ライフサイエンスコーパス: mechanoreceptor

1 t a requirement for a conventional molecular mechanoreceptor.

2 osensing without the need for a conventional mechanoreceptor.

3 hanical signaling pathway in fly campaniform mechanoreceptor.

4 a critical role in craniofacial growth as a mechanoreceptor.

5 nance and sensory function of the piloneural mechanoreceptor.

6 reted with this single-mode and self-powered mechanoreceptor.

7 alpha5beta1 integrin acting as a predominant mechanoreceptor.

8 ttribute to the presence of intact cutaneous mechanoreceptors.

9 nts but do have essentially normal cutaneous mechanoreceptors.

10 dback from stretch-sensitive cardiopulmonary mechanoreceptors.

11 force stimuli that mimics slow-adapting skin mechanoreceptors.

12 neighboring DRG neurons activates RET in RA mechanoreceptors.

13 pruritoceptive afferents and C-low threshold mechanoreceptors.

14 that larger fingers have more widely spaced mechanoreceptors.

15 al fibers innervating the lamina propria and mechanoreceptors.

16 lanceolate nerve endings of rapidly adapting mechanoreceptors.

17 criminating functional subtypes of cutaneous mechanoreceptors.

18 ng is essential for the development of these mechanoreceptors.

19 e esophagus activated from different sets of mechanoreceptors.

20 d utilizes variables easily sensed by insect mechanoreceptors.

21 that these fibers function as low-threshold mechanoreceptors.

22 agus with nociceptors in addition to tension mechanoreceptors.

23 wed that L2 neurons are Adelta-low-threshold mechanoreceptors.

24 ears use chordotonal organs as the auditory mechanoreceptors.

25 f cutaneous (SSEA4) and muscle (parvalbumin) mechanoreceptors.

26 ent with an origin from cutaneous and muscle mechanoreceptors.

27 ng information from slow- and rapid-adapting mechanoreceptors.

28 uscle spindles are complex stretch-sensitive mechanoreceptors.

29 e mechanotransduction apparatus in cutaneous mechanoreceptors.

30 of thermal-tactile integration in cutaneous mechanoreceptors.

31 termination and the specification of lingual mechanoreceptors.

32 ng signals from multiple types of peripheral mechanoreceptors.

33 , and allodynia involves TrkB(+) light-touch mechanoreceptors.

34 umber and function of regenerated fibers and mechanoreceptors.

35 Mechano-gated ion channels are cardiac mechanoreceptors.

36 strated the necessity of Abeta-low-threshold mechanoreceptors (Abeta-LTMRs) for mechanical allodynia-

37 initiated when fast conducting low-threshold mechanoreceptors (Abeta-LTMRs) generate impulses at thei

38 l reflexes may be caused by left ventricular mechanoreceptor activation.

39 Zymosan produced sensitization of colon mechanoreceptors acutely in vitro and chronic (>or=7 wee

40 ry somatosensory cortex (SI and SII) to skin mechanoreceptor afferent drive.

41 We conclude that spike-timing precision of mechanoreceptor afferents in response to dynamic stimula

42 sensory terminals, suggesting innervation by mechanoreceptor afferents.

43 between touch threshold, tactile gnosis, and mechanoreceptor and sensory fiber function after nerve r

44 and painful stimuli, perhaps contributing to mechanoreceptor and/or H+ -gated nociceptor function.

45 re consistent with those of rapidly adapting mechanoreceptors and can signal the onset, offset and in

46 The hypothesis that polymodal mechanoreceptors and capsaicin-sensitive afferent nerves

47 ns to integrate information from neighboring mechanoreceptors and generate somatosensory perception.

48 tor 5-positive (TLR5(+)) Abeta low-threshold mechanoreceptors and is directly innervated by inhibitor

49 Sensory information from mechanoreceptors and nociceptors in the skin plays key r

50 ctional classes (nociceptors/pruritoceptors, mechanoreceptors and proprioceptors) that are distinguis

51 Thus, the early Ret(+) neurons are RA mechanoreceptors and Ret signaling is required for the a

52 receptor potential vanilloid type-4 (TRPV4) mechanoreceptors and vagal afferent purinergic receptors

53 rmation coded by the different low-threshold mechanoreceptors are carried by anatomically and electro

54 Low-threshold mechanoreceptors are classified as slow-adapting (SA) or

55 The non-nociceptive vagal tension mechanoreceptors are distinguished from nociceptors by t

56 hances the pressor response seen when muscle mechanoreceptors are engaged by muscle stretch.

