalian cochlea.

143 neural circuit after interacting with neural sensory receptors in the mucosa of the intestine and tha

144 odal domains probably also gave rise to some sensory receptors in the tunicate-vertebrate ancestor.

145 Sensory receptors in the vestibular organs of birds can

146 Sensory receptors in the vestibular system (hair cells)

147 its roles in the terminal differentiation of sensory receptors in vivo, we deleted the entire gene cl

148 patterns, respectively, with their hair cell sensory receptors, indicating that very different inform

149 In humans, experimental access to single sensory receptors is difficult to achieve, yet it is cru

150 to how the sensitivity and dynamic range of sensory receptors is established, peripheral synaptic in

151 t IHC functional differentiation into mature sensory receptors is initiated in the pre-hearing cochle

152 t IHC functional differentiation into mature sensory receptors is initiated in the prehearing cochlea

153 the ionotropic receptor (IR) superfamily of sensory receptors, is up-regulated in Orco mutant legs.

154 one-to-one connections with inner hair cell sensory receptors, it has an elaborate overall morpholog

155 out dynamic head movements is transmitted by sensory receptors, known as hair cells, in the labyrinth

156 e, the accumulation of particulate matter on sensory receptors located on their antennae may have det

157 h synaptic and auditory nerve disorders from sensory receptor loss.

158 Our study implies that other rhodopsin-like sensory receptors may interact with this conserved syste

159 ferentiated sensory neurons express a single sensory receptor molecule.

160 Neither the sensory receptors nor the afferents of the ampullary org

161 Hair cells, the sensory receptors of auditory and vestibular systems, us

162 Hair cells, the sensory receptors of the inner ear, respond to mechanica

163 teins present in a lysate of hair cells, the sensory receptors of the inner ear.

164 tion to prolonged stimuli by hair cells, the sensory receptors of the inner ear.

165 Hair cells, the sensory receptors of the internal ear, subserve differen

166 Inner hair cells (IHCs), the primary sensory receptors of the mammalian cochlea, fire spontan

167 d adult inner hair cells (IHCs), the primary sensory receptors of the mammalian cochlea, is mainly ca

168 Inner hair cells (IHCs) are the primary sensory receptors of the mammalian cochlea, transducing

169 Hair cells, the sensory receptors of the mammalian inner ear, have long

170 TRACT: Type I and type II hair cells are the sensory receptors of the mammalian vestibular epithelia.

171 nation-mediated lineage tracing, as do other sensory receptors of the nose, including vomeronasal, na

172 Of these, the sensory receptors of the type I tuberous organ are S-100

173 Hair cells are the principal sensory receptors of the vertebrate auditory system, whe

174 he mechanical sensitivity of hair cells, the sensory receptors of the vestibular and auditory systems

175 se data suggest that ablation of select pain sensory receptors or the inhibition of CGRP are associat

176 g intraflagellar transport (IFT) components, sensory receptors, or other TRP channels in different ce

177 ptor subtypes depends, in part, on extrinsic sensory receptor organ-derived signals.SIGNIFICANCE STAT

178 Maturation of sensory receptor precursors is delayed, and they never a

179 cal signals detected by the large variety of sensory receptors present in the gut microbiome.

180 n other excitable cells, the ion channels of sensory receptors produce electrical signals that consti

181 Changes in the genes encoding sensory receptor proteins are an essential step in the e

182 r of neuronal subtypes that express distinct sensory receptor proteins.

183 that express only one of several alternative sensory receptor proteins.

184 cell cycle after damage-the key step toward sensory receptor regeneration blocked in mammals.

185 However, sensory receptors remain drastically understudied outsid

186 anisms underlying the ciliary homeostasis of sensory receptors remain elusive.

187 The discovery of two distinct Chlamydomonas sensory receptors responsible for phototaxis reveals add

188 Hair cells are sensory receptors responsible for transducing auditory a

189 Injury to the sensory receptors shortly after birth leads to predictab

190 wever, the necessity of optimally processing sensory receptor signals for behaviour to approach this

191 Pain results from activation of sensory receptors specialized to detect actual or impend

192 dition, betaArr1 was observed in specialized sensory receptors such as Meissner corpuscles.

193 eted from cells and subsequently detected by sensory receptors such as those belonging to the large f

194 r, and spectral frequency, as imposed by the sensory receptor surface in the cochlea, seems to be the

195 rception emphasize the topographic layout of sensory receptor surfaces, while others emphasize implic

196 that is induced by signals derived from the sensory receptors surrounding the snout whiskers and tra

197 mammalian olfactory system is unique in that sensory receptors synapse directly into the olfactory bu

198 systems, attributable to profound defects in sensory receptor terminal differentiation.

199 At the sensory receptor terminal, CsCl decreased the threshold

200 presynaptic neurons, and, potentially, other sensory receptors that activate a neuron.

201 n of taste stimuli with one or more specific sensory receptors that are generally believed to be pres

202 dermal layer, express a variety of different sensory receptors that enable them to react to various e

203 large subfamily of histidine kinase-coupled sensory receptors that possess methylation sites for use

204 Outer hair cells (OHCs) are electromotile sensory receptors that provide sound amplification withi

205 s have been modified by evolution to produce sensory receptors that relay light signals to transducer

206 indings may also have implications for other sensory receptors that respond to acids, such as nocicep

207 ic acid and characterize how the responsible sensory receptor (the variant ionotropic glutamate recep

208 Unlike any other known sensory receptor, the hair cell uses positive feedback t

209 Similar to the primary sensory receptor, the inner hair cells (IHCs), the matur

210 tein required for efficient trafficking of a sensory receptor, the receptor-type guanylate cyclase GC

211 t processed by the ENS is derived from local sensory receptors, the central nervous system, and immun

212 Each movement we make activates our own sensory receptors, thus causing a problem for the brain:

213 eptor and the anatomical restriction of this sensory receptor to the pharynx, within the oral cavity.

214 lecular mechanisms for specific targeting of sensory receptors to cilia are largely unknown.

215 such as bradykinin, which stimulates cardiac sensory receptors to evoke a sympathoexcitatory reflex.

216 logical surfaces act at the level of primary sensory receptors to inform behavior.

217 rize an entire suite of brain circuits, from sensory receptors to motor units, that are involved in c

218 mission of excitatory inputs from the airway sensory receptors to the nucleus tractus solitarius and

219 Here we describe a complete disynaptic sensory receptor-to-muscle circuit for positive feedback

220 Sensory receptors transduce physical stimuli in the envi

221 Sensory receptor TRPV4 may serve such function.

222 oscopy to demonstrate that select GFP-tagged sensory receptors undergo rapid vectorial transport alon

223 ereas gene families related to body hair and sensory receptors were contracted.

224 is sets a premium on information capacity of sensory receptors, which can be maximized by optimizing

225 d by Ionotropic Receptors (IRs), a family of sensory receptors widely studied in invertebrate chemica

226 The absence of known sensory receptors with defined ligands and biologic func

227 ake the final steps towards fully functional sensory receptors with fast graded voltage responses.

228 ractions to encode efficiently the output of sensory receptors with the fidelity and dynamic range ne

229 ve different ionotropic receptor (IR) family sensory receptors, with dry air-activated Dry Cells reli