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 he inner ear to proliferate and replace lost 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 and bitter denatonium, reliant on different sensory receptors.

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

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

11 veform into spike-timing differences between sensory receptors.

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

13 some-targeted degradative sorting of ciliary sensory receptors.

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

15 ting the proper ciliary targeting of various sensory receptors.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

32 Sensory receptors are the functional link between the en

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

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

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

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

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

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

39 provide approaches to successfully stimulate sensory receptor cell regeneration.

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

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

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

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

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

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

46 Although sensory receptor cells in the mammalian retina and inner

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

48 Sensory receptor cells of the mammalian cochlea are morp

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

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

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

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

53 ing the terminal differentiation of multiple sensory receptor cells.

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

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

56 accurate encoding of stimulus information by sensory receptor cells.

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

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

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

60 In mechanotransduction, sensory receptors convert force into electrical signals

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

62 Maps of sensory receptor epithelia and computed features of the

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

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

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

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

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

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

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

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

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

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

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

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

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

76 Cilia harbor sensory receptors for various signaling cascades critica

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

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

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

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

81 The number of sensory receptor genes varies extensively among differen

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

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

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

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

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

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

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

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

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

91 Sensory receptors in human skin transmit a wealth of tac

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

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

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

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

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

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

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

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

100 Sensory receptors in the vestibular organs of birds can

101 Sensory receptors in the vestibular system (hair cells)

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

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

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

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

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

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

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

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

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

111 ferentiated sensory neurons express a single sensory receptor molecule.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

133 Hair cells are sensory receptors responsible for transducing auditory a

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

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

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

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

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

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

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

141 At the sensory receptor terminal, CsCl decreased the threshold

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

158 Sensory receptors transduce physical stimuli in the envi

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

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

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

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

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

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

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