57 These tension mechanoreceptors are exclusively A-fibres arising from t

58 s and mechanisms of development of RA and SA mechanoreceptors are largely unknown.

59 at MSNA responses to isolated stimulation of mechanoreceptors are measurable.

60 When mechanoreceptors are stimulated, mechanically sensitive

61 currently it is not known how impulses in C-mechanoreceptors are transmitted to higher centres.

62 peripheral mechanoreceptor types, as well as mechanoreceptors at different sites in the body.

63 anical output [4-6]-arises via feedback from mechanoreceptors at the base of the wings and structures

64 regions is affected by loading low pressure mechanoreceptors at the SVC-RAJ, a manipulation that als

65 d isolectin B4 binding, suggesting that some mechanoreceptors became CGRP-IR.

66 PCs are classified as primary mechanoreceptors because there is no synapse between the

67 Whisker motion was encoded best by whisker mechanoreceptors, but also by those innervating whisker

68 th central recordings reveal that intestinal mechanoreceptors, but not other cell types, potently and

69 ts consistent with SA1 and SA2 low-threshold mechanoreceptors, but some units, which we labeled "semi

70 mmunohistochemistry and possible alternative mechanoreceptors by real-time quantitative polymerase ch

71 , suggesting the functional reinnervation of mechanoreceptors by the reinnervating afferents.

72 VGLUT3-expressing unmyelinated low-threshold mechanoreceptors (C-LTMRs) are proposed to mediate pleas

73 od population of unmyelinated, low threshold mechanoreceptors (C-LTMRs).

74 Indeed, some mechanoreceptors can detect even nanometer-scale movemen

75 verified whether isolated stimulation of the mechanoreceptors can induce responses in muscle sympathe

76 udies demonstrate that modulation of surface mechanoreceptors can regulate the sensitivity to mechani

77 Interestingly, the body touch mechanoreceptors can themselves excite the dopamine neur

78 The identity of mechanoreceptor candidates is approached, with considera

79 Mechanoreceptor cells of the somatosensory system initia

80 Mechanoreceptor cells respond to a vast span of stimulus

81 Hair cells in the inner ear are specialized mechanoreceptor cells that detect sound and head movemen

82 pose that md-L neurons are long sought after mechanoreceptor cells through which food mechanics are p

83 cochlear sensory epithelium to replace lost mechanoreceptor cells, or hair cells.

84 fruit fly larvae and that it is a bona fide mechanoreceptor channel for nematode feeding behavior.

85 een made towards identifying the elusive AHC mechanoreceptor channel.

86 e pathway requires a conserved DEG/ENaC/ASIC mechanoreceptor complex in the FLP neuron pair.

87 This mechanoreceptor complex was recognized to have an essent

88 The two-receptor system could provide this mechanoreceptor complex with a tuning mechanism to achie

89 Fingertip mechanoreceptors comprise sensory neuron endings togethe

90 stimulation in the tiny population of leech mechanoreceptors, consisting of only 10 cells of two typ

91 These papillae show the hallmarks of a mechanoreceptor, containing nerves and encapsulated nerv

92 to sympathetic outflow is attenuated and the mechanoreceptor contribution is accentuated.

93 ity and a modest decrease in the size of the mechanoreceptor current (MRC).

94 Touching e1605 animals produces a reduced mechanoreceptor current that inactivates more rapidly th

95 cesses of ALM neurons and, consequently, the mechanoreceptor current.

96 hat external force evokes rapidly activating mechanoreceptor currents (MRCs) carried mostly by Na(+)

97 onses to noxious stimuli, we found that both mechanoreceptor currents and potentials were essentially

98 ation at the central terminals of myelinated mechanoreceptors depresses synaptic input to the spinal

99 The star has the densest concentration of mechanoreceptors described for any mammal, with a centra

100 gically distinct, myelinated, nodose-derived mechanoreceptors described in animals are poorly charact

101 mice the majority of putative low threshold mechanoreceptors did not exhibit ASIC-like currents but

102 this tuning difference might be explained by mechanoreceptors' differential sensitivity to the force

103 sed the threshold pressure for initiation of mechanoreceptor discharge.

104 Thus, gastric vagal mechanoreceptors display circadian rhythm, which may act

105 e relative timing of the first spikes of two mechanoreceptors encodes stimulus location, whereas summ

106 ich the extent of lamellar cell wrappings of mechanoreceptor endings determines their force sensitivi

107 Putative low threshold mechanoreceptors exhibited rapidly adapting mechanically

108 tant potentiometric-triboelectric hybridized mechanoreceptor exhibits distinctive features that are h

109 sts that PECAM-1 may not function as a major mechanoreceptor for activation of MAPK and AKT in ECs an

110 Furthermore, the versatility of the mechanoreceptor for resolving complex stimuli in diverse

111 Meissner's corpuscles (MCs) are cutaneous mechanoreceptors found in glabrous skin and are exquisit

112 orce into excitatory current in all types of mechanoreceptors from mice and tactile-specialist birds.

113 ein-3 (STOML3), which is required for normal mechanoreceptor function.

114 al opsin Rh1 impaired photoreceptor, but not mechanoreceptor, function.

115 latory circuit downstream of the MK-specific mechanoreceptor GPIb to coordinate polarized transendoth

116 sensory-related genes such as TRPs, PPKs and mechanoreceptors had consistent levels of expression in

117 Prior studies of the PIEZO1 mechanoreceptor have suggested a possible role in glauco

118 pe similar to that of IVD cells, a number of mechanoreceptors have been identified, with alpha5beta1

119 sation is normally suppressed by inputs from mechanoreceptors; however, in many forms of chronic itch

120 y thresholds of C- and A-slow-high-threshold mechanoreceptors (HTMR) fibers but had no effect on C-LT

121 might be true for myelinated high-threshold mechanoreceptors (HTMRs).

122 Esophageal mechanoreceptors, i.e. muscular slowly adapting tension

123 these data show for the first time that the mechanoreceptor ICAM-1 is negatively regulated by an act

124 muscle spindles, which are stretch-sensitive mechanoreceptors important for proprioception.

125 The DGC likely represents a mechanoreceptor in skeletal muscle-regulating muscle gro

126 be aligned with the angular location of the mechanoreceptor in the follicle, such alignment was obse

127 acutely, zymosan sensitized muscular/mucosal mechanoreceptors in both naive and hypersensitive mice.

128 Rapidly adapting (RA) mechanoreceptors in dorsal root ganglia (DRGs) express R

129 in ECs and that there are likely to be other mechanoreceptors in ECs functioning to detect shear stre

130 tified as candidates for a spring that gates mechanoreceptors in hair cells as well as in Drosophila

131 in the primary cilia, which also function as mechanoreceptors in many cells that influence multiple b

132 It is suggested that mechanoreceptors in muscle play an important role in the

133 e whisker deformations, which in turn excite mechanoreceptors in the follicle.

134 d intake is most sensitive to stimulation of mechanoreceptors in the intestine, whereas nutrient-acti

135 or laryngeal nerve (SLN) or by deflection of mechanoreceptors in the laryngeal mucosa.

136 findings identify a key role for intestinal mechanoreceptors in the regulation of feeding.

137 formation is detected by thermoreceptors and mechanoreceptors in the skin and integrated by the centr

138 ecific vibrotactile stimulation of different mechanoreceptors in the skin.

139 istics of four different types of identified mechanoreceptors in the vibrissal follicle: ring-sinus M

140 hal ganglion and receive input from antennal mechanoreceptors in this lower region of the CNS.

141 ated currents in sensory neurons and silence mechanoreceptors in vivo.

142 romophore in the retina are also required in mechanoreceptors, including visual cycle components that

143 ical properties with those of intrapulmonary mechanoreceptors indicates that the afferent neurones me

144 The central projections of these RA mechanoreceptors innervate layers III through V of the s

145 Mechanoreceptors innervated by the internal branch of th

146 Monitoring the responses of all four mechanoreceptors innervating a patch of skin revealed st

147 ilable to the brain, we recorded spikes from mechanoreceptors innervating diverse parts of the face.

148 involves coordinated orofacial movements, so mechanoreceptors innervating facial regions other than w

149 Forepaw rapidly adapting mechanoreceptors innervating Meissner's corpuscles, reco

150 ng stimuli to identify whether low-threshold mechanoreceptor input to these neurons arises from myeli

151 -126 cm s(-1)) were used to characterize the mechanoreceptor inputs to 'wide dynamic range' neurons i

152 es, but not A-fibres, conveyed low-threshold mechanoreceptor inputs to lamina I projection neurons.

153 nsic structure, likely integrates visual and mechanoreceptor inputs.

154 cellular signaling systems on-line after the mechanoreceptor is activated are reviewed, including tho

155 ng role of the lipid membrane across various mechanoreceptors is now an accepted hypothesis.

156 of the dorsal root ganglion and in cutaneous mechanoreceptors known as Merkel-cell-neurite complexes.

157 The Pacinian corpuscle (PC), a cutaneous mechanoreceptor located deep within the dermis of the sk

158 s: arterial wall deformation, stimulation of mechanoreceptors located in the BR nerve-endings, and mo

159 that it receives substantial input from skin mechanoreceptors located on both sides of the body.

160 fferent types showed no clear alignment with mechanoreceptor location.

161 egion implicated in processing low-threshold mechanoreceptor (LTMR) information.

162 ac2(Cre)) receive direct Abeta low threshold mechanoreceptor (LTMR) input and form monosynaptic conne

163 Low-threshold mechanoreceptors (LTMRs) are believed to project extensi

164 ition and that A- and C-fibers low threshold mechanoreceptors (LTMRs) terminate in lamina IIi raise t

165 hanosensory end organs and the low-threshold mechanoreceptors (LTMRs) that innervate them.

166 To test the contribution of low-threshold mechanoreceptors (LTMRs) to nerve-injury-induced mechani

167 rmed by unique combinations of low-threshold mechanoreceptors (LTMRs), Abeta RA-LTMRs, Adelta-LTMRs,

168 ct populations of neurons, the low-threshold mechanoreceptors (LTMRs), which are classified as Abeta-

169 ialized sensory neurons termed low-threshold mechanoreceptors (LTMRs).

170 taneous sensory neurons called low-threshold mechanoreceptors (LTMRs).

171 d by sensory neurons, known as low-threshold mechanoreceptors (LTMRs).

172 sifying them as nociceptive or low-threshold-mechanoreceptors (LTMs) and as having C-, Adelta- or Aal

173 tively innervated by cutaneous low threshold mechanoreceptors (LTMs).

174 of large-diameter GG neurons expressing the mechanoreceptor marker NF200 and the GDNF coreceptor GFR

175 ted peripheral nerve fibers and reinnervated mechanoreceptors may differentially influence recovery o

176 In mechanoreceptors, mechanical stimulation by external for

177 agonists and antagonists to identify the key mechanoreceptor mediating the shear stress sensitivity o

178 ens of an artificial analogue of the natural mechanoreceptor network-can thus aid the future design o

179 Mechanoreceptor networks that provide sensory feedback a

180 Each mechanoreceptor neuron of the leech varies spike count a

181 r contribute indirectly by maintaining basic mechanoreceptor neuron physiology.

182 in amplitude than responses of low threshold mechanoreceptor neurones.

183 in control by studying responses from single mechanoreceptor neurons in Drosophila.

184 ead and nose touch using multiple classes of mechanoreceptor neurons that are electrically coupled th

185 l for survival and relies on the function of mechanoreceptor neurons that vary in their size, shape,

186 ns (nonpeptidergic and C-fiber low-threshold mechanoreceptor neurons) resistant to direct and trans-s

187 the sensory cilia of Caenorhabditis elegans mechanoreceptor neurons.

188 n the environment may impact the function of mechanoreceptor neurons.

189 and encoding of mechanical forces by primary mechanoreceptor neurons.

190 stigating the cell-surface activation of two mechanoreceptors: Notch and E-cadherin.

191 Moreover, in the duck, the expansion of mechanoreceptors occurs at the expense of thermosensors.

192 phenomenon including in bio-organisms (e.g. Mechanoreceptor of crayfish) and in environmental scienc

193 nsitivity and assessed the function of colon mechanoreceptors of hypersensitive mice.

194 Sensory hair cells are mechanoreceptors of the auditory and vestibular systems

195 Sensory hair cells, the mechanoreceptors of the auditory and vestibular systems,

196 In vertebrates, hair cells are well-known mechanoreceptors of the inner ear and lateral line, typi

197 es share expression in the neuromasts, known mechanoreceptors of the lateral line peripheral nervous

198 y of ion channel proteins coexpressed in the mechanoreceptors of worms, flies, and mice.

199 ditionally, obesity loads may be detected by mechanoreceptors on chondrocyte surfaces triggering intr

200 Mechanoreceptors on the bill of the animal were probably

201 m a variety of sensory modalities, including mechanoreceptors on their antennae, to stabilize the dir

202 sociating the sensory epithelia of the three mechanoreceptor organs, the utricle/saccule, cristae, an

203 cific role of KCNQ4 in rapidly adapting skin mechanoreceptors, our results show that different KCNQ i

204 cratica (Salpida)--to verify the presence of mechanoreceptors, particularly hair cells.

205 ciliary-associated proteins polycystin-1 (a mechanoreceptor), polycystin-2 (a Ca2+ channel), and the

206 no mechanoreceptor potential (nomp) mutations have been iso

207 The reduced mechanoreceptor potential A (rempA) locus of Drosophila

208 For example, no mechanoreceptor potential C (NOMPC), a member of transie

209 nnels, we identified Ripped Pocket (rpk), No Mechanoreceptor Potential C (nompC), and NMDA Receptors

210 We further identify NOMPC (No mechanoreceptor potential C), a member of the transient

211 d vagal axon bundles, single axons, putative mechanoreceptor precursors (intraganglionic laminar endi

212 cles and exhibit a dramatic disruption of RA mechanoreceptor projections to both the spinal cord and

213 In rodents, whisker mechanoreceptors provide a signal that informs the brain

214 Pelvic nerve mechanoreceptors recorded from zymosan-treated or naive

215 l projection deficits, but Gfralpha2 null RA mechanoreceptors recover later.

216 e identify Piezo-1 as the mainly responsible mechanoreceptor, representing a potentially druggable ta

217 Drosophila chordotonal mechanoreceptors require opsins [13, 15], and we find th

218 Sensory hair cells are mechanoreceptors required for hearing and balance functi

219 Proprioceptive mechanoreceptors reside in skeletal muscle and inform th

220 he primary afferent neurons of the haltere's mechanoreceptors respond selectively with high temporal

221 The rapidly adapting (RA) low-threshold mechanoreceptors respond to movement of the skin and vib

222 standardized mechanical stimulus to compare mechanoreceptor response before and after treatment.

223 a control preparation, suppression of type I mechanoreceptor response during 2-min, arterial infusion

224 Simulations of mechanoreceptor responses [8] suggested that the speed a

225 we have only a limited understanding of the mechanoreceptor responses that underlie tactile sensatio

226 vibration intensity and identifies candidate mechanoreceptors responsible for the cortical response.

227 riments have shown an increase in rat type I mechanoreceptor responsiveness during arterial serotonin

228 from outside the type I complex, influences mechanoreceptor responsiveness.

229 The identity of the mechanoreceptor(s) is approached, with consideration of

230 of four slowly adapting type I low-threshold mechanoreceptors (SAIs) that innervated the back skin of

231 lifying signal transduction in low-threshold mechanoreceptors (Scholz et al., 2017).

232 The beta(1) integrin, functioning as a mechanoreceptor, senses a mechanical stimulus generated

233 s of USH2A in corpuscular end-organs reduced mechanoreceptor sensitivity as well as vibration percept

234 diverse etiologies, presumably as part of a mechanoreceptor signaling complex.

235 ever, chondrocyte cilia were not the initial mechanoreceptors, since both WT and ORPK cells showed me

236 antitative activation of genetically encoded mechanoreceptors) stems from the fact that many mechanic

237 responses to both tooth pulp and facial hair mechanoreceptor stimulation are significantly attenuated

238 The mechanoreceptor stimulation model, uses circumferential

239 components produced by contralateral tactile mechanoreceptor stimulation of the tip of the index fing

240 dify reflex bronchospasm initiated by airway mechanoreceptor stimulation.

241 that the mechanosensitivity of low-threshold mechanoreceptors strongly depends on Piezo2.

242 The anatomical receptive fields of these two mechanoreceptor subtypes homotypically tile glabrous ski

243 the mechanosensitivity of most low-threshold mechanoreceptor subtypes involved in innocuous touch sen

244 at Meissner corpuscles are innervated by two mechanoreceptor subtypes that exhibit distinct responses

245 l link between loading and bone cells, where mechanoreceptors, such as integrins, initiate mechanosen

246 Mechanoreceptors surrounding each whisker encode and tra

247 nerve, we further build a power-free spiking mechanoreceptor system with a passive piezoelectric devi

248 , a new type of single-mode and self-powered mechanoreceptor that can mimic both SA and FA via seamle

249 anchored proteoglycan dystroglycan (DG) is a mechanoreceptor that transmits mechanical stretch forces

250 The skin is equipped with specialized mechanoreceptors that allow the perception of the slight

251 ptying and hypersensitivity of gastric vagal mechanoreceptors that can be normalized by an inhibitor

252 air cells of the mammalian inner ear are the mechanoreceptors that convert sound-induced vibrations i

253 atosensory system contains multiple types of mechanoreceptors that detect different mechanical stimul

254 Facial proprioception may instead rely on mechanoreceptors that encode both touch and self-motion.

255 the majority of duck trigeminal neurons are mechanoreceptors that express the Piezo2 ion channel and

256 ptor (DOR), which is expressed by myelinated mechanoreceptors that form Meissner corpuscles, Merkel c

257 ons are large- or medium-diameter myelinated mechanoreceptors that form the Merkel cell-neurite compl

258 al endings of a broad range of low-threshold mechanoreceptors that innervate both hairy and glabrous

259 d the TRPV family of cation channels as osmo-mechanoreceptors that may mediate the neuronal responses

260 r cells are exquisitely sensitive vertebrate mechanoreceptors that mediate the senses of hearing and

261 Meissner corpuscle filled the capsule of the mechanoreceptors that remained deeper in the dermis.

262 endowed with low-threshold, slowly adapting mechanoreceptors that respond to self-generated movement

263 However, the mechanoreceptors that respond to tissue stretch are poor

264 Merkel cells form slowly adapting cutaneous mechanoreceptors that transduce steady indentation in ha

265 arying stretches of two different crustacean mechanoreceptors, the gastropyloric receptor 2 in the cr

266 In fly campaniform mechanoreceptors, the mechanotransduction channels are g

267 ans and other mammals implicate one of these mechanoreceptors, the Merkel cell/neurite complex, in tw

268 ing the touch responses of the anterior-body mechanoreceptors; this modulation involves a D1-like dop

269 estimate of the sensitivity of an individual mechanoreceptor to an applied stimulus (parameterised as

270 Many arthropods use filiform hairs as mechanoreceptors to detect air motion.

271 ays relaying inputs from low-threshold Abeta mechanoreceptors to lamina I output neurons.

272 mals must integrate the activity of multiple mechanoreceptors to navigate complex environments.

273 o generate shearing forces essential for the mechanoreceptors to sense gravity and linear acceleratio

274 peripheral mechanical nociceptors and Abeta mechanoreceptors, together with spinal SOM(+) excitatory

275 Cutaneous mechanoreceptors transduce different tactile stimuli int

276 biological receptors like photoreceptors and mechanoreceptors transduce physical energy into a neural

277 Mutations disrupting the DVA mechanoreceptor (TRP-4) decreased aldicarb-induced NLP-1

278 ust combine signals from multiple peripheral mechanoreceptor types, as well as mechanoreceptors at di

279 For the two mechanoreceptor types, the transient responses of T (tou

280 ical and optogenetic stimulation of specific mechanoreceptor types.

281 carotenoid uptake and cleavage also left the mechanoreceptors unaffected, and manipulating the chromo

282 l and cisplatin administration on the type I mechanoreceptor using a skin-nerve preparation in rat an

283 te the origin of firing patterns in branched mechanoreceptors, we combined neuroanatomy, electrophysi

284 ing the leech body wall while recording from mechanoreceptors, we show that pairs of leech sensory ne

285 Recently, Merkel cell mechanoreceptors were identified as a fourth lineage der

286 urons to air puff stimulation of facial hair mechanoreceptors were significantly increased by 96% dur

287 tro single-fiber recordings of gastric vagal mechanoreceptors were taken at all time points.

288 technique, including tactile stimulation of mechanoreceptors, were followed for 2 years, and results

289 rst reconstructs the stresses experienced by mechanoreceptors when the skin is deformed and then simu

290 oural data to estimate the minimum number of mechanoreceptors which must be activated to elicit a beh

291 equire facilitation by additional nose touch mechanoreceptors, which couple electrically to the nocic

292 d that the "early Ret(+)" DRG neurons are RA mechanoreceptors, which form Meissner corpuscles, Pacini

293 pressed in muscle spindles-stretch-sensitive mechanoreceptors, while muscle denervation induces exten

294 that early-born Ret+ sensory neurons are RA mechanoreceptors, whose peripheral nerve terminals are a

295 We present a power-efficient skin-inspired mechanoreceptor with a flexible organic transistor circu

296 ion (control), during stimulation of forearm mechanoreceptors with venous congestion, and during isch

297 receiving inputs from nociceptors and Abeta mechanoreceptors, with Abeta inputs gated through feed-f

298 , the AMI allows proprioceptive signals from mechanoreceptors within both muscles to be communicated

299 Sensory hair cells (HCs) are the mechanoreceptors within the inner ear responsible for ou

300 inly in TrkB-expressing (TrkB(+)) and Ret(+) mechanoreceptors within the TG during embryogenesis.